| Symbol | ABBV |
|---|---|
| Name | ABBVIE INC. |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Biotechnology: Pharmaceutical Preparations |
| Address | 1 NORTH WAUKEGAN ROAD, NORTH CHICAGO, Illinois, 60064-6400, United States |
| Telephone | +1 847 932-7900 |
| Fax | — |
| — | |
| Website | https://www.abbvie.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001551152 |
| Description | AbbVie Inc. is a pharmaceutical company headquartered in North Chicago, Illinois. It is ranked 6th on the list of largest biomedical companies by revenue. The companys primary product is Humira, administered via injection. Additional info from NASDAQ: |
Allergan Aesthetics receives approval for Boey® (trenibotulinumtoxinE), for use in Europe: the first and only rapid-onset, short-duration neurotoxin for the temporary improvement of frown lines in adult patients
Read moreAbbVie Announces TEPKINLY® (epcoritamab) in Combination with Lenalidomide and Rituximab is Approved by the European Commission for the Treatment of Relapsed or Refractory Follicular Lymphoma
Read moreQuaggin Susan E 🟢 acquired 62 shares (1 derivative) of AbbVie Inc. (ABBV) at $251.64 Transaction Date: Jun 30, 2026 | Filing ID: 000008
Read moreAbbVie Announces Positive Phase 3 Results for Epcoritamab Plus Lenalidomide in Patients with Relapsed or Refractory Diffuse Large B-Cell Lymphoma
Read moreAbbVie Announces Positive Phase 3 Results for Epcoritamab Plus Lenalidomide in Patients with Relapsed or Refractory Diffuse Large B-Cell Lymphoma
Read moreAbbVie Receives Positive CHMP Opinion for Upadacitinib (RINVOQ®) for the Treatment of Adults and Adolescents with Severe Alopecia Areata
Read moreAbbVie Receives Positive CHMP Opinion for Upadacitinib (RINVOQ®) for the Treatment of Adults and Adolescents with Non-segmental Vitiligo
Read moreSKYRIZI® (risankizumab-rzaa) Now FDA Approved for Pediatric Use in Psoriatic Disease
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT03123211 | Expanded Access to Veliparib | — | Solid Tumors With Documented BRCA, BARD, or PALB or Other Acceptable DNA Mutations or Anomalies That Are Scientifically Sound | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123029 | Expanded Access to Venetoclax | — | Chronic Lymphocytic Leukemia (CLL) | Available | — | — | ClinicalTrials.gov |
| NCT04159597 | Expanded Access to Upadacitinib | — | Crohn Disease | Available | — | — | ClinicalTrials.gov |
| NCT03592576 | Expanded Access to Navitoclax | — | Myelofibrosis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03914261 | Expanded Access to Risankizumab | — | Crohn's Disease | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03503890 | Expanded Access to Rovalpituzumab Tesirine | — | Small Cell Lung Cancer | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03744546 | Expanded Access to ABBV-8E12 | — | Primary Tauopathy Corticobasal Degeneration Syndrome (CBD) | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123965 | Expanded Access to Glecaprevir/ Pibrentasvir | — | Hepatitis C Virus Infection | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT03123952 | Expanded Access to ABT-414 | — | Glioblastoma or Solid Tumors, Epidermal Growth Factor Receptor (EGFR) Diagnosis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123211 | Expanded Access to Veliparib | — | Solid Tumors With Documented BRCA, BARD, or PALB or Other Acceptable DNA Mutations or Anomalies That Are Scientifically Sound | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03592576 | Expanded Access to Navitoclax | — | Myelofibrosis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123029 | Expanded Access to Venetoclax | — | Chronic Lymphocytic Leukemia (CLL) | Available | — | — | ClinicalTrials.gov |
| NCT02985658 | Expanded Access With ABT-888 (Veliparib) to Treat Metastatic Breast Cancer | — | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03503890 | Expanded Access to Rovalpituzumab Tesirine | — | Small Cell Lung Cancer | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT02856438 | Early Patient Access Treatment Use Protocol CA204-220 | — | Multiple Myeloma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT01789151 | 99m-Technetium- Glucosamine in Arthritis | — | Rheumatoid Arthritis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT07310277 | Expanded Access to ABBV-706 | — | Small Cell Lung Cancer | Available | — | — | ClinicalTrials.gov |
| NCT07158827 | Expanded Access to Tavapadon | — | Parkinson Disease | Available | — | — | ClinicalTrials.gov |
| NCT05338606 | Expanded Access to Bimatoprost (Durysta) | — | Open-angle Glaucoma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT01789151 | 99m-Technetium- Glucosamine in Arthritis | — | Rheumatoid Arthritis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT04830202 | Expanded Access to Telisotuzumab Vedotin | — | Non-Small Cell Lung Cancer (NSCLC) | Temporarily_Not_Available | — | — | ClinicalTrials.gov |
| NCT03123965 | Expanded Access to Glecaprevir/ Pibrentasvir | — | Hepatitis C Virus Infection | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT03123952 | Expanded Access to ABT-414 | — | Glioblastoma or Solid Tumors, Epidermal Growth Factor Receptor (EGFR) Diagnosis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123211 | Expanded Access to Veliparib | — | Solid Tumors With Documented BRCA, BARD, or PALB or Other Acceptable DNA Mutations or Anomalies That Are Scientifically Sound | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123029 | Expanded Access to Venetoclax | — | Chronic Lymphocytic Leukemia (CLL) | Available | — | — | ClinicalTrials.gov |
| NCT04278235 | Expanded Access to Elezanumab | — | Acute Spinal Cord Injury (SCI) | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05338606 | Expanded Access to Bimatoprost (Durysta) | — | Open-angle Glaucoma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT04830202 | Expanded Access to Telisotuzumab Vedotin | — | Non-Small Cell Lung Cancer (NSCLC) | Temporarily_Not_Available | — | — | ClinicalTrials.gov |
| NCT05692050 | Expanded Access to Epcoritamab | — | Lymphoma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05733650 | Expanded Access Program for Epcoritamab | — | Large B-cell Lymphoma | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT04278235 | Expanded Access to Elezanumab | — | Acute Spinal Cord Injury (SCI) | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT04830202 | Expanded Access to Telisotuzumab Vedotin | — | Non-Small Cell Lung Cancer (NSCLC) | Temporarily_Not_Available | — | — | ClinicalTrials.gov |
| NCT05692050 | Expanded Access to Epcoritamab | — | Lymphoma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05733650 | Expanded Access Program for Epcoritamab | — | Large B-cell Lymphoma | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT04278235 | Expanded Access to Elezanumab | — | Acute Spinal Cord Injury (SCI) | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05982873 | Expanded Access to Telisotuzumab Adizutecan | — | Solid Tumors | Available | — | — | ClinicalTrials.gov |
| NCT06439966 | Expanded Access to ABBV-787 | — | Acute Myeloid Leukemia | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT06594016 | Expanded Access to Fosigotifator | — | Vanishing White Matter | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT07310277 | Expanded Access to ABBV-706 | — | Small Cell Lung Cancer | Available | — | — | ClinicalTrials.gov |
| NCT01789151 | 99m-Technetium- Glucosamine in Arthritis | — | Rheumatoid Arthritis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT07158827 | Expanded Access to Tavapadon | — | Parkinson Disease | Available | — | — | ClinicalTrials.gov |
| NCT07310277 | Expanded Access to ABBV-706 | — | Small Cell Lung Cancer | Available | — | — | ClinicalTrials.gov |
| NCT03914261 | Expanded Access to Risankizumab | — | Crohn's Disease | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT06594016 | Expanded Access to Fosigotifator | — | Vanishing White Matter | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT07158827 | Expanded Access to Tavapadon | — | Parkinson Disease | Available | — | — | ClinicalTrials.gov |
| NCT06439966 | Expanded Access to ABBV-787 | — | Acute Myeloid Leukemia | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05982873 | Expanded Access to Telisotuzumab Adizutecan | — | Solid Tumors | Available | — | — | ClinicalTrials.gov |
| NCT05733650 | Expanded Access Program for Epcoritamab | — | Large B-cell Lymphoma | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT05692050 | Expanded Access to Epcoritamab | — | Lymphoma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05338606 | Expanded Access to Bimatoprost (Durysta) | — | Open-angle Glaucoma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT04159597 | Expanded Access to Upadacitinib | — | Crohn Disease | Available | — | — | ClinicalTrials.gov |
| NCT03744546 | Expanded Access to ABBV-8E12 | — | Primary Tauopathy Corticobasal Degeneration Syndrome (CBD) | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT04278235 | Expanded Access to Elezanumab | — | Acute Spinal Cord Injury (SCI) | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT01789151 | 99m-Technetium- Glucosamine in Arthritis | — | Rheumatoid Arthritis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03914261 | Expanded Access to Risankizumab | — | Crohn's Disease | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT04830202 | Expanded Access to Telisotuzumab Vedotin | — | Non-Small Cell Lung Cancer (NSCLC) | Temporarily_Not_Available | — | — | ClinicalTrials.gov |
| NCT02856438 | Early Patient Access Treatment Use Protocol CA204-220 | — | Multiple Myeloma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT02985658 | Expanded Access With ABT-888 (Veliparib) to Treat Metastatic Breast Cancer | — | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123029 | Expanded Access to Venetoclax | — | Chronic Lymphocytic Leukemia (CLL) | Available | — | — | ClinicalTrials.gov |
| NCT03123211 | Expanded Access to Veliparib | — | Solid Tumors With Documented BRCA, BARD, or PALB or Other Acceptable DNA Mutations or Anomalies That Are Scientifically Sound | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123952 | Expanded Access to ABT-414 | — | Glioblastoma or Solid Tumors, Epidermal Growth Factor Receptor (EGFR) Diagnosis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03123965 | Expanded Access to Glecaprevir/ Pibrentasvir | — | Hepatitis C Virus Infection | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT03503890 | Expanded Access to Rovalpituzumab Tesirine | — | Small Cell Lung Cancer | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03592576 | Expanded Access to Navitoclax | — | Myelofibrosis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT02856438 | Early Patient Access Treatment Use Protocol CA204-220 | — | Multiple Myeloma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT06594016 | Expanded Access to Fosigotifator | — | Vanishing White Matter | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03744546 | Expanded Access to ABBV-8E12 | — | Primary Tauopathy Corticobasal Degeneration Syndrome (CBD) | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT07310277 | Expanded Access to ABBV-706 | — | Small Cell Lung Cancer | Available | — | — | ClinicalTrials.gov |
| NCT06439966 | Expanded Access to ABBV-787 | — | Acute Myeloid Leukemia | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT07158827 | Expanded Access to Tavapadon | — | Parkinson Disease | Available | — | — | ClinicalTrials.gov |
| NCT02985658 | Expanded Access With ABT-888 (Veliparib) to Treat Metastatic Breast Cancer | — | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT06594016 | Expanded Access to Fosigotifator | — | Vanishing White Matter | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT06439966 | Expanded Access to ABBV-787 | — | Acute Myeloid Leukemia | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT04159597 | Expanded Access to Upadacitinib | — | Crohn Disease | Available | — | — | ClinicalTrials.gov |
| NCT02856438 | Early Patient Access Treatment Use Protocol CA204-220 | — | Multiple Myeloma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03914261 | Expanded Access to Risankizumab | — | Crohn's Disease | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05338606 | Expanded Access to Bimatoprost (Durysta) | — | Open-angle Glaucoma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05982873 | Expanded Access to Telisotuzumab Adizutecan | — | Solid Tumors | Available | — | — | ClinicalTrials.gov |
| NCT03744546 | Expanded Access to ABBV-8E12 | — | Primary Tauopathy Corticobasal Degeneration Syndrome (CBD) | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT02985658 | Expanded Access With ABT-888 (Veliparib) to Treat Metastatic Breast Cancer | — | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT04159597 | Expanded Access to Upadacitinib | — | Crohn Disease | Available | — | — | ClinicalTrials.gov |
| NCT03592576 | Expanded Access to Navitoclax | — | Myelofibrosis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT03503890 | Expanded Access to Rovalpituzumab Tesirine | — | Small Cell Lung Cancer | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05692050 | Expanded Access to Epcoritamab | — | Lymphoma | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT05733650 | Expanded Access Program for Epcoritamab | — | Large B-cell Lymphoma | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT05982873 | Expanded Access to Telisotuzumab Adizutecan | — | Solid Tumors | Available | — | — | ClinicalTrials.gov |
| NCT03123965 | Expanded Access to Glecaprevir/ Pibrentasvir | — | Hepatitis C Virus Infection | Approved_For_Marketing | — | — | ClinicalTrials.gov |
| NCT03123952 | Expanded Access to ABT-414 | — | Glioblastoma or Solid Tumors, Epidermal Growth Factor Receptor (EGFR) Diagnosis | No_Longer_Available | — | — | ClinicalTrials.gov |
| NCT07600151 | Etenta-Isa-VRd in Newly Diagnosed High-Risk Multiple Myeloma | Phase1 | Myeloma Multiple | Not_Yet_Recruiting | 2026-12-01 | 2036-12-31 | ClinicalTrials.gov |
| NCT07600151 | Etenta-Isa-VRd in Newly Diagnosed High-Risk Multiple Myeloma | Phase1 | Myeloma Multiple | Not_Yet_Recruiting | 2026-12-01 | 2036-12-31 | ClinicalTrials.gov |
| NCT07600151 | Etenta-Isa-VRd in Newly Diagnosed High-Risk Multiple Myeloma | Phase1 | Myeloma Multiple | Not_Yet_Recruiting | 2026-12-01 | 2036-12-31 | ClinicalTrials.gov |
| NCT07600151 | Etenta-Isa-VRd in Newly Diagnosed High-Risk Multiple Myeloma | Phase1 | Myeloma Multiple | Not_Yet_Recruiting | 2026-12-01 | 2036-12-31 | ClinicalTrials.gov |
| NCT07175415 | HEM-iSMART E: Capivasertib + Venetoclax + Dexamethasone in Pediatric Patients W… | Phase1 | Acute Lymphoblastic Leukemia | Not_Yet_Recruiting | 2026-10-01 | 2032-10-01 | ClinicalTrials.gov |
| NCT07175415 | HEM-iSMART E: Capivasertib + Venetoclax + Dexamethasone in Pediatric Patients W… | Phase1 | Acute Lymphoblastic Leukemia | Not_Yet_Recruiting | 2026-10-01 | 2032-10-01 | ClinicalTrials.gov |
| NCT07175415 | HEM-iSMART E: Capivasertib + Venetoclax + Dexamethasone in Pediatric Patients W… | Phase1 | Acute Lymphoblastic Leukemia | Not_Yet_Recruiting | 2026-10-01 | 2032-10-01 | ClinicalTrials.gov |
| NCT07175415 | HEM-iSMART E: Capivasertib + Venetoclax + Dexamethasone in Pediatric Patients W… | Phase1 | Acute Lymphoblastic Leukemia | Not_Yet_Recruiting | 2026-10-01 | 2032-10-01 | ClinicalTrials.gov |
| NCT07690215 | Study to Assess Effectiveness of Oral Atogepant in Adult Participants For Preve… | — | Migraine | Not_Yet_Recruiting | 2026-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT07690215 | Study to Assess Effectiveness of Oral Atogepant in Adult Participants For Preve… | — | Migraine | Not_Yet_Recruiting | 2026-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT07690215 | Study to Assess Effectiveness of Oral Atogepant in Adult Participants For Preve… | — | Migraine | Not_Yet_Recruiting | 2026-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT07690215 | Study to Assess Effectiveness of Oral Atogepant in Adult Participants For Preve… | — | Migraine | Not_Yet_Recruiting | 2026-09-01 | 2028-03-01 | ClinicalTrials.gov |
| NCT07670156 | Upadacitinib in Treatment of JAK/STAT Pathway Disorders With Activating Mutatio… | Phase1 | JAK1 GOF | Not_Yet_Recruiting | 2026-08-01 | 2028-08-01 | ClinicalTrials.gov |
| NCT07670156 | Upadacitinib in Treatment of JAK/STAT Pathway Disorders With Activating Mutatio… | Phase1 | JAK1 GOF | Not_Yet_Recruiting | 2026-08-01 | 2028-08-01 | ClinicalTrials.gov |
| NCT07670156 | Upadacitinib in Treatment of JAK/STAT Pathway Disorders With Activating Mutatio… | Phase1 | JAK1 GOF | Not_Yet_Recruiting | 2026-08-01 | 2028-08-01 | ClinicalTrials.gov |
| NCT07670156 | Upadacitinib in Treatment of JAK/STAT Pathway Disorders With Activating Mutatio… | Phase1 | JAK1 GOF | Not_Yet_Recruiting | 2026-08-01 | 2028-08-01 | ClinicalTrials.gov |
| NCT07581002 | A Study to Assess Adverse Events and Change in Disease Activity When Intravenou… | Phase2 | Acute Myeloid Leukemia | Not_Yet_Recruiting | 2026-07-22 | 2032-06-01 | ClinicalTrials.gov |
| NCT07581002 | A Study to Assess Adverse Events and Change in Disease Activity When Intravenou… | Phase2 | Acute Myeloid Leukemia | Not_Yet_Recruiting | 2026-07-22 | 2032-06-01 | ClinicalTrials.gov |
| NCT07581002 | A Study to Assess Adverse Events and Change in Disease Activity When Intravenou… | Phase2 | Acute Myeloid Leukemia | Not_Yet_Recruiting | 2026-07-22 | 2032-06-01 | ClinicalTrials.gov |
| NCT07581002 | A Study to Assess Adverse Events and Change in Disease Activity When Intravenou… | Phase2 | Acute Myeloid Leukemia | Not_Yet_Recruiting | 2026-07-22 | 2032-06-01 | ClinicalTrials.gov |
| NCT07502339 | Upadacitinib in Patients Hospitalized With Acute Severe Ulcerative Colitis | Phase4 | UC - Ulcerative Colitis | Not_Yet_Recruiting | 2026-07-01 | 2028-08-01 | ClinicalTrials.gov |
| NCT07588568 | A Trial of Upadacitinib for Non-responsive Eosinophilic Esophagitis | Phase2 | EoE | Not_Yet_Recruiting | 2026-07-01 | 2030-06-01 | ClinicalTrials.gov |
| NCT07588568 | A Trial of Upadacitinib for Non-responsive Eosinophilic Esophagitis | Phase2 | EoE | Not_Yet_Recruiting | 2026-07-01 | 2030-06-01 | ClinicalTrials.gov |
| NCT07502339 | Upadacitinib in Patients Hospitalized With Acute Severe Ulcerative Colitis | Phase4 | UC - Ulcerative Colitis | Not_Yet_Recruiting | 2026-07-01 | 2028-08-01 | ClinicalTrials.gov |
| NCT07502339 | Upadacitinib in Patients Hospitalized With Acute Severe Ulcerative Colitis | Phase4 | UC - Ulcerative Colitis | Not_Yet_Recruiting | 2026-07-01 | 2028-08-01 | ClinicalTrials.gov |
| NCT07502339 | Upadacitinib in Patients Hospitalized With Acute Severe Ulcerative Colitis | Phase4 | UC - Ulcerative Colitis | Not_Yet_Recruiting | 2026-07-01 | 2028-08-01 | ClinicalTrials.gov |
| NCT07588568 | A Trial of Upadacitinib for Non-responsive Eosinophilic Esophagitis | Phase2 | EoE | Not_Yet_Recruiting | 2026-07-01 | 2030-06-01 | ClinicalTrials.gov |
| NCT07588568 | A Trial of Upadacitinib for Non-responsive Eosinophilic Esophagitis | Phase2 | EoE | Not_Yet_Recruiting | 2026-07-01 | 2030-06-01 | ClinicalTrials.gov |
| NCT07687602 | A Study to Evaluate Adverse Events and Change in Disease Activity of Mirvetuxim… | — | Folate Receptor-Alpha Positive Platinum-Resistant High-Grade Serous Epithelial Ovarian Cancer | Not_Yet_Recruiting | 2026-06-30 | 2031-08-01 | ClinicalTrials.gov |
| NCT07687602 | A Study to Evaluate Adverse Events and Change in Disease Activity of Mirvetuxim… | — | Folate Receptor-Alpha Positive Platinum-Resistant High-Grade Serous Epithelial Ovarian Cancer | Not_Yet_Recruiting | 2026-06-30 | 2031-08-01 | ClinicalTrials.gov |
| NCT07680686 | Study to Assess How Different Oral Formulations of Ubrogepant Move Through the … | Phase1 | Healthy Volunteer | Not_Yet_Recruiting | 2026-06-30 | 2026-10-01 | ClinicalTrials.gov |
| NCT07680686 | Study to Assess How Different Oral Formulations of Ubrogepant Move Through the … | Phase1 | Healthy Volunteer | Not_Yet_Recruiting | 2026-06-30 | 2026-10-01 | ClinicalTrials.gov |
| NCT07687602 | A Study to Evaluate Adverse Events and Change in Disease Activity of Mirvetuxim… | — | Folate Receptor-Alpha Positive Platinum-Resistant High-Grade Serous Epithelial Ovarian Cancer | Not_Yet_Recruiting | 2026-06-30 | 2031-08-01 | ClinicalTrials.gov |
| NCT07680686 | Study to Assess How Different Oral Formulations of Ubrogepant Move Through the … | Phase1 | Healthy Volunteer | Not_Yet_Recruiting | 2026-06-30 | 2026-10-01 | ClinicalTrials.gov |
| NCT07687602 | A Study to Evaluate Adverse Events and Change in Disease Activity of Mirvetuxim… | — | Folate Receptor-Alpha Positive Platinum-Resistant High-Grade Serous Epithelial Ovarian Cancer | Not_Yet_Recruiting | 2026-06-30 | 2031-08-01 | ClinicalTrials.gov |
| NCT07680686 | Study to Assess How Different Oral Formulations of Ubrogepant Move Through the … | Phase1 | Healthy Volunteer | Not_Yet_Recruiting | 2026-06-30 | 2026-10-01 | ClinicalTrials.gov |
| NCT07649954 | A Study to Evaluate How Multiple Doses of Itraconazole Interacts With Nacresert… | Phase1 | Healthy Volunteer | Not_Yet_Recruiting | 2026-06-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT07649954 | A Study to Evaluate How Multiple Doses of Itraconazole Interacts With Nacresert… | Phase1 | Healthy Volunteer | Not_Yet_Recruiting | 2026-06-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT07649954 | A Study to Evaluate How Multiple Doses of Itraconazole Interacts With Nacresert… | Phase1 | Healthy Volunteer | Not_Yet_Recruiting | 2026-06-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT07649954 | A Study to Evaluate How Multiple Doses of Itraconazole Interacts With Nacresert… | Phase1 | Healthy Volunteer | Not_Yet_Recruiting | 2026-06-28 | 2026-09-01 | ClinicalTrials.gov |
| NCT07040319 | Study of the Pharmacokinetics and Safety of Glecaprevir/Pibrentasvir Initiated … | Phase1 | Hepatitis C | Recruiting | 2026-06-25 | 2027-10-30 | ClinicalTrials.gov |
| NCT07040319 | Study of the Pharmacokinetics and Safety of Glecaprevir/Pibrentasvir Initiated … | Phase1 | Hepatitis C | Recruiting | 2026-06-25 | 2027-10-30 | ClinicalTrials.gov |
| NCT07040319 | Study of the Pharmacokinetics and Safety of Glecaprevir/Pibrentasvir Initiated … | Phase1 | Hepatitis C | Recruiting | 2026-06-25 | 2027-10-30 | ClinicalTrials.gov |
| NCT07040319 | Study of the Pharmacokinetics and Safety of Glecaprevir/Pibrentasvir Initiated … | Phase1 | Hepatitis C | Recruiting | 2026-06-25 | 2027-10-30 | ClinicalTrials.gov |
| NCT07673120 | A Study to Assess Safety, Tolerability, and How Single and Multiple Injections … | Phase1 | Healthy Volunteers | Recruiting | 2026-06-22 | 2028-02-01 | ClinicalTrials.gov |
| NCT07673120 | A Study to Assess Safety, Tolerability, and How Single and Multiple Injections … | Phase1 | Healthy Volunteers | Recruiting | 2026-06-22 | 2028-02-01 | ClinicalTrials.gov |
| NCT07673120 | A Study to Assess Safety, Tolerability, and How Single and Multiple Injections … | Phase1 | Healthy Volunteers | Recruiting | 2026-06-22 | 2028-02-01 | ClinicalTrials.gov |
| NCT07673120 | A Study to Assess Safety, Tolerability, and How Single and Multiple Injections … | Phase1 | Healthy Volunteers | Recruiting | 2026-06-22 | 2028-02-01 | ClinicalTrials.gov |
| NCT07673107 | Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity … | Phase2 | Upper Limb Essential Tremor | Recruiting | 2026-06-18 | 2028-11-01 | ClinicalTrials.gov |
| NCT07673107 | Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity … | Phase2 | Upper Limb Essential Tremor | Recruiting | 2026-06-18 | 2028-11-01 | ClinicalTrials.gov |
| NCT07673107 | Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity … | Phase2 | Upper Limb Essential Tremor | Recruiting | 2026-06-18 | 2028-11-01 | ClinicalTrials.gov |
| NCT07673107 | Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity … | Phase2 | Upper Limb Essential Tremor | Recruiting | 2026-06-18 | 2028-11-01 | ClinicalTrials.gov |
| NCT07639632 | Reduce Inefficiencies in Management of Spasticity | Na | Stroke | Not_Yet_Recruiting | 2026-06-15 | 2029-11-30 | ClinicalTrials.gov |
| NCT07639632 | Reduce Inefficiencies in Management of Spasticity | Na | Stroke | Not_Yet_Recruiting | 2026-06-15 | 2029-11-30 | ClinicalTrials.gov |
| NCT07639632 | Reduce Inefficiencies in Management of Spasticity | Na | Stroke | Not_Yet_Recruiting | 2026-06-15 | 2029-11-30 | ClinicalTrials.gov |
| NCT07639632 | Reduce Inefficiencies in Management of Spasticity | Na | Stroke | Not_Yet_Recruiting | 2026-06-15 | 2029-11-30 | ClinicalTrials.gov |
| NCT07466550 | A Study to Assess How Intravenous and Subcutaneous Administrations of Risankizu… | Phase1 | Healthy Volunteer | Recruiting | 2026-06-04 | 2027-01-01 | ClinicalTrials.gov |
| NCT07466550 | A Study to Assess How Intravenous and Subcutaneous Administrations of Risankizu… | Phase1 | Healthy Volunteer | Recruiting | 2026-06-04 | 2027-01-01 | ClinicalTrials.gov |
| NCT07466550 | A Study to Assess How Intravenous and Subcutaneous Administrations of Risankizu… | Phase1 | Healthy Volunteer | Recruiting | 2026-06-04 | 2027-01-01 | ClinicalTrials.gov |
| NCT07466550 | A Study to Assess How Intravenous and Subcutaneous Administrations of Risankizu… | Phase1 | Healthy Volunteer | Recruiting | 2026-06-04 | 2027-01-01 | ClinicalTrials.gov |
| NCT07592273 | Surabgene Lomparvovec Administered in the Suprachoroidal Space in Adult Partici… | Phase2 | Diabetic Retinopathy | Recruiting | 2026-06-01 | 2036-01-01 | ClinicalTrials.gov |
| NCT07592273 | Surabgene Lomparvovec Administered in the Suprachoroidal Space in Adult Partici… | Phase2 | Diabetic Retinopathy | Recruiting | 2026-06-01 | 2036-01-01 | ClinicalTrials.gov |
| NCT07592273 | Surabgene Lomparvovec Administered in the Suprachoroidal Space in Adult Partici… | Phase2 | Diabetic Retinopathy | Recruiting | 2026-06-01 | 2036-01-01 | ClinicalTrials.gov |
| NCT07592273 | Surabgene Lomparvovec Administered in the Suprachoroidal Space in Adult Partici… | Phase2 | Diabetic Retinopathy | Recruiting | 2026-06-01 | 2036-01-01 | ClinicalTrials.gov |
| NCT07604545 | A Study to Assess the Use of Artificial Intellignce to Predict Eye Treatment Ch… | — | Diabetic Macular Edema | Not_Yet_Recruiting | 2026-05-30 | 2027-03-01 | ClinicalTrials.gov |
| NCT07604545 | A Study to Assess the Use of Artificial Intellignce to Predict Eye Treatment Ch… | — | Diabetic Macular Edema | Not_Yet_Recruiting | 2026-05-30 | 2027-03-01 | ClinicalTrials.gov |
| NCT07604545 | A Study to Assess the Use of Artificial Intellignce to Predict Eye Treatment Ch… | — | Diabetic Macular Edema | Not_Yet_Recruiting | 2026-05-30 | 2027-03-01 | ClinicalTrials.gov |
| NCT07604545 | A Study to Assess the Use of Artificial Intellignce to Predict Eye Treatment Ch… | — | Diabetic Macular Edema | Not_Yet_Recruiting | 2026-05-30 | 2027-03-01 | ClinicalTrials.gov |
| NCT07607964 | A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effec… | Phase1 | Systemic Lupus Erythematosus | Recruiting | 2026-05-28 | 2029-01-01 | ClinicalTrials.gov |
| NCT07607964 | A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effec… | Phase1 | Systemic Lupus Erythematosus | Recruiting | 2026-05-28 | 2029-01-01 | ClinicalTrials.gov |
| NCT07607964 | A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effec… | Phase1 | Systemic Lupus Erythematosus | Recruiting | 2026-05-28 | 2029-01-01 | ClinicalTrials.gov |
| NCT07607964 | A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effec… | Phase1 | Systemic Lupus Erythematosus | Recruiting | 2026-05-28 | 2029-01-01 | ClinicalTrials.gov |
| NCT07604558 | A Study to Assess the Adverse Events and How Bretisilocin Intramuscular Injecti… | Phase1 | Healthy Volunteer | Recruiting | 2026-05-26 | 2026-09-01 | ClinicalTrials.gov |
| NCT07604558 | A Study to Assess the Adverse Events and How Bretisilocin Intramuscular Injecti… | Phase1 | Healthy Volunteer | Recruiting | 2026-05-26 | 2026-09-01 | ClinicalTrials.gov |
| NCT07604558 | A Study to Assess the Adverse Events and How Bretisilocin Intramuscular Injecti… | Phase1 | Healthy Volunteer | Recruiting | 2026-05-26 | 2026-09-01 | ClinicalTrials.gov |
| NCT07604558 | A Study to Assess the Adverse Events and How Bretisilocin Intramuscular Injecti… | Phase1 | Healthy Volunteer | Recruiting | 2026-05-26 | 2026-09-01 | ClinicalTrials.gov |
| NCT07525206 | A Study to Access Intravenous (IV) Telisotuzumab Adizutecan in Combination With… | Phase3 | Colorectal Cancer | Recruiting | 2026-05-22 | 2030-03-01 | ClinicalTrials.gov |
| NCT07525206 | A Study to Access Intravenous (IV) Telisotuzumab Adizutecan in Combination With… | Phase3 | Colorectal Cancer | Recruiting | 2026-05-22 | 2030-03-01 | ClinicalTrials.gov |
| NCT07525206 | A Study to Access Intravenous (IV) Telisotuzumab Adizutecan in Combination With… | Phase3 | Colorectal Cancer | Recruiting | 2026-05-22 | 2030-03-01 | ClinicalTrials.gov |
| NCT07525206 | A Study to Access Intravenous (IV) Telisotuzumab Adizutecan in Combination With… | Phase3 | Colorectal Cancer | Recruiting | 2026-05-22 | 2030-03-01 | ClinicalTrials.gov |
| NCT07306832 | A Study to Assess Adverse Events and How Intravenous (IV) Pivekimab Sunirine Mo… | Phase1 | Acute Myeloid Leukemia | Recruiting | 2026-05-20 | 2030-03-01 | ClinicalTrials.gov |
| NCT07306832 | A Study to Assess Adverse Events and How Intravenous (IV) Pivekimab Sunirine Mo… | Phase1 | Acute Myeloid Leukemia | Recruiting | 2026-05-20 | 2030-03-01 | ClinicalTrials.gov |
| NCT07306832 | A Study to Assess Adverse Events and How Intravenous (IV) Pivekimab Sunirine Mo… | Phase1 | Acute Myeloid Leukemia | Recruiting | 2026-05-20 | 2030-03-01 | ClinicalTrials.gov |
| NCT07306832 | A Study to Assess Adverse Events and How Intravenous (IV) Pivekimab Sunirine Mo… | Phase1 | Acute Myeloid Leukemia | Recruiting | 2026-05-20 | 2030-03-01 | ClinicalTrials.gov |
| NCT07599670 | A Study to Assess the Safety and Effects of ABBV-1758 Following Subcutaneous or… | Phase1 | Alzheimer's Disease | Recruiting | 2026-05-15 | 2030-10-01 | ClinicalTrials.gov |
| NCT07599670 | A Study to Assess the Safety and Effects of ABBV-1758 Following Subcutaneous or… | Phase1 | Alzheimer's Disease | Recruiting | 2026-05-15 | 2030-10-01 | ClinicalTrials.gov |
| NCT07599670 | A Study to Assess the Safety and Effects of ABBV-1758 Following Subcutaneous or… | Phase1 | Alzheimer's Disease | Recruiting | 2026-05-15 | 2030-10-01 | ClinicalTrials.gov |
| NCT07599670 | A Study to Assess the Safety and Effects of ABBV-1758 Following Subcutaneous or… | Phase1 | Alzheimer's Disease | Recruiting | 2026-05-15 | 2030-10-01 | ClinicalTrials.gov |
| NCT07587008 | Study to Assess Adverse Events and How Oral Emraclidine Moves Through the Body … | Phase1 | Healthy Volunteers | Recruiting | 2026-05-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07587008 | Study to Assess Adverse Events and How Oral Emraclidine Moves Through the Body … | Phase1 | Healthy Volunteers | Recruiting | 2026-05-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07587008 | Study to Assess Adverse Events and How Oral Emraclidine Moves Through the Body … | Phase1 | Healthy Volunteers | Recruiting | 2026-05-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07587008 | Study to Assess Adverse Events and How Oral Emraclidine Moves Through the Body … | Phase1 | Healthy Volunteers | Recruiting | 2026-05-12 | 2026-07-01 | ClinicalTrials.gov |
| NCT07599761 | A Phase 1 Study to Assess the Effect of Itraconazole on ABBV-722 in Healthy Adu… | Phase1 | Healthy Volunteers | Recruiting | 2026-05-05 | 2026-07-01 | ClinicalTrials.gov |
| NCT07599761 | A Phase 1 Study to Assess the Effect of Itraconazole on ABBV-722 in Healthy Adu… | Phase1 | Healthy Volunteers | Recruiting | 2026-05-05 | 2026-07-01 | ClinicalTrials.gov |
| NCT07599761 | A Phase 1 Study to Assess the Effect of Itraconazole on ABBV-722 in Healthy Adu… | Phase1 | Healthy Volunteers | Recruiting | 2026-05-05 | 2026-07-01 | ClinicalTrials.gov |
| NCT07599761 | A Phase 1 Study to Assess the Effect of Itraconazole on ABBV-722 in Healthy Adu… | Phase1 | Healthy Volunteers | Recruiting | 2026-05-05 | 2026-07-01 | ClinicalTrials.gov |
| NCT06953934 | A Mass Balance Study of Oral [14C] ABBV-932 in Healthy Adult Male Participants | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-05-04 | 2026-09-01 | ClinicalTrials.gov |
| NCT06953934 | A Mass Balance Study of Oral [14C] ABBV-932 in Healthy Adult Male Participants | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-05-04 | 2026-09-01 | ClinicalTrials.gov |
| NCT06953934 | A Mass Balance Study of Oral [14C] ABBV-932 in Healthy Adult Male Participants | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-05-04 | 2026-09-01 | ClinicalTrials.gov |
| NCT06953934 | A Mass Balance Study of Oral [14C] ABBV-932 in Healthy Adult Male Participants | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-05-04 | 2026-09-01 | ClinicalTrials.gov |
| NCT07570147 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Single As… | Phase1 | Healthy Volunteer | Recruiting | 2026-05-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07539844 | Study to Assess Prevalence of the Folate Receptor Alpha (FRa) in Adult Female P… | — | Ovarian Cancer | Not_Yet_Recruiting | 2026-05-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT07570147 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Single As… | Phase1 | Healthy Volunteer | Recruiting | 2026-05-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07539844 | Study to Assess Prevalence of the Folate Receptor Alpha (FRa) in Adult Female P… | — | Ovarian Cancer | Not_Yet_Recruiting | 2026-05-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT07570147 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Single As… | Phase1 | Healthy Volunteer | Recruiting | 2026-05-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07539844 | Study to Assess Prevalence of the Folate Receptor Alpha (FRa) in Adult Female P… | — | Ovarian Cancer | Not_Yet_Recruiting | 2026-05-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT07539844 | Study to Assess Prevalence of the Folate Receptor Alpha (FRa) in Adult Female P… | — | Ovarian Cancer | Not_Yet_Recruiting | 2026-05-01 | 2027-03-01 | ClinicalTrials.gov |
| NCT07570147 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Single As… | Phase1 | Healthy Volunteer | Recruiting | 2026-05-01 | 2027-04-01 | ClinicalTrials.gov |
| NCT07490301 | A Study to Assess Intravenous (IV) Telisotuzumab Adizutecan in Combination With… | Phase2 | Metastatic Pancreatic Ductal Adenocarcinoma | Recruiting | 2026-04-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07567781 | A Phase 1 Study to Assess the Effect of ABBV-722 on Midazolam, Digoxin, Pitavas… | Phase1 | Healthy Volunteers | Active_Not_Recruiting | 2026-04-30 | 2026-07-01 | ClinicalTrials.gov |
| NCT07567781 | A Phase 1 Study to Assess the Effect of ABBV-722 on Midazolam, Digoxin, Pitavas… | Phase1 | Healthy Volunteers | Active_Not_Recruiting | 2026-04-30 | 2026-07-01 | ClinicalTrials.gov |
| NCT07490301 | A Study to Assess Intravenous (IV) Telisotuzumab Adizutecan in Combination With… | Phase2 | Metastatic Pancreatic Ductal Adenocarcinoma | Recruiting | 2026-04-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07567781 | A Phase 1 Study to Assess the Effect of ABBV-722 on Midazolam, Digoxin, Pitavas… | Phase1 | Healthy Volunteers | Active_Not_Recruiting | 2026-04-30 | 2026-07-01 | ClinicalTrials.gov |
| NCT07490301 | A Study to Assess Intravenous (IV) Telisotuzumab Adizutecan in Combination With… | Phase2 | Metastatic Pancreatic Ductal Adenocarcinoma | Recruiting | 2026-04-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07490301 | A Study to Assess Intravenous (IV) Telisotuzumab Adizutecan in Combination With… | Phase2 | Metastatic Pancreatic Ductal Adenocarcinoma | Recruiting | 2026-04-30 | 2031-06-01 | ClinicalTrials.gov |
| NCT07567781 | A Phase 1 Study to Assess the Effect of ABBV-722 on Midazolam, Digoxin, Pitavas… | Phase1 | Healthy Volunteers | Active_Not_Recruiting | 2026-04-30 | 2026-07-01 | ClinicalTrials.gov |
| NCT07600762 | A Study to Assess Adverse Events, Tolerability and How a Single Oral Dose of Na… | Phase1 | Healthy Volunteer | Completed | 2026-04-21 | 2026-06-17 | ClinicalTrials.gov |
| NCT07600762 | A Study to Assess Adverse Events, Tolerability and How a Single Oral Dose of Na… | Phase1 | Healthy Volunteer | Completed | 2026-04-21 | 2026-06-17 | ClinicalTrials.gov |
| NCT07600762 | A Study to Assess Adverse Events, Tolerability and How a Single Oral Dose of Na… | Phase1 | Healthy Volunteer | Completed | 2026-04-21 | 2026-06-17 | ClinicalTrials.gov |
| NCT07600762 | A Study to Assess Adverse Events, Tolerability and How a Single Oral Dose of Na… | Phase1 | Healthy Volunteer | Completed | 2026-04-21 | 2026-06-17 | ClinicalTrials.gov |
| NCT07365241 | A Study to Evaluate Adverse Events and Change in Disease Activity of Intravenou… | Phase3 | Small Cell Lung Cancer | Not_Yet_Recruiting | 2026-04-14 | 2030-09-01 | ClinicalTrials.gov |
| NCT07365241 | A Study to Evaluate Adverse Events and Change in Disease Activity of Intravenou… | Phase3 | Small Cell Lung Cancer | Not_Yet_Recruiting | 2026-04-14 | 2030-09-01 | ClinicalTrials.gov |
| NCT07365241 | A Study to Evaluate Adverse Events and Change in Disease Activity of Intravenou… | Phase3 | Small Cell Lung Cancer | Not_Yet_Recruiting | 2026-04-14 | 2030-09-01 | ClinicalTrials.gov |
| NCT07365241 | A Study to Evaluate Adverse Events and Change in Disease Activity of Intravenou… | Phase3 | Small Cell Lung Cancer | Not_Yet_Recruiting | 2026-04-14 | 2030-09-01 | ClinicalTrials.gov |
| NCT07514260 | A Study to Assess Adverse Events, Tolerability, and Pharmacokinetics of Subcuta… | Phase1 | Healthy Volunteer | Recruiting | 2026-03-31 | 2027-01-01 | ClinicalTrials.gov |
| NCT07514260 | A Study to Assess Adverse Events, Tolerability, and Pharmacokinetics of Subcuta… | Phase1 | Healthy Volunteer | Recruiting | 2026-03-31 | 2027-01-01 | ClinicalTrials.gov |
| NCT07514260 | A Study to Assess Adverse Events, Tolerability, and Pharmacokinetics of Subcuta… | Phase1 | Healthy Volunteer | Recruiting | 2026-03-31 | 2027-01-01 | ClinicalTrials.gov |
| NCT07514260 | A Study to Assess Adverse Events, Tolerability, and Pharmacokinetics of Subcuta… | Phase1 | Healthy Volunteer | Recruiting | 2026-03-31 | 2027-01-01 | ClinicalTrials.gov |
| NCT07502417 | A Phase 1 Study to Assess the Effect of ABBV-722 on Ethinyl Estradiol and Levon… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-03-27 | 2026-07-01 | ClinicalTrials.gov |
| NCT07502417 | A Phase 1 Study to Assess the Effect of ABBV-722 on Ethinyl Estradiol and Levon… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-03-27 | 2026-07-01 | ClinicalTrials.gov |
| NCT07502417 | A Phase 1 Study to Assess the Effect of ABBV-722 on Ethinyl Estradiol and Levon… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-03-27 | 2026-07-01 | ClinicalTrials.gov |
| NCT07502417 | A Phase 1 Study to Assess the Effect of ABBV-722 on Ethinyl Estradiol and Levon… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-03-27 | 2026-07-01 | ClinicalTrials.gov |
| NCT07387471 | Study to Assess Change in Disease Activity of Oral Venetoclax in Adult Particip… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2026-03-17 | 2028-07-01 | ClinicalTrials.gov |
| NCT07387471 | Study to Assess Change in Disease Activity of Oral Venetoclax in Adult Particip… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2026-03-17 | 2028-07-01 | ClinicalTrials.gov |
| NCT07387471 | Study to Assess Change in Disease Activity of Oral Venetoclax in Adult Particip… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2026-03-17 | 2028-07-01 | ClinicalTrials.gov |
| NCT07387471 | Study to Assess Change in Disease Activity of Oral Venetoclax in Adult Particip… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2026-03-17 | 2028-07-01 | ClinicalTrials.gov |
| NCT07382440 | A Study to Assess Change in Disease Symptoms in Adult Participants With Advance… | — | Parkinson's Disease | Recruiting | 2026-03-09 | 2028-09-01 | ClinicalTrials.gov |
| NCT07382440 | A Study to Assess Change in Disease Symptoms in Adult Participants With Advance… | — | Parkinson's Disease | Recruiting | 2026-03-09 | 2028-09-01 | ClinicalTrials.gov |
| NCT07382440 | A Study to Assess Change in Disease Symptoms in Adult Participants With Advance… | — | Parkinson's Disease | Recruiting | 2026-03-09 | 2028-09-01 | ClinicalTrials.gov |
| NCT07382440 | A Study to Assess Change in Disease Symptoms in Adult Participants With Advance… | — | Parkinson's Disease | Recruiting | 2026-03-09 | 2028-09-01 | ClinicalTrials.gov |
| NCT07227896 | Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes… | — | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2027-10-01 | ClinicalTrials.gov |
| NCT07227896 | Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes… | — | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2027-10-01 | ClinicalTrials.gov |
| NCT07227896 | Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes… | — | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2027-10-01 | ClinicalTrials.gov |
| NCT07227896 | Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes… | — | Parkinson's Disease | Not_Yet_Recruiting | 2026-03-01 | 2027-10-01 | ClinicalTrials.gov |
| NCT07407062 | A Study to Evaluate Folate Receptor Alpha (FRα) Expression in Adult Participant… | — | Cancer - Ovarian | Not_Yet_Recruiting | 2026-02-28 | 2026-07-01 | ClinicalTrials.gov |
| NCT07407062 | A Study to Evaluate Folate Receptor Alpha (FRα) Expression in Adult Participant… | — | Cancer - Ovarian | Not_Yet_Recruiting | 2026-02-28 | 2026-07-01 | ClinicalTrials.gov |
| NCT07407062 | A Study to Evaluate Folate Receptor Alpha (FRα) Expression in Adult Participant… | — | Cancer - Ovarian | Not_Yet_Recruiting | 2026-02-28 | 2026-07-01 | ClinicalTrials.gov |
| NCT07407062 | A Study to Evaluate Folate Receptor Alpha (FRα) Expression in Adult Participant… | — | Cancer - Ovarian | Not_Yet_Recruiting | 2026-02-28 | 2026-07-01 | ClinicalTrials.gov |
| NCT07409246 | A Study to Evaluate Adverse Events, Change in Disease Activity, Tolerability, a… | Phase1 | Multiple Myeloma | Recruiting | 2026-02-27 | 2031-11-01 | ClinicalTrials.gov |
| NCT07419347 | Study of Glecaprevir/Pibrentasvir to Assess Safety Through Real-World Data | — | Hepatitis C Virus (HCV) | Recruiting | 2026-02-27 | 2026-06-01 | ClinicalTrials.gov |
| NCT07419347 | Study of Glecaprevir/Pibrentasvir to Assess Safety Through Real-World Data | — | Hepatitis C Virus (HCV) | Recruiting | 2026-02-27 | 2026-06-01 | ClinicalTrials.gov |
| NCT07409246 | A Study to Evaluate Adverse Events, Change in Disease Activity, Tolerability, a… | Phase1 | Multiple Myeloma | Recruiting | 2026-02-27 | 2031-11-01 | ClinicalTrials.gov |
| NCT07409246 | A Study to Evaluate Adverse Events, Change in Disease Activity, Tolerability, a… | Phase1 | Multiple Myeloma | Recruiting | 2026-02-27 | 2031-11-01 | ClinicalTrials.gov |
| NCT07419347 | Study of Glecaprevir/Pibrentasvir to Assess Safety Through Real-World Data | — | Hepatitis C Virus (HCV) | Recruiting | 2026-02-27 | 2026-06-01 | ClinicalTrials.gov |
| NCT07409246 | A Study to Evaluate Adverse Events, Change in Disease Activity, Tolerability, a… | Phase1 | Multiple Myeloma | Recruiting | 2026-02-27 | 2031-11-01 | ClinicalTrials.gov |
| NCT07419347 | Study of Glecaprevir/Pibrentasvir to Assess Safety Through Real-World Data | — | Hepatitis C Virus (HCV) | Recruiting | 2026-02-27 | 2026-06-01 | ClinicalTrials.gov |
| NCT07425899 | A Phase 1 Study of the Safety and How the Body Processes ABBV-722 and Upadaciti… | Phase1 | Healthy Volunteer | Recruiting | 2026-02-26 | 2026-08-01 | ClinicalTrials.gov |
| NCT07425899 | A Phase 1 Study of the Safety and How the Body Processes ABBV-722 and Upadaciti… | Phase1 | Healthy Volunteer | Recruiting | 2026-02-26 | 2026-08-01 | ClinicalTrials.gov |
| NCT07425899 | A Phase 1 Study of the Safety and How the Body Processes ABBV-722 and Upadaciti… | Phase1 | Healthy Volunteer | Recruiting | 2026-02-26 | 2026-08-01 | ClinicalTrials.gov |
| NCT07425899 | A Phase 1 Study of the Safety and How the Body Processes ABBV-722 and Upadaciti… | Phase1 | Healthy Volunteer | Recruiting | 2026-02-26 | 2026-08-01 | ClinicalTrials.gov |
| NCT07323641 | Telisotuzumab Vedotin and Osimertinib for the Treatment of Progressive, Incurab… | Phase2 | Lung Non-Small Cell Carcinoma | Recruiting | 2026-02-19 | 2028-02-01 | ClinicalTrials.gov |
| NCT07323641 | Telisotuzumab Vedotin and Osimertinib for the Treatment of Progressive, Incurab… | Phase2 | Lung Non-Small Cell Carcinoma | Recruiting | 2026-02-19 | 2028-02-01 | ClinicalTrials.gov |
| NCT07323641 | Telisotuzumab Vedotin and Osimertinib for the Treatment of Progressive, Incurab… | Phase2 | Lung Non-Small Cell Carcinoma | Recruiting | 2026-02-19 | 2028-02-01 | ClinicalTrials.gov |
| NCT07323641 | Telisotuzumab Vedotin and Osimertinib for the Treatment of Progressive, Incurab… | Phase2 | Lung Non-Small Cell Carcinoma | Recruiting | 2026-02-19 | 2028-02-01 | ClinicalTrials.gov |
| NCT06510309 | Rituximab Plus Venetoclax in Front Line Marginal Zone Lymphoma | Phase2 | Lymphoma | Recruiting | 2026-02-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07414784 | A Study of ABBV-295 Subcutaneous Injections to Assess Pharmacokinetics and Adve… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-02-11 | 2026-07-01 | ClinicalTrials.gov |
| NCT07413133 | A Study to Assess How the Body Absorbs ABBV-8736 Subcutaneous Injections Relati… | Phase1 | Healthy Volunteer | Completed | 2026-02-11 | 2026-06-19 | ClinicalTrials.gov |
| NCT07413133 | A Study to Assess How the Body Absorbs ABBV-8736 Subcutaneous Injections Relati… | Phase1 | Healthy Volunteer | Completed | 2026-02-11 | 2026-06-19 | ClinicalTrials.gov |
| NCT07414784 | A Study of ABBV-295 Subcutaneous Injections to Assess Pharmacokinetics and Adve… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-02-11 | 2026-07-01 | ClinicalTrials.gov |
| NCT07413133 | A Study to Assess How the Body Absorbs ABBV-8736 Subcutaneous Injections Relati… | Phase1 | Healthy Volunteer | Completed | 2026-02-11 | 2026-06-19 | ClinicalTrials.gov |
| NCT07414784 | A Study of ABBV-295 Subcutaneous Injections to Assess Pharmacokinetics and Adve… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-02-11 | 2026-07-01 | ClinicalTrials.gov |
| NCT06510309 | Rituximab Plus Venetoclax in Front Line Marginal Zone Lymphoma | Phase2 | Lymphoma | Recruiting | 2026-02-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07414784 | A Study of ABBV-295 Subcutaneous Injections to Assess Pharmacokinetics and Adve… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2026-02-11 | 2026-07-01 | ClinicalTrials.gov |
| NCT06510309 | Rituximab Plus Venetoclax in Front Line Marginal Zone Lymphoma | Phase2 | Lymphoma | Recruiting | 2026-02-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07413133 | A Study to Assess How the Body Absorbs ABBV-8736 Subcutaneous Injections Relati… | Phase1 | Healthy Volunteer | Completed | 2026-02-11 | 2026-06-19 | ClinicalTrials.gov |
| NCT06510309 | Rituximab Plus Venetoclax in Front Line Marginal Zone Lymphoma | Phase2 | Lymphoma | Recruiting | 2026-02-11 | 2031-10-01 | ClinicalTrials.gov |
| NCT07217678 | Biomarkers of Ocular Surface Damage in the Setting of Topical Ocular Hypotensiv… | Phase4 | Glaucoma | Recruiting | 2026-02-09 | 2028-01-31 | ClinicalTrials.gov |
| NCT07421258 | A Retrospective Study to Evaluate Treat-to-Target and Disease Modification in A… | — | Crohn's Disease | Recruiting | 2026-02-09 | 2026-09-01 | ClinicalTrials.gov |
| NCT07421258 | A Retrospective Study to Evaluate Treat-to-Target and Disease Modification in A… | — | Crohn's Disease | Recruiting | 2026-02-09 | 2026-09-01 | ClinicalTrials.gov |
| NCT07217678 | Biomarkers of Ocular Surface Damage in the Setting of Topical Ocular Hypotensiv… | Phase4 | Glaucoma | Recruiting | 2026-02-09 | 2028-01-31 | ClinicalTrials.gov |
| NCT07217678 | Biomarkers of Ocular Surface Damage in the Setting of Topical Ocular Hypotensiv… | Phase4 | Glaucoma | Recruiting | 2026-02-09 | 2028-01-31 | ClinicalTrials.gov |
| NCT07421258 | A Retrospective Study to Evaluate Treat-to-Target and Disease Modification in A… | — | Crohn's Disease | Recruiting | 2026-02-09 | 2026-09-01 | ClinicalTrials.gov |
| NCT07421258 | A Retrospective Study to Evaluate Treat-to-Target and Disease Modification in A… | — | Crohn's Disease | Recruiting | 2026-02-09 | 2026-09-01 | ClinicalTrials.gov |
| NCT07217678 | Biomarkers of Ocular Surface Damage in the Setting of Topical Ocular Hypotensiv… | Phase4 | Glaucoma | Recruiting | 2026-02-09 | 2028-01-31 | ClinicalTrials.gov |
| NCT07226791 | Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity … | Phase2 | Ventral Hernia | Recruiting | 2026-02-04 | 2030-05-01 | ClinicalTrials.gov |
| NCT07226791 | Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity … | Phase2 | Ventral Hernia | Recruiting | 2026-02-04 | 2030-05-01 | ClinicalTrials.gov |
| NCT07226791 | Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity … | Phase2 | Ventral Hernia | Recruiting | 2026-02-04 | 2030-05-01 | ClinicalTrials.gov |
| NCT07226791 | Study of AGN-151607-DP to Assess Adverse Events and Change in Disease Activity … | Phase2 | Ventral Hernia | Recruiting | 2026-02-04 | 2030-05-01 | ClinicalTrials.gov |
| NCT06696755 | A Study to Assess Adverse Events and Change in Disease Activity of Oral Icalcap… | Phase2 | Bipolar I Disorder | Recruiting | 2026-02-03 | 2027-11-01 | ClinicalTrials.gov |
| NCT06696755 | A Study to Assess Adverse Events and Change in Disease Activity of Oral Icalcap… | Phase2 | Bipolar I Disorder | Recruiting | 2026-02-03 | 2027-11-01 | ClinicalTrials.gov |
| NCT06696755 | A Study to Assess Adverse Events and Change in Disease Activity of Oral Icalcap… | Phase2 | Bipolar I Disorder | Recruiting | 2026-02-03 | 2027-11-01 | ClinicalTrials.gov |
| NCT06696755 | A Study to Assess Adverse Events and Change in Disease Activity of Oral Icalcap… | Phase2 | Bipolar I Disorder | Recruiting | 2026-02-03 | 2027-11-01 | ClinicalTrials.gov |
| NCT07310290 | Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participant… | — | Migraine | Recruiting | 2026-01-27 | 2027-03-01 | ClinicalTrials.gov |
| NCT07310290 | Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participant… | — | Migraine | Recruiting | 2026-01-27 | 2027-03-01 | ClinicalTrials.gov |
| NCT07310290 | Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participant… | — | Migraine | Recruiting | 2026-01-27 | 2027-03-01 | ClinicalTrials.gov |
| NCT07310290 | Study to Assess the Real-World Effectiveness of Ubrogepant in Adult Participant… | — | Migraine | Recruiting | 2026-01-27 | 2027-03-01 | ClinicalTrials.gov |
| NCT07230288 | Study of ABBV-142 to Assess Adverse Events and Change in Disease Activity in Ad… | Phase2 | Idiopathic Pulmonary Fibrosis | Recruiting | 2026-01-23 | 2029-09-01 | ClinicalTrials.gov |
| NCT07230288 | Study of ABBV-142 to Assess Adverse Events and Change in Disease Activity in Ad… | Phase2 | Idiopathic Pulmonary Fibrosis | Recruiting | 2026-01-23 | 2029-09-01 | ClinicalTrials.gov |
| NCT07230288 | Study of ABBV-142 to Assess Adverse Events and Change in Disease Activity in Ad… | Phase2 | Idiopathic Pulmonary Fibrosis | Recruiting | 2026-01-23 | 2029-09-01 | ClinicalTrials.gov |
| NCT07230288 | Study of ABBV-142 to Assess Adverse Events and Change in Disease Activity in Ad… | Phase2 | Idiopathic Pulmonary Fibrosis | Recruiting | 2026-01-23 | 2029-09-01 | ClinicalTrials.gov |
| NCT07258771 | Upadacitinib Combined With Corticosteroids vs Corticosteroid Monotherapy Induct… | Phase4 | Ulcerative Colitis Acute | Recruiting | 2026-01-16 | 2030-12-01 | ClinicalTrials.gov |
| NCT07258771 | Upadacitinib Combined With Corticosteroids vs Corticosteroid Monotherapy Induct… | Phase4 | Ulcerative Colitis Acute | Recruiting | 2026-01-16 | 2030-12-01 | ClinicalTrials.gov |
| NCT07258771 | Upadacitinib Combined With Corticosteroids vs Corticosteroid Monotherapy Induct… | Phase4 | Ulcerative Colitis Acute | Recruiting | 2026-01-16 | 2030-12-01 | ClinicalTrials.gov |
| NCT07258771 | Upadacitinib Combined With Corticosteroids vs Corticosteroid Monotherapy Induct… | Phase4 | Ulcerative Colitis Acute | Recruiting | 2026-01-16 | 2030-12-01 | ClinicalTrials.gov |
| NCT07361367 | A Phase 1 Study of a Tablet Form of ABBV-722 Taken With and Without Food in Hea… | Phase1 | Healthy Volunteers | Completed | 2026-01-15 | 2026-03-23 | ClinicalTrials.gov |
| NCT07361367 | A Phase 1 Study of a Tablet Form of ABBV-722 Taken With and Without Food in Hea… | Phase1 | Healthy Volunteers | Completed | 2026-01-15 | 2026-03-23 | ClinicalTrials.gov |
| NCT07361367 | A Phase 1 Study of a Tablet Form of ABBV-722 Taken With and Without Food in Hea… | Phase1 | Healthy Volunteers | Completed | 2026-01-15 | 2026-03-23 | ClinicalTrials.gov |
| NCT07361367 | A Phase 1 Study of a Tablet Form of ABBV-722 Taken With and Without Food in Hea… | Phase1 | Healthy Volunteers | Completed | 2026-01-15 | 2026-03-23 | ClinicalTrials.gov |
| NCT07095452 | A Study to Assess A Change in Disease Activity and Adverse Events of Intravenou… | Phase2 | Multiple Myeloma | Recruiting | 2026-01-08 | 2042-01-01 | ClinicalTrials.gov |
| NCT07095452 | A Study to Assess A Change in Disease Activity and Adverse Events of Intravenou… | Phase2 | Multiple Myeloma | Recruiting | 2026-01-08 | 2042-01-01 | ClinicalTrials.gov |
| NCT07095452 | A Study to Assess A Change in Disease Activity and Adverse Events of Intravenou… | Phase2 | Multiple Myeloma | Recruiting | 2026-01-08 | 2042-01-01 | ClinicalTrials.gov |
| NCT07095452 | A Study to Assess A Change in Disease Activity and Adverse Events of Intravenou… | Phase2 | Multiple Myeloma | Recruiting | 2026-01-08 | 2042-01-01 | ClinicalTrials.gov |
| NCT07276997 | A Study to Assess Change in Disease Activity and Adverse Events of Oral Icalcap… | Phase2 | Major Depressive Disorder | Recruiting | 2025-12-18 | 2027-09-01 | ClinicalTrials.gov |
| NCT07276997 | A Study to Assess Change in Disease Activity and Adverse Events of Oral Icalcap… | Phase2 | Major Depressive Disorder | Recruiting | 2025-12-18 | 2027-09-01 | ClinicalTrials.gov |
| NCT07276997 | A Study to Assess Change in Disease Activity and Adverse Events of Oral Icalcap… | Phase2 | Major Depressive Disorder | Recruiting | 2025-12-18 | 2027-09-01 | ClinicalTrials.gov |
| NCT07276997 | A Study to Assess Change in Disease Activity and Adverse Events of Oral Icalcap… | Phase2 | Major Depressive Disorder | Recruiting | 2025-12-18 | 2027-09-01 | ClinicalTrials.gov |
| NCT07306754 | A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of ABBV-243 in Heal… | Phase1 | Healthy Volunteers | Recruiting | 2025-12-17 | 2027-05-01 | ClinicalTrials.gov |
| NCT07306754 | A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of ABBV-243 in Heal… | Phase1 | Healthy Volunteers | Recruiting | 2025-12-17 | 2027-05-01 | ClinicalTrials.gov |
| NCT07306754 | A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of ABBV-243 in Heal… | Phase1 | Healthy Volunteers | Recruiting | 2025-12-17 | 2027-05-01 | ClinicalTrials.gov |
| NCT07306754 | A Phase 1 Study to Evaluate the Safety and Pharmacokinetics of ABBV-243 in Heal… | Phase1 | Healthy Volunteers | Recruiting | 2025-12-17 | 2027-05-01 | ClinicalTrials.gov |
| NCT07284381 | A Clinical Study to Evaluate the Effect and Side Effect of a New Artificial Tea… | Phase3 | Dry Eye Disease | Active_Not_Recruiting | 2025-12-15 | 2026-08-01 | ClinicalTrials.gov |
| NCT07284381 | A Clinical Study to Evaluate the Effect and Side Effect of a New Artificial Tea… | Phase3 | Dry Eye Disease | Active_Not_Recruiting | 2025-12-15 | 2026-08-01 | ClinicalTrials.gov |
| NCT07284381 | A Clinical Study to Evaluate the Effect and Side Effect of a New Artificial Tea… | Phase3 | Dry Eye Disease | Active_Not_Recruiting | 2025-12-15 | 2026-08-01 | ClinicalTrials.gov |
| NCT07284381 | A Clinical Study to Evaluate the Effect and Side Effect of a New Artificial Tea… | Phase3 | Dry Eye Disease | Active_Not_Recruiting | 2025-12-15 | 2026-08-01 | ClinicalTrials.gov |
| NCT07007052 | Phase II Study Evaluating the Efficacy and Safety of the Combination of Tagraxo… | Phase2 | Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) | Recruiting | 2025-12-11 | 2031-10-02 | ClinicalTrials.gov |
| NCT07007052 | Phase II Study Evaluating the Efficacy and Safety of the Combination of Tagraxo… | Phase2 | Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) | Recruiting | 2025-12-11 | 2031-10-02 | ClinicalTrials.gov |
| NCT07007052 | Phase II Study Evaluating the Efficacy and Safety of the Combination of Tagraxo… | Phase2 | Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) | Recruiting | 2025-12-11 | 2031-10-02 | ClinicalTrials.gov |
| NCT07007052 | Phase II Study Evaluating the Efficacy and Safety of the Combination of Tagraxo… | Phase2 | Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) | Recruiting | 2025-12-11 | 2031-10-02 | ClinicalTrials.gov |
| NCT07155187 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenous … | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2025-12-10 | 2030-09-01 | ClinicalTrials.gov |
| NCT07155187 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenous … | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2025-12-10 | 2030-09-01 | ClinicalTrials.gov |
| NCT07155187 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenous … | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2025-12-10 | 2030-09-01 | ClinicalTrials.gov |
| NCT07155187 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenous … | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2025-12-10 | 2030-09-01 | ClinicalTrials.gov |
| NCT07097363 | Epcoritamab With Dose Adjusted Etoposide, Cyclophosphamide, Vincristine, Doxoru… | Phase2 | B-Cell Non-Hodgkin Lymphoma | Recruiting | 2025-12-07 | 2030-05-31 | ClinicalTrials.gov |
| NCT07097363 | Epcoritamab With Dose Adjusted Etoposide, Cyclophosphamide, Vincristine, Doxoru… | Phase2 | B-Cell Non-Hodgkin Lymphoma | Recruiting | 2025-12-07 | 2030-05-31 | ClinicalTrials.gov |
| NCT07097363 | Epcoritamab With Dose Adjusted Etoposide, Cyclophosphamide, Vincristine, Doxoru… | Phase2 | B-Cell Non-Hodgkin Lymphoma | Recruiting | 2025-12-07 | 2030-05-31 | ClinicalTrials.gov |
| NCT07097363 | Epcoritamab With Dose Adjusted Etoposide, Cyclophosphamide, Vincristine, Doxoru… | Phase2 | B-Cell Non-Hodgkin Lymphoma | Recruiting | 2025-12-07 | 2030-05-31 | ClinicalTrials.gov |
| NCT06958705 | Venetoclax as Consolidation in CLL Patients Treated With BTK Inhibitor Monother… | Phase2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | Recruiting | 2025-12-01 | 2028-02-01 | ClinicalTrials.gov |
| NCT06958705 | Venetoclax as Consolidation in CLL Patients Treated With BTK Inhibitor Monother… | Phase2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | Recruiting | 2025-12-01 | 2028-02-01 | ClinicalTrials.gov |
| NCT07196644 | A Study to Assess Adverse Events and Change in Disease Activity in Participants… | Phase2 | Solid Tumors Harboring MET Amplification | Recruiting | 2025-12-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT06958705 | Venetoclax as Consolidation in CLL Patients Treated With BTK Inhibitor Monother… | Phase2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | Recruiting | 2025-12-01 | 2028-02-01 | ClinicalTrials.gov |
| NCT06958705 | Venetoclax as Consolidation in CLL Patients Treated With BTK Inhibitor Monother… | Phase2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | Recruiting | 2025-12-01 | 2028-02-01 | ClinicalTrials.gov |
| NCT07196644 | A Study to Assess Adverse Events and Change in Disease Activity in Participants… | Phase2 | Solid Tumors Harboring MET Amplification | Recruiting | 2025-12-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07196644 | A Study to Assess Adverse Events and Change in Disease Activity in Participants… | Phase2 | Solid Tumors Harboring MET Amplification | Recruiting | 2025-12-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07196644 | A Study to Assess Adverse Events and Change in Disease Activity in Participants… | Phase2 | Solid Tumors Harboring MET Amplification | Recruiting | 2025-12-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT07278336 | A Study to Assess Adverse Events, Change in Disease Activity and How Intravenou… | Phase1 | Ovarian Cancer | Recruiting | 2025-11-27 | 2029-01-01 | ClinicalTrials.gov |
| NCT07278336 | A Study to Assess Adverse Events, Change in Disease Activity and How Intravenou… | Phase1 | Ovarian Cancer | Recruiting | 2025-11-27 | 2029-01-01 | ClinicalTrials.gov |
| NCT07278336 | A Study to Assess Adverse Events, Change in Disease Activity and How Intravenou… | Phase1 | Ovarian Cancer | Recruiting | 2025-11-27 | 2029-01-01 | ClinicalTrials.gov |
| NCT07278336 | A Study to Assess Adverse Events, Change in Disease Activity and How Intravenou… | Phase1 | Ovarian Cancer | Recruiting | 2025-11-27 | 2029-01-01 | ClinicalTrials.gov |
| NCT07155174 | A Study to Evaluate the Optimal Dose, Adverse Events and Change in Disease Acti… | Phase2 | Small Cell Lung Cancer | Recruiting | 2025-11-25 | 2031-09-01 | ClinicalTrials.gov |
| NCT07155174 | A Study to Evaluate the Optimal Dose, Adverse Events and Change in Disease Acti… | Phase2 | Small Cell Lung Cancer | Recruiting | 2025-11-25 | 2031-09-01 | ClinicalTrials.gov |
| NCT07155174 | A Study to Evaluate the Optimal Dose, Adverse Events and Change in Disease Acti… | Phase2 | Small Cell Lung Cancer | Recruiting | 2025-11-25 | 2031-09-01 | ClinicalTrials.gov |
| NCT07155174 | A Study to Evaluate the Optimal Dose, Adverse Events and Change in Disease Acti… | Phase2 | Small Cell Lung Cancer | Recruiting | 2025-11-25 | 2031-09-01 | ClinicalTrials.gov |
| NCT07232004 | A Study to Evaluate How the Study Drug Moves Through the Body, Adverse Events, … | Phase1 | Healthy Volunteer | Recruiting | 2025-11-24 | 2027-08-01 | ClinicalTrials.gov |
| NCT07232004 | A Study to Evaluate How the Study Drug Moves Through the Body, Adverse Events, … | Phase1 | Healthy Volunteer | Recruiting | 2025-11-24 | 2027-08-01 | ClinicalTrials.gov |
| NCT07232004 | A Study to Evaluate How the Study Drug Moves Through the Body, Adverse Events, … | Phase1 | Healthy Volunteer | Recruiting | 2025-11-24 | 2027-08-01 | ClinicalTrials.gov |
| NCT07232004 | A Study to Evaluate How the Study Drug Moves Through the Body, Adverse Events, … | Phase1 | Healthy Volunteer | Recruiting | 2025-11-24 | 2027-08-01 | ClinicalTrials.gov |
| NCT06890338 | A Study to Assess Anti-Tumor Activity of Intravenously (IV) Infused Carboplatin… | Phase2 | Epithelial Ovarian Cancer | Recruiting | 2025-11-21 | 2030-02-01 | ClinicalTrials.gov |
| NCT06890338 | A Study to Assess Anti-Tumor Activity of Intravenously (IV) Infused Carboplatin… | Phase2 | Epithelial Ovarian Cancer | Recruiting | 2025-11-21 | 2030-02-01 | ClinicalTrials.gov |
| NCT06890338 | A Study to Assess Anti-Tumor Activity of Intravenously (IV) Infused Carboplatin… | Phase2 | Epithelial Ovarian Cancer | Recruiting | 2025-11-21 | 2030-02-01 | ClinicalTrials.gov |
| NCT06890338 | A Study to Assess Anti-Tumor Activity of Intravenously (IV) Infused Carboplatin… | Phase2 | Epithelial Ovarian Cancer | Recruiting | 2025-11-21 | 2030-02-01 | ClinicalTrials.gov |
| NCT07241039 | A Study to Assess the Adverse Events, Change in Disease Activity, and How Oral … | Phase1 | Advanced Squamous Tumors | Recruiting | 2025-11-20 | 2030-10-01 | ClinicalTrials.gov |
| NCT07241039 | A Study to Assess the Adverse Events, Change in Disease Activity, and How Oral … | Phase1 | Advanced Squamous Tumors | Recruiting | 2025-11-20 | 2030-10-01 | ClinicalTrials.gov |
| NCT07241039 | A Study to Assess the Adverse Events, Change in Disease Activity, and How Oral … | Phase1 | Advanced Squamous Tumors | Recruiting | 2025-11-20 | 2030-10-01 | ClinicalTrials.gov |
| NCT07241039 | A Study to Assess the Adverse Events, Change in Disease Activity, and How Oral … | Phase1 | Advanced Squamous Tumors | Recruiting | 2025-11-20 | 2030-10-01 | ClinicalTrials.gov |
| NCT07291232 | A Study of ABBV-295 Subcutaneous Injections to Assess Adverse Events and Pharma… | Phase1 | Obesity | Recruiting | 2025-11-19 | 2026-10-01 | ClinicalTrials.gov |
| NCT07291232 | A Study of ABBV-295 Subcutaneous Injections to Assess Adverse Events and Pharma… | Phase1 | Obesity | Recruiting | 2025-11-19 | 2026-10-01 | ClinicalTrials.gov |
| NCT07291232 | A Study of ABBV-295 Subcutaneous Injections to Assess Adverse Events and Pharma… | Phase1 | Obesity | Recruiting | 2025-11-19 | 2026-10-01 | ClinicalTrials.gov |
| NCT07291232 | A Study of ABBV-295 Subcutaneous Injections to Assess Adverse Events and Pharma… | Phase1 | Obesity | Recruiting | 2025-11-19 | 2026-10-01 | ClinicalTrials.gov |
| NCT07284342 | A Study to Assess Change in Sleep Disturbances of Adult Participants With Advan… | — | Advanced Parkinson's Disease | Recruiting | 2025-11-17 | 2027-01-01 | ClinicalTrials.gov |
| NCT07284342 | A Study to Assess Change in Sleep Disturbances of Adult Participants With Advan… | — | Advanced Parkinson's Disease | Recruiting | 2025-11-17 | 2027-01-01 | ClinicalTrials.gov |
| NCT07284342 | A Study to Assess Change in Sleep Disturbances of Adult Participants With Advan… | — | Advanced Parkinson's Disease | Recruiting | 2025-11-17 | 2027-01-01 | ClinicalTrials.gov |
| NCT07284342 | A Study to Assess Change in Sleep Disturbances of Adult Participants With Advan… | — | Advanced Parkinson's Disease | Recruiting | 2025-11-17 | 2027-01-01 | ClinicalTrials.gov |
| NCT07059845 | A Study to Assess Adverse Events and Change in Disease Activity of Multiple Tre… | Phase2 | Ovarian Cancer | Recruiting | 2025-11-13 | 2029-01-01 | ClinicalTrials.gov |
| NCT07059845 | A Study to Assess Adverse Events and Change in Disease Activity of Multiple Tre… | Phase2 | Ovarian Cancer | Recruiting | 2025-11-13 | 2029-01-01 | ClinicalTrials.gov |
| NCT07059845 | A Study to Assess Adverse Events and Change in Disease Activity of Multiple Tre… | Phase2 | Ovarian Cancer | Recruiting | 2025-11-13 | 2029-01-01 | ClinicalTrials.gov |
| NCT07059845 | A Study to Assess Adverse Events and Change in Disease Activity of Multiple Tre… | Phase2 | Ovarian Cancer | Recruiting | 2025-11-13 | 2029-01-01 | ClinicalTrials.gov |
| NCT07231952 | A Study of Pirtobrutinib, Venetoclax, and Rituximab in People With Waldenström'… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2025-11-11 | 2028-04-11 | ClinicalTrials.gov |
| NCT07231952 | A Study of Pirtobrutinib, Venetoclax, and Rituximab in People With Waldenström'… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2025-11-11 | 2028-04-11 | ClinicalTrials.gov |
| NCT07231952 | A Study of Pirtobrutinib, Venetoclax, and Rituximab in People With Waldenström'… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2025-11-11 | 2028-04-11 | ClinicalTrials.gov |
| NCT07231952 | A Study of Pirtobrutinib, Venetoclax, and Rituximab in People With Waldenström'… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2025-11-11 | 2028-04-11 | ClinicalTrials.gov |
| NCT07007065 | Study to Assess the Injection Burden, Adverse Events, Change in Disease Activit… | Phase3 | Neovascular Age-related Macular Degeneration | Recruiting | 2025-11-05 | 2033-03-01 | ClinicalTrials.gov |
| NCT07007065 | Study to Assess the Injection Burden, Adverse Events, Change in Disease Activit… | Phase3 | Neovascular Age-related Macular Degeneration | Recruiting | 2025-11-05 | 2033-03-01 | ClinicalTrials.gov |
| NCT07007065 | Study to Assess the Injection Burden, Adverse Events, Change in Disease Activit… | Phase3 | Neovascular Age-related Macular Degeneration | Recruiting | 2025-11-05 | 2033-03-01 | ClinicalTrials.gov |
| NCT07007065 | Study to Assess the Injection Burden, Adverse Events, Change in Disease Activit… | Phase3 | Neovascular Age-related Macular Degeneration | Recruiting | 2025-11-05 | 2033-03-01 | ClinicalTrials.gov |
| NCT07222709 | A Study to Assess the Adverse Events and How Oral ABBV-1042 Moves Through the B… | Phase1 | Healthy Volunteer | Recruiting | 2025-10-27 | 2026-05-01 | ClinicalTrials.gov |
| NCT07222709 | A Study to Assess the Adverse Events and How Oral ABBV-1042 Moves Through the B… | Phase1 | Healthy Volunteer | Recruiting | 2025-10-27 | 2026-05-01 | ClinicalTrials.gov |
| NCT07222709 | A Study to Assess the Adverse Events and How Oral ABBV-1042 Moves Through the B… | Phase1 | Healthy Volunteer | Recruiting | 2025-10-27 | 2026-05-01 | ClinicalTrials.gov |
| NCT07222709 | A Study to Assess the Adverse Events and How Oral ABBV-1042 Moves Through the B… | Phase1 | Healthy Volunteer | Recruiting | 2025-10-27 | 2026-05-01 | ClinicalTrials.gov |
| NCT07207369 | A Study to Assess the Safety and Effectiveness of ELAPR002f Injectable Gel in A… | Phase3 | Acne Scars | Recruiting | 2025-10-24 | 2029-11-01 | ClinicalTrials.gov |
| NCT07207369 | A Study to Assess the Safety and Effectiveness of ELAPR002f Injectable Gel in A… | Phase3 | Acne Scars | Recruiting | 2025-10-24 | 2029-11-01 | ClinicalTrials.gov |
| NCT07207369 | A Study to Assess the Safety and Effectiveness of ELAPR002f Injectable Gel in A… | Phase3 | Acne Scars | Recruiting | 2025-10-24 | 2029-11-01 | ClinicalTrials.gov |
| NCT07207369 | A Study to Assess the Safety and Effectiveness of ELAPR002f Injectable Gel in A… | Phase3 | Acne Scars | Recruiting | 2025-10-24 | 2029-11-01 | ClinicalTrials.gov |
| NCT07219017 | A Study to Assess the Mass Balance of Oral ABBV-1354 in Healthy Adult Male Part… | Phase1 | Healthy Volunteer | Completed | 2025-10-15 | 2025-12-09 | ClinicalTrials.gov |
| NCT07197307 | Combining Loncastuximab Tesirine and Epcoritamab in Relapsed/Refractory Diffuse… | Phase2 | Aggressive Diffuse Large B-cell Lymphoma | Not_Yet_Recruiting | 2025-10-15 | 2030-01-15 | ClinicalTrials.gov |
| NCT07197307 | Combining Loncastuximab Tesirine and Epcoritamab in Relapsed/Refractory Diffuse… | Phase2 | Aggressive Diffuse Large B-cell Lymphoma | Not_Yet_Recruiting | 2025-10-15 | 2030-01-15 | ClinicalTrials.gov |
| NCT07219017 | A Study to Assess the Mass Balance of Oral ABBV-1354 in Healthy Adult Male Part… | Phase1 | Healthy Volunteer | Completed | 2025-10-15 | 2025-12-09 | ClinicalTrials.gov |
| NCT07197307 | Combining Loncastuximab Tesirine and Epcoritamab in Relapsed/Refractory Diffuse… | Phase2 | Aggressive Diffuse Large B-cell Lymphoma | Not_Yet_Recruiting | 2025-10-15 | 2030-01-15 | ClinicalTrials.gov |
| NCT07219017 | A Study to Assess the Mass Balance of Oral ABBV-1354 in Healthy Adult Male Part… | Phase1 | Healthy Volunteer | Completed | 2025-10-15 | 2025-12-09 | ClinicalTrials.gov |
| NCT07197307 | Combining Loncastuximab Tesirine and Epcoritamab in Relapsed/Refractory Diffuse… | Phase2 | Aggressive Diffuse Large B-cell Lymphoma | Not_Yet_Recruiting | 2025-10-15 | 2030-01-15 | ClinicalTrials.gov |
| NCT07219017 | A Study to Assess the Mass Balance of Oral ABBV-1354 in Healthy Adult Male Part… | Phase1 | Healthy Volunteer | Completed | 2025-10-15 | 2025-12-09 | ClinicalTrials.gov |
| NCT06796998 | Epcoritamab in Patients With Newly Diagnosed Marginal Zone Lymphoma (MZL) | Phase2 | Marginal Zone Lymphoma | Recruiting | 2025-10-13 | 2031-04-15 | ClinicalTrials.gov |
| NCT06796998 | Epcoritamab in Patients With Newly Diagnosed Marginal Zone Lymphoma (MZL) | Phase2 | Marginal Zone Lymphoma | Recruiting | 2025-10-13 | 2031-04-15 | ClinicalTrials.gov |
| NCT06796998 | Epcoritamab in Patients With Newly Diagnosed Marginal Zone Lymphoma (MZL) | Phase2 | Marginal Zone Lymphoma | Recruiting | 2025-10-13 | 2031-04-15 | ClinicalTrials.gov |
| NCT06796998 | Epcoritamab in Patients With Newly Diagnosed Marginal Zone Lymphoma (MZL) | Phase2 | Marginal Zone Lymphoma | Recruiting | 2025-10-13 | 2031-04-15 | ClinicalTrials.gov |
| NCT07136116 | Study to Assess Change in Disease Activity of Risankizumab Treatment in Japanes… | — | Ulcerative Colitis | Recruiting | 2025-10-09 | 2030-02-01 | ClinicalTrials.gov |
| NCT07136116 | Study to Assess Change in Disease Activity of Risankizumab Treatment in Japanes… | — | Ulcerative Colitis | Recruiting | 2025-10-09 | 2030-02-01 | ClinicalTrials.gov |
| NCT07136116 | Study to Assess Change in Disease Activity of Risankizumab Treatment in Japanes… | — | Ulcerative Colitis | Recruiting | 2025-10-09 | 2030-02-01 | ClinicalTrials.gov |
| NCT07136116 | Study to Assess Change in Disease Activity of Risankizumab Treatment in Japanes… | — | Ulcerative Colitis | Recruiting | 2025-10-09 | 2030-02-01 | ClinicalTrials.gov |
| NCT07219030 | A Study to Assess the Adverse Events and How Oral Emraclidine Moves Through the… | Phase1 | Healthy Volunteer | Recruiting | 2025-10-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT07219030 | A Study to Assess the Adverse Events and How Oral Emraclidine Moves Through the… | Phase1 | Healthy Volunteer | Recruiting | 2025-10-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT07219030 | A Study to Assess the Adverse Events and How Oral Emraclidine Moves Through the… | Phase1 | Healthy Volunteer | Recruiting | 2025-10-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT07219030 | A Study to Assess the Adverse Events and How Oral Emraclidine Moves Through the… | Phase1 | Healthy Volunteer | Recruiting | 2025-10-08 | 2027-03-01 | ClinicalTrials.gov |
| NCT07220460 | Study to Assess the Adverse Events of Oral ABBV-932 in Adult Participants With … | Phase2 | Bipolar I or II Disorder | Recruiting | 2025-09-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT07220460 | Study to Assess the Adverse Events of Oral ABBV-932 in Adult Participants With … | Phase2 | Bipolar I or II Disorder | Recruiting | 2025-09-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT07220460 | Study to Assess the Adverse Events of Oral ABBV-932 in Adult Participants With … | Phase2 | Bipolar I or II Disorder | Recruiting | 2025-09-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT07220460 | Study to Assess the Adverse Events of Oral ABBV-932 in Adult Participants With … | Phase2 | Bipolar I or II Disorder | Recruiting | 2025-09-30 | 2027-04-01 | ClinicalTrials.gov |
| NCT07186595 | A Study to Evaluate the Safety and Effectiveness of JUVÉDERM Products in Adult … | Phase4 | Mid Face Volume Deficit | Active_Not_Recruiting | 2025-09-25 | 2026-08-01 | ClinicalTrials.gov |
| NCT07186595 | A Study to Evaluate the Safety and Effectiveness of JUVÉDERM Products in Adult … | Phase4 | Mid Face Volume Deficit | Active_Not_Recruiting | 2025-09-25 | 2026-08-01 | ClinicalTrials.gov |
| NCT07186595 | A Study to Evaluate the Safety and Effectiveness of JUVÉDERM Products in Adult … | Phase4 | Mid Face Volume Deficit | Active_Not_Recruiting | 2025-09-25 | 2026-08-01 | ClinicalTrials.gov |
| NCT07186595 | A Study to Evaluate the Safety and Effectiveness of JUVÉDERM Products in Adult … | Phase4 | Mid Face Volume Deficit | Active_Not_Recruiting | 2025-09-25 | 2026-08-01 | ClinicalTrials.gov |
| NCT06931652 | Study of Epcoritamab in R/R Primary Diffuse Large B-cell Lymphoma of the CNS Tr… | Phase2 | Primary CNS Lymphoma (PCNSL) | Recruiting | 2025-09-22 | 2030-01-01 | ClinicalTrials.gov |
| NCT06931652 | Study of Epcoritamab in R/R Primary Diffuse Large B-cell Lymphoma of the CNS Tr… | Phase2 | Primary CNS Lymphoma (PCNSL) | Recruiting | 2025-09-22 | 2030-01-01 | ClinicalTrials.gov |
| NCT06931652 | Study of Epcoritamab in R/R Primary Diffuse Large B-cell Lymphoma of the CNS Tr… | Phase2 | Primary CNS Lymphoma (PCNSL) | Recruiting | 2025-09-22 | 2030-01-01 | ClinicalTrials.gov |
| NCT06931652 | Study of Epcoritamab in R/R Primary Diffuse Large B-cell Lymphoma of the CNS Tr… | Phase2 | Primary CNS Lymphoma (PCNSL) | Recruiting | 2025-09-22 | 2030-01-01 | ClinicalTrials.gov |
| NCT06742385 | Evaluation of a Remote Monitoring Application in the Follow-up of Patients With… | Na | Crohn Disease | Recruiting | 2025-09-18 | 2028-09-18 | ClinicalTrials.gov |
| NCT06742385 | Evaluation of a Remote Monitoring Application in the Follow-up of Patients With… | Na | Crohn Disease | Recruiting | 2025-09-18 | 2028-09-18 | ClinicalTrials.gov |
| NCT06742385 | Evaluation of a Remote Monitoring Application in the Follow-up of Patients With… | Na | Crohn Disease | Recruiting | 2025-09-18 | 2028-09-18 | ClinicalTrials.gov |
| NCT06742385 | Evaluation of a Remote Monitoring Application in the Follow-up of Patients With… | Na | Crohn Disease | Recruiting | 2025-09-18 | 2028-09-18 | ClinicalTrials.gov |
| NCT07172204 | Alternating Regimen of VA and Low-dose CHA in the Treatment of Unfit Newly Diag… | Phase2 | Intensive Chemotherapy Unfit | Recruiting | 2025-09-16 | 2029-07-31 | ClinicalTrials.gov |
| NCT07172204 | Alternating Regimen of VA and Low-dose CHA in the Treatment of Unfit Newly Diag… | Phase2 | Intensive Chemotherapy Unfit | Recruiting | 2025-09-16 | 2029-07-31 | ClinicalTrials.gov |
| NCT07172204 | Alternating Regimen of VA and Low-dose CHA in the Treatment of Unfit Newly Diag… | Phase2 | Intensive Chemotherapy Unfit | Recruiting | 2025-09-16 | 2029-07-31 | ClinicalTrials.gov |
| NCT07172204 | Alternating Regimen of VA and Low-dose CHA in the Treatment of Unfit Newly Diag… | Phase2 | Intensive Chemotherapy Unfit | Recruiting | 2025-09-16 | 2029-07-31 | ClinicalTrials.gov |
| NCT05316220 | A Study to Assess Adverse Events and Change in Disease Condition of Mesalamine … | Phase3 | Ulcerative Colitis (UC) | Withdrawn | 2025-09-15 | 2026-07-19 | ClinicalTrials.gov |
| NCT05316220 | A Study to Assess Adverse Events and Change in Disease Condition of Mesalamine … | Phase3 | Ulcerative Colitis (UC) | Withdrawn | 2025-09-15 | 2026-07-19 | ClinicalTrials.gov |
| NCT05316220 | A Study to Assess Adverse Events and Change in Disease Condition of Mesalamine … | Phase3 | Ulcerative Colitis (UC) | Withdrawn | 2025-09-15 | 2026-07-19 | ClinicalTrials.gov |
| NCT05316220 | A Study to Assess Adverse Events and Change in Disease Condition of Mesalamine … | Phase3 | Ulcerative Colitis (UC) | Withdrawn | 2025-09-15 | 2026-07-19 | ClinicalTrials.gov |
| NCT07039110 | Study to Assess Change in Quality of Life of Risankizumab Treatment in Adult Pa… | — | Plaque Psoriasis | Recruiting | 2025-09-09 | 2028-03-01 | ClinicalTrials.gov |
| NCT07039110 | Study to Assess Change in Quality of Life of Risankizumab Treatment in Adult Pa… | — | Plaque Psoriasis | Recruiting | 2025-09-09 | 2028-03-01 | ClinicalTrials.gov |
| NCT07039110 | Study to Assess Change in Quality of Life of Risankizumab Treatment in Adult Pa… | — | Plaque Psoriasis | Recruiting | 2025-09-09 | 2028-03-01 | ClinicalTrials.gov |
| NCT07039110 | Study to Assess Change in Quality of Life of Risankizumab Treatment in Adult Pa… | — | Plaque Psoriasis | Recruiting | 2025-09-09 | 2028-03-01 | ClinicalTrials.gov |
| NCT07141199 | A Study to Evaluate Adverse Events, How the Drug is Tolerated, and How the Drug… | Phase1 | Healthy Volunteer | Completed | 2025-09-02 | 2026-03-23 | ClinicalTrials.gov |
| NCT07136467 | A Real World Study to Globally Assess Disease Burden in Adolescent and Adult Pa… | — | Non-Segmental Vitiligo (NSV) | Recruiting | 2025-09-02 | 2027-08-01 | ClinicalTrials.gov |
| NCT07023289 | A Study to Assess Adverse Events and Change in Disease Activity in Adult Partic… | Phase2 | Colorectal Cancer | Recruiting | 2025-09-02 | 2029-11-01 | ClinicalTrials.gov |
| NCT07141199 | A Study to Evaluate Adverse Events, How the Drug is Tolerated, and How the Drug… | Phase1 | Healthy Volunteer | Completed | 2025-09-02 | 2026-03-23 | ClinicalTrials.gov |
| NCT07136467 | A Real World Study to Globally Assess Disease Burden in Adolescent and Adult Pa… | — | Non-Segmental Vitiligo (NSV) | Recruiting | 2025-09-02 | 2027-08-01 | ClinicalTrials.gov |
| NCT07023289 | A Study to Assess Adverse Events and Change in Disease Activity in Adult Partic… | Phase2 | Colorectal Cancer | Recruiting | 2025-09-02 | 2029-11-01 | ClinicalTrials.gov |
| NCT07023289 | A Study to Assess Adverse Events and Change in Disease Activity in Adult Partic… | Phase2 | Colorectal Cancer | Recruiting | 2025-09-02 | 2029-11-01 | ClinicalTrials.gov |
| NCT07023289 | A Study to Assess Adverse Events and Change in Disease Activity in Adult Partic… | Phase2 | Colorectal Cancer | Recruiting | 2025-09-02 | 2029-11-01 | ClinicalTrials.gov |
| NCT07136467 | A Real World Study to Globally Assess Disease Burden in Adolescent and Adult Pa… | — | Non-Segmental Vitiligo (NSV) | Recruiting | 2025-09-02 | 2027-08-01 | ClinicalTrials.gov |
| NCT07141199 | A Study to Evaluate Adverse Events, How the Drug is Tolerated, and How the Drug… | Phase1 | Healthy Volunteer | Completed | 2025-09-02 | 2026-03-23 | ClinicalTrials.gov |
| NCT07141199 | A Study to Evaluate Adverse Events, How the Drug is Tolerated, and How the Drug… | Phase1 | Healthy Volunteer | Completed | 2025-09-02 | 2026-03-23 | ClinicalTrials.gov |
| NCT07136467 | A Real World Study to Globally Assess Disease Burden in Adolescent and Adult Pa… | — | Non-Segmental Vitiligo (NSV) | Recruiting | 2025-09-02 | 2027-08-01 | ClinicalTrials.gov |
| NCT06977724 | A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effec… | Phase1 | Dry Eye Syndrome | Recruiting | 2025-08-26 | 2029-03-01 | ClinicalTrials.gov |
| NCT06977724 | A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effec… | Phase1 | Dry Eye Syndrome | Recruiting | 2025-08-26 | 2029-03-01 | ClinicalTrials.gov |
| NCT06977724 | A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effec… | Phase1 | Dry Eye Syndrome | Recruiting | 2025-08-26 | 2029-03-01 | ClinicalTrials.gov |
| NCT06977724 | A Study to Assess Adverse Events, How the Drug Moves Through the Body and Effec… | Phase1 | Dry Eye Syndrome | Recruiting | 2025-08-26 | 2029-03-01 | ClinicalTrials.gov |
| NCT07024797 | Study to Assess the Adverse Events, Tolerability, and How Oral Doses of ABBV-93… | Phase1 | Healthy Volunteer | Completed | 2025-08-21 | 2025-12-08 | ClinicalTrials.gov |
| NCT07024797 | Study to Assess the Adverse Events, Tolerability, and How Oral Doses of ABBV-93… | Phase1 | Healthy Volunteer | Completed | 2025-08-21 | 2025-12-08 | ClinicalTrials.gov |
| NCT07024797 | Study to Assess the Adverse Events, Tolerability, and How Oral Doses of ABBV-93… | Phase1 | Healthy Volunteer | Completed | 2025-08-21 | 2025-12-08 | ClinicalTrials.gov |
| NCT07024797 | Study to Assess the Adverse Events, Tolerability, and How Oral Doses of ABBV-93… | Phase1 | Healthy Volunteer | Completed | 2025-08-21 | 2025-12-08 | ClinicalTrials.gov |
| NCT07018752 | A Platform Trial Evaluating New Drugs or Combination in R/R Peripheral T-cell L… | Phase1 | Peripheral T Cells Lymphoma (PTCL) | Recruiting | 2025-08-20 | 2030-01-01 | ClinicalTrials.gov |
| NCT07018752 | A Platform Trial Evaluating New Drugs or Combination in R/R Peripheral T-cell L… | Phase1 | Peripheral T Cells Lymphoma (PTCL) | Recruiting | 2025-08-20 | 2030-01-01 | ClinicalTrials.gov |
| NCT07018752 | A Platform Trial Evaluating New Drugs or Combination in R/R Peripheral T-cell L… | Phase1 | Peripheral T Cells Lymphoma (PTCL) | Recruiting | 2025-08-20 | 2030-01-01 | ClinicalTrials.gov |
| NCT07018752 | A Platform Trial Evaluating New Drugs or Combination in R/R Peripheral T-cell L… | Phase1 | Peripheral T Cells Lymphoma (PTCL) | Recruiting | 2025-08-20 | 2030-01-01 | ClinicalTrials.gov |
| NCT07136103 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenici… | Phase1 | Healthy Volunteers | Completed | 2025-08-19 | 2026-06-11 | ClinicalTrials.gov |
| NCT07136103 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenici… | Phase1 | Healthy Volunteers | Completed | 2025-08-19 | 2026-06-11 | ClinicalTrials.gov |
| NCT07136103 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenici… | Phase1 | Healthy Volunteers | Completed | 2025-08-19 | 2026-06-11 | ClinicalTrials.gov |
| NCT07136103 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenici… | Phase1 | Healthy Volunteers | Completed | 2025-08-19 | 2026-06-11 | ClinicalTrials.gov |
| NCT07160179 | Study to Assess the Adverse Events and How Intravitreal ABBV-6628 Moves Through… | Phase1 | Geographic Atrophy | Recruiting | 2025-08-13 | 2029-10-01 | ClinicalTrials.gov |
| NCT07160179 | Study to Assess the Adverse Events and How Intravitreal ABBV-6628 Moves Through… | Phase1 | Geographic Atrophy | Recruiting | 2025-08-13 | 2029-10-01 | ClinicalTrials.gov |
| NCT07160179 | Study to Assess the Adverse Events and How Intravitreal ABBV-6628 Moves Through… | Phase1 | Geographic Atrophy | Recruiting | 2025-08-13 | 2029-10-01 | ClinicalTrials.gov |
| NCT07160179 | Study to Assess the Adverse Events and How Intravitreal ABBV-6628 Moves Through… | Phase1 | Geographic Atrophy | Recruiting | 2025-08-13 | 2029-10-01 | ClinicalTrials.gov |
| NCT06896916 | Study of Intravenously (IV) Infused Etentamig in Combination With an Oral Cereb… | Phase1 | Multiple Myeloma | Recruiting | 2025-08-07 | 2036-03-01 | ClinicalTrials.gov |
| NCT06896916 | Study of Intravenously (IV) Infused Etentamig in Combination With an Oral Cereb… | Phase1 | Multiple Myeloma | Recruiting | 2025-08-07 | 2036-03-01 | ClinicalTrials.gov |
| NCT06896916 | Study of Intravenously (IV) Infused Etentamig in Combination With an Oral Cereb… | Phase1 | Multiple Myeloma | Recruiting | 2025-08-07 | 2036-03-01 | ClinicalTrials.gov |
| NCT06896916 | Study of Intravenously (IV) Infused Etentamig in Combination With an Oral Cereb… | Phase1 | Multiple Myeloma | Recruiting | 2025-08-07 | 2036-03-01 | ClinicalTrials.gov |
| NCT07126236 | Response-adaptive to Epcoritamab In First Relapse: Study to Evaluate the Effica… | Phase2 | Large B Cell Lymphoma | Recruiting | 2025-08-04 | 2031-12-01 | ClinicalTrials.gov |
| NCT07145918 | A Study to Assess Adverse Events, Change in Disease Activity, and How Oral Emra… | Phase2 | Schizophrenia | Recruiting | 2025-08-04 | 2028-02-01 | ClinicalTrials.gov |
| NCT07145918 | A Study to Assess Adverse Events, Change in Disease Activity, and How Oral Emra… | Phase2 | Schizophrenia | Recruiting | 2025-08-04 | 2028-02-01 | ClinicalTrials.gov |
| NCT07126236 | Response-adaptive to Epcoritamab In First Relapse: Study to Evaluate the Effica… | Phase2 | Large B Cell Lymphoma | Recruiting | 2025-08-04 | 2031-12-01 | ClinicalTrials.gov |
| NCT07145918 | A Study to Assess Adverse Events, Change in Disease Activity, and How Oral Emra… | Phase2 | Schizophrenia | Recruiting | 2025-08-04 | 2028-02-01 | ClinicalTrials.gov |
| NCT07126236 | Response-adaptive to Epcoritamab In First Relapse: Study to Evaluate the Effica… | Phase2 | Large B Cell Lymphoma | Recruiting | 2025-08-04 | 2031-12-01 | ClinicalTrials.gov |
| NCT07126236 | Response-adaptive to Epcoritamab In First Relapse: Study to Evaluate the Effica… | Phase2 | Large B Cell Lymphoma | Recruiting | 2025-08-04 | 2031-12-01 | ClinicalTrials.gov |
| NCT07145918 | A Study to Assess Adverse Events, Change in Disease Activity, and How Oral Emra… | Phase2 | Schizophrenia | Recruiting | 2025-08-04 | 2028-02-01 | ClinicalTrials.gov |
| NCT07005102 | A Study to Assess Adverse Events, Change in Disease Activity of Intravenous Tel… | Phase2 | Non-Squamous Non-Small Cell Lung Cancer | Recruiting | 2025-08-03 | 2036-11-01 | ClinicalTrials.gov |
| NCT07005102 | A Study to Assess Adverse Events, Change in Disease Activity of Intravenous Tel… | Phase2 | Non-Squamous Non-Small Cell Lung Cancer | Recruiting | 2025-08-03 | 2036-11-01 | ClinicalTrials.gov |
| NCT07005102 | A Study to Assess Adverse Events, Change in Disease Activity of Intravenous Tel… | Phase2 | Non-Squamous Non-Small Cell Lung Cancer | Recruiting | 2025-08-03 | 2036-11-01 | ClinicalTrials.gov |
| NCT07005102 | A Study to Assess Adverse Events, Change in Disease Activity of Intravenous Tel… | Phase2 | Non-Squamous Non-Small Cell Lung Cancer | Recruiting | 2025-08-03 | 2036-11-01 | ClinicalTrials.gov |
| NCT07024784 | A Study to Assess Change in Disease Activity and Adverse Events in Adult Partic… | Phase2 | Gynecologic Cancers | Recruiting | 2025-07-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT07024784 | A Study to Assess Change in Disease Activity and Adverse Events in Adult Partic… | Phase2 | Gynecologic Cancers | Recruiting | 2025-07-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT07024784 | A Study to Assess Change in Disease Activity and Adverse Events in Adult Partic… | Phase2 | Gynecologic Cancers | Recruiting | 2025-07-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT07024784 | A Study to Assess Change in Disease Activity and Adverse Events in Adult Partic… | Phase2 | Gynecologic Cancers | Recruiting | 2025-07-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT07071519 | A Study to Learn More About How Risankizumab Works in Young Participants With U… | Phase3 | Ulcerative Colitis | Recruiting | 2025-07-28 | 2034-07-01 | ClinicalTrials.gov |
| NCT07071519 | A Study to Learn More About How Risankizumab Works in Young Participants With U… | Phase3 | Ulcerative Colitis | Recruiting | 2025-07-28 | 2034-07-01 | ClinicalTrials.gov |
| NCT07071519 | A Study to Learn More About How Risankizumab Works in Young Participants With U… | Phase3 | Ulcerative Colitis | Recruiting | 2025-07-28 | 2034-07-01 | ClinicalTrials.gov |
| NCT07071519 | A Study to Learn More About How Risankizumab Works in Young Participants With U… | Phase3 | Ulcerative Colitis | Recruiting | 2025-07-28 | 2034-07-01 | ClinicalTrials.gov |
| NCT07044687 | Study to Assess Adverse Events and Change in Disease Activity of Oral Venetocla… | Phase4 | Acute Myeloid Leukemia | Recruiting | 2025-07-24 | 2027-11-01 | ClinicalTrials.gov |
| NCT07044687 | Study to Assess Adverse Events and Change in Disease Activity of Oral Venetocla… | Phase4 | Acute Myeloid Leukemia | Recruiting | 2025-07-24 | 2027-11-01 | ClinicalTrials.gov |
| NCT07044687 | Study to Assess Adverse Events and Change in Disease Activity of Oral Venetocla… | Phase4 | Acute Myeloid Leukemia | Recruiting | 2025-07-24 | 2027-11-01 | ClinicalTrials.gov |
| NCT07044687 | Study to Assess Adverse Events and Change in Disease Activity of Oral Venetocla… | Phase4 | Acute Myeloid Leukemia | Recruiting | 2025-07-24 | 2027-11-01 | ClinicalTrials.gov |
| NCT06953960 | A Study to Assess Adverse Events and Change in Disease Activity of Oral Surzeto… | Phase1 | Multiple Myeloma | Recruiting | 2025-07-23 | 2030-12-01 | ClinicalTrials.gov |
| NCT06953960 | A Study to Assess Adverse Events and Change in Disease Activity of Oral Surzeto… | Phase1 | Multiple Myeloma | Recruiting | 2025-07-23 | 2030-12-01 | ClinicalTrials.gov |
| NCT06953960 | A Study to Assess Adverse Events and Change in Disease Activity of Oral Surzeto… | Phase1 | Multiple Myeloma | Recruiting | 2025-07-23 | 2030-12-01 | ClinicalTrials.gov |
| NCT06953960 | A Study to Assess Adverse Events and Change in Disease Activity of Oral Surzeto… | Phase1 | Multiple Myeloma | Recruiting | 2025-07-23 | 2030-12-01 | ClinicalTrials.gov |
| NCT07122583 | A Study to Assess Non-Invasive Subcutaneous Fat Reduction in the Submental, Inn… | Phase4 | Non-Surgical Fat Reduction | Completed | 2025-07-22 | 2026-06-03 | ClinicalTrials.gov |
| NCT07122583 | A Study to Assess Non-Invasive Subcutaneous Fat Reduction in the Submental, Inn… | Phase4 | Non-Surgical Fat Reduction | Completed | 2025-07-22 | 2026-06-03 | ClinicalTrials.gov |
| NCT07122583 | A Study to Assess Non-Invasive Subcutaneous Fat Reduction in the Submental, Inn… | Phase4 | Non-Surgical Fat Reduction | Completed | 2025-07-22 | 2026-06-03 | ClinicalTrials.gov |
| NCT07122583 | A Study to Assess Non-Invasive Subcutaneous Fat Reduction in the Submental, Inn… | Phase4 | Non-Surgical Fat Reduction | Completed | 2025-07-22 | 2026-06-03 | ClinicalTrials.gov |
| NCT07058051 | Cross-sectional Study to Characterize Real World Burden of Disease in Patients … | — | Non-Segmental Vitiligo | Completed | 2025-07-17 | 2025-11-13 | ClinicalTrials.gov |
| NCT07058051 | Cross-sectional Study to Characterize Real World Burden of Disease in Patients … | — | Non-Segmental Vitiligo | Completed | 2025-07-17 | 2025-11-13 | ClinicalTrials.gov |
| NCT07058051 | Cross-sectional Study to Characterize Real World Burden of Disease in Patients … | — | Non-Segmental Vitiligo | Completed | 2025-07-17 | 2025-11-13 | ClinicalTrials.gov |
| NCT07058051 | Cross-sectional Study to Characterize Real World Burden of Disease in Patients … | — | Non-Segmental Vitiligo | Completed | 2025-07-17 | 2025-11-13 | ClinicalTrials.gov |
| NCT07071532 | A Study to Assess Adverse Events and How Oral ABBV-932 Moves Through the Body W… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-07-15 | 2025-11-01 | ClinicalTrials.gov |
| NCT07071532 | A Study to Assess Adverse Events and How Oral ABBV-932 Moves Through the Body W… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-07-15 | 2025-11-01 | ClinicalTrials.gov |
| NCT07071532 | A Study to Assess Adverse Events and How Oral ABBV-932 Moves Through the Body W… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-07-15 | 2025-11-01 | ClinicalTrials.gov |
| NCT07071532 | A Study to Assess Adverse Events and How Oral ABBV-932 Moves Through the Body W… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-07-15 | 2025-11-01 | ClinicalTrials.gov |
| NCT07073079 | A Study to Assess the Effectiveness of Second-Line Therapy of Upadacitinib and … | — | Crohn's Disease | Recruiting | 2025-07-14 | 2027-12-01 | ClinicalTrials.gov |
| NCT07073079 | A Study to Assess the Effectiveness of Second-Line Therapy of Upadacitinib and … | — | Crohn's Disease | Recruiting | 2025-07-14 | 2027-12-01 | ClinicalTrials.gov |
| NCT07073079 | A Study to Assess the Effectiveness of Second-Line Therapy of Upadacitinib and … | — | Crohn's Disease | Recruiting | 2025-07-14 | 2027-12-01 | ClinicalTrials.gov |
| NCT07073079 | A Study to Assess the Effectiveness of Second-Line Therapy of Upadacitinib and … | — | Crohn's Disease | Recruiting | 2025-07-14 | 2027-12-01 | ClinicalTrials.gov |
| NCT06972056 | Comparative Effectiveness of Migraine Preventive Medications: The APT Compariso… | Phase4 | Migraine | Recruiting | 2025-07-09 | 2029-12-01 | ClinicalTrials.gov |
| NCT06972056 | Comparative Effectiveness of Migraine Preventive Medications: The APT Compariso… | Phase4 | Migraine | Recruiting | 2025-07-09 | 2029-12-01 | ClinicalTrials.gov |
| NCT06972056 | Comparative Effectiveness of Migraine Preventive Medications: The APT Compariso… | Phase4 | Migraine | Recruiting | 2025-07-09 | 2029-12-01 | ClinicalTrials.gov |
| NCT06972056 | Comparative Effectiveness of Migraine Preventive Medications: The APT Compariso… | Phase4 | Migraine | Recruiting | 2025-07-09 | 2029-12-01 | ClinicalTrials.gov |
| NCT06892522 | A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult … | Phase1 | Multiple Myeloma | Recruiting | 2025-06-30 | 2035-12-01 | ClinicalTrials.gov |
| NCT06892522 | A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult … | Phase1 | Multiple Myeloma | Recruiting | 2025-06-30 | 2035-12-01 | ClinicalTrials.gov |
| NCT06892522 | A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult … | Phase1 | Multiple Myeloma | Recruiting | 2025-06-30 | 2035-12-01 | ClinicalTrials.gov |
| NCT06892522 | A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult … | Phase1 | Multiple Myeloma | Recruiting | 2025-06-30 | 2035-12-01 | ClinicalTrials.gov |
| NCT06972446 | A Study to Evaluate Different Targeted Therapies for Patients With Rheumatoid A… | Phase2 | Rheumatoid Arthritis | Recruiting | 2025-06-20 | 2027-11-01 | ClinicalTrials.gov |
| NCT06972446 | A Study to Evaluate Different Targeted Therapies for Patients With Rheumatoid A… | Phase2 | Rheumatoid Arthritis | Recruiting | 2025-06-20 | 2027-11-01 | ClinicalTrials.gov |
| NCT06972446 | A Study to Evaluate Different Targeted Therapies for Patients With Rheumatoid A… | Phase2 | Rheumatoid Arthritis | Recruiting | 2025-06-20 | 2027-11-01 | ClinicalTrials.gov |
| NCT06972446 | A Study to Evaluate Different Targeted Therapies for Patients With Rheumatoid A… | Phase2 | Rheumatoid Arthritis | Recruiting | 2025-06-20 | 2027-11-01 | ClinicalTrials.gov |
| NCT07023302 | A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adu… | Phase3 | Alopecia Areata | Recruiting | 2025-06-19 | 2029-02-01 | ClinicalTrials.gov |
| NCT07023302 | A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adu… | Phase3 | Alopecia Areata | Recruiting | 2025-06-19 | 2029-02-01 | ClinicalTrials.gov |
| NCT07023302 | A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adu… | Phase3 | Alopecia Areata | Recruiting | 2025-06-19 | 2029-02-01 | ClinicalTrials.gov |
| NCT07023302 | A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adu… | Phase3 | Alopecia Areata | Recruiting | 2025-06-19 | 2029-02-01 | ClinicalTrials.gov |
| NCT06880744 | A Study to Assess the Change in Disease Activity in Adult Participants With Mod… | Phase3 | Ulcerative Colitis | Active_Not_Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT06880744 | A Study to Assess the Change in Disease Activity in Adult Participants With Mod… | Phase3 | Ulcerative Colitis | Active_Not_Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT06880744 | A Study to Assess the Change in Disease Activity in Adult Participants With Mod… | Phase3 | Ulcerative Colitis | Active_Not_Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT06880744 | A Study to Assess the Change in Disease Activity in Adult Participants With Mod… | Phase3 | Ulcerative Colitis | Active_Not_Recruiting | 2025-06-17 | 2028-09-01 | ClinicalTrials.gov |
| NCT06672705 | Epcoritamab for the Treatment of Relapsed or Refractory Post Transplant Lymphop… | Phase1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | Recruiting | 2025-06-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT06672705 | Epcoritamab for the Treatment of Relapsed or Refractory Post Transplant Lymphop… | Phase1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | Recruiting | 2025-06-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT06672705 | Epcoritamab for the Treatment of Relapsed or Refractory Post Transplant Lymphop… | Phase1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | Recruiting | 2025-06-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT06672705 | Epcoritamab for the Treatment of Relapsed or Refractory Post Transplant Lymphop… | Phase1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | Recruiting | 2025-06-16 | 2026-12-31 | ClinicalTrials.gov |
| NCT07007091 | A Study to Assess the Relative Bioavailability of Risankizumab Following Subcut… | Phase1 | Healthy Volunteers | Completed | 2025-06-12 | 2026-01-15 | ClinicalTrials.gov |
| NCT07007091 | A Study to Assess the Relative Bioavailability of Risankizumab Following Subcut… | Phase1 | Healthy Volunteers | Completed | 2025-06-12 | 2026-01-15 | ClinicalTrials.gov |
| NCT07007091 | A Study to Assess the Relative Bioavailability of Risankizumab Following Subcut… | Phase1 | Healthy Volunteers | Completed | 2025-06-12 | 2026-01-15 | ClinicalTrials.gov |
| NCT07007091 | A Study to Assess the Relative Bioavailability of Risankizumab Following Subcut… | Phase1 | Healthy Volunteers | Completed | 2025-06-12 | 2026-01-15 | ClinicalTrials.gov |
| NCT06902558 | A Study to Assess Adverse Events and Effectiveness of IntraVenous Infusions of … | Phase2 | Autosomal Dominant Polycystic Kidney Disease | Recruiting | 2025-06-09 | 2029-08-01 | ClinicalTrials.gov |
| NCT06902558 | A Study to Assess Adverse Events and Effectiveness of IntraVenous Infusions of … | Phase2 | Autosomal Dominant Polycystic Kidney Disease | Recruiting | 2025-06-09 | 2029-08-01 | ClinicalTrials.gov |
| NCT06902558 | A Study to Assess Adverse Events and Effectiveness of IntraVenous Infusions of … | Phase2 | Autosomal Dominant Polycystic Kidney Disease | Recruiting | 2025-06-09 | 2029-08-01 | ClinicalTrials.gov |
| NCT06902558 | A Study to Assess Adverse Events and Effectiveness of IntraVenous Infusions of … | Phase2 | Autosomal Dominant Polycystic Kidney Disease | Recruiting | 2025-06-09 | 2029-08-01 | ClinicalTrials.gov |
| NCT06965374 | Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes… | — | Parkinson Disease | Recruiting | 2025-06-04 | 2027-06-01 | ClinicalTrials.gov |
| NCT06965374 | Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes… | — | Parkinson Disease | Recruiting | 2025-06-04 | 2027-06-01 | ClinicalTrials.gov |
| NCT06965374 | Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes… | — | Parkinson Disease | Recruiting | 2025-06-04 | 2027-06-01 | ClinicalTrials.gov |
| NCT06965374 | Real-World Study of Foslevodopa/Foscarbidopa to Assess Quality of Life Outcomes… | — | Parkinson Disease | Recruiting | 2025-06-04 | 2027-06-01 | ClinicalTrials.gov |
| NCT06682988 | A Study to Assess Adverse Events and Change in Disease Activity in Participants… | Phase2 | Advanced High-Grade Epithelial Ovarian Cancer | Recruiting | 2025-05-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT06682988 | A Study to Assess Adverse Events and Change in Disease Activity in Participants… | Phase2 | Advanced High-Grade Epithelial Ovarian Cancer | Recruiting | 2025-05-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT06682988 | A Study to Assess Adverse Events and Change in Disease Activity in Participants… | Phase2 | Advanced High-Grade Epithelial Ovarian Cancer | Recruiting | 2025-05-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT06682988 | A Study to Assess Adverse Events and Change in Disease Activity in Participants… | Phase2 | Advanced High-Grade Epithelial Ovarian Cancer | Recruiting | 2025-05-28 | 2028-04-01 | ClinicalTrials.gov |
| NCT07032597 | A Study to Assess Safety and Effectiveness of HArmonyCa Lidocaine Injectable Ge… | Phase3 | Mid Face Volume Deficit | Active_Not_Recruiting | 2025-05-26 | 2026-10-01 | ClinicalTrials.gov |
| NCT07032597 | A Study to Assess Safety and Effectiveness of HArmonyCa Lidocaine Injectable Ge… | Phase3 | Mid Face Volume Deficit | Active_Not_Recruiting | 2025-05-26 | 2026-10-01 | ClinicalTrials.gov |
| NCT07032597 | A Study to Assess Safety and Effectiveness of HArmonyCa Lidocaine Injectable Ge… | Phase3 | Mid Face Volume Deficit | Active_Not_Recruiting | 2025-05-26 | 2026-10-01 | ClinicalTrials.gov |
| NCT07032597 | A Study to Assess Safety and Effectiveness of HArmonyCa Lidocaine Injectable Ge… | Phase3 | Mid Face Volume Deficit | Active_Not_Recruiting | 2025-05-26 | 2026-10-01 | ClinicalTrials.gov |
| NCT06946524 | A Study to Assess the Bioavailability of Risankizumab Following Subcutaneous Ad… | Phase1 | Healthy Volunteers | Completed | 2025-05-08 | 2025-11-25 | ClinicalTrials.gov |
| NCT06946524 | A Study to Assess the Bioavailability of Risankizumab Following Subcutaneous Ad… | Phase1 | Healthy Volunteers | Completed | 2025-05-08 | 2025-11-25 | ClinicalTrials.gov |
| NCT06946524 | A Study to Assess the Bioavailability of Risankizumab Following Subcutaneous Ad… | Phase1 | Healthy Volunteers | Completed | 2025-05-08 | 2025-11-25 | ClinicalTrials.gov |
| NCT06946524 | A Study to Assess the Bioavailability of Risankizumab Following Subcutaneous Ad… | Phase1 | Healthy Volunteers | Completed | 2025-05-08 | 2025-11-25 | ClinicalTrials.gov |
| NCT06916507 | Study to Assess Real Life Effectiveness of Foslevodopa/Foscarbidopa in Adult Ge… | — | Parkinson's Disease | Recruiting | 2025-05-06 | 2027-09-01 | ClinicalTrials.gov |
| NCT06916507 | Study to Assess Real Life Effectiveness of Foslevodopa/Foscarbidopa in Adult Ge… | — | Parkinson's Disease | Recruiting | 2025-05-06 | 2027-09-01 | ClinicalTrials.gov |
| NCT06916507 | Study to Assess Real Life Effectiveness of Foslevodopa/Foscarbidopa in Adult Ge… | — | Parkinson's Disease | Recruiting | 2025-05-06 | 2027-09-01 | ClinicalTrials.gov |
| NCT06916507 | Study to Assess Real Life Effectiveness of Foslevodopa/Foscarbidopa in Adult Ge… | — | Parkinson's Disease | Recruiting | 2025-05-06 | 2027-09-01 | ClinicalTrials.gov |
| NCT06846320 | Study to Assess Adverse Events and Change in Disease Activity When Oral ABBV-93… | Phase2 | Generalized Anxiety Disorder (GAD) | Recruiting | 2025-04-29 | 2026-11-01 | ClinicalTrials.gov |
| NCT06846320 | Study to Assess Adverse Events and Change in Disease Activity When Oral ABBV-93… | Phase2 | Generalized Anxiety Disorder (GAD) | Recruiting | 2025-04-29 | 2026-11-01 | ClinicalTrials.gov |
| NCT06846320 | Study to Assess Adverse Events and Change in Disease Activity When Oral ABBV-93… | Phase2 | Generalized Anxiety Disorder (GAD) | Recruiting | 2025-04-29 | 2026-11-01 | ClinicalTrials.gov |
| NCT06846320 | Study to Assess Adverse Events and Change in Disease Activity When Oral ABBV-93… | Phase2 | Generalized Anxiety Disorder (GAD) | Recruiting | 2025-04-29 | 2026-11-01 | ClinicalTrials.gov |
| NCT06820463 | A Study to Evaluate the Adverse Events, and Efficacy of Intravenous (IV) of Tel… | Phase2 | Metastatic Colorectal Cancer | Recruiting | 2025-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT06820463 | A Study to Evaluate the Adverse Events, and Efficacy of Intravenous (IV) of Tel… | Phase2 | Metastatic Colorectal Cancer | Recruiting | 2025-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT06820463 | A Study to Evaluate the Adverse Events, and Efficacy of Intravenous (IV) of Tel… | Phase2 | Metastatic Colorectal Cancer | Recruiting | 2025-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT06820463 | A Study to Evaluate the Adverse Events, and Efficacy of Intravenous (IV) of Tel… | Phase2 | Metastatic Colorectal Cancer | Recruiting | 2025-04-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT06937619 | A Study to Assess the Relative Bioavailability of Risankizumab Following Subcut… | Phase1 | Healthy Volunteer | Completed | 2025-04-21 | 2025-11-10 | ClinicalTrials.gov |
| NCT06937619 | A Study to Assess the Relative Bioavailability of Risankizumab Following Subcut… | Phase1 | Healthy Volunteer | Completed | 2025-04-21 | 2025-11-10 | ClinicalTrials.gov |
| NCT06937619 | A Study to Assess the Relative Bioavailability of Risankizumab Following Subcut… | Phase1 | Healthy Volunteer | Completed | 2025-04-21 | 2025-11-10 | ClinicalTrials.gov |
| NCT06937619 | A Study to Assess the Relative Bioavailability of Risankizumab Following Subcut… | Phase1 | Healthy Volunteer | Completed | 2025-04-21 | 2025-11-10 | ClinicalTrials.gov |
| NCT07566130 | A Study to Assess Adverse Events, Tolerability and How Single and Ascending Ora… | Phase1 | Healthy Volunteers | Completed | 2025-04-18 | 2026-05-07 | ClinicalTrials.gov |
| NCT07566130 | A Study to Assess Adverse Events, Tolerability and How Single and Ascending Ora… | Phase1 | Healthy Volunteers | Completed | 2025-04-18 | 2026-05-07 | ClinicalTrials.gov |
| NCT07566130 | A Study to Assess Adverse Events, Tolerability and How Single and Ascending Ora… | Phase1 | Healthy Volunteers | Completed | 2025-04-18 | 2026-05-07 | ClinicalTrials.gov |
| NCT07566130 | A Study to Assess Adverse Events, Tolerability and How Single and Ascending Ora… | Phase1 | Healthy Volunteers | Completed | 2025-04-18 | 2026-05-07 | ClinicalTrials.gov |
| NCT06660693 | Comparison of Medical RESCUE Strategies for Patients With Steroid-refractory Ac… | Phase3 | Colitis, Ulcerative | Recruiting | 2025-04-16 | 2027-09-01 | ClinicalTrials.gov |
| NCT06660693 | Comparison of Medical RESCUE Strategies for Patients With Steroid-refractory Ac… | Phase3 | Colitis, Ulcerative | Recruiting | 2025-04-16 | 2027-09-01 | ClinicalTrials.gov |
| NCT06660693 | Comparison of Medical RESCUE Strategies for Patients With Steroid-refractory Ac… | Phase3 | Colitis, Ulcerative | Recruiting | 2025-04-16 | 2027-09-01 | ClinicalTrials.gov |
| NCT06660693 | Comparison of Medical RESCUE Strategies for Patients With Steroid-refractory Ac… | Phase3 | Colitis, Ulcerative | Recruiting | 2025-04-16 | 2027-09-01 | ClinicalTrials.gov |
| NCT06937034 | Study on Practical ExperienceS of Treatment With Foslevodopa/foScaRbidopa in Ad… | — | Parkinson's Disease | Recruiting | 2025-04-14 | 2025-12-01 | ClinicalTrials.gov |
| NCT06858813 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenousl… | Phase1 | Hepatocellular Cancer | Recruiting | 2025-04-14 | 2030-09-01 | ClinicalTrials.gov |
| NCT06858813 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenousl… | Phase1 | Hepatocellular Cancer | Recruiting | 2025-04-14 | 2030-09-01 | ClinicalTrials.gov |
| NCT06937034 | Study on Practical ExperienceS of Treatment With Foslevodopa/foScaRbidopa in Ad… | — | Parkinson's Disease | Recruiting | 2025-04-14 | 2025-12-01 | ClinicalTrials.gov |
| NCT06937034 | Study on Practical ExperienceS of Treatment With Foslevodopa/foScaRbidopa in Ad… | — | Parkinson's Disease | Recruiting | 2025-04-14 | 2025-12-01 | ClinicalTrials.gov |
| NCT06858813 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenousl… | Phase1 | Hepatocellular Cancer | Recruiting | 2025-04-14 | 2030-09-01 | ClinicalTrials.gov |
| NCT06858813 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenousl… | Phase1 | Hepatocellular Cancer | Recruiting | 2025-04-14 | 2030-09-01 | ClinicalTrials.gov |
| NCT06937034 | Study on Practical ExperienceS of Treatment With Foslevodopa/foScaRbidopa in Ad… | — | Parkinson's Disease | Recruiting | 2025-04-14 | 2025-12-01 | ClinicalTrials.gov |
| NCT06865105 | Study of Targeted Therapies for the Treatment of Adult Participants With Active… | Phase2 | Psoriatic Arthritis | Recruiting | 2025-04-11 | 2028-01-01 | ClinicalTrials.gov |
| NCT06865105 | Study of Targeted Therapies for the Treatment of Adult Participants With Active… | Phase2 | Psoriatic Arthritis | Recruiting | 2025-04-11 | 2028-01-01 | ClinicalTrials.gov |
| NCT06865105 | Study of Targeted Therapies for the Treatment of Adult Participants With Active… | Phase2 | Psoriatic Arthritis | Recruiting | 2025-04-11 | 2028-01-01 | ClinicalTrials.gov |
| NCT06865105 | Study of Targeted Therapies for the Treatment of Adult Participants With Active… | Phase2 | Psoriatic Arthritis | Recruiting | 2025-04-11 | 2028-01-01 | ClinicalTrials.gov |
| NCT06838845 | An Observational Study to Evaluate Effectiveness and Safety of Upadacitinib in … | — | Ulcerative Colitis | Recruiting | 2025-04-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT06838845 | An Observational Study to Evaluate Effectiveness and Safety of Upadacitinib in … | — | Ulcerative Colitis | Recruiting | 2025-04-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT06838845 | An Observational Study to Evaluate Effectiveness and Safety of Upadacitinib in … | — | Ulcerative Colitis | Recruiting | 2025-04-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT06838845 | An Observational Study to Evaluate Effectiveness and Safety of Upadacitinib in … | — | Ulcerative Colitis | Recruiting | 2025-04-09 | 2026-12-01 | ClinicalTrials.gov |
| NCT06895343 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenic… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-04-03 | 2026-11-01 | ClinicalTrials.gov |
| NCT06895343 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenic… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-04-03 | 2026-11-01 | ClinicalTrials.gov |
| NCT06895343 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenic… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-04-03 | 2026-11-01 | ClinicalTrials.gov |
| NCT06895343 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenic… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-04-03 | 2026-11-01 | ClinicalTrials.gov |
| NCT06536049 | Epcoritamab Plus Ibrutinib for the Treatment of Relapsed or Refractory Aggressi… | Phase1 | Recurrent Diffuse Large B-Cell Lymphoma | Recruiting | 2025-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT06536049 | Epcoritamab Plus Ibrutinib for the Treatment of Relapsed or Refractory Aggressi… | Phase1 | Recurrent Diffuse Large B-Cell Lymphoma | Recruiting | 2025-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT06536049 | Epcoritamab Plus Ibrutinib for the Treatment of Relapsed or Refractory Aggressi… | Phase1 | Recurrent Diffuse Large B-Cell Lymphoma | Recruiting | 2025-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT06536049 | Epcoritamab Plus Ibrutinib for the Treatment of Relapsed or Refractory Aggressi… | Phase1 | Recurrent Diffuse Large B-Cell Lymphoma | Recruiting | 2025-04-02 | 2027-10-31 | ClinicalTrials.gov |
| NCT06830759 | Real-World Study to Assess Subcutaneous Epcoritamab in Adult Participants With … | — | Diffuse Large B-cell Lymphoma | Recruiting | 2025-03-28 | 2031-09-01 | ClinicalTrials.gov |
| NCT06830759 | Real-World Study to Assess Subcutaneous Epcoritamab in Adult Participants With … | — | Diffuse Large B-cell Lymphoma | Recruiting | 2025-03-28 | 2031-09-01 | ClinicalTrials.gov |
| NCT06830759 | Real-World Study to Assess Subcutaneous Epcoritamab in Adult Participants With … | — | Diffuse Large B-cell Lymphoma | Recruiting | 2025-03-28 | 2031-09-01 | ClinicalTrials.gov |
| NCT06830759 | Real-World Study to Assess Subcutaneous Epcoritamab in Adult Participants With … | — | Diffuse Large B-cell Lymphoma | Recruiting | 2025-03-28 | 2031-09-01 | ClinicalTrials.gov |
| NCT06895356 | A Study to Assess the Relative Bioavailability of Oral Tavapadon in Healthy Adu… | Phase1 | Healthy Volunteer | Completed | 2025-03-26 | 2025-06-16 | ClinicalTrials.gov |
| NCT06895356 | A Study to Assess the Relative Bioavailability of Oral Tavapadon in Healthy Adu… | Phase1 | Healthy Volunteer | Completed | 2025-03-26 | 2025-06-16 | ClinicalTrials.gov |
| NCT06895356 | A Study to Assess the Relative Bioavailability of Oral Tavapadon in Healthy Adu… | Phase1 | Healthy Volunteer | Completed | 2025-03-26 | 2025-06-16 | ClinicalTrials.gov |
| NCT06895356 | A Study to Assess the Relative Bioavailability of Oral Tavapadon in Healthy Adu… | Phase1 | Healthy Volunteer | Completed | 2025-03-26 | 2025-06-16 | ClinicalTrials.gov |
| NCT06887010 | A Study to Assess How Food Affects the Movement of Oral ABBV-101 Through the Bo… | Phase1 | Healthy Volunteer | Completed | 2025-03-25 | 2025-09-16 | ClinicalTrials.gov |
| NCT06887010 | A Study to Assess How Food Affects the Movement of Oral ABBV-101 Through the Bo… | Phase1 | Healthy Volunteer | Completed | 2025-03-25 | 2025-09-16 | ClinicalTrials.gov |
| NCT06887010 | A Study to Assess How Food Affects the Movement of Oral ABBV-101 Through the Bo… | Phase1 | Healthy Volunteer | Completed | 2025-03-25 | 2025-09-16 | ClinicalTrials.gov |
| NCT06887010 | A Study to Assess How Food Affects the Movement of Oral ABBV-101 Through the Bo… | Phase1 | Healthy Volunteer | Completed | 2025-03-25 | 2025-09-16 | ClinicalTrials.gov |
| NCT05099471 | Efficacy of Venetoclax in Combination With Rituximab in Waldenström's Macroglob… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2025-03-21 | 2033-03-01 | ClinicalTrials.gov |
| NCT05099471 | Efficacy of Venetoclax in Combination With Rituximab in Waldenström's Macroglob… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2025-03-21 | 2033-03-01 | ClinicalTrials.gov |
| NCT05099471 | Efficacy of Venetoclax in Combination With Rituximab in Waldenström's Macroglob… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2025-03-21 | 2033-03-01 | ClinicalTrials.gov |
| NCT05099471 | Efficacy of Venetoclax in Combination With Rituximab in Waldenström's Macroglob… | Phase2 | Waldenstrom Macroglobulinemia | Recruiting | 2025-03-21 | 2033-03-01 | ClinicalTrials.gov |
| NCT06772623 | Study to Evaluate Adverse Events and Efficacy of Intravenous (IV) Telisotuzumab… | Phase1 | Non Small Cell Lung Carcinoma | Recruiting | 2025-03-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06772623 | Study to Evaluate Adverse Events and Efficacy of Intravenous (IV) Telisotuzumab… | Phase1 | Non Small Cell Lung Carcinoma | Recruiting | 2025-03-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06772623 | Study to Evaluate Adverse Events and Efficacy of Intravenous (IV) Telisotuzumab… | Phase1 | Non Small Cell Lung Carcinoma | Recruiting | 2025-03-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06772623 | Study to Evaluate Adverse Events and Efficacy of Intravenous (IV) Telisotuzumab… | Phase1 | Non Small Cell Lung Carcinoma | Recruiting | 2025-03-06 | 2027-11-01 | ClinicalTrials.gov |
| NCT06764706 | Study to Assess Change in Disease Activity of Risankizumab Treatment in Adult P… | — | Ulcerative Colitis | Recruiting | 2025-02-27 | 2028-07-01 | ClinicalTrials.gov |
| NCT06764706 | Study to Assess Change in Disease Activity of Risankizumab Treatment in Adult P… | — | Ulcerative Colitis | Recruiting | 2025-02-27 | 2028-07-01 | ClinicalTrials.gov |
| NCT06764706 | Study to Assess Change in Disease Activity of Risankizumab Treatment in Adult P… | — | Ulcerative Colitis | Recruiting | 2025-02-27 | 2028-07-01 | ClinicalTrials.gov |
| NCT06764706 | Study to Assess Change in Disease Activity of Risankizumab Treatment in Adult P… | — | Ulcerative Colitis | Recruiting | 2025-02-27 | 2028-07-01 | ClinicalTrials.gov |
| NCT06849791 | A Study to Assess the Relative Bioavailability of Oral ABBV-932 in Healthy Adul… | Phase1 | Healthy Volunteer | Completed | 2025-02-26 | 2026-05-08 | ClinicalTrials.gov |
| NCT06849791 | A Study to Assess the Relative Bioavailability of Oral ABBV-932 in Healthy Adul… | Phase1 | Healthy Volunteer | Completed | 2025-02-26 | 2026-05-08 | ClinicalTrials.gov |
| NCT06849791 | A Study to Assess the Relative Bioavailability of Oral ABBV-932 in Healthy Adul… | Phase1 | Healthy Volunteer | Completed | 2025-02-26 | 2026-05-08 | ClinicalTrials.gov |
| NCT06849791 | A Study to Assess the Relative Bioavailability of Oral ABBV-932 in Healthy Adul… | Phase1 | Healthy Volunteer | Completed | 2025-02-26 | 2026-05-08 | ClinicalTrials.gov |
| NCT06834789 | A Study to Assess the Adverse Events of Intramuscular Injections of AGN-151586 … | Phase1 | Glabellar Lines | Completed | 2025-02-18 | 2025-11-03 | ClinicalTrials.gov |
| NCT06834789 | A Study to Assess the Adverse Events of Intramuscular Injections of AGN-151586 … | Phase1 | Glabellar Lines | Completed | 2025-02-18 | 2025-11-03 | ClinicalTrials.gov |
| NCT06834789 | A Study to Assess the Adverse Events of Intramuscular Injections of AGN-151586 … | Phase1 | Glabellar Lines | Completed | 2025-02-18 | 2025-11-03 | ClinicalTrials.gov |
| NCT06834789 | A Study to Assess the Adverse Events of Intramuscular Injections of AGN-151586 … | Phase1 | Glabellar Lines | Completed | 2025-02-18 | 2025-11-03 | ClinicalTrials.gov |
| NCT06810505 | A Study of Oral Atogepant Tablets to Assess Adverse Events and Change in Diseas… | Phase3 | Chronic Migraine | Recruiting | 2025-02-13 | 2031-03-01 | ClinicalTrials.gov |
| NCT06810505 | A Study of Oral Atogepant Tablets to Assess Adverse Events and Change in Diseas… | Phase3 | Chronic Migraine | Recruiting | 2025-02-13 | 2031-03-01 | ClinicalTrials.gov |
| NCT06810505 | A Study of Oral Atogepant Tablets to Assess Adverse Events and Change in Diseas… | Phase3 | Chronic Migraine | Recruiting | 2025-02-13 | 2031-03-01 | ClinicalTrials.gov |
| NCT06810505 | A Study of Oral Atogepant Tablets to Assess Adverse Events and Change in Diseas… | Phase3 | Chronic Migraine | Recruiting | 2025-02-13 | 2031-03-01 | ClinicalTrials.gov |
| NCT06692881 | Study to Assess Function and Satisfaction of Oral Ubrogepant in Adult Participa… | — | Migraine | Completed | 2025-02-12 | 2026-06-01 | ClinicalTrials.gov |
| NCT06692881 | Study to Assess Function and Satisfaction of Oral Ubrogepant in Adult Participa… | — | Migraine | Completed | 2025-02-12 | 2026-06-01 | ClinicalTrials.gov |
| NCT06692881 | Study to Assess Function and Satisfaction of Oral Ubrogepant in Adult Participa… | — | Migraine | Completed | 2025-02-12 | 2026-06-01 | ClinicalTrials.gov |
| NCT06692881 | Study to Assess Function and Satisfaction of Oral Ubrogepant in Adult Participa… | — | Migraine | Completed | 2025-02-12 | 2026-06-01 | ClinicalTrials.gov |
| NCT06822738 | A Study to Assess Adverse Events and Effectiveness of Gel Stent (XEN63) Implant… | Phase3 | Primary Open Angle Glaucoma | Recruiting | 2025-02-11 | 2028-11-01 | ClinicalTrials.gov |
| NCT06822738 | A Study to Assess Adverse Events and Effectiveness of Gel Stent (XEN63) Implant… | Phase3 | Primary Open Angle Glaucoma | Recruiting | 2025-02-11 | 2028-11-01 | ClinicalTrials.gov |
| NCT06822738 | A Study to Assess Adverse Events and Effectiveness of Gel Stent (XEN63) Implant… | Phase3 | Primary Open Angle Glaucoma | Recruiting | 2025-02-11 | 2028-11-01 | ClinicalTrials.gov |
| NCT06822738 | A Study to Assess Adverse Events and Effectiveness of Gel Stent (XEN63) Implant… | Phase3 | Primary Open Angle Glaucoma | Recruiting | 2025-02-11 | 2028-11-01 | ClinicalTrials.gov |
| NCT06806293 | Study of Oral Atogepant to Assess Adverse Events and Change in Disease Activity… | Phase3 | Menstrual Migraine (MM) | Active_Not_Recruiting | 2025-02-10 | 2027-07-01 | ClinicalTrials.gov |
| NCT06806293 | Study of Oral Atogepant to Assess Adverse Events and Change in Disease Activity… | Phase3 | Menstrual Migraine (MM) | Active_Not_Recruiting | 2025-02-10 | 2027-07-01 | ClinicalTrials.gov |
| NCT06806293 | Study of Oral Atogepant to Assess Adverse Events and Change in Disease Activity… | Phase3 | Menstrual Migraine (MM) | Active_Not_Recruiting | 2025-02-10 | 2027-07-01 | ClinicalTrials.gov |
| NCT06806293 | Study of Oral Atogepant to Assess Adverse Events and Change in Disease Activity… | Phase3 | Menstrual Migraine (MM) | Active_Not_Recruiting | 2025-02-10 | 2027-07-01 | ClinicalTrials.gov |
| NCT06764693 | An Ex-US Study to Assess Treatment Persistence With Risankizumab in Adult Parti… | — | Psoriatic Arthritis | Recruiting | 2025-01-31 | 2029-02-01 | ClinicalTrials.gov |
| NCT06764693 | An Ex-US Study to Assess Treatment Persistence With Risankizumab in Adult Parti… | — | Psoriatic Arthritis | Recruiting | 2025-01-31 | 2029-02-01 | ClinicalTrials.gov |
| NCT06764693 | An Ex-US Study to Assess Treatment Persistence With Risankizumab in Adult Parti… | — | Psoriatic Arthritis | Recruiting | 2025-01-31 | 2029-02-01 | ClinicalTrials.gov |
| NCT06764693 | An Ex-US Study to Assess Treatment Persistence With Risankizumab in Adult Parti… | — | Psoriatic Arthritis | Recruiting | 2025-01-31 | 2029-02-01 | ClinicalTrials.gov |
| NCT06291220 | A Study Assessing Adverse Event and How Oral ABBV-453 Moves Through the Body in… | Phase1 | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2025-01-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT06291220 | A Study Assessing Adverse Event and How Oral ABBV-453 Moves Through the Body in… | Phase1 | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2025-01-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT06291220 | A Study Assessing Adverse Event and How Oral ABBV-453 Moves Through the Body in… | Phase1 | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2025-01-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT06291220 | A Study Assessing Adverse Event and How Oral ABBV-453 Moves Through the Body in… | Phase1 | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2025-01-27 | 2027-07-01 | ClinicalTrials.gov |
| NCT06774313 | A Study to Assess the Adverse Events and How Subcutaneous (SC) Injections and I… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-01-22 | 2026-04-01 | ClinicalTrials.gov |
| NCT06774313 | A Study to Assess the Adverse Events and How Subcutaneous (SC) Injections and I… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-01-22 | 2026-04-01 | ClinicalTrials.gov |
| NCT06794866 | A Study to Assess Adverse Events and Effectiveness of OnabotulinumtoxinA Intram… | Phase3 | Forehead Lines | Active_Not_Recruiting | 2025-01-22 | 2026-04-01 | ClinicalTrials.gov |
| NCT06774313 | A Study to Assess the Adverse Events and How Subcutaneous (SC) Injections and I… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-01-22 | 2026-04-01 | ClinicalTrials.gov |
| NCT06794866 | A Study to Assess Adverse Events and Effectiveness of OnabotulinumtoxinA Intram… | Phase3 | Forehead Lines | Active_Not_Recruiting | 2025-01-22 | 2026-04-01 | ClinicalTrials.gov |
| NCT06774313 | A Study to Assess the Adverse Events and How Subcutaneous (SC) Injections and I… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2025-01-22 | 2026-04-01 | ClinicalTrials.gov |
| NCT06794866 | A Study to Assess Adverse Events and Effectiveness of OnabotulinumtoxinA Intram… | Phase3 | Forehead Lines | Active_Not_Recruiting | 2025-01-22 | 2026-04-01 | ClinicalTrials.gov |
| NCT06794866 | A Study to Assess Adverse Events and Effectiveness of OnabotulinumtoxinA Intram… | Phase3 | Forehead Lines | Active_Not_Recruiting | 2025-01-22 | 2026-04-01 | ClinicalTrials.gov |
| NCT06568939 | A Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzum… | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2025-01-20 | 2028-02-01 | ClinicalTrials.gov |
| NCT06568939 | A Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzum… | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2025-01-20 | 2028-02-01 | ClinicalTrials.gov |
| NCT06568939 | A Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzum… | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2025-01-20 | 2028-02-01 | ClinicalTrials.gov |
| NCT06632951 | Study to Evaluate Adverse Events and Change in Disease Activity When Intravenou… | Phase2 | Urothelial Carcinoma | Active_Not_Recruiting | 2025-01-20 | 2028-08-01 | ClinicalTrials.gov |
| NCT06568939 | A Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzum… | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2025-01-20 | 2028-02-01 | ClinicalTrials.gov |
| NCT06632951 | Study to Evaluate Adverse Events and Change in Disease Activity When Intravenou… | Phase2 | Urothelial Carcinoma | Active_Not_Recruiting | 2025-01-20 | 2028-08-01 | ClinicalTrials.gov |
| NCT06632951 | Study to Evaluate Adverse Events and Change in Disease Activity When Intravenou… | Phase2 | Urothelial Carcinoma | Active_Not_Recruiting | 2025-01-20 | 2028-08-01 | ClinicalTrials.gov |
| NCT06632951 | Study to Evaluate Adverse Events and Change in Disease Activity When Intravenou… | Phase2 | Urothelial Carcinoma | Active_Not_Recruiting | 2025-01-20 | 2028-08-01 | ClinicalTrials.gov |
| NCT06667687 | Study to Evaluate Adverse Events, Change in Disease Activity, and How Intraveno… | Phase1 | Non-Hodgkin's Lymphoma | Recruiting | 2025-01-16 | 2031-11-01 | ClinicalTrials.gov |
| NCT06783621 | A Study to Evaluate Patient Satisfaction With the Overall Face and Neck Appeara… | Phase4 | Facial Contouring | Completed | 2025-01-16 | 2026-03-20 | ClinicalTrials.gov |
| NCT06783621 | A Study to Evaluate Patient Satisfaction With the Overall Face and Neck Appeara… | Phase4 | Facial Contouring | Completed | 2025-01-16 | 2026-03-20 | ClinicalTrials.gov |
| NCT06783621 | A Study to Evaluate Patient Satisfaction With the Overall Face and Neck Appeara… | Phase4 | Facial Contouring | Completed | 2025-01-16 | 2026-03-20 | ClinicalTrials.gov |
| NCT06667687 | Study to Evaluate Adverse Events, Change in Disease Activity, and How Intraveno… | Phase1 | Non-Hodgkin's Lymphoma | Recruiting | 2025-01-16 | 2031-11-01 | ClinicalTrials.gov |
| NCT06667687 | Study to Evaluate Adverse Events, Change in Disease Activity, and How Intraveno… | Phase1 | Non-Hodgkin's Lymphoma | Recruiting | 2025-01-16 | 2031-11-01 | ClinicalTrials.gov |
| NCT06667687 | Study to Evaluate Adverse Events, Change in Disease Activity, and How Intraveno… | Phase1 | Non-Hodgkin's Lymphoma | Recruiting | 2025-01-16 | 2031-11-01 | ClinicalTrials.gov |
| NCT06783621 | A Study to Evaluate Patient Satisfaction With the Overall Face and Neck Appeara… | Phase4 | Facial Contouring | Completed | 2025-01-16 | 2026-03-20 | ClinicalTrials.gov |
| NCT06504459 | Venetoclax in Combination With Cladribine and Cytarabine Alternating With Azaci… | Phase2 | Acute Monocytic Leukemia | Recruiting | 2025-01-03 | 2028-05-01 | ClinicalTrials.gov |
| NCT06504459 | Venetoclax in Combination With Cladribine and Cytarabine Alternating With Azaci… | Phase2 | Acute Monocytic Leukemia | Recruiting | 2025-01-03 | 2028-05-01 | ClinicalTrials.gov |
| NCT06504459 | Venetoclax in Combination With Cladribine and Cytarabine Alternating With Azaci… | Phase2 | Acute Monocytic Leukemia | Recruiting | 2025-01-03 | 2028-05-01 | ClinicalTrials.gov |
| NCT06504459 | Venetoclax in Combination With Cladribine and Cytarabine Alternating With Azaci… | Phase2 | Acute Monocytic Leukemia | Recruiting | 2025-01-03 | 2028-05-01 | ClinicalTrials.gov |
| NCT06390319 | Adding Dasatinib Or Venetoclax To Improve Responses In Children With Newly Diag… | Phase2 | T-cell Acute Lymphoblastic Leukemia | Recruiting | 2024-12-27 | 2033-12-01 | ClinicalTrials.gov |
| NCT06390319 | Adding Dasatinib Or Venetoclax To Improve Responses In Children With Newly Diag… | Phase2 | T-cell Acute Lymphoblastic Leukemia | Recruiting | 2024-12-27 | 2033-12-01 | ClinicalTrials.gov |
| NCT06390319 | Adding Dasatinib Or Venetoclax To Improve Responses In Children With Newly Diag… | Phase2 | T-cell Acute Lymphoblastic Leukemia | Recruiting | 2024-12-27 | 2033-12-01 | ClinicalTrials.gov |
| NCT06390319 | Adding Dasatinib Or Venetoclax To Improve Responses In Children With Newly Diag… | Phase2 | T-cell Acute Lymphoblastic Leukemia | Recruiting | 2024-12-27 | 2033-12-01 | ClinicalTrials.gov |
| NCT06701331 | Safety and Efficacy of Upadacitinib in Combination With Topical Corticosteroids… | Phase3 | Atopic Dermatitis | Active_Not_Recruiting | 2024-12-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT06701331 | Safety and Efficacy of Upadacitinib in Combination With Topical Corticosteroids… | Phase3 | Atopic Dermatitis | Active_Not_Recruiting | 2024-12-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT06701331 | Safety and Efficacy of Upadacitinib in Combination With Topical Corticosteroids… | Phase3 | Atopic Dermatitis | Active_Not_Recruiting | 2024-12-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT06701331 | Safety and Efficacy of Upadacitinib in Combination With Topical Corticosteroids… | Phase3 | Atopic Dermatitis | Active_Not_Recruiting | 2024-12-22 | 2027-01-01 | ClinicalTrials.gov |
| NCT06718101 | A Study to Evaluate the Effectiveness and Safety of Treatments, Either Alone or… | Phase2 | Atopic Dermatitis | Active_Not_Recruiting | 2024-12-19 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742086 | A Study to Evaluate the Bioavailability and Food Effects of Oral Venetoclax New… | Phase1 | Healthy Volunteer | Completed | 2024-12-19 | 2025-10-08 | ClinicalTrials.gov |
| NCT06742086 | A Study to Evaluate the Bioavailability and Food Effects of Oral Venetoclax New… | Phase1 | Healthy Volunteer | Completed | 2024-12-19 | 2025-10-08 | ClinicalTrials.gov |
| NCT06718101 | A Study to Evaluate the Effectiveness and Safety of Treatments, Either Alone or… | Phase2 | Atopic Dermatitis | Active_Not_Recruiting | 2024-12-19 | 2027-05-01 | ClinicalTrials.gov |
| NCT06742086 | A Study to Evaluate the Bioavailability and Food Effects of Oral Venetoclax New… | Phase1 | Healthy Volunteer | Completed | 2024-12-19 | 2025-10-08 | ClinicalTrials.gov |
| NCT06742086 | A Study to Evaluate the Bioavailability and Food Effects of Oral Venetoclax New… | Phase1 | Healthy Volunteer | Completed | 2024-12-19 | 2025-10-08 | ClinicalTrials.gov |
| NCT06718101 | A Study to Evaluate the Effectiveness and Safety of Treatments, Either Alone or… | Phase2 | Atopic Dermatitis | Active_Not_Recruiting | 2024-12-19 | 2027-05-01 | ClinicalTrials.gov |
| NCT06718101 | A Study to Evaluate the Effectiveness and Safety of Treatments, Either Alone or… | Phase2 | Atopic Dermatitis | Active_Not_Recruiting | 2024-12-19 | 2027-05-01 | ClinicalTrials.gov |
| NCT06734351 | A Study to Evaluate Safety and Effectiveness of NOA VOLUME Injectable Gel in Ad… | Phase3 | Mid Face Volume Deficit | Recruiting | 2024-12-16 | 2029-07-01 | ClinicalTrials.gov |
| NCT06734351 | A Study to Evaluate Safety and Effectiveness of NOA VOLUME Injectable Gel in Ad… | Phase3 | Mid Face Volume Deficit | Recruiting | 2024-12-16 | 2029-07-01 | ClinicalTrials.gov |
| NCT06734351 | A Study to Evaluate Safety and Effectiveness of NOA VOLUME Injectable Gel in Ad… | Phase3 | Mid Face Volume Deficit | Recruiting | 2024-12-16 | 2029-07-01 | ClinicalTrials.gov |
| NCT06734351 | A Study to Evaluate Safety and Effectiveness of NOA VOLUME Injectable Gel in Ad… | Phase3 | Mid Face Volume Deficit | Recruiting | 2024-12-16 | 2029-07-01 | ClinicalTrials.gov |
| NCT06628310 | A Study to Evaluate the Adverse Events, Efficacy, and Optimal Dose of Intraveno… | Phase2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | Active_Not_Recruiting | 2024-12-13 | 2030-10-01 | ClinicalTrials.gov |
| NCT06628310 | A Study to Evaluate the Adverse Events, Efficacy, and Optimal Dose of Intraveno… | Phase2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | Active_Not_Recruiting | 2024-12-13 | 2030-10-01 | ClinicalTrials.gov |
| NCT06628310 | A Study to Evaluate the Adverse Events, Efficacy, and Optimal Dose of Intraveno… | Phase2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | Active_Not_Recruiting | 2024-12-13 | 2030-10-01 | ClinicalTrials.gov |
| NCT06628310 | A Study to Evaluate the Adverse Events, Efficacy, and Optimal Dose of Intraveno… | Phase2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | Active_Not_Recruiting | 2024-12-13 | 2030-10-01 | ClinicalTrials.gov |
| NCT06158100 | Venetoclax in Combination With Azacitidine (VEN/AZA) Followed by Donor Lymphocy… | Phase1 | Acute Myeloid Leukemia | Suspended | 2024-12-04 | 2027-12-31 | ClinicalTrials.gov |
| NCT06158100 | Venetoclax in Combination With Azacitidine (VEN/AZA) Followed by Donor Lymphocy… | Phase1 | Acute Myeloid Leukemia | Suspended | 2024-12-04 | 2027-12-31 | ClinicalTrials.gov |
| NCT06158100 | Venetoclax in Combination With Azacitidine (VEN/AZA) Followed by Donor Lymphocy… | Phase1 | Acute Myeloid Leukemia | Suspended | 2024-12-04 | 2027-12-31 | ClinicalTrials.gov |
| NCT06158100 | Venetoclax in Combination With Azacitidine (VEN/AZA) Followed by Donor Lymphocy… | Phase1 | Acute Myeloid Leukemia | Suspended | 2024-12-04 | 2027-12-31 | ClinicalTrials.gov |
| NCT06454188 | A Study to Evaluate the Impact of Upadacitinib on Spondyloarthritis Outcomes in… | Phase4 | Psoriatic Arthritis | Recruiting | 2024-12-03 | 2028-10-01 | ClinicalTrials.gov |
| NCT06454188 | A Study to Evaluate the Impact of Upadacitinib on Spondyloarthritis Outcomes in… | Phase4 | Psoriatic Arthritis | Recruiting | 2024-12-03 | 2028-10-01 | ClinicalTrials.gov |
| NCT06454188 | A Study to Evaluate the Impact of Upadacitinib on Spondyloarthritis Outcomes in… | Phase4 | Psoriatic Arthritis | Recruiting | 2024-12-03 | 2028-10-01 | ClinicalTrials.gov |
| NCT06454188 | A Study to Evaluate the Impact of Upadacitinib on Spondyloarthritis Outcomes in… | Phase4 | Psoriatic Arthritis | Recruiting | 2024-12-03 | 2028-10-01 | ClinicalTrials.gov |
| NCT06078202 | A Study to Assess the Relative Bioavailability of Three Immediate-Release Table… | Phase1 | Healthy Volunteers | Withdrawn | 2024-12-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT06078202 | A Study to Assess the Relative Bioavailability of Three Immediate-Release Table… | Phase1 | Healthy Volunteers | Withdrawn | 2024-12-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT06078202 | A Study to Assess the Relative Bioavailability of Three Immediate-Release Table… | Phase1 | Healthy Volunteers | Withdrawn | 2024-12-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT06078202 | A Study to Assess the Relative Bioavailability of Three Immediate-Release Table… | Phase1 | Healthy Volunteers | Withdrawn | 2024-12-01 | 2025-01-31 | ClinicalTrials.gov |
| NCT06660368 | BCL2i CLAG-M in R/R Acute Myeloid Leukemia | Phase2 | Relapsed or Refractory Acute Myeloid Leukemia (AML) | Recruiting | 2024-11-26 | 2027-11-01 | ClinicalTrials.gov |
| NCT06660368 | BCL2i CLAG-M in R/R Acute Myeloid Leukemia | Phase2 | Relapsed or Refractory Acute Myeloid Leukemia (AML) | Recruiting | 2024-11-26 | 2027-11-01 | ClinicalTrials.gov |
| NCT06722417 | A Single Dose Study to Assess Adverse Events and How Oral Icalcaprant Moves Thr… | Phase1 | Healthy Volunteer | Completed | 2024-11-26 | 2025-01-17 | ClinicalTrials.gov |
| NCT06722417 | A Single Dose Study to Assess Adverse Events and How Oral Icalcaprant Moves Thr… | Phase1 | Healthy Volunteer | Completed | 2024-11-26 | 2025-01-17 | ClinicalTrials.gov |
| NCT06722417 | A Single Dose Study to Assess Adverse Events and How Oral Icalcaprant Moves Thr… | Phase1 | Healthy Volunteer | Completed | 2024-11-26 | 2025-01-17 | ClinicalTrials.gov |
| NCT06660368 | BCL2i CLAG-M in R/R Acute Myeloid Leukemia | Phase2 | Relapsed or Refractory Acute Myeloid Leukemia (AML) | Recruiting | 2024-11-26 | 2027-11-01 | ClinicalTrials.gov |
| NCT06543914 | Observational Study of Oral Atogepant to Evaluate Real-World Effectiveness in A… | — | Migraine | Active_Not_Recruiting | 2024-11-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06543914 | Observational Study of Oral Atogepant to Evaluate Real-World Effectiveness in A… | — | Migraine | Active_Not_Recruiting | 2024-11-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06722417 | A Single Dose Study to Assess Adverse Events and How Oral Icalcaprant Moves Thr… | Phase1 | Healthy Volunteer | Completed | 2024-11-26 | 2025-01-17 | ClinicalTrials.gov |
| NCT06543914 | Observational Study of Oral Atogepant to Evaluate Real-World Effectiveness in A… | — | Migraine | Active_Not_Recruiting | 2024-11-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06660368 | BCL2i CLAG-M in R/R Acute Myeloid Leukemia | Phase2 | Relapsed or Refractory Acute Myeloid Leukemia (AML) | Recruiting | 2024-11-26 | 2027-11-01 | ClinicalTrials.gov |
| NCT06543914 | Observational Study of Oral Atogepant to Evaluate Real-World Effectiveness in A… | — | Migraine | Active_Not_Recruiting | 2024-11-26 | 2029-02-01 | ClinicalTrials.gov |
| NCT06548568 | A Real-world Study to Assess Safety of OZURDEX® (Dexamethasone Intravitreal Imp… | — | Diabetic Macular Edema | Active_Not_Recruiting | 2024-11-13 | 2027-04-01 | ClinicalTrials.gov |
| NCT06722430 | A Study to Assess Change in How Oral Icalcaprant With Itraconazole Moves Throug… | Phase1 | Healthy Volunteer | Completed | 2024-11-13 | 2025-01-13 | ClinicalTrials.gov |
| NCT06722430 | A Study to Assess Change in How Oral Icalcaprant With Itraconazole Moves Throug… | Phase1 | Healthy Volunteer | Completed | 2024-11-13 | 2025-01-13 | ClinicalTrials.gov |
| NCT06722430 | A Study to Assess Change in How Oral Icalcaprant With Itraconazole Moves Throug… | Phase1 | Healthy Volunteer | Completed | 2024-11-13 | 2025-01-13 | ClinicalTrials.gov |
| NCT06722430 | A Study to Assess Change in How Oral Icalcaprant With Itraconazole Moves Throug… | Phase1 | Healthy Volunteer | Completed | 2024-11-13 | 2025-01-13 | ClinicalTrials.gov |
| NCT06548568 | A Real-world Study to Assess Safety of OZURDEX® (Dexamethasone Intravitreal Imp… | — | Diabetic Macular Edema | Active_Not_Recruiting | 2024-11-13 | 2027-04-01 | ClinicalTrials.gov |
| NCT06548568 | A Real-world Study to Assess Safety of OZURDEX® (Dexamethasone Intravitreal Imp… | — | Diabetic Macular Edema | Active_Not_Recruiting | 2024-11-13 | 2027-04-01 | ClinicalTrials.gov |
| NCT06548568 | A Real-world Study to Assess Safety of OZURDEX® (Dexamethasone Intravitreal Imp… | — | Diabetic Macular Edema | Active_Not_Recruiting | 2024-11-13 | 2027-04-01 | ClinicalTrials.gov |
| NCT06639620 | Study To Assess Effectiveness and Adverse Events of Foscarbidopa/ Foslevodopa i… | — | Advanced Parkinson Disease | Active_Not_Recruiting | 2024-11-12 | 2027-03-01 | ClinicalTrials.gov |
| NCT06639620 | Study To Assess Effectiveness and Adverse Events of Foscarbidopa/ Foslevodopa i… | — | Advanced Parkinson Disease | Active_Not_Recruiting | 2024-11-12 | 2027-03-01 | ClinicalTrials.gov |
| NCT06639620 | Study To Assess Effectiveness and Adverse Events of Foscarbidopa/ Foslevodopa i… | — | Advanced Parkinson Disease | Active_Not_Recruiting | 2024-11-12 | 2027-03-01 | ClinicalTrials.gov |
| NCT06639620 | Study To Assess Effectiveness and Adverse Events of Foscarbidopa/ Foslevodopa i… | — | Advanced Parkinson Disease | Active_Not_Recruiting | 2024-11-12 | 2027-03-01 | ClinicalTrials.gov |
| NCT06698926 | A Study to Assess the Safety, Tolerability, and Interactions of ABBV-CLS-616 Or… | Phase1 | Healthy Volunteer | Completed | 2024-11-11 | 2026-01-09 | ClinicalTrials.gov |
| NCT06698926 | A Study to Assess the Safety, Tolerability, and Interactions of ABBV-CLS-616 Or… | Phase1 | Healthy Volunteer | Completed | 2024-11-11 | 2026-01-09 | ClinicalTrials.gov |
| NCT06698926 | A Study to Assess the Safety, Tolerability, and Interactions of ABBV-CLS-616 Or… | Phase1 | Healthy Volunteer | Completed | 2024-11-11 | 2026-01-09 | ClinicalTrials.gov |
| NCT06698926 | A Study to Assess the Safety, Tolerability, and Interactions of ABBV-CLS-616 Or… | Phase1 | Healthy Volunteer | Completed | 2024-11-11 | 2026-01-09 | ClinicalTrials.gov |
| NCT06614192 | A Study Assessing Adverse Events and Disease Activity of Intravenously (IV) Inf… | Phase3 | Metastatic Colorectal Cancer | Active_Not_Recruiting | 2024-11-08 | 2027-08-01 | ClinicalTrials.gov |
| NCT06614192 | A Study Assessing Adverse Events and Disease Activity of Intravenously (IV) Inf… | Phase3 | Metastatic Colorectal Cancer | Active_Not_Recruiting | 2024-11-08 | 2027-08-01 | ClinicalTrials.gov |
| NCT06614192 | A Study Assessing Adverse Events and Disease Activity of Intravenously (IV) Inf… | Phase3 | Metastatic Colorectal Cancer | Active_Not_Recruiting | 2024-11-08 | 2027-08-01 | ClinicalTrials.gov |
| NCT06614192 | A Study Assessing Adverse Events and Disease Activity of Intravenously (IV) Inf… | Phase3 | Metastatic Colorectal Cancer | Active_Not_Recruiting | 2024-11-08 | 2027-08-01 | ClinicalTrials.gov |
| NCT06712628 | A Comparison Study of Persistence of UPadacitinib vs. TNF-inhibitoRs In a Germa… | — | Moderate to Severe Rheumatoid Arthritis | Recruiting | 2024-11-07 | 2028-12-01 | ClinicalTrials.gov |
| NCT06511882 | Discontinuation of Hypomethylating Agent and Venetoclax in Patients With AML MRD | Phase2 | Acute Myeloid Leukemia | Recruiting | 2024-11-07 | 2028-08-01 | ClinicalTrials.gov |
| NCT06511882 | Discontinuation of Hypomethylating Agent and Venetoclax in Patients With AML MRD | Phase2 | Acute Myeloid Leukemia | Recruiting | 2024-11-07 | 2028-08-01 | ClinicalTrials.gov |
| NCT06511882 | Discontinuation of Hypomethylating Agent and Venetoclax in Patients With AML MRD | Phase2 | Acute Myeloid Leukemia | Recruiting | 2024-11-07 | 2028-08-01 | ClinicalTrials.gov |
| NCT06712628 | A Comparison Study of Persistence of UPadacitinib vs. TNF-inhibitoRs In a Germa… | — | Moderate to Severe Rheumatoid Arthritis | Recruiting | 2024-11-07 | 2028-12-01 | ClinicalTrials.gov |
| NCT06712628 | A Comparison Study of Persistence of UPadacitinib vs. TNF-inhibitoRs In a Germa… | — | Moderate to Severe Rheumatoid Arthritis | Recruiting | 2024-11-07 | 2028-12-01 | ClinicalTrials.gov |
| NCT06511882 | Discontinuation of Hypomethylating Agent and Venetoclax in Patients With AML MRD | Phase2 | Acute Myeloid Leukemia | Recruiting | 2024-11-07 | 2028-08-01 | ClinicalTrials.gov |
| NCT06712628 | A Comparison Study of Persistence of UPadacitinib vs. TNF-inhibitoRs In a Germa… | — | Moderate to Severe Rheumatoid Arthritis | Recruiting | 2024-11-07 | 2028-12-01 | ClinicalTrials.gov |
| NCT06575192 | Evaluation of the Safety and Effectiveness of ARTIA Reconstructive Tissue Matri… | Phase3 | Breast Reconstruction | Recruiting | 2024-11-05 | 2031-02-01 | ClinicalTrials.gov |
| NCT06575192 | Evaluation of the Safety and Effectiveness of ARTIA Reconstructive Tissue Matri… | Phase3 | Breast Reconstruction | Recruiting | 2024-11-05 | 2031-02-01 | ClinicalTrials.gov |
| NCT06575192 | Evaluation of the Safety and Effectiveness of ARTIA Reconstructive Tissue Matri… | Phase3 | Breast Reconstruction | Recruiting | 2024-11-05 | 2031-02-01 | ClinicalTrials.gov |
| NCT06575192 | Evaluation of the Safety and Effectiveness of ARTIA Reconstructive Tissue Matri… | Phase3 | Breast Reconstruction | Recruiting | 2024-11-05 | 2031-02-01 | ClinicalTrials.gov |
| NCT06644144 | P4O2 ILD Extension | — | Interstitial Lung Disease | Recruiting | 2024-11-01 | 2031-10-01 | ClinicalTrials.gov |
| NCT06644144 | P4O2 ILD Extension | — | Interstitial Lung Disease | Recruiting | 2024-11-01 | 2031-10-01 | ClinicalTrials.gov |
| NCT06644144 | P4O2 ILD Extension | — | Interstitial Lung Disease | Recruiting | 2024-11-01 | 2031-10-01 | ClinicalTrials.gov |
| NCT06644144 | P4O2 ILD Extension | — | Interstitial Lung Disease | Recruiting | 2024-11-01 | 2031-10-01 | ClinicalTrials.gov |
| NCT06673238 | A Study to Assess How the Drug Moves Through the Body, Adverse Events, and Tole… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2024-10-29 | 2026-06-01 | ClinicalTrials.gov |
| NCT06673238 | A Study to Assess How the Drug Moves Through the Body, Adverse Events, and Tole… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2024-10-29 | 2026-06-01 | ClinicalTrials.gov |
| NCT06673238 | A Study to Assess How the Drug Moves Through the Body, Adverse Events, and Tole… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2024-10-29 | 2026-06-01 | ClinicalTrials.gov |
| NCT06673238 | A Study to Assess How the Drug Moves Through the Body, Adverse Events, and Tole… | Phase1 | Healthy Volunteer | Active_Not_Recruiting | 2024-10-29 | 2026-06-01 | ClinicalTrials.gov |
| NCT06618118 | A Study to Assess Adverse Events of Fosigotifator (ABBV-CLS-7262) in Adults Wit… | Phase1 | Major Depressive Disorder (MDD) | Terminated | 2024-10-23 | 2025-09-23 | ClinicalTrials.gov |
| NCT06618118 | A Study to Assess Adverse Events of Fosigotifator (ABBV-CLS-7262) in Adults Wit… | Phase1 | Major Depressive Disorder (MDD) | Terminated | 2024-10-23 | 2025-09-23 | ClinicalTrials.gov |
| NCT06618118 | A Study to Assess Adverse Events of Fosigotifator (ABBV-CLS-7262) in Adults Wit… | Phase1 | Major Depressive Disorder (MDD) | Terminated | 2024-10-23 | 2025-09-23 | ClinicalTrials.gov |
| NCT06618118 | A Study to Assess Adverse Events of Fosigotifator (ABBV-CLS-7262) in Adults Wit… | Phase1 | Major Depressive Disorder (MDD) | Terminated | 2024-10-23 | 2025-09-23 | ClinicalTrials.gov |
| NCT06772194 | Taiwan Post-Stroke Disability Study | — | Stroke | Recruiting | 2024-10-21 | 2028-09-30 | ClinicalTrials.gov |
| NCT06772194 | Taiwan Post-Stroke Disability Study | — | Stroke | Recruiting | 2024-10-21 | 2028-09-30 | ClinicalTrials.gov |
| NCT06772194 | Taiwan Post-Stroke Disability Study | — | Stroke | Recruiting | 2024-10-21 | 2028-09-30 | ClinicalTrials.gov |
| NCT06772194 | Taiwan Post-Stroke Disability Study | — | Stroke | Recruiting | 2024-10-21 | 2028-09-30 | ClinicalTrials.gov |
| NCT06605599 | Study of Oral ABBV-932 to Assess Adverse Events and Change in Disease Activity … | Phase2 | Bipolar I Disorder | Completed | 2024-10-15 | 2025-12-10 | ClinicalTrials.gov |
| NCT06605599 | Study of Oral ABBV-932 to Assess Adverse Events and Change in Disease Activity … | Phase2 | Bipolar I Disorder | Completed | 2024-10-15 | 2025-12-10 | ClinicalTrials.gov |
| NCT06605599 | Study of Oral ABBV-932 to Assess Adverse Events and Change in Disease Activity … | Phase2 | Bipolar I Disorder | Completed | 2024-10-15 | 2025-12-10 | ClinicalTrials.gov |
| NCT06605599 | Study of Oral ABBV-932 to Assess Adverse Events and Change in Disease Activity … | Phase2 | Bipolar I Disorder | Completed | 2024-10-15 | 2025-12-10 | ClinicalTrials.gov |
| NCT06632938 | A Study to Evaluate Adverse Events and How the Drug Moves Through the Body From… | Phase1 | Healthy Volunteer | Completed | 2024-10-08 | 2025-05-15 | ClinicalTrials.gov |
| NCT06632938 | A Study to Evaluate Adverse Events and How the Drug Moves Through the Body From… | Phase1 | Healthy Volunteer | Completed | 2024-10-08 | 2025-05-15 | ClinicalTrials.gov |
| NCT06632938 | A Study to Evaluate Adverse Events and How the Drug Moves Through the Body From… | Phase1 | Healthy Volunteer | Completed | 2024-10-08 | 2025-05-15 | ClinicalTrials.gov |
| NCT06632938 | A Study to Evaluate Adverse Events and How the Drug Moves Through the Body From… | Phase1 | Healthy Volunteer | Completed | 2024-10-08 | 2025-05-15 | ClinicalTrials.gov |
| NCT06602479 | A Study to Investigate the Safety and Efficacy of MEDI0618 Compared to Placebo … | Phase2 | Migraine | Recruiting | 2024-10-07 | 2027-05-07 | ClinicalTrials.gov |
| NCT06602479 | A Study to Investigate the Safety and Efficacy of MEDI0618 Compared to Placebo … | Phase2 | Migraine | Recruiting | 2024-10-07 | 2027-05-07 | ClinicalTrials.gov |
| NCT06602479 | A Study to Investigate the Safety and Efficacy of MEDI0618 Compared to Placebo … | Phase2 | Migraine | Recruiting | 2024-10-07 | 2027-05-07 | ClinicalTrials.gov |
| NCT06602479 | A Study to Investigate the Safety and Efficacy of MEDI0618 Compared to Placebo … | Phase2 | Migraine | Recruiting | 2024-10-07 | 2027-05-07 | ClinicalTrials.gov |
| NCT06464692 | Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzumab… | Phase1 | Colorectal Cancer | Recruiting | 2024-09-30 | 2028-09-01 | ClinicalTrials.gov |
| NCT06464692 | Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzumab… | Phase1 | Colorectal Cancer | Recruiting | 2024-09-30 | 2028-09-01 | ClinicalTrials.gov |
| NCT06464692 | Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzumab… | Phase1 | Colorectal Cancer | Recruiting | 2024-09-30 | 2028-09-01 | ClinicalTrials.gov |
| NCT06464692 | Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzumab… | Phase1 | Colorectal Cancer | Recruiting | 2024-09-30 | 2028-09-01 | ClinicalTrials.gov |
| NCT06581042 | Study to Assess Treatment Patterns and Outcomes With Upadacitinib in Adult Part… | — | Ulcerative Colitis | Recruiting | 2024-09-27 | 2029-09-01 | ClinicalTrials.gov |
| NCT06581042 | Study to Assess Treatment Patterns and Outcomes With Upadacitinib in Adult Part… | — | Ulcerative Colitis | Recruiting | 2024-09-27 | 2029-09-01 | ClinicalTrials.gov |
| NCT06581042 | Study to Assess Treatment Patterns and Outcomes With Upadacitinib in Adult Part… | — | Ulcerative Colitis | Recruiting | 2024-09-27 | 2029-09-01 | ClinicalTrials.gov |
| NCT06581042 | Study to Assess Treatment Patterns and Outcomes With Upadacitinib in Adult Part… | — | Ulcerative Colitis | Recruiting | 2024-09-27 | 2029-09-01 | ClinicalTrials.gov |
| NCT06603558 | Post-Marketing Study to Assess the Safety and Effectiveness of Oral Atogepant i… | — | Chronic Migraine | Recruiting | 2024-09-24 | 2029-05-01 | ClinicalTrials.gov |
| NCT06603558 | Post-Marketing Study to Assess the Safety and Effectiveness of Oral Atogepant i… | — | Chronic Migraine | Recruiting | 2024-09-24 | 2029-05-01 | ClinicalTrials.gov |
| NCT06603558 | Post-Marketing Study to Assess the Safety and Effectiveness of Oral Atogepant i… | — | Chronic Migraine | Recruiting | 2024-09-24 | 2029-05-01 | ClinicalTrials.gov |
| NCT06603558 | Post-Marketing Study to Assess the Safety and Effectiveness of Oral Atogepant i… | — | Chronic Migraine | Recruiting | 2024-09-24 | 2029-05-01 | ClinicalTrials.gov |
| NCT06284486 | A Multi-Site Break Through Cancer Trial: Phase II Study Investigating Dual Inhi… | Phase1 | Acute Myeloid Leukemia | Recruiting | 2024-09-23 | 2028-12-30 | ClinicalTrials.gov |
| NCT06284486 | A Multi-Site Break Through Cancer Trial: Phase II Study Investigating Dual Inhi… | Phase1 | Acute Myeloid Leukemia | Recruiting | 2024-09-23 | 2028-12-30 | ClinicalTrials.gov |
| NCT06284486 | A Multi-Site Break Through Cancer Trial: Phase II Study Investigating Dual Inhi… | Phase1 | Acute Myeloid Leukemia | Recruiting | 2024-09-23 | 2028-12-30 | ClinicalTrials.gov |
| NCT06284486 | A Multi-Site Break Through Cancer Trial: Phase II Study Investigating Dual Inhi… | Phase1 | Acute Myeloid Leukemia | Recruiting | 2024-09-23 | 2028-12-30 | ClinicalTrials.gov |
| NCT06487559 | A Study to Assess the Adverse Events and How Intravenously Infused Livmoniplima… | Phase1 | Hepatocellular Carcinoma (HCC) | Recruiting | 2024-09-11 | 2027-10-01 | ClinicalTrials.gov |
| NCT06487559 | A Study to Assess the Adverse Events and How Intravenously Infused Livmoniplima… | Phase1 | Hepatocellular Carcinoma (HCC) | Recruiting | 2024-09-11 | 2027-10-01 | ClinicalTrials.gov |
| NCT06571266 | A Study to Assess the Relative Bioavailability of Two Formulations of Risankizu… | Phase1 | Healthy Volunteers | Completed | 2024-09-11 | 2025-04-16 | ClinicalTrials.gov |
| NCT06571266 | A Study to Assess the Relative Bioavailability of Two Formulations of Risankizu… | Phase1 | Healthy Volunteers | Completed | 2024-09-11 | 2025-04-16 | ClinicalTrials.gov |
| NCT06571266 | A Study to Assess the Relative Bioavailability of Two Formulations of Risankizu… | Phase1 | Healthy Volunteers | Completed | 2024-09-11 | 2025-04-16 | ClinicalTrials.gov |
| NCT06487559 | A Study to Assess the Adverse Events and How Intravenously Infused Livmoniplima… | Phase1 | Hepatocellular Carcinoma (HCC) | Recruiting | 2024-09-11 | 2027-10-01 | ClinicalTrials.gov |
| NCT06571266 | A Study to Assess the Relative Bioavailability of Two Formulations of Risankizu… | Phase1 | Healthy Volunteers | Completed | 2024-09-11 | 2025-04-16 | ClinicalTrials.gov |
| NCT06487559 | A Study to Assess the Adverse Events and How Intravenously Infused Livmoniplima… | Phase1 | Hepatocellular Carcinoma (HCC) | Recruiting | 2024-09-11 | 2027-10-01 | ClinicalTrials.gov |
| NCT06417775 | Study of Oral Ubrogepant to Assess Adverse Events and Change in Disease Activit… | Phase3 | Migraine | Active_Not_Recruiting | 2024-09-10 | 2027-09-01 | ClinicalTrials.gov |
| NCT06417775 | Study of Oral Ubrogepant to Assess Adverse Events and Change in Disease Activit… | Phase3 | Migraine | Active_Not_Recruiting | 2024-09-10 | 2027-09-01 | ClinicalTrials.gov |
| NCT06417775 | Study of Oral Ubrogepant to Assess Adverse Events and Change in Disease Activit… | Phase3 | Migraine | Active_Not_Recruiting | 2024-09-10 | 2027-09-01 | ClinicalTrials.gov |
| NCT06417775 | Study of Oral Ubrogepant to Assess Adverse Events and Change in Disease Activit… | Phase3 | Migraine | Active_Not_Recruiting | 2024-09-10 | 2027-09-01 | ClinicalTrials.gov |
| NCT06579300 | A Study to Assess Multiple Ascending Dose, Drug-Drug Interaction, and Asian Pha… | Phase1 | Healthy Volunteer | Terminated | 2024-09-04 | 2025-09-03 | ClinicalTrials.gov |
| NCT06579300 | A Study to Assess Multiple Ascending Dose, Drug-Drug Interaction, and Asian Pha… | Phase1 | Healthy Volunteer | Terminated | 2024-09-04 | 2025-09-03 | ClinicalTrials.gov |
| NCT06548542 | Study of Targeted Therapies for the Treatment of Adult Participants With Modera… | Phase2 | Crohn's Disease | Recruiting | 2024-09-04 | 2030-01-01 | ClinicalTrials.gov |
| NCT06579300 | A Study to Assess Multiple Ascending Dose, Drug-Drug Interaction, and Asian Pha… | Phase1 | Healthy Volunteer | Terminated | 2024-09-04 | 2025-09-03 | ClinicalTrials.gov |
| NCT06548542 | Study of Targeted Therapies for the Treatment of Adult Participants With Modera… | Phase2 | Crohn's Disease | Recruiting | 2024-09-04 | 2030-01-01 | ClinicalTrials.gov |
| NCT06579300 | A Study to Assess Multiple Ascending Dose, Drug-Drug Interaction, and Asian Pha… | Phase1 | Healthy Volunteer | Terminated | 2024-09-04 | 2025-09-03 | ClinicalTrials.gov |
| NCT06548542 | Study of Targeted Therapies for the Treatment of Adult Participants With Modera… | Phase2 | Crohn's Disease | Recruiting | 2024-09-04 | 2030-01-01 | ClinicalTrials.gov |
| NCT06548542 | Study of Targeted Therapies for the Treatment of Adult Participants With Modera… | Phase2 | Crohn's Disease | Recruiting | 2024-09-04 | 2030-01-01 | ClinicalTrials.gov |
| NCT06300580 | Study of Oral ABBV-932 Capsules to Evaluate Dopamine D2 and D3 Receptor Occupan… | Phase1 | Healthy Volunteers | Completed | 2024-08-21 | 2025-05-26 | ClinicalTrials.gov |
| NCT06300580 | Study of Oral ABBV-932 Capsules to Evaluate Dopamine D2 and D3 Receptor Occupan… | Phase1 | Healthy Volunteers | Completed | 2024-08-21 | 2025-05-26 | ClinicalTrials.gov |
| NCT06300580 | Study of Oral ABBV-932 Capsules to Evaluate Dopamine D2 and D3 Receptor Occupan… | Phase1 | Healthy Volunteers | Completed | 2024-08-21 | 2025-05-26 | ClinicalTrials.gov |
| NCT06300580 | Study of Oral ABBV-932 Capsules to Evaluate Dopamine D2 and D3 Receptor Occupan… | Phase1 | Healthy Volunteers | Completed | 2024-08-21 | 2025-05-26 | ClinicalTrials.gov |
| NCT06461897 | A Study to Assess Adverse Events and Change in Disease Activity Comparing Oral … | Phase3 | Atopic Dermatitis | Recruiting | 2024-08-19 | 2030-07-01 | ClinicalTrials.gov |
| NCT06461897 | A Study to Assess Adverse Events and Change in Disease Activity Comparing Oral … | Phase3 | Atopic Dermatitis | Recruiting | 2024-08-19 | 2030-07-01 | ClinicalTrials.gov |
| NCT06461897 | A Study to Assess Adverse Events and Change in Disease Activity Comparing Oral … | Phase3 | Atopic Dermatitis | Recruiting | 2024-08-19 | 2030-07-01 | ClinicalTrials.gov |
| NCT06461897 | A Study to Assess Adverse Events and Change in Disease Activity Comparing Oral … | Phase3 | Atopic Dermatitis | Recruiting | 2024-08-19 | 2030-07-01 | ClinicalTrials.gov |
| NCT06524635 | A Study to Assess Molecular Changes in Adult Participants With Moderate to Seve… | Phase2 | Hidradenitis Suppurativa | Recruiting | 2024-08-14 | 2027-02-01 | ClinicalTrials.gov |
| NCT06524635 | A Study to Assess Molecular Changes in Adult Participants With Moderate to Seve… | Phase2 | Hidradenitis Suppurativa | Recruiting | 2024-08-14 | 2027-02-01 | ClinicalTrials.gov |
| NCT06524635 | A Study to Assess Molecular Changes in Adult Participants With Moderate to Seve… | Phase2 | Hidradenitis Suppurativa | Recruiting | 2024-08-14 | 2027-02-01 | ClinicalTrials.gov |
| NCT06524635 | A Study to Assess Molecular Changes in Adult Participants With Moderate to Seve… | Phase2 | Hidradenitis Suppurativa | Recruiting | 2024-08-14 | 2027-02-01 | ClinicalTrials.gov |
| NCT06508658 | A Study of Subcutaneously Injected Epcoritamab Plus Oral Lenalidomide Tablets C… | Phase3 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2024-08-13 | 2028-03-01 | ClinicalTrials.gov |
| NCT06508658 | A Study of Subcutaneously Injected Epcoritamab Plus Oral Lenalidomide Tablets C… | Phase3 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2024-08-13 | 2028-03-01 | ClinicalTrials.gov |
| NCT06508658 | A Study of Subcutaneously Injected Epcoritamab Plus Oral Lenalidomide Tablets C… | Phase3 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2024-08-13 | 2028-03-01 | ClinicalTrials.gov |
| NCT06508658 | A Study of Subcutaneously Injected Epcoritamab Plus Oral Lenalidomide Tablets C… | Phase3 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2024-08-13 | 2028-03-01 | ClinicalTrials.gov |
| NCT06332534 | Crohn's Disease: Efficacy, Safety, and Pharmacokinetics of Upadacitinib in Pedi… | Phase3 | Crohn's Disease | Recruiting | 2024-08-08 | 2034-12-01 | ClinicalTrials.gov |
| NCT06332534 | Crohn's Disease: Efficacy, Safety, and Pharmacokinetics of Upadacitinib in Pedi… | Phase3 | Crohn's Disease | Recruiting | 2024-08-08 | 2034-12-01 | ClinicalTrials.gov |
| NCT06332534 | Crohn's Disease: Efficacy, Safety, and Pharmacokinetics of Upadacitinib in Pedi… | Phase3 | Crohn's Disease | Recruiting | 2024-08-08 | 2034-12-01 | ClinicalTrials.gov |
| NCT06332534 | Crohn's Disease: Efficacy, Safety, and Pharmacokinetics of Upadacitinib in Pedi… | Phase3 | Crohn's Disease | Recruiting | 2024-08-08 | 2034-12-01 | ClinicalTrials.gov |
| NCT06503536 | A Study to Assess Treatment Patterns, Clinical Outcomes, and Healthcare Resourc… | — | Atopic Dermatitis (AD) | Completed | 2024-08-06 | 2024-10-31 | ClinicalTrials.gov |
| NCT03938701 | Fluorescence Imaging of IBD and RA Using Adalimumab-800CW | Phase2 | IBD | Recruiting | 2024-08-06 | 2026-08-01 | ClinicalTrials.gov |
| NCT03938701 | Fluorescence Imaging of IBD and RA Using Adalimumab-800CW | Phase2 | IBD | Recruiting | 2024-08-06 | 2026-08-01 | ClinicalTrials.gov |
| NCT06503536 | A Study to Assess Treatment Patterns, Clinical Outcomes, and Healthcare Resourc… | — | Atopic Dermatitis (AD) | Completed | 2024-08-06 | 2024-10-31 | ClinicalTrials.gov |
| NCT03938701 | Fluorescence Imaging of IBD and RA Using Adalimumab-800CW | Phase2 | IBD | Recruiting | 2024-08-06 | 2026-08-01 | ClinicalTrials.gov |
| NCT06503536 | A Study to Assess Treatment Patterns, Clinical Outcomes, and Healthcare Resourc… | — | Atopic Dermatitis (AD) | Completed | 2024-08-06 | 2024-10-31 | ClinicalTrials.gov |
| NCT06503536 | A Study to Assess Treatment Patterns, Clinical Outcomes, and Healthcare Resourc… | — | Atopic Dermatitis (AD) | Completed | 2024-08-06 | 2024-10-31 | ClinicalTrials.gov |
| NCT03938701 | Fluorescence Imaging of IBD and RA Using Adalimumab-800CW | Phase2 | IBD | Recruiting | 2024-08-06 | 2026-08-01 | ClinicalTrials.gov |
| NCT06428019 | A Study to Evaluate the Risk of Tumor Lysis Syndrome (TLS) in Adult Participant… | Phase3 | Chronic Lymphocytic Leukemia | Recruiting | 2024-08-05 | 2028-03-01 | ClinicalTrials.gov |
| NCT06428019 | A Study to Evaluate the Risk of Tumor Lysis Syndrome (TLS) in Adult Participant… | Phase3 | Chronic Lymphocytic Leukemia | Recruiting | 2024-08-05 | 2028-03-01 | ClinicalTrials.gov |
| NCT06428019 | A Study to Evaluate the Risk of Tumor Lysis Syndrome (TLS) in Adult Participant… | Phase3 | Chronic Lymphocytic Leukemia | Recruiting | 2024-08-05 | 2028-03-01 | ClinicalTrials.gov |
| NCT06428019 | A Study to Evaluate the Risk of Tumor Lysis Syndrome (TLS) in Adult Participant… | Phase3 | Chronic Lymphocytic Leukemia | Recruiting | 2024-08-05 | 2028-03-01 | ClinicalTrials.gov |
| NCT05894109 | Efficacy of Zinc Supplementation on Botox Treated Forehead Rhytids | Na | Adjuvant Zinc May Increase the Efficacy of Botulinum Toxin | Withdrawn | 2024-08-01 | 2024-10-01 | ClinicalTrials.gov |
| NCT05894109 | Efficacy of Zinc Supplementation on Botox Treated Forehead Rhytids | Na | Adjuvant Zinc May Increase the Efficacy of Botulinum Toxin | Withdrawn | 2024-08-01 | 2024-10-01 | ClinicalTrials.gov |
| NCT05894109 | Efficacy of Zinc Supplementation on Botox Treated Forehead Rhytids | Na | Adjuvant Zinc May Increase the Efficacy of Botulinum Toxin | Withdrawn | 2024-08-01 | 2024-10-01 | ClinicalTrials.gov |
| NCT05894109 | Efficacy of Zinc Supplementation on Botox Treated Forehead Rhytids | Na | Adjuvant Zinc May Increase the Efficacy of Botulinum Toxin | Withdrawn | 2024-08-01 | 2024-10-01 | ClinicalTrials.gov |
| NCT06365853 | A Study of Ocular Toxicity Evaluation and Mitigation During Treatment With Mirv… | Phase2 | Recurrent Ovarian Cancer | Recruiting | 2024-07-29 | 2027-06-01 | ClinicalTrials.gov |
| NCT06365853 | A Study of Ocular Toxicity Evaluation and Mitigation During Treatment With Mirv… | Phase2 | Recurrent Ovarian Cancer | Recruiting | 2024-07-29 | 2027-06-01 | ClinicalTrials.gov |
| NCT06365853 | A Study of Ocular Toxicity Evaluation and Mitigation During Treatment With Mirv… | Phase2 | Recurrent Ovarian Cancer | Recruiting | 2024-07-29 | 2027-06-01 | ClinicalTrials.gov |
| NCT06365853 | A Study of Ocular Toxicity Evaluation and Mitigation During Treatment With Mirv… | Phase2 | Recurrent Ovarian Cancer | Recruiting | 2024-07-29 | 2027-06-01 | ClinicalTrials.gov |
| NCT06487572 | A Study to Assess Pharmacokinetic Exposures Following Intravenous and Subcutane… | Phase1 | Healthy Volunteers | Completed | 2024-07-23 | 2025-02-07 | ClinicalTrials.gov |
| NCT06487572 | A Study to Assess Pharmacokinetic Exposures Following Intravenous and Subcutane… | Phase1 | Healthy Volunteers | Completed | 2024-07-23 | 2025-02-07 | ClinicalTrials.gov |
| NCT06487572 | A Study to Assess Pharmacokinetic Exposures Following Intravenous and Subcutane… | Phase1 | Healthy Volunteers | Completed | 2024-07-23 | 2025-02-07 | ClinicalTrials.gov |
| NCT06487572 | A Study to Assess Pharmacokinetic Exposures Following Intravenous and Subcutane… | Phase1 | Healthy Volunteers | Completed | 2024-07-23 | 2025-02-07 | ClinicalTrials.gov |
| NCT06547125 | A Study to Assess Adverse Events and Effectiveness of Intradermally Injected JU… | Phase2 | Skin Quality Deficit | Completed | 2024-07-18 | 2026-02-05 | ClinicalTrials.gov |
| NCT06547125 | A Study to Assess Adverse Events and Effectiveness of Intradermally Injected JU… | Phase2 | Skin Quality Deficit | Completed | 2024-07-18 | 2026-02-05 | ClinicalTrials.gov |
| NCT06547125 | A Study to Assess Adverse Events and Effectiveness of Intradermally Injected JU… | Phase2 | Skin Quality Deficit | Completed | 2024-07-18 | 2026-02-05 | ClinicalTrials.gov |
| NCT06547125 | A Study to Assess Adverse Events and Effectiveness of Intradermally Injected JU… | Phase2 | Skin Quality Deficit | Completed | 2024-07-18 | 2026-02-05 | ClinicalTrials.gov |
| NCT06477926 | A Study to Assess Relative Bioavailability and Food Effect of ABBV-668 Extended… | Phase1 | Healthy Volunteers | Completed | 2024-07-09 | 2024-09-20 | ClinicalTrials.gov |
| NCT06477926 | A Study to Assess Relative Bioavailability and Food Effect of ABBV-668 Extended… | Phase1 | Healthy Volunteers | Completed | 2024-07-09 | 2024-09-20 | ClinicalTrials.gov |
| NCT06477926 | A Study to Assess Relative Bioavailability and Food Effect of ABBV-668 Extended… | Phase1 | Healthy Volunteers | Completed | 2024-07-09 | 2024-09-20 | ClinicalTrials.gov |
| NCT06477926 | A Study to Assess Relative Bioavailability and Food Effect of ABBV-668 Extended… | Phase1 | Healthy Volunteers | Completed | 2024-07-09 | 2024-09-20 | ClinicalTrials.gov |
| NCT06100744 | A Study to Assess Adverse Events, Change in Disease Activity, and How the Drug … | Phase3 | Juvenile Psoriatic Arthritis | Recruiting | 2024-07-08 | 2028-10-01 | ClinicalTrials.gov |
| NCT06100744 | A Study to Assess Adverse Events, Change in Disease Activity, and How the Drug … | Phase3 | Juvenile Psoriatic Arthritis | Recruiting | 2024-07-08 | 2028-10-01 | ClinicalTrials.gov |
| NCT06100744 | A Study to Assess Adverse Events, Change in Disease Activity, and How the Drug … | Phase3 | Juvenile Psoriatic Arthritis | Recruiting | 2024-07-08 | 2028-10-01 | ClinicalTrials.gov |
| NCT06100744 | A Study to Assess Adverse Events, Change in Disease Activity, and How the Drug … | Phase3 | Juvenile Psoriatic Arthritis | Recruiting | 2024-07-08 | 2028-10-01 | ClinicalTrials.gov |
| NCT06468228 | A Study to Assess Disease Activity and Safety of Lutikizumab in Adult and Adole… | Phase3 | Hidradenitis Suppurativa | Active_Not_Recruiting | 2024-06-27 | 2026-12-01 | ClinicalTrials.gov |
| NCT06468228 | A Study to Assess Disease Activity and Safety of Lutikizumab in Adult and Adole… | Phase3 | Hidradenitis Suppurativa | Active_Not_Recruiting | 2024-06-27 | 2026-12-01 | ClinicalTrials.gov |
| NCT06468228 | A Study to Assess Disease Activity and Safety of Lutikizumab in Adult and Adole… | Phase3 | Hidradenitis Suppurativa | Active_Not_Recruiting | 2024-06-27 | 2026-12-01 | ClinicalTrials.gov |
| NCT06468228 | A Study to Assess Disease Activity and Safety of Lutikizumab in Adult and Adole… | Phase3 | Hidradenitis Suppurativa | Active_Not_Recruiting | 2024-06-27 | 2026-12-01 | ClinicalTrials.gov |
| NCT06402513 | A Study in Healthy Adult Participants to Assess the Pharmacokinetics, Immunogen… | Phase1 | Healthy Volunteers | Completed | 2024-06-24 | 2024-10-08 | ClinicalTrials.gov |
| NCT06402513 | A Study in Healthy Adult Participants to Assess the Pharmacokinetics, Immunogen… | Phase1 | Healthy Volunteers | Completed | 2024-06-24 | 2024-10-08 | ClinicalTrials.gov |
| NCT06459297 | Study of Oral Upadacitinib to Assess Change in Disease Activity and Adverse Eve… | — | Ulcerative Colitis | Completed | 2024-06-24 | 2025-12-09 | ClinicalTrials.gov |
| NCT06459297 | Study of Oral Upadacitinib to Assess Change in Disease Activity and Adverse Eve… | — | Ulcerative Colitis | Completed | 2024-06-24 | 2025-12-09 | ClinicalTrials.gov |
| NCT06402513 | A Study in Healthy Adult Participants to Assess the Pharmacokinetics, Immunogen… | Phase1 | Healthy Volunteers | Completed | 2024-06-24 | 2024-10-08 | ClinicalTrials.gov |
| NCT06459297 | Study of Oral Upadacitinib to Assess Change in Disease Activity and Adverse Eve… | — | Ulcerative Colitis | Completed | 2024-06-24 | 2025-12-09 | ClinicalTrials.gov |
| NCT06459297 | Study of Oral Upadacitinib to Assess Change in Disease Activity and Adverse Eve… | — | Ulcerative Colitis | Completed | 2024-06-24 | 2025-12-09 | ClinicalTrials.gov |
| NCT06402513 | A Study in Healthy Adult Participants to Assess the Pharmacokinetics, Immunogen… | Phase1 | Healthy Volunteers | Completed | 2024-06-24 | 2024-10-08 | ClinicalTrials.gov |
| NCT06223516 | Study of ABBV-383 Assessing Adverse Events and Clinical Activity With Subcutane… | Phase1 | Multiple Myeloma | Active_Not_Recruiting | 2024-06-17 | 2027-12-01 | ClinicalTrials.gov |
| NCT06439394 | An Observational Study to Assess Optive MEGA-3 (OM3) on Dry Eye Symptoms and Qu… | — | Dry Eye | Completed | 2024-06-17 | 2024-07-18 | ClinicalTrials.gov |
| NCT06443775 | An Observational Study to Assess Next Generation Emulsion Preservative Free Eye… | — | Dry Eye | Completed | 2024-06-17 | 2024-10-14 | ClinicalTrials.gov |
| NCT06443775 | An Observational Study to Assess Next Generation Emulsion Preservative Free Eye… | — | Dry Eye | Completed | 2024-06-17 | 2024-10-14 | ClinicalTrials.gov |
| NCT06223516 | Study of ABBV-383 Assessing Adverse Events and Clinical Activity With Subcutane… | Phase1 | Multiple Myeloma | Active_Not_Recruiting | 2024-06-17 | 2027-12-01 | ClinicalTrials.gov |
| NCT06439394 | An Observational Study to Assess Optive MEGA-3 (OM3) on Dry Eye Symptoms and Qu… | — | Dry Eye | Completed | 2024-06-17 | 2024-07-18 | ClinicalTrials.gov |
| NCT06439394 | An Observational Study to Assess Optive MEGA-3 (OM3) on Dry Eye Symptoms and Qu… | — | Dry Eye | Completed | 2024-06-17 | 2024-07-18 | ClinicalTrials.gov |
| NCT06223516 | Study of ABBV-383 Assessing Adverse Events and Clinical Activity With Subcutane… | Phase1 | Multiple Myeloma | Active_Not_Recruiting | 2024-06-17 | 2027-12-01 | ClinicalTrials.gov |
| NCT06443775 | An Observational Study to Assess Next Generation Emulsion Preservative Free Eye… | — | Dry Eye | Completed | 2024-06-17 | 2024-10-14 | ClinicalTrials.gov |
| NCT06223516 | Study of ABBV-383 Assessing Adverse Events and Clinical Activity With Subcutane… | Phase1 | Multiple Myeloma | Active_Not_Recruiting | 2024-06-17 | 2027-12-01 | ClinicalTrials.gov |
| NCT06443775 | An Observational Study to Assess Next Generation Emulsion Preservative Free Eye… | — | Dry Eye | Completed | 2024-06-17 | 2024-10-14 | ClinicalTrials.gov |
| NCT06439394 | An Observational Study to Assess Optive MEGA-3 (OM3) on Dry Eye Symptoms and Qu… | — | Dry Eye | Completed | 2024-06-17 | 2024-07-18 | ClinicalTrials.gov |
| NCT06389136 | A Study of Upadacitinib in Adult Participants With Moderate-to-Severe Atopic De… | Phase3 | Atopic Dermatitis | Recruiting | 2024-06-14 | 2027-03-01 | ClinicalTrials.gov |
| NCT06389136 | A Study of Upadacitinib in Adult Participants With Moderate-to-Severe Atopic De… | Phase3 | Atopic Dermatitis | Recruiting | 2024-06-14 | 2027-03-01 | ClinicalTrials.gov |
| NCT06389136 | A Study of Upadacitinib in Adult Participants With Moderate-to-Severe Atopic De… | Phase3 | Atopic Dermatitis | Recruiting | 2024-06-14 | 2027-03-01 | ClinicalTrials.gov |
| NCT06389136 | A Study of Upadacitinib in Adult Participants With Moderate-to-Severe Atopic De… | Phase3 | Atopic Dermatitis | Recruiting | 2024-06-14 | 2027-03-01 | ClinicalTrials.gov |
| NCT06421740 | An Observational Study to Assess Real-World Use of Upadacitinib Tablets in Adol… | — | Atopic Dermatitis | Recruiting | 2024-06-07 | 2026-06-01 | ClinicalTrials.gov |
| NCT06421740 | An Observational Study to Assess Real-World Use of Upadacitinib Tablets in Adol… | — | Atopic Dermatitis | Recruiting | 2024-06-07 | 2026-06-01 | ClinicalTrials.gov |
| NCT06421740 | An Observational Study to Assess Real-World Use of Upadacitinib Tablets in Adol… | — | Atopic Dermatitis | Recruiting | 2024-06-07 | 2026-06-01 | ClinicalTrials.gov |
| NCT06421740 | An Observational Study to Assess Real-World Use of Upadacitinib Tablets in Adol… | — | Atopic Dermatitis | Recruiting | 2024-06-07 | 2026-06-01 | ClinicalTrials.gov |
| NCT05796388 | A Study of Virtual Reality and Linaclotide for IBS-C | Na | Irritable Bowel Syndrome With Constipation | Recruiting | 2024-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06093503 | Study of Intravenous Telisotuzumab Vedotin in Combination Osimertinib or Standa… | Phase3 | Non-Small Cell Lung Cancer | Withdrawn | 2024-05-31 | 2028-04-11 | ClinicalTrials.gov |
| NCT05796388 | A Study of Virtual Reality and Linaclotide for IBS-C | Na | Irritable Bowel Syndrome With Constipation | Recruiting | 2024-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT05796388 | A Study of Virtual Reality and Linaclotide for IBS-C | Na | Irritable Bowel Syndrome With Constipation | Recruiting | 2024-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06093503 | Study of Intravenous Telisotuzumab Vedotin in Combination Osimertinib or Standa… | Phase3 | Non-Small Cell Lung Cancer | Withdrawn | 2024-05-31 | 2028-04-11 | ClinicalTrials.gov |
| NCT05796388 | A Study of Virtual Reality and Linaclotide for IBS-C | Na | Irritable Bowel Syndrome With Constipation | Recruiting | 2024-05-31 | 2026-06-01 | ClinicalTrials.gov |
| NCT06093503 | Study of Intravenous Telisotuzumab Vedotin in Combination Osimertinib or Standa… | Phase3 | Non-Small Cell Lung Cancer | Withdrawn | 2024-05-31 | 2028-04-11 | ClinicalTrials.gov |
| NCT06093503 | Study of Intravenous Telisotuzumab Vedotin in Combination Osimertinib or Standa… | Phase3 | Non-Small Cell Lung Cancer | Withdrawn | 2024-05-31 | 2028-04-11 | ClinicalTrials.gov |
| NCT06390722 | A Study to Assess the Effect of Upadacitinib in Atopic Dermatitis-induced Sleep… | Phase3 | Atopic Dermatitis | Withdrawn | 2024-05-23 | 2026-07-08 | ClinicalTrials.gov |
| NCT06390722 | A Study to Assess the Effect of Upadacitinib in Atopic Dermatitis-induced Sleep… | Phase3 | Atopic Dermatitis | Withdrawn | 2024-05-23 | 2026-07-08 | ClinicalTrials.gov |
| NCT06390722 | A Study to Assess the Effect of Upadacitinib in Atopic Dermatitis-induced Sleep… | Phase3 | Atopic Dermatitis | Withdrawn | 2024-05-23 | 2026-07-08 | ClinicalTrials.gov |
| NCT06390722 | A Study to Assess the Effect of Upadacitinib in Atopic Dermatitis-induced Sleep… | Phase3 | Atopic Dermatitis | Withdrawn | 2024-05-23 | 2026-07-08 | ClinicalTrials.gov |
| NCT06425003 | Study of [14C] ABBV-CLS-7262 in Healthy Male Volunteers Following Single Oral D… | Phase1 | Healthy Volunteer | Completed | 2024-05-21 | 2024-07-12 | ClinicalTrials.gov |
| NCT06425003 | Study of [14C] ABBV-CLS-7262 in Healthy Male Volunteers Following Single Oral D… | Phase1 | Healthy Volunteer | Completed | 2024-05-21 | 2024-07-12 | ClinicalTrials.gov |
| NCT06425003 | Study of [14C] ABBV-CLS-7262 in Healthy Male Volunteers Following Single Oral D… | Phase1 | Healthy Volunteer | Completed | 2024-05-21 | 2024-07-12 | ClinicalTrials.gov |
| NCT06425003 | Study of [14C] ABBV-CLS-7262 in Healthy Male Volunteers Following Single Oral D… | Phase1 | Healthy Volunteer | Completed | 2024-05-21 | 2024-07-12 | ClinicalTrials.gov |
| NCT06158841 | Study Assessing Activity of Intravenous (IV) Etentamig Monotherapy Versus Stand… | Phase3 | Multiple Myeloma | Recruiting | 2024-05-19 | 2027-12-01 | ClinicalTrials.gov |
| NCT06158841 | Study Assessing Activity of Intravenous (IV) Etentamig Monotherapy Versus Stand… | Phase3 | Multiple Myeloma | Recruiting | 2024-05-19 | 2027-12-01 | ClinicalTrials.gov |
| NCT06158841 | Study Assessing Activity of Intravenous (IV) Etentamig Monotherapy Versus Stand… | Phase3 | Multiple Myeloma | Recruiting | 2024-05-19 | 2027-12-01 | ClinicalTrials.gov |
| NCT06158841 | Study Assessing Activity of Intravenous (IV) Etentamig Monotherapy Versus Stand… | Phase3 | Multiple Myeloma | Recruiting | 2024-05-19 | 2027-12-01 | ClinicalTrials.gov |
| NCT06414148 | MRD-Directed Consolidation With Epcor-only or Epcor-R2 Post Anti-CD19 CAR TCell… | Phase2 | Relapsed/Refractory Large B-cell Lymphoma | Recruiting | 2024-05-14 | 2028-05-01 | ClinicalTrials.gov |
| NCT06414148 | MRD-Directed Consolidation With Epcor-only or Epcor-R2 Post Anti-CD19 CAR TCell… | Phase2 | Relapsed/Refractory Large B-cell Lymphoma | Recruiting | 2024-05-14 | 2028-05-01 | ClinicalTrials.gov |
| NCT06414148 | MRD-Directed Consolidation With Epcor-only or Epcor-R2 Post Anti-CD19 CAR TCell… | Phase2 | Relapsed/Refractory Large B-cell Lymphoma | Recruiting | 2024-05-14 | 2028-05-01 | ClinicalTrials.gov |
| NCT06414148 | MRD-Directed Consolidation With Epcor-only or Epcor-R2 Post Anti-CD19 CAR TCell… | Phase2 | Relapsed/Refractory Large B-cell Lymphoma | Recruiting | 2024-05-14 | 2028-05-01 | ClinicalTrials.gov |
| NCT06414798 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of ABBV-1088 O… | Phase1 | Healthy Volunteers | Completed | 2024-05-13 | 2025-02-08 | ClinicalTrials.gov |
| NCT06414798 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of ABBV-1088 O… | Phase1 | Healthy Volunteers | Completed | 2024-05-13 | 2025-02-08 | ClinicalTrials.gov |
| NCT06414798 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of ABBV-1088 O… | Phase1 | Healthy Volunteers | Completed | 2024-05-13 | 2025-02-08 | ClinicalTrials.gov |
| NCT06414798 | A Study to Assess the Safety, Tolerability, and Pharmacokinetics of ABBV-1088 O… | Phase1 | Healthy Volunteers | Completed | 2024-05-13 | 2025-02-08 | ClinicalTrials.gov |
| NCT06333860 | A Study to Learn How Safe and Effective Risankizumab is When Compared to Deucra… | Phase4 | Moderate Plaque Psoriasis | Completed | 2024-05-10 | 2026-03-19 | ClinicalTrials.gov |
| NCT06333860 | A Study to Learn How Safe and Effective Risankizumab is When Compared to Deucra… | Phase4 | Moderate Plaque Psoriasis | Completed | 2024-05-10 | 2026-03-19 | ClinicalTrials.gov |
| NCT06333860 | A Study to Learn How Safe and Effective Risankizumab is When Compared to Deucra… | Phase4 | Moderate Plaque Psoriasis | Completed | 2024-05-10 | 2026-03-19 | ClinicalTrials.gov |
| NCT06333860 | A Study to Learn How Safe and Effective Risankizumab is When Compared to Deucra… | Phase4 | Moderate Plaque Psoriasis | Completed | 2024-05-10 | 2026-03-19 | ClinicalTrials.gov |
| NCT06406348 | A Phase 1 Trial to Assess Safety, Tolerability and Pharmacokinetics of ALIA-175… | Phase1 | Alzheimer Disease | Completed | 2024-05-09 | 2025-04-22 | ClinicalTrials.gov |
| NCT06406348 | A Phase 1 Trial to Assess Safety, Tolerability and Pharmacokinetics of ALIA-175… | Phase1 | Alzheimer Disease | Completed | 2024-05-09 | 2025-04-22 | ClinicalTrials.gov |
| NCT06406348 | A Phase 1 Trial to Assess Safety, Tolerability and Pharmacokinetics of ALIA-175… | Phase1 | Alzheimer Disease | Completed | 2024-05-09 | 2025-04-22 | ClinicalTrials.gov |
| NCT06406348 | A Phase 1 Trial to Assess Safety, Tolerability and Pharmacokinetics of ALIA-175… | Phase1 | Alzheimer Disease | Completed | 2024-05-09 | 2025-04-22 | ClinicalTrials.gov |
| NCT05606757 | A Study to Evaluate Adverse Events and Effectiveness of OnabotulinumtoxinA in P… | Phase2 | Ventral Hernia | Withdrawn | 2024-05-07 | 2025-09-26 | ClinicalTrials.gov |
| NCT05606757 | A Study to Evaluate Adverse Events and Effectiveness of OnabotulinumtoxinA in P… | Phase2 | Ventral Hernia | Withdrawn | 2024-05-07 | 2025-09-26 | ClinicalTrials.gov |
| NCT05606757 | A Study to Evaluate Adverse Events and Effectiveness of OnabotulinumtoxinA in P… | Phase2 | Ventral Hernia | Withdrawn | 2024-05-07 | 2025-09-26 | ClinicalTrials.gov |
| NCT05606757 | A Study to Evaluate Adverse Events and Effectiveness of OnabotulinumtoxinA in P… | Phase2 | Ventral Hernia | Withdrawn | 2024-05-07 | 2025-09-26 | ClinicalTrials.gov |
| NCT06399718 | A Study to Assess BOTOX Injections for the Change of Masseter Muscle Prominence… | Phase3 | Masseter Muscle Prominence | Completed | 2024-04-30 | 2025-11-10 | ClinicalTrials.gov |
| NCT06399718 | A Study to Assess BOTOX Injections for the Change of Masseter Muscle Prominence… | Phase3 | Masseter Muscle Prominence | Completed | 2024-04-30 | 2025-11-10 | ClinicalTrials.gov |
| NCT06399718 | A Study to Assess BOTOX Injections for the Change of Masseter Muscle Prominence… | Phase3 | Masseter Muscle Prominence | Completed | 2024-04-30 | 2025-11-10 | ClinicalTrials.gov |
| NCT06399718 | A Study to Assess BOTOX Injections for the Change of Masseter Muscle Prominence… | Phase3 | Masseter Muscle Prominence | Completed | 2024-04-30 | 2025-11-10 | ClinicalTrials.gov |
| NCT06247319 | Study to Evaluate the Effectiveness of Risankizumab in Participants With a Rece… | — | Moderate Plaque Psoriasis | Active_Not_Recruiting | 2024-04-29 | 2027-10-01 | ClinicalTrials.gov |
| NCT06247319 | Study to Evaluate the Effectiveness of Risankizumab in Participants With a Rece… | — | Moderate Plaque Psoriasis | Active_Not_Recruiting | 2024-04-29 | 2027-10-01 | ClinicalTrials.gov |
| NCT06247319 | Study to Evaluate the Effectiveness of Risankizumab in Participants With a Rece… | — | Moderate Plaque Psoriasis | Active_Not_Recruiting | 2024-04-29 | 2027-10-01 | ClinicalTrials.gov |
| NCT06247319 | Study to Evaluate the Effectiveness of Risankizumab in Participants With a Rece… | — | Moderate Plaque Psoriasis | Active_Not_Recruiting | 2024-04-29 | 2027-10-01 | ClinicalTrials.gov |
| NCT06345339 | A Study to Assess the Safety and Efficacy of Oral Armour Thyroid Compared to Sy… | Phase2 | Hypothyroidism | Recruiting | 2024-04-26 | 2028-06-01 | ClinicalTrials.gov |
| NCT06345339 | A Study to Assess the Safety and Efficacy of Oral Armour Thyroid Compared to Sy… | Phase2 | Hypothyroidism | Recruiting | 2024-04-26 | 2028-06-01 | ClinicalTrials.gov |
| NCT06345339 | A Study to Assess the Safety and Efficacy of Oral Armour Thyroid Compared to Sy… | Phase2 | Hypothyroidism | Recruiting | 2024-04-26 | 2028-06-01 | ClinicalTrials.gov |
| NCT06345339 | A Study to Assess the Safety and Efficacy of Oral Armour Thyroid Compared to Sy… | Phase2 | Hypothyroidism | Recruiting | 2024-04-26 | 2028-06-01 | ClinicalTrials.gov |
| NCT06346288 | A Study to Assess the Concentrations of Risankizumab in the Breast Milk of Adul… | Phase4 | Inflammatory Bowel Disease | Completed | 2024-04-24 | 2026-02-05 | ClinicalTrials.gov |
| NCT06346288 | A Study to Assess the Concentrations of Risankizumab in the Breast Milk of Adul… | Phase4 | Inflammatory Bowel Disease | Completed | 2024-04-24 | 2026-02-05 | ClinicalTrials.gov |
| NCT06346288 | A Study to Assess the Concentrations of Risankizumab in the Breast Milk of Adul… | Phase4 | Inflammatory Bowel Disease | Completed | 2024-04-24 | 2026-02-05 | ClinicalTrials.gov |
| NCT06346288 | A Study to Assess the Concentrations of Risankizumab in the Breast Milk of Adul… | Phase4 | Inflammatory Bowel Disease | Completed | 2024-04-24 | 2026-02-05 | ClinicalTrials.gov |
| NCT06387394 | A Study to Assess BOTOX Injections in Adult Participants for the Change of Mass… | Phase3 | Masseter Muscle Prominence | Completed | 2024-04-22 | 2025-11-25 | ClinicalTrials.gov |
| NCT06387394 | A Study to Assess BOTOX Injections in Adult Participants for the Change of Mass… | Phase3 | Masseter Muscle Prominence | Completed | 2024-04-22 | 2025-11-25 | ClinicalTrials.gov |
| NCT06387394 | A Study to Assess BOTOX Injections in Adult Participants for the Change of Mass… | Phase3 | Masseter Muscle Prominence | Completed | 2024-04-22 | 2025-11-25 | ClinicalTrials.gov |
| NCT06387394 | A Study to Assess BOTOX Injections in Adult Participants for the Change of Mass… | Phase3 | Masseter Muscle Prominence | Completed | 2024-04-22 | 2025-11-25 | ClinicalTrials.gov |
| NCT06256367 | Observational Study of Oral Cariprazine Capsules to Assess Change in Disease Ac… | — | Bipolar I Disorder | Completed | 2024-04-18 | 2026-01-23 | ClinicalTrials.gov |
| NCT06256367 | Observational Study of Oral Cariprazine Capsules to Assess Change in Disease Ac… | — | Bipolar I Disorder | Completed | 2024-04-18 | 2026-01-23 | ClinicalTrials.gov |
| NCT06256367 | Observational Study of Oral Cariprazine Capsules to Assess Change in Disease Ac… | — | Bipolar I Disorder | Completed | 2024-04-18 | 2026-01-23 | ClinicalTrials.gov |
| NCT06256367 | Observational Study of Oral Cariprazine Capsules to Assess Change in Disease Ac… | — | Bipolar I Disorder | Completed | 2024-04-18 | 2026-01-23 | ClinicalTrials.gov |
| NCT06236438 | Study to Evaluate Adverse Events, Optimal Dose, and Change in Disease Activity,… | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2024-04-10 | 2031-10-01 | ClinicalTrials.gov |
| NCT06236438 | Study to Evaluate Adverse Events, Optimal Dose, and Change in Disease Activity,… | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2024-04-10 | 2031-10-01 | ClinicalTrials.gov |
| NCT06236438 | Study to Evaluate Adverse Events, Optimal Dose, and Change in Disease Activity,… | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2024-04-10 | 2031-10-01 | ClinicalTrials.gov |
| NCT06236438 | Study to Evaluate Adverse Events, Optimal Dose, and Change in Disease Activity,… | Phase2 | Non-Small Cell Lung Cancer | Recruiting | 2024-04-10 | 2031-10-01 | ClinicalTrials.gov |
| NCT06773403 | Upadacitinib for Prurigo Nodularis | Phase4 | Prurigo Nodularis | Terminated | 2024-04-09 | 2025-06-06 | ClinicalTrials.gov |
| NCT06773403 | Upadacitinib for Prurigo Nodularis | Phase4 | Prurigo Nodularis | Terminated | 2024-04-09 | 2025-06-06 | ClinicalTrials.gov |
| NCT06773403 | Upadacitinib for Prurigo Nodularis | Phase4 | Prurigo Nodularis | Terminated | 2024-04-09 | 2025-06-06 | ClinicalTrials.gov |
| NCT06773403 | Upadacitinib for Prurigo Nodularis | Phase4 | Prurigo Nodularis | Terminated | 2024-04-09 | 2025-06-06 | ClinicalTrials.gov |
| NCT05904106 | Venetoclax Plus Azacitidine Versus Intensive Chemotherapy for Fit Patients With… | Phase2 | Acute Myeloid Leukemia | Recruiting | 2024-04-07 | 2028-09-01 | ClinicalTrials.gov |
| NCT05904106 | Venetoclax Plus Azacitidine Versus Intensive Chemotherapy for Fit Patients With… | Phase2 | Acute Myeloid Leukemia | Recruiting | 2024-04-07 | 2028-09-01 | ClinicalTrials.gov |
| NCT05904106 | Venetoclax Plus Azacitidine Versus Intensive Chemotherapy for Fit Patients With… | Phase2 | Acute Myeloid Leukemia | Recruiting | 2024-04-07 | 2028-09-01 | ClinicalTrials.gov |
| NCT05904106 | Venetoclax Plus Azacitidine Versus Intensive Chemotherapy for Fit Patients With… | Phase2 | Acute Myeloid Leukemia | Recruiting | 2024-04-07 | 2028-09-01 | ClinicalTrials.gov |
| NCT06158854 | A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult … | Phase1 | Immunoglobulin Light Chain (AL) Amyloidosis | Recruiting | 2024-04-01 | 2031-08-01 | ClinicalTrials.gov |
| NCT06158854 | A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult … | Phase1 | Immunoglobulin Light Chain (AL) Amyloidosis | Recruiting | 2024-04-01 | 2031-08-01 | ClinicalTrials.gov |
| NCT06158854 | A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult … | Phase1 | Immunoglobulin Light Chain (AL) Amyloidosis | Recruiting | 2024-04-01 | 2031-08-01 | ClinicalTrials.gov |
| NCT06158854 | A Study to Assess Change in Disease Activity and Adverse Events (AE)s in Adult … | Phase1 | Immunoglobulin Light Chain (AL) Amyloidosis | Recruiting | 2024-04-01 | 2031-08-01 | ClinicalTrials.gov |
| NCT06247540 | Venetoclax, Rituximab and Nivolumab in Combination for the Treatment of Richter… | Phase2 | Recurrent Transformed Chronic Lymphocytic Leukemia | Withdrawn | 2024-03-29 | 2031-12-29 | ClinicalTrials.gov |
| NCT06308198 | A Study to Evaluate AGN-151586 Intramuscular Injections in Adult Participants f… | Phase3 | Glabellar Lines | Completed | 2024-03-29 | 2025-02-26 | ClinicalTrials.gov |
| NCT06247540 | Venetoclax, Rituximab and Nivolumab in Combination for the Treatment of Richter… | Phase2 | Recurrent Transformed Chronic Lymphocytic Leukemia | Withdrawn | 2024-03-29 | 2031-12-29 | ClinicalTrials.gov |
| NCT06247540 | Venetoclax, Rituximab and Nivolumab in Combination for the Treatment of Richter… | Phase2 | Recurrent Transformed Chronic Lymphocytic Leukemia | Withdrawn | 2024-03-29 | 2031-12-29 | ClinicalTrials.gov |
| NCT06308198 | A Study to Evaluate AGN-151586 Intramuscular Injections in Adult Participants f… | Phase3 | Glabellar Lines | Completed | 2024-03-29 | 2025-02-26 | ClinicalTrials.gov |
| NCT06247540 | Venetoclax, Rituximab and Nivolumab in Combination for the Treatment of Richter… | Phase2 | Recurrent Transformed Chronic Lymphocytic Leukemia | Withdrawn | 2024-03-29 | 2031-12-29 | ClinicalTrials.gov |
| NCT06308198 | A Study to Evaluate AGN-151586 Intramuscular Injections in Adult Participants f… | Phase3 | Glabellar Lines | Completed | 2024-03-29 | 2025-02-26 | ClinicalTrials.gov |
| NCT06308198 | A Study to Evaluate AGN-151586 Intramuscular Injections in Adult Participants f… | Phase3 | Glabellar Lines | Completed | 2024-03-29 | 2025-02-26 | ClinicalTrials.gov |
| NCT06119217 | Phase 2 Study of TTX-030 and Chemotherapy With or Without Budigalimab for 1L mP… | Phase2 | Pancreatic Cancer | Completed | 2024-03-25 | 2026-03-06 | ClinicalTrials.gov |
| NCT06241313 | Study of Oral Atogepant Tablets to Assess Safety and Efficacy in Adult Particip… | Phase3 | Migraine | Active_Not_Recruiting | 2024-03-25 | 2026-11-01 | ClinicalTrials.gov |
| NCT06241313 | Study of Oral Atogepant Tablets to Assess Safety and Efficacy in Adult Particip… | Phase3 | Migraine | Active_Not_Recruiting | 2024-03-25 | 2026-11-01 | ClinicalTrials.gov |
| NCT06119217 | Phase 2 Study of TTX-030 and Chemotherapy With or Without Budigalimab for 1L mP… | Phase2 | Pancreatic Cancer | Completed | 2024-03-25 | 2026-03-06 | ClinicalTrials.gov |
| NCT06119217 | Phase 2 Study of TTX-030 and Chemotherapy With or Without Budigalimab for 1L mP… | Phase2 | Pancreatic Cancer | Completed | 2024-03-25 | 2026-03-06 | ClinicalTrials.gov |
| NCT06241313 | Study of Oral Atogepant Tablets to Assess Safety and Efficacy in Adult Particip… | Phase3 | Migraine | Active_Not_Recruiting | 2024-03-25 | 2026-11-01 | ClinicalTrials.gov |
| NCT06119217 | Phase 2 Study of TTX-030 and Chemotherapy With or Without Budigalimab for 1L mP… | Phase2 | Pancreatic Cancer | Completed | 2024-03-25 | 2026-03-06 | ClinicalTrials.gov |
| NCT06241313 | Study of Oral Atogepant Tablets to Assess Safety and Efficacy in Adult Particip… | Phase3 | Migraine | Active_Not_Recruiting | 2024-03-25 | 2026-11-01 | ClinicalTrials.gov |
| NCT06257875 | A Study to Assess Adverse Events and Change in Disease Activity From Intravenou… | Phase2 | Ulcerative Colitis | Active_Not_Recruiting | 2024-03-23 | 2027-09-01 | ClinicalTrials.gov |
| NCT06257875 | A Study to Assess Adverse Events and Change in Disease Activity From Intravenou… | Phase2 | Ulcerative Colitis | Active_Not_Recruiting | 2024-03-23 | 2027-09-01 | ClinicalTrials.gov |
| NCT06257875 | A Study to Assess Adverse Events and Change in Disease Activity From Intravenou… | Phase2 | Ulcerative Colitis | Active_Not_Recruiting | 2024-03-23 | 2027-09-01 | ClinicalTrials.gov |
| NCT06257875 | A Study to Assess Adverse Events and Change in Disease Activity From Intravenou… | Phase2 | Ulcerative Colitis | Active_Not_Recruiting | 2024-03-23 | 2027-09-01 | ClinicalTrials.gov |
| NCT06310876 | A Thorough QT Study of ABBV-CLS-7262 in Healthy Subjects | Phase1 | Healthy | Completed | 2024-03-14 | 2024-06-26 | ClinicalTrials.gov |
| NCT06310876 | A Thorough QT Study of ABBV-CLS-7262 in Healthy Subjects | Phase1 | Healthy | Completed | 2024-03-14 | 2024-06-26 | ClinicalTrials.gov |
| NCT06310876 | A Thorough QT Study of ABBV-CLS-7262 in Healthy Subjects | Phase1 | Healthy | Completed | 2024-03-14 | 2024-06-26 | ClinicalTrials.gov |
| NCT06310876 | A Thorough QT Study of ABBV-CLS-7262 in Healthy Subjects | Phase1 | Healthy | Completed | 2024-03-14 | 2024-06-26 | ClinicalTrials.gov |
| NCT06318273 | A Study to Assess Adverse Events, and How Intravenously (IV) Infused ABBV-969 M… | Phase1 | Metastatic Castration-Resistant Prostate Cancer | Active_Not_Recruiting | 2024-03-08 | 2027-05-01 | ClinicalTrials.gov |
| NCT06318273 | A Study to Assess Adverse Events, and How Intravenously (IV) Infused ABBV-969 M… | Phase1 | Metastatic Castration-Resistant Prostate Cancer | Active_Not_Recruiting | 2024-03-08 | 2027-05-01 | ClinicalTrials.gov |
| NCT06318273 | A Study to Assess Adverse Events, and How Intravenously (IV) Infused ABBV-969 M… | Phase1 | Metastatic Castration-Resistant Prostate Cancer | Active_Not_Recruiting | 2024-03-08 | 2027-05-01 | ClinicalTrials.gov |
| NCT06318273 | A Study to Assess Adverse Events, and How Intravenously (IV) Infused ABBV-969 M… | Phase1 | Metastatic Castration-Resistant Prostate Cancer | Active_Not_Recruiting | 2024-03-08 | 2027-05-01 | ClinicalTrials.gov |
| NCT06058741 | A Study to Asses Effectiveness and Treatment Management of Oral Venetoclax Tabl… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2024-03-04 | 2026-11-01 | ClinicalTrials.gov |
| NCT06058741 | A Study to Asses Effectiveness and Treatment Management of Oral Venetoclax Tabl… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2024-03-04 | 2026-11-01 | ClinicalTrials.gov |
| NCT06058741 | A Study to Asses Effectiveness and Treatment Management of Oral Venetoclax Tabl… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2024-03-04 | 2026-11-01 | ClinicalTrials.gov |
| NCT06058741 | A Study to Asses Effectiveness and Treatment Management of Oral Venetoclax Tabl… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2024-03-04 | 2026-11-01 | ClinicalTrials.gov |
| NCT06278766 | A Study to Assess the Mass Balance of [14C] ABBV-552 in Healthy Male Participan… | Phase1 | Healthy Volunteer | Completed | 2024-02-21 | 2024-04-19 | ClinicalTrials.gov |
| NCT06278766 | A Study to Assess the Mass Balance of [14C] ABBV-552 in Healthy Male Participan… | Phase1 | Healthy Volunteer | Completed | 2024-02-21 | 2024-04-19 | ClinicalTrials.gov |
| NCT06278766 | A Study to Assess the Mass Balance of [14C] ABBV-552 in Healthy Male Participan… | Phase1 | Healthy Volunteer | Completed | 2024-02-21 | 2024-04-19 | ClinicalTrials.gov |
| NCT06278766 | A Study to Assess the Mass Balance of [14C] ABBV-552 in Healthy Male Participan… | Phase1 | Healthy Volunteer | Completed | 2024-02-21 | 2024-04-19 | ClinicalTrials.gov |
| NCT05930275 | Study to Assess Speed of Onset and Durability of Effectiveness of Upadacitinib … | — | Crohn's Disease | Active_Not_Recruiting | 2024-02-19 | 2028-09-01 | ClinicalTrials.gov |
| NCT05930275 | Study to Assess Speed of Onset and Durability of Effectiveness of Upadacitinib … | — | Crohn's Disease | Active_Not_Recruiting | 2024-02-19 | 2028-09-01 | ClinicalTrials.gov |
| NCT05930275 | Study to Assess Speed of Onset and Durability of Effectiveness of Upadacitinib … | — | Crohn's Disease | Active_Not_Recruiting | 2024-02-19 | 2028-09-01 | ClinicalTrials.gov |
| NCT05930275 | Study to Assess Speed of Onset and Durability of Effectiveness of Upadacitinib … | — | Crohn's Disease | Active_Not_Recruiting | 2024-02-19 | 2028-09-01 | ClinicalTrials.gov |
| NCT06158958 | A Study to Assess the Safety, Pharmacokinetics, and Efficacy of Intravenous (IV… | Phase1 | Solid Tumors | Terminated | 2024-02-06 | 2025-10-22 | ClinicalTrials.gov |
| NCT06158958 | A Study to Assess the Safety, Pharmacokinetics, and Efficacy of Intravenous (IV… | Phase1 | Solid Tumors | Terminated | 2024-02-06 | 2025-10-22 | ClinicalTrials.gov |
| NCT06158958 | A Study to Assess the Safety, Pharmacokinetics, and Efficacy of Intravenous (IV… | Phase1 | Solid Tumors | Terminated | 2024-02-06 | 2025-10-22 | ClinicalTrials.gov |
| NCT06158958 | A Study to Assess the Safety, Pharmacokinetics, and Efficacy of Intravenous (IV… | Phase1 | Solid Tumors | Terminated | 2024-02-06 | 2025-10-22 | ClinicalTrials.gov |
| NCT06218251 | A Study to Evaluate Participant Satisfaction and Natural Outcomes Following Adm… | Phase4 | Upper Facial Lines | Completed | 2024-02-05 | 2024-12-17 | ClinicalTrials.gov |
| NCT06218251 | A Study to Evaluate Participant Satisfaction and Natural Outcomes Following Adm… | Phase4 | Upper Facial Lines | Completed | 2024-02-05 | 2024-12-17 | ClinicalTrials.gov |
| NCT06218251 | A Study to Evaluate Participant Satisfaction and Natural Outcomes Following Adm… | Phase4 | Upper Facial Lines | Completed | 2024-02-05 | 2024-12-17 | ClinicalTrials.gov |
| NCT06218251 | A Study to Evaluate Participant Satisfaction and Natural Outcomes Following Adm… | Phase4 | Upper Facial Lines | Completed | 2024-02-05 | 2024-12-17 | ClinicalTrials.gov |
| NCT06477159 | Pancreatic Enzyme Replacement Therapy for Acute Pancreatitis-Associated Exocrin… | Phase4 | Exocrine Pancreatic Insufficiency | Recruiting | 2024-02-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT06477159 | Pancreatic Enzyme Replacement Therapy for Acute Pancreatitis-Associated Exocrin… | Phase4 | Exocrine Pancreatic Insufficiency | Recruiting | 2024-02-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT06477159 | Pancreatic Enzyme Replacement Therapy for Acute Pancreatitis-Associated Exocrin… | Phase4 | Exocrine Pancreatic Insufficiency | Recruiting | 2024-02-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT06477159 | Pancreatic Enzyme Replacement Therapy for Acute Pancreatitis-Associated Exocrin… | Phase4 | Exocrine Pancreatic Insufficiency | Recruiting | 2024-02-01 | 2027-12-31 | ClinicalTrials.gov |
| NCT06148181 | A Study to Evaluate Adverse Events and How Single Ascending Doses of ABBV-141 M… | Phase1 | Healthy Volunteers | Completed | 2024-01-29 | 2024-12-30 | ClinicalTrials.gov |
| NCT06148181 | A Study to Evaluate Adverse Events and How Single Ascending Doses of ABBV-141 M… | Phase1 | Healthy Volunteers | Completed | 2024-01-29 | 2024-12-30 | ClinicalTrials.gov |
| NCT06148181 | A Study to Evaluate Adverse Events and How Single Ascending Doses of ABBV-141 M… | Phase1 | Healthy Volunteers | Completed | 2024-01-29 | 2024-12-30 | ClinicalTrials.gov |
| NCT06148181 | A Study to Evaluate Adverse Events and How Single Ascending Doses of ABBV-141 M… | Phase1 | Healthy Volunteers | Completed | 2024-01-29 | 2024-12-30 | ClinicalTrials.gov |
| NCT06107426 | Real-World Study of ABBV-951 Subcutaneous Infusion to Assess Change in Disease … | — | Parkinson's Disease (PD) | Active_Not_Recruiting | 2024-01-24 | 2029-05-01 | ClinicalTrials.gov |
| NCT06107426 | Real-World Study of ABBV-951 Subcutaneous Infusion to Assess Change in Disease … | — | Parkinson's Disease (PD) | Active_Not_Recruiting | 2024-01-24 | 2029-05-01 | ClinicalTrials.gov |
| NCT06107426 | Real-World Study of ABBV-951 Subcutaneous Infusion to Assess Change in Disease … | — | Parkinson's Disease (PD) | Active_Not_Recruiting | 2024-01-24 | 2029-05-01 | ClinicalTrials.gov |
| NCT06107426 | Real-World Study of ABBV-951 Subcutaneous Infusion to Assess Change in Disease … | — | Parkinson's Disease (PD) | Active_Not_Recruiting | 2024-01-24 | 2029-05-01 | ClinicalTrials.gov |
| NCT05956509 | Study of Intramuscular Injections of ABBV-950 to Assess Adverse Events and Chan… | Phase1 | Upper Limb Spasticity | Terminated | 2024-01-12 | 2024-06-02 | ClinicalTrials.gov |
| NCT05956509 | Study of Intramuscular Injections of ABBV-950 to Assess Adverse Events and Chan… | Phase1 | Upper Limb Spasticity | Terminated | 2024-01-12 | 2024-06-02 | ClinicalTrials.gov |
| NCT05956509 | Study of Intramuscular Injections of ABBV-950 to Assess Adverse Events and Chan… | Phase1 | Upper Limb Spasticity | Terminated | 2024-01-12 | 2024-06-02 | ClinicalTrials.gov |
| NCT05956509 | Study of Intramuscular Injections of ABBV-950 to Assess Adverse Events and Chan… | Phase1 | Upper Limb Spasticity | Terminated | 2024-01-12 | 2024-06-02 | ClinicalTrials.gov |
| NCT06109272 | A Study to Assess the Dose, Adverse Events, and Change in Disease Activity of L… | Phase2 | Hepatocellular Carcinoma | Recruiting | 2024-01-11 | 2030-09-01 | ClinicalTrials.gov |
| NCT06109272 | A Study to Assess the Dose, Adverse Events, and Change in Disease Activity of L… | Phase2 | Hepatocellular Carcinoma | Recruiting | 2024-01-11 | 2030-09-01 | ClinicalTrials.gov |
| NCT06109272 | A Study to Assess the Dose, Adverse Events, and Change in Disease Activity of L… | Phase2 | Hepatocellular Carcinoma | Recruiting | 2024-01-11 | 2030-09-01 | ClinicalTrials.gov |
| NCT06109272 | A Study to Assess the Dose, Adverse Events, and Change in Disease Activity of L… | Phase2 | Hepatocellular Carcinoma | Recruiting | 2024-01-11 | 2030-09-01 | ClinicalTrials.gov |
| NCT05821855 | A Study to Evaluate Adverse Events and Change in Disease Activity With the XEN4… | Phase4 | Open-angle Glaucoma | Active_Not_Recruiting | 2024-01-09 | 2030-07-01 | ClinicalTrials.gov |
| NCT05821855 | A Study to Evaluate Adverse Events and Change in Disease Activity With the XEN4… | Phase4 | Open-angle Glaucoma | Active_Not_Recruiting | 2024-01-09 | 2030-07-01 | ClinicalTrials.gov |
| NCT05821855 | A Study to Evaluate Adverse Events and Change in Disease Activity With the XEN4… | Phase4 | Open-angle Glaucoma | Active_Not_Recruiting | 2024-01-09 | 2030-07-01 | ClinicalTrials.gov |
| NCT05821855 | A Study to Evaluate Adverse Events and Change in Disease Activity With the XEN4… | Phase4 | Open-angle Glaucoma | Active_Not_Recruiting | 2024-01-09 | 2030-07-01 | ClinicalTrials.gov |
| NCT05486481 | Venetoclax, Daratumumab, and Dexamethasone for Systemic Light-Chain Amyloidosis… | Phase1 | AL Amyloidosis | Withdrawn | 2024-01-08 | 2028-12-31 | ClinicalTrials.gov |
| NCT05486481 | Venetoclax, Daratumumab, and Dexamethasone for Systemic Light-Chain Amyloidosis… | Phase1 | AL Amyloidosis | Withdrawn | 2024-01-08 | 2028-12-31 | ClinicalTrials.gov |
| NCT05486481 | Venetoclax, Daratumumab, and Dexamethasone for Systemic Light-Chain Amyloidosis… | Phase1 | AL Amyloidosis | Withdrawn | 2024-01-08 | 2028-12-31 | ClinicalTrials.gov |
| NCT05486481 | Venetoclax, Daratumumab, and Dexamethasone for Systemic Light-Chain Amyloidosis… | Phase1 | AL Amyloidosis | Withdrawn | 2024-01-08 | 2028-12-31 | ClinicalTrials.gov |
| NCT06151561 | Study of AGN-151586 in Japanese Participants With Moderate to Severe Glabellar … | Phase1 | Moderate to Severe Glabellar Lines | Completed | 2024-01-05 | 2024-04-03 | ClinicalTrials.gov |
| NCT06151561 | Study of AGN-151586 in Japanese Participants With Moderate to Severe Glabellar … | Phase1 | Moderate to Severe Glabellar Lines | Completed | 2024-01-05 | 2024-04-03 | ClinicalTrials.gov |
| NCT06151561 | Study of AGN-151586 in Japanese Participants With Moderate to Severe Glabellar … | Phase1 | Moderate to Severe Glabellar Lines | Completed | 2024-01-05 | 2024-04-03 | ClinicalTrials.gov |
| NCT06151561 | Study of AGN-151586 in Japanese Participants With Moderate to Severe Glabellar … | Phase1 | Moderate to Severe Glabellar Lines | Completed | 2024-01-05 | 2024-04-03 | ClinicalTrials.gov |
| NCT06058728 | A Study to Evaluate Changes in Hair in Adult Participants Taking Oral Oriahnn C… | — | Uterine Fibroids (UF) | Withdrawn | 2023-12-20 | 2026-08-01 | ClinicalTrials.gov |
| NCT06058728 | A Study to Evaluate Changes in Hair in Adult Participants Taking Oral Oriahnn C… | — | Uterine Fibroids (UF) | Withdrawn | 2023-12-20 | 2026-08-01 | ClinicalTrials.gov |
| NCT06058728 | A Study to Evaluate Changes in Hair in Adult Participants Taking Oral Oriahnn C… | — | Uterine Fibroids (UF) | Withdrawn | 2023-12-20 | 2026-08-01 | ClinicalTrials.gov |
| NCT06058728 | A Study to Evaluate Changes in Hair in Adult Participants Taking Oral Oriahnn C… | — | Uterine Fibroids (UF) | Withdrawn | 2023-12-20 | 2026-08-01 | ClinicalTrials.gov |
| NCT06118411 | A Study To Assess Adverse Events and Effectiveness of Upadacitinib Oral Tablets… | Phase3 | Vitiligo | Active_Not_Recruiting | 2023-12-19 | 2028-03-01 | ClinicalTrials.gov |
| NCT06145607 | A Phase 1 Study Assessing the Effect of Food on the Pharmacokinetics of ABBV- C… | Phase1 | Healthy | Completed | 2023-12-19 | 2024-02-26 | ClinicalTrials.gov |
| NCT06151535 | A Study to Evaluate the Safety and Effectiveness of ELAPR002f Injectable Gel fo… | Phase2 | Skin Quality Deficit | Completed | 2023-12-19 | 2025-02-24 | ClinicalTrials.gov |
| NCT06145607 | A Phase 1 Study Assessing the Effect of Food on the Pharmacokinetics of ABBV- C… | Phase1 | Healthy | Completed | 2023-12-19 | 2024-02-26 | ClinicalTrials.gov |
| NCT06145607 | A Phase 1 Study Assessing the Effect of Food on the Pharmacokinetics of ABBV- C… | Phase1 | Healthy | Completed | 2023-12-19 | 2024-02-26 | ClinicalTrials.gov |
| NCT06118411 | A Study To Assess Adverse Events and Effectiveness of Upadacitinib Oral Tablets… | Phase3 | Vitiligo | Active_Not_Recruiting | 2023-12-19 | 2028-03-01 | ClinicalTrials.gov |
| NCT06151535 | A Study to Evaluate the Safety and Effectiveness of ELAPR002f Injectable Gel fo… | Phase2 | Skin Quality Deficit | Completed | 2023-12-19 | 2025-02-24 | ClinicalTrials.gov |
| NCT06118411 | A Study To Assess Adverse Events and Effectiveness of Upadacitinib Oral Tablets… | Phase3 | Vitiligo | Active_Not_Recruiting | 2023-12-19 | 2028-03-01 | ClinicalTrials.gov |
| NCT06151535 | A Study to Evaluate the Safety and Effectiveness of ELAPR002f Injectable Gel fo… | Phase2 | Skin Quality Deficit | Completed | 2023-12-19 | 2025-02-24 | ClinicalTrials.gov |
| NCT06145607 | A Phase 1 Study Assessing the Effect of Food on the Pharmacokinetics of ABBV- C… | Phase1 | Healthy | Completed | 2023-12-19 | 2024-02-26 | ClinicalTrials.gov |
| NCT06151535 | A Study to Evaluate the Safety and Effectiveness of ELAPR002f Injectable Gel fo… | Phase2 | Skin Quality Deficit | Completed | 2023-12-19 | 2025-02-24 | ClinicalTrials.gov |
| NCT06118411 | A Study To Assess Adverse Events and Effectiveness of Upadacitinib Oral Tablets… | Phase3 | Vitiligo | Active_Not_Recruiting | 2023-12-19 | 2028-03-01 | ClinicalTrials.gov |
| NCT06034470 | Combination Chemotherapy (FLAG-Ida) With Pivekimab Sunirine (PVEK [IMGN632]) fo… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2023-12-18 | 2029-05-31 | ClinicalTrials.gov |
| NCT06034470 | Combination Chemotherapy (FLAG-Ida) With Pivekimab Sunirine (PVEK [IMGN632]) fo… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2023-12-18 | 2029-05-31 | ClinicalTrials.gov |
| NCT06034470 | Combination Chemotherapy (FLAG-Ida) With Pivekimab Sunirine (PVEK [IMGN632]) fo… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2023-12-18 | 2029-05-31 | ClinicalTrials.gov |
| NCT06034470 | Combination Chemotherapy (FLAG-Ida) With Pivekimab Sunirine (PVEK [IMGN632]) fo… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2023-12-18 | 2029-05-31 | ClinicalTrials.gov |
| NCT06174688 | A Study to Assess the Adverse Events and Effectiveness of BOTOX Injections for … | Phase3 | Forehead Lines | Completed | 2023-12-12 | 2024-09-13 | ClinicalTrials.gov |
| NCT06174688 | A Study to Assess the Adverse Events and Effectiveness of BOTOX Injections for … | Phase3 | Forehead Lines | Completed | 2023-12-12 | 2024-09-13 | ClinicalTrials.gov |
| NCT06174688 | A Study to Assess the Adverse Events and Effectiveness of BOTOX Injections for … | Phase3 | Forehead Lines | Completed | 2023-12-12 | 2024-09-13 | ClinicalTrials.gov |
| NCT06174688 | A Study to Assess the Adverse Events and Effectiveness of BOTOX Injections for … | Phase3 | Forehead Lines | Completed | 2023-12-12 | 2024-09-13 | ClinicalTrials.gov |
| NCT05995353 | A Study to Assess Adverse Events, Change in Disease Activity, and How Intraveno… | Phase3 | Crohn's Disease | Recruiting | 2023-12-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT05995353 | A Study to Assess Adverse Events, Change in Disease Activity, and How Intraveno… | Phase3 | Crohn's Disease | Recruiting | 2023-12-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT05995353 | A Study to Assess Adverse Events, Change in Disease Activity, and How Intraveno… | Phase3 | Crohn's Disease | Recruiting | 2023-12-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT05995353 | A Study to Assess Adverse Events, Change in Disease Activity, and How Intraveno… | Phase3 | Crohn's Disease | Recruiting | 2023-12-11 | 2029-04-01 | ClinicalTrials.gov |
| NCT05782127 | Oral Azacitidine Combined With Venetoclax in Previously Untreated Higher-risk M… | Phase1 | Untreated Myelodysplastic Syndrome | Active_Not_Recruiting | 2023-12-06 | 2028-11-01 | ClinicalTrials.gov |
| NCT05782127 | Oral Azacitidine Combined With Venetoclax in Previously Untreated Higher-risk M… | Phase1 | Untreated Myelodysplastic Syndrome | Active_Not_Recruiting | 2023-12-06 | 2028-11-01 | ClinicalTrials.gov |
| NCT05782127 | Oral Azacitidine Combined With Venetoclax in Previously Untreated Higher-risk M… | Phase1 | Untreated Myelodysplastic Syndrome | Active_Not_Recruiting | 2023-12-06 | 2028-11-01 | ClinicalTrials.gov |
| NCT05782127 | Oral Azacitidine Combined With Venetoclax in Previously Untreated Higher-risk M… | Phase1 | Untreated Myelodysplastic Syndrome | Active_Not_Recruiting | 2023-12-06 | 2028-11-01 | ClinicalTrials.gov |
| NCT05956483 | Study to Assess Accuracy of Rapid Mood Screener in Adult Participants With Unip… | — | Bipolar I Disorder | Completed | 2023-12-04 | 2024-08-16 | ClinicalTrials.gov |
| NCT05956483 | Study to Assess Accuracy of Rapid Mood Screener in Adult Participants With Unip… | — | Bipolar I Disorder | Completed | 2023-12-04 | 2024-08-16 | ClinicalTrials.gov |
| NCT05956483 | Study to Assess Accuracy of Rapid Mood Screener in Adult Participants With Unip… | — | Bipolar I Disorder | Completed | 2023-12-04 | 2024-08-16 | ClinicalTrials.gov |
| NCT05956483 | Study to Assess Accuracy of Rapid Mood Screener in Adult Participants With Unip… | — | Bipolar I Disorder | Completed | 2023-12-04 | 2024-08-16 | ClinicalTrials.gov |
| NCT05916157 | An Observational Study of Subcutaneous Infusion of ABBV-951 to Assess Change in… | — | Parkinson's Disease (PD) | Active_Not_Recruiting | 2023-11-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT05587049 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Recruiting | 2023-11-30 | 2026-11-01 | ClinicalTrials.gov |
| NCT05916157 | An Observational Study of Subcutaneous Infusion of ABBV-951 to Assess Change in… | — | Parkinson's Disease (PD) | Active_Not_Recruiting | 2023-11-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT05916157 | An Observational Study of Subcutaneous Infusion of ABBV-951 to Assess Change in… | — | Parkinson's Disease (PD) | Active_Not_Recruiting | 2023-11-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT05587049 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Recruiting | 2023-11-30 | 2026-11-01 | ClinicalTrials.gov |
| NCT05916157 | An Observational Study of Subcutaneous Infusion of ABBV-951 to Assess Change in… | — | Parkinson's Disease (PD) | Active_Not_Recruiting | 2023-11-30 | 2027-01-01 | ClinicalTrials.gov |
| NCT05587049 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Recruiting | 2023-11-30 | 2026-11-01 | ClinicalTrials.gov |
| NCT05587049 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Recruiting | 2023-11-30 | 2026-11-01 | ClinicalTrials.gov |
| NCT06144684 | A Two-Part First-In-Human Study to Assess the Safety, Tolerability, Pharmacokin… | Phase1 | Healthy Volunteers | Completed | 2023-11-29 | 2026-01-05 | ClinicalTrials.gov |
| NCT06144684 | A Two-Part First-In-Human Study to Assess the Safety, Tolerability, Pharmacokin… | Phase1 | Healthy Volunteers | Completed | 2023-11-29 | 2026-01-05 | ClinicalTrials.gov |
| NCT06144684 | A Two-Part First-In-Human Study to Assess the Safety, Tolerability, Pharmacokin… | Phase1 | Healthy Volunteers | Completed | 2023-11-29 | 2026-01-05 | ClinicalTrials.gov |
| NCT06144684 | A Two-Part First-In-Human Study to Assess the Safety, Tolerability, Pharmacokin… | Phase1 | Healthy Volunteers | Completed | 2023-11-29 | 2026-01-05 | ClinicalTrials.gov |
| NCT06137287 | A Study to Assess Adverse Events and Change of Masseter Muscle Prominence Using… | Phase3 | Masseter Muscle Prominence | Completed | 2023-11-22 | 2025-07-31 | ClinicalTrials.gov |
| NCT06137287 | A Study to Assess Adverse Events and Change of Masseter Muscle Prominence Using… | Phase3 | Masseter Muscle Prominence | Completed | 2023-11-22 | 2025-07-31 | ClinicalTrials.gov |
| NCT06137287 | A Study to Assess Adverse Events and Change of Masseter Muscle Prominence Using… | Phase3 | Masseter Muscle Prominence | Completed | 2023-11-22 | 2025-07-31 | ClinicalTrials.gov |
| NCT06137287 | A Study to Assess Adverse Events and Change of Masseter Muscle Prominence Using… | Phase3 | Masseter Muscle Prominence | Completed | 2023-11-22 | 2025-07-31 | ClinicalTrials.gov |
| NCT05995340 | ELAPR002f Injectable Gel in the Treatment of Atrophic Acne Scars | Phase3 | Atrophic Acne Scars | Active_Not_Recruiting | 2023-11-21 | 2026-08-01 | ClinicalTrials.gov |
| NCT05995340 | ELAPR002f Injectable Gel in the Treatment of Atrophic Acne Scars | Phase3 | Atrophic Acne Scars | Active_Not_Recruiting | 2023-11-21 | 2026-08-01 | ClinicalTrials.gov |
| NCT05995340 | ELAPR002f Injectable Gel in the Treatment of Atrophic Acne Scars | Phase3 | Atrophic Acne Scars | Active_Not_Recruiting | 2023-11-21 | 2026-08-01 | ClinicalTrials.gov |
| NCT05995340 | ELAPR002f Injectable Gel in the Treatment of Atrophic Acne Scars | Phase3 | Atrophic Acne Scars | Active_Not_Recruiting | 2023-11-21 | 2026-08-01 | ClinicalTrials.gov |
| NCT06054425 | A Study to Compare the Bioavailability of Intravenously Infused Risankizumab Ma… | Phase1 | Healthy Volunteers | Completed | 2023-11-20 | 2024-05-06 | ClinicalTrials.gov |
| NCT06054425 | A Study to Compare the Bioavailability of Intravenously Infused Risankizumab Ma… | Phase1 | Healthy Volunteers | Completed | 2023-11-20 | 2024-05-06 | ClinicalTrials.gov |
| NCT06054425 | A Study to Compare the Bioavailability of Intravenously Infused Risankizumab Ma… | Phase1 | Healthy Volunteers | Completed | 2023-11-20 | 2024-05-06 | ClinicalTrials.gov |
| NCT06054425 | A Study to Compare the Bioavailability of Intravenously Infused Risankizumab Ma… | Phase1 | Healthy Volunteers | Completed | 2023-11-20 | 2024-05-06 | ClinicalTrials.gov |
| NCT06063967 | A Study to Assess Adverse Events and Change in Disease Activity of Risankizumab… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2023-11-15 | 2027-03-01 | ClinicalTrials.gov |
| NCT06063967 | A Study to Assess Adverse Events and Change in Disease Activity of Risankizumab… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2023-11-15 | 2027-03-01 | ClinicalTrials.gov |
| NCT06063967 | A Study to Assess Adverse Events and Change in Disease Activity of Risankizumab… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2023-11-15 | 2027-03-01 | ClinicalTrials.gov |
| NCT06063967 | A Study to Assess Adverse Events and Change in Disease Activity of Risankizumab… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2023-11-15 | 2027-03-01 | ClinicalTrials.gov |
| NCT06068868 | Study to Evaluate Adverse Events and Movement of Intravenously (IV) Infused ABB… | Phase1 | Acute Myeloid Leukemia | Terminated | 2023-11-13 | 2025-02-25 | ClinicalTrials.gov |
| NCT06068868 | Study to Evaluate Adverse Events and Movement of Intravenously (IV) Infused ABB… | Phase1 | Acute Myeloid Leukemia | Terminated | 2023-11-13 | 2025-02-25 | ClinicalTrials.gov |
| NCT06068868 | Study to Evaluate Adverse Events and Movement of Intravenously (IV) Infused ABB… | Phase1 | Acute Myeloid Leukemia | Terminated | 2023-11-13 | 2025-02-25 | ClinicalTrials.gov |
| NCT06068868 | Study to Evaluate Adverse Events and Movement of Intravenously (IV) Infused ABB… | Phase1 | Acute Myeloid Leukemia | Terminated | 2023-11-13 | 2025-02-25 | ClinicalTrials.gov |
| NCT06107413 | Study to Assess Adverse Events and Change in Disease Activity in Previously Tre… | Phase2 | Unresectable Metastatic Colorectal Cancer | Active_Not_Recruiting | 2023-11-12 | 2026-12-01 | ClinicalTrials.gov |
| NCT06107413 | Study to Assess Adverse Events and Change in Disease Activity in Previously Tre… | Phase2 | Unresectable Metastatic Colorectal Cancer | Active_Not_Recruiting | 2023-11-12 | 2026-12-01 | ClinicalTrials.gov |
| NCT06107413 | Study to Assess Adverse Events and Change in Disease Activity in Previously Tre… | Phase2 | Unresectable Metastatic Colorectal Cancer | Active_Not_Recruiting | 2023-11-12 | 2026-12-01 | ClinicalTrials.gov |
| NCT06107413 | Study to Assess Adverse Events and Change in Disease Activity in Previously Tre… | Phase2 | Unresectable Metastatic Colorectal Cancer | Active_Not_Recruiting | 2023-11-12 | 2026-12-01 | ClinicalTrials.gov |
| NCT05959070 | An Observational Study to Validate the Cumulative Life Course Impairment (CLCI)… | — | Psoriasis | Completed | 2023-11-09 | 2025-03-21 | ClinicalTrials.gov |
| NCT06084481 | Study to Assess Adverse Events and Change in Disease Activity in Adult Particip… | Phase1 | Hepatocellular Carcinoma | Active_Not_Recruiting | 2023-11-09 | 2026-07-01 | ClinicalTrials.gov |
| NCT05959070 | An Observational Study to Validate the Cumulative Life Course Impairment (CLCI)… | — | Psoriasis | Completed | 2023-11-09 | 2025-03-21 | ClinicalTrials.gov |
| NCT05959070 | An Observational Study to Validate the Cumulative Life Course Impairment (CLCI)… | — | Psoriasis | Completed | 2023-11-09 | 2025-03-21 | ClinicalTrials.gov |
| NCT06084481 | Study to Assess Adverse Events and Change in Disease Activity in Adult Particip… | Phase1 | Hepatocellular Carcinoma | Active_Not_Recruiting | 2023-11-09 | 2026-07-01 | ClinicalTrials.gov |
| NCT05959070 | An Observational Study to Validate the Cumulative Life Course Impairment (CLCI)… | — | Psoriasis | Completed | 2023-11-09 | 2025-03-21 | ClinicalTrials.gov |
| NCT06084481 | Study to Assess Adverse Events and Change in Disease Activity in Adult Particip… | Phase1 | Hepatocellular Carcinoma | Active_Not_Recruiting | 2023-11-09 | 2026-07-01 | ClinicalTrials.gov |
| NCT06084481 | Study to Assess Adverse Events and Change in Disease Activity in Adult Particip… | Phase1 | Hepatocellular Carcinoma | Active_Not_Recruiting | 2023-11-09 | 2026-07-01 | ClinicalTrials.gov |
| NCT06125795 | A Study to Assess Change in Functioning and Health Related Quality of Life in A… | — | Chronic Lymphocytic Leukemia | Recruiting | 2023-11-06 | 2026-07-01 | ClinicalTrials.gov |
| NCT06125795 | A Study to Assess Change in Functioning and Health Related Quality of Life in A… | — | Chronic Lymphocytic Leukemia | Recruiting | 2023-11-06 | 2026-07-01 | ClinicalTrials.gov |
| NCT05782907 | Study to Assess Adverse Events, Change in Disease Activity, and How Oral Upadac… | Phase3 | Ulcerative Colitis | Active_Not_Recruiting | 2023-11-06 | 2031-10-01 | ClinicalTrials.gov |
| NCT06125795 | A Study to Assess Change in Functioning and Health Related Quality of Life in A… | — | Chronic Lymphocytic Leukemia | Recruiting | 2023-11-06 | 2026-07-01 | ClinicalTrials.gov |
| NCT05782907 | Study to Assess Adverse Events, Change in Disease Activity, and How Oral Upadac… | Phase3 | Ulcerative Colitis | Active_Not_Recruiting | 2023-11-06 | 2031-10-01 | ClinicalTrials.gov |
| NCT05782907 | Study to Assess Adverse Events, Change in Disease Activity, and How Oral Upadac… | Phase3 | Ulcerative Colitis | Active_Not_Recruiting | 2023-11-06 | 2031-10-01 | ClinicalTrials.gov |
| NCT06125795 | A Study to Assess Change in Functioning and Health Related Quality of Life in A… | — | Chronic Lymphocytic Leukemia | Recruiting | 2023-11-06 | 2026-07-01 | ClinicalTrials.gov |
| NCT05782907 | Study to Assess Adverse Events, Change in Disease Activity, and How Oral Upadac… | Phase3 | Ulcerative Colitis | Active_Not_Recruiting | 2023-11-06 | 2031-10-01 | ClinicalTrials.gov |
| NCT06068842 | A Study to Assess Prevalence of a Specific Protein Overexpression in Adult Part… | — | Non Small Cell Lung Cancer | Completed | 2023-11-03 | 2024-12-31 | ClinicalTrials.gov |
| NCT06068842 | A Study to Assess Prevalence of a Specific Protein Overexpression in Adult Part… | — | Non Small Cell Lung Cancer | Completed | 2023-11-03 | 2024-12-31 | ClinicalTrials.gov |
| NCT06068842 | A Study to Assess Prevalence of a Specific Protein Overexpression in Adult Part… | — | Non Small Cell Lung Cancer | Completed | 2023-11-03 | 2024-12-31 | ClinicalTrials.gov |
| NCT06068842 | A Study to Assess Prevalence of a Specific Protein Overexpression in Adult Part… | — | Non Small Cell Lung Cancer | Completed | 2023-11-03 | 2024-12-31 | ClinicalTrials.gov |
| NCT05978622 | Observational Study of Adult Participants With Diabetic Macular Edema and Subop… | — | Diabetic Macular Edema | Active_Not_Recruiting | 2023-10-30 | 2026-06-01 | ClinicalTrials.gov |
| NCT05978622 | Observational Study of Adult Participants With Diabetic Macular Edema and Subop… | — | Diabetic Macular Edema | Active_Not_Recruiting | 2023-10-30 | 2026-06-01 | ClinicalTrials.gov |
| NCT05978622 | Observational Study of Adult Participants With Diabetic Macular Edema and Subop… | — | Diabetic Macular Edema | Active_Not_Recruiting | 2023-10-30 | 2026-06-01 | ClinicalTrials.gov |
| NCT05978622 | Observational Study of Adult Participants With Diabetic Macular Edema and Subop… | — | Diabetic Macular Edema | Active_Not_Recruiting | 2023-10-30 | 2026-06-01 | ClinicalTrials.gov |
| NCT06126146 | An Observational Study to Assess Participant-Reported Real-World Experience of … | — | Crohn's Disease | Completed | 2023-10-26 | 2024-05-16 | ClinicalTrials.gov |
| NCT06126146 | An Observational Study to Assess Participant-Reported Real-World Experience of … | — | Crohn's Disease | Completed | 2023-10-26 | 2024-05-16 | ClinicalTrials.gov |
| NCT06126146 | An Observational Study to Assess Participant-Reported Real-World Experience of … | — | Crohn's Disease | Completed | 2023-10-26 | 2024-05-16 | ClinicalTrials.gov |
| NCT06126146 | An Observational Study to Assess Participant-Reported Real-World Experience of … | — | Crohn's Disease | Completed | 2023-10-26 | 2024-05-16 | ClinicalTrials.gov |
| NCT06332690 | OCT and OCT-Angiography Biomarkers of Treatment Response to Dexamethasone Impla… | — | Diabetic Macular Edema | Unknown | 2023-10-17 | 2025-12-01 | ClinicalTrials.gov |
| NCT06332690 | OCT and OCT-Angiography Biomarkers of Treatment Response to Dexamethasone Impla… | — | Diabetic Macular Edema | Unknown | 2023-10-17 | 2025-12-01 | ClinicalTrials.gov |
| NCT06332690 | OCT and OCT-Angiography Biomarkers of Treatment Response to Dexamethasone Impla… | — | Diabetic Macular Edema | Unknown | 2023-10-17 | 2025-12-01 | ClinicalTrials.gov |
| NCT06068855 | A Study to Assess the Effectiveness of BOTOX (Botulinum Toxin Type A) Injection… | Phase3 | Masseter Muscle Prominence | Completed | 2023-10-17 | 2025-11-20 | ClinicalTrials.gov |
| NCT06068855 | A Study to Assess the Effectiveness of BOTOX (Botulinum Toxin Type A) Injection… | Phase3 | Masseter Muscle Prominence | Completed | 2023-10-17 | 2025-11-20 | ClinicalTrials.gov |
| NCT06068855 | A Study to Assess the Effectiveness of BOTOX (Botulinum Toxin Type A) Injection… | Phase3 | Masseter Muscle Prominence | Completed | 2023-10-17 | 2025-11-20 | ClinicalTrials.gov |
| NCT06332690 | OCT and OCT-Angiography Biomarkers of Treatment Response to Dexamethasone Impla… | — | Diabetic Macular Edema | Unknown | 2023-10-17 | 2025-12-01 | ClinicalTrials.gov |
| NCT06068855 | A Study to Assess the Effectiveness of BOTOX (Botulinum Toxin Type A) Injection… | Phase3 | Masseter Muscle Prominence | Completed | 2023-10-17 | 2025-11-20 | ClinicalTrials.gov |
| NCT06032546 | A Study to Assess Change in Disease Activity, Adverse Events, and How the Drug … | Phase2 | Human Immuno-deficiency Virus (HIV) Disease | Terminated | 2023-10-12 | 2025-09-22 | ClinicalTrials.gov |
| NCT06032546 | A Study to Assess Change in Disease Activity, Adverse Events, and How the Drug … | Phase2 | Human Immuno-deficiency Virus (HIV) Disease | Terminated | 2023-10-12 | 2025-09-22 | ClinicalTrials.gov |
| NCT06032546 | A Study to Assess Change in Disease Activity, Adverse Events, and How the Drug … | Phase2 | Human Immuno-deficiency Virus (HIV) Disease | Terminated | 2023-10-12 | 2025-09-22 | ClinicalTrials.gov |
| NCT06032546 | A Study to Assess Change in Disease Activity, Adverse Events, and How the Drug … | Phase2 | Human Immuno-deficiency Virus (HIV) Disease | Terminated | 2023-10-12 | 2025-09-22 | ClinicalTrials.gov |
| NCT06012240 | A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adu… | Phase3 | Alopecia Areata | Recruiting | 2023-10-11 | 2030-04-01 | ClinicalTrials.gov |
| NCT06012240 | A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adu… | Phase3 | Alopecia Areata | Recruiting | 2023-10-11 | 2030-04-01 | ClinicalTrials.gov |
| NCT06012240 | A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adu… | Phase3 | Alopecia Areata | Recruiting | 2023-10-11 | 2030-04-01 | ClinicalTrials.gov |
| NCT06012240 | A Study to Evaluate the Safety and Effectiveness of Upadacitinib Tablets in Adu… | Phase3 | Alopecia Areata | Recruiting | 2023-10-11 | 2030-04-01 | ClinicalTrials.gov |
| NCT05748483 | Comparative Study of Oral Atogepant Versus Oral Topiramate to Assess Adverse Ev… | Phase3 | Migraine | Completed | 2023-10-07 | 2026-06-02 | ClinicalTrials.gov |
| NCT05748483 | Comparative Study of Oral Atogepant Versus Oral Topiramate to Assess Adverse Ev… | Phase3 | Migraine | Completed | 2023-10-07 | 2026-06-02 | ClinicalTrials.gov |
| NCT05748483 | Comparative Study of Oral Atogepant Versus Oral Topiramate to Assess Adverse Ev… | Phase3 | Migraine | Completed | 2023-10-07 | 2026-06-02 | ClinicalTrials.gov |
| NCT05748483 | Comparative Study of Oral Atogepant Versus Oral Topiramate to Assess Adverse Ev… | Phase3 | Migraine | Completed | 2023-10-07 | 2026-06-02 | ClinicalTrials.gov |
| NCT06070948 | A Study to Assess Food Effect of Venetoclax New Tablet Formulation in Healthy F… | Phase1 | Healthy Volunteers | Withdrawn | 2023-10-05 | 2025-07-28 | ClinicalTrials.gov |
| NCT06070948 | A Study to Assess Food Effect of Venetoclax New Tablet Formulation in Healthy F… | Phase1 | Healthy Volunteers | Withdrawn | 2023-10-05 | 2025-07-28 | ClinicalTrials.gov |
| NCT06070948 | A Study to Assess Food Effect of Venetoclax New Tablet Formulation in Healthy F… | Phase1 | Healthy Volunteers | Withdrawn | 2023-10-05 | 2025-07-28 | ClinicalTrials.gov |
| NCT06070948 | A Study to Assess Food Effect of Venetoclax New Tablet Formulation in Healthy F… | Phase1 | Healthy Volunteers | Withdrawn | 2023-10-05 | 2025-07-28 | ClinicalTrials.gov |
| NCT05768711 | Azacitidine Combined With Venetoclax in Patients With Higher-risk Chronic Myelo… | Phase2 | Chronic Myeloid Leukemia | Active_Not_Recruiting | 2023-10-04 | 2028-10-01 | ClinicalTrials.gov |
| NCT05768711 | Azacitidine Combined With Venetoclax in Patients With Higher-risk Chronic Myelo… | Phase2 | Chronic Myeloid Leukemia | Active_Not_Recruiting | 2023-10-04 | 2028-10-01 | ClinicalTrials.gov |
| NCT05768711 | Azacitidine Combined With Venetoclax in Patients With Higher-risk Chronic Myelo… | Phase2 | Chronic Myeloid Leukemia | Active_Not_Recruiting | 2023-10-04 | 2028-10-01 | ClinicalTrials.gov |
| NCT05768711 | Azacitidine Combined With Venetoclax in Patients With Higher-risk Chronic Myelo… | Phase2 | Chronic Myeloid Leukemia | Active_Not_Recruiting | 2023-10-04 | 2028-10-01 | ClinicalTrials.gov |
| NCT05887609 | An Evaluation of Maintenance Therapy Combination Mirvetuximab Soravtansine and … | Phase2 | Ovary Cancer | Recruiting | 2023-10-03 | 2031-01-31 | ClinicalTrials.gov |
| NCT05887609 | An Evaluation of Maintenance Therapy Combination Mirvetuximab Soravtansine and … | Phase2 | Ovary Cancer | Recruiting | 2023-10-03 | 2031-01-31 | ClinicalTrials.gov |
| NCT05887609 | An Evaluation of Maintenance Therapy Combination Mirvetuximab Soravtansine and … | Phase2 | Ovary Cancer | Recruiting | 2023-10-03 | 2031-01-31 | ClinicalTrials.gov |
| NCT05887609 | An Evaluation of Maintenance Therapy Combination Mirvetuximab Soravtansine and … | Phase2 | Ovary Cancer | Recruiting | 2023-10-03 | 2031-01-31 | ClinicalTrials.gov |
| NCT05609630 | Study of Oral Upadacitinib and Subcutaneous/Intravenous Tocilizumab to Evaluate… | Phase3 | Juvenile Idiopathic Arthritis | Recruiting | 2023-10-02 | 2029-06-01 | ClinicalTrials.gov |
| NCT05609630 | Study of Oral Upadacitinib and Subcutaneous/Intravenous Tocilizumab to Evaluate… | Phase3 | Juvenile Idiopathic Arthritis | Recruiting | 2023-10-02 | 2029-06-01 | ClinicalTrials.gov |
| NCT05609630 | Study of Oral Upadacitinib and Subcutaneous/Intravenous Tocilizumab to Evaluate… | Phase3 | Juvenile Idiopathic Arthritis | Recruiting | 2023-10-02 | 2029-06-01 | ClinicalTrials.gov |
| NCT05609630 | Study of Oral Upadacitinib and Subcutaneous/Intravenous Tocilizumab to Evaluate… | Phase3 | Juvenile Idiopathic Arthritis | Recruiting | 2023-10-02 | 2029-06-01 | ClinicalTrials.gov |
| NCT05990829 | Compare the Efficacy of VItrectomy Combined With DExamethasone Implant Versus W… | Phase4 | Diabetic Macular Edema | Unknown | 2023-10-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT05990829 | Compare the Efficacy of VItrectomy Combined With DExamethasone Implant Versus W… | Phase4 | Diabetic Macular Edema | Unknown | 2023-10-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT05990829 | Compare the Efficacy of VItrectomy Combined With DExamethasone Implant Versus W… | Phase4 | Diabetic Macular Edema | Unknown | 2023-10-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT05990829 | Compare the Efficacy of VItrectomy Combined With DExamethasone Implant Versus W… | Phase4 | Diabetic Macular Edema | Unknown | 2023-10-01 | 2025-04-01 | ClinicalTrials.gov |
| NCT06067568 | Relative Bioavailability of Two Lutikizumab Formulations and Pharmacokinetics, … | Phase1 | Healthy Volunteers | Completed | 2023-09-28 | 2024-02-26 | ClinicalTrials.gov |
| NCT06067568 | Relative Bioavailability of Two Lutikizumab Formulations and Pharmacokinetics, … | Phase1 | Healthy Volunteers | Completed | 2023-09-28 | 2024-02-26 | ClinicalTrials.gov |
| NCT06067568 | Relative Bioavailability of Two Lutikizumab Formulations and Pharmacokinetics, … | Phase1 | Healthy Volunteers | Completed | 2023-09-28 | 2024-02-26 | ClinicalTrials.gov |
| NCT06067568 | Relative Bioavailability of Two Lutikizumab Formulations and Pharmacokinetics, … | Phase1 | Healthy Volunteers | Completed | 2023-09-28 | 2024-02-26 | ClinicalTrials.gov |
| NCT05822752 | Study to Evaluate Adverse Events, and Change in Disease Activity, When Intraven… | Phase2 | Hepatocellular Carcinoma | Active_Not_Recruiting | 2023-09-21 | 2026-11-01 | ClinicalTrials.gov |
| NCT05822752 | Study to Evaluate Adverse Events, and Change in Disease Activity, When Intraven… | Phase2 | Hepatocellular Carcinoma | Active_Not_Recruiting | 2023-09-21 | 2026-11-01 | ClinicalTrials.gov |
| NCT05822752 | Study to Evaluate Adverse Events, and Change in Disease Activity, When Intraven… | Phase2 | Hepatocellular Carcinoma | Active_Not_Recruiting | 2023-09-21 | 2026-11-01 | ClinicalTrials.gov |
| NCT05822752 | Study to Evaluate Adverse Events, and Change in Disease Activity, When Intraven… | Phase2 | Hepatocellular Carcinoma | Active_Not_Recruiting | 2023-09-21 | 2026-11-01 | ClinicalTrials.gov |
| NCT06150729 | Study of Intramuscular Injections of OnabotulinumtoxinA to Assess Change in Dis… | — | Spasticity | Completed | 2023-09-08 | 2025-05-30 | ClinicalTrials.gov |
| NCT06150729 | Study of Intramuscular Injections of OnabotulinumtoxinA to Assess Change in Dis… | — | Spasticity | Completed | 2023-09-08 | 2025-05-30 | ClinicalTrials.gov |
| NCT06150729 | Study of Intramuscular Injections of OnabotulinumtoxinA to Assess Change in Dis… | — | Spasticity | Completed | 2023-09-08 | 2025-05-30 | ClinicalTrials.gov |
| NCT06150729 | Study of Intramuscular Injections of OnabotulinumtoxinA to Assess Change in Dis… | — | Spasticity | Completed | 2023-09-08 | 2025-05-30 | ClinicalTrials.gov |
| NCT06018987 | A Study to Assess Adverse Events and Effectiveness of HAC 20L Injections in Adu… | Phase2 | Nasolabial Folds | Completed | 2023-09-05 | 2025-02-03 | ClinicalTrials.gov |
| NCT06018987 | A Study to Assess Adverse Events and Effectiveness of HAC 20L Injections in Adu… | Phase2 | Nasolabial Folds | Completed | 2023-09-05 | 2025-02-03 | ClinicalTrials.gov |
| NCT06018987 | A Study to Assess Adverse Events and Effectiveness of HAC 20L Injections in Adu… | Phase2 | Nasolabial Folds | Completed | 2023-09-05 | 2025-02-03 | ClinicalTrials.gov |
| NCT06018987 | A Study to Assess Adverse Events and Effectiveness of HAC 20L Injections in Adu… | Phase2 | Nasolabial Folds | Completed | 2023-09-05 | 2025-02-03 | ClinicalTrials.gov |
| NCT05701215 | Venetoclax After TKI to Target Persisting Stem Cells in CML | Phase2 | Chronic Myeloid Leukemia | Active_Not_Recruiting | 2023-08-31 | 2026-01-31 | ClinicalTrials.gov |
| NCT05701215 | Venetoclax After TKI to Target Persisting Stem Cells in CML | Phase2 | Chronic Myeloid Leukemia | Active_Not_Recruiting | 2023-08-31 | 2026-01-31 | ClinicalTrials.gov |
| NCT06024239 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of ABBV-932 … | Phase1 | Healthy Volunteers | Completed | 2023-08-31 | 2025-03-04 | ClinicalTrials.gov |
| NCT05701215 | Venetoclax After TKI to Target Persisting Stem Cells in CML | Phase2 | Chronic Myeloid Leukemia | Active_Not_Recruiting | 2023-08-31 | 2026-01-31 | ClinicalTrials.gov |
| NCT05701215 | Venetoclax After TKI to Target Persisting Stem Cells in CML | Phase2 | Chronic Myeloid Leukemia | Active_Not_Recruiting | 2023-08-31 | 2026-01-31 | ClinicalTrials.gov |
| NCT06024239 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of ABBV-932 … | Phase1 | Healthy Volunteers | Completed | 2023-08-31 | 2025-03-04 | ClinicalTrials.gov |
| NCT06024239 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of ABBV-932 … | Phase1 | Healthy Volunteers | Completed | 2023-08-31 | 2025-03-04 | ClinicalTrials.gov |
| NCT06024239 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of ABBV-932 … | Phase1 | Healthy Volunteers | Completed | 2023-08-31 | 2025-03-04 | ClinicalTrials.gov |
| NCT06009237 | A Study to Assess Pharmacokinetics, Safety, and Tolerability of ABBV-903 in Hea… | Phase1 | Healthy Volunteers | Terminated | 2023-08-23 | 2023-10-30 | ClinicalTrials.gov |
| NCT06009237 | A Study to Assess Pharmacokinetics, Safety, and Tolerability of ABBV-903 in Hea… | Phase1 | Healthy Volunteers | Terminated | 2023-08-23 | 2023-10-30 | ClinicalTrials.gov |
| NCT06009237 | A Study to Assess Pharmacokinetics, Safety, and Tolerability of ABBV-903 in Hea… | Phase1 | Healthy Volunteers | Terminated | 2023-08-23 | 2023-10-30 | ClinicalTrials.gov |
| NCT06009237 | A Study to Assess Pharmacokinetics, Safety, and Tolerability of ABBV-903 in Hea… | Phase1 | Healthy Volunteers | Terminated | 2023-08-23 | 2023-10-30 | ClinicalTrials.gov |
| NCT05995366 | A Study to Assess the Mass Balance of [14C] ABBV-903 in Healthy Male Participan… | Phase1 | Healthy Volunteer | Completed | 2023-08-18 | 2023-10-13 | ClinicalTrials.gov |
| NCT05959083 | Real World Study of Oral Upadacitinib Tablets to Assess Adverse Events and Chan… | — | Atopic Dermatitis (AD) | Completed | 2023-08-18 | 2026-05-07 | ClinicalTrials.gov |
| NCT05959083 | Real World Study of Oral Upadacitinib Tablets to Assess Adverse Events and Chan… | — | Atopic Dermatitis (AD) | Completed | 2023-08-18 | 2026-05-07 | ClinicalTrials.gov |
| NCT05995366 | A Study to Assess the Mass Balance of [14C] ABBV-903 in Healthy Male Participan… | Phase1 | Healthy Volunteer | Completed | 2023-08-18 | 2023-10-13 | ClinicalTrials.gov |
| NCT05995366 | A Study to Assess the Mass Balance of [14C] ABBV-903 in Healthy Male Participan… | Phase1 | Healthy Volunteer | Completed | 2023-08-18 | 2023-10-13 | ClinicalTrials.gov |
| NCT05959083 | Real World Study of Oral Upadacitinib Tablets to Assess Adverse Events and Chan… | — | Atopic Dermatitis (AD) | Completed | 2023-08-18 | 2026-05-07 | ClinicalTrials.gov |
| NCT05995366 | A Study to Assess the Mass Balance of [14C] ABBV-903 in Healthy Male Participan… | Phase1 | Healthy Volunteer | Completed | 2023-08-18 | 2023-10-13 | ClinicalTrials.gov |
| NCT05959083 | Real World Study of Oral Upadacitinib Tablets to Assess Adverse Events and Chan… | — | Atopic Dermatitis (AD) | Completed | 2023-08-18 | 2026-05-07 | ClinicalTrials.gov |
| NCT05969223 | Study to Assess the Safety and Efficacy of Subcutaneously Injected Risankizumab… | Phase4 | Genital Psoriasis | Completed | 2023-08-10 | 2025-11-28 | ClinicalTrials.gov |
| NCT05969223 | Study to Assess the Safety and Efficacy of Subcutaneously Injected Risankizumab… | Phase4 | Genital Psoriasis | Completed | 2023-08-10 | 2025-11-28 | ClinicalTrials.gov |
| NCT05969223 | Study to Assess the Safety and Efficacy of Subcutaneously Injected Risankizumab… | Phase4 | Genital Psoriasis | Completed | 2023-08-10 | 2025-11-28 | ClinicalTrials.gov |
| NCT05969223 | Study to Assess the Safety and Efficacy of Subcutaneously Injected Risankizumab… | Phase4 | Genital Psoriasis | Completed | 2023-08-10 | 2025-11-28 | ClinicalTrials.gov |
| NCT05941442 | A Study to Evaluate Efficacy, Safety, and Tolerability of Darigabat in Particip… | Phase2 | Panic Disorder | Completed | 2023-07-31 | 2025-03-31 | ClinicalTrials.gov |
| NCT05941442 | A Study to Evaluate Efficacy, Safety, and Tolerability of Darigabat in Particip… | Phase2 | Panic Disorder | Completed | 2023-07-31 | 2025-03-31 | ClinicalTrials.gov |
| NCT05941442 | A Study to Evaluate Efficacy, Safety, and Tolerability of Darigabat in Particip… | Phase2 | Panic Disorder | Completed | 2023-07-31 | 2025-03-31 | ClinicalTrials.gov |
| NCT05941442 | A Study to Evaluate Efficacy, Safety, and Tolerability of Darigabat in Particip… | Phase2 | Panic Disorder | Completed | 2023-07-31 | 2025-03-31 | ClinicalTrials.gov |
| NCT06023030 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Crohn's Disease | Recruiting | 2023-07-28 | 2027-05-01 | ClinicalTrials.gov |
| NCT06023030 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Crohn's Disease | Recruiting | 2023-07-28 | 2027-05-01 | ClinicalTrials.gov |
| NCT06023030 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Crohn's Disease | Recruiting | 2023-07-28 | 2027-05-01 | ClinicalTrials.gov |
| NCT06023030 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Crohn's Disease | Recruiting | 2023-07-28 | 2027-05-01 | ClinicalTrials.gov |
| NCT05955261 | A Study of Venetoclax in Combination With Conventional Chemotherapy in Pediatri… | Phase2 | Acute Myeloid Leukemia | Suspended | 2023-07-25 | 2034-03-01 | ClinicalTrials.gov |
| NCT05955261 | A Study of Venetoclax in Combination With Conventional Chemotherapy in Pediatri… | Phase2 | Acute Myeloid Leukemia | Suspended | 2023-07-25 | 2034-03-01 | ClinicalTrials.gov |
| NCT05843643 | Program to Assess Adverse Events and Change in Disease Activity of Oral Upadaci… | Phase3 | Systemic Lupus Erythematosus | Active_Not_Recruiting | 2023-07-25 | 2027-10-01 | ClinicalTrials.gov |
| NCT05843643 | Program to Assess Adverse Events and Change in Disease Activity of Oral Upadaci… | Phase3 | Systemic Lupus Erythematosus | Active_Not_Recruiting | 2023-07-25 | 2027-10-01 | ClinicalTrials.gov |
| NCT05843643 | Program to Assess Adverse Events and Change in Disease Activity of Oral Upadaci… | Phase3 | Systemic Lupus Erythematosus | Active_Not_Recruiting | 2023-07-25 | 2027-10-01 | ClinicalTrials.gov |
| NCT05843643 | Program to Assess Adverse Events and Change in Disease Activity of Oral Upadaci… | Phase3 | Systemic Lupus Erythematosus | Active_Not_Recruiting | 2023-07-25 | 2027-10-01 | ClinicalTrials.gov |
| NCT05955261 | A Study of Venetoclax in Combination With Conventional Chemotherapy in Pediatri… | Phase2 | Acute Myeloid Leukemia | Suspended | 2023-07-25 | 2034-03-01 | ClinicalTrials.gov |
| NCT05955261 | A Study of Venetoclax in Combination With Conventional Chemotherapy in Pediatri… | Phase2 | Acute Myeloid Leukemia | Suspended | 2023-07-25 | 2034-03-01 | ClinicalTrials.gov |
| NCT05940402 | A Study to Evaluate Pharmacokinetic and Safety Trial of Emraclidine in Particip… | Phase1 | Renal Impairment | Completed | 2023-07-24 | 2024-12-19 | ClinicalTrials.gov |
| NCT05940402 | A Study to Evaluate Pharmacokinetic and Safety Trial of Emraclidine in Particip… | Phase1 | Renal Impairment | Completed | 2023-07-24 | 2024-12-19 | ClinicalTrials.gov |
| NCT05940402 | A Study to Evaluate Pharmacokinetic and Safety Trial of Emraclidine in Particip… | Phase1 | Renal Impairment | Completed | 2023-07-24 | 2024-12-19 | ClinicalTrials.gov |
| NCT05940402 | A Study to Evaluate Pharmacokinetic and Safety Trial of Emraclidine in Particip… | Phase1 | Renal Impairment | Completed | 2023-07-24 | 2024-12-19 | ClinicalTrials.gov |
| NCT05861427 | Study of Oral Atogepant Tablets to Assess Change in Disease Activity in Adult J… | Phase3 | Migraine | Completed | 2023-07-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT05861427 | Study of Oral Atogepant Tablets to Assess Change in Disease Activity in Adult J… | Phase3 | Migraine | Completed | 2023-07-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT05861427 | Study of Oral Atogepant Tablets to Assess Change in Disease Activity in Adult J… | Phase3 | Migraine | Completed | 2023-07-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT05861427 | Study of Oral Atogepant Tablets to Assess Change in Disease Activity in Adult J… | Phase3 | Migraine | Completed | 2023-07-12 | 2025-03-01 | ClinicalTrials.gov |
| NCT05892757 | Study to Assess Adverse Events and Compare How Oral Ubrogepant and Oral Atogepa… | Phase1 | Healthy Volunteers | Completed | 2023-07-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT05892757 | Study to Assess Adverse Events and Compare How Oral Ubrogepant and Oral Atogepa… | Phase1 | Healthy Volunteers | Completed | 2023-07-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT05892757 | Study to Assess Adverse Events and Compare How Oral Ubrogepant and Oral Atogepa… | Phase1 | Healthy Volunteers | Completed | 2023-07-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT05892757 | Study to Assess Adverse Events and Compare How Oral Ubrogepant and Oral Atogepa… | Phase1 | Healthy Volunteers | Completed | 2023-07-11 | 2024-02-22 | ClinicalTrials.gov |
| NCT05935033 | A Study to Evaluate the Effect of Hepatic Impairment on the Pharmacokinetics of… | Phase1 | Hepatic Impairment | Completed | 2023-06-30 | 2025-02-21 | ClinicalTrials.gov |
| NCT05935033 | A Study to Evaluate the Effect of Hepatic Impairment on the Pharmacokinetics of… | Phase1 | Hepatic Impairment | Completed | 2023-06-30 | 2025-02-21 | ClinicalTrials.gov |
| NCT05935033 | A Study to Evaluate the Effect of Hepatic Impairment on the Pharmacokinetics of… | Phase1 | Hepatic Impairment | Completed | 2023-06-30 | 2025-02-21 | ClinicalTrials.gov |
| NCT05935033 | A Study to Evaluate the Effect of Hepatic Impairment on the Pharmacokinetics of… | Phase1 | Hepatic Impairment | Completed | 2023-06-30 | 2025-02-21 | ClinicalTrials.gov |
| NCT05878067 | A Study to Assess Symptom Relief and Product Tolerability of ABBV-444 Drops in … | Phase3 | Dry Eye Syndrome | Completed | 2023-06-27 | 2023-10-06 | ClinicalTrials.gov |
| NCT05878067 | A Study to Assess Symptom Relief and Product Tolerability of ABBV-444 Drops in … | Phase3 | Dry Eye Syndrome | Completed | 2023-06-27 | 2023-10-06 | ClinicalTrials.gov |
| NCT05878067 | A Study to Assess Symptom Relief and Product Tolerability of ABBV-444 Drops in … | Phase3 | Dry Eye Syndrome | Completed | 2023-06-27 | 2023-10-06 | ClinicalTrials.gov |
| NCT05878067 | A Study to Assess Symptom Relief and Product Tolerability of ABBV-444 Drops in … | Phase3 | Dry Eye Syndrome | Completed | 2023-06-27 | 2023-10-06 | ClinicalTrials.gov |
| NCT05827887 | An Observational Study to Assess Ubrogepant Tablets and Atogepant Tablets to Tr… | — | Migraine | Completed | 2023-06-25 | 2026-01-28 | ClinicalTrials.gov |
| NCT05827887 | An Observational Study to Assess Ubrogepant Tablets and Atogepant Tablets to Tr… | — | Migraine | Completed | 2023-06-25 | 2026-01-28 | ClinicalTrials.gov |
| NCT05827887 | An Observational Study to Assess Ubrogepant Tablets and Atogepant Tablets to Tr… | — | Migraine | Completed | 2023-06-25 | 2026-01-28 | ClinicalTrials.gov |
| NCT05827887 | An Observational Study to Assess Ubrogepant Tablets and Atogepant Tablets to Tr… | — | Migraine | Completed | 2023-06-25 | 2026-01-28 | ClinicalTrials.gov |
| NCT05895266 | A Study to Assess Drug-Drug Interaction Between ABBV-903 and Midazolam in Adult… | Phase1 | Healthy Volunteer | Completed | 2023-06-23 | 2023-11-02 | ClinicalTrials.gov |
| NCT05895266 | A Study to Assess Drug-Drug Interaction Between ABBV-903 and Midazolam in Adult… | Phase1 | Healthy Volunteer | Completed | 2023-06-23 | 2023-11-02 | ClinicalTrials.gov |
| NCT05895266 | A Study to Assess Drug-Drug Interaction Between ABBV-903 and Midazolam in Adult… | Phase1 | Healthy Volunteer | Completed | 2023-06-23 | 2023-11-02 | ClinicalTrials.gov |
| NCT05895266 | A Study to Assess Drug-Drug Interaction Between ABBV-903 and Midazolam in Adult… | Phase1 | Healthy Volunteer | Completed | 2023-06-23 | 2023-11-02 | ClinicalTrials.gov |
| NCT05889182 | A Study to Assess Change in Disease Activity and Adverse Events of Oral Upadaci… | Phase3 | Hidradenitis Suppurativa | Recruiting | 2023-06-21 | 2028-09-01 | ClinicalTrials.gov |
| NCT05889182 | A Study to Assess Change in Disease Activity and Adverse Events of Oral Upadaci… | Phase3 | Hidradenitis Suppurativa | Recruiting | 2023-06-21 | 2028-09-01 | ClinicalTrials.gov |
| NCT05889182 | A Study to Assess Change in Disease Activity and Adverse Events of Oral Upadaci… | Phase3 | Hidradenitis Suppurativa | Recruiting | 2023-06-21 | 2028-09-01 | ClinicalTrials.gov |
| NCT05889182 | A Study to Assess Change in Disease Activity and Adverse Events of Oral Upadaci… | Phase3 | Hidradenitis Suppurativa | Recruiting | 2023-06-21 | 2028-09-01 | ClinicalTrials.gov |
| NCT05909553 | Study to Assess Adverse Events and Compare How Crushed, Ground, and Intact Oral… | Phase1 | Healthy Volunteers | Completed | 2023-06-15 | 2023-09-22 | ClinicalTrials.gov |
| NCT05814627 | Study to Assess Change in Disease Activity and Adverse Events of Oral Upadaciti… | Phase3 | Rheumatoid Arthritis | Active_Not_Recruiting | 2023-06-15 | 2026-07-01 | ClinicalTrials.gov |
| NCT05814627 | Study to Assess Change in Disease Activity and Adverse Events of Oral Upadaciti… | Phase3 | Rheumatoid Arthritis | Active_Not_Recruiting | 2023-06-15 | 2026-07-01 | ClinicalTrials.gov |
| NCT05909553 | Study to Assess Adverse Events and Compare How Crushed, Ground, and Intact Oral… | Phase1 | Healthy Volunteers | Completed | 2023-06-15 | 2023-09-22 | ClinicalTrials.gov |
| NCT05909553 | Study to Assess Adverse Events and Compare How Crushed, Ground, and Intact Oral… | Phase1 | Healthy Volunteers | Completed | 2023-06-15 | 2023-09-22 | ClinicalTrials.gov |
| NCT05909553 | Study to Assess Adverse Events and Compare How Crushed, Ground, and Intact Oral… | Phase1 | Healthy Volunteers | Completed | 2023-06-15 | 2023-09-22 | ClinicalTrials.gov |
| NCT05814627 | Study to Assess Change in Disease Activity and Adverse Events of Oral Upadaciti… | Phase3 | Rheumatoid Arthritis | Active_Not_Recruiting | 2023-06-15 | 2026-07-01 | ClinicalTrials.gov |
| NCT05814627 | Study to Assess Change in Disease Activity and Adverse Events of Oral Upadaciti… | Phase3 | Rheumatoid Arthritis | Active_Not_Recruiting | 2023-06-15 | 2026-07-01 | ClinicalTrials.gov |
| NCT05818709 | A Study to Assess Adverse Events and Effectiveness of HAC 22L Injection for Mid… | Phase3 | Facial Volume Deficit | Completed | 2023-06-14 | 2025-12-05 | ClinicalTrials.gov |
| NCT05818709 | A Study to Assess Adverse Events and Effectiveness of HAC 22L Injection for Mid… | Phase3 | Facial Volume Deficit | Completed | 2023-06-14 | 2025-12-05 | ClinicalTrials.gov |
| NCT05818709 | A Study to Assess Adverse Events and Effectiveness of HAC 22L Injection for Mid… | Phase3 | Facial Volume Deficit | Completed | 2023-06-14 | 2025-12-05 | ClinicalTrials.gov |
| NCT05818709 | A Study to Assess Adverse Events and Effectiveness of HAC 22L Injection for Mid… | Phase3 | Facial Volume Deficit | Completed | 2023-06-14 | 2025-12-05 | ClinicalTrials.gov |
| NCT05938985 | Croatian Version of the Ocular Surface Disease Index Questionnaire (OSDI) | — | Dry Eye | Unknown | 2023-06-12 | 2023-11-02 | ClinicalTrials.gov |
| NCT05938985 | Croatian Version of the Ocular Surface Disease Index Questionnaire (OSDI) | — | Dry Eye | Unknown | 2023-06-12 | 2023-11-02 | ClinicalTrials.gov |
| NCT05938985 | Croatian Version of the Ocular Surface Disease Index Questionnaire (OSDI) | — | Dry Eye | Unknown | 2023-06-12 | 2023-11-02 | ClinicalTrials.gov |
| NCT05938985 | Croatian Version of the Ocular Surface Disease Index Questionnaire (OSDI) | — | Dry Eye | Unknown | 2023-06-12 | 2023-11-02 | ClinicalTrials.gov |
| NCT05841537 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Crohn's Disease | Active_Not_Recruiting | 2023-06-09 | 2028-07-01 | ClinicalTrials.gov |
| NCT05753501 | Study to Evaluate Adverse Events, Change in Disease Activity, and How Oral ABBV… | Phase1 | Hematologic Cancer | Active_Not_Recruiting | 2023-06-09 | 2031-03-01 | ClinicalTrials.gov |
| NCT05753501 | Study to Evaluate Adverse Events, Change in Disease Activity, and How Oral ABBV… | Phase1 | Hematologic Cancer | Active_Not_Recruiting | 2023-06-09 | 2031-03-01 | ClinicalTrials.gov |
| NCT05841537 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Crohn's Disease | Active_Not_Recruiting | 2023-06-09 | 2028-07-01 | ClinicalTrials.gov |
| NCT05841537 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Crohn's Disease | Active_Not_Recruiting | 2023-06-09 | 2028-07-01 | ClinicalTrials.gov |
| NCT05753501 | Study to Evaluate Adverse Events, Change in Disease Activity, and How Oral ABBV… | Phase1 | Hematologic Cancer | Active_Not_Recruiting | 2023-06-09 | 2031-03-01 | ClinicalTrials.gov |
| NCT05841537 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Crohn's Disease | Active_Not_Recruiting | 2023-06-09 | 2028-07-01 | ClinicalTrials.gov |
| NCT05753501 | Study to Evaluate Adverse Events, Change in Disease Activity, and How Oral ABBV… | Phase1 | Hematologic Cancer | Active_Not_Recruiting | 2023-06-09 | 2031-03-01 | ClinicalTrials.gov |
| NCT06362044 | A Study to Assess Frequency of Undetectable Minimal Residual Disease (uMRD) in … | — | Chronic Lymphocytic Leukemia | Completed | 2023-06-07 | 2024-12-31 | ClinicalTrials.gov |
| NCT06362044 | A Study to Assess Frequency of Undetectable Minimal Residual Disease (uMRD) in … | — | Chronic Lymphocytic Leukemia | Completed | 2023-06-07 | 2024-12-31 | ClinicalTrials.gov |
| NCT06362044 | A Study to Assess Frequency of Undetectable Minimal Residual Disease (uMRD) in … | — | Chronic Lymphocytic Leukemia | Completed | 2023-06-07 | 2024-12-31 | ClinicalTrials.gov |
| NCT06362044 | A Study to Assess Frequency of Undetectable Minimal Residual Disease (uMRD) in … | — | Chronic Lymphocytic Leukemia | Completed | 2023-06-07 | 2024-12-31 | ClinicalTrials.gov |
| NCT05707949 | Long-term Extension Study to Assess Adverse Events of Oral Atogepant Tablets in… | Phase3 | Migraine Prophylaxis | Enrolling_By_Invitation | 2023-06-05 | 2032-04-01 | ClinicalTrials.gov |
| NCT05707949 | Long-term Extension Study to Assess Adverse Events of Oral Atogepant Tablets in… | Phase3 | Migraine Prophylaxis | Enrolling_By_Invitation | 2023-06-05 | 2032-04-01 | ClinicalTrials.gov |
| NCT05771428 | Study to Assess Adverse Events, Change in Disease Activity and How Oral ABBV-55… | Phase2 | Alzheimer's Disease (AD) | Completed | 2023-06-05 | 2024-09-12 | ClinicalTrials.gov |
| NCT05771428 | Study to Assess Adverse Events, Change in Disease Activity and How Oral ABBV-55… | Phase2 | Alzheimer's Disease (AD) | Completed | 2023-06-05 | 2024-09-12 | ClinicalTrials.gov |
| NCT05707949 | Long-term Extension Study to Assess Adverse Events of Oral Atogepant Tablets in… | Phase3 | Migraine Prophylaxis | Enrolling_By_Invitation | 2023-06-05 | 2032-04-01 | ClinicalTrials.gov |
| NCT05771428 | Study to Assess Adverse Events, Change in Disease Activity and How Oral ABBV-55… | Phase2 | Alzheimer's Disease (AD) | Completed | 2023-06-05 | 2024-09-12 | ClinicalTrials.gov |
| NCT05707949 | Long-term Extension Study to Assess Adverse Events of Oral Atogepant Tablets in… | Phase3 | Migraine Prophylaxis | Enrolling_By_Invitation | 2023-06-05 | 2032-04-01 | ClinicalTrials.gov |
| NCT05771428 | Study to Assess Adverse Events, Change in Disease Activity and How Oral ABBV-55… | Phase2 | Alzheimer's Disease (AD) | Completed | 2023-06-05 | 2024-09-12 | ClinicalTrials.gov |
| NCT06362031 | A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource … | — | Acute Myeloid Leukemia | Withdrawn | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT06362031 | A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource … | — | Acute Myeloid Leukemia | Withdrawn | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT06362031 | A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource … | — | Acute Myeloid Leukemia | Withdrawn | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT06362031 | A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource … | — | Acute Myeloid Leukemia | Withdrawn | 2023-06-01 | 2024-04-30 | ClinicalTrials.gov |
| NCT05630885 | A Study to Evaluate the Effects of Cenicriviroc Mesylate on Arterial Inflammati… | Phase2 | HIV-1-infection | Completed | 2023-05-30 | 2024-06-19 | ClinicalTrials.gov |
| NCT05630885 | A Study to Evaluate the Effects of Cenicriviroc Mesylate on Arterial Inflammati… | Phase2 | HIV-1-infection | Completed | 2023-05-30 | 2024-06-19 | ClinicalTrials.gov |
| NCT05630885 | A Study to Evaluate the Effects of Cenicriviroc Mesylate on Arterial Inflammati… | Phase2 | HIV-1-infection | Completed | 2023-05-30 | 2024-06-19 | ClinicalTrials.gov |
| NCT05630885 | A Study to Evaluate the Effects of Cenicriviroc Mesylate on Arterial Inflammati… | Phase2 | HIV-1-infection | Completed | 2023-05-30 | 2024-06-19 | ClinicalTrials.gov |
| NCT05507580 | A Study to Assess Treat-to-Target and Dosing Flexibility of Oral Upadacitinib T… | Phase4 | Atopic Dermatitis | Completed | 2023-05-29 | 2024-08-15 | ClinicalTrials.gov |
| NCT05507580 | A Study to Assess Treat-to-Target and Dosing Flexibility of Oral Upadacitinib T… | Phase4 | Atopic Dermatitis | Completed | 2023-05-29 | 2024-08-15 | ClinicalTrials.gov |
| NCT05507580 | A Study to Assess Treat-to-Target and Dosing Flexibility of Oral Upadacitinib T… | Phase4 | Atopic Dermatitis | Completed | 2023-05-29 | 2024-08-15 | ClinicalTrials.gov |
| NCT05507580 | A Study to Assess Treat-to-Target and Dosing Flexibility of Oral Upadacitinib T… | Phase4 | Atopic Dermatitis | Completed | 2023-05-29 | 2024-08-15 | ClinicalTrials.gov |
| NCT05833438 | Venetoclax in Combination with 5 Days Azacitidine in Untreated AML Patients, No… | Phase2 | Acute Myeloid Leukemia (AML) | Recruiting | 2023-05-17 | 2025-07-01 | ClinicalTrials.gov |
| NCT05833438 | Venetoclax in Combination with 5 Days Azacitidine in Untreated AML Patients, No… | Phase2 | Acute Myeloid Leukemia (AML) | Recruiting | 2023-05-17 | 2025-07-01 | ClinicalTrials.gov |
| NCT05833438 | Venetoclax in Combination with 5 Days Azacitidine in Untreated AML Patients, No… | Phase2 | Acute Myeloid Leukemia (AML) | Recruiting | 2023-05-17 | 2025-07-01 | ClinicalTrials.gov |
| NCT05833438 | Venetoclax in Combination with 5 Days Azacitidine in Untreated AML Patients, No… | Phase2 | Acute Myeloid Leukemia (AML) | Recruiting | 2023-05-17 | 2025-07-01 | ClinicalTrials.gov |
| NCT05711394 | A Study to Assess the Adverse Events and Change in Disease Activity of Oral Ato… | Phase3 | Episodic Migraine | Recruiting | 2023-05-01 | 2028-05-01 | ClinicalTrials.gov |
| NCT05711394 | A Study to Assess the Adverse Events and Change in Disease Activity of Oral Ato… | Phase3 | Episodic Migraine | Recruiting | 2023-05-01 | 2028-05-01 | ClinicalTrials.gov |
| NCT05711394 | A Study to Assess the Adverse Events and Change in Disease Activity of Oral Ato… | Phase3 | Episodic Migraine | Recruiting | 2023-05-01 | 2028-05-01 | ClinicalTrials.gov |
| NCT05711394 | A Study to Assess the Adverse Events and Change in Disease Activity of Oral Ato… | Phase3 | Episodic Migraine | Recruiting | 2023-05-01 | 2028-05-01 | ClinicalTrials.gov |
| NCT05760313 | A Study to Assess Adverse Events and Change in Disease Activity in Pediatric Pa… | Phase2 | Functional Constipation | Completed | 2023-04-27 | 2025-06-09 | ClinicalTrials.gov |
| NCT05760313 | A Study to Assess Adverse Events and Change in Disease Activity in Pediatric Pa… | Phase2 | Functional Constipation | Completed | 2023-04-27 | 2025-06-09 | ClinicalTrials.gov |
| NCT05760313 | A Study to Assess Adverse Events and Change in Disease Activity in Pediatric Pa… | Phase2 | Functional Constipation | Completed | 2023-04-27 | 2025-06-09 | ClinicalTrials.gov |
| NCT05760313 | A Study to Assess Adverse Events and Change in Disease Activity in Pediatric Pa… | Phase2 | Functional Constipation | Completed | 2023-04-27 | 2025-06-09 | ClinicalTrials.gov |
| NCT05512390 | A Study to Assess the Adverse Events, Change in Disease Activity, and How Intra… | Phase1 | Diffuse Large B-Cell Lymphoma | Recruiting | 2023-04-26 | 2027-02-01 | ClinicalTrials.gov |
| NCT05512390 | A Study to Assess the Adverse Events, Change in Disease Activity, and How Intra… | Phase1 | Diffuse Large B-Cell Lymphoma | Recruiting | 2023-04-26 | 2027-02-01 | ClinicalTrials.gov |
| NCT05512390 | A Study to Assess the Adverse Events, Change in Disease Activity, and How Intra… | Phase1 | Diffuse Large B-Cell Lymphoma | Recruiting | 2023-04-26 | 2027-02-01 | ClinicalTrials.gov |
| NCT05512390 | A Study to Assess the Adverse Events, Change in Disease Activity, and How Intra… | Phase1 | Diffuse Large B-Cell Lymphoma | Recruiting | 2023-04-26 | 2027-02-01 | ClinicalTrials.gov |
| NCT05785715 | Study to Evaluate the Clinical Activity and Safety of Oral NX-13 in Moderate to… | Phase2 | Ulcerative Colitis | Terminated | 2023-04-24 | 2025-05-30 | ClinicalTrials.gov |
| NCT05785715 | Study to Evaluate the Clinical Activity and Safety of Oral NX-13 in Moderate to… | Phase2 | Ulcerative Colitis | Terminated | 2023-04-24 | 2025-05-30 | ClinicalTrials.gov |
| NCT05785715 | Study to Evaluate the Clinical Activity and Safety of Oral NX-13 in Moderate to… | Phase2 | Ulcerative Colitis | Terminated | 2023-04-24 | 2025-05-30 | ClinicalTrials.gov |
| NCT05785715 | Study to Evaluate the Clinical Activity and Safety of Oral NX-13 in Moderate to… | Phase2 | Ulcerative Colitis | Terminated | 2023-04-24 | 2025-05-30 | ClinicalTrials.gov |
| NCT05836506 | A Study to Assess the Relative Bioavailability of Immediate Release Formulation… | Phase1 | Healthy Volunteer | Completed | 2023-04-18 | 2023-06-20 | ClinicalTrials.gov |
| NCT05836506 | A Study to Assess the Relative Bioavailability of Immediate Release Formulation… | Phase1 | Healthy Volunteer | Completed | 2023-04-18 | 2023-06-20 | ClinicalTrials.gov |
| NCT05836506 | A Study to Assess the Relative Bioavailability of Immediate Release Formulation… | Phase1 | Healthy Volunteer | Completed | 2023-04-18 | 2023-06-20 | ClinicalTrials.gov |
| NCT05836506 | A Study to Assess the Relative Bioavailability of Immediate Release Formulation… | Phase1 | Healthy Volunteer | Completed | 2023-04-18 | 2023-06-20 | ClinicalTrials.gov |
| NCT05741034 | A Study to Assess Adverse Events and Effectiveness of Injected JUVÉDERM® VOLITE… | Phase3 | Neck Lines | Completed | 2023-04-07 | 2024-12-09 | ClinicalTrials.gov |
| NCT05741034 | A Study to Assess Adverse Events and Effectiveness of Injected JUVÉDERM® VOLITE… | Phase3 | Neck Lines | Completed | 2023-04-07 | 2024-12-09 | ClinicalTrials.gov |
| NCT05741034 | A Study to Assess Adverse Events and Effectiveness of Injected JUVÉDERM® VOLITE… | Phase3 | Neck Lines | Completed | 2023-04-07 | 2024-12-09 | ClinicalTrials.gov |
| NCT05741034 | A Study to Assess Adverse Events and Effectiveness of Injected JUVÉDERM® VOLITE… | Phase3 | Neck Lines | Completed | 2023-04-07 | 2024-12-09 | ClinicalTrials.gov |
| NCT05618028 | Study to Evaluate Adverse Events and Change in Disease Activity in Adult Partic… | Phase1 | Diffuse Large B-Cell Lymphoma | Recruiting | 2023-04-04 | 2029-07-01 | ClinicalTrials.gov |
| NCT05618028 | Study to Evaluate Adverse Events and Change in Disease Activity in Adult Partic… | Phase1 | Diffuse Large B-Cell Lymphoma | Recruiting | 2023-04-04 | 2029-07-01 | ClinicalTrials.gov |
| NCT05618028 | Study to Evaluate Adverse Events and Change in Disease Activity in Adult Partic… | Phase1 | Diffuse Large B-Cell Lymphoma | Recruiting | 2023-04-04 | 2029-07-01 | ClinicalTrials.gov |
| NCT05618028 | Study to Evaluate Adverse Events and Change in Disease Activity in Adult Partic… | Phase1 | Diffuse Large B-Cell Lymphoma | Recruiting | 2023-04-04 | 2029-07-01 | ClinicalTrials.gov |
| NCT05292664 | Venetoclax Basket Trial for High Risk Hematologic Malignancies | Phase1 | Myelodysplastic Syndromes, de Novo | Recruiting | 2023-03-29 | 2030-07-02 | ClinicalTrials.gov |
| NCT05292664 | Venetoclax Basket Trial for High Risk Hematologic Malignancies | Phase1 | Myelodysplastic Syndromes, de Novo | Recruiting | 2023-03-29 | 2030-07-02 | ClinicalTrials.gov |
| NCT05292664 | Venetoclax Basket Trial for High Risk Hematologic Malignancies | Phase1 | Myelodysplastic Syndromes, de Novo | Recruiting | 2023-03-29 | 2030-07-02 | ClinicalTrials.gov |
| NCT05292664 | Venetoclax Basket Trial for High Risk Hematologic Malignancies | Phase1 | Myelodysplastic Syndromes, de Novo | Recruiting | 2023-03-29 | 2030-07-02 | ClinicalTrials.gov |
| NCT05763459 | A Phase 1 Study of ABBV-CLS-7262, Rosuvastatin, and Digoxin in Healthy Subjects | Phase1 | Healthy | Completed | 2023-03-24 | 2023-06-02 | ClinicalTrials.gov |
| NCT05763459 | A Phase 1 Study of ABBV-CLS-7262, Rosuvastatin, and Digoxin in Healthy Subjects | Phase1 | Healthy | Completed | 2023-03-24 | 2023-06-02 | ClinicalTrials.gov |
| NCT05763459 | A Phase 1 Study of ABBV-CLS-7262, Rosuvastatin, and Digoxin in Healthy Subjects | Phase1 | Healthy | Completed | 2023-03-24 | 2023-06-02 | ClinicalTrials.gov |
| NCT05763459 | A Phase 1 Study of ABBV-CLS-7262, Rosuvastatin, and Digoxin in Healthy Subjects | Phase1 | Healthy | Completed | 2023-03-24 | 2023-06-02 | ClinicalTrials.gov |
| NCT05650632 | A Study to Assess Adverse Events of Intravenously (IV) Infused Etentamig (ABBV-… | Phase1 | Multiple Myeloma | Recruiting | 2023-03-21 | 2029-08-01 | ClinicalTrials.gov |
| NCT05650632 | A Study to Assess Adverse Events of Intravenously (IV) Infused Etentamig (ABBV-… | Phase1 | Multiple Myeloma | Recruiting | 2023-03-21 | 2029-08-01 | ClinicalTrials.gov |
| NCT05650632 | A Study to Assess Adverse Events of Intravenously (IV) Infused Etentamig (ABBV-… | Phase1 | Multiple Myeloma | Recruiting | 2023-03-21 | 2029-08-01 | ClinicalTrials.gov |
| NCT05650632 | A Study to Assess Adverse Events of Intravenously (IV) Infused Etentamig (ABBV-… | Phase1 | Multiple Myeloma | Recruiting | 2023-03-21 | 2029-08-01 | ClinicalTrials.gov |
| NCT05570006 | Study of ABBV-668 Oral Capsules to Assess Adverse Events and Change in Disease … | Phase2 | Ulcerative Colitis | Completed | 2023-03-16 | 2024-12-23 | ClinicalTrials.gov |
| NCT05570006 | Study of ABBV-668 Oral Capsules to Assess Adverse Events and Change in Disease … | Phase2 | Ulcerative Colitis | Completed | 2023-03-16 | 2024-12-23 | ClinicalTrials.gov |
| NCT05570006 | Study of ABBV-668 Oral Capsules to Assess Adverse Events and Change in Disease … | Phase2 | Ulcerative Colitis | Completed | 2023-03-16 | 2024-12-23 | ClinicalTrials.gov |
| NCT05570006 | Study of ABBV-668 Oral Capsules to Assess Adverse Events and Change in Disease … | Phase2 | Ulcerative Colitis | Completed | 2023-03-16 | 2024-12-23 | ClinicalTrials.gov |
| NCT05445778 | Mirvetuximab Soravtansine With Bevacizumab Versus Bevacizumab as Maintenance in… | Phase3 | Ovarian Cancer | Active_Not_Recruiting | 2023-03-15 | 2032-05-01 | ClinicalTrials.gov |
| NCT05445778 | Mirvetuximab Soravtansine With Bevacizumab Versus Bevacizumab as Maintenance in… | Phase3 | Ovarian Cancer | Active_Not_Recruiting | 2023-03-15 | 2032-05-01 | ClinicalTrials.gov |
| NCT05445778 | Mirvetuximab Soravtansine With Bevacizumab Versus Bevacizumab as Maintenance in… | Phase3 | Ovarian Cancer | Active_Not_Recruiting | 2023-03-15 | 2032-05-01 | ClinicalTrials.gov |
| NCT05445778 | Mirvetuximab Soravtansine With Bevacizumab Versus Bevacizumab as Maintenance in… | Phase3 | Ovarian Cancer | Active_Not_Recruiting | 2023-03-15 | 2032-05-01 | ClinicalTrials.gov |
| NCT05605756 | BOTOX Effects on Seizure Severity and Susceptibility | Phase4 | Drug-resistant Focal Seizure | Terminated | 2023-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05605756 | BOTOX Effects on Seizure Severity and Susceptibility | Phase4 | Drug-resistant Focal Seizure | Terminated | 2023-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05605756 | BOTOX Effects on Seizure Severity and Susceptibility | Phase4 | Drug-resistant Focal Seizure | Terminated | 2023-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05605756 | BOTOX Effects on Seizure Severity and Susceptibility | Phase4 | Drug-resistant Focal Seizure | Terminated | 2023-03-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT05669794 | An Observational Study to Assess Change in Disease Activity and Use of Upadacit… | — | Atopic Dermatitis | Active_Not_Recruiting | 2023-02-21 | 2027-02-01 | ClinicalTrials.gov |
| NCT05669794 | An Observational Study to Assess Change in Disease Activity and Use of Upadacit… | — | Atopic Dermatitis | Active_Not_Recruiting | 2023-02-21 | 2027-02-01 | ClinicalTrials.gov |
| NCT05669794 | An Observational Study to Assess Change in Disease Activity and Use of Upadacit… | — | Atopic Dermatitis | Active_Not_Recruiting | 2023-02-21 | 2027-02-01 | ClinicalTrials.gov |
| NCT05669794 | An Observational Study to Assess Change in Disease Activity and Use of Upadacit… | — | Atopic Dermatitis | Active_Not_Recruiting | 2023-02-21 | 2027-02-01 | ClinicalTrials.gov |
| NCT05738850 | Study to Assess Adverse Events and How ABBV-932 Oral Capsules Moves Through the… | Phase1 | Generalized Anxiety Disorder (GAD) | Completed | 2023-02-15 | 2024-05-31 | ClinicalTrials.gov |
| NCT05738850 | Study to Assess Adverse Events and How ABBV-932 Oral Capsules Moves Through the… | Phase1 | Generalized Anxiety Disorder (GAD) | Completed | 2023-02-15 | 2024-05-31 | ClinicalTrials.gov |
| NCT05738850 | Study to Assess Adverse Events and How ABBV-932 Oral Capsules Moves Through the… | Phase1 | Generalized Anxiety Disorder (GAD) | Completed | 2023-02-15 | 2024-05-31 | ClinicalTrials.gov |
| NCT05738850 | Study to Assess Adverse Events and How ABBV-932 Oral Capsules Moves Through the… | Phase1 | Generalized Anxiety Disorder (GAD) | Completed | 2023-02-15 | 2024-05-31 | ClinicalTrials.gov |
| NCT05555953 | Effect of Long-term Psoriasis on Patients' Life - CORONATE | — | Psoriasis | Completed | 2023-01-26 | 2024-10-17 | ClinicalTrials.gov |
| NCT05555953 | Effect of Long-term Psoriasis on Patients' Life - CORONATE | — | Psoriasis | Completed | 2023-01-26 | 2024-10-17 | ClinicalTrials.gov |
| NCT05555953 | Effect of Long-term Psoriasis on Patients' Life - CORONATE | — | Psoriasis | Completed | 2023-01-26 | 2024-10-17 | ClinicalTrials.gov |
| NCT05555953 | Effect of Long-term Psoriasis on Patients' Life - CORONATE | — | Psoriasis | Completed | 2023-01-26 | 2024-10-17 | ClinicalTrials.gov |
| NCT05686980 | A Study to Assess the Adverse Events and How Oral ABBV-552 Capsules Moves Throu… | Phase1 | Healthy Volunteers | Completed | 2023-01-17 | 2023-03-30 | ClinicalTrials.gov |
| NCT05686980 | A Study to Assess the Adverse Events and How Oral ABBV-552 Capsules Moves Throu… | Phase1 | Healthy Volunteers | Completed | 2023-01-17 | 2023-03-30 | ClinicalTrials.gov |
| NCT05686980 | A Study to Assess the Adverse Events and How Oral ABBV-552 Capsules Moves Throu… | Phase1 | Healthy Volunteers | Completed | 2023-01-17 | 2023-03-30 | ClinicalTrials.gov |
| NCT05686980 | A Study to Assess the Adverse Events and How Oral ABBV-552 Capsules Moves Throu… | Phase1 | Healthy Volunteers | Completed | 2023-01-17 | 2023-03-30 | ClinicalTrials.gov |
| NCT05564650 | Navitoclax in Relapsed or Refractory High-Risk Myelodysplastic Syndrome | Phase1 | Myelodysplastic Syndrome | Completed | 2023-01-12 | 2026-05-08 | ClinicalTrials.gov |
| NCT05564650 | Navitoclax in Relapsed or Refractory High-Risk Myelodysplastic Syndrome | Phase1 | Myelodysplastic Syndrome | Completed | 2023-01-12 | 2026-05-08 | ClinicalTrials.gov |
| NCT05564650 | Navitoclax in Relapsed or Refractory High-Risk Myelodysplastic Syndrome | Phase1 | Myelodysplastic Syndrome | Completed | 2023-01-12 | 2026-05-08 | ClinicalTrials.gov |
| NCT05564650 | Navitoclax in Relapsed or Refractory High-Risk Myelodysplastic Syndrome | Phase1 | Myelodysplastic Syndrome | Completed | 2023-01-12 | 2026-05-08 | ClinicalTrials.gov |
| NCT05527184 | First in Human Study of IMGN151 in Recurrent Gynaecological Cancers | Phase1 | Endometrial Cancer | Active_Not_Recruiting | 2023-01-11 | 2027-02-01 | ClinicalTrials.gov |
| NCT05527184 | First in Human Study of IMGN151 in Recurrent Gynaecological Cancers | Phase1 | Endometrial Cancer | Active_Not_Recruiting | 2023-01-11 | 2027-02-01 | ClinicalTrials.gov |
| NCT05527184 | First in Human Study of IMGN151 in Recurrent Gynaecological Cancers | Phase1 | Endometrial Cancer | Active_Not_Recruiting | 2023-01-11 | 2027-02-01 | ClinicalTrials.gov |
| NCT05527184 | First in Human Study of IMGN151 in Recurrent Gynaecological Cancers | Phase1 | Endometrial Cancer | Active_Not_Recruiting | 2023-01-11 | 2027-02-01 | ClinicalTrials.gov |
| NCT05158894 | Observational Study to Assess Adverse Events When Adult Female Participants Are… | — | Migraine | Recruiting | 2023-01-10 | 2036-01-01 | ClinicalTrials.gov |
| NCT05158894 | Observational Study to Assess Adverse Events When Adult Female Participants Are… | — | Migraine | Recruiting | 2023-01-10 | 2036-01-01 | ClinicalTrials.gov |
| NCT05158894 | Observational Study to Assess Adverse Events When Adult Female Participants Are… | — | Migraine | Recruiting | 2023-01-10 | 2036-01-01 | ClinicalTrials.gov |
| NCT05158894 | Observational Study to Assess Adverse Events When Adult Female Participants Are… | — | Migraine | Recruiting | 2023-01-10 | 2036-01-01 | ClinicalTrials.gov |
| NCT05647551 | A Study to Evaluate Satisfaction in Adult Participants With the Aesthetics of t… | Phase4 | Facial Corrections | Completed | 2023-01-05 | 2023-10-05 | ClinicalTrials.gov |
| NCT05647551 | A Study to Evaluate Satisfaction in Adult Participants With the Aesthetics of t… | Phase4 | Facial Corrections | Completed | 2023-01-05 | 2023-10-05 | ClinicalTrials.gov |
| NCT05647551 | A Study to Evaluate Satisfaction in Adult Participants With the Aesthetics of t… | Phase4 | Facial Corrections | Completed | 2023-01-05 | 2023-10-05 | ClinicalTrials.gov |
| NCT05647551 | A Study to Evaluate Satisfaction in Adult Participants With the Aesthetics of t… | Phase4 | Facial Corrections | Completed | 2023-01-05 | 2023-10-05 | ClinicalTrials.gov |
| NCT05744401 | A Long-term Extension Study to Evaluate Safety, Tolerability, and Efficacy of A… | Phase2 | Alzheimer's Disease | Terminated | 2023-01-04 | 2025-02-05 | ClinicalTrials.gov |
| NCT05744401 | A Long-term Extension Study to Evaluate Safety, Tolerability, and Efficacy of A… | Phase2 | Alzheimer's Disease | Terminated | 2023-01-04 | 2025-02-05 | ClinicalTrials.gov |
| NCT05744401 | A Long-term Extension Study to Evaluate Safety, Tolerability, and Efficacy of A… | Phase2 | Alzheimer's Disease | Terminated | 2023-01-04 | 2025-02-05 | ClinicalTrials.gov |
| NCT05744401 | A Long-term Extension Study to Evaluate Safety, Tolerability, and Efficacy of A… | Phase2 | Alzheimer's Disease | Terminated | 2023-01-04 | 2025-02-05 | ClinicalTrials.gov |
| NCT05691699 | A Study to Assess Adverse Events and How Single and Multiple Ascending Doses of… | Phase1 | Healthy Volunteer | Completed | 2023-01-03 | 2023-10-23 | ClinicalTrials.gov |
| NCT05691699 | A Study to Assess Adverse Events and How Single and Multiple Ascending Doses of… | Phase1 | Healthy Volunteer | Completed | 2023-01-03 | 2023-10-23 | ClinicalTrials.gov |
| NCT05691699 | A Study to Assess Adverse Events and How Single and Multiple Ascending Doses of… | Phase1 | Healthy Volunteer | Completed | 2023-01-03 | 2023-10-23 | ClinicalTrials.gov |
| NCT05691699 | A Study to Assess Adverse Events and How Single and Multiple Ascending Doses of… | Phase1 | Healthy Volunteer | Completed | 2023-01-03 | 2023-10-23 | ClinicalTrials.gov |
| NCT05652205 | A Study to Assess Adverse Events and Change in Symptoms With Linaclotide Versus… | Phase3 | Functional Constipation (FC) | Completed | 2022-12-29 | 2025-09-02 | ClinicalTrials.gov |
| NCT05652205 | A Study to Assess Adverse Events and Change in Symptoms With Linaclotide Versus… | Phase3 | Functional Constipation (FC) | Completed | 2022-12-29 | 2025-09-02 | ClinicalTrials.gov |
| NCT05652205 | A Study to Assess Adverse Events and Change in Symptoms With Linaclotide Versus… | Phase3 | Functional Constipation (FC) | Completed | 2022-12-29 | 2025-09-02 | ClinicalTrials.gov |
| NCT05652205 | A Study to Assess Adverse Events and Change in Symptoms With Linaclotide Versus… | Phase3 | Functional Constipation (FC) | Completed | 2022-12-29 | 2025-09-02 | ClinicalTrials.gov |
| NCT05791526 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Ulcerative Colitis | Completed | 2022-12-19 | 2025-12-09 | ClinicalTrials.gov |
| NCT05791526 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Ulcerative Colitis | Completed | 2022-12-19 | 2025-12-09 | ClinicalTrials.gov |
| NCT05791526 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Ulcerative Colitis | Completed | 2022-12-19 | 2025-12-09 | ClinicalTrials.gov |
| NCT05791526 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Ulcerative Colitis | Completed | 2022-12-19 | 2025-12-09 | ClinicalTrials.gov |
| NCT05653986 | An Observational Study to Assess Change in Disease Activity When Ubrogepant Tab… | — | Migraine | Completed | 2022-12-18 | 2024-08-05 | ClinicalTrials.gov |
| NCT05653986 | An Observational Study to Assess Change in Disease Activity When Ubrogepant Tab… | — | Migraine | Completed | 2022-12-18 | 2024-08-05 | ClinicalTrials.gov |
| NCT05653986 | An Observational Study to Assess Change in Disease Activity When Ubrogepant Tab… | — | Migraine | Completed | 2022-12-18 | 2024-08-05 | ClinicalTrials.gov |
| NCT05653986 | An Observational Study to Assess Change in Disease Activity When Ubrogepant Tab… | — | Migraine | Completed | 2022-12-18 | 2024-08-05 | ClinicalTrials.gov |
| NCT05616871 | An Observational Study to Assess Change in Disease Activity and Treatment Patte… | — | Psoriatic Arthritis | Active_Not_Recruiting | 2022-12-15 | 2027-07-01 | ClinicalTrials.gov |
| NCT05616871 | An Observational Study to Assess Change in Disease Activity and Treatment Patte… | — | Psoriatic Arthritis | Active_Not_Recruiting | 2022-12-15 | 2027-07-01 | ClinicalTrials.gov |
| NCT05616871 | An Observational Study to Assess Change in Disease Activity and Treatment Patte… | — | Psoriatic Arthritis | Active_Not_Recruiting | 2022-12-15 | 2027-07-01 | ClinicalTrials.gov |
| NCT05616871 | An Observational Study to Assess Change in Disease Activity and Treatment Patte… | — | Psoriatic Arthritis | Active_Not_Recruiting | 2022-12-15 | 2027-07-01 | ClinicalTrials.gov |
| NCT05555979 | A Study to Assess Change in Patient Experience in Adult Participants With Chron… | — | Chronic Lymphocytic Leukemia | Completed | 2022-12-14 | 2024-04-10 | ClinicalTrials.gov |
| NCT05555979 | A Study to Assess Change in Patient Experience in Adult Participants With Chron… | — | Chronic Lymphocytic Leukemia | Completed | 2022-12-14 | 2024-04-10 | ClinicalTrials.gov |
| NCT05555979 | A Study to Assess Change in Patient Experience in Adult Participants With Chron… | — | Chronic Lymphocytic Leukemia | Completed | 2022-12-14 | 2024-04-10 | ClinicalTrials.gov |
| NCT05555979 | A Study to Assess Change in Patient Experience in Adult Participants With Chron… | — | Chronic Lymphocytic Leukemia | Completed | 2022-12-14 | 2024-04-10 | ClinicalTrials.gov |
| NCT05451316 | A Study to Assess Change in Disease Activity in Adolescents and Adults With Mod… | — | Atopic Dermatitis | Completed | 2022-12-08 | 2024-11-02 | ClinicalTrials.gov |
| NCT05451316 | A Study to Assess Change in Disease Activity in Adolescents and Adults With Mod… | — | Atopic Dermatitis | Completed | 2022-12-08 | 2024-11-02 | ClinicalTrials.gov |
| NCT05451316 | A Study to Assess Change in Disease Activity in Adolescents and Adults With Mod… | — | Atopic Dermatitis | Completed | 2022-12-08 | 2024-11-02 | ClinicalTrials.gov |
| NCT05451316 | A Study to Assess Change in Disease Activity in Adolescents and Adults With Mod… | — | Atopic Dermatitis | Completed | 2022-12-08 | 2024-11-02 | ClinicalTrials.gov |
| NCT05599984 | Study to Evaluate Adverse Events, Change in Disease Activity, and How ABBV-706 … | Phase1 | Advanced Solid Tumors | Active_Not_Recruiting | 2022-12-05 | 2026-06-01 | ClinicalTrials.gov |
| NCT05599984 | Study to Evaluate Adverse Events, Change in Disease Activity, and How ABBV-706 … | Phase1 | Advanced Solid Tumors | Active_Not_Recruiting | 2022-12-05 | 2026-06-01 | ClinicalTrials.gov |
| NCT05599984 | Study to Evaluate Adverse Events, Change in Disease Activity, and How ABBV-706 … | Phase1 | Advanced Solid Tumors | Active_Not_Recruiting | 2022-12-05 | 2026-06-01 | ClinicalTrials.gov |
| NCT05599984 | Study to Evaluate Adverse Events, Change in Disease Activity, and How ABBV-706 … | Phase1 | Advanced Solid Tumors | Active_Not_Recruiting | 2022-12-05 | 2026-06-01 | ClinicalTrials.gov |
| NCT05644977 | A Multiple Dose Trial of Emraclidine in Elderly Participants and in Participant… | Phase1 | Healthy Participants | Completed | 2022-12-02 | 2025-04-14 | ClinicalTrials.gov |
| NCT05644977 | A Multiple Dose Trial of Emraclidine in Elderly Participants and in Participant… | Phase1 | Healthy Participants | Completed | 2022-12-02 | 2025-04-14 | ClinicalTrials.gov |
| NCT05644977 | A Multiple Dose Trial of Emraclidine in Elderly Participants and in Participant… | Phase1 | Healthy Participants | Completed | 2022-12-02 | 2025-04-14 | ClinicalTrials.gov |
| NCT05644977 | A Multiple Dose Trial of Emraclidine in Elderly Participants and in Participant… | Phase1 | Healthy Participants | Completed | 2022-12-02 | 2025-04-14 | ClinicalTrials.gov |
| NCT05624320 | Using AGN-190584 in Subjects Utilizing Single -Use Daily, Contact Lenses | Phase4 | Presbyopia | Withdrawn | 2022-12-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT05624320 | Using AGN-190584 in Subjects Utilizing Single -Use Daily, Contact Lenses | Phase4 | Presbyopia | Withdrawn | 2022-12-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT05624320 | Using AGN-190584 in Subjects Utilizing Single -Use Daily, Contact Lenses | Phase4 | Presbyopia | Withdrawn | 2022-12-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT05624320 | Using AGN-190584 in Subjects Utilizing Single -Use Daily, Contact Lenses | Phase4 | Presbyopia | Withdrawn | 2022-12-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT05601882 | A Study to Evaluate Adverse Events and Change in Disease Activity Comparing Ora… | Phase3 | Atopic Dermatitis | Completed | 2022-11-28 | 2024-08-08 | ClinicalTrials.gov |
| NCT05601882 | A Study to Evaluate Adverse Events and Change in Disease Activity Comparing Ora… | Phase3 | Atopic Dermatitis | Completed | 2022-11-28 | 2024-08-08 | ClinicalTrials.gov |
| NCT05601882 | A Study to Evaluate Adverse Events and Change in Disease Activity Comparing Ora… | Phase3 | Atopic Dermatitis | Completed | 2022-11-28 | 2024-08-08 | ClinicalTrials.gov |
| NCT05601882 | A Study to Evaluate Adverse Events and Change in Disease Activity Comparing Ora… | Phase3 | Atopic Dermatitis | Completed | 2022-11-28 | 2024-08-08 | ClinicalTrials.gov |
| NCT05226455 | Venetoclax in Patients With MDS or AML in Relapse After AHSCT | Phase1 | MDS | Active_Not_Recruiting | 2022-11-23 | 2027-09-01 | ClinicalTrials.gov |
| NCT05226455 | Venetoclax in Patients With MDS or AML in Relapse After AHSCT | Phase1 | MDS | Active_Not_Recruiting | 2022-11-23 | 2027-09-01 | ClinicalTrials.gov |
| NCT05226455 | Venetoclax in Patients With MDS or AML in Relapse After AHSCT | Phase1 | MDS | Active_Not_Recruiting | 2022-11-23 | 2027-09-01 | ClinicalTrials.gov |
| NCT05226455 | Venetoclax in Patients With MDS or AML in Relapse After AHSCT | Phase1 | MDS | Active_Not_Recruiting | 2022-11-23 | 2027-09-01 | ClinicalTrials.gov |
| NCT04334915 | Study to Evaluate the Effects of Cenicriviroc Mesylate on Arterial Inflammation… | Phase2 | HIV Infections | Withdrawn | 2022-11-22 | 2024-08-15 | ClinicalTrials.gov |
| NCT04334915 | Study to Evaluate the Effects of Cenicriviroc Mesylate on Arterial Inflammation… | Phase2 | HIV Infections | Withdrawn | 2022-11-22 | 2024-08-15 | ClinicalTrials.gov |
| NCT04334915 | Study to Evaluate the Effects of Cenicriviroc Mesylate on Arterial Inflammation… | Phase2 | HIV Infections | Withdrawn | 2022-11-22 | 2024-08-15 | ClinicalTrials.gov |
| NCT04334915 | Study to Evaluate the Effects of Cenicriviroc Mesylate on Arterial Inflammation… | Phase2 | HIV Infections | Withdrawn | 2022-11-22 | 2024-08-15 | ClinicalTrials.gov |
| NCT05513703 | A Study to Assess Disease Activity of Intravenously (IV) Infused Telisotuzumab … | Phase2 | Non Small Cell Lung Cancer | Terminated | 2022-11-21 | 2024-10-28 | ClinicalTrials.gov |
| NCT05513703 | A Study to Assess Disease Activity of Intravenously (IV) Infused Telisotuzumab … | Phase2 | Non Small Cell Lung Cancer | Terminated | 2022-11-21 | 2024-10-28 | ClinicalTrials.gov |
| NCT05513703 | A Study to Assess Disease Activity of Intravenously (IV) Infused Telisotuzumab … | Phase2 | Non Small Cell Lung Cancer | Terminated | 2022-11-21 | 2024-10-28 | ClinicalTrials.gov |
| NCT05513703 | A Study to Assess Disease Activity of Intravenously (IV) Infused Telisotuzumab … | Phase2 | Non Small Cell Lung Cancer | Terminated | 2022-11-21 | 2024-10-28 | ClinicalTrials.gov |
| NCT05582681 | HCV Test and Treat Utilizing Simplified HCV Patient Education | Phase4 | Hepatitis C | Terminated | 2022-11-11 | 2024-11-22 | ClinicalTrials.gov |
| NCT05582681 | HCV Test and Treat Utilizing Simplified HCV Patient Education | Phase4 | Hepatitis C | Terminated | 2022-11-11 | 2024-11-22 | ClinicalTrials.gov |
| NCT05590702 | French Observational Study of Patients With Chronic Lymphocytic Leukemia Or Sma… | — | CLL/SLL | Active_Not_Recruiting | 2022-11-11 | 2032-12-01 | ClinicalTrials.gov |
| NCT05582681 | HCV Test and Treat Utilizing Simplified HCV Patient Education | Phase4 | Hepatitis C | Terminated | 2022-11-11 | 2024-11-22 | ClinicalTrials.gov |
| NCT05590702 | French Observational Study of Patients With Chronic Lymphocytic Leukemia Or Sma… | — | CLL/SLL | Active_Not_Recruiting | 2022-11-11 | 2032-12-01 | ClinicalTrials.gov |
| NCT05582681 | HCV Test and Treat Utilizing Simplified HCV Patient Education | Phase4 | Hepatitis C | Terminated | 2022-11-11 | 2024-11-22 | ClinicalTrials.gov |
| NCT05590702 | French Observational Study of Patients With Chronic Lymphocytic Leukemia Or Sma… | — | CLL/SLL | Active_Not_Recruiting | 2022-11-11 | 2032-12-01 | ClinicalTrials.gov |
| NCT05590702 | French Observational Study of Patients With Chronic Lymphocytic Leukemia Or Sma… | — | CLL/SLL | Active_Not_Recruiting | 2022-11-11 | 2032-12-01 | ClinicalTrials.gov |
| NCT05411211 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Polyarticular Juvenile Idiopathic Arthritis | Completed | 2022-11-10 | 2024-09-08 | ClinicalTrials.gov |
| NCT05411211 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Polyarticular Juvenile Idiopathic Arthritis | Completed | 2022-11-10 | 2024-09-08 | ClinicalTrials.gov |
| NCT05411211 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Polyarticular Juvenile Idiopathic Arthritis | Completed | 2022-11-10 | 2024-09-08 | ClinicalTrials.gov |
| NCT05411211 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Polyarticular Juvenile Idiopathic Arthritis | Completed | 2022-11-10 | 2024-09-08 | ClinicalTrials.gov |
| NCT05259839 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenousl… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-10-20 | 2033-09-01 | ClinicalTrials.gov |
| NCT05259839 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenousl… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-10-20 | 2033-09-01 | ClinicalTrials.gov |
| NCT05259839 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenousl… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-10-20 | 2033-09-01 | ClinicalTrials.gov |
| NCT05496348 | Study of Oral Upadacitinib to Assess Change in Disease Activity in Adult Partic… | — | Ulcerative Colitis | Active_Not_Recruiting | 2022-10-20 | 2027-08-01 | ClinicalTrials.gov |
| NCT05496348 | Study of Oral Upadacitinib to Assess Change in Disease Activity in Adult Partic… | — | Ulcerative Colitis | Active_Not_Recruiting | 2022-10-20 | 2027-08-01 | ClinicalTrials.gov |
| NCT05496348 | Study of Oral Upadacitinib to Assess Change in Disease Activity in Adult Partic… | — | Ulcerative Colitis | Active_Not_Recruiting | 2022-10-20 | 2027-08-01 | ClinicalTrials.gov |
| NCT05259839 | A Study to Assess Adverse Events and Change in Disease Activity of Intravenousl… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-10-20 | 2033-09-01 | ClinicalTrials.gov |
| NCT05496348 | Study of Oral Upadacitinib to Assess Change in Disease Activity in Adult Partic… | — | Ulcerative Colitis | Active_Not_Recruiting | 2022-10-20 | 2027-08-01 | ClinicalTrials.gov |
| NCT05556226 | Study to Assess Adverse Events and Compare How Two Subcutaneous ABBV-154 Inject… | Phase1 | ABBV-154 | Completed | 2022-10-18 | 2023-02-17 | ClinicalTrials.gov |
| NCT05556226 | Study to Assess Adverse Events and Compare How Two Subcutaneous ABBV-154 Inject… | Phase1 | ABBV-154 | Completed | 2022-10-18 | 2023-02-17 | ClinicalTrials.gov |
| NCT05556226 | Study to Assess Adverse Events and Compare How Two Subcutaneous ABBV-154 Inject… | Phase1 | ABBV-154 | Completed | 2022-10-18 | 2023-02-17 | ClinicalTrials.gov |
| NCT05556226 | Study to Assess Adverse Events and Compare How Two Subcutaneous ABBV-154 Inject… | Phase1 | ABBV-154 | Completed | 2022-10-18 | 2023-02-17 | ClinicalTrials.gov |
| NCT07226752 | A Sub-study Trial of Epcoritamab vs Investigator's Choice Chemotherapy in Relap… | Phase3 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2022-10-08 | 2028-06-14 | ClinicalTrials.gov |
| NCT07226752 | A Sub-study Trial of Epcoritamab vs Investigator's Choice Chemotherapy in Relap… | Phase3 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2022-10-08 | 2028-06-14 | ClinicalTrials.gov |
| NCT07226752 | A Sub-study Trial of Epcoritamab vs Investigator's Choice Chemotherapy in Relap… | Phase3 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2022-10-08 | 2028-06-14 | ClinicalTrials.gov |
| NCT07226752 | A Sub-study Trial of Epcoritamab vs Investigator's Choice Chemotherapy in Relap… | Phase3 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2022-10-08 | 2028-06-14 | ClinicalTrials.gov |
| NCT05206357 | Study of the Adverse Events and Change in Disease State of Pediatric Participan… | Phase1 | Non-hodgkin Lymphoma | Active_Not_Recruiting | 2022-10-04 | 2028-11-01 | ClinicalTrials.gov |
| NCT05206357 | Study of the Adverse Events and Change in Disease State of Pediatric Participan… | Phase1 | Non-hodgkin Lymphoma | Active_Not_Recruiting | 2022-10-04 | 2028-11-01 | ClinicalTrials.gov |
| NCT05206357 | Study of the Adverse Events and Change in Disease State of Pediatric Participan… | Phase1 | Non-hodgkin Lymphoma | Active_Not_Recruiting | 2022-10-04 | 2028-11-01 | ClinicalTrials.gov |
| NCT05206357 | Study of the Adverse Events and Change in Disease State of Pediatric Participan… | Phase1 | Non-hodgkin Lymphoma | Active_Not_Recruiting | 2022-10-04 | 2028-11-01 | ClinicalTrials.gov |
| NCT05183035 | Venetoclax in Children With Relapsed Acute Myeloid Leukemia (AML) | Phase3 | Acute Myeloid Leukemia | Recruiting | 2022-10-01 | 2031-04-01 | ClinicalTrials.gov |
| NCT05183035 | Venetoclax in Children With Relapsed Acute Myeloid Leukemia (AML) | Phase3 | Acute Myeloid Leukemia | Recruiting | 2022-10-01 | 2031-04-01 | ClinicalTrials.gov |
| NCT05183035 | Venetoclax in Children With Relapsed Acute Myeloid Leukemia (AML) | Phase3 | Acute Myeloid Leukemia | Recruiting | 2022-10-01 | 2031-04-01 | ClinicalTrials.gov |
| NCT05183035 | Venetoclax in Children With Relapsed Acute Myeloid Leukemia (AML) | Phase3 | Acute Myeloid Leukemia | Recruiting | 2022-10-01 | 2031-04-01 | ClinicalTrials.gov |
| NCT05456685 | Mirvetuximab Soravtansine (MIRV) With Carboplatin in Second-line Treatment of F… | Phase2 | High Grade Ovarian Cancer | Active_Not_Recruiting | 2022-09-28 | 2026-11-01 | ClinicalTrials.gov |
| NCT05567029 | Study to Evaluate the Relative Bioavailability of Two Risankizumab Drug Product… | Phase1 | Healthy Volunteers | Completed | 2022-09-28 | 2023-04-20 | ClinicalTrials.gov |
| NCT05567029 | Study to Evaluate the Relative Bioavailability of Two Risankizumab Drug Product… | Phase1 | Healthy Volunteers | Completed | 2022-09-28 | 2023-04-20 | ClinicalTrials.gov |
| NCT05567029 | Study to Evaluate the Relative Bioavailability of Two Risankizumab Drug Product… | Phase1 | Healthy Volunteers | Completed | 2022-09-28 | 2023-04-20 | ClinicalTrials.gov |
| NCT05456685 | Mirvetuximab Soravtansine (MIRV) With Carboplatin in Second-line Treatment of F… | Phase2 | High Grade Ovarian Cancer | Active_Not_Recruiting | 2022-09-28 | 2026-11-01 | ClinicalTrials.gov |
| NCT05456685 | Mirvetuximab Soravtansine (MIRV) With Carboplatin in Second-line Treatment of F… | Phase2 | High Grade Ovarian Cancer | Active_Not_Recruiting | 2022-09-28 | 2026-11-01 | ClinicalTrials.gov |
| NCT05567029 | Study to Evaluate the Relative Bioavailability of Two Risankizumab Drug Product… | Phase1 | Healthy Volunteers | Completed | 2022-09-28 | 2023-04-20 | ClinicalTrials.gov |
| NCT05456685 | Mirvetuximab Soravtansine (MIRV) With Carboplatin in Second-line Treatment of F… | Phase2 | High Grade Ovarian Cancer | Active_Not_Recruiting | 2022-09-28 | 2026-11-01 | ClinicalTrials.gov |
| NCT05538585 | A Study to Assess How Food Affects the Safety and Pharmacokinetics of Galicafto… | Phase1 | Healthy Volunteers | Completed | 2022-09-27 | 2022-12-21 | ClinicalTrials.gov |
| NCT05538585 | A Study to Assess How Food Affects the Safety and Pharmacokinetics of Galicafto… | Phase1 | Healthy Volunteers | Completed | 2022-09-27 | 2022-12-21 | ClinicalTrials.gov |
| NCT05538585 | A Study to Assess How Food Affects the Safety and Pharmacokinetics of Galicafto… | Phase1 | Healthy Volunteers | Completed | 2022-09-27 | 2022-12-21 | ClinicalTrials.gov |
| NCT05538585 | A Study to Assess How Food Affects the Safety and Pharmacokinetics of Galicafto… | Phase1 | Healthy Volunteers | Completed | 2022-09-27 | 2022-12-21 | ClinicalTrials.gov |
| NCT05530278 | A Study to Assess the Pharmacokinetics and Safety of Co-administered Oral Galic… | Phase1 | Healthy Volunteers | Completed | 2022-09-20 | 2022-11-29 | ClinicalTrials.gov |
| NCT05530278 | A Study to Assess the Pharmacokinetics and Safety of Co-administered Oral Galic… | Phase1 | Healthy Volunteers | Completed | 2022-09-20 | 2022-11-29 | ClinicalTrials.gov |
| NCT05530278 | A Study to Assess the Pharmacokinetics and Safety of Co-administered Oral Galic… | Phase1 | Healthy Volunteers | Completed | 2022-09-20 | 2022-11-29 | ClinicalTrials.gov |
| NCT05530278 | A Study to Assess the Pharmacokinetics and Safety of Co-administered Oral Galic… | Phase1 | Healthy Volunteers | Completed | 2022-09-20 | 2022-11-29 | ClinicalTrials.gov |
| NCT05424562 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2022-09-07 | 2027-03-01 | ClinicalTrials.gov |
| NCT05454033 | A Study to Assess Adverse Events and Effectiveness of Intradermally Injected JU… | Phase3 | Perioral Lines | Completed | 2022-09-07 | 2024-09-03 | ClinicalTrials.gov |
| NCT05424562 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2022-09-07 | 2027-03-01 | ClinicalTrials.gov |
| NCT05454033 | A Study to Assess Adverse Events and Effectiveness of Intradermally Injected JU… | Phase3 | Perioral Lines | Completed | 2022-09-07 | 2024-09-03 | ClinicalTrials.gov |
| NCT05454033 | A Study to Assess Adverse Events and Effectiveness of Intradermally Injected JU… | Phase3 | Perioral Lines | Completed | 2022-09-07 | 2024-09-03 | ClinicalTrials.gov |
| NCT05424562 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2022-09-07 | 2027-03-01 | ClinicalTrials.gov |
| NCT05424562 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2022-09-07 | 2027-03-01 | ClinicalTrials.gov |
| NCT05454033 | A Study to Assess Adverse Events and Effectiveness of Intradermally Injected JU… | Phase3 | Perioral Lines | Completed | 2022-09-07 | 2024-09-03 | ClinicalTrials.gov |
| NCT05503082 | Ubrogepant treatmeNt in mIgraine Patients Utilizing mOnoclonal aNtibodies | Phase4 | Headache, Migraine | Active_Not_Recruiting | 2022-09-06 | 2024-11-01 | ClinicalTrials.gov |
| NCT05503082 | Ubrogepant treatmeNt in mIgraine Patients Utilizing mOnoclonal aNtibodies | Phase4 | Headache, Migraine | Active_Not_Recruiting | 2022-09-06 | 2024-11-01 | ClinicalTrials.gov |
| NCT05503082 | Ubrogepant treatmeNt in mIgraine Patients Utilizing mOnoclonal aNtibodies | Phase4 | Headache, Migraine | Active_Not_Recruiting | 2022-09-06 | 2024-11-01 | ClinicalTrials.gov |
| NCT05503082 | Ubrogepant treatmeNt in mIgraine Patients Utilizing mOnoclonal aNtibodies | Phase4 | Headache, Migraine | Active_Not_Recruiting | 2022-09-06 | 2024-11-01 | ClinicalTrials.gov |
| NCT04872790 | Venetoclax, Dasatinib, Prednisone, Rituximab and Blinatumomab for the Treatment… | Phase1 | B Acute Lymphoblastic Leukemia | Recruiting | 2022-09-02 | 2026-12-02 | ClinicalTrials.gov |
| NCT04872790 | Venetoclax, Dasatinib, Prednisone, Rituximab and Blinatumomab for the Treatment… | Phase1 | B Acute Lymphoblastic Leukemia | Recruiting | 2022-09-02 | 2026-12-02 | ClinicalTrials.gov |
| NCT05443724 | A Study to Evaluate Safety and Tolerability of CVL-231 (Emraclidine) in Adult P… | Phase2 | Schizophrenia | Completed | 2022-09-02 | 2025-06-25 | ClinicalTrials.gov |
| NCT05452070 | A Study to Assess Adverse Events and Change in Disease Activity of HArmonyCa Li… | Phase3 | Mid Face Volume Deficit | Completed | 2022-09-02 | 2025-05-08 | ClinicalTrials.gov |
| NCT05443724 | A Study to Evaluate Safety and Tolerability of CVL-231 (Emraclidine) in Adult P… | Phase2 | Schizophrenia | Completed | 2022-09-02 | 2025-06-25 | ClinicalTrials.gov |
| NCT04872790 | Venetoclax, Dasatinib, Prednisone, Rituximab and Blinatumomab for the Treatment… | Phase1 | B Acute Lymphoblastic Leukemia | Recruiting | 2022-09-02 | 2026-12-02 | ClinicalTrials.gov |
| NCT05443724 | A Study to Evaluate Safety and Tolerability of CVL-231 (Emraclidine) in Adult P… | Phase2 | Schizophrenia | Completed | 2022-09-02 | 2025-06-25 | ClinicalTrials.gov |
| NCT05443724 | A Study to Evaluate Safety and Tolerability of CVL-231 (Emraclidine) in Adult P… | Phase2 | Schizophrenia | Completed | 2022-09-02 | 2025-06-25 | ClinicalTrials.gov |
| NCT05452070 | A Study to Assess Adverse Events and Change in Disease Activity of HArmonyCa Li… | Phase3 | Mid Face Volume Deficit | Completed | 2022-09-02 | 2025-05-08 | ClinicalTrials.gov |
| NCT04872790 | Venetoclax, Dasatinib, Prednisone, Rituximab and Blinatumomab for the Treatment… | Phase1 | B Acute Lymphoblastic Leukemia | Recruiting | 2022-09-02 | 2026-12-02 | ClinicalTrials.gov |
| NCT05452070 | A Study to Assess Adverse Events and Change in Disease Activity of HArmonyCa Li… | Phase3 | Mid Face Volume Deficit | Completed | 2022-09-02 | 2025-05-08 | ClinicalTrials.gov |
| NCT05452070 | A Study to Assess Adverse Events and Change in Disease Activity of HArmonyCa Li… | Phase3 | Mid Face Volume Deficit | Completed | 2022-09-02 | 2025-05-08 | ClinicalTrials.gov |
| NCT05496335 | A Study to Evaluate Sequential Administration of AGN-151586 and Onabotulinumtox… | Phase1 | Glabellar Lines | Completed | 2022-08-30 | 2023-05-30 | ClinicalTrials.gov |
| NCT05496335 | A Study to Evaluate Sequential Administration of AGN-151586 and Onabotulinumtox… | Phase1 | Glabellar Lines | Completed | 2022-08-30 | 2023-05-30 | ClinicalTrials.gov |
| NCT05496335 | A Study to Evaluate Sequential Administration of AGN-151586 and Onabotulinumtox… | Phase1 | Glabellar Lines | Completed | 2022-08-30 | 2023-05-30 | ClinicalTrials.gov |
| NCT05496335 | A Study to Evaluate Sequential Administration of AGN-151586 and Onabotulinumtox… | Phase1 | Glabellar Lines | Completed | 2022-08-30 | 2023-05-30 | ClinicalTrials.gov |
| NCT05192889 | Trial Treating Relapsed Acute Lymphoblastic Leukemia With Venetoclax and Navito… | Phase1 | Refractory Acute Lymphoblastic Leukemia | Active_Not_Recruiting | 2022-08-25 | 2027-02-01 | ClinicalTrials.gov |
| NCT05192889 | Trial Treating Relapsed Acute Lymphoblastic Leukemia With Venetoclax and Navito… | Phase1 | Refractory Acute Lymphoblastic Leukemia | Active_Not_Recruiting | 2022-08-25 | 2027-02-01 | ClinicalTrials.gov |
| NCT05192889 | Trial Treating Relapsed Acute Lymphoblastic Leukemia With Venetoclax and Navito… | Phase1 | Refractory Acute Lymphoblastic Leukemia | Active_Not_Recruiting | 2022-08-25 | 2027-02-01 | ClinicalTrials.gov |
| NCT05192889 | Trial Treating Relapsed Acute Lymphoblastic Leukemia With Venetoclax and Navito… | Phase1 | Refractory Acute Lymphoblastic Leukemia | Active_Not_Recruiting | 2022-08-25 | 2027-02-01 | ClinicalTrials.gov |
| NCT05444972 | A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource … | — | Myelofibrosis | Completed | 2022-08-23 | 2023-11-14 | ClinicalTrials.gov |
| NCT05413785 | Hepatitis C Treatment in Probation and Parole Office | Na | Hepatitis C | Completed | 2022-08-23 | 2024-05-31 | ClinicalTrials.gov |
| NCT05444972 | A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource … | — | Myelofibrosis | Completed | 2022-08-23 | 2023-11-14 | ClinicalTrials.gov |
| NCT05413785 | Hepatitis C Treatment in Probation and Parole Office | Na | Hepatitis C | Completed | 2022-08-23 | 2024-05-31 | ClinicalTrials.gov |
| NCT05444972 | A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource … | — | Myelofibrosis | Completed | 2022-08-23 | 2023-11-14 | ClinicalTrials.gov |
| NCT05413785 | Hepatitis C Treatment in Probation and Parole Office | Na | Hepatitis C | Completed | 2022-08-23 | 2024-05-31 | ClinicalTrials.gov |
| NCT05444972 | A Study to Explore Treatment Patterns, Treatment Outcomes, Healthcare Resource … | — | Myelofibrosis | Completed | 2022-08-23 | 2023-11-14 | ClinicalTrials.gov |
| NCT05413785 | Hepatitis C Treatment in Probation and Parole Office | Na | Hepatitis C | Completed | 2022-08-23 | 2024-05-31 | ClinicalTrials.gov |
| NCT05368558 | Study to Assess Adverse Events and Change in Disease Activity of Oral Cariprazi… | Phase3 | Schizophrenia | Terminated | 2022-08-18 | 2024-09-20 | ClinicalTrials.gov |
| NCT05368558 | Study to Assess Adverse Events and Change in Disease Activity of Oral Cariprazi… | Phase3 | Schizophrenia | Terminated | 2022-08-18 | 2024-09-20 | ClinicalTrials.gov |
| NCT05368558 | Study to Assess Adverse Events and Change in Disease Activity of Oral Cariprazi… | Phase3 | Schizophrenia | Terminated | 2022-08-18 | 2024-09-20 | ClinicalTrials.gov |
| NCT05368558 | Study to Assess Adverse Events and Change in Disease Activity of Oral Cariprazi… | Phase3 | Schizophrenia | Terminated | 2022-08-18 | 2024-09-20 | ClinicalTrials.gov |
| NCT05451810 | A Study to Evaluate Adverse Events of Subcutaneous (SC) Epcoritamab Administere… | Phase2 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2022-08-17 | 2027-03-01 | ClinicalTrials.gov |
| NCT05451810 | A Study to Evaluate Adverse Events of Subcutaneous (SC) Epcoritamab Administere… | Phase2 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2022-08-17 | 2027-03-01 | ClinicalTrials.gov |
| NCT05451810 | A Study to Evaluate Adverse Events of Subcutaneous (SC) Epcoritamab Administere… | Phase2 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2022-08-17 | 2027-03-01 | ClinicalTrials.gov |
| NCT05451810 | A Study to Evaluate Adverse Events of Subcutaneous (SC) Epcoritamab Administere… | Phase2 | Diffuse Large B-Cell Lymphoma | Active_Not_Recruiting | 2022-08-17 | 2027-03-01 | ClinicalTrials.gov |
| NCT05291234 | A Study to Assess Safety of ABBV-916 and How Intravenous ABBV-916 Moves Through… | Phase2 | Alzheimer's Disease (AD) | Completed | 2022-08-15 | 2025-11-19 | ClinicalTrials.gov |
| NCT05291234 | A Study to Assess Safety of ABBV-916 and How Intravenous ABBV-916 Moves Through… | Phase2 | Alzheimer's Disease (AD) | Completed | 2022-08-15 | 2025-11-19 | ClinicalTrials.gov |
| NCT05494606 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Ulcerative Colitis | Active_Not_Recruiting | 2022-08-15 | 2028-03-01 | ClinicalTrials.gov |
| NCT05494606 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Ulcerative Colitis | Active_Not_Recruiting | 2022-08-15 | 2028-03-01 | ClinicalTrials.gov |
| NCT05291234 | A Study to Assess Safety of ABBV-916 and How Intravenous ABBV-916 Moves Through… | Phase2 | Alzheimer's Disease (AD) | Completed | 2022-08-15 | 2025-11-19 | ClinicalTrials.gov |
| NCT05291234 | A Study to Assess Safety of ABBV-916 and How Intravenous ABBV-916 Moves Through… | Phase2 | Alzheimer's Disease (AD) | Completed | 2022-08-15 | 2025-11-19 | ClinicalTrials.gov |
| NCT05494606 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Ulcerative Colitis | Active_Not_Recruiting | 2022-08-15 | 2028-03-01 | ClinicalTrials.gov |
| NCT05494606 | An Observational Study to Assess Change in Disease Activity and Adverse Events … | — | Ulcerative Colitis | Active_Not_Recruiting | 2022-08-15 | 2028-03-01 | ClinicalTrials.gov |
| NCT05475821 | Study to Assess Adverse Events and How Oral ABBV-990 Moves Through the Body of … | Phase1 | Healthy Volunteers | Terminated | 2022-07-25 | 2022-09-26 | ClinicalTrials.gov |
| NCT05475821 | Study to Assess Adverse Events and How Oral ABBV-990 Moves Through the Body of … | Phase1 | Healthy Volunteers | Terminated | 2022-07-25 | 2022-09-26 | ClinicalTrials.gov |
| NCT05475821 | Study to Assess Adverse Events and How Oral ABBV-990 Moves Through the Body of … | Phase1 | Healthy Volunteers | Terminated | 2022-07-25 | 2022-09-26 | ClinicalTrials.gov |
| NCT05475821 | Study to Assess Adverse Events and How Oral ABBV-990 Moves Through the Body of … | Phase1 | Healthy Volunteers | Terminated | 2022-07-25 | 2022-09-26 | ClinicalTrials.gov |
| NCT05411198 | Study to Assess Change in Disease Activity and Adverse Events of Ab Externo App… | Phase3 | Open-Angle Glaucoma | Completed | 2022-07-22 | 2026-02-04 | ClinicalTrials.gov |
| NCT05411198 | Study to Assess Change in Disease Activity and Adverse Events of Ab Externo App… | Phase3 | Open-Angle Glaucoma | Completed | 2022-07-22 | 2026-02-04 | ClinicalTrials.gov |
| NCT05411198 | Study to Assess Change in Disease Activity and Adverse Events of Ab Externo App… | Phase3 | Open-Angle Glaucoma | Completed | 2022-07-22 | 2026-02-04 | ClinicalTrials.gov |
| NCT05411198 | Study to Assess Change in Disease Activity and Adverse Events of Ab Externo App… | Phase3 | Open-Angle Glaucoma | Completed | 2022-07-22 | 2026-02-04 | ClinicalTrials.gov |
| NCT05455294 | Combination Navitoclax, Venetoclax and Decitabine for Advanced Myeloid Neoplasms | Phase1 | Myeloid Malignancy | Active_Not_Recruiting | 2022-07-18 | 2026-12-31 | ClinicalTrials.gov |
| NCT05384483 | Cariprazine Versus Placebo for Social Anxiety Disorder | Phase4 | Social Anxiety Disorder | Completed | 2022-07-18 | 2024-04-15 | ClinicalTrials.gov |
| NCT05384483 | Cariprazine Versus Placebo for Social Anxiety Disorder | Phase4 | Social Anxiety Disorder | Completed | 2022-07-18 | 2024-04-15 | ClinicalTrials.gov |
| NCT05455294 | Combination Navitoclax, Venetoclax and Decitabine for Advanced Myeloid Neoplasms | Phase1 | Myeloid Malignancy | Active_Not_Recruiting | 2022-07-18 | 2026-12-31 | ClinicalTrials.gov |
| NCT05384483 | Cariprazine Versus Placebo for Social Anxiety Disorder | Phase4 | Social Anxiety Disorder | Completed | 2022-07-18 | 2024-04-15 | ClinicalTrials.gov |
| NCT05384483 | Cariprazine Versus Placebo for Social Anxiety Disorder | Phase4 | Social Anxiety Disorder | Completed | 2022-07-18 | 2024-04-15 | ClinicalTrials.gov |
| NCT05455294 | Combination Navitoclax, Venetoclax and Decitabine for Advanced Myeloid Neoplasms | Phase1 | Myeloid Malignancy | Active_Not_Recruiting | 2022-07-18 | 2026-12-31 | ClinicalTrials.gov |
| NCT05455294 | Combination Navitoclax, Venetoclax and Decitabine for Advanced Myeloid Neoplasms | Phase1 | Myeloid Malignancy | Active_Not_Recruiting | 2022-07-18 | 2026-12-31 | ClinicalTrials.gov |
| NCT05414201 | A Study to Assess Change in Disease Activity and Adverse Events of Adalimumab i… | Phase4 | Non-infectious Intermediate Posterior- or Pan-uveitis | Completed | 2022-07-07 | 2024-06-10 | ClinicalTrials.gov |
| NCT05414201 | A Study to Assess Change in Disease Activity and Adverse Events of Adalimumab i… | Phase4 | Non-infectious Intermediate Posterior- or Pan-uveitis | Completed | 2022-07-07 | 2024-06-10 | ClinicalTrials.gov |
| NCT05439616 | Study of Cariprazine Oral Capsules or Solution to Assess Adverse Events and Cha… | Phase3 | Autism Spectrum Disorder | Completed | 2022-07-07 | 2024-10-04 | ClinicalTrials.gov |
| NCT05414201 | A Study to Assess Change in Disease Activity and Adverse Events of Adalimumab i… | Phase4 | Non-infectious Intermediate Posterior- or Pan-uveitis | Completed | 2022-07-07 | 2024-06-10 | ClinicalTrials.gov |
| NCT05439616 | Study of Cariprazine Oral Capsules or Solution to Assess Adverse Events and Cha… | Phase3 | Autism Spectrum Disorder | Completed | 2022-07-07 | 2024-10-04 | ClinicalTrials.gov |
| NCT05439616 | Study of Cariprazine Oral Capsules or Solution to Assess Adverse Events and Cha… | Phase3 | Autism Spectrum Disorder | Completed | 2022-07-07 | 2024-10-04 | ClinicalTrials.gov |
| NCT05414201 | A Study to Assess Change in Disease Activity and Adverse Events of Adalimumab i… | Phase4 | Non-infectious Intermediate Posterior- or Pan-uveitis | Completed | 2022-07-07 | 2024-06-10 | ClinicalTrials.gov |
| NCT05439616 | Study of Cariprazine Oral Capsules or Solution to Assess Adverse Events and Cha… | Phase3 | Autism Spectrum Disorder | Completed | 2022-07-07 | 2024-10-04 | ClinicalTrials.gov |
| NCT05609643 | Study to Assess Change in Disease Activity and Adverse Events of RINVOQ in Adul… | — | Ankylosing Spondylitis | Completed | 2022-07-06 | 2026-01-29 | ClinicalTrials.gov |
| NCT05376839 | A Study to Assess Safety of Cedirogant and How Cedirogant Moves Through the Bod… | Phase1 | Hepatic Impairment | Terminated | 2022-07-06 | 2022-11-08 | ClinicalTrials.gov |
| NCT05376839 | A Study to Assess Safety of Cedirogant and How Cedirogant Moves Through the Bod… | Phase1 | Hepatic Impairment | Terminated | 2022-07-06 | 2022-11-08 | ClinicalTrials.gov |
| NCT05609643 | Study to Assess Change in Disease Activity and Adverse Events of RINVOQ in Adul… | — | Ankylosing Spondylitis | Completed | 2022-07-06 | 2026-01-29 | ClinicalTrials.gov |
| NCT05376839 | A Study to Assess Safety of Cedirogant and How Cedirogant Moves Through the Bod… | Phase1 | Hepatic Impairment | Terminated | 2022-07-06 | 2022-11-08 | ClinicalTrials.gov |
| NCT05609643 | Study to Assess Change in Disease Activity and Adverse Events of RINVOQ in Adul… | — | Ankylosing Spondylitis | Completed | 2022-07-06 | 2026-01-29 | ClinicalTrials.gov |
| NCT05609643 | Study to Assess Change in Disease Activity and Adverse Events of RINVOQ in Adul… | — | Ankylosing Spondylitis | Completed | 2022-07-06 | 2026-01-29 | ClinicalTrials.gov |
| NCT05376839 | A Study to Assess Safety of Cedirogant and How Cedirogant Moves Through the Bod… | Phase1 | Hepatic Impairment | Terminated | 2022-07-06 | 2022-11-08 | ClinicalTrials.gov |
| NCT05227703 | A Trial of 15 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Sch… | Phase2 | Schizophrenia | Completed | 2022-07-05 | 2024-09-11 | ClinicalTrials.gov |
| NCT05227703 | A Trial of 15 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Sch… | Phase2 | Schizophrenia | Completed | 2022-07-05 | 2024-09-11 | ClinicalTrials.gov |
| NCT05227703 | A Trial of 15 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Sch… | Phase2 | Schizophrenia | Completed | 2022-07-05 | 2024-09-11 | ClinicalTrials.gov |
| NCT05227703 | A Trial of 15 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Sch… | Phase2 | Schizophrenia | Completed | 2022-07-05 | 2024-09-11 | ClinicalTrials.gov |
| NCT05227690 | A Trial of 10 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Sch… | Phase2 | Schizophrenia | Completed | 2022-06-30 | 2024-08-26 | ClinicalTrials.gov |
| NCT05227690 | A Trial of 10 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Sch… | Phase2 | Schizophrenia | Completed | 2022-06-30 | 2024-08-26 | ClinicalTrials.gov |
| NCT05227690 | A Trial of 10 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Sch… | Phase2 | Schizophrenia | Completed | 2022-06-30 | 2024-08-26 | ClinicalTrials.gov |
| NCT05227690 | A Trial of 10 and 30 mg Doses of CVL-231 (Emraclidine) in Participants With Sch… | Phase2 | Schizophrenia | Completed | 2022-06-30 | 2024-08-26 | ClinicalTrials.gov |
| NCT05394805 | A Study of Subcutaneous HUMIRA (Adalimumab) Injection to Assess Adverse Events … | — | Crohn's Disease | Completed | 2022-06-29 | 2024-12-26 | ClinicalTrials.gov |
| NCT05394805 | A Study of Subcutaneous HUMIRA (Adalimumab) Injection to Assess Adverse Events … | — | Crohn's Disease | Completed | 2022-06-29 | 2024-12-26 | ClinicalTrials.gov |
| NCT05394805 | A Study of Subcutaneous HUMIRA (Adalimumab) Injection to Assess Adverse Events … | — | Crohn's Disease | Completed | 2022-06-29 | 2024-12-26 | ClinicalTrials.gov |
| NCT05394805 | A Study of Subcutaneous HUMIRA (Adalimumab) Injection to Assess Adverse Events … | — | Crohn's Disease | Completed | 2022-06-29 | 2024-12-26 | ClinicalTrials.gov |
| NCT05025423 | Phase II Trial of Venetoclax and Rituximab as Initial Therapy in Older Patients… | Phase2 | Mantle Cell Lymphoma | Terminated | 2022-06-21 | 2025-05-14 | ClinicalTrials.gov |
| NCT05025423 | Phase II Trial of Venetoclax and Rituximab as Initial Therapy in Older Patients… | Phase2 | Mantle Cell Lymphoma | Terminated | 2022-06-21 | 2025-05-14 | ClinicalTrials.gov |
| NCT05025423 | Phase II Trial of Venetoclax and Rituximab as Initial Therapy in Older Patients… | Phase2 | Mantle Cell Lymphoma | Terminated | 2022-06-21 | 2025-05-14 | ClinicalTrials.gov |
| NCT05025423 | Phase II Trial of Venetoclax and Rituximab as Initial Therapy in Older Patients… | Phase2 | Mantle Cell Lymphoma | Terminated | 2022-06-21 | 2025-05-14 | ClinicalTrials.gov |
| NCT05394792 | An Observational Study of Upadacitinib to Assess Change in Disease Activity in … | — | Atopic Dermatitis | Completed | 2022-06-01 | 2024-08-15 | ClinicalTrials.gov |
| NCT05394792 | An Observational Study of Upadacitinib to Assess Change in Disease Activity in … | — | Atopic Dermatitis | Completed | 2022-06-01 | 2024-08-15 | ClinicalTrials.gov |
| NCT05394792 | An Observational Study of Upadacitinib to Assess Change in Disease Activity in … | — | Atopic Dermatitis | Completed | 2022-06-01 | 2024-08-15 | ClinicalTrials.gov |
| NCT05394792 | An Observational Study of Upadacitinib to Assess Change in Disease Activity in … | — | Atopic Dermatitis | Completed | 2022-06-01 | 2024-08-15 | ClinicalTrials.gov |
| NCT05317494 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Recruiting | 2022-05-26 | 2026-12-01 | ClinicalTrials.gov |
| NCT05317494 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Recruiting | 2022-05-26 | 2026-12-01 | ClinicalTrials.gov |
| NCT05317494 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Recruiting | 2022-05-26 | 2026-12-01 | ClinicalTrials.gov |
| NCT05317494 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Recruiting | 2022-05-26 | 2026-12-01 | ClinicalTrials.gov |
| NCT05342584 | Venetoclax Plus Intensive Chemotherapy in AML and Advanced MDS | Phase1 | Acute Myeloid Leukemia | Recruiting | 2022-05-25 | 2028-12-01 | ClinicalTrials.gov |
| NCT05342584 | Venetoclax Plus Intensive Chemotherapy in AML and Advanced MDS | Phase1 | Acute Myeloid Leukemia | Recruiting | 2022-05-25 | 2028-12-01 | ClinicalTrials.gov |
| NCT05342584 | Venetoclax Plus Intensive Chemotherapy in AML and Advanced MDS | Phase1 | Acute Myeloid Leukemia | Recruiting | 2022-05-25 | 2028-12-01 | ClinicalTrials.gov |
| NCT05342584 | Venetoclax Plus Intensive Chemotherapy in AML and Advanced MDS | Phase1 | Acute Myeloid Leukemia | Recruiting | 2022-05-25 | 2028-12-01 | ClinicalTrials.gov |
| NCT05308654 | A Study to Assess the Adverse Events and Change in Disease Activity in Adult Pa… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-05-17 | 2025-12-01 | ClinicalTrials.gov |
| NCT05308654 | A Study to Assess the Adverse Events and Change in Disease Activity in Adult Pa… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-05-17 | 2025-12-01 | ClinicalTrials.gov |
| NCT05308654 | A Study to Assess the Adverse Events and Change in Disease Activity in Adult Pa… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-05-17 | 2025-12-01 | ClinicalTrials.gov |
| NCT05308654 | A Study to Assess the Adverse Events and Change in Disease Activity in Adult Pa… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-05-17 | 2025-12-01 | ClinicalTrials.gov |
| NCT05316233 | A Study to Assess Adverse Events and Change in Disease Activity of JUVÉDERM® VO… | Phase3 | Neck Lines | Completed | 2022-05-02 | 2024-09-12 | ClinicalTrials.gov |
| NCT05316233 | A Study to Assess Adverse Events and Change in Disease Activity of JUVÉDERM® VO… | Phase3 | Neck Lines | Completed | 2022-05-02 | 2024-09-12 | ClinicalTrials.gov |
| NCT05316233 | A Study to Assess Adverse Events and Change in Disease Activity of JUVÉDERM® VO… | Phase3 | Neck Lines | Completed | 2022-05-02 | 2024-09-12 | ClinicalTrials.gov |
| NCT05316233 | A Study to Assess Adverse Events and Change in Disease Activity of JUVÉDERM® VO… | Phase3 | Neck Lines | Completed | 2022-05-02 | 2024-09-12 | ClinicalTrials.gov |
| NCT05327920 | An Observational Study to Assess the Impact of Upadacitinib in Adult Hungarian … | — | Rheumatoid Arthritis | Completed | 2022-04-20 | 2024-04-22 | ClinicalTrials.gov |
| NCT05327920 | An Observational Study to Assess the Impact of Upadacitinib in Adult Hungarian … | — | Rheumatoid Arthritis | Completed | 2022-04-20 | 2024-04-22 | ClinicalTrials.gov |
| NCT05327920 | An Observational Study to Assess the Impact of Upadacitinib in Adult Hungarian … | — | Rheumatoid Arthritis | Completed | 2022-04-20 | 2024-04-22 | ClinicalTrials.gov |
| NCT05327920 | An Observational Study to Assess the Impact of Upadacitinib in Adult Hungarian … | — | Rheumatoid Arthritis | Completed | 2022-04-20 | 2024-04-22 | ClinicalTrials.gov |
| NCT05216250 | Study of BOTOX Injections to Assess Change in Disease Symptoms in Adult Partici… | Phase2 | Upper Limb Essential Tremor (UL ET) | Completed | 2022-04-12 | 2025-02-03 | ClinicalTrials.gov |
| NCT05216250 | Study of BOTOX Injections to Assess Change in Disease Symptoms in Adult Partici… | Phase2 | Upper Limb Essential Tremor (UL ET) | Completed | 2022-04-12 | 2025-02-03 | ClinicalTrials.gov |
| NCT05216250 | Study of BOTOX Injections to Assess Change in Disease Symptoms in Adult Partici… | Phase2 | Upper Limb Essential Tremor (UL ET) | Completed | 2022-04-12 | 2025-02-03 | ClinicalTrials.gov |
| NCT05216250 | Study of BOTOX Injections to Assess Change in Disease Symptoms in Adult Partici… | Phase2 | Upper Limb Essential Tremor (UL ET) | Completed | 2022-04-12 | 2025-02-03 | ClinicalTrials.gov |
| NCT05296447 | Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space f… | — | Diabetic Retinopathy, DR | Enrolling_By_Invitation | 2022-04-04 | 2028-05-01 | ClinicalTrials.gov |
| NCT05296447 | Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space f… | — | Diabetic Retinopathy, DR | Enrolling_By_Invitation | 2022-04-04 | 2028-05-01 | ClinicalTrials.gov |
| NCT05296447 | Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space f… | — | Diabetic Retinopathy, DR | Enrolling_By_Invitation | 2022-04-04 | 2028-05-01 | ClinicalTrials.gov |
| NCT05296447 | Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space f… | — | Diabetic Retinopathy, DR | Enrolling_By_Invitation | 2022-04-04 | 2028-05-01 | ClinicalTrials.gov |
| NCT05141006 | Study of BOTOX Injections to Assess Change in Disease Activity and Adverse Even… | Phase2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | Completed | 2022-03-29 | 2024-12-06 | ClinicalTrials.gov |
| NCT05141006 | Study of BOTOX Injections to Assess Change in Disease Activity and Adverse Even… | Phase2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | Completed | 2022-03-29 | 2024-12-06 | ClinicalTrials.gov |
| NCT05141006 | Study of BOTOX Injections to Assess Change in Disease Activity and Adverse Even… | Phase2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | Completed | 2022-03-29 | 2024-12-06 | ClinicalTrials.gov |
| NCT05141006 | Study of BOTOX Injections to Assess Change in Disease Activity and Adverse Even… | Phase2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | Completed | 2022-03-29 | 2024-12-06 | ClinicalTrials.gov |
| NCT04895436 | Study to Assess Change in Disease Activity and Adverse Events of Oral Venetocla… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2022-03-28 | 2029-01-01 | ClinicalTrials.gov |
| NCT04895436 | Study to Assess Change in Disease Activity and Adverse Events of Oral Venetocla… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2022-03-28 | 2029-01-01 | ClinicalTrials.gov |
| NCT04895436 | Study to Assess Change in Disease Activity and Adverse Events of Oral Venetocla… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2022-03-28 | 2029-01-01 | ClinicalTrials.gov |
| NCT04895436 | Study to Assess Change in Disease Activity and Adverse Events of Oral Venetocla… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2022-03-28 | 2029-01-01 | ClinicalTrials.gov |
| NCT04928846 | A Study to Assess Disease Activity and Adverse Events of Intravenous (IV) Telis… | Phase3 | Non Small Cell Lung Cancer | Recruiting | 2022-03-25 | 2029-02-01 | ClinicalTrials.gov |
| NCT04928846 | A Study to Assess Disease Activity and Adverse Events of Intravenous (IV) Telis… | Phase3 | Non Small Cell Lung Cancer | Recruiting | 2022-03-25 | 2029-02-01 | ClinicalTrials.gov |
| NCT04928846 | A Study to Assess Disease Activity and Adverse Events of Intravenous (IV) Telis… | Phase3 | Non Small Cell Lung Cancer | Recruiting | 2022-03-25 | 2029-02-01 | ClinicalTrials.gov |
| NCT04928846 | A Study to Assess Disease Activity and Adverse Events of Intravenous (IV) Telis… | Phase3 | Non Small Cell Lung Cancer | Recruiting | 2022-03-25 | 2029-02-01 | ClinicalTrials.gov |
| NCT05286229 | A Study to Assess Adverse Events and Change in Disease State of Intravenously (… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-03-24 | 2026-03-01 | ClinicalTrials.gov |
| NCT05286229 | A Study to Assess Adverse Events and Change in Disease State of Intravenously (… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-03-24 | 2026-03-01 | ClinicalTrials.gov |
| NCT05286229 | A Study to Assess Adverse Events and Change in Disease State of Intravenously (… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-03-24 | 2026-03-01 | ClinicalTrials.gov |
| NCT05286229 | A Study to Assess Adverse Events and Change in Disease State of Intravenously (… | Phase1 | Relapsed/Refractory Multiple Myeloma | Active_Not_Recruiting | 2022-03-24 | 2026-03-01 | ClinicalTrials.gov |
| NCT05216263 | Study of Oral Atogepant When Added to OnabotulinumtoxinA (BOTOX) to Assess Adve… | Phase3 | Chronic Migraine | Completed | 2022-03-22 | 2025-05-02 | ClinicalTrials.gov |
| NCT05216263 | Study of Oral Atogepant When Added to OnabotulinumtoxinA (BOTOX) to Assess Adve… | Phase3 | Chronic Migraine | Completed | 2022-03-22 | 2025-05-02 | ClinicalTrials.gov |
| NCT05216263 | Study of Oral Atogepant When Added to OnabotulinumtoxinA (BOTOX) to Assess Adve… | Phase3 | Chronic Migraine | Completed | 2022-03-22 | 2025-05-02 | ClinicalTrials.gov |
| NCT05216263 | Study of Oral Atogepant When Added to OnabotulinumtoxinA (BOTOX) to Assess Adve… | Phase3 | Chronic Migraine | Completed | 2022-03-22 | 2025-05-02 | ClinicalTrials.gov |
| NCT05248867 | A Study to Assess Adverse Events and Change in Disease Activity of Intramuscula… | Phase3 | Glabellar Lines | Completed | 2022-03-16 | 2023-03-17 | ClinicalTrials.gov |
| NCT05248867 | A Study to Assess Adverse Events and Change in Disease Activity of Intramuscula… | Phase3 | Glabellar Lines | Completed | 2022-03-16 | 2023-03-17 | ClinicalTrials.gov |
| NCT05248867 | A Study to Assess Adverse Events and Change in Disease Activity of Intramuscula… | Phase3 | Glabellar Lines | Completed | 2022-03-16 | 2023-03-17 | ClinicalTrials.gov |
| NCT05248867 | A Study to Assess Adverse Events and Change in Disease Activity of Intramuscula… | Phase3 | Glabellar Lines | Completed | 2022-03-16 | 2023-03-17 | ClinicalTrials.gov |
| NCT05170646 | An Observational Study to Assess the Real-World Effectiveness of Upadacitinib i… | — | Rheumatoid Arthritis | Completed | 2022-03-14 | 2024-01-31 | ClinicalTrials.gov |
| NCT05170646 | An Observational Study to Assess the Real-World Effectiveness of Upadacitinib i… | — | Rheumatoid Arthritis | Completed | 2022-03-14 | 2024-01-31 | ClinicalTrials.gov |
| NCT05170646 | An Observational Study to Assess the Real-World Effectiveness of Upadacitinib i… | — | Rheumatoid Arthritis | Completed | 2022-03-14 | 2024-01-31 | ClinicalTrials.gov |
| NCT05170646 | An Observational Study to Assess the Real-World Effectiveness of Upadacitinib i… | — | Rheumatoid Arthritis | Completed | 2022-03-14 | 2024-01-31 | ClinicalTrials.gov |
| NCT05201248 | A Study to Evaluate Adverse Events and Change in Disease Activity of Subcutaneo… | Phase1 | B-Cell Non-Hodgkin Lymphoma | Active_Not_Recruiting | 2022-03-10 | 2025-04-01 | ClinicalTrials.gov |
| NCT05201248 | A Study to Evaluate Adverse Events and Change in Disease Activity of Subcutaneo… | Phase1 | B-Cell Non-Hodgkin Lymphoma | Active_Not_Recruiting | 2022-03-10 | 2025-04-01 | ClinicalTrials.gov |
| NCT05201248 | A Study to Evaluate Adverse Events and Change in Disease Activity of Subcutaneo… | Phase1 | B-Cell Non-Hodgkin Lymphoma | Active_Not_Recruiting | 2022-03-10 | 2025-04-01 | ClinicalTrials.gov |
| NCT05201248 | A Study to Evaluate Adverse Events and Change in Disease Activity of Subcutaneo… | Phase1 | B-Cell Non-Hodgkin Lymphoma | Active_Not_Recruiting | 2022-03-10 | 2025-04-01 | ClinicalTrials.gov |
| NCT05248880 | A Study to Assess Adverse Events and Change in Disease Activity of Intramuscula… | Phase3 | Glabellar Lines | Completed | 2022-03-08 | 2023-02-01 | ClinicalTrials.gov |
| NCT05248880 | A Study to Assess Adverse Events and Change in Disease Activity of Intramuscula… | Phase3 | Glabellar Lines | Completed | 2022-03-08 | 2023-02-01 | ClinicalTrials.gov |
| NCT05248880 | A Study to Assess Adverse Events and Change in Disease Activity of Intramuscula… | Phase3 | Glabellar Lines | Completed | 2022-03-08 | 2023-02-01 | ClinicalTrials.gov |
| NCT05248880 | A Study to Assess Adverse Events and Change in Disease Activity of Intramuscula… | Phase3 | Glabellar Lines | Completed | 2022-03-08 | 2023-02-01 | ClinicalTrials.gov |
| NCT05264129 | Study to Assess Adverse Events When Ubrogepant Tablets in Combination With Atog… | Phase4 | Episodic Migraine | Completed | 2022-03-07 | 2023-04-04 | ClinicalTrials.gov |
| NCT05264129 | Study to Assess Adverse Events When Ubrogepant Tablets in Combination With Atog… | Phase4 | Episodic Migraine | Completed | 2022-03-07 | 2023-04-04 | ClinicalTrials.gov |
| NCT05264129 | Study to Assess Adverse Events When Ubrogepant Tablets in Combination With Atog… | Phase4 | Episodic Migraine | Completed | 2022-03-07 | 2023-04-04 | ClinicalTrials.gov |
| NCT05264129 | Study to Assess Adverse Events When Ubrogepant Tablets in Combination With Atog… | Phase4 | Episodic Migraine | Completed | 2022-03-07 | 2023-04-04 | ClinicalTrials.gov |
| NCT05283135 | High Dose Risankizumab for Psoriasis | Phase2 | Psoriasis | Completed | 2022-03-01 | 2024-07-10 | ClinicalTrials.gov |
| NCT05283135 | High Dose Risankizumab for Psoriasis | Phase2 | Psoriasis | Completed | 2022-03-01 | 2024-07-10 | ClinicalTrials.gov |
| NCT05283135 | High Dose Risankizumab for Psoriasis | Phase2 | Psoriasis | Completed | 2022-03-01 | 2024-07-10 | ClinicalTrials.gov |
| NCT05283135 | High Dose Risankizumab for Psoriasis | Phase2 | Psoriasis | Completed | 2022-03-01 | 2024-07-10 | ClinicalTrials.gov |
| NCT05248893 | A Study to Assess Adverse Events of Intramuscular AGN-151586 Injection in Adult… | Phase3 | Glabellar Lines | Completed | 2022-02-25 | 2023-06-26 | ClinicalTrials.gov |
| NCT05248893 | A Study to Assess Adverse Events of Intramuscular AGN-151586 Injection in Adult… | Phase3 | Glabellar Lines | Completed | 2022-02-25 | 2023-06-26 | ClinicalTrials.gov |
| NCT05248893 | A Study to Assess Adverse Events of Intramuscular AGN-151586 Injection in Adult… | Phase3 | Glabellar Lines | Completed | 2022-02-25 | 2023-06-26 | ClinicalTrials.gov |
| NCT05248893 | A Study to Assess Adverse Events of Intramuscular AGN-151586 Injection in Adult… | Phase3 | Glabellar Lines | Completed | 2022-02-25 | 2023-06-26 | ClinicalTrials.gov |
| NCT04984317 | Feasibility of BOTOX Injection on Improving Female Stress Urinary Incontinence | Early_Phase1 | Stress Urinary Incontinence | Suspended | 2022-02-14 | 2027-08-01 | ClinicalTrials.gov |
| NCT04984317 | Feasibility of BOTOX Injection on Improving Female Stress Urinary Incontinence | Early_Phase1 | Stress Urinary Incontinence | Suspended | 2022-02-14 | 2027-08-01 | ClinicalTrials.gov |
| NCT04984317 | Feasibility of BOTOX Injection on Improving Female Stress Urinary Incontinence | Early_Phase1 | Stress Urinary Incontinence | Suspended | 2022-02-14 | 2027-08-01 | ClinicalTrials.gov |
| NCT04984317 | Feasibility of BOTOX Injection on Improving Female Stress Urinary Incontinence | Early_Phase1 | Stress Urinary Incontinence | Suspended | 2022-02-14 | 2027-08-01 | ClinicalTrials.gov |
| NCT04905810 | Azacitidine or Decitabine With Venetoclax for Acute Myeloid Leukemia With Prior… | Phase2 | Acute Myeloid Leukemia | Recruiting | 2022-02-09 | 2025-12-01 | ClinicalTrials.gov |
| NCT04905810 | Azacitidine or Decitabine With Venetoclax for Acute Myeloid Leukemia With Prior… | Phase2 | Acute Myeloid Leukemia | Recruiting | 2022-02-09 | 2025-12-01 | ClinicalTrials.gov |
| NCT04905810 | Azacitidine or Decitabine With Venetoclax for Acute Myeloid Leukemia With Prior… | Phase2 | Acute Myeloid Leukemia | Recruiting | 2022-02-09 | 2025-12-01 | ClinicalTrials.gov |
| NCT04905810 | Azacitidine or Decitabine With Venetoclax for Acute Myeloid Leukemia With Prior… | Phase2 | Acute Myeloid Leukemia | Recruiting | 2022-02-09 | 2025-12-01 | ClinicalTrials.gov |
| NCT04797767 | Venetoclax and CLAG-M for the Treatment of Acute Myeloid Leukemia and High-Grad… | Phase1 | Acute Biphenotypic Leukemia | Recruiting | 2022-02-04 | 2028-12-31 | ClinicalTrials.gov |
| NCT04797767 | Venetoclax and CLAG-M for the Treatment of Acute Myeloid Leukemia and High-Grad… | Phase1 | Acute Biphenotypic Leukemia | Recruiting | 2022-02-04 | 2028-12-31 | ClinicalTrials.gov |
| NCT04797767 | Venetoclax and CLAG-M for the Treatment of Acute Myeloid Leukemia and High-Grad… | Phase1 | Acute Biphenotypic Leukemia | Recruiting | 2022-02-04 | 2028-12-31 | ClinicalTrials.gov |
| NCT04797767 | Venetoclax and CLAG-M for the Treatment of Acute Myeloid Leukemia and High-Grad… | Phase1 | Acute Biphenotypic Leukemia | Recruiting | 2022-02-04 | 2028-12-31 | ClinicalTrials.gov |
| NCT05068284 | A Study to Evaluate Adverse Events and Change in Disease Activity in Participan… | Phase2 | Crohn's Disease | Terminated | 2022-01-31 | 2023-07-20 | ClinicalTrials.gov |
| NCT05068284 | A Study to Evaluate Adverse Events and Change in Disease Activity in Participan… | Phase2 | Crohn's Disease | Terminated | 2022-01-31 | 2023-07-20 | ClinicalTrials.gov |
| NCT05068284 | A Study to Evaluate Adverse Events and Change in Disease Activity in Participan… | Phase2 | Crohn's Disease | Terminated | 2022-01-31 | 2023-07-20 | ClinicalTrials.gov |
| NCT05068284 | A Study to Evaluate Adverse Events and Change in Disease Activity in Participan… | Phase2 | Crohn's Disease | Terminated | 2022-01-31 | 2023-07-20 | ClinicalTrials.gov |
| NCT05094050 | Study to Assess How ABBV-951 is Absorbed When Administered at Different Subcuta… | Phase1 | Parkinson's Disease | Completed | 2022-01-18 | 2023-03-17 | ClinicalTrials.gov |
| NCT05094050 | Study to Assess How ABBV-951 is Absorbed When Administered at Different Subcuta… | Phase1 | Parkinson's Disease | Completed | 2022-01-18 | 2023-03-17 | ClinicalTrials.gov |
| NCT05094050 | Study to Assess How ABBV-951 is Absorbed When Administered at Different Subcuta… | Phase1 | Parkinson's Disease | Completed | 2022-01-18 | 2023-03-17 | ClinicalTrials.gov |
| NCT05094050 | Study to Assess How ABBV-951 is Absorbed When Administered at Different Subcuta… | Phase1 | Parkinson's Disease | Completed | 2022-01-18 | 2023-03-17 | ClinicalTrials.gov |
| NCT04895410 | Study to Assess Adverse Events and Change in Disease Activity of Intravenous (I… | Phase1 | Multiple Myeloma | Terminated | 2022-01-17 | 2022-06-24 | ClinicalTrials.gov |
| NCT04895410 | Study to Assess Adverse Events and Change in Disease Activity of Intravenous (I… | Phase1 | Multiple Myeloma | Terminated | 2022-01-17 | 2022-06-24 | ClinicalTrials.gov |
| NCT04895410 | Study to Assess Adverse Events and Change in Disease Activity of Intravenous (I… | Phase1 | Multiple Myeloma | Terminated | 2022-01-17 | 2022-06-24 | ClinicalTrials.gov |
| NCT04895410 | Study to Assess Adverse Events and Change in Disease Activity of Intravenous (I… | Phase1 | Multiple Myeloma | Terminated | 2022-01-17 | 2022-06-24 | ClinicalTrials.gov |
| NCT05127954 | Long-term Extension Study to Assess Safety and Tolerability of Oral Ubrogepant … | Phase3 | Migraine | Enrolling_By_Invitation | 2022-01-14 | 2028-01-01 | ClinicalTrials.gov |
| NCT05127954 | Long-term Extension Study to Assess Safety and Tolerability of Oral Ubrogepant … | Phase3 | Migraine | Enrolling_By_Invitation | 2022-01-14 | 2028-01-01 | ClinicalTrials.gov |
| NCT05127954 | Long-term Extension Study to Assess Safety and Tolerability of Oral Ubrogepant … | Phase3 | Migraine | Enrolling_By_Invitation | 2022-01-14 | 2028-01-01 | ClinicalTrials.gov |
| NCT05127954 | Long-term Extension Study to Assess Safety and Tolerability of Oral Ubrogepant … | Phase3 | Migraine | Enrolling_By_Invitation | 2022-01-14 | 2028-01-01 | ClinicalTrials.gov |
| NCT05125302 | Study to Assess Adverse Events and Disease Activity of Oral Ubrogepant Tablets … | Phase3 | Migraine | Recruiting | 2022-01-13 | 2027-05-01 | ClinicalTrials.gov |
| NCT05407636 | Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD | Phase3 | AMD | Recruiting | 2022-01-13 | 2027-11-01 | ClinicalTrials.gov |
| NCT05125302 | Study to Assess Adverse Events and Disease Activity of Oral Ubrogepant Tablets … | Phase3 | Migraine | Recruiting | 2022-01-13 | 2027-05-01 | ClinicalTrials.gov |
| NCT05407636 | Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD | Phase3 | AMD | Recruiting | 2022-01-13 | 2027-11-01 | ClinicalTrials.gov |
| NCT05125302 | Study to Assess Adverse Events and Disease Activity of Oral Ubrogepant Tablets … | Phase3 | Migraine | Recruiting | 2022-01-13 | 2027-05-01 | ClinicalTrials.gov |
| NCT05125302 | Study to Assess Adverse Events and Disease Activity of Oral Ubrogepant Tablets … | Phase3 | Migraine | Recruiting | 2022-01-13 | 2027-05-01 | ClinicalTrials.gov |
| NCT05407636 | Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD | Phase3 | AMD | Recruiting | 2022-01-13 | 2027-11-01 | ClinicalTrials.gov |
| NCT05407636 | Pivotal 2 Study of RGX-314 Gene Therapy in Participants With nAMD | Phase3 | AMD | Recruiting | 2022-01-13 | 2027-11-01 | ClinicalTrials.gov |
| NCT04464187 | A Study to Evaluate Pregnancy Outcomes in Females Treated With Oral Elagolix Ta… | — | Endometriosis | Terminated | 2022-01-06 | 2025-07-11 | ClinicalTrials.gov |
| NCT04464187 | A Study to Evaluate Pregnancy Outcomes in Females Treated With Oral Elagolix Ta… | — | Endometriosis | Terminated | 2022-01-06 | 2025-07-11 | ClinicalTrials.gov |
| NCT05144243 | Study to Assess Adverse Events and Change in Disease State of Oral Venetoclax i… | Phase4 | Acute Myeloid Leukemia (AML) | Active_Not_Recruiting | 2022-01-06 | 2026-03-01 | ClinicalTrials.gov |
| NCT05144243 | Study to Assess Adverse Events and Change in Disease State of Oral Venetoclax i… | Phase4 | Acute Myeloid Leukemia (AML) | Active_Not_Recruiting | 2022-01-06 | 2026-03-01 | ClinicalTrials.gov |
| NCT04464187 | A Study to Evaluate Pregnancy Outcomes in Females Treated With Oral Elagolix Ta… | — | Endometriosis | Terminated | 2022-01-06 | 2025-07-11 | ClinicalTrials.gov |
| NCT05144243 | Study to Assess Adverse Events and Change in Disease State of Oral Venetoclax i… | Phase4 | Acute Myeloid Leukemia (AML) | Active_Not_Recruiting | 2022-01-06 | 2026-03-01 | ClinicalTrials.gov |
| NCT04464187 | A Study to Evaluate Pregnancy Outcomes in Females Treated With Oral Elagolix Ta… | — | Endometriosis | Terminated | 2022-01-06 | 2025-07-11 | ClinicalTrials.gov |
| NCT05144243 | Study to Assess Adverse Events and Change in Disease State of Oral Venetoclax i… | Phase4 | Acute Myeloid Leukemia (AML) | Active_Not_Recruiting | 2022-01-06 | 2026-03-01 | ClinicalTrials.gov |
| NCT05139602 | A Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-… | Phase2 | Hidradenitis Suppurativa | Active_Not_Recruiting | 2021-12-28 | 2027-12-01 | ClinicalTrials.gov |
| NCT05139602 | A Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-… | Phase2 | Hidradenitis Suppurativa | Active_Not_Recruiting | 2021-12-28 | 2027-12-01 | ClinicalTrials.gov |
| NCT05139602 | A Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-… | Phase2 | Hidradenitis Suppurativa | Active_Not_Recruiting | 2021-12-28 | 2027-12-01 | ClinicalTrials.gov |
| NCT05139602 | A Study to Assess Disease Activity and Safety of Subcutaneous Lutikizumab (ABT-… | Phase2 | Hidradenitis Suppurativa | Active_Not_Recruiting | 2021-12-28 | 2027-12-01 | ClinicalTrials.gov |
| NCT05215639 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Completed | 2021-12-27 | 2025-11-24 | ClinicalTrials.gov |
| NCT05215639 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Completed | 2021-12-27 | 2025-11-24 | ClinicalTrials.gov |
| NCT05215639 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Completed | 2021-12-27 | 2025-11-24 | ClinicalTrials.gov |
| NCT05215639 | A Study to Assess Change in Disease State in Adult Participants With Acute Myel… | — | Acute Myeloid Leukemia | Completed | 2021-12-27 | 2025-11-24 | ClinicalTrials.gov |
| NCT05210803 | Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space f… | — | Neovascular Age-Related Macular Degeneration (nAMD) | Enrolling_By_Invitation | 2021-12-20 | 2028-03-01 | ClinicalTrials.gov |
| NCT05210803 | Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space f… | — | Neovascular Age-Related Macular Degeneration (nAMD) | Enrolling_By_Invitation | 2021-12-20 | 2028-03-01 | ClinicalTrials.gov |
| NCT05210803 | Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space f… | — | Neovascular Age-Related Macular Degeneration (nAMD) | Enrolling_By_Invitation | 2021-12-20 | 2028-03-01 | ClinicalTrials.gov |
| NCT05210803 | Long-Term Follow-Up Study of RGX-314 Administered in the Suprachoroidal Space f… | — | Neovascular Age-Related Macular Degeneration (nAMD) | Enrolling_By_Invitation | 2021-12-20 | 2028-03-01 | ClinicalTrials.gov |
| NCT05139836 | A Study to Assess Disease Activity in Adolescent and Adult Participants With At… | — | Atopic Dermatitis | Active_Not_Recruiting | 2021-12-13 | 2027-09-01 | ClinicalTrials.gov |
| NCT05139836 | A Study to Assess Disease Activity in Adolescent and Adult Participants With At… | — | Atopic Dermatitis | Active_Not_Recruiting | 2021-12-13 | 2027-09-01 | ClinicalTrials.gov |
| NCT05139836 | A Study to Assess Disease Activity in Adolescent and Adult Participants With At… | — | Atopic Dermatitis | Active_Not_Recruiting | 2021-12-13 | 2027-09-01 | ClinicalTrials.gov |
| NCT05139836 | A Study to Assess Disease Activity in Adolescent and Adult Participants With At… | — | Atopic Dermatitis | Active_Not_Recruiting | 2021-12-13 | 2027-09-01 | ClinicalTrials.gov |
| NCT05048732 | Imaging Apoptosis for Lymphoma Treatment Response | Early_Phase1 | Diffuse Large B Cell Lymphoma | Terminated | 2021-12-06 | 2024-02-10 | ClinicalTrials.gov |
| NCT05048732 | Imaging Apoptosis for Lymphoma Treatment Response | Early_Phase1 | Diffuse Large B Cell Lymphoma | Terminated | 2021-12-06 | 2024-02-10 | ClinicalTrials.gov |
| NCT05048732 | Imaging Apoptosis for Lymphoma Treatment Response | Early_Phase1 | Diffuse Large B Cell Lymphoma | Terminated | 2021-12-06 | 2024-02-10 | ClinicalTrials.gov |
| NCT05048732 | Imaging Apoptosis for Lymphoma Treatment Response | Early_Phase1 | Diffuse Large B Cell Lymphoma | Terminated | 2021-12-06 | 2024-02-10 | ClinicalTrials.gov |
| NCT04887857 | A Study to Assess Safety and Tolerability of CC-486 (ONUREG®, Oral Azacitidine)… | Phase1 | Leukemia, Myeloid, Acute | Completed | 2021-12-01 | 2024-01-08 | ClinicalTrials.gov |
| NCT04887857 | A Study to Assess Safety and Tolerability of CC-486 (ONUREG®, Oral Azacitidine)… | Phase1 | Leukemia, Myeloid, Acute | Completed | 2021-12-01 | 2024-01-08 | ClinicalTrials.gov |
| NCT04887857 | A Study to Assess Safety and Tolerability of CC-486 (ONUREG®, Oral Azacitidine)… | Phase1 | Leukemia, Myeloid, Acute | Completed | 2021-12-01 | 2024-01-08 | ClinicalTrials.gov |
| NCT04887857 | A Study to Assess Safety and Tolerability of CC-486 (ONUREG®, Oral Azacitidine)… | Phase1 | Leukemia, Myeloid, Acute | Completed | 2021-12-01 | 2024-01-08 | ClinicalTrials.gov |
| NCT05152576 | A Study To Assess the Adverse Effects and Change in Condition of Onabotulinumto… | Phase2 | Forehead Lines | Completed | 2021-11-29 | 2022-09-06 | ClinicalTrials.gov |
| NCT05152576 | A Study To Assess the Adverse Effects and Change in Condition of Onabotulinumto… | Phase2 | Forehead Lines | Completed | 2021-11-29 | 2022-09-06 | ClinicalTrials.gov |
| NCT05152576 | A Study To Assess the Adverse Effects and Change in Condition of Onabotulinumto… | Phase2 | Forehead Lines | Completed | 2021-11-29 | 2022-09-06 | ClinicalTrials.gov |
| NCT05152576 | A Study To Assess the Adverse Effects and Change in Condition of Onabotulinumto… | Phase2 | Forehead Lines | Completed | 2021-11-29 | 2022-09-06 | ClinicalTrials.gov |
| NCT05164783 | Multicenter Implementation of E-monitoring in Parkinson's Disease | Na | Parkinson Disease | Active_Not_Recruiting | 2021-11-23 | 2025-06-27 | ClinicalTrials.gov |
| NCT05164783 | Multicenter Implementation of E-monitoring in Parkinson's Disease | Na | Parkinson Disease | Active_Not_Recruiting | 2021-11-23 | 2025-06-27 | ClinicalTrials.gov |
| NCT05164783 | Multicenter Implementation of E-monitoring in Parkinson's Disease | Na | Parkinson Disease | Active_Not_Recruiting | 2021-11-23 | 2025-06-27 | ClinicalTrials.gov |
| NCT05164783 | Multicenter Implementation of E-monitoring in Parkinson's Disease | Na | Parkinson Disease | Active_Not_Recruiting | 2021-11-23 | 2025-06-27 | ClinicalTrials.gov |
| NCT05094128 | A Study to Assess Disease Activity in Adult Participants With Axial Spondyloart… | — | Axial Spondylarthritis (r-axSpA) | Active_Not_Recruiting | 2021-11-22 | 2027-04-01 | ClinicalTrials.gov |
| NCT05094128 | A Study to Assess Disease Activity in Adult Participants With Axial Spondyloart… | — | Axial Spondylarthritis (r-axSpA) | Active_Not_Recruiting | 2021-11-22 | 2027-04-01 | ClinicalTrials.gov |
| NCT05094128 | A Study to Assess Disease Activity in Adult Participants With Axial Spondyloart… | — | Axial Spondylarthritis (r-axSpA) | Active_Not_Recruiting | 2021-11-22 | 2027-04-01 | ClinicalTrials.gov |
| NCT05094128 | A Study to Assess Disease Activity in Adult Participants With Axial Spondyloart… | — | Axial Spondylarthritis (r-axSpA) | Active_Not_Recruiting | 2021-11-22 | 2027-04-01 | ClinicalTrials.gov |
| NCT05081557 | A Study to Assess Real-World Use, Safety, and Effectiveness of Oral Upadacitini… | — | Atopic Dermatitis | Active_Not_Recruiting | 2021-11-17 | 2026-10-01 | ClinicalTrials.gov |
| NCT05081557 | A Study to Assess Real-World Use, Safety, and Effectiveness of Oral Upadacitini… | — | Atopic Dermatitis | Active_Not_Recruiting | 2021-11-17 | 2026-10-01 | ClinicalTrials.gov |
| NCT05081557 | A Study to Assess Real-World Use, Safety, and Effectiveness of Oral Upadacitini… | — | Atopic Dermatitis | Active_Not_Recruiting | 2021-11-17 | 2026-10-01 | ClinicalTrials.gov |
| NCT05081557 | A Study to Assess Real-World Use, Safety, and Effectiveness of Oral Upadacitini… | — | Atopic Dermatitis | Active_Not_Recruiting | 2021-11-17 | 2026-10-01 | ClinicalTrials.gov |
| NCT05134649 | A Study To Assess the Safety of OnabotulinumtoxinA (BOTOX) Intramuscular Inject… | Phase3 | Platysma Prominence | Completed | 2021-11-16 | 2023-08-18 | ClinicalTrials.gov |
| NCT05134649 | A Study To Assess the Safety of OnabotulinumtoxinA (BOTOX) Intramuscular Inject… | Phase3 | Platysma Prominence | Completed | 2021-11-16 | 2023-08-18 | ClinicalTrials.gov |
| NCT05044234 | A Study to Assess Adverse Events and Disease Activity With Cedirogant (ABBV-157… | Phase2 | Psoriasis | Terminated | 2021-11-16 | 2022-11-30 | ClinicalTrials.gov |
| NCT05134649 | A Study To Assess the Safety of OnabotulinumtoxinA (BOTOX) Intramuscular Inject… | Phase3 | Platysma Prominence | Completed | 2021-11-16 | 2023-08-18 | ClinicalTrials.gov |
| NCT05044234 | A Study to Assess Adverse Events and Disease Activity With Cedirogant (ABBV-157… | Phase2 | Psoriasis | Terminated | 2021-11-16 | 2022-11-30 | ClinicalTrials.gov |
| NCT05134649 | A Study To Assess the Safety of OnabotulinumtoxinA (BOTOX) Intramuscular Inject… | Phase3 | Platysma Prominence | Completed | 2021-11-16 | 2023-08-18 | ClinicalTrials.gov |
| NCT05044234 | A Study to Assess Adverse Events and Disease Activity With Cedirogant (ABBV-157… | Phase2 | Psoriasis | Terminated | 2021-11-16 | 2022-11-30 | ClinicalTrials.gov |
| NCT05044234 | A Study to Assess Adverse Events and Disease Activity With Cedirogant (ABBV-157… | Phase2 | Psoriasis | Terminated | 2021-11-16 | 2022-11-30 | ClinicalTrials.gov |
| NCT03400306 | A Study Evaluating the Bioavailability and Food Effect of Veliparib Tablets Fol… | Phase1 | Cancer - Ovarian | Withdrawn | 2021-11-15 | 2021-11-16 | ClinicalTrials.gov |
| NCT03400306 | A Study Evaluating the Bioavailability and Food Effect of Veliparib Tablets Fol… | Phase1 | Cancer - Ovarian | Withdrawn | 2021-11-15 | 2021-11-16 | ClinicalTrials.gov |
| NCT03400306 | A Study Evaluating the Bioavailability and Food Effect of Veliparib Tablets Fol… | Phase1 | Cancer - Ovarian | Withdrawn | 2021-11-15 | 2021-11-16 | ClinicalTrials.gov |
| NCT03400306 | A Study Evaluating the Bioavailability and Food Effect of Veliparib Tablets Fol… | Phase1 | Cancer - Ovarian | Withdrawn | 2021-11-15 | 2021-11-16 | ClinicalTrials.gov |
| NCT04898894 | Study of Selinexor and Venetoclax in Combination With Chemotherapy in Pediatric… | Phase1 | Acute Leukemia of Ambiguous Lineage in Relapse | Active_Not_Recruiting | 2021-11-15 | 2027-09-01 | ClinicalTrials.gov |
| NCT05080218 | COVID-19 VaccinE Response in Rheumatology Patients | Phase4 | Rheumatoid Arthritis | Completed | 2021-11-15 | 2024-05-28 | ClinicalTrials.gov |
| NCT04898894 | Study of Selinexor and Venetoclax in Combination With Chemotherapy in Pediatric… | Phase1 | Acute Leukemia of Ambiguous Lineage in Relapse | Active_Not_Recruiting | 2021-11-15 | 2027-09-01 | ClinicalTrials.gov |
| NCT05080218 | COVID-19 VaccinE Response in Rheumatology Patients | Phase4 | Rheumatoid Arthritis | Completed | 2021-11-15 | 2024-05-28 | ClinicalTrials.gov |
| NCT04898894 | Study of Selinexor and Venetoclax in Combination With Chemotherapy in Pediatric… | Phase1 | Acute Leukemia of Ambiguous Lineage in Relapse | Active_Not_Recruiting | 2021-11-15 | 2027-09-01 | ClinicalTrials.gov |
| NCT04898894 | Study of Selinexor and Venetoclax in Combination With Chemotherapy in Pediatric… | Phase1 | Acute Leukemia of Ambiguous Lineage in Relapse | Active_Not_Recruiting | 2021-11-15 | 2027-09-01 | ClinicalTrials.gov |
| NCT05080218 | COVID-19 VaccinE Response in Rheumatology Patients | Phase4 | Rheumatoid Arthritis | Completed | 2021-11-15 | 2024-05-28 | ClinicalTrials.gov |
| NCT05080218 | COVID-19 VaccinE Response in Rheumatology Patients | Phase4 | Rheumatoid Arthritis | Completed | 2021-11-15 | 2024-05-28 | ClinicalTrials.gov |
| NCT05105841 | Study to Assess Change in Disease Activity and Adverse Events of Oral Venetocla… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2021-11-08 | 2025-10-09 | ClinicalTrials.gov |
| NCT05105841 | Study to Assess Change in Disease Activity and Adverse Events of Oral Venetocla… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2021-11-08 | 2025-10-09 | ClinicalTrials.gov |
| NCT05105841 | Study to Assess Change in Disease Activity and Adverse Events of Oral Venetocla… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2021-11-08 | 2025-10-09 | ClinicalTrials.gov |
| NCT05105841 | Study to Assess Change in Disease Activity and Adverse Events of Oral Venetocla… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2021-11-08 | 2025-10-09 | ClinicalTrials.gov |
| NCT05130554 | XEN45 in the Treatment of Chinese Patients With Primary Open-angle Glaucoma | Na | Glaucoma | Unknown | 2021-11-07 | 2022-09-30 | ClinicalTrials.gov |
| NCT05130554 | XEN45 in the Treatment of Chinese Patients With Primary Open-angle Glaucoma | Na | Glaucoma | Unknown | 2021-11-07 | 2022-09-30 | ClinicalTrials.gov |
| NCT05130554 | XEN45 in the Treatment of Chinese Patients With Primary Open-angle Glaucoma | Na | Glaucoma | Unknown | 2021-11-07 | 2022-09-30 | ClinicalTrials.gov |
| NCT05130554 | XEN45 in the Treatment of Chinese Patients With Primary Open-angle Glaucoma | Na | Glaucoma | Unknown | 2021-11-07 | 2022-09-30 | ClinicalTrials.gov |
| NCT05028569 | Study of BOTOX Injections in Prevention of Migraine in Adult Participants With … | Phase3 | Episodic Migraine | Terminated | 2021-11-05 | 2024-11-06 | ClinicalTrials.gov |
| NCT05028569 | Study of BOTOX Injections in Prevention of Migraine in Adult Participants With … | Phase3 | Episodic Migraine | Terminated | 2021-11-05 | 2024-11-06 | ClinicalTrials.gov |
| NCT05028569 | Study of BOTOX Injections in Prevention of Migraine in Adult Participants With … | Phase3 | Episodic Migraine | Terminated | 2021-11-05 | 2024-11-06 | ClinicalTrials.gov |
| NCT05028569 | Study of BOTOX Injections in Prevention of Migraine in Adult Participants With … | Phase3 | Episodic Migraine | Terminated | 2021-11-05 | 2024-11-06 | ClinicalTrials.gov |
| NCT05005403 | Study to Assess Adverse Events and Pharmacokinetics in Adult Participants With … | Phase1 | Non-Small Cell Lung Cancer | Recruiting | 2021-11-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT05005403 | Study to Assess Adverse Events and Pharmacokinetics in Adult Participants With … | Phase1 | Non-Small Cell Lung Cancer | Recruiting | 2021-11-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT05005403 | Study to Assess Adverse Events and Pharmacokinetics in Adult Participants With … | Phase1 | Non-Small Cell Lung Cancer | Recruiting | 2021-11-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT05005403 | Study to Assess Adverse Events and Pharmacokinetics in Adult Participants With … | Phase1 | Non-Small Cell Lung Cancer | Recruiting | 2021-11-01 | 2027-07-01 | ClinicalTrials.gov |
| NCT05083286 | Duration of Botox Using OLD Versus COLD for Treatment of Glabellar Lines | Early_Phase1 | Glabellar Frown Lines | Unknown | 2021-10-20 | 2022-08-01 | ClinicalTrials.gov |
| NCT05083286 | Duration of Botox Using OLD Versus COLD for Treatment of Glabellar Lines | Early_Phase1 | Glabellar Frown Lines | Unknown | 2021-10-20 | 2022-08-01 | ClinicalTrials.gov |
| NCT05083286 | Duration of Botox Using OLD Versus COLD for Treatment of Glabellar Lines | Early_Phase1 | Glabellar Frown Lines | Unknown | 2021-10-20 | 2022-08-01 | ClinicalTrials.gov |
| NCT05083286 | Duration of Botox Using OLD Versus COLD for Treatment of Glabellar Lines | Early_Phase1 | Glabellar Frown Lines | Unknown | 2021-10-20 | 2022-08-01 | ClinicalTrials.gov |
| NCT05041257 | Mirvetuximab Soravtansine Monotherapy in Platinum-Sensitive Epithelial, Periton… | Phase2 | Ovarian Cancer | Completed | 2021-10-19 | 2024-12-12 | ClinicalTrials.gov |
| NCT05041257 | Mirvetuximab Soravtansine Monotherapy in Platinum-Sensitive Epithelial, Periton… | Phase2 | Ovarian Cancer | Completed | 2021-10-19 | 2024-12-12 | ClinicalTrials.gov |
| NCT05088980 | Study to Assess Effectiveness and Adverse Events of JUVEDERM VOLBELLA With Lido… | Phase3 | Infraorbital Hollowing | Completed | 2021-10-19 | 2023-11-29 | ClinicalTrials.gov |
| NCT05088980 | Study to Assess Effectiveness and Adverse Events of JUVEDERM VOLBELLA With Lido… | Phase3 | Infraorbital Hollowing | Completed | 2021-10-19 | 2023-11-29 | ClinicalTrials.gov |
| NCT05041257 | Mirvetuximab Soravtansine Monotherapy in Platinum-Sensitive Epithelial, Periton… | Phase2 | Ovarian Cancer | Completed | 2021-10-19 | 2024-12-12 | ClinicalTrials.gov |
| NCT05088980 | Study to Assess Effectiveness and Adverse Events of JUVEDERM VOLBELLA With Lido… | Phase3 | Infraorbital Hollowing | Completed | 2021-10-19 | 2023-11-29 | ClinicalTrials.gov |
| NCT05041257 | Mirvetuximab Soravtansine Monotherapy in Platinum-Sensitive Epithelial, Periton… | Phase2 | Ovarian Cancer | Completed | 2021-10-19 | 2024-12-12 | ClinicalTrials.gov |
| NCT05088980 | Study to Assess Effectiveness and Adverse Events of JUVEDERM VOLBELLA With Lido… | Phase3 | Infraorbital Hollowing | Completed | 2021-10-19 | 2023-11-29 | ClinicalTrials.gov |
| NCT05577000 | Anti-BCMA Chimeric Antigen Receptor T Cells for Relapsed or Refractory Multiple… | Phase1 | Refractory Multiple Myeloma | Active_Not_Recruiting | 2021-10-18 | 2038-08-31 | ClinicalTrials.gov |
| NCT05577000 | Anti-BCMA Chimeric Antigen Receptor T Cells for Relapsed or Refractory Multiple… | Phase1 | Refractory Multiple Myeloma | Active_Not_Recruiting | 2021-10-18 | 2038-08-31 | ClinicalTrials.gov |
| NCT05577000 | Anti-BCMA Chimeric Antigen Receptor T Cells for Relapsed or Refractory Multiple… | Phase1 | Refractory Multiple Myeloma | Active_Not_Recruiting | 2021-10-18 | 2038-08-31 | ClinicalTrials.gov |
| NCT05577000 | Anti-BCMA Chimeric Antigen Receptor T Cells for Relapsed or Refractory Multiple… | Phase1 | Refractory Multiple Myeloma | Active_Not_Recruiting | 2021-10-18 | 2038-08-31 | ClinicalTrials.gov |
| NCT05069597 | Study to Evaluate Symptoms of Exocrine Pancreatic Insufficiency in Adult Partic… | Phase4 | Cystic Fibrosis | Completed | 2021-10-14 | 2023-08-28 | ClinicalTrials.gov |
| NCT05069597 | Study to Evaluate Symptoms of Exocrine Pancreatic Insufficiency in Adult Partic… | Phase4 | Cystic Fibrosis | Completed | 2021-10-14 | 2023-08-28 | ClinicalTrials.gov |
| NCT05069597 | Study to Evaluate Symptoms of Exocrine Pancreatic Insufficiency in Adult Partic… | Phase4 | Cystic Fibrosis | Completed | 2021-10-14 | 2023-08-28 | ClinicalTrials.gov |
| NCT05069597 | Study to Evaluate Symptoms of Exocrine Pancreatic Insufficiency in Adult Partic… | Phase4 | Cystic Fibrosis | Completed | 2021-10-14 | 2023-08-28 | ClinicalTrials.gov |
| NCT05029882 | Study to Assess Adverse Events and Change in Disease Activity in Adult Particip… | Phase1 | Non-Small Cell Lung Cancer | Active_Not_Recruiting | 2021-10-13 | 2027-11-01 | ClinicalTrials.gov |
| NCT05119777 | HArmonyCa Injectable Gel for Mid Face Soft Tissue Augmentation | Phase4 | Soft Tissue Augmentation | Completed | 2021-10-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT05119777 | HArmonyCa Injectable Gel for Mid Face Soft Tissue Augmentation | Phase4 | Soft Tissue Augmentation | Completed | 2021-10-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT05119777 | HArmonyCa Injectable Gel for Mid Face Soft Tissue Augmentation | Phase4 | Soft Tissue Augmentation | Completed | 2021-10-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT05029882 | Study to Assess Adverse Events and Change in Disease Activity in Adult Particip… | Phase1 | Non-Small Cell Lung Cancer | Active_Not_Recruiting | 2021-10-13 | 2027-11-01 | ClinicalTrials.gov |
| NCT05119777 | HArmonyCa Injectable Gel for Mid Face Soft Tissue Augmentation | Phase4 | Soft Tissue Augmentation | Completed | 2021-10-13 | 2023-09-15 | ClinicalTrials.gov |
| NCT05029882 | Study to Assess Adverse Events and Change in Disease Activity in Adult Particip… | Phase1 | Non-Small Cell Lung Cancer | Active_Not_Recruiting | 2021-10-13 | 2027-11-01 | ClinicalTrials.gov |
| NCT05029882 | Study to Assess Adverse Events and Change in Disease Activity in Adult Particip… | Phase1 | Non-Small Cell Lung Cancer | Active_Not_Recruiting | 2021-10-13 | 2027-11-01 | ClinicalTrials.gov |
| NCT04976777 | A Study to Evaluate an Updated Dexamethasone Intravitreal (Into the Eye) Applic… | Phase3 | Macular Edema | Completed | 2021-10-12 | 2022-02-09 | ClinicalTrials.gov |
| NCT04976777 | A Study to Evaluate an Updated Dexamethasone Intravitreal (Into the Eye) Applic… | Phase3 | Macular Edema | Completed | 2021-10-12 | 2022-02-09 | ClinicalTrials.gov |
| NCT04976777 | A Study to Evaluate an Updated Dexamethasone Intravitreal (Into the Eye) Applic… | Phase3 | Macular Edema | Completed | 2021-10-12 | 2022-02-09 | ClinicalTrials.gov |
| NCT04976777 | A Study to Evaluate an Updated Dexamethasone Intravitreal (Into the Eye) Applic… | Phase3 | Macular Edema | Completed | 2021-10-12 | 2022-02-09 | ClinicalTrials.gov |
| NCT05100199 | A Study to the Assess the Change in Condition and Adverse Events of Onabotulinu… | Phase2 | Glabellar Lines | Completed | 2021-10-06 | 2022-12-02 | ClinicalTrials.gov |
| NCT05100199 | A Study to the Assess the Change in Condition and Adverse Events of Onabotulinu… | Phase2 | Glabellar Lines | Completed | 2021-10-06 | 2022-12-02 | ClinicalTrials.gov |
| NCT05100199 | A Study to the Assess the Change in Condition and Adverse Events of Onabotulinu… | Phase2 | Glabellar Lines | Completed | 2021-10-06 | 2022-12-02 | ClinicalTrials.gov |
| NCT05100199 | A Study to the Assess the Change in Condition and Adverse Events of Onabotulinu… | Phase2 | Glabellar Lines | Completed | 2021-10-06 | 2022-12-02 | ClinicalTrials.gov |
| NCT05026502 | A Study to Assess Patient-Reported Quality of Life and Effectiveness on Control… | — | Heavy Menstrual Bleeding | Terminated | 2021-10-05 | 2022-08-30 | ClinicalTrials.gov |
| NCT05026502 | A Study to Assess Patient-Reported Quality of Life and Effectiveness on Control… | — | Heavy Menstrual Bleeding | Terminated | 2021-10-05 | 2022-08-30 | ClinicalTrials.gov |
| NCT05026502 | A Study to Assess Patient-Reported Quality of Life and Effectiveness on Control… | — | Heavy Menstrual Bleeding | Terminated | 2021-10-05 | 2022-08-30 | ClinicalTrials.gov |
| NCT05026502 | A Study to Assess Patient-Reported Quality of Life and Effectiveness on Control… | — | Heavy Menstrual Bleeding | Terminated | 2021-10-05 | 2022-08-30 | ClinicalTrials.gov |
| NCT05029895 | A Study to Evaluate Adverse Events and Change in Disease State of Oral Upadacit… | — | Atopic Dermatitis | Completed | 2021-09-29 | 2025-09-17 | ClinicalTrials.gov |
| NCT05029895 | A Study to Evaluate Adverse Events and Change in Disease State of Oral Upadacit… | — | Atopic Dermatitis | Completed | 2021-09-29 | 2025-09-17 | ClinicalTrials.gov |
| NCT05029895 | A Study to Evaluate Adverse Events and Change in Disease State of Oral Upadacit… | — | Atopic Dermatitis | Completed | 2021-09-29 | 2025-09-17 | ClinicalTrials.gov |
| NCT05029895 | A Study to Evaluate Adverse Events and Change in Disease State of Oral Upadacit… | — | Atopic Dermatitis | Completed | 2021-09-29 | 2025-09-17 | ClinicalTrials.gov |
| NCT05016947 | Venetoclax Plus Inotuzumab for B-ALL | Phase1 | B-cell Acute Lymphoblastic Leukemia | Active_Not_Recruiting | 2021-09-24 | 2026-12-23 | ClinicalTrials.gov |
| NCT05016947 | Venetoclax Plus Inotuzumab for B-ALL | Phase1 | B-cell Acute Lymphoblastic Leukemia | Active_Not_Recruiting | 2021-09-24 | 2026-12-23 | ClinicalTrials.gov |
| NCT05016947 | Venetoclax Plus Inotuzumab for B-ALL | Phase1 | B-cell Acute Lymphoblastic Leukemia | Active_Not_Recruiting | 2021-09-24 | 2026-12-23 | ClinicalTrials.gov |
| NCT05016947 | Venetoclax Plus Inotuzumab for B-ALL | Phase1 | B-cell Acute Lymphoblastic Leukemia | Active_Not_Recruiting | 2021-09-24 | 2026-12-23 | ClinicalTrials.gov |
| NCT04948645 | A Phase 1 Study to Investigate the Safety and Pharmacokinetics of Fosigotifator… | Phase1 | ALS | Terminated | 2021-09-22 | 2025-07-15 | ClinicalTrials.gov |
| NCT04948645 | A Phase 1 Study to Investigate the Safety and Pharmacokinetics of Fosigotifator… | Phase1 | ALS | Terminated | 2021-09-22 | 2025-07-15 | ClinicalTrials.gov |
| NCT04948645 | A Phase 1 Study to Investigate the Safety and Pharmacokinetics of Fosigotifator… | Phase1 | ALS | Terminated | 2021-09-22 | 2025-07-15 | ClinicalTrials.gov |
| NCT04948645 | A Phase 1 Study to Investigate the Safety and Pharmacokinetics of Fosigotifator… | Phase1 | ALS | Terminated | 2021-09-22 | 2025-07-15 | ClinicalTrials.gov |
| NCT04853368 | Study to Evaluate Adverse Events and Change in Disease Activity With Oral Capsu… | Phase2 | Cystic Fibrosis (CF) | Terminated | 2021-09-20 | 2023-06-05 | ClinicalTrials.gov |
| NCT04853368 | Study to Evaluate Adverse Events and Change in Disease Activity With Oral Capsu… | Phase2 | Cystic Fibrosis (CF) | Terminated | 2021-09-20 | 2023-06-05 | ClinicalTrials.gov |
| NCT04853368 | Study to Evaluate Adverse Events and Change in Disease Activity With Oral Capsu… | Phase2 | Cystic Fibrosis (CF) | Terminated | 2021-09-20 | 2023-06-05 | ClinicalTrials.gov |
| NCT04853368 | Study to Evaluate Adverse Events and Change in Disease Activity With Oral Capsu… | Phase2 | Cystic Fibrosis (CF) | Terminated | 2021-09-20 | 2023-06-05 | ClinicalTrials.gov |
| NCT04949828 | Effect of CREON on Exocrine Pancreatic Insufficiency (EPI) Symptoms | — | Chronic Pancreatitis | Completed | 2021-09-16 | 2024-02-29 | ClinicalTrials.gov |
| NCT04949828 | Effect of CREON on Exocrine Pancreatic Insufficiency (EPI) Symptoms | — | Chronic Pancreatitis | Completed | 2021-09-16 | 2024-02-29 | ClinicalTrials.gov |
| NCT04949828 | Effect of CREON on Exocrine Pancreatic Insufficiency (EPI) Symptoms | — | Chronic Pancreatitis | Completed | 2021-09-16 | 2024-02-29 | ClinicalTrials.gov |
| NCT04949828 | Effect of CREON on Exocrine Pancreatic Insufficiency (EPI) Symptoms | — | Chronic Pancreatitis | Completed | 2021-09-16 | 2024-02-29 | ClinicalTrials.gov |
| NCT05077488 | VFORM: Prospective, Open Label, Study to Evaluate VOLIFT With Lidocaine Treatme… | Phase4 | Marionette Lines Forehead Contouring | Completed | 2021-09-15 | 2022-11-08 | ClinicalTrials.gov |
| NCT05077488 | VFORM: Prospective, Open Label, Study to Evaluate VOLIFT With Lidocaine Treatme… | Phase4 | Marionette Lines Forehead Contouring | Completed | 2021-09-15 | 2022-11-08 | ClinicalTrials.gov |
| NCT05077488 | VFORM: Prospective, Open Label, Study to Evaluate VOLIFT With Lidocaine Treatme… | Phase4 | Marionette Lines Forehead Contouring | Completed | 2021-09-15 | 2022-11-08 | ClinicalTrials.gov |
| NCT05077488 | VFORM: Prospective, Open Label, Study to Evaluate VOLIFT With Lidocaine Treatme… | Phase4 | Marionette Lines Forehead Contouring | Completed | 2021-09-15 | 2022-11-08 | ClinicalTrials.gov |
| NCT04972968 | A Study to Evaluate the Change in Disease State and Adverse Events in Adult Par… | Phase2 | Polymyalgia Rheumatica | Terminated | 2021-09-09 | 2023-07-24 | ClinicalTrials.gov |
| NCT04972968 | A Study to Evaluate the Change in Disease State and Adverse Events in Adult Par… | Phase2 | Polymyalgia Rheumatica | Terminated | 2021-09-09 | 2023-07-24 | ClinicalTrials.gov |
| NCT04972968 | A Study to Evaluate the Change in Disease State and Adverse Events in Adult Par… | Phase2 | Polymyalgia Rheumatica | Terminated | 2021-09-09 | 2023-07-24 | ClinicalTrials.gov |
| NCT04972968 | A Study to Evaluate the Change in Disease State and Adverse Events in Adult Par… | Phase2 | Polymyalgia Rheumatica | Terminated | 2021-09-09 | 2023-07-24 | ClinicalTrials.gov |
| NCT04572763 | Copanlisib Plus Venetoclax in R/R DLBCL | Phase1 | Diffuse Large B Cell Lymphoma | Active_Not_Recruiting | 2021-09-08 | 2026-07-29 | ClinicalTrials.gov |
| NCT04572763 | Copanlisib Plus Venetoclax in R/R DLBCL | Phase1 | Diffuse Large B Cell Lymphoma | Active_Not_Recruiting | 2021-09-08 | 2026-07-29 | ClinicalTrials.gov |
| NCT04572763 | Copanlisib Plus Venetoclax in R/R DLBCL | Phase1 | Diffuse Large B Cell Lymphoma | Active_Not_Recruiting | 2021-09-08 | 2026-07-29 | ClinicalTrials.gov |
| NCT04572763 | Copanlisib Plus Venetoclax in R/R DLBCL | Phase1 | Diffuse Large B Cell Lymphoma | Active_Not_Recruiting | 2021-09-08 | 2026-07-29 | ClinicalTrials.gov |
| NCT04983589 | A Study to Assess Safety and Efficacy in Participants Age 40 to 55 With Presbyo… | Phase3 | Presbyopia | Completed | 2021-09-02 | 2022-02-11 | ClinicalTrials.gov |
| NCT04983589 | A Study to Assess Safety and Efficacy in Participants Age 40 to 55 With Presbyo… | Phase3 | Presbyopia | Completed | 2021-09-02 | 2022-02-11 | ClinicalTrials.gov |
| NCT04983589 | A Study to Assess Safety and Efficacy in Participants Age 40 to 55 With Presbyo… | Phase3 | Presbyopia | Completed | 2021-09-02 | 2022-02-11 | ClinicalTrials.gov |
| NCT04983589 | A Study to Assess Safety and Efficacy in Participants Age 40 to 55 With Presbyo… | Phase3 | Presbyopia | Completed | 2021-09-02 | 2022-02-11 | ClinicalTrials.gov |
| NCT05013424 | A Study of OnabotulinumtoxinA X Injection in Adult Participants With Glabellar … | Phase2 | Glabellar Lines | Completed | 2021-09-01 | 2022-07-07 | ClinicalTrials.gov |
| NCT05013424 | A Study of OnabotulinumtoxinA X Injection in Adult Participants With Glabellar … | Phase2 | Glabellar Lines | Completed | 2021-09-01 | 2022-07-07 | ClinicalTrials.gov |
| NCT05013424 | A Study of OnabotulinumtoxinA X Injection in Adult Participants With Glabellar … | Phase2 | Glabellar Lines | Completed | 2021-09-01 | 2022-07-07 | ClinicalTrials.gov |
| NCT05013424 | A Study of OnabotulinumtoxinA X Injection in Adult Participants With Glabellar … | Phase2 | Glabellar Lines | Completed | 2021-09-01 | 2022-07-07 | ClinicalTrials.gov |
| NCT04903626 | Study to Evaluate Adverse Events and Change in Disease Activity in Adult and Ad… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2021-08-24 | 2024-09-17 | ClinicalTrials.gov |
| NCT04903626 | Study to Evaluate Adverse Events and Change in Disease Activity in Adult and Ad… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2021-08-24 | 2024-09-17 | ClinicalTrials.gov |
| NCT04903626 | Study to Evaluate Adverse Events and Change in Disease Activity in Adult and Ad… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2021-08-24 | 2024-09-17 | ClinicalTrials.gov |
| NCT04903626 | Study to Evaluate Adverse Events and Change in Disease Activity in Adult and Ad… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2021-08-24 | 2024-09-17 | ClinicalTrials.gov |
| NCT04965272 | A Study To Assess Adverse Events and Change in Disease Activity With Oral Carip… | Phase2 | Generalized Anxiety Disorder | Withdrawn | 2021-08-18 | 2021-08-24 | ClinicalTrials.gov |
| NCT04965272 | A Study To Assess Adverse Events and Change in Disease Activity With Oral Carip… | Phase2 | Generalized Anxiety Disorder | Withdrawn | 2021-08-18 | 2021-08-24 | ClinicalTrials.gov |
| NCT04965272 | A Study To Assess Adverse Events and Change in Disease Activity With Oral Carip… | Phase2 | Generalized Anxiety Disorder | Withdrawn | 2021-08-18 | 2021-08-24 | ClinicalTrials.gov |
| NCT04965272 | A Study To Assess Adverse Events and Change in Disease Activity With Oral Carip… | Phase2 | Generalized Anxiety Disorder | Withdrawn | 2021-08-18 | 2021-08-24 | ClinicalTrials.gov |
| NCT04880876 | A Study Evaluating Oral Eluxadoline Administered to Pediatric Participants With… | Phase3 | Irritable Bowel Syndrome | Enrolling_By_Invitation | 2021-08-13 | 2032-12-01 | ClinicalTrials.gov |
| NCT04880876 | A Study Evaluating Oral Eluxadoline Administered to Pediatric Participants With… | Phase3 | Irritable Bowel Syndrome | Enrolling_By_Invitation | 2021-08-13 | 2032-12-01 | ClinicalTrials.gov |
| NCT04880876 | A Study Evaluating Oral Eluxadoline Administered to Pediatric Participants With… | Phase3 | Irritable Bowel Syndrome | Enrolling_By_Invitation | 2021-08-13 | 2032-12-01 | ClinicalTrials.gov |
| NCT04880876 | A Study Evaluating Oral Eluxadoline Administered to Pediatric Participants With… | Phase3 | Irritable Bowel Syndrome | Enrolling_By_Invitation | 2021-08-13 | 2032-12-01 | ClinicalTrials.gov |
| NCT04994535 | A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramus… | Phase3 | Platysma Prominence | Completed | 2021-08-10 | 2023-06-14 | ClinicalTrials.gov |
| NCT04994535 | A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramus… | Phase3 | Platysma Prominence | Completed | 2021-08-10 | 2023-06-14 | ClinicalTrials.gov |
| NCT04994535 | A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramus… | Phase3 | Platysma Prominence | Completed | 2021-08-10 | 2023-06-14 | ClinicalTrials.gov |
| NCT04994535 | A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramus… | Phase3 | Platysma Prominence | Completed | 2021-08-10 | 2023-06-14 | ClinicalTrials.gov |
| NCT04677153 | Rapid HCV Treatment Access for Persons Who Use Drugs | Na | Hepatitis C Virus Infection, Response to Therapy of | Completed | 2021-08-06 | 2024-09-23 | ClinicalTrials.gov |
| NCT04677153 | Rapid HCV Treatment Access for Persons Who Use Drugs | Na | Hepatitis C Virus Infection, Response to Therapy of | Completed | 2021-08-06 | 2024-09-23 | ClinicalTrials.gov |
| NCT04677153 | Rapid HCV Treatment Access for Persons Who Use Drugs | Na | Hepatitis C Virus Infection, Response to Therapy of | Completed | 2021-08-06 | 2024-09-23 | ClinicalTrials.gov |
| NCT04677153 | Rapid HCV Treatment Access for Persons Who Use Drugs | Na | Hepatitis C Virus Infection, Response to Therapy of | Completed | 2021-08-06 | 2024-09-23 | ClinicalTrials.gov |
| NCT04829747 | Study to Assess Adverse Events (AEs) When Oral Atogepant Tablet is Given to Adu… | Phase3 | Chronic Migraine | Completed | 2021-08-02 | 2022-01-20 | ClinicalTrials.gov |
| NCT04829747 | Study to Assess Adverse Events (AEs) When Oral Atogepant Tablet is Given to Adu… | Phase3 | Chronic Migraine | Completed | 2021-08-02 | 2022-01-20 | ClinicalTrials.gov |
| NCT04829747 | Study to Assess Adverse Events (AEs) When Oral Atogepant Tablet is Given to Adu… | Phase3 | Chronic Migraine | Completed | 2021-08-02 | 2022-01-20 | ClinicalTrials.gov |
| NCT04829747 | Study to Assess Adverse Events (AEs) When Oral Atogepant Tablet is Given to Adu… | Phase3 | Chronic Migraine | Completed | 2021-08-02 | 2022-01-20 | ClinicalTrials.gov |
| NCT05420233 | The CROCO Study: CROhn's Disease COhort Study | Na | Crohn Disease | Recruiting | 2021-08-01 | 2030-07-01 | ClinicalTrials.gov |
| NCT05420233 | The CROCO Study: CROhn's Disease COhort Study | Na | Crohn Disease | Recruiting | 2021-08-01 | 2030-07-01 | ClinicalTrials.gov |
| NCT05420233 | The CROCO Study: CROhn's Disease COhort Study | Na | Crohn Disease | Recruiting | 2021-08-01 | 2030-07-01 | ClinicalTrials.gov |
| NCT05420233 | The CROCO Study: CROhn's Disease COhort Study | Na | Crohn Disease | Recruiting | 2021-08-01 | 2030-07-01 | ClinicalTrials.gov |
| NCT04846959 | Study to Evaluate Pregnancy Outcomes in Risankizumab Exposed Pregnancies Relati… | — | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | Recruiting | 2021-07-30 | 2032-06-01 | ClinicalTrials.gov |
| NCT04846959 | Study to Evaluate Pregnancy Outcomes in Risankizumab Exposed Pregnancies Relati… | — | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | Recruiting | 2021-07-30 | 2032-06-01 | ClinicalTrials.gov |
| NCT04846959 | Study to Evaluate Pregnancy Outcomes in Risankizumab Exposed Pregnancies Relati… | — | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | Recruiting | 2021-07-30 | 2032-06-01 | ClinicalTrials.gov |
| NCT04846959 | Study to Evaluate Pregnancy Outcomes in Risankizumab Exposed Pregnancies Relati… | — | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | Recruiting | 2021-07-30 | 2032-06-01 | ClinicalTrials.gov |
| NCT04862286 | Study to Evaluate Adverse Events and Change in Disease Activity in Participants… | Phase3 | Psoriasis | Active_Not_Recruiting | 2021-07-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT04862286 | Study to Evaluate Adverse Events and Change in Disease Activity in Participants… | Phase3 | Psoriasis | Active_Not_Recruiting | 2021-07-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT04862286 | Study to Evaluate Adverse Events and Change in Disease Activity in Participants… | Phase3 | Psoriasis | Active_Not_Recruiting | 2021-07-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT04862286 | Study to Evaluate Adverse Events and Change in Disease Activity in Participants… | Phase3 | Psoriasis | Active_Not_Recruiting | 2021-07-24 | 2028-04-01 | ClinicalTrials.gov |
| NCT04891419 | JUVÉDERM® VOLUMA® With Lidocaine for Correction of Temple Hollowing in Chinese … | Phase3 | Temple Hollowing | Completed | 2021-07-20 | 2023-11-22 | ClinicalTrials.gov |
| NCT04891419 | JUVÉDERM® VOLUMA® With Lidocaine for Correction of Temple Hollowing in Chinese … | Phase3 | Temple Hollowing | Completed | 2021-07-20 | 2023-11-22 | ClinicalTrials.gov |
| NCT04891419 | JUVÉDERM® VOLUMA® With Lidocaine for Correction of Temple Hollowing in Chinese … | Phase3 | Temple Hollowing | Completed | 2021-07-20 | 2023-11-22 | ClinicalTrials.gov |
| NCT04891419 | JUVÉDERM® VOLUMA® With Lidocaine for Correction of Temple Hollowing in Chinese … | Phase3 | Temple Hollowing | Completed | 2021-07-20 | 2023-11-22 | ClinicalTrials.gov |
| NCT04918823 | Novel Use of Cyclosporine Ophthalmic Emulsion 0.05% in a PROSE Device | Phase1 | Ocular Surface Disease | Completed | 2021-07-15 | 2023-04-14 | ClinicalTrials.gov |
| NCT04918823 | Novel Use of Cyclosporine Ophthalmic Emulsion 0.05% in a PROSE Device | Phase1 | Ocular Surface Disease | Completed | 2021-07-15 | 2023-04-14 | ClinicalTrials.gov |
| NCT04918823 | Novel Use of Cyclosporine Ophthalmic Emulsion 0.05% in a PROSE Device | Phase1 | Ocular Surface Disease | Completed | 2021-07-15 | 2023-04-14 | ClinicalTrials.gov |
| NCT04918823 | Novel Use of Cyclosporine Ophthalmic Emulsion 0.05% in a PROSE Device | Phase1 | Ocular Surface Disease | Completed | 2021-07-15 | 2023-04-14 | ClinicalTrials.gov |
| NCT04810598 | Study to Assess Adverse Events and the Movement of Oral Venetoclax Tablet Throu… | Phase1 | Renal Impairment | Completed | 2021-07-08 | 2022-08-16 | ClinicalTrials.gov |
| NCT04949399 | A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramus… | Phase3 | Platysma Prominence | Completed | 2021-07-08 | 2022-12-20 | ClinicalTrials.gov |
| NCT04810598 | Study to Assess Adverse Events and the Movement of Oral Venetoclax Tablet Throu… | Phase1 | Renal Impairment | Completed | 2021-07-08 | 2022-08-16 | ClinicalTrials.gov |
| NCT04810598 | Study to Assess Adverse Events and the Movement of Oral Venetoclax Tablet Throu… | Phase1 | Renal Impairment | Completed | 2021-07-08 | 2022-08-16 | ClinicalTrials.gov |
| NCT04810598 | Study to Assess Adverse Events and the Movement of Oral Venetoclax Tablet Throu… | Phase1 | Renal Impairment | Completed | 2021-07-08 | 2022-08-16 | ClinicalTrials.gov |
| NCT04949399 | A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramus… | Phase3 | Platysma Prominence | Completed | 2021-07-08 | 2022-12-20 | ClinicalTrials.gov |
| NCT04949399 | A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramus… | Phase3 | Platysma Prominence | Completed | 2021-07-08 | 2022-12-20 | ClinicalTrials.gov |
| NCT04949399 | A Study To Assess the Safety and Effects of OnabotulinumtoxinA (BOTOX) Intramus… | Phase3 | Platysma Prominence | Completed | 2021-07-08 | 2022-12-20 | ClinicalTrials.gov |
| NCT04721002 | Study to Evaluate t(11;14) Status and BCL2 Expression in Adult Participants Wit… | — | Multiple Myeloma (MM) | Completed | 2021-07-07 | 2023-09-30 | ClinicalTrials.gov |
| NCT04721002 | Study to Evaluate t(11;14) Status and BCL2 Expression in Adult Participants Wit… | — | Multiple Myeloma (MM) | Completed | 2021-07-07 | 2023-09-30 | ClinicalTrials.gov |
| NCT04721002 | Study to Evaluate t(11;14) Status and BCL2 Expression in Adult Participants Wit… | — | Multiple Myeloma (MM) | Completed | 2021-07-07 | 2023-09-30 | ClinicalTrials.gov |
| NCT04721002 | Study to Evaluate t(11;14) Status and BCL2 Expression in Adult Participants Wit… | — | Multiple Myeloma (MM) | Completed | 2021-07-07 | 2023-09-30 | ClinicalTrials.gov |
| NCT05038878 | An Oral GnRH Antagonist to Treat Mild Autonomous Cortisol Excess (MACE) Due to … | Phase4 | Mild Autonomous Cortisol Excess | Terminated | 2021-07-06 | 2022-06-24 | ClinicalTrials.gov |
| NCT05038878 | An Oral GnRH Antagonist to Treat Mild Autonomous Cortisol Excess (MACE) Due to … | Phase4 | Mild Autonomous Cortisol Excess | Terminated | 2021-07-06 | 2022-06-24 | ClinicalTrials.gov |
| NCT05038878 | An Oral GnRH Antagonist to Treat Mild Autonomous Cortisol Excess (MACE) Due to … | Phase4 | Mild Autonomous Cortisol Excess | Terminated | 2021-07-06 | 2022-06-24 | ClinicalTrials.gov |
| NCT05038878 | An Oral GnRH Antagonist to Treat Mild Autonomous Cortisol Excess (MACE) Due to … | Phase4 | Mild Autonomous Cortisol Excess | Terminated | 2021-07-06 | 2022-06-24 | ClinicalTrials.gov |
| NCT04543916 | Venetoclax and Irinotecan in Relapsed/Refractory SCLC | Phase1 | Relapsed Small Cell Lung Cancer | Withdrawn | 2021-06-30 | 2028-06-30 | ClinicalTrials.gov |
| NCT04543916 | Venetoclax and Irinotecan in Relapsed/Refractory SCLC | Phase1 | Relapsed Small Cell Lung Cancer | Withdrawn | 2021-06-30 | 2028-06-30 | ClinicalTrials.gov |
| NCT04543916 | Venetoclax and Irinotecan in Relapsed/Refractory SCLC | Phase1 | Relapsed Small Cell Lung Cancer | Withdrawn | 2021-06-30 | 2028-06-30 | ClinicalTrials.gov |
| NCT04927975 | Study to Evaluate Adverse Events and Change in Disease Activity With Oral Table… | Phase2 | Non-Segmental Vitiligo | Completed | 2021-06-30 | 2023-08-29 | ClinicalTrials.gov |
| NCT04927975 | Study to Evaluate Adverse Events and Change in Disease Activity With Oral Table… | Phase2 | Non-Segmental Vitiligo | Completed | 2021-06-30 | 2023-08-29 | ClinicalTrials.gov |
| NCT04927975 | Study to Evaluate Adverse Events and Change in Disease Activity With Oral Table… | Phase2 | Non-Segmental Vitiligo | Completed | 2021-06-30 | 2023-08-29 | ClinicalTrials.gov |
| NCT04927975 | Study to Evaluate Adverse Events and Change in Disease Activity With Oral Table… | Phase2 | Non-Segmental Vitiligo | Completed | 2021-06-30 | 2023-08-29 | ClinicalTrials.gov |
| NCT04543916 | Venetoclax and Irinotecan in Relapsed/Refractory SCLC | Phase1 | Relapsed Small Cell Lung Cancer | Withdrawn | 2021-06-30 | 2028-06-30 | ClinicalTrials.gov |
| NCT04912063 | Study to Evaluate Adverse Events and Movement of Lemzoparlimab in Body When Use… | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2021-06-25 | 2023-05-09 | ClinicalTrials.gov |
| NCT04912063 | Study to Evaluate Adverse Events and Movement of Lemzoparlimab in Body When Use… | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2021-06-25 | 2023-05-09 | ClinicalTrials.gov |
| NCT04912063 | Study to Evaluate Adverse Events and Movement of Lemzoparlimab in Body When Use… | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2021-06-25 | 2023-05-09 | ClinicalTrials.gov |
| NCT04912063 | Study to Evaluate Adverse Events and Movement of Lemzoparlimab in Body When Use… | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2021-06-25 | 2023-05-09 | ClinicalTrials.gov |
| NCT04888585 | Study to Evaluate Adverse Events and Change in Disease Activity in Participants… | Phase2 | Rheumatoid Arthritis (RA) | Terminated | 2021-06-23 | 2023-08-04 | ClinicalTrials.gov |
| NCT04799990 | Study to Assess Adverse Events When Subcutaneous Risankizumab Injection is Give… | — | Psoriasis | Withdrawn | 2021-06-23 | 2022-03-10 | ClinicalTrials.gov |
| NCT04888585 | Study to Evaluate Adverse Events and Change in Disease Activity in Participants… | Phase2 | Rheumatoid Arthritis (RA) | Terminated | 2021-06-23 | 2023-08-04 | ClinicalTrials.gov |
| NCT04799990 | Study to Assess Adverse Events When Subcutaneous Risankizumab Injection is Give… | — | Psoriasis | Withdrawn | 2021-06-23 | 2022-03-10 | ClinicalTrials.gov |
| NCT04888585 | Study to Evaluate Adverse Events and Change in Disease Activity in Participants… | Phase2 | Rheumatoid Arthritis (RA) | Terminated | 2021-06-23 | 2023-08-04 | ClinicalTrials.gov |
| NCT04799990 | Study to Assess Adverse Events When Subcutaneous Risankizumab Injection is Give… | — | Psoriasis | Withdrawn | 2021-06-23 | 2022-03-10 | ClinicalTrials.gov |
| NCT04888585 | Study to Evaluate Adverse Events and Change in Disease Activity in Participants… | Phase2 | Rheumatoid Arthritis (RA) | Terminated | 2021-06-23 | 2023-08-04 | ClinicalTrials.gov |
| NCT04799990 | Study to Assess Adverse Events When Subcutaneous Risankizumab Injection is Give… | — | Psoriasis | Withdrawn | 2021-06-23 | 2022-03-10 | ClinicalTrials.gov |
| NCT04958031 | A Trial of the Safety, Tolerability, and Pharmacodynamics of CVL-871 in Subject… | Phase2 | Apathy in Dementia | Terminated | 2021-06-22 | 2025-02-12 | ClinicalTrials.gov |
| NCT04958031 | A Trial of the Safety, Tolerability, and Pharmacodynamics of CVL-871 in Subject… | Phase2 | Apathy in Dementia | Terminated | 2021-06-22 | 2025-02-12 | ClinicalTrials.gov |
| NCT04958031 | A Trial of the Safety, Tolerability, and Pharmacodynamics of CVL-871 in Subject… | Phase2 | Apathy in Dementia | Terminated | 2021-06-22 | 2025-02-12 | ClinicalTrials.gov |
| NCT04958031 | A Trial of the Safety, Tolerability, and Pharmacodynamics of CVL-871 in Subject… | Phase2 | Apathy in Dementia | Terminated | 2021-06-22 | 2025-02-12 | ClinicalTrials.gov |
| NCT04908475 | Study of Subcutaneous Risankizumab Injection Compared to Oral Apremilast Tablet… | Phase4 | Psoriasis | Completed | 2021-06-09 | 2023-04-20 | ClinicalTrials.gov |
| NCT04908475 | Study of Subcutaneous Risankizumab Injection Compared to Oral Apremilast Tablet… | Phase4 | Psoriasis | Completed | 2021-06-09 | 2023-04-20 | ClinicalTrials.gov |
| NCT04908475 | Study of Subcutaneous Risankizumab Injection Compared to Oral Apremilast Tablet… | Phase4 | Psoriasis | Completed | 2021-06-09 | 2023-04-20 | ClinicalTrials.gov |
| NCT04908475 | Study of Subcutaneous Risankizumab Injection Compared to Oral Apremilast Tablet… | Phase4 | Psoriasis | Completed | 2021-06-09 | 2023-04-20 | ClinicalTrials.gov |
| NCT04818385 | Study to Assess the Change in Disease State When Subcutaneous Risankizumab Inje… | — | Psoriasis | Completed | 2021-05-31 | 2025-08-01 | ClinicalTrials.gov |
| NCT04818385 | Study to Assess the Change in Disease State When Subcutaneous Risankizumab Inje… | — | Psoriasis | Completed | 2021-05-31 | 2025-08-01 | ClinicalTrials.gov |
| NCT04818385 | Study to Assess the Change in Disease State When Subcutaneous Risankizumab Inje… | — | Psoriasis | Completed | 2021-05-31 | 2025-08-01 | ClinicalTrials.gov |
| NCT04818385 | Study to Assess the Change in Disease State When Subcutaneous Risankizumab Inje… | — | Psoriasis | Completed | 2021-05-31 | 2025-08-01 | ClinicalTrials.gov |
| NCT04813263 | Study of Oral Venetoclax Tablets to Evaluate Adverse Events and Change in Disea… | — | Acute Myeloid Leukemia (AML) | Completed | 2021-05-28 | 2024-04-30 | ClinicalTrials.gov |
| NCT04807972 | Study to Evaluate Adverse Events and Change in Disease Activity When Intravenou… | Phase1 | Pancreatic Cancer | Terminated | 2021-05-28 | 2024-03-25 | ClinicalTrials.gov |
| NCT04807972 | Study to Evaluate Adverse Events and Change in Disease Activity When Intravenou… | Phase1 | Pancreatic Cancer | Terminated | 2021-05-28 | 2024-03-25 | ClinicalTrials.gov |
| NCT04813263 | Study of Oral Venetoclax Tablets to Evaluate Adverse Events and Change in Disea… | — | Acute Myeloid Leukemia (AML) | Completed | 2021-05-28 | 2024-04-30 | ClinicalTrials.gov |
| NCT04807972 | Study to Evaluate Adverse Events and Change in Disease Activity When Intravenou… | Phase1 | Pancreatic Cancer | Terminated | 2021-05-28 | 2024-03-25 | ClinicalTrials.gov |
| NCT04807972 | Study to Evaluate Adverse Events and Change in Disease Activity When Intravenou… | Phase1 | Pancreatic Cancer | Terminated | 2021-05-28 | 2024-03-25 | ClinicalTrials.gov |
| NCT04813263 | Study of Oral Venetoclax Tablets to Evaluate Adverse Events and Change in Disea… | — | Acute Myeloid Leukemia (AML) | Completed | 2021-05-28 | 2024-04-30 | ClinicalTrials.gov |
| NCT04813263 | Study of Oral Venetoclax Tablets to Evaluate Adverse Events and Change in Disea… | — | Acute Myeloid Leukemia (AML) | Completed | 2021-05-28 | 2024-04-30 | ClinicalTrials.gov |
| NCT04913610 | Study to Assess Adverse Events, Change in Disease Activity and How Oral ABBV-40… | Phase2 | Onchocerciasis | Terminated | 2021-05-22 | 2023-08-29 | ClinicalTrials.gov |
| NCT04913610 | Study to Assess Adverse Events, Change in Disease Activity and How Oral ABBV-40… | Phase2 | Onchocerciasis | Terminated | 2021-05-22 | 2023-08-29 | ClinicalTrials.gov |
| NCT04913610 | Study to Assess Adverse Events, Change in Disease Activity and How Oral ABBV-40… | Phase2 | Onchocerciasis | Terminated | 2021-05-22 | 2023-08-29 | ClinicalTrials.gov |
| NCT04913610 | Study to Assess Adverse Events, Change in Disease Activity and How Oral ABBV-40… | Phase2 | Onchocerciasis | Terminated | 2021-05-22 | 2023-08-29 | ClinicalTrials.gov |
| NCT04801797 | Venetoclax + Azacitidine vs. Induction Chemotherapy in AML | Phase2 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2021-05-20 | 2028-01-01 | ClinicalTrials.gov |
| NCT04801797 | Venetoclax + Azacitidine vs. Induction Chemotherapy in AML | Phase2 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2021-05-20 | 2028-01-01 | ClinicalTrials.gov |
| NCT04801797 | Venetoclax + Azacitidine vs. Induction Chemotherapy in AML | Phase2 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2021-05-20 | 2028-01-01 | ClinicalTrials.gov |
| NCT04801797 | Venetoclax + Azacitidine vs. Induction Chemotherapy in AML | Phase2 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2021-05-20 | 2028-01-01 | ClinicalTrials.gov |
| NCT04837482 | A Study to Assess the Impact and Adverse Events of Topical Eyedrops of AGN-1905… | Phase3 | Presbyopia | Completed | 2021-05-14 | 2021-12-07 | ClinicalTrials.gov |
| NCT04837482 | A Study to Assess the Impact and Adverse Events of Topical Eyedrops of AGN-1905… | Phase3 | Presbyopia | Completed | 2021-05-14 | 2021-12-07 | ClinicalTrials.gov |
| NCT04837482 | A Study to Assess the Impact and Adverse Events of Topical Eyedrops of AGN-1905… | Phase3 | Presbyopia | Completed | 2021-05-14 | 2021-12-07 | ClinicalTrials.gov |
| NCT04837482 | A Study to Assess the Impact and Adverse Events of Topical Eyedrops of AGN-1905… | Phase3 | Presbyopia | Completed | 2021-05-14 | 2021-12-07 | ClinicalTrials.gov |
| NCT04416451 | A Phase II Study Using Rituximab Plus Venetoclax in the Front Line Treatment of… | Phase2 | Marginal Zone Lymphoma | Active_Not_Recruiting | 2021-05-04 | 2027-06-01 | ClinicalTrials.gov |
| NCT04416451 | A Phase II Study Using Rituximab Plus Venetoclax in the Front Line Treatment of… | Phase2 | Marginal Zone Lymphoma | Active_Not_Recruiting | 2021-05-04 | 2027-06-01 | ClinicalTrials.gov |
| NCT04416451 | A Phase II Study Using Rituximab Plus Venetoclax in the Front Line Treatment of… | Phase2 | Marginal Zone Lymphoma | Active_Not_Recruiting | 2021-05-04 | 2027-06-01 | ClinicalTrials.gov |
| NCT04416451 | A Phase II Study Using Rituximab Plus Venetoclax in the Front Line Treatment of… | Phase2 | Marginal Zone Lymphoma | Active_Not_Recruiting | 2021-05-04 | 2027-06-01 | ClinicalTrials.gov |
| NCT04846244 | A Study of the Change in Early and Sustained Pain Control in Axial Spondylarthr… | — | Axial Spondylarthritis (axSpA) | Completed | 2021-04-30 | 2025-03-24 | ClinicalTrials.gov |
| NCT04846244 | A Study of the Change in Early and Sustained Pain Control in Axial Spondylarthr… | — | Axial Spondylarthritis (axSpA) | Completed | 2021-04-30 | 2025-03-24 | ClinicalTrials.gov |
| NCT04846244 | A Study of the Change in Early and Sustained Pain Control in Axial Spondylarthr… | — | Axial Spondylarthritis (axSpA) | Completed | 2021-04-30 | 2025-03-24 | ClinicalTrials.gov |
| NCT04846244 | A Study of the Change in Early and Sustained Pain Control in Axial Spondylarthr… | — | Axial Spondylarthritis (axSpA) | Completed | 2021-04-30 | 2025-03-24 | ClinicalTrials.gov |
| NCT04777357 | A Study to Assess Change in Disease Activity and Adverse Events (AEs) With Cari… | Phase3 | Depression | Recruiting | 2021-04-28 | 2027-03-01 | ClinicalTrials.gov |
| NCT04777357 | A Study to Assess Change in Disease Activity and Adverse Events (AEs) With Cari… | Phase3 | Depression | Recruiting | 2021-04-28 | 2027-03-01 | ClinicalTrials.gov |
| NCT04777357 | A Study to Assess Change in Disease Activity and Adverse Events (AEs) With Cari… | Phase3 | Depression | Recruiting | 2021-04-28 | 2027-03-01 | ClinicalTrials.gov |
| NCT04777357 | A Study to Assess Change in Disease Activity and Adverse Events (AEs) With Cari… | Phase3 | Depression | Recruiting | 2021-04-28 | 2027-03-01 | ClinicalTrials.gov |
| NCT04804254 | Study to Evaluate Adverse Events, Change in Disease Activity, Movement of Oral … | Phase1 | B-cell Lymphoma | Terminated | 2021-04-27 | 2023-01-11 | ClinicalTrials.gov |
| NCT04804254 | Study to Evaluate Adverse Events, Change in Disease Activity, Movement of Oral … | Phase1 | B-cell Lymphoma | Terminated | 2021-04-27 | 2023-01-11 | ClinicalTrials.gov |
| NCT04804254 | Study to Evaluate Adverse Events, Change in Disease Activity, Movement of Oral … | Phase1 | B-cell Lymphoma | Terminated | 2021-04-27 | 2023-01-11 | ClinicalTrials.gov |
| NCT04804254 | Study to Evaluate Adverse Events, Change in Disease Activity, Movement of Oral … | Phase1 | B-cell Lymphoma | Terminated | 2021-04-27 | 2023-01-11 | ClinicalTrials.gov |
| NCT04780516 | Study to Assess Change in Disease Symptoms in Adult Participants With Moderate … | — | Psoriasis | Active_Not_Recruiting | 2021-04-26 | 2026-12-01 | ClinicalTrials.gov |
| NCT04780516 | Study to Assess Change in Disease Symptoms in Adult Participants With Moderate … | — | Psoriasis | Active_Not_Recruiting | 2021-04-26 | 2026-12-01 | ClinicalTrials.gov |
| NCT04780516 | Study to Assess Change in Disease Symptoms in Adult Participants With Moderate … | — | Psoriasis | Active_Not_Recruiting | 2021-04-26 | 2026-12-01 | ClinicalTrials.gov |
| NCT04780516 | Study to Assess Change in Disease Symptoms in Adult Participants With Moderate … | — | Psoriasis | Active_Not_Recruiting | 2021-04-26 | 2026-12-01 | ClinicalTrials.gov |
| NCT04721223 | JAB-3068 Activity in Adult Patients With Advanced Solid Tumors | Phase1 | Advanced Solid Tumor | Completed | 2021-04-26 | 2023-12-29 | ClinicalTrials.gov |
| NCT04721223 | JAB-3068 Activity in Adult Patients With Advanced Solid Tumors | Phase1 | Advanced Solid Tumor | Completed | 2021-04-26 | 2023-12-29 | ClinicalTrials.gov |
| NCT04721223 | JAB-3068 Activity in Adult Patients With Advanced Solid Tumors | Phase1 | Advanced Solid Tumor | Completed | 2021-04-26 | 2023-12-29 | ClinicalTrials.gov |
| NCT04721223 | JAB-3068 Activity in Adult Patients With Advanced Solid Tumors | Phase1 | Advanced Solid Tumor | Completed | 2021-04-26 | 2023-12-29 | ClinicalTrials.gov |
| NCT04500106 | Study to Assess Participant/Caregiver/Investigator Satisfaction of Video-Assist… | — | Parkinson's Disease | Completed | 2021-04-22 | 2021-10-14 | ClinicalTrials.gov |
| NCT04500106 | Study to Assess Participant/Caregiver/Investigator Satisfaction of Video-Assist… | — | Parkinson's Disease | Completed | 2021-04-22 | 2021-10-14 | ClinicalTrials.gov |
| NCT04500106 | Study to Assess Participant/Caregiver/Investigator Satisfaction of Video-Assist… | — | Parkinson's Disease | Completed | 2021-04-22 | 2021-10-14 | ClinicalTrials.gov |
| NCT04500106 | Study to Assess Participant/Caregiver/Investigator Satisfaction of Video-Assist… | — | Parkinson's Disease | Completed | 2021-04-22 | 2021-10-14 | ClinicalTrials.gov |
| NCT04554966 | Study to Assess Adverse Events and How Intravenous (IV) or Subcutaneous (SC) AB… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2021-04-16 | 2023-08-14 | ClinicalTrials.gov |
| NCT04554966 | Study to Assess Adverse Events and How Intravenous (IV) or Subcutaneous (SC) AB… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2021-04-16 | 2023-08-14 | ClinicalTrials.gov |
| NCT04554966 | Study to Assess Adverse Events and How Intravenous (IV) or Subcutaneous (SC) AB… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2021-04-16 | 2023-08-14 | ClinicalTrials.gov |
| NCT04554966 | Study to Assess Adverse Events and How Intravenous (IV) or Subcutaneous (SC) AB… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2021-04-16 | 2023-08-14 | ClinicalTrials.gov |
| NCT04630652 | Risankizumab Long-term Remission Study | Phase4 | Psoriasis | Completed | 2021-04-07 | 2025-05-13 | ClinicalTrials.gov |
| NCT04630652 | Risankizumab Long-term Remission Study | Phase4 | Psoriasis | Completed | 2021-04-07 | 2025-05-13 | ClinicalTrials.gov |
| NCT04630652 | Risankizumab Long-term Remission Study | Phase4 | Psoriasis | Completed | 2021-04-07 | 2025-05-13 | ClinicalTrials.gov |
| NCT04630652 | Risankizumab Long-term Remission Study | Phase4 | Psoriasis | Completed | 2021-04-07 | 2025-05-13 | ClinicalTrials.gov |
| NCT04826523 | Study of Oral Venetoclax Tablets to Evaluate Adverse Events and Change in Disea… | — | Acute Myeloid Leukemia (AML) | Completed | 2021-04-05 | 2025-10-20 | ClinicalTrials.gov |
| NCT04826523 | Study of Oral Venetoclax Tablets to Evaluate Adverse Events and Change in Disea… | — | Acute Myeloid Leukemia (AML) | Completed | 2021-04-05 | 2025-10-20 | ClinicalTrials.gov |
| NCT04826523 | Study of Oral Venetoclax Tablets to Evaluate Adverse Events and Change in Disea… | — | Acute Myeloid Leukemia (AML) | Completed | 2021-04-05 | 2025-10-20 | ClinicalTrials.gov |
| NCT04826523 | Study of Oral Venetoclax Tablets to Evaluate Adverse Events and Change in Disea… | — | Acute Myeloid Leukemia (AML) | Completed | 2021-04-05 | 2025-10-20 | ClinicalTrials.gov |
| NCT04720976 | JAB-3312 Based Combination Therapy in Adult Patients With Advanced Solid Tumors | Phase1 | Solid Tumor | Completed | 2021-03-23 | 2023-12-19 | ClinicalTrials.gov |
| NCT04720976 | JAB-3312 Based Combination Therapy in Adult Patients With Advanced Solid Tumors | Phase1 | Solid Tumor | Completed | 2021-03-23 | 2023-12-19 | ClinicalTrials.gov |
| NCT04720976 | JAB-3312 Based Combination Therapy in Adult Patients With Advanced Solid Tumors | Phase1 | Solid Tumor | Completed | 2021-03-23 | 2023-12-19 | ClinicalTrials.gov |
| NCT04720976 | JAB-3312 Based Combination Therapy in Adult Patients With Advanced Solid Tumors | Phase1 | Solid Tumor | Completed | 2021-03-23 | 2023-12-19 | ClinicalTrials.gov |
| NCT04827368 | Volatile Organic Compounds (VOCs) in Active Inflammatory Bowel Disease | — | IBD | Active_Not_Recruiting | 2021-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT04827368 | Volatile Organic Compounds (VOCs) in Active Inflammatory Bowel Disease | — | IBD | Active_Not_Recruiting | 2021-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT04827368 | Volatile Organic Compounds (VOCs) in Active Inflammatory Bowel Disease | — | IBD | Active_Not_Recruiting | 2021-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT04827368 | Volatile Organic Compounds (VOCs) in Active Inflammatory Bowel Disease | — | IBD | Active_Not_Recruiting | 2021-03-22 | 2026-06-30 | ClinicalTrials.gov |
| NCT04480086 | Safety and Tolerability Study of Mivebresib Tablet Alone or in Combination With… | Phase1 | Myelofibrosis (MF) | Terminated | 2021-03-17 | 2023-07-28 | ClinicalTrials.gov |
| NCT04480086 | Safety and Tolerability Study of Mivebresib Tablet Alone or in Combination With… | Phase1 | Myelofibrosis (MF) | Terminated | 2021-03-17 | 2023-07-28 | ClinicalTrials.gov |
| NCT04818515 | Study To Assess Adverse Events and Drug to Drug Interaction of Oral Tablet Atog… | Phase1 | Migraine | Completed | 2021-03-17 | 2021-06-18 | ClinicalTrials.gov |
| NCT04818515 | Study To Assess Adverse Events and Drug to Drug Interaction of Oral Tablet Atog… | Phase1 | Migraine | Completed | 2021-03-17 | 2021-06-18 | ClinicalTrials.gov |
| NCT04480086 | Safety and Tolerability Study of Mivebresib Tablet Alone or in Combination With… | Phase1 | Myelofibrosis (MF) | Terminated | 2021-03-17 | 2023-07-28 | ClinicalTrials.gov |
| NCT04818515 | Study To Assess Adverse Events and Drug to Drug Interaction of Oral Tablet Atog… | Phase1 | Migraine | Completed | 2021-03-17 | 2021-06-18 | ClinicalTrials.gov |
| NCT04480086 | Safety and Tolerability Study of Mivebresib Tablet Alone or in Combination With… | Phase1 | Myelofibrosis (MF) | Terminated | 2021-03-17 | 2023-07-28 | ClinicalTrials.gov |
| NCT04818515 | Study To Assess Adverse Events and Drug to Drug Interaction of Oral Tablet Atog… | Phase1 | Migraine | Completed | 2021-03-17 | 2021-06-18 | ClinicalTrials.gov |
| NCT04799353 | Study to Evaluate the Safety and How the Body Handles a Single Dose of Subcutan… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2021-03-15 | 2022-10-11 | ClinicalTrials.gov |
| NCT04799353 | Study to Evaluate the Safety and How the Body Handles a Single Dose of Subcutan… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2021-03-15 | 2022-10-11 | ClinicalTrials.gov |
| NCT04799353 | Study to Evaluate the Safety and How the Body Handles a Single Dose of Subcutan… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2021-03-15 | 2022-10-11 | ClinicalTrials.gov |
| NCT04799353 | Study to Evaluate the Safety and How the Body Handles a Single Dose of Subcutan… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2021-03-15 | 2022-10-11 | ClinicalTrials.gov |
| NCT04755595 | Combination Facial Aesthetic Treatment in Millennials | Phase2 | Dermatological Non-Disease | Completed | 2021-03-09 | 2021-05-19 | ClinicalTrials.gov |
| NCT04755595 | Combination Facial Aesthetic Treatment in Millennials | Phase2 | Dermatological Non-Disease | Completed | 2021-03-09 | 2021-05-19 | ClinicalTrials.gov |
| NCT04755595 | Combination Facial Aesthetic Treatment in Millennials | Phase2 | Dermatological Non-Disease | Completed | 2021-03-09 | 2021-05-19 | ClinicalTrials.gov |
| NCT04755595 | Combination Facial Aesthetic Treatment in Millennials | Phase2 | Dermatological Non-Disease | Completed | 2021-03-09 | 2021-05-19 | ClinicalTrials.gov |
| NCT04740827 | Atogepant for Prophylaxis of Migraine in Participants Who Failed Previous Oral … | Phase3 | Episodic Migraine | Completed | 2021-03-05 | 2022-08-04 | ClinicalTrials.gov |
| NCT04740827 | Atogepant for Prophylaxis of Migraine in Participants Who Failed Previous Oral … | Phase3 | Episodic Migraine | Completed | 2021-03-05 | 2022-08-04 | ClinicalTrials.gov |
| NCT04740827 | Atogepant for Prophylaxis of Migraine in Participants Who Failed Previous Oral … | Phase3 | Episodic Migraine | Completed | 2021-03-05 | 2022-08-04 | ClinicalTrials.gov |
| NCT04740827 | Atogepant for Prophylaxis of Migraine in Participants Who Failed Previous Oral … | Phase3 | Episodic Migraine | Completed | 2021-03-05 | 2022-08-04 | ClinicalTrials.gov |
| NCT04647214 | 18 Month Prospective Efficacy and Safety Study of Bimatoprost Intracameral Impl… | — | Open-angle Glaucoma | Completed | 2021-03-03 | 2024-07-12 | ClinicalTrials.gov |
| NCT04647214 | 18 Month Prospective Efficacy and Safety Study of Bimatoprost Intracameral Impl… | — | Open-angle Glaucoma | Completed | 2021-03-03 | 2024-07-12 | ClinicalTrials.gov |
| NCT04647214 | 18 Month Prospective Efficacy and Safety Study of Bimatoprost Intracameral Impl… | — | Open-angle Glaucoma | Completed | 2021-03-03 | 2024-07-12 | ClinicalTrials.gov |
| NCT04647214 | 18 Month Prospective Efficacy and Safety Study of Bimatoprost Intracameral Impl… | — | Open-angle Glaucoma | Completed | 2021-03-03 | 2024-07-12 | ClinicalTrials.gov |
| NCT04608318 | Ibrutinib Monotherapy Versus Fixed-duration Venetoclax Plus Obinutuzumab Versus… | Phase3 | Chronic Lymphoid Leukemia | Active_Not_Recruiting | 2021-03-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT04608318 | Ibrutinib Monotherapy Versus Fixed-duration Venetoclax Plus Obinutuzumab Versus… | Phase3 | Chronic Lymphoid Leukemia | Active_Not_Recruiting | 2021-03-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT04608318 | Ibrutinib Monotherapy Versus Fixed-duration Venetoclax Plus Obinutuzumab Versus… | Phase3 | Chronic Lymphoid Leukemia | Active_Not_Recruiting | 2021-03-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT04608318 | Ibrutinib Monotherapy Versus Fixed-duration Venetoclax Plus Obinutuzumab Versus… | Phase3 | Chronic Lymphoid Leukemia | Active_Not_Recruiting | 2021-03-01 | 2027-09-01 | ClinicalTrials.gov |
| NCT04713592 | Study of Subcutaneous (Injected Under the Skin) Risankizumab to Assess Change i… | Phase3 | Psoriasis | Completed | 2021-02-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT04713592 | Study of Subcutaneous (Injected Under the Skin) Risankizumab to Assess Change i… | Phase3 | Psoriasis | Completed | 2021-02-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT04713592 | Study of Subcutaneous (Injected Under the Skin) Risankizumab to Assess Change i… | Phase3 | Psoriasis | Completed | 2021-02-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT04713592 | Study of Subcutaneous (Injected Under the Skin) Risankizumab to Assess Change i… | Phase3 | Psoriasis | Completed | 2021-02-26 | 2023-04-20 | ClinicalTrials.gov |
| NCT04760769 | Open-label Trial in Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2021-02-24 | 2025-12-01 | ClinicalTrials.gov |
| NCT04760769 | Open-label Trial in Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2021-02-24 | 2025-12-01 | ClinicalTrials.gov |
| NCT04760769 | Open-label Trial in Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2021-02-24 | 2025-12-01 | ClinicalTrials.gov |
| NCT04760769 | Open-label Trial in Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2021-02-24 | 2025-12-01 | ClinicalTrials.gov |
| NCT04721015 | Study of Intravenous (IV) ABBV-637 Alone or in Combination With IV Docetaxel/Os… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2021-02-23 | 2026-02-01 | ClinicalTrials.gov |
| NCT04721015 | Study of Intravenous (IV) ABBV-637 Alone or in Combination With IV Docetaxel/Os… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2021-02-23 | 2026-02-01 | ClinicalTrials.gov |
| NCT04721015 | Study of Intravenous (IV) ABBV-637 Alone or in Combination With IV Docetaxel/Os… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2021-02-23 | 2026-02-01 | ClinicalTrials.gov |
| NCT04721015 | Study of Intravenous (IV) ABBV-637 Alone or in Combination With IV Docetaxel/Os… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2021-02-23 | 2026-02-01 | ClinicalTrials.gov |
| NCT04832724 | RGX-314 Gene Therapy Pharmacodynamic Study for Neovascular Age-related Macular … | Phase2 | Neovascular Age-related Macular Degeneration | Completed | 2021-02-22 | 2024-03-18 | ClinicalTrials.gov |
| NCT04832724 | RGX-314 Gene Therapy Pharmacodynamic Study for Neovascular Age-related Macular … | Phase2 | Neovascular Age-related Macular Degeneration | Completed | 2021-02-22 | 2024-03-18 | ClinicalTrials.gov |
| NCT04832724 | RGX-314 Gene Therapy Pharmacodynamic Study for Neovascular Age-related Macular … | Phase2 | Neovascular Age-related Macular Degeneration | Completed | 2021-02-22 | 2024-03-18 | ClinicalTrials.gov |
| NCT04832724 | RGX-314 Gene Therapy Pharmacodynamic Study for Neovascular Age-related Macular … | Phase2 | Neovascular Age-related Macular Degeneration | Completed | 2021-02-22 | 2024-03-18 | ClinicalTrials.gov |
| NCT04686136 | A Long-Term Safety and Tolerability Extension Study Evaluating Atogepant for th… | Phase3 | Episodic Migraine | Completed | 2021-02-19 | 2025-10-20 | ClinicalTrials.gov |
| NCT04686136 | A Long-Term Safety and Tolerability Extension Study Evaluating Atogepant for th… | Phase3 | Episodic Migraine | Completed | 2021-02-19 | 2025-10-20 | ClinicalTrials.gov |
| NCT04686136 | A Long-Term Safety and Tolerability Extension Study Evaluating Atogepant for th… | Phase3 | Episodic Migraine | Completed | 2021-02-19 | 2025-10-20 | ClinicalTrials.gov |
| NCT04686136 | A Long-Term Safety and Tolerability Extension Study Evaluating Atogepant for th… | Phase3 | Episodic Migraine | Completed | 2021-02-19 | 2025-10-20 | ClinicalTrials.gov |
| NCT04750226 | Study To Assess Adverse Events and Change in Disease Activity Of 24-hour Contin… | Phase3 | Parkinson's Disease (PD) | Completed | 2021-02-18 | 2026-04-27 | ClinicalTrials.gov |
| NCT04750226 | Study To Assess Adverse Events and Change in Disease Activity Of 24-hour Contin… | Phase3 | Parkinson's Disease (PD) | Completed | 2021-02-18 | 2026-04-27 | ClinicalTrials.gov |
| NCT04750226 | Study To Assess Adverse Events and Change in Disease Activity Of 24-hour Contin… | Phase3 | Parkinson's Disease (PD) | Completed | 2021-02-18 | 2026-04-27 | ClinicalTrials.gov |
| NCT04750226 | Study To Assess Adverse Events and Change in Disease Activity Of 24-hour Contin… | Phase3 | Parkinson's Disease (PD) | Completed | 2021-02-18 | 2026-04-27 | ClinicalTrials.gov |
| NCT04750213 | A Study to Assess Adverse Events and Change in Disease State in Adult Participa… | — | Pyoderma Gangrenosum | Completed | 2021-02-12 | 2024-11-11 | ClinicalTrials.gov |
| NCT04750213 | A Study to Assess Adverse Events and Change in Disease State in Adult Participa… | — | Pyoderma Gangrenosum | Completed | 2021-02-12 | 2024-11-11 | ClinicalTrials.gov |
| NCT04750213 | A Study to Assess Adverse Events and Change in Disease State in Adult Participa… | — | Pyoderma Gangrenosum | Completed | 2021-02-12 | 2024-11-11 | ClinicalTrials.gov |
| NCT04750213 | A Study to Assess Adverse Events and Change in Disease State in Adult Participa… | — | Pyoderma Gangrenosum | Completed | 2021-02-12 | 2024-11-11 | ClinicalTrials.gov |
| NCT04758117 | A Study to Assess the Change in Disease State in Adult Participants Being Treat… | — | Psoriatic Arthritis | Completed | 2021-02-04 | 2023-07-26 | ClinicalTrials.gov |
| NCT04687046 | A Study of JUVÉDERM VOLUX® Injectable Gel for Chin Enhancement in Chinese Adult… | — | Chin Retrusion | Completed | 2021-02-04 | 2022-02-28 | ClinicalTrials.gov |
| NCT04687046 | A Study of JUVÉDERM VOLUX® Injectable Gel for Chin Enhancement in Chinese Adult… | — | Chin Retrusion | Completed | 2021-02-04 | 2022-02-28 | ClinicalTrials.gov |
| NCT04758117 | A Study to Assess the Change in Disease State in Adult Participants Being Treat… | — | Psoriatic Arthritis | Completed | 2021-02-04 | 2023-07-26 | ClinicalTrials.gov |
| NCT04758117 | A Study to Assess the Change in Disease State in Adult Participants Being Treat… | — | Psoriatic Arthritis | Completed | 2021-02-04 | 2023-07-26 | ClinicalTrials.gov |
| NCT04687046 | A Study of JUVÉDERM VOLUX® Injectable Gel for Chin Enhancement in Chinese Adult… | — | Chin Retrusion | Completed | 2021-02-04 | 2022-02-28 | ClinicalTrials.gov |
| NCT04758117 | A Study to Assess the Change in Disease State in Adult Participants Being Treat… | — | Psoriatic Arthritis | Completed | 2021-02-04 | 2023-07-26 | ClinicalTrials.gov |
| NCT04687046 | A Study of JUVÉDERM VOLUX® Injectable Gel for Chin Enhancement in Chinese Adult… | — | Chin Retrusion | Completed | 2021-02-04 | 2022-02-28 | ClinicalTrials.gov |
| NCT04578756 | Open-Label, Flexible-dose Study to Evaluate the Long-Term Safety and Tolerabili… | Phase3 | Schizophrenia | Completed | 2021-02-01 | 2025-10-06 | ClinicalTrials.gov |
| NCT04578756 | Open-Label, Flexible-dose Study to Evaluate the Long-Term Safety and Tolerabili… | Phase3 | Schizophrenia | Completed | 2021-02-01 | 2025-10-06 | ClinicalTrials.gov |
| NCT04578756 | Open-Label, Flexible-dose Study to Evaluate the Long-Term Safety and Tolerabili… | Phase3 | Schizophrenia | Completed | 2021-02-01 | 2025-10-06 | ClinicalTrials.gov |
| NCT04578756 | Open-Label, Flexible-dose Study to Evaluate the Long-Term Safety and Tolerabili… | Phase3 | Schizophrenia | Completed | 2021-02-01 | 2025-10-06 | ClinicalTrials.gov |
| NCT04541810 | A Study of Oral Upadacitinib (RINVOQ) Tablets to Assess Adverse Events and Chan… | — | Rheumatoid Arthritis (RA) | Completed | 2021-01-26 | 2025-12-31 | ClinicalTrials.gov |
| NCT04541810 | A Study of Oral Upadacitinib (RINVOQ) Tablets to Assess Adverse Events and Chan… | — | Rheumatoid Arthritis (RA) | Completed | 2021-01-26 | 2025-12-31 | ClinicalTrials.gov |
| NCT04541810 | A Study of Oral Upadacitinib (RINVOQ) Tablets to Assess Adverse Events and Chan… | — | Rheumatoid Arthritis (RA) | Completed | 2021-01-26 | 2025-12-31 | ClinicalTrials.gov |
| NCT04541810 | A Study of Oral Upadacitinib (RINVOQ) Tablets to Assess Adverse Events and Chan… | — | Rheumatoid Arthritis (RA) | Completed | 2021-01-26 | 2025-12-31 | ClinicalTrials.gov |
| NCT04655300 | Evaluation of Age-related Skin Changes Using Clinical Probe Measurements and Im… | — | Age-related Skin Changes | Completed | 2021-01-16 | 2021-02-05 | ClinicalTrials.gov |
| NCT04655300 | Evaluation of Age-related Skin Changes Using Clinical Probe Measurements and Im… | — | Age-related Skin Changes | Completed | 2021-01-16 | 2021-02-05 | ClinicalTrials.gov |
| NCT04655300 | Evaluation of Age-related Skin Changes Using Clinical Probe Measurements and Im… | — | Age-related Skin Changes | Completed | 2021-01-16 | 2021-02-05 | ClinicalTrials.gov |
| NCT04655300 | Evaluation of Age-related Skin Changes Using Clinical Probe Measurements and Im… | — | Age-related Skin Changes | Completed | 2021-01-16 | 2021-02-05 | ClinicalTrials.gov |
| NCT04277247 | Botulinum Toxin Type A for Foot Dystonia-associated Pain in Parkinson's Disease | Phase2 | Dystonia Disorder | Unknown | 2021-01-12 | 2022-12-01 | ClinicalTrials.gov |
| NCT05121298 | Discontinuation of Methotrexate in Rheumatoid Arthritis Patients Achieving Clin… | Phase3 | Rheumatoid Arthritis | Unknown | 2021-01-12 | 2024-09-30 | ClinicalTrials.gov |
| NCT04277247 | Botulinum Toxin Type A for Foot Dystonia-associated Pain in Parkinson's Disease | Phase2 | Dystonia Disorder | Unknown | 2021-01-12 | 2022-12-01 | ClinicalTrials.gov |
| NCT05121298 | Discontinuation of Methotrexate in Rheumatoid Arthritis Patients Achieving Clin… | Phase3 | Rheumatoid Arthritis | Unknown | 2021-01-12 | 2024-09-30 | ClinicalTrials.gov |
| NCT04277247 | Botulinum Toxin Type A for Foot Dystonia-associated Pain in Parkinson's Disease | Phase2 | Dystonia Disorder | Unknown | 2021-01-12 | 2022-12-01 | ClinicalTrials.gov |
| NCT05121298 | Discontinuation of Methotrexate in Rheumatoid Arthritis Patients Achieving Clin… | Phase3 | Rheumatoid Arthritis | Unknown | 2021-01-12 | 2024-09-30 | ClinicalTrials.gov |
| NCT05121298 | Discontinuation of Methotrexate in Rheumatoid Arthritis Patients Achieving Clin… | Phase3 | Rheumatoid Arthritis | Unknown | 2021-01-12 | 2024-09-30 | ClinicalTrials.gov |
| NCT04277247 | Botulinum Toxin Type A for Foot Dystonia-associated Pain in Parkinson's Disease | Phase2 | Dystonia Disorder | Unknown | 2021-01-12 | 2022-12-01 | ClinicalTrials.gov |
| NCT04704921 | Pivotal 1 Study of ABBV-RGX-314 (Also Known as RGX-314) Gene Therapy Administer… | Phase2 | AMD | Active_Not_Recruiting | 2020-12-29 | 2027-11-01 | ClinicalTrials.gov |
| NCT04704921 | Pivotal 1 Study of ABBV-RGX-314 (Also Known as RGX-314) Gene Therapy Administer… | Phase2 | AMD | Active_Not_Recruiting | 2020-12-29 | 2027-11-01 | ClinicalTrials.gov |
| NCT04704921 | Pivotal 1 Study of ABBV-RGX-314 (Also Known as RGX-314) Gene Therapy Administer… | Phase2 | AMD | Active_Not_Recruiting | 2020-12-29 | 2027-11-01 | ClinicalTrials.gov |
| NCT04704921 | Pivotal 1 Study of ABBV-RGX-314 (Also Known as RGX-314) Gene Therapy Administer… | Phase2 | AMD | Active_Not_Recruiting | 2020-12-29 | 2027-11-01 | ClinicalTrials.gov |
| NCT03580044 | Efficacy, Safety, and Tolerability of ATM-AVI in the Treatment of Serious Infec… | Phase3 | Serious Bacterial Infection | Terminated | 2020-12-25 | 2023-01-23 | ClinicalTrials.gov |
| NCT03580044 | Efficacy, Safety, and Tolerability of ATM-AVI in the Treatment of Serious Infec… | Phase3 | Serious Bacterial Infection | Terminated | 2020-12-25 | 2023-01-23 | ClinicalTrials.gov |
| NCT03580044 | Efficacy, Safety, and Tolerability of ATM-AVI in the Treatment of Serious Infec… | Phase3 | Serious Bacterial Infection | Terminated | 2020-12-25 | 2023-01-23 | ClinicalTrials.gov |
| NCT03580044 | Efficacy, Safety, and Tolerability of ATM-AVI in the Treatment of Serious Infec… | Phase3 | Serious Bacterial Infection | Terminated | 2020-12-25 | 2023-01-23 | ClinicalTrials.gov |
| NCT04666675 | A Study of Oral Upadacitinib Tablets to Assess Change in Disease State in Parti… | Phase3 | Atopic Dermatitis (AD) | Withdrawn | 2020-12-24 | 2021-03-23 | ClinicalTrials.gov |
| NCT04666675 | A Study of Oral Upadacitinib Tablets to Assess Change in Disease State in Parti… | Phase3 | Atopic Dermatitis (AD) | Withdrawn | 2020-12-24 | 2021-03-23 | ClinicalTrials.gov |
| NCT04666675 | A Study of Oral Upadacitinib Tablets to Assess Change in Disease State in Parti… | Phase3 | Atopic Dermatitis (AD) | Withdrawn | 2020-12-24 | 2021-03-23 | ClinicalTrials.gov |
| NCT04666675 | A Study of Oral Upadacitinib Tablets to Assess Change in Disease State in Parti… | Phase3 | Atopic Dermatitis (AD) | Withdrawn | 2020-12-24 | 2021-03-23 | ClinicalTrials.gov |
| NCT04843839 | CHED - Congenital Hereditary Endothelial Dystrophy: New Paradigm Shift in Thera… | Phase2 | Congenital Hereditary Endothelial Dystrophy of Cornea | Unknown | 2020-12-15 | 2022-12-15 | ClinicalTrials.gov |
| NCT04843839 | CHED - Congenital Hereditary Endothelial Dystrophy: New Paradigm Shift in Thera… | Phase2 | Congenital Hereditary Endothelial Dystrophy of Cornea | Unknown | 2020-12-15 | 2022-12-15 | ClinicalTrials.gov |
| NCT04843839 | CHED - Congenital Hereditary Endothelial Dystrophy: New Paradigm Shift in Thera… | Phase2 | Congenital Hereditary Endothelial Dystrophy of Cornea | Unknown | 2020-12-15 | 2022-12-15 | ClinicalTrials.gov |
| NCT04843839 | CHED - Congenital Hereditary Endothelial Dystrophy: New Paradigm Shift in Thera… | Phase2 | Congenital Hereditary Endothelial Dystrophy of Cornea | Unknown | 2020-12-15 | 2022-12-15 | ClinicalTrials.gov |
| NCT04630990 | Study Of Oral Elagolix Tablets To Assess the Tolerability and Change in Disease… | — | Endometriosis | Completed | 2020-12-14 | 2024-03-26 | ClinicalTrials.gov |
| NCT04630990 | Study Of Oral Elagolix Tablets To Assess the Tolerability and Change in Disease… | — | Endometriosis | Completed | 2020-12-14 | 2024-03-26 | ClinicalTrials.gov |
| NCT04630990 | Study Of Oral Elagolix Tablets To Assess the Tolerability and Change in Disease… | — | Endometriosis | Completed | 2020-12-14 | 2024-03-26 | ClinicalTrials.gov |
| NCT04630990 | Study Of Oral Elagolix Tablets To Assess the Tolerability and Change in Disease… | — | Endometriosis | Completed | 2020-12-14 | 2024-03-26 | ClinicalTrials.gov |
| NCT04655261 | Study of Oral Venetoclax Tablets in Combination With Intravenous Obinutuzumab I… | — | Chronic Lymphocytic Leukemia (CLL) | Terminated | 2020-12-12 | 2021-11-09 | ClinicalTrials.gov |
| NCT04655261 | Study of Oral Venetoclax Tablets in Combination With Intravenous Obinutuzumab I… | — | Chronic Lymphocytic Leukemia (CLL) | Terminated | 2020-12-12 | 2021-11-09 | ClinicalTrials.gov |
| NCT04655261 | Study of Oral Venetoclax Tablets in Combination With Intravenous Obinutuzumab I… | — | Chronic Lymphocytic Leukemia (CLL) | Terminated | 2020-12-12 | 2021-11-09 | ClinicalTrials.gov |
| NCT04655261 | Study of Oral Venetoclax Tablets in Combination With Intravenous Obinutuzumab I… | — | Chronic Lymphocytic Leukemia (CLL) | Terminated | 2020-12-12 | 2021-11-09 | ClinicalTrials.gov |
| NCT04644120 | Study to Assess Adverse Events and How Intravenous (IV) ABBV-47D11 and IV ABBV-… | Phase1 | CoronaVirus Disease-2019 (COVID-19) | Completed | 2020-12-10 | 2021-08-24 | ClinicalTrials.gov |
| NCT04644120 | Study to Assess Adverse Events and How Intravenous (IV) ABBV-47D11 and IV ABBV-… | Phase1 | CoronaVirus Disease-2019 (COVID-19) | Completed | 2020-12-10 | 2021-08-24 | ClinicalTrials.gov |
| NCT04644120 | Study to Assess Adverse Events and How Intravenous (IV) ABBV-47D11 and IV ABBV-… | Phase1 | CoronaVirus Disease-2019 (COVID-19) | Completed | 2020-12-10 | 2021-08-24 | ClinicalTrials.gov |
| NCT04644120 | Study to Assess Adverse Events and How Intravenous (IV) ABBV-47D11 and IV ABBV-… | Phase1 | CoronaVirus Disease-2019 (COVID-19) | Completed | 2020-12-10 | 2021-08-24 | ClinicalTrials.gov |
| NCT04686786 | An Open-label Extension Trial of CVL-865 as Adjunctive Therapy in the Treatment… | Phase2 | Seizures | Terminated | 2020-12-08 | 2024-12-05 | ClinicalTrials.gov |
| NCT04686786 | An Open-label Extension Trial of CVL-865 as Adjunctive Therapy in the Treatment… | Phase2 | Seizures | Terminated | 2020-12-08 | 2024-12-05 | ClinicalTrials.gov |
| NCT04686786 | An Open-label Extension Trial of CVL-865 as Adjunctive Therapy in the Treatment… | Phase2 | Seizures | Terminated | 2020-12-08 | 2024-12-05 | ClinicalTrials.gov |
| NCT04686786 | An Open-label Extension Trial of CVL-865 as Adjunctive Therapy in the Treatment… | Phase2 | Seizures | Terminated | 2020-12-08 | 2024-12-05 | ClinicalTrials.gov |
| NCT04567550 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants … | Phase2 | Diabetic Retinopathy (DR) | Active_Not_Recruiting | 2020-11-20 | 2026-12-01 | ClinicalTrials.gov |
| NCT04567550 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants … | Phase2 | Diabetic Retinopathy (DR) | Active_Not_Recruiting | 2020-11-20 | 2026-12-01 | ClinicalTrials.gov |
| NCT04567550 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants … | Phase2 | Diabetic Retinopathy (DR) | Active_Not_Recruiting | 2020-11-20 | 2026-12-01 | ClinicalTrials.gov |
| NCT04567550 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants … | Phase2 | Diabetic Retinopathy (DR) | Active_Not_Recruiting | 2020-11-20 | 2026-12-01 | ClinicalTrials.gov |
| NCT04610762 | HCV RNA Fingerstick Assay as Useful Point of Care of Diagnostic Tool for Drug U… | — | Hepatitis C, Chronic | Completed | 2020-11-17 | 2022-11-17 | ClinicalTrials.gov |
| NCT04610762 | HCV RNA Fingerstick Assay as Useful Point of Care of Diagnostic Tool for Drug U… | — | Hepatitis C, Chronic | Completed | 2020-11-17 | 2022-11-17 | ClinicalTrials.gov |
| NCT04610762 | HCV RNA Fingerstick Assay as Useful Point of Care of Diagnostic Tool for Drug U… | — | Hepatitis C, Chronic | Completed | 2020-11-17 | 2022-11-17 | ClinicalTrials.gov |
| NCT04610762 | HCV RNA Fingerstick Assay as Useful Point of Care of Diagnostic Tool for Drug U… | — | Hepatitis C, Chronic | Completed | 2020-11-17 | 2022-11-17 | ClinicalTrials.gov |
| NCT04631588 | Intradermal (ID) BOTOX in the Treatment of Facial Fine Lines | Phase1 | Facial Fine Lines | Completed | 2020-11-16 | 2021-11-03 | ClinicalTrials.gov |
| NCT04631588 | Intradermal (ID) BOTOX in the Treatment of Facial Fine Lines | Phase1 | Facial Fine Lines | Completed | 2020-11-16 | 2021-11-03 | ClinicalTrials.gov |
| NCT04499248 | AGN-193408 SR in the Treatment of Open-angle Glaucoma or Ocular Hypertension | Phase1 | Open-angle Glaucoma | Active_Not_Recruiting | 2020-11-16 | 2029-04-01 | ClinicalTrials.gov |
| NCT04631588 | Intradermal (ID) BOTOX in the Treatment of Facial Fine Lines | Phase1 | Facial Fine Lines | Completed | 2020-11-16 | 2021-11-03 | ClinicalTrials.gov |
| NCT04499248 | AGN-193408 SR in the Treatment of Open-angle Glaucoma or Ocular Hypertension | Phase1 | Open-angle Glaucoma | Active_Not_Recruiting | 2020-11-16 | 2029-04-01 | ClinicalTrials.gov |
| NCT04499248 | AGN-193408 SR in the Treatment of Open-angle Glaucoma or Ocular Hypertension | Phase1 | Open-angle Glaucoma | Active_Not_Recruiting | 2020-11-16 | 2029-04-01 | ClinicalTrials.gov |
| NCT04499248 | AGN-193408 SR in the Treatment of Open-angle Glaucoma or Ocular Hypertension | Phase1 | Open-angle Glaucoma | Active_Not_Recruiting | 2020-11-16 | 2029-04-01 | ClinicalTrials.gov |
| NCT04631588 | Intradermal (ID) BOTOX in the Treatment of Facial Fine Lines | Phase1 | Facial Fine Lines | Completed | 2020-11-16 | 2021-11-03 | ClinicalTrials.gov |
| NCT04454658 | Safety and Tolerability Study of Oral ABBV-744 Tablet Alone or in Combination W… | Phase1 | Myelofibrosis (MF) | Active_Not_Recruiting | 2020-11-11 | 2027-01-01 | ClinicalTrials.gov |
| NCT04454658 | Safety and Tolerability Study of Oral ABBV-744 Tablet Alone or in Combination W… | Phase1 | Myelofibrosis (MF) | Active_Not_Recruiting | 2020-11-11 | 2027-01-01 | ClinicalTrials.gov |
| NCT04454658 | Safety and Tolerability Study of Oral ABBV-744 Tablet Alone or in Combination W… | Phase1 | Myelofibrosis (MF) | Active_Not_Recruiting | 2020-11-11 | 2027-01-01 | ClinicalTrials.gov |
| NCT04454658 | Safety and Tolerability Study of Oral ABBV-744 Tablet Alone or in Combination W… | Phase1 | Myelofibrosis (MF) | Active_Not_Recruiting | 2020-11-11 | 2027-01-01 | ClinicalTrials.gov |
| NCT04505566 | INflammatory MediatorS in the PathophysIology of Diabetic REtinopathy Study | Phase1 | Diabetic Retinopathy | Completed | 2020-11-09 | 2026-04-21 | ClinicalTrials.gov |
| NCT04309474 | A Safety and Efficacy Study of Intravenous (IV) Elezanumab Assessing Change in … | Phase2 | Acute Ischemic Stroke | Completed | 2020-11-09 | 2024-12-23 | ClinicalTrials.gov |
| NCT04505566 | INflammatory MediatorS in the PathophysIology of Diabetic REtinopathy Study | Phase1 | Diabetic Retinopathy | Completed | 2020-11-09 | 2026-04-21 | ClinicalTrials.gov |
| NCT04309474 | A Safety and Efficacy Study of Intravenous (IV) Elezanumab Assessing Change in … | Phase2 | Acute Ischemic Stroke | Completed | 2020-11-09 | 2024-12-23 | ClinicalTrials.gov |
| NCT04309474 | A Safety and Efficacy Study of Intravenous (IV) Elezanumab Assessing Change in … | Phase2 | Acute Ischemic Stroke | Completed | 2020-11-09 | 2024-12-23 | ClinicalTrials.gov |
| NCT04309474 | A Safety and Efficacy Study of Intravenous (IV) Elezanumab Assessing Change in … | Phase2 | Acute Ischemic Stroke | Completed | 2020-11-09 | 2024-12-23 | ClinicalTrials.gov |
| NCT04505566 | INflammatory MediatorS in the PathophysIology of Diabetic REtinopathy Study | Phase1 | Diabetic Retinopathy | Completed | 2020-11-09 | 2026-04-21 | ClinicalTrials.gov |
| NCT04505566 | INflammatory MediatorS in the PathophysIology of Diabetic REtinopathy Study | Phase1 | Diabetic Retinopathy | Completed | 2020-11-09 | 2026-04-21 | ClinicalTrials.gov |
| NCT04611230 | A Study to Assess Infection Rate of Severe Acute Respiratory Syndrome - CoronaV… | — | Severe Acute Respiratory Syndrome - CoronaVirus 2 (SARS-CoV-2) | Completed | 2020-11-05 | 2021-10-27 | ClinicalTrials.gov |
| NCT04570631 | Study to Determine Recommended Phase 2 Dose of Intravenous (IV) Eftozanermin Al… | Phase1 | Multiple Myeloma | Terminated | 2020-11-05 | 2025-05-05 | ClinicalTrials.gov |
| NCT04092179 | Study of Enasidenib and Venetoclax in IDH2-Mutated Blood Cancers | Phase1 | Acute Myeloid Leukemia | Terminated | 2020-11-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT04092179 | Study of Enasidenib and Venetoclax in IDH2-Mutated Blood Cancers | Phase1 | Acute Myeloid Leukemia | Terminated | 2020-11-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT04092179 | Study of Enasidenib and Venetoclax in IDH2-Mutated Blood Cancers | Phase1 | Acute Myeloid Leukemia | Terminated | 2020-11-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT04092179 | Study of Enasidenib and Venetoclax in IDH2-Mutated Blood Cancers | Phase1 | Acute Myeloid Leukemia | Terminated | 2020-11-05 | 2023-10-26 | ClinicalTrials.gov |
| NCT04570631 | Study to Determine Recommended Phase 2 Dose of Intravenous (IV) Eftozanermin Al… | Phase1 | Multiple Myeloma | Terminated | 2020-11-05 | 2025-05-05 | ClinicalTrials.gov |
| NCT04611230 | A Study to Assess Infection Rate of Severe Acute Respiratory Syndrome - CoronaV… | — | Severe Acute Respiratory Syndrome - CoronaVirus 2 (SARS-CoV-2) | Completed | 2020-11-05 | 2021-10-27 | ClinicalTrials.gov |
| NCT04570631 | Study to Determine Recommended Phase 2 Dose of Intravenous (IV) Eftozanermin Al… | Phase1 | Multiple Myeloma | Terminated | 2020-11-05 | 2025-05-05 | ClinicalTrials.gov |
| NCT04570631 | Study to Determine Recommended Phase 2 Dose of Intravenous (IV) Eftozanermin Al… | Phase1 | Multiple Myeloma | Terminated | 2020-11-05 | 2025-05-05 | ClinicalTrials.gov |
| NCT04611230 | A Study to Assess Infection Rate of Severe Acute Respiratory Syndrome - CoronaV… | — | Severe Acute Respiratory Syndrome - CoronaVirus 2 (SARS-CoV-2) | Completed | 2020-11-05 | 2021-10-27 | ClinicalTrials.gov |
| NCT04611230 | A Study to Assess Infection Rate of Severe Acute Respiratory Syndrome - CoronaV… | — | Severe Acute Respiratory Syndrome - CoronaVirus 2 (SARS-CoV-2) | Completed | 2020-11-05 | 2021-10-27 | ClinicalTrials.gov |
| NCT04602923 | Keratometric Change After XEN, Trabeculectomy and Tube Shunts | Na | Glaucoma, Open-Angle | Completed | 2020-11-04 | 2024-08-07 | ClinicalTrials.gov |
| NCT04602923 | Keratometric Change After XEN, Trabeculectomy and Tube Shunts | Na | Glaucoma, Open-Angle | Completed | 2020-11-04 | 2024-08-07 | ClinicalTrials.gov |
| NCT04602923 | Keratometric Change After XEN, Trabeculectomy and Tube Shunts | Na | Glaucoma, Open-Angle | Completed | 2020-11-04 | 2024-08-07 | ClinicalTrials.gov |
| NCT04602923 | Keratometric Change After XEN, Trabeculectomy and Tube Shunts | Na | Glaucoma, Open-Angle | Completed | 2020-11-04 | 2024-08-07 | ClinicalTrials.gov |
| NCT04380142 | Study Comparing Continuous Subcutaneous Infusion Of ABBV-951 With Oral Carbidop… | Phase3 | Parkinson's Disease (PD) | Completed | 2020-10-19 | 2021-09-29 | ClinicalTrials.gov |
| NCT04380142 | Study Comparing Continuous Subcutaneous Infusion Of ABBV-951 With Oral Carbidop… | Phase3 | Parkinson's Disease (PD) | Completed | 2020-10-19 | 2021-09-29 | ClinicalTrials.gov |
| NCT04380142 | Study Comparing Continuous Subcutaneous Infusion Of ABBV-951 With Oral Carbidop… | Phase3 | Parkinson's Disease (PD) | Completed | 2020-10-19 | 2021-09-29 | ClinicalTrials.gov |
| NCT04380142 | Study Comparing Continuous Subcutaneous Infusion Of ABBV-951 With Oral Carbidop… | Phase3 | Parkinson's Disease (PD) | Completed | 2020-10-19 | 2021-09-29 | ClinicalTrials.gov |
| NCT04497597 | A Study of Oral Upadacitinib Tablets to Assess Treatment Patterns, Achievement … | — | Rheumatoid Arthritis (RA) | Completed | 2020-10-16 | 2024-05-15 | ClinicalTrials.gov |
| NCT04497597 | A Study of Oral Upadacitinib Tablets to Assess Treatment Patterns, Achievement … | — | Rheumatoid Arthritis (RA) | Completed | 2020-10-16 | 2024-05-15 | ClinicalTrials.gov |
| NCT04497597 | A Study of Oral Upadacitinib Tablets to Assess Treatment Patterns, Achievement … | — | Rheumatoid Arthritis (RA) | Completed | 2020-10-16 | 2024-05-15 | ClinicalTrials.gov |
| NCT04497597 | A Study of Oral Upadacitinib Tablets to Assess Treatment Patterns, Achievement … | — | Rheumatoid Arthritis (RA) | Completed | 2020-10-16 | 2024-05-15 | ClinicalTrials.gov |
| NCT04559984 | JUVÉDERM VOLUX® for Chin Retrusion in China | Phase3 | Chin Retrusion | Completed | 2020-10-15 | 2022-08-26 | ClinicalTrials.gov |
| NCT04559984 | JUVÉDERM VOLUX® for Chin Retrusion in China | Phase3 | Chin Retrusion | Completed | 2020-10-15 | 2022-08-26 | ClinicalTrials.gov |
| NCT04559984 | JUVÉDERM VOLUX® for Chin Retrusion in China | Phase3 | Chin Retrusion | Completed | 2020-10-15 | 2022-08-26 | ClinicalTrials.gov |
| NCT04559984 | JUVÉDERM VOLUX® for Chin Retrusion in China | Phase3 | Chin Retrusion | Completed | 2020-10-15 | 2022-08-26 | ClinicalTrials.gov |
| NCT04577482 | Study of Oral Glecaprevir/Pibrentasvir Tablets in Participants Aged 12 Years or… | — | Hepatitis C Virus (HCV) | Completed | 2020-10-07 | 2022-09-03 | ClinicalTrials.gov |
| NCT04577482 | Study of Oral Glecaprevir/Pibrentasvir Tablets in Participants Aged 12 Years or… | — | Hepatitis C Virus (HCV) | Completed | 2020-10-07 | 2022-09-03 | ClinicalTrials.gov |
| NCT04574492 | A Study of Oral Upadacitinib Tablets to Assess the Change in Disease Symptoms i… | — | Rheumatoid Arthritis (RA) | Completed | 2020-10-07 | 2024-07-30 | ClinicalTrials.gov |
| NCT04574492 | A Study of Oral Upadacitinib Tablets to Assess the Change in Disease Symptoms i… | — | Rheumatoid Arthritis (RA) | Completed | 2020-10-07 | 2024-07-30 | ClinicalTrials.gov |
| NCT04574492 | A Study of Oral Upadacitinib Tablets to Assess the Change in Disease Symptoms i… | — | Rheumatoid Arthritis (RA) | Completed | 2020-10-07 | 2024-07-30 | ClinicalTrials.gov |
| NCT04577482 | Study of Oral Glecaprevir/Pibrentasvir Tablets in Participants Aged 12 Years or… | — | Hepatitis C Virus (HCV) | Completed | 2020-10-07 | 2022-09-03 | ClinicalTrials.gov |
| NCT04577482 | Study of Oral Glecaprevir/Pibrentasvir Tablets in Participants Aged 12 Years or… | — | Hepatitis C Virus (HCV) | Completed | 2020-10-07 | 2022-09-03 | ClinicalTrials.gov |
| NCT04574492 | A Study of Oral Upadacitinib Tablets to Assess the Change in Disease Symptoms i… | — | Rheumatoid Arthritis (RA) | Completed | 2020-10-07 | 2024-07-30 | ClinicalTrials.gov |
| NCT04509622 | A Study of Oral Venetoclax Tablet in Combination With Subcutaneous Low-Dose Cyt… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2020-10-05 | 2021-04-15 | ClinicalTrials.gov |
| NCT04509622 | A Study of Oral Venetoclax Tablet in Combination With Subcutaneous Low-Dose Cyt… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2020-10-05 | 2021-04-15 | ClinicalTrials.gov |
| NCT04509622 | A Study of Oral Venetoclax Tablet in Combination With Subcutaneous Low-Dose Cyt… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2020-10-05 | 2021-04-15 | ClinicalTrials.gov |
| NCT04509622 | A Study of Oral Venetoclax Tablet in Combination With Subcutaneous Low-Dose Cyt… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2020-10-05 | 2021-04-15 | ClinicalTrials.gov |
| NCT04524611 | Study Comparing Intravenous (IV)/Subcutaneous (SC) Risankizumab to IV/SC Usteki… | Phase3 | Crohn's Disease (CD) | Active_Not_Recruiting | 2020-09-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT04567589 | A Study to Evaluate Awareness and Knowledge of the Fibristal Additional Risk Mi… | — | Uterine Fibroids | Withdrawn | 2020-09-30 | 2021-02-28 | ClinicalTrials.gov |
| NCT04567589 | A Study to Evaluate Awareness and Knowledge of the Fibristal Additional Risk Mi… | — | Uterine Fibroids | Withdrawn | 2020-09-30 | 2021-02-28 | ClinicalTrials.gov |
| NCT04524611 | Study Comparing Intravenous (IV)/Subcutaneous (SC) Risankizumab to IV/SC Usteki… | Phase3 | Crohn's Disease (CD) | Active_Not_Recruiting | 2020-09-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT04567589 | A Study to Evaluate Awareness and Knowledge of the Fibristal Additional Risk Mi… | — | Uterine Fibroids | Withdrawn | 2020-09-30 | 2021-02-28 | ClinicalTrials.gov |
| NCT04524611 | Study Comparing Intravenous (IV)/Subcutaneous (SC) Risankizumab to IV/SC Usteki… | Phase3 | Crohn's Disease (CD) | Active_Not_Recruiting | 2020-09-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT04524611 | Study Comparing Intravenous (IV)/Subcutaneous (SC) Risankizumab to IV/SC Usteki… | Phase3 | Crohn's Disease (CD) | Active_Not_Recruiting | 2020-09-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT04567589 | A Study to Evaluate Awareness and Knowledge of the Fibristal Additional Risk Mi… | — | Uterine Fibroids | Withdrawn | 2020-09-30 | 2021-02-28 | ClinicalTrials.gov |
| NCT04472598 | Study of Oral Navitoclax Tablet In Combination With Oral Ruxolitinib Tablet Whe… | Phase3 | Myelofibrosis (MF) | Completed | 2020-09-29 | 2025-01-29 | ClinicalTrials.gov |
| NCT04472598 | Study of Oral Navitoclax Tablet In Combination With Oral Ruxolitinib Tablet Whe… | Phase3 | Myelofibrosis (MF) | Completed | 2020-09-29 | 2025-01-29 | ClinicalTrials.gov |
| NCT04472598 | Study of Oral Navitoclax Tablet In Combination With Oral Ruxolitinib Tablet Whe… | Phase3 | Myelofibrosis (MF) | Completed | 2020-09-29 | 2025-01-29 | ClinicalTrials.gov |
| NCT04472598 | Study of Oral Navitoclax Tablet In Combination With Oral Ruxolitinib Tablet Whe… | Phase3 | Myelofibrosis (MF) | Completed | 2020-09-29 | 2025-01-29 | ClinicalTrials.gov |
| NCT04542499 | Flexible-Dose, Adjunctive Therapy Trial in Adults With Parkinson's Disease With… | Phase3 | Parkinson Disease | Completed | 2020-09-23 | 2024-02-15 | ClinicalTrials.gov |
| NCT04542499 | Flexible-Dose, Adjunctive Therapy Trial in Adults With Parkinson's Disease With… | Phase3 | Parkinson Disease | Completed | 2020-09-23 | 2024-02-15 | ClinicalTrials.gov |
| NCT04477486 | Study to Assess Effect of Oral Venetoclax Tablet in Combination With Oral Ibrut… | Phase2 | Mantle Cell Lymphoma (MCL) | Completed | 2020-09-23 | 2025-05-28 | ClinicalTrials.gov |
| NCT04542499 | Flexible-Dose, Adjunctive Therapy Trial in Adults With Parkinson's Disease With… | Phase3 | Parkinson Disease | Completed | 2020-09-23 | 2024-02-15 | ClinicalTrials.gov |
| NCT04477486 | Study to Assess Effect of Oral Venetoclax Tablet in Combination With Oral Ibrut… | Phase2 | Mantle Cell Lymphoma (MCL) | Completed | 2020-09-23 | 2025-05-28 | ClinicalTrials.gov |
| NCT04477486 | Study to Assess Effect of Oral Venetoclax Tablet in Combination With Oral Ibrut… | Phase2 | Mantle Cell Lymphoma (MCL) | Completed | 2020-09-23 | 2025-05-28 | ClinicalTrials.gov |
| NCT04542499 | Flexible-Dose, Adjunctive Therapy Trial in Adults With Parkinson's Disease With… | Phase3 | Parkinson Disease | Completed | 2020-09-23 | 2024-02-15 | ClinicalTrials.gov |
| NCT04477486 | Study to Assess Effect of Oral Venetoclax Tablet in Combination With Oral Ibrut… | Phase2 | Mantle Cell Lymphoma (MCL) | Completed | 2020-09-23 | 2025-05-28 | ClinicalTrials.gov |
| NCT04552249 | Evaluation of Age-related Skin Changes and Instrument Reliability Using Clinica… | — | Age-related Skin Changes | Completed | 2020-09-22 | 2020-12-18 | ClinicalTrials.gov |
| NCT04552249 | Evaluation of Age-related Skin Changes and Instrument Reliability Using Clinica… | — | Age-related Skin Changes | Completed | 2020-09-22 | 2020-12-18 | ClinicalTrials.gov |
| NCT04552249 | Evaluation of Age-related Skin Changes and Instrument Reliability Using Clinica… | — | Age-related Skin Changes | Completed | 2020-09-22 | 2020-12-18 | ClinicalTrials.gov |
| NCT04552249 | Evaluation of Age-related Skin Changes and Instrument Reliability Using Clinica… | — | Age-related Skin Changes | Completed | 2020-09-22 | 2020-12-18 | ClinicalTrials.gov |
| NCT04064827 | A Study to Evaluate Safety, Efficacy and Pharmacokinetics of Paricalcitol For T… | Phase3 | Chronic Kidney Disease (CKD) | Terminated | 2020-09-16 | 2025-06-09 | ClinicalTrials.gov |
| NCT04064827 | A Study to Evaluate Safety, Efficacy and Pharmacokinetics of Paricalcitol For T… | Phase3 | Chronic Kidney Disease (CKD) | Terminated | 2020-09-16 | 2025-06-09 | ClinicalTrials.gov |
| NCT04064827 | A Study to Evaluate Safety, Efficacy and Pharmacokinetics of Paricalcitol For T… | Phase3 | Chronic Kidney Disease (CKD) | Terminated | 2020-09-16 | 2025-06-09 | ClinicalTrials.gov |
| NCT04064827 | A Study to Evaluate Safety, Efficacy and Pharmacokinetics of Paricalcitol For T… | Phase3 | Chronic Kidney Disease (CKD) | Terminated | 2020-09-16 | 2025-06-09 | ClinicalTrials.gov |
| NCT05274087 | Study to Evaluate the Effect of Different Warm-Up Times of Risankizumab Autoinj… | Phase1 | Healthy Volunteers | Completed | 2020-09-15 | 2021-04-07 | ClinicalTrials.gov |
| NCT05274087 | Study to Evaluate the Effect of Different Warm-Up Times of Risankizumab Autoinj… | Phase1 | Healthy Volunteers | Completed | 2020-09-15 | 2021-04-07 | ClinicalTrials.gov |
| NCT05274087 | Study to Evaluate the Effect of Different Warm-Up Times of Risankizumab Autoinj… | Phase1 | Healthy Volunteers | Completed | 2020-09-15 | 2021-04-07 | ClinicalTrials.gov |
| NCT05274087 | Study to Evaluate the Effect of Different Warm-Up Times of Risankizumab Autoinj… | Phase1 | Healthy Volunteers | Completed | 2020-09-15 | 2021-04-07 | ClinicalTrials.gov |
| NCT04401748 | Study Of Venetoclax Tablet With Intravenous or Subcutaneous Azacitidine to Asse… | Phase3 | Myelodysplastic Syndrome (MDS) | Active_Not_Recruiting | 2020-09-10 | 2026-03-01 | ClinicalTrials.gov |
| NCT04401748 | Study Of Venetoclax Tablet With Intravenous or Subcutaneous Azacitidine to Asse… | Phase3 | Myelodysplastic Syndrome (MDS) | Active_Not_Recruiting | 2020-09-10 | 2026-03-01 | ClinicalTrials.gov |
| NCT04401748 | Study Of Venetoclax Tablet With Intravenous or Subcutaneous Azacitidine to Asse… | Phase3 | Myelodysplastic Syndrome (MDS) | Active_Not_Recruiting | 2020-09-10 | 2026-03-01 | ClinicalTrials.gov |
| NCT04401748 | Study Of Venetoclax Tablet With Intravenous or Subcutaneous Azacitidine to Asse… | Phase3 | Myelodysplastic Syndrome (MDS) | Active_Not_Recruiting | 2020-09-10 | 2026-03-01 | ClinicalTrials.gov |
| NCT04295538 | Safety And Efficacy Study Of Intravenous (IV) Administration Of Elezanumab To A… | Phase2 | Spinal Cord Injury (SCI) | Completed | 2020-09-06 | 2026-01-26 | ClinicalTrials.gov |
| NCT04295538 | Safety And Efficacy Study Of Intravenous (IV) Administration Of Elezanumab To A… | Phase2 | Spinal Cord Injury (SCI) | Completed | 2020-09-06 | 2026-01-26 | ClinicalTrials.gov |
| NCT04295538 | Safety And Efficacy Study Of Intravenous (IV) Administration Of Elezanumab To A… | Phase2 | Spinal Cord Injury (SCI) | Completed | 2020-09-06 | 2026-01-26 | ClinicalTrials.gov |
| NCT04295538 | Safety And Efficacy Study Of Intravenous (IV) Administration Of Elezanumab To A… | Phase2 | Spinal Cord Injury (SCI) | Completed | 2020-09-06 | 2026-01-26 | ClinicalTrials.gov |
| NCT05274100 | Study of Intravenous and Subcutaneous Administration of Risankizumab in Healthy… | Phase1 | Healthy Volunteers | Completed | 2020-09-01 | 2021-07-06 | ClinicalTrials.gov |
| NCT04445025 | Comparison Elagolix vs Depot Leuprolide Prior to Frozen Embryo Transfers in Pat… | Early_Phase1 | Infertility | Completed | 2020-09-01 | 2024-12-30 | ClinicalTrials.gov |
| NCT05274100 | Study of Intravenous and Subcutaneous Administration of Risankizumab in Healthy… | Phase1 | Healthy Volunteers | Completed | 2020-09-01 | 2021-07-06 | ClinicalTrials.gov |
| NCT04445025 | Comparison Elagolix vs Depot Leuprolide Prior to Frozen Embryo Transfers in Pat… | Early_Phase1 | Infertility | Completed | 2020-09-01 | 2024-12-30 | ClinicalTrials.gov |
| NCT05274100 | Study of Intravenous and Subcutaneous Administration of Risankizumab in Healthy… | Phase1 | Healthy Volunteers | Completed | 2020-09-01 | 2021-07-06 | ClinicalTrials.gov |
| NCT04445025 | Comparison Elagolix vs Depot Leuprolide Prior to Frozen Embryo Transfers in Pat… | Early_Phase1 | Infertility | Completed | 2020-09-01 | 2024-12-30 | ClinicalTrials.gov |
| NCT05274100 | Study of Intravenous and Subcutaneous Administration of Risankizumab in Healthy… | Phase1 | Healthy Volunteers | Completed | 2020-09-01 | 2021-07-06 | ClinicalTrials.gov |
| NCT04445025 | Comparison Elagolix vs Depot Leuprolide Prior to Frozen Embryo Transfers in Pat… | Early_Phase1 | Infertility | Completed | 2020-09-01 | 2024-12-30 | ClinicalTrials.gov |
| NCT04468984 | Study of Oral Navitoclax Tablet in Combination With Oral Ruxolitinib Tablet Ver… | Phase3 | Myelofibrosis (MF) | Active_Not_Recruiting | 2020-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04468984 | Study of Oral Navitoclax Tablet in Combination With Oral Ruxolitinib Tablet Ver… | Phase3 | Myelofibrosis (MF) | Active_Not_Recruiting | 2020-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04468984 | Study of Oral Navitoclax Tablet in Combination With Oral Ruxolitinib Tablet Ver… | Phase3 | Myelofibrosis (MF) | Active_Not_Recruiting | 2020-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04468984 | Study of Oral Navitoclax Tablet in Combination With Oral Ruxolitinib Tablet Ver… | Phase3 | Myelofibrosis (MF) | Active_Not_Recruiting | 2020-08-31 | 2026-12-01 | ClinicalTrials.gov |
| NCT04500418 | Charité Trial of Cenicriviroc (CVC) Treatment for COVID-19 Patients | Phase2 | Covid19 | Terminated | 2020-08-25 | 2021-07-27 | ClinicalTrials.gov |
| NCT04514653 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants … | Phase2 | Neovascular Age-Related Macular Degeneration (nAMD) | Active_Not_Recruiting | 2020-08-25 | 2027-02-01 | ClinicalTrials.gov |
| NCT04514653 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants … | Phase2 | Neovascular Age-Related Macular Degeneration (nAMD) | Active_Not_Recruiting | 2020-08-25 | 2027-02-01 | ClinicalTrials.gov |
| NCT04500418 | Charité Trial of Cenicriviroc (CVC) Treatment for COVID-19 Patients | Phase2 | Covid19 | Terminated | 2020-08-25 | 2021-07-27 | ClinicalTrials.gov |
| NCT04514653 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants … | Phase2 | Neovascular Age-Related Macular Degeneration (nAMD) | Active_Not_Recruiting | 2020-08-25 | 2027-02-01 | ClinicalTrials.gov |
| NCT04500418 | Charité Trial of Cenicriviroc (CVC) Treatment for COVID-19 Patients | Phase2 | Covid19 | Terminated | 2020-08-25 | 2021-07-27 | ClinicalTrials.gov |
| NCT04500418 | Charité Trial of Cenicriviroc (CVC) Treatment for COVID-19 Patients | Phase2 | Covid19 | Terminated | 2020-08-25 | 2021-07-27 | ClinicalTrials.gov |
| NCT04514653 | RGX-314 Gene Therapy Administered in the Suprachoroidal Space for Participants … | Phase2 | Neovascular Age-Related Macular Degeneration (nAMD) | Active_Not_Recruiting | 2020-08-25 | 2027-02-01 | ClinicalTrials.gov |
| NCT04492020 | Study to Evaluate Oral Ubrogepant in the Acute Treatment of Migraine During the… | Phase3 | Migraine | Completed | 2020-08-21 | 2022-04-19 | ClinicalTrials.gov |
| NCT04492020 | Study to Evaluate Oral Ubrogepant in the Acute Treatment of Migraine During the… | Phase3 | Migraine | Completed | 2020-08-21 | 2022-04-19 | ClinicalTrials.gov |
| NCT04492020 | Study to Evaluate Oral Ubrogepant in the Acute Treatment of Migraine During the… | Phase3 | Migraine | Completed | 2020-08-21 | 2022-04-19 | ClinicalTrials.gov |
| NCT04492020 | Study to Evaluate Oral Ubrogepant in the Acute Treatment of Migraine During the… | Phase3 | Migraine | Completed | 2020-08-21 | 2022-04-19 | ClinicalTrials.gov |
| NCT04333576 | Study Of Oral Elagolix Tablets In Combination With Combined Oral Contraceptive … | Phase3 | Endometriosis | Active_Not_Recruiting | 2020-08-10 | 2027-07-01 | ClinicalTrials.gov |
| NCT04333576 | Study Of Oral Elagolix Tablets In Combination With Combined Oral Contraceptive … | Phase3 | Endometriosis | Active_Not_Recruiting | 2020-08-10 | 2027-07-01 | ClinicalTrials.gov |
| NCT04333576 | Study Of Oral Elagolix Tablets In Combination With Combined Oral Contraceptive … | Phase3 | Endometriosis | Active_Not_Recruiting | 2020-08-10 | 2027-07-01 | ClinicalTrials.gov |
| NCT04333576 | Study Of Oral Elagolix Tablets In Combination With Combined Oral Contraceptive … | Phase3 | Endometriosis | Active_Not_Recruiting | 2020-08-10 | 2027-07-01 | ClinicalTrials.gov |
| NCT04336982 | A Safety and Efficacy Study of CC-90009 Combinations in Subjects With Acute Mye… | Phase1 | Leukemia, Myeloid, Acute | Terminated | 2020-08-05 | 2024-04-05 | ClinicalTrials.gov |
| NCT04336982 | A Safety and Efficacy Study of CC-90009 Combinations in Subjects With Acute Mye… | Phase1 | Leukemia, Myeloid, Acute | Terminated | 2020-08-05 | 2024-04-05 | ClinicalTrials.gov |
| NCT04336982 | A Safety and Efficacy Study of CC-90009 Combinations in Subjects With Acute Mye… | Phase1 | Leukemia, Myeloid, Acute | Terminated | 2020-08-05 | 2024-04-05 | ClinicalTrials.gov |
| NCT04336982 | A Safety and Efficacy Study of CC-90009 Combinations in Subjects With Acute Mye… | Phase1 | Leukemia, Myeloid, Acute | Terminated | 2020-08-05 | 2024-04-05 | ClinicalTrials.gov |
| NCT04433442 | Study to Assess the Safety and Change in Disease Symptoms of Risankizumab (Skyr… | — | Psoriasis | Completed | 2020-08-04 | 2025-06-13 | ClinicalTrials.gov |
| NCT04433442 | Study to Assess the Safety and Change in Disease Symptoms of Risankizumab (Skyr… | — | Psoriasis | Completed | 2020-08-04 | 2025-06-13 | ClinicalTrials.gov |
| NCT04433442 | Study to Assess the Safety and Change in Disease Symptoms of Risankizumab (Skyr… | — | Psoriasis | Completed | 2020-08-04 | 2025-06-13 | ClinicalTrials.gov |
| NCT04433442 | Study to Assess the Safety and Change in Disease Symptoms of Risankizumab (Skyr… | — | Psoriasis | Completed | 2020-08-04 | 2025-06-13 | ClinicalTrials.gov |
| NCT04403763 | Phase 1/2 Study of AGN-241622 in Healthy Participants and Participants With Pre… | Phase1 | Presbyopia | Terminated | 2020-07-27 | 2022-12-05 | ClinicalTrials.gov |
| NCT04403763 | Phase 1/2 Study of AGN-241622 in Healthy Participants and Participants With Pre… | Phase1 | Presbyopia | Terminated | 2020-07-27 | 2022-12-05 | ClinicalTrials.gov |
| NCT04403763 | Phase 1/2 Study of AGN-241622 in Healthy Participants and Participants With Pre… | Phase1 | Presbyopia | Terminated | 2020-07-27 | 2022-12-05 | ClinicalTrials.gov |
| NCT04451772 | A Study of the Safety of Oral Elsubrutinib Capsules and Oral Upadacitinib Table… | Phase2 | Systemic Lupus Erythematosus (SLE) | Completed | 2020-07-27 | 2024-01-03 | ClinicalTrials.gov |
| NCT04403763 | Phase 1/2 Study of AGN-241622 in Healthy Participants and Participants With Pre… | Phase1 | Presbyopia | Terminated | 2020-07-27 | 2022-12-05 | ClinicalTrials.gov |
| NCT04451772 | A Study of the Safety of Oral Elsubrutinib Capsules and Oral Upadacitinib Table… | Phase2 | Systemic Lupus Erythematosus (SLE) | Completed | 2020-07-27 | 2024-01-03 | ClinicalTrials.gov |
| NCT04451772 | A Study of the Safety of Oral Elsubrutinib Capsules and Oral Upadacitinib Table… | Phase2 | Systemic Lupus Erythematosus (SLE) | Completed | 2020-07-27 | 2024-01-03 | ClinicalTrials.gov |
| NCT04451772 | A Study of the Safety of Oral Elsubrutinib Capsules and Oral Upadacitinib Table… | Phase2 | Systemic Lupus Erythematosus (SLE) | Completed | 2020-07-27 | 2024-01-03 | ClinicalTrials.gov |
| NCT04451720 | Study of Subcutaneous Risankizumab Injection to Assess Change in Palmoplantar P… | Phase3 | Palmoplantar Pustulosis (PPP) | Completed | 2020-07-20 | 2022-11-21 | ClinicalTrials.gov |
| NCT04451720 | Study of Subcutaneous Risankizumab Injection to Assess Change in Palmoplantar P… | Phase3 | Palmoplantar Pustulosis (PPP) | Completed | 2020-07-20 | 2022-11-21 | ClinicalTrials.gov |
| NCT04451720 | Study of Subcutaneous Risankizumab Injection to Assess Change in Palmoplantar P… | Phase3 | Palmoplantar Pustulosis (PPP) | Completed | 2020-07-20 | 2022-11-21 | ClinicalTrials.gov |
| NCT04451720 | Study of Subcutaneous Risankizumab Injection to Assess Change in Palmoplantar P… | Phase3 | Palmoplantar Pustulosis (PPP) | Completed | 2020-07-20 | 2022-11-21 | ClinicalTrials.gov |
| NCT04424641 | A Study on the Safety of GEN1044 (DuoBody®-CD3x5T4) in Patients With Malignant … | Phase1 | Locally Advanced or Metastatic Solid Tumor(s) | Terminated | 2020-07-15 | 2021-10-29 | ClinicalTrials.gov |
| NCT04424641 | A Study on the Safety of GEN1044 (DuoBody®-CD3x5T4) in Patients With Malignant … | Phase1 | Locally Advanced or Metastatic Solid Tumor(s) | Terminated | 2020-07-15 | 2021-10-29 | ClinicalTrials.gov |
| NCT04553627 | Feasibility of Producing the Appearance of a Gluteal Lift Post Cryolipolysis | Na | Subcutaneous Fat | Unknown | 2020-07-15 | 2021-05-30 | ClinicalTrials.gov |
| NCT04553627 | Feasibility of Producing the Appearance of a Gluteal Lift Post Cryolipolysis | Na | Subcutaneous Fat | Unknown | 2020-07-15 | 2021-05-30 | ClinicalTrials.gov |
| NCT04424641 | A Study on the Safety of GEN1044 (DuoBody®-CD3x5T4) in Patients With Malignant … | Phase1 | Locally Advanced or Metastatic Solid Tumor(s) | Terminated | 2020-07-15 | 2021-10-29 | ClinicalTrials.gov |
| NCT03832361 | Evaluation of Mirvetuximab Soravtansine (IMGN853) in Women With Folate Receptor… | Phase2 | Endometrial Cancer | Recruiting | 2020-07-15 | 2028-10-01 | ClinicalTrials.gov |
| NCT04424641 | A Study on the Safety of GEN1044 (DuoBody®-CD3x5T4) in Patients With Malignant … | Phase1 | Locally Advanced or Metastatic Solid Tumor(s) | Terminated | 2020-07-15 | 2021-10-29 | ClinicalTrials.gov |
| NCT04553627 | Feasibility of Producing the Appearance of a Gluteal Lift Post Cryolipolysis | Na | Subcutaneous Fat | Unknown | 2020-07-15 | 2021-05-30 | ClinicalTrials.gov |
| NCT03832361 | Evaluation of Mirvetuximab Soravtansine (IMGN853) in Women With Folate Receptor… | Phase2 | Endometrial Cancer | Recruiting | 2020-07-15 | 2028-10-01 | ClinicalTrials.gov |
| NCT03832361 | Evaluation of Mirvetuximab Soravtansine (IMGN853) in Women With Folate Receptor… | Phase2 | Endometrial Cancer | Recruiting | 2020-07-15 | 2028-10-01 | ClinicalTrials.gov |
| NCT03832361 | Evaluation of Mirvetuximab Soravtansine (IMGN853) in Women With Folate Receptor… | Phase2 | Endometrial Cancer | Recruiting | 2020-07-15 | 2028-10-01 | ClinicalTrials.gov |
| NCT04553627 | Feasibility of Producing the Appearance of a Gluteal Lift Post Cryolipolysis | Na | Subcutaneous Fat | Unknown | 2020-07-15 | 2021-05-30 | ClinicalTrials.gov |
| NCT04430855 | A Study of Oral Upadacitinib Tablet Compared to Placebo in Adult Participants W… | Phase2 | Hidradenitis Suppurativa (HS) | Completed | 2020-07-14 | 2022-01-25 | ClinicalTrials.gov |
| NCT04430855 | A Study of Oral Upadacitinib Tablet Compared to Placebo in Adult Participants W… | Phase2 | Hidradenitis Suppurativa (HS) | Completed | 2020-07-14 | 2022-01-25 | ClinicalTrials.gov |
| NCT04435600 | A Study of Subcutaneous Risankizumab Injection for Pediatric Participants With … | Phase3 | Psoriasis | Completed | 2020-07-14 | 2024-10-15 | ClinicalTrials.gov |
| NCT04430855 | A Study of Oral Upadacitinib Tablet Compared to Placebo in Adult Participants W… | Phase2 | Hidradenitis Suppurativa (HS) | Completed | 2020-07-14 | 2022-01-25 | ClinicalTrials.gov |
| NCT04435600 | A Study of Subcutaneous Risankizumab Injection for Pediatric Participants With … | Phase3 | Psoriasis | Completed | 2020-07-14 | 2024-10-15 | ClinicalTrials.gov |
| NCT04435600 | A Study of Subcutaneous Risankizumab Injection for Pediatric Participants With … | Phase3 | Psoriasis | Completed | 2020-07-14 | 2024-10-15 | ClinicalTrials.gov |
| NCT04430855 | A Study of Oral Upadacitinib Tablet Compared to Placebo in Adult Participants W… | Phase2 | Hidradenitis Suppurativa (HS) | Completed | 2020-07-14 | 2022-01-25 | ClinicalTrials.gov |
| NCT04435600 | A Study of Subcutaneous Risankizumab Injection for Pediatric Participants With … | Phase3 | Psoriasis | Completed | 2020-07-14 | 2024-10-15 | ClinicalTrials.gov |
| NCT04273139 | Ibrutinib + Venetoclax in Untreated WM | Phase2 | Waldenstrom Macroglobulinemia | Active_Not_Recruiting | 2020-07-09 | 2028-02-01 | ClinicalTrials.gov |
| NCT04273139 | Ibrutinib + Venetoclax in Untreated WM | Phase2 | Waldenstrom Macroglobulinemia | Active_Not_Recruiting | 2020-07-09 | 2028-02-01 | ClinicalTrials.gov |
| NCT04273139 | Ibrutinib + Venetoclax in Untreated WM | Phase2 | Waldenstrom Macroglobulinemia | Active_Not_Recruiting | 2020-07-09 | 2028-02-01 | ClinicalTrials.gov |
| NCT04273139 | Ibrutinib + Venetoclax in Untreated WM | Phase2 | Waldenstrom Macroglobulinemia | Active_Not_Recruiting | 2020-07-09 | 2028-02-01 | ClinicalTrials.gov |
| NCT04274907 | A Safety Study of Oral Venetoclax in Combination With Intravenous Pembrolizumab… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2020-06-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT04274907 | A Safety Study of Oral Venetoclax in Combination With Intravenous Pembrolizumab… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2020-06-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT04274907 | A Safety Study of Oral Venetoclax in Combination With Intravenous Pembrolizumab… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2020-06-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT04274907 | A Safety Study of Oral Venetoclax in Combination With Intravenous Pembrolizumab… | Phase1 | Non Small Cell Lung Cancer | Terminated | 2020-06-30 | 2021-02-02 | ClinicalTrials.gov |
| NCT04382885 | Cariprazine Pediatric ASD PK Study | Phase1 | Autism Spectrum Disorder | Completed | 2020-06-26 | 2021-12-10 | ClinicalTrials.gov |
| NCT04382885 | Cariprazine Pediatric ASD PK Study | Phase1 | Autism Spectrum Disorder | Completed | 2020-06-26 | 2021-12-10 | ClinicalTrials.gov |
| NCT04382885 | Cariprazine Pediatric ASD PK Study | Phase1 | Autism Spectrum Disorder | Completed | 2020-06-26 | 2021-12-10 | ClinicalTrials.gov |
| NCT04382885 | Cariprazine Pediatric ASD PK Study | Phase1 | Autism Spectrum Disorder | Completed | 2020-06-26 | 2021-12-10 | ClinicalTrials.gov |
| NCT04437433 | A Study Evaluating Oral Atogepant for the Prevention of Migraine in Japanese Pa… | Phase3 | Chronic Migraine | Completed | 2020-06-18 | 2024-06-11 | ClinicalTrials.gov |
| NCT04437433 | A Study Evaluating Oral Atogepant for the Prevention of Migraine in Japanese Pa… | Phase3 | Chronic Migraine | Completed | 2020-06-18 | 2024-06-11 | ClinicalTrials.gov |
| NCT04437433 | A Study Evaluating Oral Atogepant for the Prevention of Migraine in Japanese Pa… | Phase3 | Chronic Migraine | Completed | 2020-06-18 | 2024-06-11 | ClinicalTrials.gov |
| NCT04437433 | A Study Evaluating Oral Atogepant for the Prevention of Migraine in Japanese Pa… | Phase3 | Chronic Migraine | Completed | 2020-06-18 | 2024-06-11 | ClinicalTrials.gov |
| NCT04040621 | Single-dose PK Study of Ceftazidime-Avibactam In Hospitalized Children Receivin… | Phase1 | Hospitalized Children With Suspected or Confirmed Nosocomial Pneumonia | Terminated | 2020-06-15 | 2021-05-07 | ClinicalTrials.gov |
| NCT04040621 | Single-dose PK Study of Ceftazidime-Avibactam In Hospitalized Children Receivin… | Phase1 | Hospitalized Children With Suspected or Confirmed Nosocomial Pneumonia | Terminated | 2020-06-15 | 2021-05-07 | ClinicalTrials.gov |
| NCT04040621 | Single-dose PK Study of Ceftazidime-Avibactam In Hospitalized Children Receivin… | Phase1 | Hospitalized Children With Suspected or Confirmed Nosocomial Pneumonia | Terminated | 2020-06-15 | 2021-05-07 | ClinicalTrials.gov |
| NCT04040621 | Single-dose PK Study of Ceftazidime-Avibactam In Hospitalized Children Receivin… | Phase1 | Hospitalized Children With Suspected or Confirmed Nosocomial Pneumonia | Terminated | 2020-06-15 | 2021-05-07 | ClinicalTrials.gov |
| NCT04285580 | A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of… | Phase3 | Open-Angle Glaucoma | Completed | 2020-06-11 | 2022-05-14 | ClinicalTrials.gov |
| NCT04285580 | A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of… | Phase3 | Open-Angle Glaucoma | Completed | 2020-06-11 | 2022-05-14 | ClinicalTrials.gov |
| NCT04285580 | A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of… | Phase3 | Open-Angle Glaucoma | Completed | 2020-06-11 | 2022-05-14 | ClinicalTrials.gov |
| NCT04285580 | A Phase 3b Study Evaluating the 24-Hour Intraocular Pressure Lowering Effect of… | Phase3 | Open-Angle Glaucoma | Completed | 2020-06-11 | 2022-05-14 | ClinicalTrials.gov |
| NCT04379050 | Extension Study To Evaluate Safety And Tolerability Of 24-Hour Daily Exposure O… | Phase3 | Parkinson's Disease (PD) | Completed | 2020-06-08 | 2026-04-17 | ClinicalTrials.gov |
| NCT04379050 | Extension Study To Evaluate Safety And Tolerability Of 24-Hour Daily Exposure O… | Phase3 | Parkinson's Disease (PD) | Completed | 2020-06-08 | 2026-04-17 | ClinicalTrials.gov |
| NCT04379050 | Extension Study To Evaluate Safety And Tolerability Of 24-Hour Daily Exposure O… | Phase3 | Parkinson's Disease (PD) | Completed | 2020-06-08 | 2026-04-17 | ClinicalTrials.gov |
| NCT04379050 | Extension Study To Evaluate Safety And Tolerability Of 24-Hour Daily Exposure O… | Phase3 | Parkinson's Disease (PD) | Completed | 2020-06-08 | 2026-04-17 | ClinicalTrials.gov |
| NCT04375397 | Study of Oral Ibrutinib Capsules to Assess Respiratory Failure in Adult Partici… | Phase2 | CoronaVirus Induced Disease-2019 (COVID-19) | Completed | 2020-06-06 | 2021-06-08 | ClinicalTrials.gov |
| NCT04375397 | Study of Oral Ibrutinib Capsules to Assess Respiratory Failure in Adult Partici… | Phase2 | CoronaVirus Induced Disease-2019 (COVID-19) | Completed | 2020-06-06 | 2021-06-08 | ClinicalTrials.gov |
| NCT04375397 | Study of Oral Ibrutinib Capsules to Assess Respiratory Failure in Adult Partici… | Phase2 | CoronaVirus Induced Disease-2019 (COVID-19) | Completed | 2020-06-06 | 2021-06-08 | ClinicalTrials.gov |
| NCT04375397 | Study of Oral Ibrutinib Capsules to Assess Respiratory Failure in Adult Partici… | Phase2 | CoronaVirus Induced Disease-2019 (COVID-19) | Completed | 2020-06-06 | 2021-06-08 | ClinicalTrials.gov |
| NCT04417465 | First In Human Study With ABBV-CLS-579 When Given Alone and In Combination In P… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2020-06-03 | 2025-08-21 | ClinicalTrials.gov |
| NCT04417465 | First In Human Study With ABBV-CLS-579 When Given Alone and In Combination In P… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2020-06-03 | 2025-08-21 | ClinicalTrials.gov |
| NCT04417465 | First In Human Study With ABBV-CLS-579 When Given Alone and In Combination In P… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2020-06-03 | 2025-08-21 | ClinicalTrials.gov |
| NCT04417465 | First In Human Study With ABBV-CLS-579 When Given Alone and In Combination In P… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2020-06-03 | 2025-08-21 | ClinicalTrials.gov |
| NCT04372628 | Trial of Early Therapies During Non-hospitalized Outpatient Window for COVID-19 | Phase2 | COVID-19 | Completed | 2020-06-01 | 2022-01-18 | ClinicalTrials.gov |
| NCT04372628 | Trial of Early Therapies During Non-hospitalized Outpatient Window for COVID-19 | Phase2 | COVID-19 | Completed | 2020-06-01 | 2022-01-18 | ClinicalTrials.gov |
| NCT04372628 | Trial of Early Therapies During Non-hospitalized Outpatient Window for COVID-19 | Phase2 | COVID-19 | Completed | 2020-06-01 | 2022-01-18 | ClinicalTrials.gov |
| NCT04372628 | Trial of Early Therapies During Non-hospitalized Outpatient Window for COVID-19 | Phase2 | COVID-19 | Completed | 2020-06-01 | 2022-01-18 | ClinicalTrials.gov |
| NCT04352309 | Efficacy Study Of Oral Glecaprevir/Pibrentasvir Tablet In Pediatric (12 Years a… | — | Hepatitis C Virus (HCV) | Completed | 2020-05-29 | 2021-06-11 | ClinicalTrials.gov |
| NCT04352309 | Efficacy Study Of Oral Glecaprevir/Pibrentasvir Tablet In Pediatric (12 Years a… | — | Hepatitis C Virus (HCV) | Completed | 2020-05-29 | 2021-06-11 | ClinicalTrials.gov |
| NCT04352309 | Efficacy Study Of Oral Glecaprevir/Pibrentasvir Tablet In Pediatric (12 Years a… | — | Hepatitis C Virus (HCV) | Completed | 2020-05-29 | 2021-06-11 | ClinicalTrials.gov |
| NCT04352309 | Efficacy Study Of Oral Glecaprevir/Pibrentasvir Tablet In Pediatric (12 Years a… | — | Hepatitis C Virus (HCV) | Completed | 2020-05-29 | 2021-06-11 | ClinicalTrials.gov |
| NCT04414397 | A Study Evaluating JUVÉDERM® VOLUMA® XC Injectable Gel for Correction of Temple… | Phase3 | Temple Hollowing | Completed | 2020-05-28 | 2022-10-17 | ClinicalTrials.gov |
| NCT04414397 | A Study Evaluating JUVÉDERM® VOLUMA® XC Injectable Gel for Correction of Temple… | Phase3 | Temple Hollowing | Completed | 2020-05-28 | 2022-10-17 | ClinicalTrials.gov |
| NCT04414397 | A Study Evaluating JUVÉDERM® VOLUMA® XC Injectable Gel for Correction of Temple… | Phase3 | Temple Hollowing | Completed | 2020-05-28 | 2022-10-17 | ClinicalTrials.gov |
| NCT04414397 | A Study Evaluating JUVÉDERM® VOLUMA® XC Injectable Gel for Correction of Temple… | Phase3 | Temple Hollowing | Completed | 2020-05-28 | 2022-10-17 | ClinicalTrials.gov |
| NCT04254783 | A Study to Evaluate the Effect of Intravenous (IV) Infusions of Risankizumab on… | Phase1 | Ulcerative Colitis (UC) | Completed | 2020-05-27 | 2022-10-14 | ClinicalTrials.gov |
| NCT04254783 | A Study to Evaluate the Effect of Intravenous (IV) Infusions of Risankizumab on… | Phase1 | Ulcerative Colitis (UC) | Completed | 2020-05-27 | 2022-10-14 | ClinicalTrials.gov |
| NCT04254783 | A Study to Evaluate the Effect of Intravenous (IV) Infusions of Risankizumab on… | Phase1 | Ulcerative Colitis (UC) | Completed | 2020-05-27 | 2022-10-14 | ClinicalTrials.gov |
| NCT04254783 | A Study to Evaluate the Effect of Intravenous (IV) Infusions of Risankizumab on… | Phase1 | Ulcerative Colitis (UC) | Completed | 2020-05-27 | 2022-10-14 | ClinicalTrials.gov |
| NCT04366973 | A Study Describing the Care Cascade and Effectiveness and Safety of Glecaprevir… | — | Hepatitis C Virus (HCV) | Completed | 2020-05-26 | 2023-12-31 | ClinicalTrials.gov |
| NCT04366973 | A Study Describing the Care Cascade and Effectiveness and Safety of Glecaprevir… | — | Hepatitis C Virus (HCV) | Completed | 2020-05-26 | 2023-12-31 | ClinicalTrials.gov |
| NCT04366973 | A Study Describing the Care Cascade and Effectiveness and Safety of Glecaprevir… | — | Hepatitis C Virus (HCV) | Completed | 2020-05-26 | 2023-12-31 | ClinicalTrials.gov |
| NCT04366973 | A Study Describing the Care Cascade and Effectiveness and Safety of Glecaprevir… | — | Hepatitis C Virus (HCV) | Completed | 2020-05-26 | 2023-12-31 | ClinicalTrials.gov |
| NCT04274933 | A Study to Evaluate the Safety and Tolerability of Venetoclax Tablets in Combin… | Phase1 | Breast Cancer | Terminated | 2020-05-21 | 2020-10-08 | ClinicalTrials.gov |
| NCT04274933 | A Study to Evaluate the Safety and Tolerability of Venetoclax Tablets in Combin… | Phase1 | Breast Cancer | Terminated | 2020-05-21 | 2020-10-08 | ClinicalTrials.gov |
| NCT04274933 | A Study to Evaluate the Safety and Tolerability of Venetoclax Tablets in Combin… | Phase1 | Breast Cancer | Terminated | 2020-05-21 | 2020-10-08 | ClinicalTrials.gov |
| NCT04274933 | A Study to Evaluate the Safety and Tolerability of Venetoclax Tablets in Combin… | Phase1 | Breast Cancer | Terminated | 2020-05-21 | 2020-10-08 | ClinicalTrials.gov |
| NCT04390581 | A Study to Evaluate the Effect of Juvederm Volift With Lidocaine on Aging Hands… | Phase4 | Skin Depressions | Completed | 2020-05-20 | 2022-12-06 | ClinicalTrials.gov |
| NCT04390581 | A Study to Evaluate the Effect of Juvederm Volift With Lidocaine on Aging Hands… | Phase4 | Skin Depressions | Completed | 2020-05-20 | 2022-12-06 | ClinicalTrials.gov |
| NCT04390581 | A Study to Evaluate the Effect of Juvederm Volift With Lidocaine on Aging Hands… | Phase4 | Skin Depressions | Completed | 2020-05-20 | 2022-12-06 | ClinicalTrials.gov |
| NCT04390581 | A Study to Evaluate the Effect of Juvederm Volift With Lidocaine on Aging Hands… | Phase4 | Skin Depressions | Completed | 2020-05-20 | 2022-12-06 | ClinicalTrials.gov |
| NCT04178902 | A Study of the Safety and Tolerability of ABBV-467 in Adult Participants With R… | Phase1 | Multiple Myeloma (MM) | Terminated | 2020-05-19 | 2021-04-16 | ClinicalTrials.gov |
| NCT04178902 | A Study of the Safety and Tolerability of ABBV-467 in Adult Participants With R… | Phase1 | Multiple Myeloma (MM) | Terminated | 2020-05-19 | 2021-04-16 | ClinicalTrials.gov |
| NCT04178902 | A Study of the Safety and Tolerability of ABBV-467 in Adult Participants With R… | Phase1 | Multiple Myeloma (MM) | Terminated | 2020-05-19 | 2021-04-16 | ClinicalTrials.gov |
| NCT04320745 | A Study to Evaluate Androderm®'s Effect on Blood Pressure in Adult Hypogonodal … | Phase4 | Hypogonadism | Completed | 2020-05-19 | 2021-06-24 | ClinicalTrials.gov |
| NCT04320745 | A Study to Evaluate Androderm®'s Effect on Blood Pressure in Adult Hypogonodal … | Phase4 | Hypogonadism | Completed | 2020-05-19 | 2021-06-24 | ClinicalTrials.gov |
| NCT04320745 | A Study to Evaluate Androderm®'s Effect on Blood Pressure in Adult Hypogonodal … | Phase4 | Hypogonadism | Completed | 2020-05-19 | 2021-06-24 | ClinicalTrials.gov |
| NCT04320745 | A Study to Evaluate Androderm®'s Effect on Blood Pressure in Adult Hypogonodal … | Phase4 | Hypogonadism | Completed | 2020-05-19 | 2021-06-24 | ClinicalTrials.gov |
| NCT04178902 | A Study of the Safety and Tolerability of ABBV-467 in Adult Participants With R… | Phase1 | Multiple Myeloma (MM) | Terminated | 2020-05-19 | 2021-04-16 | ClinicalTrials.gov |
| NCT04274894 | A Study of the Effect of Topical Testosterone Replacement Therapy on Blood Pres… | Phase4 | Hypogonadism | Completed | 2020-05-12 | 2022-01-07 | ClinicalTrials.gov |
| NCT04274894 | A Study of the Effect of Topical Testosterone Replacement Therapy on Blood Pres… | Phase4 | Hypogonadism | Completed | 2020-05-12 | 2022-01-07 | ClinicalTrials.gov |
| NCT04274894 | A Study of the Effect of Topical Testosterone Replacement Therapy on Blood Pres… | Phase4 | Hypogonadism | Completed | 2020-05-12 | 2022-01-07 | ClinicalTrials.gov |
| NCT04274894 | A Study of the Effect of Topical Testosterone Replacement Therapy on Blood Pres… | Phase4 | Hypogonadism | Completed | 2020-05-12 | 2022-01-07 | ClinicalTrials.gov |
| NCT04315311 | Study Of Effects Of Oral CREON Capsules In Adult Participants With Exocrine Pan… | Phase4 | Exocrine Pancreatic Insufficiency (EPI) | Withdrawn | 2020-05-06 | 2021-09-22 | ClinicalTrials.gov |
| NCT04315311 | Study Of Effects Of Oral CREON Capsules In Adult Participants With Exocrine Pan… | Phase4 | Exocrine Pancreatic Insufficiency (EPI) | Withdrawn | 2020-05-06 | 2021-09-22 | ClinicalTrials.gov |
| NCT04315311 | Study Of Effects Of Oral CREON Capsules In Adult Participants With Exocrine Pan… | Phase4 | Exocrine Pancreatic Insufficiency (EPI) | Withdrawn | 2020-05-06 | 2021-09-22 | ClinicalTrials.gov |
| NCT04315311 | Study Of Effects Of Oral CREON Capsules In Adult Participants With Exocrine Pan… | Phase4 | Exocrine Pancreatic Insufficiency (EPI) | Withdrawn | 2020-05-06 | 2021-09-22 | ClinicalTrials.gov |
| NCT04272203 | A Study to Determine Safety, Tolerability, Pharmacokinetics, and Recommended Ph… | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2020-05-05 | 2022-06-27 | ClinicalTrials.gov |
| NCT04272203 | A Study to Determine Safety, Tolerability, Pharmacokinetics, and Recommended Ph… | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2020-05-05 | 2022-06-27 | ClinicalTrials.gov |
| NCT04272203 | A Study to Determine Safety, Tolerability, Pharmacokinetics, and Recommended Ph… | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2020-05-05 | 2022-06-27 | ClinicalTrials.gov |
| NCT04272203 | A Study to Determine Safety, Tolerability, Pharmacokinetics, and Recommended Ph… | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2020-05-05 | 2022-06-27 | ClinicalTrials.gov |
| NCT04340115 | Study To Assess Frequency Of Serious Infections In Clinical Practice In Japan F… | — | Rheumatoid Arthritis (RA) | Completed | 2020-04-24 | 2025-08-15 | ClinicalTrials.gov |
| NCT04340115 | Study To Assess Frequency Of Serious Infections In Clinical Practice In Japan F… | — | Rheumatoid Arthritis (RA) | Completed | 2020-04-24 | 2025-08-15 | ClinicalTrials.gov |
| NCT04340115 | Study To Assess Frequency Of Serious Infections In Clinical Practice In Japan F… | — | Rheumatoid Arthritis (RA) | Completed | 2020-04-24 | 2025-08-15 | ClinicalTrials.gov |
| NCT04340115 | Study To Assess Frequency Of Serious Infections In Clinical Practice In Japan F… | — | Rheumatoid Arthritis (RA) | Completed | 2020-04-24 | 2025-08-15 | ClinicalTrials.gov |
| NCT04411693 | Comparative Study of Dexamethasone Implant to Intravitreal Aflibercept in Subje… | Phase4 | Diabetic Macular Edema | Completed | 2020-04-10 | 2024-01-31 | ClinicalTrials.gov |
| NCT04411693 | Comparative Study of Dexamethasone Implant to Intravitreal Aflibercept in Subje… | Phase4 | Diabetic Macular Edema | Completed | 2020-04-10 | 2024-01-31 | ClinicalTrials.gov |
| NCT04411693 | Comparative Study of Dexamethasone Implant to Intravitreal Aflibercept in Subje… | Phase4 | Diabetic Macular Edema | Completed | 2020-04-10 | 2024-01-31 | ClinicalTrials.gov |
| NCT04411693 | Comparative Study of Dexamethasone Implant to Intravitreal Aflibercept in Subje… | Phase4 | Diabetic Macular Edema | Completed | 2020-04-10 | 2024-01-31 | ClinicalTrials.gov |
| NCT04330820 | Trial for Relapsed or Refractory AML Patients Combining Cytarabine and Mitoxant… | Phase1 | Relapsed Adult AML | Unknown | 2020-04-06 | 2025-08-01 | ClinicalTrials.gov |
| NCT04330820 | Trial for Relapsed or Refractory AML Patients Combining Cytarabine and Mitoxant… | Phase1 | Relapsed Adult AML | Unknown | 2020-04-06 | 2025-08-01 | ClinicalTrials.gov |
| NCT04330820 | Trial for Relapsed or Refractory AML Patients Combining Cytarabine and Mitoxant… | Phase1 | Relapsed Adult AML | Unknown | 2020-04-06 | 2025-08-01 | ClinicalTrials.gov |
| NCT04330820 | Trial for Relapsed or Refractory AML Patients Combining Cytarabine and Mitoxant… | Phase1 | Relapsed Adult AML | Unknown | 2020-04-06 | 2025-08-01 | ClinicalTrials.gov |
| NCT04178317 | A Study of the Safety and Efficacy of Venetoclax for Participants With Chronic … | — | Cancer, Chronic Lymphocytic Leukemia (CLL) | Completed | 2020-04-02 | 2025-08-18 | ClinicalTrials.gov |
| NCT04178317 | A Study of the Safety and Efficacy of Venetoclax for Participants With Chronic … | — | Cancer, Chronic Lymphocytic Leukemia (CLL) | Completed | 2020-04-02 | 2025-08-18 | ClinicalTrials.gov |
| NCT04261608 | A Retrospective Chart Review Study to Evaluate Safety of McGhan Single Lumen Ge… | — | Breast Augmentation | Completed | 2020-04-02 | 2020-07-04 | ClinicalTrials.gov |
| NCT04261608 | A Retrospective Chart Review Study to Evaluate Safety of McGhan Single Lumen Ge… | — | Breast Augmentation | Completed | 2020-04-02 | 2020-07-04 | ClinicalTrials.gov |
| NCT04261608 | A Retrospective Chart Review Study to Evaluate Safety of McGhan Single Lumen Ge… | — | Breast Augmentation | Completed | 2020-04-02 | 2020-07-04 | ClinicalTrials.gov |
| NCT04178317 | A Study of the Safety and Efficacy of Venetoclax for Participants With Chronic … | — | Cancer, Chronic Lymphocytic Leukemia (CLL) | Completed | 2020-04-02 | 2025-08-18 | ClinicalTrials.gov |
| NCT04261608 | A Retrospective Chart Review Study to Evaluate Safety of McGhan Single Lumen Ge… | — | Breast Augmentation | Completed | 2020-04-02 | 2020-07-04 | ClinicalTrials.gov |
| NCT04178317 | A Study of the Safety and Efficacy of Venetoclax for Participants With Chronic … | — | Cancer, Chronic Lymphocytic Leukemia (CLL) | Completed | 2020-04-02 | 2025-08-18 | ClinicalTrials.gov |
| NCT04306900 | TTX-030 in Combination With Immunotherapy and/or Chemotherapy in Subjects With … | Phase1 | Solid Tumor, Adult | Completed | 2020-03-30 | 2024-03-27 | ClinicalTrials.gov |
| NCT04306900 | TTX-030 in Combination With Immunotherapy and/or Chemotherapy in Subjects With … | Phase1 | Solid Tumor, Adult | Completed | 2020-03-30 | 2024-03-27 | ClinicalTrials.gov |
| NCT04306900 | TTX-030 in Combination With Immunotherapy and/or Chemotherapy in Subjects With … | Phase1 | Solid Tumor, Adult | Completed | 2020-03-30 | 2024-03-27 | ClinicalTrials.gov |
| NCT04306900 | TTX-030 in Combination With Immunotherapy and/or Chemotherapy in Subjects With … | Phase1 | Solid Tumor, Adult | Completed | 2020-03-30 | 2024-03-27 | ClinicalTrials.gov |
| NCT04102020 | A Study of Oral Venetoclax Tablets and Oral Azacitidine as Maintenance Therapy … | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2020-03-26 | 2026-02-20 | ClinicalTrials.gov |
| NCT04102020 | A Study of Oral Venetoclax Tablets and Oral Azacitidine as Maintenance Therapy … | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2020-03-26 | 2026-02-20 | ClinicalTrials.gov |
| NCT04102020 | A Study of Oral Venetoclax Tablets and Oral Azacitidine as Maintenance Therapy … | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2020-03-26 | 2026-02-20 | ClinicalTrials.gov |
| NCT04102020 | A Study of Oral Venetoclax Tablets and Oral Azacitidine as Maintenance Therapy … | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2020-03-26 | 2026-02-20 | ClinicalTrials.gov |
| NCT04330690 | Treatments for COVID-19: Canadian Arm of the SOLIDARITY Trial | Phase3 | COVID-19 | Unknown | 2020-03-18 | 2024-05-18 | ClinicalTrials.gov |
| NCT04330690 | Treatments for COVID-19: Canadian Arm of the SOLIDARITY Trial | Phase3 | COVID-19 | Unknown | 2020-03-18 | 2024-05-18 | ClinicalTrials.gov |
| NCT04330690 | Treatments for COVID-19: Canadian Arm of the SOLIDARITY Trial | Phase3 | COVID-19 | Unknown | 2020-03-18 | 2024-05-18 | ClinicalTrials.gov |
| NCT04330690 | Treatments for COVID-19: Canadian Arm of the SOLIDARITY Trial | Phase3 | COVID-19 | Unknown | 2020-03-18 | 2024-05-18 | ClinicalTrials.gov |
| NCT04253314 | A Study of the Effectiveness of Venetoclax Tablets in Adult Acute Myeloid Leuke… | — | Acute Myeloid Leukemia (AML) | Completed | 2020-03-13 | 2023-02-16 | ClinicalTrials.gov |
| NCT04253314 | A Study of the Effectiveness of Venetoclax Tablets in Adult Acute Myeloid Leuke… | — | Acute Myeloid Leukemia (AML) | Completed | 2020-03-13 | 2023-02-16 | ClinicalTrials.gov |
| NCT04253314 | A Study of the Effectiveness of Venetoclax Tablets in Adult Acute Myeloid Leuke… | — | Acute Myeloid Leukemia (AML) | Completed | 2020-03-13 | 2023-02-16 | ClinicalTrials.gov |
| NCT04253314 | A Study of the Effectiveness of Venetoclax Tablets in Adult Acute Myeloid Leuke… | — | Acute Myeloid Leukemia (AML) | Completed | 2020-03-13 | 2023-02-16 | ClinicalTrials.gov |
| NCT05217472 | An Efficacy and Safety Study of Injectable Ravagalimab to Assess Change in EULA… | Phase2 | Sjogren's Syndrome (SS) | Withdrawn | 2020-03-06 | 2022-05-15 | ClinicalTrials.gov |
| NCT05217472 | An Efficacy and Safety Study of Injectable Ravagalimab to Assess Change in EULA… | Phase2 | Sjogren's Syndrome (SS) | Withdrawn | 2020-03-06 | 2022-05-15 | ClinicalTrials.gov |
| NCT05217472 | An Efficacy and Safety Study of Injectable Ravagalimab to Assess Change in EULA… | Phase2 | Sjogren's Syndrome (SS) | Withdrawn | 2020-03-06 | 2022-05-15 | ClinicalTrials.gov |
| NCT05217472 | An Efficacy and Safety Study of Injectable Ravagalimab to Assess Change in EULA… | Phase2 | Sjogren's Syndrome (SS) | Withdrawn | 2020-03-06 | 2022-05-15 | ClinicalTrials.gov |
| NCT04030962 | A Study of the Drugs AGN-242428 and AGN-231868 in Participants With Dry Eye Dis… | Phase1 | Dry Eye Disease | Completed | 2020-03-04 | 2022-03-18 | ClinicalTrials.gov |
| NCT04030962 | A Study of the Drugs AGN-242428 and AGN-231868 in Participants With Dry Eye Dis… | Phase1 | Dry Eye Disease | Completed | 2020-03-04 | 2022-03-18 | ClinicalTrials.gov |
| NCT04030962 | A Study of the Drugs AGN-242428 and AGN-231868 in Participants With Dry Eye Dis… | Phase1 | Dry Eye Disease | Completed | 2020-03-04 | 2022-03-18 | ClinicalTrials.gov |
| NCT04030962 | A Study of the Drugs AGN-242428 and AGN-231868 in Participants With Dry Eye Dis… | Phase1 | Dry Eye Disease | Completed | 2020-03-04 | 2022-03-18 | ClinicalTrials.gov |
| NCT04127695 | A Study to Evaluate the Safety and Tolerability of ABBV-0805 in Patients With P… | Phase1 | Parkinson's Disease | Withdrawn | 2020-03-03 | 2020-06-16 | ClinicalTrials.gov |
| NCT04127695 | A Study to Evaluate the Safety and Tolerability of ABBV-0805 in Patients With P… | Phase1 | Parkinson's Disease | Withdrawn | 2020-03-03 | 2020-06-16 | ClinicalTrials.gov |
| NCT04127695 | A Study to Evaluate the Safety and Tolerability of ABBV-0805 in Patients With P… | Phase1 | Parkinson's Disease | Withdrawn | 2020-03-03 | 2020-06-16 | ClinicalTrials.gov |
| NCT04127695 | A Study to Evaluate the Safety and Tolerability of ABBV-0805 in Patients With P… | Phase1 | Parkinson's Disease | Withdrawn | 2020-03-03 | 2020-06-16 | ClinicalTrials.gov |
| NCT05401136 | Evaluating the Chain of Addiction Care (CAC) | — | Hepatitis C, Chronic | Unknown | 2020-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT05401136 | Evaluating the Chain of Addiction Care (CAC) | — | Hepatitis C, Chronic | Unknown | 2020-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT05401136 | Evaluating the Chain of Addiction Care (CAC) | — | Hepatitis C, Chronic | Unknown | 2020-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT05401136 | Evaluating the Chain of Addiction Care (CAC) | — | Hepatitis C, Chronic | Unknown | 2020-03-01 | 2023-12-01 | ClinicalTrials.gov |
| NCT04161885 | A Study Evaluating Safety and Efficacy of Venetoclax in Combination With Azacit… | Phase3 | Acute Myeloid Leukemia (AML) | Terminated | 2020-02-26 | 2025-09-23 | ClinicalTrials.gov |
| NCT04161885 | A Study Evaluating Safety and Efficacy of Venetoclax in Combination With Azacit… | Phase3 | Acute Myeloid Leukemia (AML) | Terminated | 2020-02-26 | 2025-09-23 | ClinicalTrials.gov |
| NCT04161885 | A Study Evaluating Safety and Efficacy of Venetoclax in Combination With Azacit… | Phase3 | Acute Myeloid Leukemia (AML) | Terminated | 2020-02-26 | 2025-09-23 | ClinicalTrials.gov |
| NCT04161885 | A Study Evaluating Safety and Efficacy of Venetoclax in Combination With Azacit… | Phase3 | Acute Myeloid Leukemia (AML) | Terminated | 2020-02-26 | 2025-09-23 | ClinicalTrials.gov |
| NCT03859869 | A Study of Creon (Pancrelipase) in Resected and Non-resected Pancreatic Cancer … | Phase4 | Exocrine Pancreatic Insufficiency (EPI) | Terminated | 2020-02-25 | 2022-03-23 | ClinicalTrials.gov |
| NCT03859869 | A Study of Creon (Pancrelipase) in Resected and Non-resected Pancreatic Cancer … | Phase4 | Exocrine Pancreatic Insufficiency (EPI) | Terminated | 2020-02-25 | 2022-03-23 | ClinicalTrials.gov |
| NCT03859869 | A Study of Creon (Pancrelipase) in Resected and Non-resected Pancreatic Cancer … | Phase4 | Exocrine Pancreatic Insufficiency (EPI) | Terminated | 2020-02-25 | 2022-03-23 | ClinicalTrials.gov |
| NCT03859869 | A Study of Creon (Pancrelipase) in Resected and Non-resected Pancreatic Cancer … | Phase4 | Exocrine Pancreatic Insufficiency (EPI) | Terminated | 2020-02-25 | 2022-03-23 | ClinicalTrials.gov |
| NCT04189627 | A Study of the Effectiveness and Clinical Practice Use of Glecaprevir/Pibrentas… | — | Hepatitis C Virus (HCV) | Completed | 2020-02-17 | 2021-06-24 | ClinicalTrials.gov |
| NCT04262791 | A Non-Drug Study Detecting And Quantifying Nocturnal Scratch Behaviors From Wri… | Phase1 | Atopic Dermatitis | Terminated | 2020-02-17 | 2022-01-31 | ClinicalTrials.gov |
| NCT04189627 | A Study of the Effectiveness and Clinical Practice Use of Glecaprevir/Pibrentas… | — | Hepatitis C Virus (HCV) | Completed | 2020-02-17 | 2021-06-24 | ClinicalTrials.gov |
| NCT04262791 | A Non-Drug Study Detecting And Quantifying Nocturnal Scratch Behaviors From Wri… | Phase1 | Atopic Dermatitis | Terminated | 2020-02-17 | 2022-01-31 | ClinicalTrials.gov |
| NCT04262791 | A Non-Drug Study Detecting And Quantifying Nocturnal Scratch Behaviors From Wri… | Phase1 | Atopic Dermatitis | Terminated | 2020-02-17 | 2022-01-31 | ClinicalTrials.gov |
| NCT04189627 | A Study of the Effectiveness and Clinical Practice Use of Glecaprevir/Pibrentas… | — | Hepatitis C Virus (HCV) | Completed | 2020-02-17 | 2021-06-24 | ClinicalTrials.gov |
| NCT04189627 | A Study of the Effectiveness and Clinical Practice Use of Glecaprevir/Pibrentas… | — | Hepatitis C Virus (HCV) | Completed | 2020-02-17 | 2021-06-24 | ClinicalTrials.gov |
| NCT04262791 | A Non-Drug Study Detecting And Quantifying Nocturnal Scratch Behaviors From Wri… | Phase1 | Atopic Dermatitis | Terminated | 2020-02-17 | 2022-01-31 | ClinicalTrials.gov |
| NCT04189614 | An Efficacy and Safety Study of Cofetuzumab Pelidotin in Participants With PTK7… | Phase1 | Cancer | Terminated | 2020-02-13 | 2026-05-07 | ClinicalTrials.gov |
| NCT04189614 | An Efficacy and Safety Study of Cofetuzumab Pelidotin in Participants With PTK7… | Phase1 | Cancer | Terminated | 2020-02-13 | 2026-05-07 | ClinicalTrials.gov |
| NCT04189614 | An Efficacy and Safety Study of Cofetuzumab Pelidotin in Participants With PTK7… | Phase1 | Cancer | Terminated | 2020-02-13 | 2026-05-07 | ClinicalTrials.gov |
| NCT04189614 | An Efficacy and Safety Study of Cofetuzumab Pelidotin in Participants With PTK7… | Phase1 | Cancer | Terminated | 2020-02-13 | 2026-05-07 | ClinicalTrials.gov |
| NCT04197141 | Hypofractionated Whole-Pelvis Radiotherapy (WPRT) vs Conventionally-Fractionate… | Phase2 | Prostate Cancer | Active_Not_Recruiting | 2020-02-07 | 2027-03-01 | ClinicalTrials.gov |
| NCT04197141 | Hypofractionated Whole-Pelvis Radiotherapy (WPRT) vs Conventionally-Fractionate… | Phase2 | Prostate Cancer | Active_Not_Recruiting | 2020-02-07 | 2027-03-01 | ClinicalTrials.gov |
| NCT04197141 | Hypofractionated Whole-Pelvis Radiotherapy (WPRT) vs Conventionally-Fractionate… | Phase2 | Prostate Cancer | Active_Not_Recruiting | 2020-02-07 | 2027-03-01 | ClinicalTrials.gov |
| NCT04197141 | Hypofractionated Whole-Pelvis Radiotherapy (WPRT) vs Conventionally-Fractionate… | Phase2 | Prostate Cancer | Active_Not_Recruiting | 2020-02-07 | 2027-03-01 | ClinicalTrials.gov |
| NCT04267536 | An Observational Study to Evaluate Impact of CRP-Level on Real World Effectiven… | — | Rheumatoid Arthritis (RA) | Completed | 2020-02-06 | 2022-02-01 | ClinicalTrials.gov |
| NCT04267536 | An Observational Study to Evaluate Impact of CRP-Level on Real World Effectiven… | — | Rheumatoid Arthritis (RA) | Completed | 2020-02-06 | 2022-02-01 | ClinicalTrials.gov |
| NCT04267536 | An Observational Study to Evaluate Impact of CRP-Level on Real World Effectiven… | — | Rheumatoid Arthritis (RA) | Completed | 2020-02-06 | 2022-02-01 | ClinicalTrials.gov |
| NCT04267536 | An Observational Study to Evaluate Impact of CRP-Level on Real World Effectiven… | — | Rheumatoid Arthritis (RA) | Completed | 2020-02-06 | 2022-02-01 | ClinicalTrials.gov |
| NCT04161898 | A Study to Evaluate the Efficacy and Safety of Upadacitinib in Participants Wit… | Phase3 | Takayasu Arteritis (TAK) | Active_Not_Recruiting | 2020-02-04 | 2028-08-01 | ClinicalTrials.gov |
| NCT04161898 | A Study to Evaluate the Efficacy and Safety of Upadacitinib in Participants Wit… | Phase3 | Takayasu Arteritis (TAK) | Active_Not_Recruiting | 2020-02-04 | 2028-08-01 | ClinicalTrials.gov |
| NCT04161898 | A Study to Evaluate the Efficacy and Safety of Upadacitinib in Participants Wit… | Phase3 | Takayasu Arteritis (TAK) | Active_Not_Recruiting | 2020-02-04 | 2028-08-01 | ClinicalTrials.gov |
| NCT04161898 | A Study to Evaluate the Efficacy and Safety of Upadacitinib in Participants Wit… | Phase3 | Takayasu Arteritis (TAK) | Active_Not_Recruiting | 2020-02-04 | 2028-08-01 | ClinicalTrials.gov |
| NCT04198415 | A Study of the Safety and Efficacy of Venetoclax in Japanese Participants With … | — | Cancer | Completed | 2020-02-03 | 2022-10-21 | ClinicalTrials.gov |
| NCT04198415 | A Study of the Safety and Efficacy of Venetoclax in Japanese Participants With … | — | Cancer | Completed | 2020-02-03 | 2022-10-21 | ClinicalTrials.gov |
| NCT04198415 | A Study of the Safety and Efficacy of Venetoclax in Japanese Participants With … | — | Cancer | Completed | 2020-02-03 | 2022-10-21 | ClinicalTrials.gov |
| NCT04198415 | A Study of the Safety and Efficacy of Venetoclax in Japanese Participants With … | — | Cancer | Completed | 2020-02-03 | 2022-10-21 | ClinicalTrials.gov |
| NCT04223804 | A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-1… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2020-01-30 | 2023-02-27 | ClinicalTrials.gov |
| NCT04223804 | A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-1… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2020-01-30 | 2023-02-27 | ClinicalTrials.gov |
| NCT04223804 | A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-1… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2020-01-30 | 2023-02-27 | ClinicalTrials.gov |
| NCT04223804 | A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of ABBV-1… | Phase1 | Human Immunodeficiency Virus (HIV) | Completed | 2020-01-30 | 2023-02-27 | ClinicalTrials.gov |
| NCT04244175 | A Trial of the Efficacy and Safety of CVL-865 as Adjunctive Therapy in the Trea… | Phase2 | Seizures | Completed | 2020-01-27 | 2024-05-21 | ClinicalTrials.gov |
| NCT04244175 | A Trial of the Efficacy and Safety of CVL-865 as Adjunctive Therapy in the Trea… | Phase2 | Seizures | Completed | 2020-01-27 | 2024-05-21 | ClinicalTrials.gov |
| NCT04244175 | A Trial of the Efficacy and Safety of CVL-865 as Adjunctive Therapy in the Trea… | Phase2 | Seizures | Completed | 2020-01-27 | 2024-05-21 | ClinicalTrials.gov |
| NCT04244175 | A Trial of the Efficacy and Safety of CVL-865 as Adjunctive Therapy in the Trea… | Phase2 | Seizures | Completed | 2020-01-27 | 2024-05-21 | ClinicalTrials.gov |
| NCT04196283 | A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminar… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2020-01-22 | 2022-10-27 | ClinicalTrials.gov |
| NCT04196283 | A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminar… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2020-01-22 | 2022-10-27 | ClinicalTrials.gov |
| NCT03818542 | A Study to Assess the Effects of Multiple Study Drug Regimens in Subjects With … | Phase1 | Head and Neck Cancer | Terminated | 2020-01-22 | 2020-09-23 | ClinicalTrials.gov |
| NCT04196283 | A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminar… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2020-01-22 | 2022-10-27 | ClinicalTrials.gov |
| NCT03818542 | A Study to Assess the Effects of Multiple Study Drug Regimens in Subjects With … | Phase1 | Head and Neck Cancer | Terminated | 2020-01-22 | 2020-09-23 | ClinicalTrials.gov |
| NCT03818542 | A Study to Assess the Effects of Multiple Study Drug Regimens in Subjects With … | Phase1 | Head and Neck Cancer | Terminated | 2020-01-22 | 2020-09-23 | ClinicalTrials.gov |
| NCT04196283 | A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminar… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2020-01-22 | 2022-10-27 | ClinicalTrials.gov |
| NCT03818542 | A Study to Assess the Effects of Multiple Study Drug Regimens in Subjects With … | Phase1 | Head and Neck Cancer | Terminated | 2020-01-22 | 2020-09-23 | ClinicalTrials.gov |
| NCT04140175 | A Study of Women Receiving Standard of Care (SOC) for the Treatment of Pelvic P… | — | Endometriosis | Terminated | 2020-01-20 | 2020-11-19 | ClinicalTrials.gov |
| NCT04140175 | A Study of Women Receiving Standard of Care (SOC) for the Treatment of Pelvic P… | — | Endometriosis | Terminated | 2020-01-20 | 2020-11-19 | ClinicalTrials.gov |
| NCT04140175 | A Study of Women Receiving Standard of Care (SOC) for the Treatment of Pelvic P… | — | Endometriosis | Terminated | 2020-01-20 | 2020-11-19 | ClinicalTrials.gov |
| NCT04140175 | A Study of Women Receiving Standard of Care (SOC) for the Treatment of Pelvic P… | — | Endometriosis | Terminated | 2020-01-20 | 2020-11-19 | ClinicalTrials.gov |
| NCT04195698 | Open-Label Extension Study of Upadacitinib in Adult Participants With Moderate … | Phase3 | Atopic Dermatitis | Completed | 2020-01-15 | 2023-09-11 | ClinicalTrials.gov |
| NCT04195698 | Open-Label Extension Study of Upadacitinib in Adult Participants With Moderate … | Phase3 | Atopic Dermatitis | Completed | 2020-01-15 | 2023-09-11 | ClinicalTrials.gov |
| NCT04195698 | Open-Label Extension Study of Upadacitinib in Adult Participants With Moderate … | Phase3 | Atopic Dermatitis | Completed | 2020-01-15 | 2023-09-11 | ClinicalTrials.gov |
| NCT04195698 | Open-Label Extension Study of Upadacitinib in Adult Participants With Moderate … | Phase3 | Atopic Dermatitis | Completed | 2020-01-15 | 2023-09-11 | ClinicalTrials.gov |
| NCT04126031 | Evaluation of Pharmacokinetics, Safety, and Tolerability of Ceftazidime-avibact… | Phase2 | Gram-negative Bacterial Infection | Terminated | 2020-01-14 | 2022-12-30 | ClinicalTrials.gov |
| NCT04183608 | A Trial COmparing staNdard of Care Versus Treat to Target With telemonitoRing a… | Phase4 | Ulcerative Colitis | Recruiting | 2020-01-14 | 2028-05-01 | ClinicalTrials.gov |
| NCT04126031 | Evaluation of Pharmacokinetics, Safety, and Tolerability of Ceftazidime-avibact… | Phase2 | Gram-negative Bacterial Infection | Terminated | 2020-01-14 | 2022-12-30 | ClinicalTrials.gov |
| NCT04183608 | A Trial COmparing staNdard of Care Versus Treat to Target With telemonitoRing a… | Phase4 | Ulcerative Colitis | Recruiting | 2020-01-14 | 2028-05-01 | ClinicalTrials.gov |
| NCT03873493 | A Study Evaluating the Efficacy of Venetoclax Plus Ibrutinib in Participants Wi… | Phase2 | Leukemia | Completed | 2020-01-14 | 2021-11-04 | ClinicalTrials.gov |
| NCT04183608 | A Trial COmparing staNdard of Care Versus Treat to Target With telemonitoRing a… | Phase4 | Ulcerative Colitis | Recruiting | 2020-01-14 | 2028-05-01 | ClinicalTrials.gov |
| NCT03873493 | A Study Evaluating the Efficacy of Venetoclax Plus Ibrutinib in Participants Wi… | Phase2 | Leukemia | Completed | 2020-01-14 | 2021-11-04 | ClinicalTrials.gov |
| NCT03873493 | A Study Evaluating the Efficacy of Venetoclax Plus Ibrutinib in Participants Wi… | Phase2 | Leukemia | Completed | 2020-01-14 | 2021-11-04 | ClinicalTrials.gov |
| NCT04183608 | A Trial COmparing staNdard of Care Versus Treat to Target With telemonitoRing a… | Phase4 | Ulcerative Colitis | Recruiting | 2020-01-14 | 2028-05-01 | ClinicalTrials.gov |
| NCT04126031 | Evaluation of Pharmacokinetics, Safety, and Tolerability of Ceftazidime-avibact… | Phase2 | Gram-negative Bacterial Infection | Terminated | 2020-01-14 | 2022-12-30 | ClinicalTrials.gov |
| NCT03873493 | A Study Evaluating the Efficacy of Venetoclax Plus Ibrutinib in Participants Wi… | Phase2 | Leukemia | Completed | 2020-01-14 | 2021-11-04 | ClinicalTrials.gov |
| NCT04126031 | Evaluation of Pharmacokinetics, Safety, and Tolerability of Ceftazidime-avibact… | Phase2 | Gram-negative Bacterial Infection | Terminated | 2020-01-14 | 2022-12-30 | ClinicalTrials.gov |
| NCT04159779 | A Study of Clinical Outcomes in Chronic Lymphocytic Leukemia (CLL) Patients Tre… | — | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2020-01-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT04159779 | A Study of Clinical Outcomes in Chronic Lymphocytic Leukemia (CLL) Patients Tre… | — | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2020-01-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT04159779 | A Study of Clinical Outcomes in Chronic Lymphocytic Leukemia (CLL) Patients Tre… | — | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2020-01-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT04159779 | A Study of Clinical Outcomes in Chronic Lymphocytic Leukemia (CLL) Patients Tre… | — | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2020-01-13 | 2026-06-30 | ClinicalTrials.gov |
| NCT04223193 | Flexible-Dose Trial in Early Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2020-01-06 | 2024-10-01 | ClinicalTrials.gov |
| NCT04223193 | Flexible-Dose Trial in Early Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2020-01-06 | 2024-10-01 | ClinicalTrials.gov |
| NCT04223193 | Flexible-Dose Trial in Early Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2020-01-06 | 2024-10-01 | ClinicalTrials.gov |
| NCT04223193 | Flexible-Dose Trial in Early Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2020-01-06 | 2024-10-01 | ClinicalTrials.gov |
| NCT04240535 | Evaluation of the Safety and Efficacy of OnabotulinumtoxinA to the Depressor An… | Phase4 | Aging | Not_Yet_Recruiting | 2020-01-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT04240535 | Evaluation of the Safety and Efficacy of OnabotulinumtoxinA to the Depressor An… | Phase4 | Aging | Not_Yet_Recruiting | 2020-01-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT04240535 | Evaluation of the Safety and Efficacy of OnabotulinumtoxinA to the Depressor An… | Phase4 | Aging | Not_Yet_Recruiting | 2020-01-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT04240535 | Evaluation of the Safety and Efficacy of OnabotulinumtoxinA to the Depressor An… | Phase4 | Aging | Not_Yet_Recruiting | 2020-01-01 | 2020-07-01 | ClinicalTrials.gov |
| NCT04209855 | A Study of Mirvetuximab Soravtansine vs. Investigator's Choice (IC) of Chemothe… | Phase3 | Epithelial Ovarian Cancer | Completed | 2019-12-31 | 2024-10-29 | ClinicalTrials.gov |
| NCT04209855 | A Study of Mirvetuximab Soravtansine vs. Investigator's Choice (IC) of Chemothe… | Phase3 | Epithelial Ovarian Cancer | Completed | 2019-12-31 | 2024-10-29 | ClinicalTrials.gov |
| NCT04209855 | A Study of Mirvetuximab Soravtansine vs. Investigator's Choice (IC) of Chemothe… | Phase3 | Epithelial Ovarian Cancer | Completed | 2019-12-31 | 2024-10-29 | ClinicalTrials.gov |
| NCT04209855 | A Study of Mirvetuximab Soravtansine vs. Investigator's Choice (IC) of Chemothe… | Phase3 | Epithelial Ovarian Cancer | Completed | 2019-12-31 | 2024-10-29 | ClinicalTrials.gov |
| NCT04214028 | A Study of the Safety, Effectiveness and Clinical Use of Maviret in Adolescent … | — | Hepatitis C Virus (HCV) | Completed | 2019-12-26 | 2024-08-01 | ClinicalTrials.gov |
| NCT04214028 | A Study of the Safety, Effectiveness and Clinical Use of Maviret in Adolescent … | — | Hepatitis C Virus (HCV) | Completed | 2019-12-26 | 2024-08-01 | ClinicalTrials.gov |
| NCT04214028 | A Study of the Safety, Effectiveness and Clinical Use of Maviret in Adolescent … | — | Hepatitis C Virus (HCV) | Completed | 2019-12-26 | 2024-08-01 | ClinicalTrials.gov |
| NCT04214028 | A Study of the Safety, Effectiveness and Clinical Use of Maviret in Adolescent … | — | Hepatitis C Virus (HCV) | Completed | 2019-12-26 | 2024-08-01 | ClinicalTrials.gov |
| NCT04303897 | Real-world Evidence Study of XEN in Chinese Patients With Refractory Glaucoma | — | Refractory Glaucoma | Completed | 2019-12-19 | 2022-03-03 | ClinicalTrials.gov |
| NCT04303897 | Real-world Evidence Study of XEN in Chinese Patients With Refractory Glaucoma | — | Refractory Glaucoma | Completed | 2019-12-19 | 2022-03-03 | ClinicalTrials.gov |
| NCT04303897 | Real-world Evidence Study of XEN in Chinese Patients With Refractory Glaucoma | — | Refractory Glaucoma | Completed | 2019-12-19 | 2022-03-03 | ClinicalTrials.gov |
| NCT04303897 | Real-world Evidence Study of XEN in Chinese Patients With Refractory Glaucoma | — | Refractory Glaucoma | Completed | 2019-12-19 | 2022-03-03 | ClinicalTrials.gov |
| NCT04201093 | Fixed-Dose Trial in Early Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2019-12-13 | 2024-06-28 | ClinicalTrials.gov |
| NCT04201093 | Fixed-Dose Trial in Early Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2019-12-13 | 2024-06-28 | ClinicalTrials.gov |
| NCT04201093 | Fixed-Dose Trial in Early Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2019-12-13 | 2024-06-28 | ClinicalTrials.gov |
| NCT04201093 | Fixed-Dose Trial in Early Parkinson's Disease (PD) | Phase3 | Parkinson Disease | Completed | 2019-12-13 | 2024-06-28 | ClinicalTrials.gov |
| NCT03969888 | A Phase 2 Study of ABBV-3067 Alone and in Combination With ABBV-2222 | Phase2 | Cystic Fibrosis | Completed | 2019-12-11 | 2022-06-09 | ClinicalTrials.gov |
| NCT03969888 | A Phase 2 Study of ABBV-3067 Alone and in Combination With ABBV-2222 | Phase2 | Cystic Fibrosis | Completed | 2019-12-11 | 2022-06-09 | ClinicalTrials.gov |
| NCT03969888 | A Phase 2 Study of ABBV-3067 Alone and in Combination With ABBV-2222 | Phase2 | Cystic Fibrosis | Completed | 2019-12-11 | 2022-06-09 | ClinicalTrials.gov |
| NCT03969888 | A Phase 2 Study of ABBV-3067 Alone and in Combination With ABBV-2222 | Phase2 | Cystic Fibrosis | Completed | 2019-12-11 | 2022-06-09 | ClinicalTrials.gov |
| NCT04080856 | Real-World Experience Study of Elagolix For the Treatment of Endometriosis in C… | — | Endometriosis | Completed | 2019-12-04 | 2021-09-27 | ClinicalTrials.gov |
| NCT04080856 | Real-World Experience Study of Elagolix For the Treatment of Endometriosis in C… | — | Endometriosis | Completed | 2019-12-04 | 2021-09-27 | ClinicalTrials.gov |
| NCT03993847 | CLassification of Axial SpondyloarthritiS Inception Cohort | — | Spondyloarthritis | Completed | 2019-12-04 | 2022-08-22 | ClinicalTrials.gov |
| NCT03993847 | CLassification of Axial SpondyloarthritiS Inception Cohort | — | Spondyloarthritis | Completed | 2019-12-04 | 2022-08-22 | ClinicalTrials.gov |
| NCT03993847 | CLassification of Axial SpondyloarthritiS Inception Cohort | — | Spondyloarthritis | Completed | 2019-12-04 | 2022-08-22 | ClinicalTrials.gov |
| NCT04080856 | Real-World Experience Study of Elagolix For the Treatment of Endometriosis in C… | — | Endometriosis | Completed | 2019-12-04 | 2021-09-27 | ClinicalTrials.gov |
| NCT04080856 | Real-World Experience Study of Elagolix For the Treatment of Endometriosis in C… | — | Endometriosis | Completed | 2019-12-04 | 2021-09-27 | ClinicalTrials.gov |
| NCT03993847 | CLassification of Axial SpondyloarthritiS Inception Cohort | — | Spondyloarthritis | Completed | 2019-12-04 | 2022-08-22 | ClinicalTrials.gov |
| NCT04169373 | A Study to Evaluate Efficacy and Safety of Upadacitinib in Adults With Axial Sp… | Phase3 | Spondyloarthritis | Completed | 2019-11-26 | 2025-02-28 | ClinicalTrials.gov |
| NCT04169373 | A Study to Evaluate Efficacy and Safety of Upadacitinib in Adults With Axial Sp… | Phase3 | Spondyloarthritis | Completed | 2019-11-26 | 2025-02-28 | ClinicalTrials.gov |
| NCT04169373 | A Study to Evaluate Efficacy and Safety of Upadacitinib in Adults With Axial Sp… | Phase3 | Spondyloarthritis | Completed | 2019-11-26 | 2025-02-28 | ClinicalTrials.gov |
| NCT04169373 | A Study to Evaluate Efficacy and Safety of Upadacitinib in Adults With Axial Sp… | Phase3 | Spondyloarthritis | Completed | 2019-11-26 | 2025-02-28 | ClinicalTrials.gov |
| NCT04042740 | Glecaprevir/Pibrentasvir Fixed-dose Combination Treatment for Acute Hepatitis C… | Phase2 | Hepatitis C Infection | Completed | 2019-11-20 | 2023-08-22 | ClinicalTrials.gov |
| NCT04042740 | Glecaprevir/Pibrentasvir Fixed-dose Combination Treatment for Acute Hepatitis C… | Phase2 | Hepatitis C Infection | Completed | 2019-11-20 | 2023-08-22 | ClinicalTrials.gov |
| NCT04042740 | Glecaprevir/Pibrentasvir Fixed-dose Combination Treatment for Acute Hepatitis C… | Phase2 | Hepatitis C Infection | Completed | 2019-11-20 | 2023-08-22 | ClinicalTrials.gov |
| NCT04042740 | Glecaprevir/Pibrentasvir Fixed-dose Combination Treatment for Acute Hepatitis C… | Phase2 | Hepatitis C Infection | Completed | 2019-11-20 | 2023-08-22 | ClinicalTrials.gov |
| NCT04166058 | Long-term Safety of Linaclotide in Pediatric Participants With FC or IBS-C | Phase3 | Irritable Bowel Syndrome With Constipation | Completed | 2019-11-19 | 2025-06-05 | ClinicalTrials.gov |
| NCT04166058 | Long-term Safety of Linaclotide in Pediatric Participants With FC or IBS-C | Phase3 | Irritable Bowel Syndrome With Constipation | Completed | 2019-11-19 | 2025-06-05 | ClinicalTrials.gov |
| NCT04166058 | Long-term Safety of Linaclotide in Pediatric Participants With FC or IBS-C | Phase3 | Irritable Bowel Syndrome With Constipation | Completed | 2019-11-19 | 2025-06-05 | ClinicalTrials.gov |
| NCT04166058 | Long-term Safety of Linaclotide in Pediatric Participants With FC or IBS-C | Phase3 | Irritable Bowel Syndrome With Constipation | Completed | 2019-11-19 | 2025-06-05 | ClinicalTrials.gov |
| NCT03844815 | Study of Venetoclax in Combination With Decitabine in Subjects With Acute Myelo… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-11-18 | 2027-12-10 | ClinicalTrials.gov |
| NCT03844815 | Study of Venetoclax in Combination With Decitabine in Subjects With Acute Myelo… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-11-18 | 2027-12-10 | ClinicalTrials.gov |
| NCT03844815 | Study of Venetoclax in Combination With Decitabine in Subjects With Acute Myelo… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-11-18 | 2027-12-10 | ClinicalTrials.gov |
| NCT03844815 | Study of Venetoclax in Combination With Decitabine in Subjects With Acute Myelo… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-11-18 | 2027-12-10 | ClinicalTrials.gov |
| NCT04102007 | A Study of the Safety and Efficacy of Risankizumab in Adult Participants With P… | Phase3 | Plaque Psoriasis | Completed | 2019-11-12 | 2022-11-07 | ClinicalTrials.gov |
| NCT04102007 | A Study of the Safety and Efficacy of Risankizumab in Adult Participants With P… | Phase3 | Plaque Psoriasis | Completed | 2019-11-12 | 2022-11-07 | ClinicalTrials.gov |
| NCT04102007 | A Study of the Safety and Efficacy of Risankizumab in Adult Participants With P… | Phase3 | Plaque Psoriasis | Completed | 2019-11-12 | 2022-11-07 | ClinicalTrials.gov |
| NCT04102007 | A Study of the Safety and Efficacy of Risankizumab in Adult Participants With P… | Phase3 | Plaque Psoriasis | Completed | 2019-11-12 | 2022-11-07 | ClinicalTrials.gov |
| NCT04041050 | A Study Evaluating Safety and Tolerability, and Pharmacokinetics of Navitoclax … | Phase1 | Myeloproliferative Neoplasm | Active_Not_Recruiting | 2019-11-08 | 2026-12-31 | ClinicalTrials.gov |
| NCT04041050 | A Study Evaluating Safety and Tolerability, and Pharmacokinetics of Navitoclax … | Phase1 | Myeloproliferative Neoplasm | Active_Not_Recruiting | 2019-11-08 | 2026-12-31 | ClinicalTrials.gov |
| NCT04041050 | A Study Evaluating Safety and Tolerability, and Pharmacokinetics of Navitoclax … | Phase1 | Myeloproliferative Neoplasm | Active_Not_Recruiting | 2019-11-08 | 2026-12-31 | ClinicalTrials.gov |
| NCT04041050 | A Study Evaluating Safety and Tolerability, and Pharmacokinetics of Navitoclax … | Phase1 | Myeloproliferative Neoplasm | Active_Not_Recruiting | 2019-11-08 | 2026-12-31 | ClinicalTrials.gov |
| NCT04086264 | IMGN632 as Monotherapy or With Venetoclax and/or Azacitidine for Participants W… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-11-06 | 2027-02-01 | ClinicalTrials.gov |
| NCT04086264 | IMGN632 as Monotherapy or With Venetoclax and/or Azacitidine for Participants W… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-11-06 | 2027-02-01 | ClinicalTrials.gov |
| NCT04086264 | IMGN632 as Monotherapy or With Venetoclax and/or Azacitidine for Participants W… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-11-06 | 2027-02-01 | ClinicalTrials.gov |
| NCT04086264 | IMGN632 as Monotherapy or With Venetoclax and/or Azacitidine for Participants W… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-11-06 | 2027-02-01 | ClinicalTrials.gov |
| NCT05247294 | Assessment of Fluctuating Parkinson's Disease With Sensor-based Home Monitoring | — | Parkinson Disease | Completed | 2019-11-03 | 2021-02-24 | ClinicalTrials.gov |
| NCT05247294 | Assessment of Fluctuating Parkinson's Disease With Sensor-based Home Monitoring | — | Parkinson Disease | Completed | 2019-11-03 | 2021-02-24 | ClinicalTrials.gov |
| NCT05247294 | Assessment of Fluctuating Parkinson's Disease With Sensor-based Home Monitoring | — | Parkinson Disease | Completed | 2019-11-03 | 2021-02-24 | ClinicalTrials.gov |
| NCT05247294 | Assessment of Fluctuating Parkinson's Disease With Sensor-based Home Monitoring | — | Parkinson Disease | Completed | 2019-11-03 | 2021-02-24 | ClinicalTrials.gov |
| NCT04138199 | A Study to Assess Effectiveness and Safety of Fixed Dose Combination of Lopinav… | — | HIV-1 Infection | Terminated | 2019-11-01 | 2020-07-08 | ClinicalTrials.gov |
| NCT03044795 | Response to PARP Inhibitor Predicted by the RAD51 Assay | Phase2 | Cancer | Withdrawn | 2019-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT04138199 | A Study to Assess Effectiveness and Safety of Fixed Dose Combination of Lopinav… | — | HIV-1 Infection | Terminated | 2019-11-01 | 2020-07-08 | ClinicalTrials.gov |
| NCT03044795 | Response to PARP Inhibitor Predicted by the RAD51 Assay | Phase2 | Cancer | Withdrawn | 2019-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT04138199 | A Study to Assess Effectiveness and Safety of Fixed Dose Combination of Lopinav… | — | HIV-1 Infection | Terminated | 2019-11-01 | 2020-07-08 | ClinicalTrials.gov |
| NCT04138199 | A Study to Assess Effectiveness and Safety of Fixed Dose Combination of Lopinav… | — | HIV-1 Infection | Terminated | 2019-11-01 | 2020-07-08 | ClinicalTrials.gov |
| NCT03044795 | Response to PARP Inhibitor Predicted by the RAD51 Assay | Phase2 | Cancer | Withdrawn | 2019-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT03044795 | Response to PARP Inhibitor Predicted by the RAD51 Assay | Phase2 | Cancer | Withdrawn | 2019-11-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT04142450 | CoolSculpting® the Upper Arms and Inner Thighs in Participants of Chinese Desce… | Na | Body Fat Disorder | Completed | 2019-10-27 | 2020-02-24 | ClinicalTrials.gov |
| NCT04142450 | CoolSculpting® the Upper Arms and Inner Thighs in Participants of Chinese Desce… | Na | Body Fat Disorder | Completed | 2019-10-27 | 2020-02-24 | ClinicalTrials.gov |
| NCT04142450 | CoolSculpting® the Upper Arms and Inner Thighs in Participants of Chinese Desce… | Na | Body Fat Disorder | Completed | 2019-10-27 | 2020-02-24 | ClinicalTrials.gov |
| NCT04142450 | CoolSculpting® the Upper Arms and Inner Thighs in Participants of Chinese Desce… | Na | Body Fat Disorder | Completed | 2019-10-27 | 2020-02-24 | ClinicalTrials.gov |
| NCT03924947 | A Study to Compare US Marketed Creon Manufactured With a Modernized Process at … | Phase4 | Cystic Fibrosis | Completed | 2019-10-23 | 2022-07-11 | ClinicalTrials.gov |
| NCT03924947 | A Study to Compare US Marketed Creon Manufactured With a Modernized Process at … | Phase4 | Cystic Fibrosis | Completed | 2019-10-23 | 2022-07-11 | ClinicalTrials.gov |
| NCT03924947 | A Study to Compare US Marketed Creon Manufactured With a Modernized Process at … | Phase4 | Cystic Fibrosis | Completed | 2019-10-23 | 2022-07-11 | ClinicalTrials.gov |
| NCT03924947 | A Study to Compare US Marketed Creon Manufactured With a Modernized Process at … | Phase4 | Cystic Fibrosis | Completed | 2019-10-23 | 2022-07-11 | ClinicalTrials.gov |
| NCT04110145 | Linaclotide Safety and Efficacy in 2 to 5-Year-Old Participants With Functional… | Phase2 | Functional Constipation | Completed | 2019-10-14 | 2021-04-20 | ClinicalTrials.gov |
| NCT04110145 | Linaclotide Safety and Efficacy in 2 to 5-Year-Old Participants With Functional… | Phase2 | Functional Constipation | Completed | 2019-10-14 | 2021-04-20 | ClinicalTrials.gov |
| NCT04110145 | Linaclotide Safety and Efficacy in 2 to 5-Year-Old Participants With Functional… | Phase2 | Functional Constipation | Completed | 2019-10-14 | 2021-04-20 | ClinicalTrials.gov |
| NCT04110145 | Linaclotide Safety and Efficacy in 2 to 5-Year-Old Participants With Functional… | Phase2 | Functional Constipation | Completed | 2019-10-14 | 2021-04-20 | ClinicalTrials.gov |
| NCT04124705 | A Study of Armour® Thyroid Compared to Synthetic T4 (Levothyroxine) in Previous… | Phase2 | Hypothyroidism | Completed | 2019-10-11 | 2021-06-22 | ClinicalTrials.gov |
| NCT04124705 | A Study of Armour® Thyroid Compared to Synthetic T4 (Levothyroxine) in Previous… | Phase2 | Hypothyroidism | Completed | 2019-10-11 | 2021-06-22 | ClinicalTrials.gov |
| NCT04124705 | A Study of Armour® Thyroid Compared to Synthetic T4 (Levothyroxine) in Previous… | Phase2 | Hypothyroidism | Completed | 2019-10-11 | 2021-06-22 | ClinicalTrials.gov |
| NCT04124705 | A Study of Armour® Thyroid Compared to Synthetic T4 (Levothyroxine) in Previous… | Phase2 | Hypothyroidism | Completed | 2019-10-11 | 2021-06-22 | ClinicalTrials.gov |
| NCT04206293 | A Study to Evaluate The Impact on Skin Quality Attributes by Juvederm® Volite I… | Na | Healthy Adults | Completed | 2019-10-08 | 2020-07-29 | ClinicalTrials.gov |
| NCT04206293 | A Study to Evaluate The Impact on Skin Quality Attributes by Juvederm® Volite I… | Na | Healthy Adults | Completed | 2019-10-08 | 2020-07-29 | ClinicalTrials.gov |
| NCT04206293 | A Study to Evaluate The Impact on Skin Quality Attributes by Juvederm® Volite I… | Na | Healthy Adults | Completed | 2019-10-08 | 2020-07-29 | ClinicalTrials.gov |
| NCT04206293 | A Study to Evaluate The Impact on Skin Quality Attributes by Juvederm® Volite I… | Na | Healthy Adults | Completed | 2019-10-08 | 2020-07-29 | ClinicalTrials.gov |
| NCT04026113 | Linaclotide Safety and Efficacy in Pediatric Participants, 6 to 17 Years of Age… | Phase3 | Functional Constipation | Completed | 2019-10-01 | 2024-05-29 | ClinicalTrials.gov |
| NCT04026113 | Linaclotide Safety and Efficacy in Pediatric Participants, 6 to 17 Years of Age… | Phase3 | Functional Constipation | Completed | 2019-10-01 | 2024-05-29 | ClinicalTrials.gov |
| NCT04026113 | Linaclotide Safety and Efficacy in Pediatric Participants, 6 to 17 Years of Age… | Phase3 | Functional Constipation | Completed | 2019-10-01 | 2024-05-29 | ClinicalTrials.gov |
| NCT04026113 | Linaclotide Safety and Efficacy in Pediatric Participants, 6 to 17 Years of Age… | Phase3 | Functional Constipation | Completed | 2019-10-01 | 2024-05-29 | ClinicalTrials.gov |
| NCT04010968 | Evaluation of Risk-Adapted and MRD-Driven Strategy for Untreated Fit Patients W… | Phase2 | Intermediate Risk Chronic Lymphocytic Leukemia | Completed | 2019-09-27 | 2025-01-30 | ClinicalTrials.gov |
| NCT04010968 | Evaluation of Risk-Adapted and MRD-Driven Strategy for Untreated Fit Patients W… | Phase2 | Intermediate Risk Chronic Lymphocytic Leukemia | Completed | 2019-09-27 | 2025-01-30 | ClinicalTrials.gov |
| NCT04010968 | Evaluation of Risk-Adapted and MRD-Driven Strategy for Untreated Fit Patients W… | Phase2 | Intermediate Risk Chronic Lymphocytic Leukemia | Completed | 2019-09-27 | 2025-01-30 | ClinicalTrials.gov |
| NCT04010968 | Evaluation of Risk-Adapted and MRD-Driven Strategy for Untreated Fit Patients W… | Phase2 | Intermediate Risk Chronic Lymphocytic Leukemia | Completed | 2019-09-27 | 2025-01-30 | ClinicalTrials.gov |
| NCT04096326 | AGN-151586 Dose-Ranging Study for Treatment of Glabellar Lines | Phase2 | Glabellar Lines | Completed | 2019-09-26 | 2020-09-09 | ClinicalTrials.gov |
| NCT04179474 | Safety, Tolerability and Drug- Drug Interaction Study of Ubrogepant With Erenum… | Phase1 | Migraine | Completed | 2019-09-26 | 2019-12-23 | ClinicalTrials.gov |
| NCT04096326 | AGN-151586 Dose-Ranging Study for Treatment of Glabellar Lines | Phase2 | Glabellar Lines | Completed | 2019-09-26 | 2020-09-09 | ClinicalTrials.gov |
| NCT04096326 | AGN-151586 Dose-Ranging Study for Treatment of Glabellar Lines | Phase2 | Glabellar Lines | Completed | 2019-09-26 | 2020-09-09 | ClinicalTrials.gov |
| NCT04179474 | Safety, Tolerability and Drug- Drug Interaction Study of Ubrogepant With Erenum… | Phase1 | Migraine | Completed | 2019-09-26 | 2019-12-23 | ClinicalTrials.gov |
| NCT04096326 | AGN-151586 Dose-Ranging Study for Treatment of Glabellar Lines | Phase2 | Glabellar Lines | Completed | 2019-09-26 | 2020-09-09 | ClinicalTrials.gov |
| NCT04179474 | Safety, Tolerability and Drug- Drug Interaction Study of Ubrogepant With Erenum… | Phase1 | Migraine | Completed | 2019-09-26 | 2019-12-23 | ClinicalTrials.gov |
| NCT04179474 | Safety, Tolerability and Drug- Drug Interaction Study of Ubrogepant With Erenum… | Phase1 | Migraine | Completed | 2019-09-26 | 2019-12-23 | ClinicalTrials.gov |
| NCT03848143 | Intraoral Administration of Botox in Patients With Dentoalveolar Neuropathic Pa… | Phase2 | Neuropathic Pain | Completed | 2019-09-11 | 2025-06-30 | ClinicalTrials.gov |
| NCT03848143 | Intraoral Administration of Botox in Patients With Dentoalveolar Neuropathic Pa… | Phase2 | Neuropathic Pain | Completed | 2019-09-11 | 2025-06-30 | ClinicalTrials.gov |
| NCT03848143 | Intraoral Administration of Botox in Patients With Dentoalveolar Neuropathic Pa… | Phase2 | Neuropathic Pain | Completed | 2019-09-11 | 2025-06-30 | ClinicalTrials.gov |
| NCT03848143 | Intraoral Administration of Botox in Patients With Dentoalveolar Neuropathic Pa… | Phase2 | Neuropathic Pain | Completed | 2019-09-11 | 2025-06-30 | ClinicalTrials.gov |
| NCT04070768 | Study of the Safety and Efficacy of Gemtuzumab Ozogamicin (GO) and Venetoclax i… | Phase1 | Acute Myeloid Leukemia | Completed | 2019-09-06 | 2024-02-20 | ClinicalTrials.gov |
| NCT03844048 | An Extension Study of Venetoclax for Subjects Who Have Completed a Prior Veneto… | Phase3 | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2019-09-06 | 2027-08-01 | ClinicalTrials.gov |
| NCT03844048 | An Extension Study of Venetoclax for Subjects Who Have Completed a Prior Veneto… | Phase3 | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2019-09-06 | 2027-08-01 | ClinicalTrials.gov |
| NCT03844048 | An Extension Study of Venetoclax for Subjects Who Have Completed a Prior Veneto… | Phase3 | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2019-09-06 | 2027-08-01 | ClinicalTrials.gov |
| NCT04070768 | Study of the Safety and Efficacy of Gemtuzumab Ozogamicin (GO) and Venetoclax i… | Phase1 | Acute Myeloid Leukemia | Completed | 2019-09-06 | 2024-02-20 | ClinicalTrials.gov |
| NCT03844048 | An Extension Study of Venetoclax for Subjects Who Have Completed a Prior Veneto… | Phase3 | Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2019-09-06 | 2027-08-01 | ClinicalTrials.gov |
| NCT04070768 | Study of the Safety and Efficacy of Gemtuzumab Ozogamicin (GO) and Venetoclax i… | Phase1 | Acute Myeloid Leukemia | Completed | 2019-09-06 | 2024-02-20 | ClinicalTrials.gov |
| NCT04070768 | Study of the Safety and Efficacy of Gemtuzumab Ozogamicin (GO) and Venetoclax i… | Phase1 | Acute Myeloid Leukemia | Completed | 2019-09-06 | 2024-02-20 | ClinicalTrials.gov |
| NCT04073303 | BOTOX® Treatment for Adults With a Wide Lower Face Due to Masseter Muscle Promi… | Phase3 | Masseter Muscle Prominence | Completed | 2019-08-29 | 2022-11-10 | ClinicalTrials.gov |
| NCT04073303 | BOTOX® Treatment for Adults With a Wide Lower Face Due to Masseter Muscle Promi… | Phase3 | Masseter Muscle Prominence | Completed | 2019-08-29 | 2022-11-10 | ClinicalTrials.gov |
| NCT04073303 | BOTOX® Treatment for Adults With a Wide Lower Face Due to Masseter Muscle Promi… | Phase3 | Masseter Muscle Prominence | Completed | 2019-08-29 | 2022-11-10 | ClinicalTrials.gov |
| NCT04073303 | BOTOX® Treatment for Adults With a Wide Lower Face Due to Masseter Muscle Promi… | Phase3 | Masseter Muscle Prominence | Completed | 2019-08-29 | 2022-11-10 | ClinicalTrials.gov |
| NCT03874052 | Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Trea… | Phase1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | Recruiting | 2019-08-16 | 2027-12-31 | ClinicalTrials.gov |
| NCT03874052 | Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Trea… | Phase1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | Recruiting | 2019-08-16 | 2027-12-31 | ClinicalTrials.gov |
| NCT03874052 | Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Trea… | Phase1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | Recruiting | 2019-08-16 | 2027-12-31 | ClinicalTrials.gov |
| NCT03874052 | Ruxolitinib in Combination With Venetoclax With and Without Azacitidine in Trea… | Phase1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | Recruiting | 2019-08-16 | 2027-12-31 | ClinicalTrials.gov |
| NCT03941964 | A Study of the Effectiveness of Venetoclax in Combination With Azacitidine or D… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2019-08-15 | 2022-03-14 | ClinicalTrials.gov |
| NCT03941964 | A Study of the Effectiveness of Venetoclax in Combination With Azacitidine or D… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2019-08-15 | 2022-03-14 | ClinicalTrials.gov |
| NCT03941964 | A Study of the Effectiveness of Venetoclax in Combination With Azacitidine or D… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2019-08-15 | 2022-03-14 | ClinicalTrials.gov |
| NCT03941964 | A Study of the Effectiveness of Venetoclax in Combination With Azacitidine or D… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2019-08-15 | 2022-03-14 | ClinicalTrials.gov |
| NCT03951077 | Study of the Safety and Efficacy of Elagolix in Women With Polycystic Ovary Syn… | Phase2 | Polycystic Ovary Syndrome | Completed | 2019-08-12 | 2021-02-10 | ClinicalTrials.gov |
| NCT03951077 | Study of the Safety and Efficacy of Elagolix in Women With Polycystic Ovary Syn… | Phase2 | Polycystic Ovary Syndrome | Completed | 2019-08-12 | 2021-02-10 | ClinicalTrials.gov |
| NCT03951077 | Study of the Safety and Efficacy of Elagolix in Women With Polycystic Ovary Syn… | Phase2 | Polycystic Ovary Syndrome | Completed | 2019-08-12 | 2021-02-10 | ClinicalTrials.gov |
| NCT03951077 | Study of the Safety and Efficacy of Elagolix in Women With Polycystic Ovary Syn… | Phase2 | Polycystic Ovary Syndrome | Completed | 2019-08-12 | 2021-02-10 | ClinicalTrials.gov |
| NCT03987958 | A Study to Describe the Safety and Effectiveness of Venetoclax in Acute Myeloid… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-08-08 | 2027-07-01 | ClinicalTrials.gov |
| NCT03987958 | A Study to Describe the Safety and Effectiveness of Venetoclax in Acute Myeloid… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-08-08 | 2027-07-01 | ClinicalTrials.gov |
| NCT03987958 | A Study to Describe the Safety and Effectiveness of Venetoclax in Acute Myeloid… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-08-08 | 2027-07-01 | ClinicalTrials.gov |
| NCT03987958 | A Study to Describe the Safety and Effectiveness of Venetoclax in Acute Myeloid… | — | Acute Myeloid Leukemia | Active_Not_Recruiting | 2019-08-08 | 2027-07-01 | ClinicalTrials.gov |
| NCT03751436 | Enzalutamide With Venetoclax in Treating Patients With Metastatic Castration Re… | Phase1 | Castration Levels of Testosterone | Completed | 2019-08-02 | 2023-08-11 | ClinicalTrials.gov |
| NCT03751436 | Enzalutamide With Venetoclax in Treating Patients With Metastatic Castration Re… | Phase1 | Castration Levels of Testosterone | Completed | 2019-08-02 | 2023-08-11 | ClinicalTrials.gov |
| NCT03751436 | Enzalutamide With Venetoclax in Treating Patients With Metastatic Castration Re… | Phase1 | Castration Levels of Testosterone | Completed | 2019-08-02 | 2023-08-11 | ClinicalTrials.gov |
| NCT03751436 | Enzalutamide With Venetoclax in Treating Patients With Metastatic Castration Re… | Phase1 | Castration Levels of Testosterone | Completed | 2019-08-02 | 2023-08-11 | ClinicalTrials.gov |
| NCT03557619 | A Study to Assess the Effect of Venetoclax on Ethinyl Estradiol and Levonorgest… | Phase1 | Hematologic Malignancies | Recruiting | 2019-07-30 | 2026-03-21 | ClinicalTrials.gov |
| NCT03557619 | A Study to Assess the Effect of Venetoclax on Ethinyl Estradiol and Levonorgest… | Phase1 | Hematologic Malignancies | Recruiting | 2019-07-30 | 2026-03-21 | ClinicalTrials.gov |
| NCT03557619 | A Study to Assess the Effect of Venetoclax on Ethinyl Estradiol and Levonorgest… | Phase1 | Hematologic Malignancies | Recruiting | 2019-07-30 | 2026-03-21 | ClinicalTrials.gov |
| NCT03557619 | A Study to Assess the Effect of Venetoclax on Ethinyl Estradiol and Levonorgest… | Phase1 | Hematologic Malignancies | Recruiting | 2019-07-30 | 2026-03-21 | ClinicalTrials.gov |
| NCT03909100 | International CoolSculpting: Study to Evaluate Patient Satisfaction for Non-Inv… | Na | Non-invasive Fat Reduction | Completed | 2019-07-29 | 2020-02-28 | ClinicalTrials.gov |
| NCT03909100 | International CoolSculpting: Study to Evaluate Patient Satisfaction for Non-Inv… | Na | Non-invasive Fat Reduction | Completed | 2019-07-29 | 2020-02-28 | ClinicalTrials.gov |
| NCT03909100 | International CoolSculpting: Study to Evaluate Patient Satisfaction for Non-Inv… | Na | Non-invasive Fat Reduction | Completed | 2019-07-29 | 2020-02-28 | ClinicalTrials.gov |
| NCT03909100 | International CoolSculpting: Study to Evaluate Patient Satisfaction for Non-Inv… | Na | Non-invasive Fat Reduction | Completed | 2019-07-29 | 2020-02-28 | ClinicalTrials.gov |
| NCT04089722 | Efficacy and Safety of Deoxycholic Acid Injections for Removal of Adipose Tissu… | Phase4 | Brassiere Strap Fat (BSF) | Completed | 2019-07-26 | 2020-10-22 | ClinicalTrials.gov |
| NCT04089722 | Efficacy and Safety of Deoxycholic Acid Injections for Removal of Adipose Tissu… | Phase4 | Brassiere Strap Fat (BSF) | Completed | 2019-07-26 | 2020-10-22 | ClinicalTrials.gov |
| NCT04089722 | Efficacy and Safety of Deoxycholic Acid Injections for Removal of Adipose Tissu… | Phase4 | Brassiere Strap Fat (BSF) | Completed | 2019-07-26 | 2020-10-22 | ClinicalTrials.gov |
| NCT04089722 | Efficacy and Safety of Deoxycholic Acid Injections for Removal of Adipose Tissu… | Phase4 | Brassiere Strap Fat (BSF) | Completed | 2019-07-26 | 2020-10-22 | ClinicalTrials.gov |
| NCT03978520 | A Study to Investigate the Safety and Efficacy of Elsubrutinib and Upadacitinib… | Phase2 | Systemic Lupus Erythematosus (SLE) | Completed | 2019-07-25 | 2022-07-14 | ClinicalTrials.gov |
| NCT03978520 | A Study to Investigate the Safety and Efficacy of Elsubrutinib and Upadacitinib… | Phase2 | Systemic Lupus Erythematosus (SLE) | Completed | 2019-07-25 | 2022-07-14 | ClinicalTrials.gov |
| NCT03908307 | Evaluation of OZURDEX® in Patients With Macular Edema Secondary to Retinal Vein… | Phase4 | Macular Edema | Completed | 2019-07-25 | 2021-09-26 | ClinicalTrials.gov |
| NCT03978520 | A Study to Investigate the Safety and Efficacy of Elsubrutinib and Upadacitinib… | Phase2 | Systemic Lupus Erythematosus (SLE) | Completed | 2019-07-25 | 2022-07-14 | ClinicalTrials.gov |
| NCT03908307 | Evaluation of OZURDEX® in Patients With Macular Edema Secondary to Retinal Vein… | Phase4 | Macular Edema | Completed | 2019-07-25 | 2021-09-26 | ClinicalTrials.gov |
| NCT03908307 | Evaluation of OZURDEX® in Patients With Macular Edema Secondary to Retinal Vein… | Phase4 | Macular Edema | Completed | 2019-07-25 | 2021-09-26 | ClinicalTrials.gov |
| NCT03978520 | A Study to Investigate the Safety and Efficacy of Elsubrutinib and Upadacitinib… | Phase2 | Systemic Lupus Erythematosus (SLE) | Completed | 2019-07-25 | 2022-07-14 | ClinicalTrials.gov |
| NCT03908307 | Evaluation of OZURDEX® in Patients With Macular Edema Secondary to Retinal Vein… | Phase4 | Macular Edema | Completed | 2019-07-25 | 2021-09-26 | ClinicalTrials.gov |
| NCT03855865 | Study of Rapastinel as Monotherapy in Major Depressive Disorder (MDD) | Phase3 | Depressive Disorder, Major | Withdrawn | 2019-07-01 | 2020-12-31 | ClinicalTrials.gov |
| NCT03982394 | Observational Study of Patients With Moderate to Severe Chronic Plaque Psoriasis | — | Chronic Plaque Psoriasis | Completed | 2019-07-01 | 2025-09-02 | ClinicalTrials.gov |
| NCT03855865 | Study of Rapastinel as Monotherapy in Major Depressive Disorder (MDD) | Phase3 | Depressive Disorder, Major | Withdrawn | 2019-07-01 | 2020-12-31 | ClinicalTrials.gov |
| NCT03982394 | Observational Study of Patients With Moderate to Severe Chronic Plaque Psoriasis | — | Chronic Plaque Psoriasis | Completed | 2019-07-01 | 2025-09-02 | ClinicalTrials.gov |
| NCT03982394 | Observational Study of Patients With Moderate to Severe Chronic Plaque Psoriasis | — | Chronic Plaque Psoriasis | Completed | 2019-07-01 | 2025-09-02 | ClinicalTrials.gov |
| NCT03855865 | Study of Rapastinel as Monotherapy in Major Depressive Disorder (MDD) | Phase3 | Depressive Disorder, Major | Withdrawn | 2019-07-01 | 2020-12-31 | ClinicalTrials.gov |
| NCT03982394 | Observational Study of Patients With Moderate to Severe Chronic Plaque Psoriasis | — | Chronic Plaque Psoriasis | Completed | 2019-07-01 | 2025-09-02 | ClinicalTrials.gov |
| NCT03855865 | Study of Rapastinel as Monotherapy in Major Depressive Disorder (MDD) | Phase3 | Depressive Disorder, Major | Withdrawn | 2019-07-01 | 2020-12-31 | ClinicalTrials.gov |
| NCT05268068 | A Study of Intravenously (IV) Infused or Subcutaneously (SC) Injected Risankizu… | Phase1 | Healthy Volunteers | Completed | 2019-06-27 | 2020-04-26 | ClinicalTrials.gov |
| NCT05268068 | A Study of Intravenously (IV) Infused or Subcutaneously (SC) Injected Risankizu… | Phase1 | Healthy Volunteers | Completed | 2019-06-27 | 2020-04-26 | ClinicalTrials.gov |
| NCT05268068 | A Study of Intravenously (IV) Infused or Subcutaneously (SC) Injected Risankizu… | Phase1 | Healthy Volunteers | Completed | 2019-06-27 | 2020-04-26 | ClinicalTrials.gov |
| NCT05268068 | A Study of Intravenously (IV) Infused or Subcutaneously (SC) Injected Risankizu… | Phase1 | Healthy Volunteers | Completed | 2019-06-27 | 2020-04-26 | ClinicalTrials.gov |
| NCT03925441 | Post-Marketing Surveillance Study of Adalimumab in Pediatric Chronic Severe Pla… | — | Psoriasis | Completed | 2019-06-25 | 2019-08-06 | ClinicalTrials.gov |
| NCT03925441 | Post-Marketing Surveillance Study of Adalimumab in Pediatric Chronic Severe Pla… | — | Psoriasis | Completed | 2019-06-25 | 2019-08-06 | ClinicalTrials.gov |
| NCT03925441 | Post-Marketing Surveillance Study of Adalimumab in Pediatric Chronic Severe Pla… | — | Psoriasis | Completed | 2019-06-25 | 2019-08-06 | ClinicalTrials.gov |
| NCT03925441 | Post-Marketing Surveillance Study of Adalimumab in Pediatric Chronic Severe Pla… | — | Psoriasis | Completed | 2019-06-25 | 2019-08-06 | ClinicalTrials.gov |
| NCT03725007 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Upadaciti… | Phase1 | Juvenile Idiopathic Arthritis (JIA) | Active_Not_Recruiting | 2019-06-24 | 2027-05-01 | ClinicalTrials.gov |
| NCT03827564 | Goblet Cell Degranulation Produced by Intranasal Tear Neurostimulator (ITN) in … | Na | Dry Eye Syndromes | Terminated | 2019-06-24 | 2020-06-08 | ClinicalTrials.gov |
| NCT03933735 | A Study of TNB-383B in Participants With Relapsed or Refractory Multiple Myeloma | Phase1 | Multiple Myeloma | Active_Not_Recruiting | 2019-06-24 | 2026-05-01 | ClinicalTrials.gov |
| NCT03725007 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Upadaciti… | Phase1 | Juvenile Idiopathic Arthritis (JIA) | Active_Not_Recruiting | 2019-06-24 | 2027-05-01 | ClinicalTrials.gov |
| NCT03933735 | A Study of TNB-383B in Participants With Relapsed or Refractory Multiple Myeloma | Phase1 | Multiple Myeloma | Active_Not_Recruiting | 2019-06-24 | 2026-05-01 | ClinicalTrials.gov |
| NCT03725007 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Upadaciti… | Phase1 | Juvenile Idiopathic Arthritis (JIA) | Active_Not_Recruiting | 2019-06-24 | 2027-05-01 | ClinicalTrials.gov |
| NCT03827564 | Goblet Cell Degranulation Produced by Intranasal Tear Neurostimulator (ITN) in … | Na | Dry Eye Syndromes | Terminated | 2019-06-24 | 2020-06-08 | ClinicalTrials.gov |
| NCT03933735 | A Study of TNB-383B in Participants With Relapsed or Refractory Multiple Myeloma | Phase1 | Multiple Myeloma | Active_Not_Recruiting | 2019-06-24 | 2026-05-01 | ClinicalTrials.gov |
| NCT03933735 | A Study of TNB-383B in Participants With Relapsed or Refractory Multiple Myeloma | Phase1 | Multiple Myeloma | Active_Not_Recruiting | 2019-06-24 | 2026-05-01 | ClinicalTrials.gov |
| NCT03827564 | Goblet Cell Degranulation Produced by Intranasal Tear Neurostimulator (ITN) in … | Na | Dry Eye Syndromes | Terminated | 2019-06-24 | 2020-06-08 | ClinicalTrials.gov |
| NCT03827564 | Goblet Cell Degranulation Produced by Intranasal Tear Neurostimulator (ITN) in … | Na | Dry Eye Syndromes | Terminated | 2019-06-24 | 2020-06-08 | ClinicalTrials.gov |
| NCT03725007 | A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Upadaciti… | Phase1 | Juvenile Idiopathic Arthritis (JIA) | Active_Not_Recruiting | 2019-06-24 | 2027-05-01 | ClinicalTrials.gov |
| NCT03955783 | Venetoclax and Selinexor in Treating Patients with Relapsed or Refractory High … | Phase1 | Diffuse Large B-cell Lymphoma | Completed | 2019-06-21 | 2024-09-01 | ClinicalTrials.gov |
| NCT03955783 | Venetoclax and Selinexor in Treating Patients with Relapsed or Refractory High … | Phase1 | Diffuse Large B-cell Lymphoma | Completed | 2019-06-21 | 2024-09-01 | ClinicalTrials.gov |
| NCT03955783 | Venetoclax and Selinexor in Treating Patients with Relapsed or Refractory High … | Phase1 | Diffuse Large B-cell Lymphoma | Completed | 2019-06-21 | 2024-09-01 | ClinicalTrials.gov |
| NCT03955783 | Venetoclax and Selinexor in Treating Patients with Relapsed or Refractory High … | Phase1 | Diffuse Large B-cell Lymphoma | Completed | 2019-06-21 | 2024-09-01 | ClinicalTrials.gov |
| NCT03922607 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-157 i… | Phase1 | Psoriasis | Completed | 2019-06-11 | 2021-04-13 | ClinicalTrials.gov |
| NCT03757533 | Health Coaching as a Tool for Improving Medication Adherence in Adult Patients … | Na | Inflammatory Bowel Diseases | Completed | 2019-06-11 | 2023-07-21 | ClinicalTrials.gov |
| NCT03757533 | Health Coaching as a Tool for Improving Medication Adherence in Adult Patients … | Na | Inflammatory Bowel Diseases | Completed | 2019-06-11 | 2023-07-21 | ClinicalTrials.gov |
| NCT03922607 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-157 i… | Phase1 | Psoriasis | Completed | 2019-06-11 | 2021-04-13 | ClinicalTrials.gov |
| NCT03922607 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-157 i… | Phase1 | Psoriasis | Completed | 2019-06-11 | 2021-04-13 | ClinicalTrials.gov |
| NCT03922607 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-157 i… | Phase1 | Psoriasis | Completed | 2019-06-11 | 2021-04-13 | ClinicalTrials.gov |
| NCT03757533 | Health Coaching as a Tool for Improving Medication Adherence in Adult Patients … | Na | Inflammatory Bowel Diseases | Completed | 2019-06-11 | 2023-07-21 | ClinicalTrials.gov |
| NCT03757533 | Health Coaching as a Tool for Improving Medication Adherence in Adult Patients … | Na | Inflammatory Bowel Diseases | Completed | 2019-06-11 | 2023-07-21 | ClinicalTrials.gov |
| NCT03875508 | A Study to Assess Usability of Risankizumab Autoinjector Combination Product in… | Phase3 | Psoriasis | Completed | 2019-06-04 | 2020-08-25 | ClinicalTrials.gov |
| NCT03875508 | A Study to Assess Usability of Risankizumab Autoinjector Combination Product in… | Phase3 | Psoriasis | Completed | 2019-06-04 | 2020-08-25 | ClinicalTrials.gov |
| NCT03875508 | A Study to Assess Usability of Risankizumab Autoinjector Combination Product in… | Phase3 | Psoriasis | Completed | 2019-06-04 | 2020-08-25 | ClinicalTrials.gov |
| NCT03875508 | A Study to Assess Usability of Risankizumab Autoinjector Combination Product in… | Phase3 | Psoriasis | Completed | 2019-06-04 | 2020-08-25 | ClinicalTrials.gov |
| NCT03926169 | A Global Study Comparing Risankizumab to Placebo in Adult Participants With Mod… | Phase2 | Hidradenitis Suppurativa | Completed | 2019-06-03 | 2021-08-02 | ClinicalTrials.gov |
| NCT03926169 | A Global Study Comparing Risankizumab to Placebo in Adult Participants With Mod… | Phase2 | Hidradenitis Suppurativa | Completed | 2019-06-03 | 2021-08-02 | ClinicalTrials.gov |
| NCT03926169 | A Global Study Comparing Risankizumab to Placebo in Adult Participants With Mod… | Phase2 | Hidradenitis Suppurativa | Completed | 2019-06-03 | 2021-08-02 | ClinicalTrials.gov |
| NCT03926169 | A Global Study Comparing Risankizumab to Placebo in Adult Participants With Mod… | Phase2 | Hidradenitis Suppurativa | Completed | 2019-06-03 | 2021-08-02 | ClinicalTrials.gov |
| NCT03999801 | Long-term Follow-Up Study of RGX-314 and Fellow Eye Substudy | Phase2 | Neovascular Age-related Macular Degeneration | Enrolling_By_Invitation | 2019-05-31 | 2028-12-01 | ClinicalTrials.gov |
| NCT03999801 | Long-term Follow-Up Study of RGX-314 and Fellow Eye Substudy | Phase2 | Neovascular Age-related Macular Degeneration | Enrolling_By_Invitation | 2019-05-31 | 2028-12-01 | ClinicalTrials.gov |
| NCT03999801 | Long-term Follow-Up Study of RGX-314 and Fellow Eye Substudy | Phase2 | Neovascular Age-related Macular Degeneration | Enrolling_By_Invitation | 2019-05-31 | 2028-12-01 | ClinicalTrials.gov |
| NCT03999801 | Long-term Follow-Up Study of RGX-314 and Fellow Eye Substudy | Phase2 | Neovascular Age-related Macular Degeneration | Enrolling_By_Invitation | 2019-05-31 | 2028-12-01 | ClinicalTrials.gov |
| NCT03924323 | A Study of Escitalopram in the Treatment of Children and Adolescents With Gener… | Phase4 | Anxiety Disorders,Generalized Anxiety Disorder | Completed | 2019-05-30 | 2021-09-20 | ClinicalTrials.gov |
| NCT03924323 | A Study of Escitalopram in the Treatment of Children and Adolescents With Gener… | Phase4 | Anxiety Disorders,Generalized Anxiety Disorder | Completed | 2019-05-30 | 2021-09-20 | ClinicalTrials.gov |
| NCT03924323 | A Study of Escitalopram in the Treatment of Children and Adolescents With Gener… | Phase4 | Anxiety Disorders,Generalized Anxiety Disorder | Completed | 2019-05-30 | 2021-09-20 | ClinicalTrials.gov |
| NCT03924323 | A Study of Escitalopram in the Treatment of Children and Adolescents With Gener… | Phase4 | Anxiety Disorders,Generalized Anxiety Disorder | Completed | 2019-05-30 | 2021-09-20 | ClinicalTrials.gov |
| NCT03893955 | A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminar… | Phase1 | Cancer | Active_Not_Recruiting | 2019-05-21 | 2026-03-01 | ClinicalTrials.gov |
| NCT03893955 | A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminar… | Phase1 | Cancer | Active_Not_Recruiting | 2019-05-21 | 2026-03-01 | ClinicalTrials.gov |
| NCT03893955 | A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminar… | Phase1 | Cancer | Active_Not_Recruiting | 2019-05-21 | 2026-03-01 | ClinicalTrials.gov |
| NCT03893955 | A Study to Determine the Safety, Tolerability, Pharmacokinetics, and Preliminar… | Phase1 | Cancer | Active_Not_Recruiting | 2019-05-21 | 2026-03-01 | ClinicalTrials.gov |
| NCT03861936 | BOTOX® (onabotulinumtoxinA) Treatment of Masseter Muscle Prominence | Phase2 | Masseter Muscle Prominence | Completed | 2019-05-16 | 2020-07-02 | ClinicalTrials.gov |
| NCT03861936 | BOTOX® (onabotulinumtoxinA) Treatment of Masseter Muscle Prominence | Phase2 | Masseter Muscle Prominence | Completed | 2019-05-16 | 2020-07-02 | ClinicalTrials.gov |
| NCT03861936 | BOTOX® (onabotulinumtoxinA) Treatment of Masseter Muscle Prominence | Phase2 | Masseter Muscle Prominence | Completed | 2019-05-16 | 2020-07-02 | ClinicalTrials.gov |
| NCT03861936 | BOTOX® (onabotulinumtoxinA) Treatment of Masseter Muscle Prominence | Phase2 | Masseter Muscle Prominence | Completed | 2019-05-16 | 2020-07-02 | ClinicalTrials.gov |
| NCT03875482 | A Study to Assess Safety and Efficacy of Risankizumab Using a New Formulation i… | Phase3 | Psoriasis | Completed | 2019-05-13 | 2020-07-15 | ClinicalTrials.gov |
| NCT03823378 | A Study in Rheumatoid Arthritis Patients Who Have Completed a Preceding Study W… | Phase2 | Rheumatoid Arthritis (RA) | Terminated | 2019-05-13 | 2020-09-09 | ClinicalTrials.gov |
| NCT03875482 | A Study to Assess Safety and Efficacy of Risankizumab Using a New Formulation i… | Phase3 | Psoriasis | Completed | 2019-05-13 | 2020-07-15 | ClinicalTrials.gov |
| NCT03823378 | A Study in Rheumatoid Arthritis Patients Who Have Completed a Preceding Study W… | Phase2 | Rheumatoid Arthritis (RA) | Terminated | 2019-05-13 | 2020-09-09 | ClinicalTrials.gov |
| NCT03875482 | A Study to Assess Safety and Efficacy of Risankizumab Using a New Formulation i… | Phase3 | Psoriasis | Completed | 2019-05-13 | 2020-07-15 | ClinicalTrials.gov |
| NCT03875482 | A Study to Assess Safety and Efficacy of Risankizumab Using a New Formulation i… | Phase3 | Psoriasis | Completed | 2019-05-13 | 2020-07-15 | ClinicalTrials.gov |
| NCT03823378 | A Study in Rheumatoid Arthritis Patients Who Have Completed a Preceding Study W… | Phase2 | Rheumatoid Arthritis (RA) | Terminated | 2019-05-13 | 2020-09-09 | ClinicalTrials.gov |
| NCT03823378 | A Study in Rheumatoid Arthritis Patients Who Have Completed a Preceding Study W… | Phase2 | Rheumatoid Arthritis (RA) | Terminated | 2019-05-13 | 2020-09-09 | ClinicalTrials.gov |
| NCT03939312 | Extension Study to Evaluate the Long-Term Safety and Tolerability of Oral Atoge… | Phase3 | Episodic Migraine | Completed | 2019-05-06 | 2021-03-31 | ClinicalTrials.gov |
| NCT03939312 | Extension Study to Evaluate the Long-Term Safety and Tolerability of Oral Atoge… | Phase3 | Episodic Migraine | Completed | 2019-05-06 | 2021-03-31 | ClinicalTrials.gov |
| NCT03939312 | Extension Study to Evaluate the Long-Term Safety and Tolerability of Oral Atoge… | Phase3 | Episodic Migraine | Completed | 2019-05-06 | 2021-03-31 | ClinicalTrials.gov |
| NCT03939312 | Extension Study to Evaluate the Long-Term Safety and Tolerability of Oral Atoge… | Phase3 | Episodic Migraine | Completed | 2019-05-06 | 2021-03-31 | ClinicalTrials.gov |
| NCT03894956 | Observational Study Evaluating Long-Term Safety and Effectiveness of Humira in … | — | Hidradenitis Suppurativa (HS) | Completed | 2019-05-02 | 2021-11-10 | ClinicalTrials.gov |
| NCT03894956 | Observational Study Evaluating Long-Term Safety and Effectiveness of Humira in … | — | Hidradenitis Suppurativa (HS) | Completed | 2019-05-02 | 2021-11-10 | ClinicalTrials.gov |
| NCT03894956 | Observational Study Evaluating Long-Term Safety and Effectiveness of Humira in … | — | Hidradenitis Suppurativa (HS) | Completed | 2019-05-02 | 2021-11-10 | ClinicalTrials.gov |
| NCT03894956 | Observational Study Evaluating Long-Term Safety and Effectiveness of Humira in … | — | Hidradenitis Suppurativa (HS) | Completed | 2019-05-02 | 2021-11-10 | ClinicalTrials.gov |
| NCT03785184 | A Study of Venetoclax Plus Lenalidomide and Dexamethasone for the Treatment of … | Phase2 | Multiple Myeloma | Withdrawn | 2019-04-29 | 2019-08-22 | ClinicalTrials.gov |
| NCT03781167 | A Study to Evaluate the Safety and Tolerability of ABBV-951 in Subjects With Pa… | Phase3 | Parkinson's Disease (PD) | Completed | 2019-04-29 | 2022-08-17 | ClinicalTrials.gov |
| NCT03785184 | A Study of Venetoclax Plus Lenalidomide and Dexamethasone for the Treatment of … | Phase2 | Multiple Myeloma | Withdrawn | 2019-04-29 | 2019-08-22 | ClinicalTrials.gov |
| NCT03785184 | A Study of Venetoclax Plus Lenalidomide and Dexamethasone for the Treatment of … | Phase2 | Multiple Myeloma | Withdrawn | 2019-04-29 | 2019-08-22 | ClinicalTrials.gov |
| NCT03785184 | A Study of Venetoclax Plus Lenalidomide and Dexamethasone for the Treatment of … | Phase2 | Multiple Myeloma | Withdrawn | 2019-04-29 | 2019-08-22 | ClinicalTrials.gov |
| NCT03781167 | A Study to Evaluate the Safety and Tolerability of ABBV-951 in Subjects With Pa… | Phase3 | Parkinson's Disease (PD) | Completed | 2019-04-29 | 2022-08-17 | ClinicalTrials.gov |
| NCT03781167 | A Study to Evaluate the Safety and Tolerability of ABBV-951 in Subjects With Pa… | Phase3 | Parkinson's Disease (PD) | Completed | 2019-04-29 | 2022-08-17 | ClinicalTrials.gov |
| NCT03781167 | A Study to Evaluate the Safety and Tolerability of ABBV-951 in Subjects With Pa… | Phase3 | Parkinson's Disease (PD) | Completed | 2019-04-29 | 2022-08-17 | ClinicalTrials.gov |
| NCT03915067 | BOTOX® for the Treatment of Platysma Prominence | Phase2 | Platysma Prominence | Completed | 2019-04-23 | 2020-04-16 | ClinicalTrials.gov |
| NCT03915067 | BOTOX® for the Treatment of Platysma Prominence | Phase2 | Platysma Prominence | Completed | 2019-04-23 | 2020-04-16 | ClinicalTrials.gov |
| NCT03915067 | BOTOX® for the Treatment of Platysma Prominence | Phase2 | Platysma Prominence | Completed | 2019-04-23 | 2020-04-16 | ClinicalTrials.gov |
| NCT03915067 | BOTOX® for the Treatment of Platysma Prominence | Phase2 | Platysma Prominence | Completed | 2019-04-23 | 2020-04-16 | ClinicalTrials.gov |
| NCT03842566 | Evaluation of Age-Related Skin Changes | — | Age-related Skin Changes | Completed | 2019-04-18 | 2019-07-12 | ClinicalTrials.gov |
| NCT03842566 | Evaluation of Age-Related Skin Changes | — | Age-related Skin Changes | Completed | 2019-04-18 | 2019-07-12 | ClinicalTrials.gov |
| NCT03842566 | Evaluation of Age-Related Skin Changes | — | Age-related Skin Changes | Completed | 2019-04-18 | 2019-07-12 | ClinicalTrials.gov |
| NCT03842566 | Evaluation of Age-Related Skin Changes | — | Age-related Skin Changes | Completed | 2019-04-18 | 2019-07-12 | ClinicalTrials.gov |
| NCT03954444 | A Clinical Endpoint Bioequivalence Study of "Oxymetazoline Hydrochloride Cream" | Phase3 | Rosacea | Completed | 2019-04-15 | 2020-02-27 | ClinicalTrials.gov |
| NCT03954444 | A Clinical Endpoint Bioequivalence Study of "Oxymetazoline Hydrochloride Cream" | Phase3 | Rosacea | Completed | 2019-04-15 | 2020-02-27 | ClinicalTrials.gov |
| NCT03954444 | A Clinical Endpoint Bioequivalence Study of "Oxymetazoline Hydrochloride Cream" | Phase3 | Rosacea | Completed | 2019-04-15 | 2020-02-27 | ClinicalTrials.gov |
| NCT03954444 | A Clinical Endpoint Bioequivalence Study of "Oxymetazoline Hydrochloride Cream" | Phase3 | Rosacea | Completed | 2019-04-15 | 2020-02-27 | ClinicalTrials.gov |
| NCT03886220 | A Study to Evaluate the Safety and Efficacy of Elagolix for the Management of H… | Phase4 | Uterine Fibroids | Completed | 2019-04-12 | 2021-04-28 | ClinicalTrials.gov |
| NCT03886220 | A Study to Evaluate the Safety and Efficacy of Elagolix for the Management of H… | Phase4 | Uterine Fibroids | Completed | 2019-04-12 | 2021-04-28 | ClinicalTrials.gov |
| NCT03886220 | A Study to Evaluate the Safety and Efficacy of Elagolix for the Management of H… | Phase4 | Uterine Fibroids | Completed | 2019-04-12 | 2021-04-28 | ClinicalTrials.gov |
| NCT03886220 | A Study to Evaluate the Safety and Efficacy of Elagolix for the Management of H… | Phase4 | Uterine Fibroids | Completed | 2019-04-12 | 2021-04-28 | ClinicalTrials.gov |
| NCT03781726 | Multi-center Study to Transplant Hepatitis-C Infected Kidneys | Phase4 | Renal Failure Chronic | Completed | 2019-04-10 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781726 | Multi-center Study to Transplant Hepatitis-C Infected Kidneys | Phase4 | Renal Failure Chronic | Completed | 2019-04-10 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781726 | Multi-center Study to Transplant Hepatitis-C Infected Kidneys | Phase4 | Renal Failure Chronic | Completed | 2019-04-10 | 2021-12-31 | ClinicalTrials.gov |
| NCT03781726 | Multi-center Study to Transplant Hepatitis-C Infected Kidneys | Phase4 | Renal Failure Chronic | Completed | 2019-04-10 | 2021-12-31 | ClinicalTrials.gov |
| NCT03868254 | Chart Review of XEN 45 Gel Stent: Long Term Performance and Safety Assessment (… | — | Glaucoma | Completed | 2019-04-05 | 2019-10-25 | ClinicalTrials.gov |
| NCT03868254 | Chart Review of XEN 45 Gel Stent: Long Term Performance and Safety Assessment (… | — | Glaucoma | Completed | 2019-04-05 | 2019-10-25 | ClinicalTrials.gov |
| NCT03868254 | Chart Review of XEN 45 Gel Stent: Long Term Performance and Safety Assessment (… | — | Glaucoma | Completed | 2019-04-05 | 2019-10-25 | ClinicalTrials.gov |
| NCT03868254 | Chart Review of XEN 45 Gel Stent: Long Term Performance and Safety Assessment (… | — | Glaucoma | Completed | 2019-04-05 | 2019-10-25 | ClinicalTrials.gov |
| NCT05283681 | A Study to Evaluate the Bioavailability of Risankizumab in Pre-filled Syringe o… | Phase1 | Healthy Volunteers | Completed | 2019-04-02 | 2019-11-11 | ClinicalTrials.gov |
| NCT05283681 | A Study to Evaluate the Bioavailability of Risankizumab in Pre-filled Syringe o… | Phase1 | Healthy Volunteers | Completed | 2019-04-02 | 2019-11-11 | ClinicalTrials.gov |
| NCT05283681 | A Study to Evaluate the Bioavailability of Risankizumab in Pre-filled Syringe o… | Phase1 | Healthy Volunteers | Completed | 2019-04-02 | 2019-11-11 | ClinicalTrials.gov |
| NCT05283681 | A Study to Evaluate the Bioavailability of Risankizumab in Pre-filled Syringe o… | Phase1 | Healthy Volunteers | Completed | 2019-04-02 | 2019-11-11 | ClinicalTrials.gov |
| NCT03732703 | Myeloma-Developing Regimens Using Genomics (MyDRUG) | Phase1 | Relapsed Refractory Multiple Myeloma | Completed | 2019-04-01 | 2024-12-31 | ClinicalTrials.gov |
| NCT03732703 | Myeloma-Developing Regimens Using Genomics (MyDRUG) | Phase1 | Relapsed Refractory Multiple Myeloma | Completed | 2019-04-01 | 2024-12-31 | ClinicalTrials.gov |
| NCT03732703 | Myeloma-Developing Regimens Using Genomics (MyDRUG) | Phase1 | Relapsed Refractory Multiple Myeloma | Completed | 2019-04-01 | 2024-12-31 | ClinicalTrials.gov |
| NCT03489265 | Effects of Eluxadoline (Viberzi®) 100 mg Twice Daily on Diarrhea-Associated Fec… | Phase2 | Fecal Incontinence | Withdrawn | 2019-04-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03489265 | Effects of Eluxadoline (Viberzi®) 100 mg Twice Daily on Diarrhea-Associated Fec… | Phase2 | Fecal Incontinence | Withdrawn | 2019-04-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03969537 | Telemedicine Follow-up for Patients With Cervical Dystonia Treated With Neuroto… | — | Cervical Dystonia | Completed | 2019-04-01 | 2020-06-04 | ClinicalTrials.gov |
| NCT03732703 | Myeloma-Developing Regimens Using Genomics (MyDRUG) | Phase1 | Relapsed Refractory Multiple Myeloma | Completed | 2019-04-01 | 2024-12-31 | ClinicalTrials.gov |
| NCT03969537 | Telemedicine Follow-up for Patients With Cervical Dystonia Treated With Neuroto… | — | Cervical Dystonia | Completed | 2019-04-01 | 2020-06-04 | ClinicalTrials.gov |
| NCT03489265 | Effects of Eluxadoline (Viberzi®) 100 mg Twice Daily on Diarrhea-Associated Fec… | Phase2 | Fecal Incontinence | Withdrawn | 2019-04-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03969537 | Telemedicine Follow-up for Patients With Cervical Dystonia Treated With Neuroto… | — | Cervical Dystonia | Completed | 2019-04-01 | 2020-06-04 | ClinicalTrials.gov |
| NCT03489265 | Effects of Eluxadoline (Viberzi®) 100 mg Twice Daily on Diarrhea-Associated Fec… | Phase2 | Fecal Incontinence | Withdrawn | 2019-04-01 | 2020-03-01 | ClinicalTrials.gov |
| NCT03969537 | Telemedicine Follow-up for Patients With Cervical Dystonia Treated With Neuroto… | — | Cervical Dystonia | Completed | 2019-04-01 | 2020-06-04 | ClinicalTrials.gov |
| NCT03823391 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of… | Phase2 | Rheumatoid Arthritis (RA) | Completed | 2019-03-27 | 2020-08-26 | ClinicalTrials.gov |
| NCT03823391 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of… | Phase2 | Rheumatoid Arthritis (RA) | Completed | 2019-03-27 | 2020-08-26 | ClinicalTrials.gov |
| NCT03891446 | Long-term Safety and Efficacy Extension Trial of Bimatoprost SR | Phase3 | Open-Angle Glaucoma | Completed | 2019-03-27 | 2026-06-19 | ClinicalTrials.gov |
| NCT03891446 | Long-term Safety and Efficacy Extension Trial of Bimatoprost SR | Phase3 | Open-Angle Glaucoma | Completed | 2019-03-27 | 2026-06-19 | ClinicalTrials.gov |
| NCT03823391 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of… | Phase2 | Rheumatoid Arthritis (RA) | Completed | 2019-03-27 | 2020-08-26 | ClinicalTrials.gov |
| NCT03891446 | Long-term Safety and Efficacy Extension Trial of Bimatoprost SR | Phase3 | Open-Angle Glaucoma | Completed | 2019-03-27 | 2026-06-19 | ClinicalTrials.gov |
| NCT03823391 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of… | Phase2 | Rheumatoid Arthritis (RA) | Completed | 2019-03-27 | 2020-08-26 | ClinicalTrials.gov |
| NCT03891446 | Long-term Safety and Efficacy Extension Trial of Bimatoprost SR | Phase3 | Open-Angle Glaucoma | Completed | 2019-03-27 | 2026-06-19 | ClinicalTrials.gov |
| NCT03695185 | A Study to Investigate How Well Ravagalimab (ABBV-323) Works and How Safe it is… | Phase2 | Ulcerative Colitis (UC) | Completed | 2019-03-26 | 2022-01-10 | ClinicalTrials.gov |
| NCT03695185 | A Study to Investigate How Well Ravagalimab (ABBV-323) Works and How Safe it is… | Phase2 | Ulcerative Colitis (UC) | Completed | 2019-03-26 | 2022-01-10 | ClinicalTrials.gov |
| NCT03695185 | A Study to Investigate How Well Ravagalimab (ABBV-323) Works and How Safe it is… | Phase2 | Ulcerative Colitis (UC) | Completed | 2019-03-26 | 2022-01-10 | ClinicalTrials.gov |
| NCT03695185 | A Study to Investigate How Well Ravagalimab (ABBV-323) Works and How Safe it is… | Phase2 | Ulcerative Colitis (UC) | Completed | 2019-03-26 | 2022-01-10 | ClinicalTrials.gov |
| NCT03675308 | A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic… | Phase3 | Psoriatic Arthritis | Active_Not_Recruiting | 2019-03-25 | 2026-09-28 | ClinicalTrials.gov |
| NCT03675308 | A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic… | Phase3 | Psoriatic Arthritis | Active_Not_Recruiting | 2019-03-25 | 2026-09-28 | ClinicalTrials.gov |
| NCT03879837 | Therapeutic Equivalence of Fluticasone Propionate Pressurized Metered Dose Inha… | Phase3 | Asthma | Completed | 2019-03-25 | 2021-07-09 | ClinicalTrials.gov |
| NCT03879837 | Therapeutic Equivalence of Fluticasone Propionate Pressurized Metered Dose Inha… | Phase3 | Asthma | Completed | 2019-03-25 | 2021-07-09 | ClinicalTrials.gov |
| NCT03675308 | A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic… | Phase3 | Psoriatic Arthritis | Active_Not_Recruiting | 2019-03-25 | 2026-09-28 | ClinicalTrials.gov |
| NCT03879837 | Therapeutic Equivalence of Fluticasone Propionate Pressurized Metered Dose Inha… | Phase3 | Asthma | Completed | 2019-03-25 | 2021-07-09 | ClinicalTrials.gov |
| NCT03675308 | A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic… | Phase3 | Psoriatic Arthritis | Active_Not_Recruiting | 2019-03-25 | 2026-09-28 | ClinicalTrials.gov |
| NCT03879837 | Therapeutic Equivalence of Fluticasone Propionate Pressurized Metered Dose Inha… | Phase3 | Asthma | Completed | 2019-03-25 | 2021-07-09 | ClinicalTrials.gov |
| NCT03712787 | An Extension Study of ABBV-8E12 in Early Alzheimer's Disease (AD) | Phase2 | Alzheimer's Disease | Terminated | 2019-03-22 | 2021-09-30 | ClinicalTrials.gov |
| NCT03712787 | An Extension Study of ABBV-8E12 in Early Alzheimer's Disease (AD) | Phase2 | Alzheimer's Disease | Terminated | 2019-03-22 | 2021-09-30 | ClinicalTrials.gov |
| NCT03712787 | An Extension Study of ABBV-8E12 in Early Alzheimer's Disease (AD) | Phase2 | Alzheimer's Disease | Terminated | 2019-03-22 | 2021-09-30 | ClinicalTrials.gov |
| NCT03712787 | An Extension Study of ABBV-8E12 in Early Alzheimer's Disease (AD) | Phase2 | Alzheimer's Disease | Terminated | 2019-03-22 | 2021-09-30 | ClinicalTrials.gov |
| NCT03797261 | A Study of Venetoclax and AMG 176 in Patients With Relapsed/Refractory Hematolo… | Phase1 | Acute Myeloid Leukemia | Terminated | 2019-03-18 | 2019-12-30 | ClinicalTrials.gov |
| NCT03797261 | A Study of Venetoclax and AMG 176 in Patients With Relapsed/Refractory Hematolo… | Phase1 | Acute Myeloid Leukemia | Terminated | 2019-03-18 | 2019-12-30 | ClinicalTrials.gov |
| NCT03797261 | A Study of Venetoclax and AMG 176 in Patients With Relapsed/Refractory Hematolo… | Phase1 | Acute Myeloid Leukemia | Terminated | 2019-03-18 | 2019-12-30 | ClinicalTrials.gov |
| NCT03797261 | A Study of Venetoclax and AMG 176 in Patients With Relapsed/Refractory Hematolo… | Phase1 | Acute Myeloid Leukemia | Terminated | 2019-03-18 | 2019-12-30 | ClinicalTrials.gov |
| NCT05486195 | A Single Ascending Oral Dose Study of SDI-118 in Healthy Male Subjects Includin… | Phase1 | Cognitive Disorders | Completed | 2019-03-14 | 2020-03-11 | ClinicalTrials.gov |
| NCT05486195 | A Single Ascending Oral Dose Study of SDI-118 in Healthy Male Subjects Includin… | Phase1 | Cognitive Disorders | Completed | 2019-03-14 | 2020-03-11 | ClinicalTrials.gov |
| NCT05486195 | A Single Ascending Oral Dose Study of SDI-118 in Healthy Male Subjects Includin… | Phase1 | Cognitive Disorders | Completed | 2019-03-14 | 2020-03-11 | ClinicalTrials.gov |
| NCT05486195 | A Single Ascending Oral Dose Study of SDI-118 in Healthy Male Subjects Includin… | Phase1 | Cognitive Disorders | Completed | 2019-03-14 | 2020-03-11 | ClinicalTrials.gov |
| NCT03855137 | Efficacy, Safety, and Tolerability of Atogepant for the Prevention of Chronic M… | Phase3 | Chronic Migraine | Completed | 2019-03-11 | 2022-01-20 | ClinicalTrials.gov |
| NCT03855137 | Efficacy, Safety, and Tolerability of Atogepant for the Prevention of Chronic M… | Phase3 | Chronic Migraine | Completed | 2019-03-11 | 2022-01-20 | ClinicalTrials.gov |
| NCT03855137 | Efficacy, Safety, and Tolerability of Atogepant for the Prevention of Chronic M… | Phase3 | Chronic Migraine | Completed | 2019-03-11 | 2022-01-20 | ClinicalTrials.gov |
| NCT03855137 | Efficacy, Safety, and Tolerability of Atogepant for the Prevention of Chronic M… | Phase3 | Chronic Migraine | Completed | 2019-03-11 | 2022-01-20 | ClinicalTrials.gov |
| NCT03671148 | A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic… | Phase3 | Psoriatic Arthritis (PsA) | Completed | 2019-03-07 | 2026-06-04 | ClinicalTrials.gov |
| NCT03671148 | A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic… | Phase3 | Psoriatic Arthritis (PsA) | Completed | 2019-03-07 | 2026-06-04 | ClinicalTrials.gov |
| NCT03671148 | A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic… | Phase3 | Psoriatic Arthritis (PsA) | Completed | 2019-03-07 | 2026-06-04 | ClinicalTrials.gov |
| NCT03671148 | A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic… | Phase3 | Psoriatic Arthritis (PsA) | Completed | 2019-03-07 | 2026-06-04 | ClinicalTrials.gov |
| NCT03372941 | Hospital Avoidance Strategies for ABSSSI | Phase4 | Skin Infection | Terminated | 2019-03-04 | 2021-10-14 | ClinicalTrials.gov |
| NCT03372941 | Hospital Avoidance Strategies for ABSSSI | Phase4 | Skin Infection | Terminated | 2019-03-04 | 2021-10-14 | ClinicalTrials.gov |
| NCT03372941 | Hospital Avoidance Strategies for ABSSSI | Phase4 | Skin Infection | Terminated | 2019-03-04 | 2021-10-14 | ClinicalTrials.gov |
| NCT03372941 | Hospital Avoidance Strategies for ABSSSI | Phase4 | Skin Infection | Terminated | 2019-03-04 | 2021-10-14 | ClinicalTrials.gov |
| NCT03779841 | Botulinum Toxin Type A (AGN-151607) for the Prevention of Post-operative Atrial… | Phase2 | Post-Operative Atrial Fibrillation | Completed | 2019-03-01 | 2023-03-06 | ClinicalTrials.gov |
| NCT03857542 | A Phase 3 Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in… | Phase3 | Presbyopia | Completed | 2019-03-01 | 2020-09-10 | ClinicalTrials.gov |
| NCT03779841 | Botulinum Toxin Type A (AGN-151607) for the Prevention of Post-operative Atrial… | Phase2 | Post-Operative Atrial Fibrillation | Completed | 2019-03-01 | 2023-03-06 | ClinicalTrials.gov |
| NCT03779841 | Botulinum Toxin Type A (AGN-151607) for the Prevention of Post-operative Atrial… | Phase2 | Post-Operative Atrial Fibrillation | Completed | 2019-03-01 | 2023-03-06 | ClinicalTrials.gov |
| NCT03779841 | Botulinum Toxin Type A (AGN-151607) for the Prevention of Post-operative Atrial… | Phase2 | Post-Operative Atrial Fibrillation | Completed | 2019-03-01 | 2023-03-06 | ClinicalTrials.gov |
| NCT03857542 | A Phase 3 Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in… | Phase3 | Presbyopia | Completed | 2019-03-01 | 2020-09-10 | ClinicalTrials.gov |
| NCT03857542 | A Phase 3 Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in… | Phase3 | Presbyopia | Completed | 2019-03-01 | 2020-09-10 | ClinicalTrials.gov |
| NCT03857542 | A Phase 3 Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in… | Phase3 | Presbyopia | Completed | 2019-03-01 | 2020-09-10 | ClinicalTrials.gov |
| NCT03868163 | Real World Evidence of the Effectiveness and Clinical Practice Use of Glecaprev… | — | Chronic Hepatitis C (CHC) | Completed | 2019-02-28 | 2020-09-04 | ClinicalTrials.gov |
| NCT03850782 | Evaluation of the Duration of Effect of Bimatoprost SR in Participants With Ope… | Phase3 | Open-Angle Glaucoma | Completed | 2019-02-28 | 2025-08-08 | ClinicalTrials.gov |
| NCT03850782 | Evaluation of the Duration of Effect of Bimatoprost SR in Participants With Ope… | Phase3 | Open-Angle Glaucoma | Completed | 2019-02-28 | 2025-08-08 | ClinicalTrials.gov |
| NCT03868163 | Real World Evidence of the Effectiveness and Clinical Practice Use of Glecaprev… | — | Chronic Hepatitis C (CHC) | Completed | 2019-02-28 | 2020-09-04 | ClinicalTrials.gov |
| NCT03868163 | Real World Evidence of the Effectiveness and Clinical Practice Use of Glecaprev… | — | Chronic Hepatitis C (CHC) | Completed | 2019-02-28 | 2020-09-04 | ClinicalTrials.gov |
| NCT03850782 | Evaluation of the Duration of Effect of Bimatoprost SR in Participants With Ope… | Phase3 | Open-Angle Glaucoma | Completed | 2019-02-28 | 2025-08-08 | ClinicalTrials.gov |
| NCT03850782 | Evaluation of the Duration of Effect of Bimatoprost SR in Participants With Ope… | Phase3 | Open-Angle Glaucoma | Completed | 2019-02-28 | 2025-08-08 | ClinicalTrials.gov |
| NCT03868163 | Real World Evidence of the Effectiveness and Clinical Practice Use of Glecaprev… | — | Chronic Hepatitis C (CHC) | Completed | 2019-02-28 | 2020-09-04 | ClinicalTrials.gov |
| NCT03737812 | A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard … | Phase2 | Multiple Sclerosis (MS) | Completed | 2019-02-27 | 2021-08-30 | ClinicalTrials.gov |
| NCT03737812 | A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard … | Phase2 | Multiple Sclerosis (MS) | Completed | 2019-02-27 | 2021-08-30 | ClinicalTrials.gov |
| NCT03737812 | A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard … | Phase2 | Multiple Sclerosis (MS) | Completed | 2019-02-27 | 2021-08-30 | ClinicalTrials.gov |
| NCT03737812 | A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard … | Phase2 | Multiple Sclerosis (MS) | Completed | 2019-02-27 | 2021-08-30 | ClinicalTrials.gov |
| NCT03873857 | A Study to Assess Effectiveness of Venclexta (Venetoclax) in Patients With Rela… | — | Chronic Lymphocytic Leukemia (CLL) | Completed | 2019-02-25 | 2022-09-12 | ClinicalTrials.gov |
| NCT03852810 | Satisfaction With XEN Gel Stent Versus Trabeculectomy for the Treatment of Glau… | — | Glaucoma | Completed | 2019-02-25 | 2020-12-09 | ClinicalTrials.gov |
| NCT03873857 | A Study to Assess Effectiveness of Venclexta (Venetoclax) in Patients With Rela… | — | Chronic Lymphocytic Leukemia (CLL) | Completed | 2019-02-25 | 2022-09-12 | ClinicalTrials.gov |
| NCT03852810 | Satisfaction With XEN Gel Stent Versus Trabeculectomy for the Treatment of Glau… | — | Glaucoma | Completed | 2019-02-25 | 2020-12-09 | ClinicalTrials.gov |
| NCT03873857 | A Study to Assess Effectiveness of Venclexta (Venetoclax) in Patients With Rela… | — | Chronic Lymphocytic Leukemia (CLL) | Completed | 2019-02-25 | 2022-09-12 | ClinicalTrials.gov |
| NCT03852810 | Satisfaction With XEN Gel Stent Versus Trabeculectomy for the Treatment of Glau… | — | Glaucoma | Completed | 2019-02-25 | 2020-12-09 | ClinicalTrials.gov |
| NCT03852810 | Satisfaction With XEN Gel Stent Versus Trabeculectomy for the Treatment of Glau… | — | Glaucoma | Completed | 2019-02-25 | 2020-12-09 | ClinicalTrials.gov |
| NCT03873857 | A Study to Assess Effectiveness of Venclexta (Venetoclax) in Patients With Rela… | — | Chronic Lymphocytic Leukemia (CLL) | Completed | 2019-02-25 | 2022-09-12 | ClinicalTrials.gov |
| NCT03738397 | A Study to Compare Safety and Efficacy of Upadacitinib to Dupilumab in Adult Pa… | Phase3 | Atopic Dermatitis | Completed | 2019-02-21 | 2020-12-09 | ClinicalTrials.gov |
| NCT03821935 | Study to Determine the Safety, Tolerability, Pharmacokinetics and Recommended P… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2019-02-21 | 2027-06-01 | ClinicalTrials.gov |
| NCT03738397 | A Study to Compare Safety and Efficacy of Upadacitinib to Dupilumab in Adult Pa… | Phase3 | Atopic Dermatitis | Completed | 2019-02-21 | 2020-12-09 | ClinicalTrials.gov |
| NCT03821935 | Study to Determine the Safety, Tolerability, Pharmacokinetics and Recommended P… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2019-02-21 | 2027-06-01 | ClinicalTrials.gov |
| NCT03738397 | A Study to Compare Safety and Efficacy of Upadacitinib to Dupilumab in Adult Pa… | Phase3 | Atopic Dermatitis | Completed | 2019-02-21 | 2020-12-09 | ClinicalTrials.gov |
| NCT03738397 | A Study to Compare Safety and Efficacy of Upadacitinib to Dupilumab in Adult Pa… | Phase3 | Atopic Dermatitis | Completed | 2019-02-21 | 2020-12-09 | ClinicalTrials.gov |
| NCT03821935 | Study to Determine the Safety, Tolerability, Pharmacokinetics and Recommended P… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2019-02-21 | 2027-06-01 | ClinicalTrials.gov |
| NCT03821935 | Study to Determine the Safety, Tolerability, Pharmacokinetics and Recommended P… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2019-02-21 | 2027-06-01 | ClinicalTrials.gov |
| NCT03659669 | A Study to Describe the Effectiveness and Safety of Venetoclax Treatment in Chr… | — | Chronic Lymphocytic Leukemia (CLL) | Suspended | 2019-02-10 | 2027-02-28 | ClinicalTrials.gov |
| NCT03659669 | A Study to Describe the Effectiveness and Safety of Venetoclax Treatment in Chr… | — | Chronic Lymphocytic Leukemia (CLL) | Suspended | 2019-02-10 | 2027-02-28 | ClinicalTrials.gov |
| NCT03659669 | A Study to Describe the Effectiveness and Safety of Venetoclax Treatment in Chr… | — | Chronic Lymphocytic Leukemia (CLL) | Suspended | 2019-02-10 | 2027-02-28 | ClinicalTrials.gov |
| NCT03659669 | A Study to Describe the Effectiveness and Safety of Venetoclax Treatment in Chr… | — | Chronic Lymphocytic Leukemia (CLL) | Suspended | 2019-02-10 | 2027-02-28 | ClinicalTrials.gov |
| NCT03646604 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Upadacitin… | Phase1 | Atopic Dermatitis | Completed | 2019-01-31 | 2024-08-29 | ClinicalTrials.gov |
| NCT03646604 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Upadacitin… | Phase1 | Atopic Dermatitis | Completed | 2019-01-31 | 2024-08-29 | ClinicalTrials.gov |
| NCT03646604 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Upadacitin… | Phase1 | Atopic Dermatitis | Completed | 2019-01-31 | 2024-08-29 | ClinicalTrials.gov |
| NCT03646604 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Upadacitin… | Phase1 | Atopic Dermatitis | Completed | 2019-01-31 | 2024-08-29 | ClinicalTrials.gov |
| NCT03725202 | A Study to Evaluate the Safety and Efficacy of Upadacitinib in Participants Wit… | Phase3 | Giant Cell Arteritis (GCA) | Completed | 2019-01-24 | 2025-03-11 | ClinicalTrials.gov |
| NCT03725202 | A Study to Evaluate the Safety and Efficacy of Upadacitinib in Participants Wit… | Phase3 | Giant Cell Arteritis (GCA) | Completed | 2019-01-24 | 2025-03-11 | ClinicalTrials.gov |
| NCT03725202 | A Study to Evaluate the Safety and Efficacy of Upadacitinib in Participants Wit… | Phase3 | Giant Cell Arteritis (GCA) | Completed | 2019-01-24 | 2025-03-11 | ClinicalTrials.gov |
| NCT03725202 | A Study to Evaluate the Safety and Efficacy of Upadacitinib in Participants Wit… | Phase3 | Giant Cell Arteritis (GCA) | Completed | 2019-01-24 | 2025-03-11 | ClinicalTrials.gov |
| NCT03712449 | A Study to Evaluate Participant Satisfaction With Facial Appearance Overall and… | Phase4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | Completed | 2019-01-22 | 2020-07-29 | ClinicalTrials.gov |
| NCT03712449 | A Study to Evaluate Participant Satisfaction With Facial Appearance Overall and… | Phase4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | Completed | 2019-01-22 | 2020-07-29 | ClinicalTrials.gov |
| NCT03712449 | A Study to Evaluate Participant Satisfaction With Facial Appearance Overall and… | Phase4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | Completed | 2019-01-22 | 2020-07-29 | ClinicalTrials.gov |
| NCT03712449 | A Study to Evaluate Participant Satisfaction With Facial Appearance Overall and… | Phase4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | Completed | 2019-01-22 | 2020-07-29 | ClinicalTrials.gov |
| NCT03701919 | Botulinum Toxin Pyloroplasty to Reduce Postoperative Nausea and Vomiting After … | Phase4 | Bariatric Surgery | Completed | 2019-01-07 | 2022-11-11 | ClinicalTrials.gov |
| NCT03701919 | Botulinum Toxin Pyloroplasty to Reduce Postoperative Nausea and Vomiting After … | Phase4 | Bariatric Surgery | Completed | 2019-01-07 | 2022-11-11 | ClinicalTrials.gov |
| NCT03701919 | Botulinum Toxin Pyloroplasty to Reduce Postoperative Nausea and Vomiting After … | Phase4 | Bariatric Surgery | Completed | 2019-01-07 | 2022-11-11 | ClinicalTrials.gov |
| NCT03701919 | Botulinum Toxin Pyloroplasty to Reduce Postoperative Nausea and Vomiting After … | Phase4 | Bariatric Surgery | Completed | 2019-01-07 | 2022-11-11 | ClinicalTrials.gov |
| NCT03706040 | A Study to Evaluate Risankizumab in Adults and Adolescents With Moderate to Sev… | Phase2 | Dermatitis | Completed | 2018-12-27 | 2021-04-26 | ClinicalTrials.gov |
| NCT03706040 | A Study to Evaluate Risankizumab in Adults and Adolescents With Moderate to Sev… | Phase2 | Dermatitis | Completed | 2018-12-27 | 2021-04-26 | ClinicalTrials.gov |
| NCT03706040 | A Study to Evaluate Risankizumab in Adults and Adolescents With Moderate to Sev… | Phase2 | Dermatitis | Completed | 2018-12-27 | 2021-04-26 | ClinicalTrials.gov |
| NCT03706040 | A Study to Evaluate Risankizumab in Adults and Adolescents With Moderate to Sev… | Phase2 | Dermatitis | Completed | 2018-12-27 | 2021-04-26 | ClinicalTrials.gov |
| NCT03804268 | Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in Participa… | Phase3 | Presbyopia | Completed | 2018-12-21 | 2019-10-31 | ClinicalTrials.gov |
| NCT03804268 | Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in Participa… | Phase3 | Presbyopia | Completed | 2018-12-21 | 2019-10-31 | ClinicalTrials.gov |
| NCT03804268 | Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in Participa… | Phase3 | Presbyopia | Completed | 2018-12-21 | 2019-10-31 | ClinicalTrials.gov |
| NCT03804268 | Efficacy Study of Pilocarpine HCl Ophthalmic Solution (AGN-190584) in Participa… | Phase3 | Presbyopia | Completed | 2018-12-21 | 2019-10-31 | ClinicalTrials.gov |
| NCT03786380 | Diabetic Gastroparesis Study 05 | Phase3 | Gastroparesis | Terminated | 2018-12-20 | 2020-10-05 | ClinicalTrials.gov |
| NCT03786380 | Diabetic Gastroparesis Study 05 | Phase3 | Gastroparesis | Terminated | 2018-12-20 | 2020-10-05 | ClinicalTrials.gov |
| NCT03786380 | Diabetic Gastroparesis Study 05 | Phase3 | Gastroparesis | Terminated | 2018-12-20 | 2020-10-05 | ClinicalTrials.gov |
| NCT03786380 | Diabetic Gastroparesis Study 05 | Phase3 | Gastroparesis | Terminated | 2018-12-20 | 2020-10-05 | ClinicalTrials.gov |
| NCT03796728 | A Study to Evaluate the Effectiveness of Juvéderm® VOLIFT™ With Lidocaine for L… | Phase4 | Lip Augmentation | Completed | 2018-12-19 | 2020-06-09 | ClinicalTrials.gov |
| NCT03796728 | A Study to Evaluate the Effectiveness of Juvéderm® VOLIFT™ With Lidocaine for L… | Phase4 | Lip Augmentation | Completed | 2018-12-19 | 2020-06-09 | ClinicalTrials.gov |
| NCT03796728 | A Study to Evaluate the Effectiveness of Juvéderm® VOLIFT™ With Lidocaine for L… | Phase4 | Lip Augmentation | Completed | 2018-12-19 | 2020-06-09 | ClinicalTrials.gov |
| NCT03796728 | A Study to Evaluate the Effectiveness of Juvéderm® VOLIFT™ With Lidocaine for L… | Phase4 | Lip Augmentation | Completed | 2018-12-19 | 2020-06-09 | ClinicalTrials.gov |
| NCT03777059 | 12-Week Placebo-controlled Study of Atogepant for the Preventive Treatment of M… | Phase3 | Episodic Migraine | Completed | 2018-12-14 | 2020-06-19 | ClinicalTrials.gov |
| NCT03777059 | 12-Week Placebo-controlled Study of Atogepant for the Preventive Treatment of M… | Phase3 | Episodic Migraine | Completed | 2018-12-14 | 2020-06-19 | ClinicalTrials.gov |
| NCT03777059 | 12-Week Placebo-controlled Study of Atogepant for the Preventive Treatment of M… | Phase3 | Episodic Migraine | Completed | 2018-12-14 | 2020-06-19 | ClinicalTrials.gov |
| NCT03777059 | 12-Week Placebo-controlled Study of Atogepant for the Preventive Treatment of M… | Phase3 | Episodic Migraine | Completed | 2018-12-14 | 2020-06-19 | ClinicalTrials.gov |
| NCT03737851 | A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard … | Phase2 | Multiple Sclerosis (MS) | Completed | 2018-12-11 | 2021-09-09 | ClinicalTrials.gov |
| NCT03737851 | A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard … | Phase2 | Multiple Sclerosis (MS) | Completed | 2018-12-11 | 2021-09-09 | ClinicalTrials.gov |
| NCT03737851 | A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard … | Phase2 | Multiple Sclerosis (MS) | Completed | 2018-12-11 | 2021-09-09 | ClinicalTrials.gov |
| NCT03737851 | A Study to Assess the Safety and Efficacy of Elezanumab When Added to Standard … | Phase2 | Multiple Sclerosis (MS) | Completed | 2018-12-11 | 2021-09-09 | ClinicalTrials.gov |
| NCT03767400 | Dynamic Optical Coherence Tomography(D-OCT) Aging Study: A Preliminary Evaluati… | — | Skin Care | Completed | 2018-12-07 | 2019-07-30 | ClinicalTrials.gov |
| NCT03767400 | Dynamic Optical Coherence Tomography(D-OCT) Aging Study: A Preliminary Evaluati… | — | Skin Care | Completed | 2018-12-07 | 2019-07-30 | ClinicalTrials.gov |
| NCT03767400 | Dynamic Optical Coherence Tomography(D-OCT) Aging Study: A Preliminary Evaluati… | — | Skin Care | Completed | 2018-12-07 | 2019-07-30 | ClinicalTrials.gov |
| NCT03767400 | Dynamic Optical Coherence Tomography(D-OCT) Aging Study: A Preliminary Evaluati… | — | Skin Care | Completed | 2018-12-07 | 2019-07-30 | ClinicalTrials.gov |
| NCT03653026 | A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants Wi… | Phase3 | Ulcerative Colitis (UC) | Completed | 2018-12-06 | 2021-01-14 | ClinicalTrials.gov |
| NCT03653026 | A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants Wi… | Phase3 | Ulcerative Colitis (UC) | Completed | 2018-12-06 | 2021-01-14 | ClinicalTrials.gov |
| NCT03653026 | A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants Wi… | Phase3 | Ulcerative Colitis (UC) | Completed | 2018-12-06 | 2021-01-14 | ClinicalTrials.gov |
| NCT03653026 | A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants Wi… | Phase3 | Ulcerative Colitis (UC) | Completed | 2018-12-06 | 2021-01-14 | ClinicalTrials.gov |
| NCT03756883 | Therapeutic Equivalence of Two Formulations of Fluticasone Propionate and Salme… | Phase3 | Asthma | Completed | 2018-12-03 | 2019-11-10 | ClinicalTrials.gov |
| NCT03756883 | Therapeutic Equivalence of Two Formulations of Fluticasone Propionate and Salme… | Phase3 | Asthma | Completed | 2018-12-03 | 2019-11-10 | ClinicalTrials.gov |
| NCT03756883 | Therapeutic Equivalence of Two Formulations of Fluticasone Propionate and Salme… | Phase3 | Asthma | Completed | 2018-12-03 | 2019-11-10 | ClinicalTrials.gov |
| NCT03756883 | Therapeutic Equivalence of Two Formulations of Fluticasone Propionate and Salme… | Phase3 | Asthma | Completed | 2018-12-03 | 2019-11-10 | ClinicalTrials.gov |
| NCT03719885 | TrueTear in Sjogren's Disease Patients | Na | Dry Eye Syndromes | Completed | 2018-12-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT03719885 | TrueTear in Sjogren's Disease Patients | Na | Dry Eye Syndromes | Completed | 2018-12-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT03719885 | TrueTear in Sjogren's Disease Patients | Na | Dry Eye Syndromes | Completed | 2018-12-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT03719885 | TrueTear in Sjogren's Disease Patients | Na | Dry Eye Syndromes | Completed | 2018-12-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT03573024 | Venetoclax and Azacitidine for Non-Elderly Adult Patients With Acute Myeloid Le… | Phase2 | Acute Myeloid Leukemia | Completed | 2018-11-28 | 2026-02-19 | ClinicalTrials.gov |
| NCT03573024 | Venetoclax and Azacitidine for Non-Elderly Adult Patients With Acute Myeloid Le… | Phase2 | Acute Myeloid Leukemia | Completed | 2018-11-28 | 2026-02-19 | ClinicalTrials.gov |
| NCT03573024 | Venetoclax and Azacitidine for Non-Elderly Adult Patients With Acute Myeloid Le… | Phase2 | Acute Myeloid Leukemia | Completed | 2018-11-28 | 2026-02-19 | ClinicalTrials.gov |
| NCT03573024 | Venetoclax and Azacitidine for Non-Elderly Adult Patients With Acute Myeloid Le… | Phase2 | Acute Myeloid Leukemia | Completed | 2018-11-28 | 2026-02-19 | ClinicalTrials.gov |
| NCT03832179 | Steroid vs. Anti-vascular Endothelial Growth Factor for Diabetic Macular Edema … | Phase4 | Diabetic Macular Edema | Completed | 2018-11-15 | 2024-03-30 | ClinicalTrials.gov |
| NCT03832179 | Steroid vs. Anti-vascular Endothelial Growth Factor for Diabetic Macular Edema … | Phase4 | Diabetic Macular Edema | Completed | 2018-11-15 | 2024-03-30 | ClinicalTrials.gov |
| NCT03832179 | Steroid vs. Anti-vascular Endothelial Growth Factor for Diabetic Macular Edema … | Phase4 | Diabetic Macular Edema | Completed | 2018-11-15 | 2024-03-30 | ClinicalTrials.gov |
| NCT03832179 | Steroid vs. Anti-vascular Endothelial Growth Factor for Diabetic Macular Edema … | Phase4 | Diabetic Macular Edema | Completed | 2018-11-15 | 2024-03-30 | ClinicalTrials.gov |
| NCT03712137 | Study of the Safety and Effectiveness of JUVÉDERM VOLUX™ XC Injectable Gel for … | Phase3 | Jawline Definition | Completed | 2018-11-12 | 2021-01-26 | ClinicalTrials.gov |
| NCT03712137 | Study of the Safety and Effectiveness of JUVÉDERM VOLUX™ XC Injectable Gel for … | Phase3 | Jawline Definition | Completed | 2018-11-12 | 2021-01-26 | ClinicalTrials.gov |
| NCT03712137 | Study of the Safety and Effectiveness of JUVÉDERM VOLUX™ XC Injectable Gel for … | Phase3 | Jawline Definition | Completed | 2018-11-12 | 2021-01-26 | ClinicalTrials.gov |
| NCT03712137 | Study of the Safety and Effectiveness of JUVÉDERM VOLUX™ XC Injectable Gel for … | Phase3 | Jawline Definition | Completed | 2018-11-12 | 2021-01-26 | ClinicalTrials.gov |
| NCT03739203 | The Objective of This Study is to Evaluate the Efficacy, Safety and Tolerabilit… | Phase3 | Major Depressive Disorder | Completed | 2018-11-10 | 2021-09-06 | ClinicalTrials.gov |
| NCT03739203 | The Objective of This Study is to Evaluate the Efficacy, Safety and Tolerabilit… | Phase3 | Major Depressive Disorder | Completed | 2018-11-10 | 2021-09-06 | ClinicalTrials.gov |
| NCT03739203 | The Objective of This Study is to Evaluate the Efficacy, Safety and Tolerabilit… | Phase3 | Major Depressive Disorder | Completed | 2018-11-10 | 2021-09-06 | ClinicalTrials.gov |
| NCT03739203 | The Objective of This Study is to Evaluate the Efficacy, Safety and Tolerabilit… | Phase3 | Major Depressive Disorder | Completed | 2018-11-10 | 2021-09-06 | ClinicalTrials.gov |
| NCT03738215 | Efficacy, Safety and Tolerability of Cariprazine as an Adjunctive Treatment to … | Phase3 | Major Depressive Disorder | Completed | 2018-11-09 | 2021-09-30 | ClinicalTrials.gov |
| NCT03738215 | Efficacy, Safety and Tolerability of Cariprazine as an Adjunctive Treatment to … | Phase3 | Major Depressive Disorder | Completed | 2018-11-09 | 2021-09-30 | ClinicalTrials.gov |
| NCT03738215 | Efficacy, Safety and Tolerability of Cariprazine as an Adjunctive Treatment to … | Phase3 | Major Depressive Disorder | Completed | 2018-11-09 | 2021-09-30 | ClinicalTrials.gov |
| NCT03738215 | Efficacy, Safety and Tolerability of Cariprazine as an Adjunctive Treatment to … | Phase3 | Major Depressive Disorder | Completed | 2018-11-09 | 2021-09-30 | ClinicalTrials.gov |
| NCT03814733 | Assessment of Effect of Rapastinel on Driving Performance | Phase1 | Driving Performance | Completed | 2018-11-05 | 2019-04-03 | ClinicalTrials.gov |
| NCT03814733 | Assessment of Effect of Rapastinel on Driving Performance | Phase1 | Driving Performance | Completed | 2018-11-05 | 2019-04-03 | ClinicalTrials.gov |
| NCT03814733 | Assessment of Effect of Rapastinel on Driving Performance | Phase1 | Driving Performance | Completed | 2018-11-05 | 2019-04-03 | ClinicalTrials.gov |
| NCT03814733 | Assessment of Effect of Rapastinel on Driving Performance | Phase1 | Driving Performance | Completed | 2018-11-05 | 2019-04-03 | ClinicalTrials.gov |
| NCT03799900 | Assessment of Abuse Potential of Rapastinel in Humans | Phase1 | Human Abuse Potential | Completed | 2018-11-01 | 2019-03-29 | ClinicalTrials.gov |
| NCT03799900 | Assessment of Abuse Potential of Rapastinel in Humans | Phase1 | Human Abuse Potential | Completed | 2018-11-01 | 2019-03-29 | ClinicalTrials.gov |
| NCT03799900 | Assessment of Abuse Potential of Rapastinel in Humans | Phase1 | Human Abuse Potential | Completed | 2018-11-01 | 2019-03-29 | ClinicalTrials.gov |
| NCT03799900 | Assessment of Abuse Potential of Rapastinel in Humans | Phase1 | Human Abuse Potential | Completed | 2018-11-01 | 2019-03-29 | ClinicalTrials.gov |
| NCT03675776 | Study of Rapastinel as Monotherapy in Patients With Major Depressive Disorder (… | Phase3 | Depressive Disorder, Major | Terminated | 2018-10-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03675776 | Study of Rapastinel as Monotherapy in Patients With Major Depressive Disorder (… | Phase3 | Depressive Disorder, Major | Terminated | 2018-10-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03675776 | Study of Rapastinel as Monotherapy in Patients With Major Depressive Disorder (… | Phase3 | Depressive Disorder, Major | Terminated | 2018-10-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03675776 | Study of Rapastinel as Monotherapy in Patients With Major Depressive Disorder (… | Phase3 | Depressive Disorder, Major | Terminated | 2018-10-30 | 2019-07-11 | ClinicalTrials.gov |
| NCT03661138 | A Study to Evaluate Safety of Upadacitinib in Combination With Topical Corticos… | Phase3 | Atopic Dermatitis | Completed | 2018-10-27 | 2022-08-19 | ClinicalTrials.gov |
| NCT03661138 | A Study to Evaluate Safety of Upadacitinib in Combination With Topical Corticos… | Phase3 | Atopic Dermatitis | Completed | 2018-10-27 | 2022-08-19 | ClinicalTrials.gov |
| NCT03661138 | A Study to Evaluate Safety of Upadacitinib in Combination With Topical Corticos… | Phase3 | Atopic Dermatitis | Completed | 2018-10-27 | 2022-08-19 | ClinicalTrials.gov |
| NCT03661138 | A Study to Evaluate Safety of Upadacitinib in Combination With Topical Corticos… | Phase3 | Atopic Dermatitis | Completed | 2018-10-27 | 2022-08-19 | ClinicalTrials.gov |
| NCT03695237 | A Study to Evaluate Leuprolide Acetate 45 mg 6-Month Formulation in Children Wi… | Phase3 | Central Precocious Puberty (CPP) | Completed | 2018-10-24 | 2023-11-29 | ClinicalTrials.gov |
| NCT03639194 | A Study of ABBV-011 Alone and in Combination With Budigalimab (ABBV-181) in Par… | Phase1 | Small Cell Lung Cancer | Completed | 2018-10-24 | 2024-01-25 | ClinicalTrials.gov |
| NCT03695237 | A Study to Evaluate Leuprolide Acetate 45 mg 6-Month Formulation in Children Wi… | Phase3 | Central Precocious Puberty (CPP) | Completed | 2018-10-24 | 2023-11-29 | ClinicalTrials.gov |
| NCT03639194 | A Study of ABBV-011 Alone and in Combination With Budigalimab (ABBV-181) in Par… | Phase1 | Small Cell Lung Cancer | Completed | 2018-10-24 | 2024-01-25 | ClinicalTrials.gov |
| NCT03639194 | A Study of ABBV-011 Alone and in Combination With Budigalimab (ABBV-181) in Par… | Phase1 | Small Cell Lung Cancer | Completed | 2018-10-24 | 2024-01-25 | ClinicalTrials.gov |
| NCT03639194 | A Study of ABBV-011 Alone and in Combination With Budigalimab (ABBV-181) in Par… | Phase1 | Small Cell Lung Cancer | Completed | 2018-10-24 | 2024-01-25 | ClinicalTrials.gov |
| NCT03695237 | A Study to Evaluate Leuprolide Acetate 45 mg 6-Month Formulation in Children Wi… | Phase3 | Central Precocious Puberty (CPP) | Completed | 2018-10-24 | 2023-11-29 | ClinicalTrials.gov |
| NCT03695237 | A Study to Evaluate Leuprolide Acetate 45 mg 6-Month Formulation in Children Wi… | Phase3 | Central Precocious Puberty (CPP) | Completed | 2018-10-24 | 2023-11-29 | ClinicalTrials.gov |
| NCT03539744 | A Study Designed to Evaluate the Safety and Efficacy of Venetoclax Plus Dexamet… | Phase3 | Multiple Myeloma | Active_Not_Recruiting | 2018-10-22 | 2027-11-01 | ClinicalTrials.gov |
| NCT03539744 | A Study Designed to Evaluate the Safety and Efficacy of Venetoclax Plus Dexamet… | Phase3 | Multiple Myeloma | Active_Not_Recruiting | 2018-10-22 | 2027-11-01 | ClinicalTrials.gov |
| NCT03539744 | A Study Designed to Evaluate the Safety and Efficacy of Venetoclax Plus Dexamet… | Phase3 | Multiple Myeloma | Active_Not_Recruiting | 2018-10-22 | 2027-11-01 | ClinicalTrials.gov |
| NCT03539744 | A Study Designed to Evaluate the Safety and Efficacy of Venetoclax Plus Dexamet… | Phase3 | Multiple Myeloma | Active_Not_Recruiting | 2018-10-22 | 2027-11-01 | ClinicalTrials.gov |
| NCT03693586 | Study to Determine the Hepatitis C Virus Infection Prevalence Among Patients At… | — | Chronic Hepatitis c | Completed | 2018-10-19 | 2022-03-08 | ClinicalTrials.gov |
| NCT03693586 | Study to Determine the Hepatitis C Virus Infection Prevalence Among Patients At… | — | Chronic Hepatitis c | Completed | 2018-10-19 | 2022-03-08 | ClinicalTrials.gov |
| NCT03693586 | Study to Determine the Hepatitis C Virus Infection Prevalence Among Patients At… | — | Chronic Hepatitis c | Completed | 2018-10-19 | 2022-03-08 | ClinicalTrials.gov |
| NCT03693586 | Study to Determine the Hepatitis C Virus Infection Prevalence Among Patients At… | — | Chronic Hepatitis c | Completed | 2018-10-19 | 2022-03-08 | ClinicalTrials.gov |
| NCT03567616 | A Study of Venetoclax in Combination With Pomalidomide and Dexamethasone in Par… | Phase2 | Multiple Myeloma | Terminated | 2018-10-18 | 2020-06-18 | ClinicalTrials.gov |
| NCT03625505 | A Study to Assess Safety and Efficacy of Venetoclax in Combination With Gilteri… | Phase1 | Acute Myeloid Leukemia (AML) | Completed | 2018-10-18 | 2021-08-31 | ClinicalTrials.gov |
| NCT03567616 | A Study of Venetoclax in Combination With Pomalidomide and Dexamethasone in Par… | Phase2 | Multiple Myeloma | Terminated | 2018-10-18 | 2020-06-18 | ClinicalTrials.gov |
| NCT03567616 | A Study of Venetoclax in Combination With Pomalidomide and Dexamethasone in Par… | Phase2 | Multiple Myeloma | Terminated | 2018-10-18 | 2020-06-18 | ClinicalTrials.gov |
| NCT03625505 | A Study to Assess Safety and Efficacy of Venetoclax in Combination With Gilteri… | Phase1 | Acute Myeloid Leukemia (AML) | Completed | 2018-10-18 | 2021-08-31 | ClinicalTrials.gov |
| NCT03625505 | A Study to Assess Safety and Efficacy of Venetoclax in Combination With Gilteri… | Phase1 | Acute Myeloid Leukemia (AML) | Completed | 2018-10-18 | 2021-08-31 | ClinicalTrials.gov |
| NCT03625505 | A Study to Assess Safety and Efficacy of Venetoclax in Combination With Gilteri… | Phase1 | Acute Myeloid Leukemia (AML) | Completed | 2018-10-18 | 2021-08-31 | ClinicalTrials.gov |
| NCT03567616 | A Study of Venetoclax in Combination With Pomalidomide and Dexamethasone in Par… | Phase2 | Multiple Myeloma | Terminated | 2018-10-18 | 2020-06-18 | ClinicalTrials.gov |
| NCT03709758 | Venetoclax in Combination With Intensive Induction and Consolidation Chemothera… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2018-10-17 | 2026-09-01 | ClinicalTrials.gov |
| NCT03709758 | Venetoclax in Combination With Intensive Induction and Consolidation Chemothera… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2018-10-17 | 2026-09-01 | ClinicalTrials.gov |
| NCT03709758 | Venetoclax in Combination With Intensive Induction and Consolidation Chemothera… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2018-10-17 | 2026-09-01 | ClinicalTrials.gov |
| NCT03709758 | Venetoclax in Combination With Intensive Induction and Consolidation Chemothera… | Phase1 | Acute Myeloid Leukemia | Active_Not_Recruiting | 2018-10-17 | 2026-09-01 | ClinicalTrials.gov |
| NCT03539536 | Study of Telisotuzumab Vedotin (ABBV-399) in Participants With Previously Treat… | Phase2 | Non-small Cell Lung Cancer | Active_Not_Recruiting | 2018-10-10 | 2026-08-01 | ClinicalTrials.gov |
| NCT03539536 | Study of Telisotuzumab Vedotin (ABBV-399) in Participants With Previously Treat… | Phase2 | Non-small Cell Lung Cancer | Active_Not_Recruiting | 2018-10-10 | 2026-08-01 | ClinicalTrials.gov |
| NCT03661697 | Combination Versus Laser Treatment Only | Na | Photoaging | Completed | 2018-10-10 | 2019-03-07 | ClinicalTrials.gov |
| NCT03661697 | Combination Versus Laser Treatment Only | Na | Photoaging | Completed | 2018-10-10 | 2019-03-07 | ClinicalTrials.gov |
| NCT03661697 | Combination Versus Laser Treatment Only | Na | Photoaging | Completed | 2018-10-10 | 2019-03-07 | ClinicalTrials.gov |
| NCT03539536 | Study of Telisotuzumab Vedotin (ABBV-399) in Participants With Previously Treat… | Phase2 | Non-small Cell Lung Cancer | Active_Not_Recruiting | 2018-10-10 | 2026-08-01 | ClinicalTrials.gov |
| NCT03539536 | Study of Telisotuzumab Vedotin (ABBV-399) in Participants With Previously Treat… | Phase2 | Non-small Cell Lung Cancer | Active_Not_Recruiting | 2018-10-10 | 2026-08-01 | ClinicalTrials.gov |
| NCT03661697 | Combination Versus Laser Treatment Only | Na | Photoaging | Completed | 2018-10-10 | 2019-03-07 | ClinicalTrials.gov |
| NCT03682705 | A Study to Investigate the Safety and Efficacy of ABBV-105 Alone or in Combinat… | Phase2 | Rheumatoid Arthritis (RA) | Completed | 2018-10-08 | 2020-03-26 | ClinicalTrials.gov |
| NCT03700320 | Study to Evaluate the Safety and Tolerability of Treatment With Atogepant 60 mg… | Phase3 | Episodic Migraine | Completed | 2018-10-08 | 2020-05-21 | ClinicalTrials.gov |
| NCT03700320 | Study to Evaluate the Safety and Tolerability of Treatment With Atogepant 60 mg… | Phase3 | Episodic Migraine | Completed | 2018-10-08 | 2020-05-21 | ClinicalTrials.gov |
| NCT03682705 | A Study to Investigate the Safety and Efficacy of ABBV-105 Alone or in Combinat… | Phase2 | Rheumatoid Arthritis (RA) | Completed | 2018-10-08 | 2020-03-26 | ClinicalTrials.gov |
| NCT03700320 | Study to Evaluate the Safety and Tolerability of Treatment With Atogepant 60 mg… | Phase3 | Episodic Migraine | Completed | 2018-10-08 | 2020-05-21 | ClinicalTrials.gov |
| NCT03682705 | A Study to Investigate the Safety and Efficacy of ABBV-105 Alone or in Combinat… | Phase2 | Rheumatoid Arthritis (RA) | Completed | 2018-10-08 | 2020-03-26 | ClinicalTrials.gov |
| NCT03700320 | Study to Evaluate the Safety and Tolerability of Treatment With Atogepant 60 mg… | Phase3 | Episodic Migraine | Completed | 2018-10-08 | 2020-05-21 | ClinicalTrials.gov |
| NCT03682705 | A Study to Investigate the Safety and Efficacy of ABBV-105 Alone or in Combinat… | Phase2 | Rheumatoid Arthritis (RA) | Completed | 2018-10-08 | 2020-03-26 | ClinicalTrials.gov |
| NCT03637517 | Malaria: Relative Bioavailability and Food Effect of DSM265 | Phase1 | Healthy Volunteers | Completed | 2018-10-03 | 2018-11-19 | ClinicalTrials.gov |
| NCT03637517 | Malaria: Relative Bioavailability and Food Effect of DSM265 | Phase1 | Healthy Volunteers | Completed | 2018-10-03 | 2018-11-19 | ClinicalTrials.gov |
| NCT03637517 | Malaria: Relative Bioavailability and Food Effect of DSM265 | Phase1 | Healthy Volunteers | Completed | 2018-10-03 | 2018-11-19 | ClinicalTrials.gov |
| NCT03637517 | Malaria: Relative Bioavailability and Food Effect of DSM265 | Phase1 | Healthy Volunteers | Completed | 2018-10-03 | 2018-11-19 | ClinicalTrials.gov |
| NCT03654885 | XEN-45 Gel Stent Versus Trabeculectomy in Glaucoma: Gold-Standard Pathway Study… | Phase4 | Glaucoma | Completed | 2018-10-01 | 2021-05-13 | ClinicalTrials.gov |
| NCT03631368 | Treatment of Hypertrophic Scars With Intradermal Botox | Phase2 | Hypertrophic Scar | Unknown | 2018-10-01 | 2019-05-31 | ClinicalTrials.gov |
| NCT03654885 | XEN-45 Gel Stent Versus Trabeculectomy in Glaucoma: Gold-Standard Pathway Study… | Phase4 | Glaucoma | Completed | 2018-10-01 | 2021-05-13 | ClinicalTrials.gov |
| NCT03631368 | Treatment of Hypertrophic Scars With Intradermal Botox | Phase2 | Hypertrophic Scar | Unknown | 2018-10-01 | 2019-05-31 | ClinicalTrials.gov |
| NCT03654885 | XEN-45 Gel Stent Versus Trabeculectomy in Glaucoma: Gold-Standard Pathway Study… | Phase4 | Glaucoma | Completed | 2018-10-01 | 2021-05-13 | ClinicalTrials.gov |
| NCT03654885 | XEN-45 Gel Stent Versus Trabeculectomy in Glaucoma: Gold-Standard Pathway Study… | Phase4 | Glaucoma | Completed | 2018-10-01 | 2021-05-13 | ClinicalTrials.gov |
| NCT03631368 | Treatment of Hypertrophic Scars With Intradermal Botox | Phase2 | Hypertrophic Scar | Unknown | 2018-10-01 | 2019-05-31 | ClinicalTrials.gov |
| NCT03631368 | Treatment of Hypertrophic Scars With Intradermal Botox | Phase2 | Hypertrophic Scar | Unknown | 2018-10-01 | 2019-05-31 | ClinicalTrials.gov |
| NCT02786563 | Changes in Ultrasonographic Assessment of Inflammation Upon Initiation of Adali… | — | Rheumatoid Arthritis (RA) | Withdrawn | 2018-09-30 | 2018-11-21 | ClinicalTrials.gov |
| NCT02786563 | Changes in Ultrasonographic Assessment of Inflammation Upon Initiation of Adali… | — | Rheumatoid Arthritis (RA) | Withdrawn | 2018-09-30 | 2018-11-21 | ClinicalTrials.gov |
| NCT02786563 | Changes in Ultrasonographic Assessment of Inflammation Upon Initiation of Adali… | — | Rheumatoid Arthritis (RA) | Withdrawn | 2018-09-30 | 2018-11-21 | ClinicalTrials.gov |
| NCT02786563 | Changes in Ultrasonographic Assessment of Inflammation Upon Initiation of Adali… | — | Rheumatoid Arthritis (RA) | Withdrawn | 2018-09-30 | 2018-11-21 | ClinicalTrials.gov |
| NCT03740230 | An Observational Study of Maviret (Glecaprevir/Pibrentasvir) for Korean Chronic… | — | Hepatitis C | Completed | 2018-09-26 | 2023-07-21 | ClinicalTrials.gov |
| NCT03740230 | An Observational Study of Maviret (Glecaprevir/Pibrentasvir) for Korean Chronic… | — | Hepatitis C | Completed | 2018-09-26 | 2023-07-21 | ClinicalTrials.gov |
| NCT03740230 | An Observational Study of Maviret (Glecaprevir/Pibrentasvir) for Korean Chronic… | — | Hepatitis C | Completed | 2018-09-26 | 2023-07-21 | ClinicalTrials.gov |
| NCT03740230 | An Observational Study of Maviret (Glecaprevir/Pibrentasvir) for Korean Chronic… | — | Hepatitis C | Completed | 2018-09-26 | 2023-07-21 | ClinicalTrials.gov |
| NCT03517540 | Study of Safety, Tolerability, and Efficacy of a Combination Treatment of LJN45… | Phase2 | Non-alcoholic Steatohepatitis (NASH) | Completed | 2018-09-11 | 2020-10-15 | ClinicalTrials.gov |
| NCT03517540 | Study of Safety, Tolerability, and Efficacy of a Combination Treatment of LJN45… | Phase2 | Non-alcoholic Steatohepatitis (NASH) | Completed | 2018-09-11 | 2020-10-15 | ClinicalTrials.gov |
| NCT03517540 | Study of Safety, Tolerability, and Efficacy of a Combination Treatment of LJN45… | Phase2 | Non-alcoholic Steatohepatitis (NASH) | Completed | 2018-09-11 | 2020-10-15 | ClinicalTrials.gov |
| NCT03517540 | Study of Safety, Tolerability, and Efficacy of a Combination Treatment of LJN45… | Phase2 | Non-alcoholic Steatohepatitis (NASH) | Completed | 2018-09-11 | 2020-10-15 | ClinicalTrials.gov |
| NCT03543358 | A Long-Term Study of Rovalpituzumab Tesirine | Phase2 | Cancer | Completed | 2018-09-10 | 2019-11-26 | ClinicalTrials.gov |
| NCT03543358 | A Long-Term Study of Rovalpituzumab Tesirine | Phase2 | Cancer | Completed | 2018-09-10 | 2019-11-26 | ClinicalTrials.gov |
| NCT03543358 | A Long-Term Study of Rovalpituzumab Tesirine | Phase2 | Cancer | Completed | 2018-09-10 | 2019-11-26 | ClinicalTrials.gov |
| NCT03543358 | A Long-Term Study of Rovalpituzumab Tesirine | Phase2 | Cancer | Completed | 2018-09-10 | 2019-11-26 | ClinicalTrials.gov |
| NCT03567876 | Rituximab, Bendamustine and Cytarabine Followed by Venetoclax in High Risk Elde… | Phase2 | Lymphoma, Mantle-Cell | Completed | 2018-09-03 | 2025-10-15 | ClinicalTrials.gov |
| NCT03567876 | Rituximab, Bendamustine and Cytarabine Followed by Venetoclax in High Risk Elde… | Phase2 | Lymphoma, Mantle-Cell | Completed | 2018-09-03 | 2025-10-15 | ClinicalTrials.gov |
| NCT03567876 | Rituximab, Bendamustine and Cytarabine Followed by Venetoclax in High Risk Elde… | Phase2 | Lymphoma, Mantle-Cell | Completed | 2018-09-03 | 2025-10-15 | ClinicalTrials.gov |
| NCT03567876 | Rituximab, Bendamustine and Cytarabine Followed by Venetoclax in High Risk Elde… | Phase2 | Lymphoma, Mantle-Cell | Completed | 2018-09-03 | 2025-10-15 | ClinicalTrials.gov |
| NCT03398135 | A Study to Assess the Efficacy and Safety of Risankizumab in Participants With … | Phase3 | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2018-08-28 | 2029-02-01 | ClinicalTrials.gov |
| NCT03398135 | A Study to Assess the Efficacy and Safety of Risankizumab in Participants With … | Phase3 | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2018-08-28 | 2029-02-01 | ClinicalTrials.gov |
| NCT03398135 | A Study to Assess the Efficacy and Safety of Risankizumab in Participants With … | Phase3 | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2018-08-28 | 2029-02-01 | ClinicalTrials.gov |
| NCT03398135 | A Study to Assess the Efficacy and Safety of Risankizumab in Participants With … | Phase3 | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2018-08-28 | 2029-02-01 | ClinicalTrials.gov |
| NCT03485547 | Study of Venetoclax, a BCL2 Antagonist, for Patients With Blastic Plasmacytoid … | Phase1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | Completed | 2018-08-23 | 2025-04-16 | ClinicalTrials.gov |
| NCT03668600 | Study of Adjunctive or Monotherapy Rapastinel Treatment in Patients With Major … | Phase3 | Depressive Disorder, Major | Terminated | 2018-08-23 | 2019-07-03 | ClinicalTrials.gov |
| NCT03668600 | Study of Adjunctive or Monotherapy Rapastinel Treatment in Patients With Major … | Phase3 | Depressive Disorder, Major | Terminated | 2018-08-23 | 2019-07-03 | ClinicalTrials.gov |
| NCT03485547 | Study of Venetoclax, a BCL2 Antagonist, for Patients With Blastic Plasmacytoid … | Phase1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | Completed | 2018-08-23 | 2025-04-16 | ClinicalTrials.gov |
| NCT03485547 | Study of Venetoclax, a BCL2 Antagonist, for Patients With Blastic Plasmacytoid … | Phase1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | Completed | 2018-08-23 | 2025-04-16 | ClinicalTrials.gov |
| NCT03668600 | Study of Adjunctive or Monotherapy Rapastinel Treatment in Patients With Major … | Phase3 | Depressive Disorder, Major | Terminated | 2018-08-23 | 2019-07-03 | ClinicalTrials.gov |
| NCT03485547 | Study of Venetoclax, a BCL2 Antagonist, for Patients With Blastic Plasmacytoid … | Phase1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | Completed | 2018-08-23 | 2025-04-16 | ClinicalTrials.gov |
| NCT03668600 | Study of Adjunctive or Monotherapy Rapastinel Treatment in Patients With Major … | Phase3 | Depressive Disorder, Major | Terminated | 2018-08-23 | 2019-07-03 | ClinicalTrials.gov |
| NCT03637348 | Effect of TrueTear Corneal Surface Imaging | Na | Cataract | Completed | 2018-08-13 | 2019-07-08 | ClinicalTrials.gov |
| NCT03569293 | Evaluation of Upadacitinib in Adolescent and Adult Patients With Moderate to Se… | Phase3 | Atopic Dermatitis | Completed | 2018-08-13 | 2025-10-10 | ClinicalTrials.gov |
| NCT03569293 | Evaluation of Upadacitinib in Adolescent and Adult Patients With Moderate to Se… | Phase3 | Atopic Dermatitis | Completed | 2018-08-13 | 2025-10-10 | ClinicalTrials.gov |
| NCT03637348 | Effect of TrueTear Corneal Surface Imaging | Na | Cataract | Completed | 2018-08-13 | 2019-07-08 | ClinicalTrials.gov |
| NCT03637348 | Effect of TrueTear Corneal Surface Imaging | Na | Cataract | Completed | 2018-08-13 | 2019-07-08 | ClinicalTrials.gov |
| NCT03569293 | Evaluation of Upadacitinib in Adolescent and Adult Patients With Moderate to Se… | Phase3 | Atopic Dermatitis | Completed | 2018-08-13 | 2025-10-10 | ClinicalTrials.gov |
| NCT03569293 | Evaluation of Upadacitinib in Adolescent and Adult Patients With Moderate to Se… | Phase3 | Atopic Dermatitis | Completed | 2018-08-13 | 2025-10-10 | ClinicalTrials.gov |
| NCT03637348 | Effect of TrueTear Corneal Surface Imaging | Na | Cataract | Completed | 2018-08-13 | 2019-07-08 | ClinicalTrials.gov |
| NCT03406156 | A Study in Previously Untreated Chronic Lymphocytic Leukemia (CLL) Subjects, Ex… | Phase3 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2018-08-10 | 2023-07-12 | ClinicalTrials.gov |
| NCT03406156 | A Study in Previously Untreated Chronic Lymphocytic Leukemia (CLL) Subjects, Ex… | Phase3 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2018-08-10 | 2023-07-12 | ClinicalTrials.gov |
| NCT03406156 | A Study in Previously Untreated Chronic Lymphocytic Leukemia (CLL) Subjects, Ex… | Phase3 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2018-08-10 | 2023-07-12 | ClinicalTrials.gov |
| NCT03406156 | A Study in Previously Untreated Chronic Lymphocytic Leukemia (CLL) Subjects, Ex… | Phase3 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2018-08-10 | 2023-07-12 | ClinicalTrials.gov |
| NCT03568318 | A Study to Evaluate Upadacitinib in Combination With Topical Corticosteroids in… | Phase3 | Atopic Dermatitis | Active_Not_Recruiting | 2018-08-09 | 2030-10-23 | ClinicalTrials.gov |
| NCT03568318 | A Study to Evaluate Upadacitinib in Combination With Topical Corticosteroids in… | Phase3 | Atopic Dermatitis | Active_Not_Recruiting | 2018-08-09 | 2030-10-23 | ClinicalTrials.gov |
| NCT03568318 | A Study to Evaluate Upadacitinib in Combination With Topical Corticosteroids in… | Phase3 | Atopic Dermatitis | Active_Not_Recruiting | 2018-08-09 | 2030-10-23 | ClinicalTrials.gov |
| NCT03568318 | A Study to Evaluate Upadacitinib in Combination With Topical Corticosteroids in… | Phase3 | Atopic Dermatitis | Active_Not_Recruiting | 2018-08-09 | 2030-10-23 | ClinicalTrials.gov |
| NCT03594721 | Clinical Trial Evaluation of a Test Serum Post HEV (High Energy Visible) Light … | Na | Blue Light Damage | Completed | 2018-08-06 | 2018-08-30 | ClinicalTrials.gov |
| NCT03594721 | Clinical Trial Evaluation of a Test Serum Post HEV (High Energy Visible) Light … | Na | Blue Light Damage | Completed | 2018-08-06 | 2018-08-30 | ClinicalTrials.gov |
| NCT03594721 | Clinical Trial Evaluation of a Test Serum Post HEV (High Energy Visible) Light … | Na | Blue Light Damage | Completed | 2018-08-06 | 2018-08-30 | ClinicalTrials.gov |
| NCT03594721 | Clinical Trial Evaluation of a Test Serum Post HEV (High Energy Visible) Light … | Na | Blue Light Damage | Completed | 2018-08-06 | 2018-08-30 | ClinicalTrials.gov |
| NCT03614156 | Study of Monotherapy Rapastinel in the Prevention of Relapse in Patients With M… | Phase3 | Depressive Disorder, Major | Terminated | 2018-08-02 | 2019-07-11 | ClinicalTrials.gov |
| NCT03614156 | Study of Monotherapy Rapastinel in the Prevention of Relapse in Patients With M… | Phase3 | Depressive Disorder, Major | Terminated | 2018-08-02 | 2019-07-11 | ClinicalTrials.gov |
| NCT03614156 | Study of Monotherapy Rapastinel in the Prevention of Relapse in Patients With M… | Phase3 | Depressive Disorder, Major | Terminated | 2018-08-02 | 2019-07-11 | ClinicalTrials.gov |
| NCT03614156 | Study of Monotherapy Rapastinel in the Prevention of Relapse in Patients With M… | Phase3 | Depressive Disorder, Major | Terminated | 2018-08-02 | 2019-07-11 | ClinicalTrials.gov |
| NCT03584958 | Comparing Refractive and Visual Outcomes of MIGS and Traditional Surgeries | — | Glaucoma | Unknown | 2018-08-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT03584958 | Comparing Refractive and Visual Outcomes of MIGS and Traditional Surgeries | — | Glaucoma | Unknown | 2018-08-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT03584958 | Comparing Refractive and Visual Outcomes of MIGS and Traditional Surgeries | — | Glaucoma | Unknown | 2018-08-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT03584958 | Comparing Refractive and Visual Outcomes of MIGS and Traditional Surgeries | — | Glaucoma | Unknown | 2018-08-01 | 2023-06-30 | ClinicalTrials.gov |
| NCT03593213 | Clinical Trial Evaluating the Efficacy, Safety, and Tolerability of Cariprazine… | Phase3 | Schizophrenia | Terminated | 2018-07-30 | 2021-02-11 | ClinicalTrials.gov |
| NCT03419403 | UNITE Study: Understanding New Interventions With GBM ThErapy | Phase3 | Glioblastoma Multiforme | Terminated | 2018-07-30 | 2020-03-03 | ClinicalTrials.gov |
| NCT03219437 | A Study Comparing the Safety and Efficacy of Risankizumab to Methotrexate in Su… | Phase3 | Psoriasis | Completed | 2018-07-30 | 2021-11-26 | ClinicalTrials.gov |
| NCT03419403 | UNITE Study: Understanding New Interventions With GBM ThErapy | Phase3 | Glioblastoma Multiforme | Terminated | 2018-07-30 | 2020-03-03 | ClinicalTrials.gov |
| NCT03593213 | Clinical Trial Evaluating the Efficacy, Safety, and Tolerability of Cariprazine… | Phase3 | Schizophrenia | Terminated | 2018-07-30 | 2021-02-11 | ClinicalTrials.gov |
| NCT03219437 | A Study Comparing the Safety and Efficacy of Risankizumab to Methotrexate in Su… | Phase3 | Psoriasis | Completed | 2018-07-30 | 2021-11-26 | ClinicalTrials.gov |
| NCT03593213 | Clinical Trial Evaluating the Efficacy, Safety, and Tolerability of Cariprazine… | Phase3 | Schizophrenia | Terminated | 2018-07-30 | 2021-02-11 | ClinicalTrials.gov |
| NCT03593213 | Clinical Trial Evaluating the Efficacy, Safety, and Tolerability of Cariprazine… | Phase3 | Schizophrenia | Terminated | 2018-07-30 | 2021-02-11 | ClinicalTrials.gov |
| NCT03419403 | UNITE Study: Understanding New Interventions With GBM ThErapy | Phase3 | Glioblastoma Multiforme | Terminated | 2018-07-30 | 2020-03-03 | ClinicalTrials.gov |
| NCT03219437 | A Study Comparing the Safety and Efficacy of Risankizumab to Methotrexate in Su… | Phase3 | Psoriasis | Completed | 2018-07-30 | 2021-11-26 | ClinicalTrials.gov |
| NCT03219437 | A Study Comparing the Safety and Efficacy of Risankizumab to Methotrexate in Su… | Phase3 | Psoriasis | Completed | 2018-07-30 | 2021-11-26 | ClinicalTrials.gov |
| NCT03419403 | UNITE Study: Understanding New Interventions With GBM ThErapy | Phase3 | Glioblastoma Multiforme | Terminated | 2018-07-30 | 2020-03-03 | ClinicalTrials.gov |
| NCT03607422 | A Study to Evaluate Upadacitinib in Adolescents and Adults With Moderate to Sev… | Phase3 | Atopic Dermatitis | Completed | 2018-07-27 | 2025-11-11 | ClinicalTrials.gov |
| NCT03607422 | A Study to Evaluate Upadacitinib in Adolescents and Adults With Moderate to Sev… | Phase3 | Atopic Dermatitis | Completed | 2018-07-27 | 2025-11-11 | ClinicalTrials.gov |
| NCT03607422 | A Study to Evaluate Upadacitinib in Adolescents and Adults With Moderate to Sev… | Phase3 | Atopic Dermatitis | Completed | 2018-07-27 | 2025-11-11 | ClinicalTrials.gov |
| NCT03607422 | A Study to Evaluate Upadacitinib in Adolescents and Adults With Moderate to Sev… | Phase3 | Atopic Dermatitis | Completed | 2018-07-27 | 2025-11-11 | ClinicalTrials.gov |
| NCT03484520 | A Study of Venetoclax and Dinaciclib (MK7965) in Patients With Relapsed/Refract… | Phase1 | Cancer - Acute Myeloid Leukemia | Terminated | 2018-07-23 | 2022-12-01 | ClinicalTrials.gov |
| NCT03484520 | A Study of Venetoclax and Dinaciclib (MK7965) in Patients With Relapsed/Refract… | Phase1 | Cancer - Acute Myeloid Leukemia | Terminated | 2018-07-23 | 2022-12-01 | ClinicalTrials.gov |
| NCT03484520 | A Study of Venetoclax and Dinaciclib (MK7965) in Patients With Relapsed/Refract… | Phase1 | Cancer - Acute Myeloid Leukemia | Terminated | 2018-07-23 | 2022-12-01 | ClinicalTrials.gov |
| NCT03484520 | A Study of Venetoclax and Dinaciclib (MK7965) in Patients With Relapsed/Refract… | Phase1 | Cancer - Acute Myeloid Leukemia | Terminated | 2018-07-23 | 2022-12-01 | ClinicalTrials.gov |
| NCT03518047 | Risankizumab Therapy Versus Placebo for Subjects With Psoriasis in the Russian … | Phase3 | Psoriasis | Completed | 2018-07-19 | 2020-02-11 | ClinicalTrials.gov |
| NCT03362931 | Safety and Effectiveness of the XEN45 Glaucoma Treatment System in Patients Wit… | Phase3 | Glaucoma | Completed | 2018-07-19 | 2022-03-18 | ClinicalTrials.gov |
| NCT03362931 | Safety and Effectiveness of the XEN45 Glaucoma Treatment System in Patients Wit… | Phase3 | Glaucoma | Completed | 2018-07-19 | 2022-03-18 | ClinicalTrials.gov |
| NCT03518047 | Risankizumab Therapy Versus Placebo for Subjects With Psoriasis in the Russian … | Phase3 | Psoriasis | Completed | 2018-07-19 | 2020-02-11 | ClinicalTrials.gov |
| NCT03362931 | Safety and Effectiveness of the XEN45 Glaucoma Treatment System in Patients Wit… | Phase3 | Glaucoma | Completed | 2018-07-19 | 2022-03-18 | ClinicalTrials.gov |
| NCT03518047 | Risankizumab Therapy Versus Placebo for Subjects With Psoriasis in the Russian … | Phase3 | Psoriasis | Completed | 2018-07-19 | 2020-02-11 | ClinicalTrials.gov |
| NCT03518047 | Risankizumab Therapy Versus Placebo for Subjects With Psoriasis in the Russian … | Phase3 | Psoriasis | Completed | 2018-07-19 | 2020-02-11 | ClinicalTrials.gov |
| NCT03362931 | Safety and Effectiveness of the XEN45 Glaucoma Treatment System in Patients Wit… | Phase3 | Glaucoma | Completed | 2018-07-19 | 2022-03-18 | ClinicalTrials.gov |
| NCT03595059 | A Study With ABBV-155 Alone and in Combination With Taxane Therapy in Adults Wi… | Phase1 | Advanced Solid Tumors | Completed | 2018-07-13 | 2025-09-12 | ClinicalTrials.gov |
| NCT03595059 | A Study With ABBV-155 Alone and in Combination With Taxane Therapy in Adults Wi… | Phase1 | Advanced Solid Tumors | Completed | 2018-07-13 | 2025-09-12 | ClinicalTrials.gov |
| NCT03595059 | A Study With ABBV-155 Alone and in Combination With Taxane Therapy in Adults Wi… | Phase1 | Advanced Solid Tumors | Completed | 2018-07-13 | 2025-09-12 | ClinicalTrials.gov |
| NCT03595059 | A Study With ABBV-155 Alone and in Combination With Taxane Therapy in Adults Wi… | Phase1 | Advanced Solid Tumors | Completed | 2018-07-13 | 2025-09-12 | ClinicalTrials.gov |
| NCT03367429 | The Movement of Botulinum Toxin Through the Lateral Gastrocnemius Muscle in Hum… | Phase4 | Stroke | Terminated | 2018-06-15 | 2019-09-18 | ClinicalTrials.gov |
| NCT03573297 | A Cariprazine Study in the Prevention of Relapse in Bipolar I Disorder Patients… | Phase3 | Bipolar I Disorder | Completed | 2018-06-15 | 2022-09-05 | ClinicalTrials.gov |
| NCT03367429 | The Movement of Botulinum Toxin Through the Lateral Gastrocnemius Muscle in Hum… | Phase4 | Stroke | Terminated | 2018-06-15 | 2019-09-18 | ClinicalTrials.gov |
| NCT03560518 | Study of Rapastinel as Monotherapy in Patients With MDD | Phase3 | Depressive Disorder, Major | Terminated | 2018-06-15 | 2019-07-08 | ClinicalTrials.gov |
| NCT03560518 | Study of Rapastinel as Monotherapy in Patients With MDD | Phase3 | Depressive Disorder, Major | Terminated | 2018-06-15 | 2019-07-08 | ClinicalTrials.gov |
| NCT03560518 | Study of Rapastinel as Monotherapy in Patients With MDD | Phase3 | Depressive Disorder, Major | Terminated | 2018-06-15 | 2019-07-08 | ClinicalTrials.gov |
| NCT03573297 | A Cariprazine Study in the Prevention of Relapse in Bipolar I Disorder Patients… | Phase3 | Bipolar I Disorder | Completed | 2018-06-15 | 2022-09-05 | ClinicalTrials.gov |
| NCT03573297 | A Cariprazine Study in the Prevention of Relapse in Bipolar I Disorder Patients… | Phase3 | Bipolar I Disorder | Completed | 2018-06-15 | 2022-09-05 | ClinicalTrials.gov |
| NCT03367429 | The Movement of Botulinum Toxin Through the Lateral Gastrocnemius Muscle in Hum… | Phase4 | Stroke | Terminated | 2018-06-15 | 2019-09-18 | ClinicalTrials.gov |
| NCT03367429 | The Movement of Botulinum Toxin Through the Lateral Gastrocnemius Muscle in Hum… | Phase4 | Stroke | Terminated | 2018-06-15 | 2019-09-18 | ClinicalTrials.gov |
| NCT03573297 | A Cariprazine Study in the Prevention of Relapse in Bipolar I Disorder Patients… | Phase3 | Bipolar I Disorder | Completed | 2018-06-15 | 2022-09-05 | ClinicalTrials.gov |
| NCT03560518 | Study of Rapastinel as Monotherapy in Patients With MDD | Phase3 | Depressive Disorder, Major | Terminated | 2018-06-15 | 2019-07-08 | ClinicalTrials.gov |
| NCT03219216 | A Study to Evaluate the Efficacy and Safety of Glecaprevir (GLE)/Pibrentasvir (… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2018-06-06 | 2019-03-11 | ClinicalTrials.gov |
| NCT03219216 | A Study to Evaluate the Efficacy and Safety of Glecaprevir (GLE)/Pibrentasvir (… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2018-06-06 | 2019-03-11 | ClinicalTrials.gov |
| NCT03219216 | A Study to Evaluate the Efficacy and Safety of Glecaprevir (GLE)/Pibrentasvir (… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2018-06-06 | 2019-03-11 | ClinicalTrials.gov |
| NCT03219216 | A Study to Evaluate the Efficacy and Safety of Glecaprevir (GLE)/Pibrentasvir (… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2018-06-06 | 2019-03-11 | ClinicalTrials.gov |
| NCT03505892 | A Study to Investigate the Clinical REsponses in Ankylosing Spondylitis Patient… | — | Ankylosing Spondylitis (AS) | Completed | 2018-06-05 | 2021-10-25 | ClinicalTrials.gov |
| NCT03505892 | A Study to Investigate the Clinical REsponses in Ankylosing Spondylitis Patient… | — | Ankylosing Spondylitis (AS) | Completed | 2018-06-05 | 2021-10-25 | ClinicalTrials.gov |
| NCT03505892 | A Study to Investigate the Clinical REsponses in Ankylosing Spondylitis Patient… | — | Ankylosing Spondylitis (AS) | Completed | 2018-06-05 | 2021-10-25 | ClinicalTrials.gov |
| NCT03505892 | A Study to Investigate the Clinical REsponses in Ankylosing Spondylitis Patient… | — | Ankylosing Spondylitis (AS) | Completed | 2018-06-05 | 2021-10-25 | ClinicalTrials.gov |
| NCT03559972 | Study to Evaluate Efficacy and Tolerability of Two Topical Regimens in Subjects… | Na | Facial Photodamage | Completed | 2018-06-04 | 2018-12-03 | ClinicalTrials.gov |
| NCT03559972 | Study to Evaluate Efficacy and Tolerability of Two Topical Regimens in Subjects… | Na | Facial Photodamage | Completed | 2018-06-04 | 2018-12-03 | ClinicalTrials.gov |
| NCT03559972 | Study to Evaluate Efficacy and Tolerability of Two Topical Regimens in Subjects… | Na | Facial Photodamage | Completed | 2018-06-04 | 2018-12-03 | ClinicalTrials.gov |
| NCT03559972 | Study to Evaluate Efficacy and Tolerability of Two Topical Regimens in Subjects… | Na | Facial Photodamage | Completed | 2018-06-04 | 2018-12-03 | ClinicalTrials.gov |
| NCT03441555 | A Study of Venetoclax and Alvocidib in Patients With Relapsed/Refractory Acute … | Phase1 | Acute Myeloid Leukemia (AML) | Completed | 2018-05-30 | 2021-01-25 | ClinicalTrials.gov |
| NCT03441555 | A Study of Venetoclax and Alvocidib in Patients With Relapsed/Refractory Acute … | Phase1 | Acute Myeloid Leukemia (AML) | Completed | 2018-05-30 | 2021-01-25 | ClinicalTrials.gov |
| NCT03441555 | A Study of Venetoclax and Alvocidib in Patients With Relapsed/Refractory Acute … | Phase1 | Acute Myeloid Leukemia (AML) | Completed | 2018-05-30 | 2021-01-25 | ClinicalTrials.gov |
| NCT03441555 | A Study of Venetoclax and Alvocidib in Patients With Relapsed/Refractory Acute … | Phase1 | Acute Myeloid Leukemia (AML) | Completed | 2018-05-30 | 2021-01-25 | ClinicalTrials.gov |
| NCT03539549 | A Study to Evaluate Abicipar Pegol for Safety and Treatment Effect in Participa… | Phase2 | Macular Degeneration | Completed | 2018-05-25 | 2019-02-27 | ClinicalTrials.gov |
| NCT03539549 | A Study to Evaluate Abicipar Pegol for Safety and Treatment Effect in Participa… | Phase2 | Macular Degeneration | Completed | 2018-05-25 | 2019-02-27 | ClinicalTrials.gov |
| NCT03539549 | A Study to Evaluate Abicipar Pegol for Safety and Treatment Effect in Participa… | Phase2 | Macular Degeneration | Completed | 2018-05-25 | 2019-02-27 | ClinicalTrials.gov |
| NCT03539549 | A Study to Evaluate Abicipar Pegol for Safety and Treatment Effect in Participa… | Phase2 | Macular Degeneration | Completed | 2018-05-25 | 2019-02-27 | ClinicalTrials.gov |
| NCT03543566 | Bladder Antimuscarinic Medication and Accidental Bowel Leakage | — | Urinary Incontinence, Urge | Completed | 2018-05-21 | 2019-01-18 | ClinicalTrials.gov |
| NCT03543566 | Bladder Antimuscarinic Medication and Accidental Bowel Leakage | — | Urinary Incontinence, Urge | Completed | 2018-05-21 | 2019-01-18 | ClinicalTrials.gov |
| NCT03543566 | Bladder Antimuscarinic Medication and Accidental Bowel Leakage | — | Urinary Incontinence, Urge | Completed | 2018-05-21 | 2019-01-18 | ClinicalTrials.gov |
| NCT03543566 | Bladder Antimuscarinic Medication and Accidental Bowel Leakage | — | Urinary Incontinence, Urge | Completed | 2018-05-21 | 2019-01-18 | ClinicalTrials.gov |
| NCT03339089 | Real-world Effectiveness of Adalimumab on Health Outcomes in Chinese Patients W… | — | Ankylosing Spondylitis (AS) | Completed | 2018-05-18 | 2021-07-08 | ClinicalTrials.gov |
| NCT03339089 | Real-world Effectiveness of Adalimumab on Health Outcomes in Chinese Patients W… | — | Ankylosing Spondylitis (AS) | Completed | 2018-05-18 | 2021-07-08 | ClinicalTrials.gov |
| NCT03339089 | Real-world Effectiveness of Adalimumab on Health Outcomes in Chinese Patients W… | — | Ankylosing Spondylitis (AS) | Completed | 2018-05-18 | 2021-07-08 | ClinicalTrials.gov |
| NCT03339089 | Real-world Effectiveness of Adalimumab on Health Outcomes in Chinese Patients W… | — | Ankylosing Spondylitis (AS) | Completed | 2018-05-18 | 2021-07-08 | ClinicalTrials.gov |
| NCT03478787 | Risankizumab Versus Secukinumab for Participants With Moderate to Severe Plaque… | Phase3 | Psoriasis | Completed | 2018-05-08 | 2020-07-08 | ClinicalTrials.gov |
| NCT03478787 | Risankizumab Versus Secukinumab for Participants With Moderate to Severe Plaque… | Phase3 | Psoriasis | Completed | 2018-05-08 | 2020-07-08 | ClinicalTrials.gov |
| NCT03478787 | Risankizumab Versus Secukinumab for Participants With Moderate to Severe Plaque… | Phase3 | Psoriasis | Completed | 2018-05-08 | 2020-07-08 | ClinicalTrials.gov |
| NCT03478787 | Risankizumab Versus Secukinumab for Participants With Moderate to Severe Plaque… | Phase3 | Psoriasis | Completed | 2018-05-08 | 2020-07-08 | ClinicalTrials.gov |
| NCT03383263 | A Study to Assess Persistence, Adherence and Changes in Disease Activity in the… | — | Polyarticular Juvenile Arthritis | Completed | 2018-05-04 | 2020-09-14 | ClinicalTrials.gov |
| NCT03383263 | A Study to Assess Persistence, Adherence and Changes in Disease Activity in the… | — | Polyarticular Juvenile Arthritis | Completed | 2018-05-04 | 2020-09-14 | ClinicalTrials.gov |
| NCT03383263 | A Study to Assess Persistence, Adherence and Changes in Disease Activity in the… | — | Polyarticular Juvenile Arthritis | Completed | 2018-05-04 | 2020-09-14 | ClinicalTrials.gov |
| NCT03383263 | A Study to Assess Persistence, Adherence and Changes in Disease Activity in the… | — | Polyarticular Juvenile Arthritis | Completed | 2018-05-04 | 2020-09-14 | ClinicalTrials.gov |
| NCT03518034 | A Study to Evaluate the Effect of Testosterone Replacement Therapy (TRT) on the… | Phase4 | Hypogonadism | Completed | 2018-05-03 | 2023-01-19 | ClinicalTrials.gov |
| NCT03518034 | A Study to Evaluate the Effect of Testosterone Replacement Therapy (TRT) on the… | Phase4 | Hypogonadism | Completed | 2018-05-03 | 2023-01-19 | ClinicalTrials.gov |
| NCT03518034 | A Study to Evaluate the Effect of Testosterone Replacement Therapy (TRT) on the… | Phase4 | Hypogonadism | Completed | 2018-05-03 | 2023-01-19 | ClinicalTrials.gov |
| NCT03518034 | A Study to Evaluate the Effect of Testosterone Replacement Therapy (TRT) on the… | Phase4 | Hypogonadism | Completed | 2018-05-03 | 2023-01-19 | ClinicalTrials.gov |
| NCT03374917 | A Study in Subjects With Parkinson's Disease to Evaluate the Safety and Tolerab… | Phase1 | Parkinson's Disease (PD) | Completed | 2018-04-18 | 2019-03-04 | ClinicalTrials.gov |
| NCT03374917 | A Study in Subjects With Parkinson's Disease to Evaluate the Safety and Tolerab… | Phase1 | Parkinson's Disease (PD) | Completed | 2018-04-18 | 2019-03-04 | ClinicalTrials.gov |
| NCT03374917 | A Study in Subjects With Parkinson's Disease to Evaluate the Safety and Tolerab… | Phase1 | Parkinson's Disease (PD) | Completed | 2018-04-18 | 2019-03-04 | ClinicalTrials.gov |
| NCT03374917 | A Study in Subjects With Parkinson's Disease to Evaluate the Safety and Tolerab… | Phase1 | Parkinson's Disease (PD) | Completed | 2018-04-18 | 2019-03-04 | ClinicalTrials.gov |
| NCT03413319 | Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (P… | Phase1 | Progressive Supranuclear Palsy (PSP) | Completed | 2018-04-17 | 2019-11-20 | ClinicalTrials.gov |
| NCT03413319 | Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (P… | Phase1 | Progressive Supranuclear Palsy (PSP) | Completed | 2018-04-17 | 2019-11-20 | ClinicalTrials.gov |
| NCT03413319 | Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (P… | Phase1 | Progressive Supranuclear Palsy (PSP) | Completed | 2018-04-17 | 2019-11-20 | ClinicalTrials.gov |
| NCT03413319 | Extension Study of ABBV-8E12 in Patients With Progressive Supranuclear Palsy (P… | Phase1 | Progressive Supranuclear Palsy (PSP) | Completed | 2018-04-17 | 2019-11-20 | ClinicalTrials.gov |
| NCT03469258 | Study of Pancreatic Enzyme Replacement on Completion of Adjuvant Chemotherapy f… | Phase2 | Pancreatic Cancer | Terminated | 2018-04-13 | 2019-10-01 | ClinicalTrials.gov |
| NCT03469258 | Study of Pancreatic Enzyme Replacement on Completion of Adjuvant Chemotherapy f… | Phase2 | Pancreatic Cancer | Terminated | 2018-04-13 | 2019-10-01 | ClinicalTrials.gov |
| NCT03469258 | Study of Pancreatic Enzyme Replacement on Completion of Adjuvant Chemotherapy f… | Phase2 | Pancreatic Cancer | Terminated | 2018-04-13 | 2019-10-01 | ClinicalTrials.gov |
| NCT03469258 | Study of Pancreatic Enzyme Replacement on Completion of Adjuvant Chemotherapy f… | Phase2 | Pancreatic Cancer | Terminated | 2018-04-13 | 2019-10-01 | ClinicalTrials.gov |
| NCT03105102 | A Study of the Efficacy and Safety of Risankizumab in Participants With Crohn's… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2018-04-09 | 2026-05-01 | ClinicalTrials.gov |
| NCT03105102 | A Study of the Efficacy and Safety of Risankizumab in Participants With Crohn's… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2018-04-09 | 2026-05-01 | ClinicalTrials.gov |
| NCT03105102 | A Study of the Efficacy and Safety of Risankizumab in Participants With Crohn's… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2018-04-09 | 2026-05-01 | ClinicalTrials.gov |
| NCT03105102 | A Study of the Efficacy and Safety of Risankizumab in Participants With Crohn's… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2018-04-09 | 2026-05-01 | ClinicalTrials.gov |
| NCT03314181 | A Study of Combination Therapy With Venetoclax, Daratumumab and Dexamethasone (… | Phase2 | Multiple Myeloma | Active_Not_Recruiting | 2018-04-02 | 2031-05-01 | ClinicalTrials.gov |
| NCT03314181 | A Study of Combination Therapy With Venetoclax, Daratumumab and Dexamethasone (… | Phase2 | Multiple Myeloma | Active_Not_Recruiting | 2018-04-02 | 2031-05-01 | ClinicalTrials.gov |
| NCT03314181 | A Study of Combination Therapy With Venetoclax, Daratumumab and Dexamethasone (… | Phase2 | Multiple Myeloma | Active_Not_Recruiting | 2018-04-02 | 2031-05-01 | ClinicalTrials.gov |
| NCT03314181 | A Study of Combination Therapy With Venetoclax, Daratumumab and Dexamethasone (… | Phase2 | Multiple Myeloma | Active_Not_Recruiting | 2018-04-02 | 2031-05-01 | ClinicalTrials.gov |
| NCT03361176 | Kybella With Triamcinolone | Phase4 | Adiposity | Completed | 2018-03-26 | 2018-12-18 | ClinicalTrials.gov |
| NCT03361176 | Kybella With Triamcinolone | Phase4 | Adiposity | Completed | 2018-03-26 | 2018-12-18 | ClinicalTrials.gov |
| NCT03361176 | Kybella With Triamcinolone | Phase4 | Adiposity | Completed | 2018-03-26 | 2018-12-18 | ClinicalTrials.gov |
| NCT03361176 | Kybella With Triamcinolone | Phase4 | Adiposity | Completed | 2018-03-26 | 2018-12-18 | ClinicalTrials.gov |
| NCT03345823 | A Maintenance and Long-Term Extension Study of the Efficacy and Safety of Upada… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2018-03-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT03345823 | A Maintenance and Long-Term Extension Study of the Efficacy and Safety of Upada… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2018-03-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT03345823 | A Maintenance and Long-Term Extension Study of the Efficacy and Safety of Upada… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2018-03-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT03345823 | A Maintenance and Long-Term Extension Study of the Efficacy and Safety of Upada… | Phase3 | Crohn's Disease | Active_Not_Recruiting | 2018-03-21 | 2027-09-01 | ClinicalTrials.gov |
| NCT03368859 | A Study of ABT-165 Plus FOLFIRI vs Bevacizumab Plus FOLFIRI in Subjects With Me… | Phase2 | Cancer | Terminated | 2018-03-20 | 2019-12-18 | ClinicalTrials.gov |
| NCT03368859 | A Study of ABT-165 Plus FOLFIRI vs Bevacizumab Plus FOLFIRI in Subjects With Me… | Phase2 | Cancer | Terminated | 2018-03-20 | 2019-12-18 | ClinicalTrials.gov |
| NCT03368859 | A Study of ABT-165 Plus FOLFIRI vs Bevacizumab Plus FOLFIRI in Subjects With Me… | Phase2 | Cancer | Terminated | 2018-03-20 | 2019-12-18 | ClinicalTrials.gov |
| NCT03368859 | A Study of ABT-165 Plus FOLFIRI vs Bevacizumab Plus FOLFIRI in Subjects With Me… | Phase2 | Cancer | Terminated | 2018-03-20 | 2019-12-18 | ClinicalTrials.gov |
| NCT03360006 | A Study Evaluating the Safety and Pharmacokinetics of ABBV-744 in Participants … | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2018-03-16 | 2020-12-19 | ClinicalTrials.gov |
| NCT03360006 | A Study Evaluating the Safety and Pharmacokinetics of ABBV-744 in Participants … | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2018-03-16 | 2020-12-19 | ClinicalTrials.gov |
| NCT03360006 | A Study Evaluating the Safety and Pharmacokinetics of ABBV-744 in Participants … | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2018-03-16 | 2020-12-19 | ClinicalTrials.gov |
| NCT03360006 | A Study Evaluating the Safety and Pharmacokinetics of ABBV-744 in Participants … | Phase1 | Acute Myeloid Leukemia (AML) | Terminated | 2018-03-16 | 2020-12-19 | ClinicalTrials.gov |
| NCT03334487 | Study Evaluating the Safety of Rovalpituzumab Tesirine for Third-Line and Later… | Phase3 | Small Cell Lung Cancer | Withdrawn | 2018-03-15 | 2018-12-20 | ClinicalTrials.gov |
| NCT03334487 | Study Evaluating the Safety of Rovalpituzumab Tesirine for Third-Line and Later… | Phase3 | Small Cell Lung Cancer | Withdrawn | 2018-03-15 | 2018-12-20 | ClinicalTrials.gov |
| NCT03334487 | Study Evaluating the Safety of Rovalpituzumab Tesirine for Third-Line and Later… | Phase3 | Small Cell Lung Cancer | Withdrawn | 2018-03-15 | 2018-12-20 | ClinicalTrials.gov |
| NCT03334487 | Study Evaluating the Safety of Rovalpituzumab Tesirine for Third-Line and Later… | Phase3 | Small Cell Lung Cancer | Withdrawn | 2018-03-15 | 2018-12-20 | ClinicalTrials.gov |
| NCT03065582 | The Effect of Topical Sunscreen Plus Antioxidant Against the Visible Light Biol… | Na | Pigmentation | Completed | 2018-03-13 | 2019-04-22 | ClinicalTrials.gov |
| NCT03487900 | Is the Endoscopic Remission Evaluation, Using the CREDO 1 Index / Score in CD P… | Na | CD | Unknown | 2018-03-13 | 2023-12-31 | ClinicalTrials.gov |
| NCT03065582 | The Effect of Topical Sunscreen Plus Antioxidant Against the Visible Light Biol… | Na | Pigmentation | Completed | 2018-03-13 | 2019-04-22 | ClinicalTrials.gov |
| NCT03487900 | Is the Endoscopic Remission Evaluation, Using the CREDO 1 Index / Score in CD P… | Na | CD | Unknown | 2018-03-13 | 2023-12-31 | ClinicalTrials.gov |
| NCT03065582 | The Effect of Topical Sunscreen Plus Antioxidant Against the Visible Light Biol… | Na | Pigmentation | Completed | 2018-03-13 | 2019-04-22 | ClinicalTrials.gov |
| NCT03065582 | The Effect of Topical Sunscreen Plus Antioxidant Against the Visible Light Biol… | Na | Pigmentation | Completed | 2018-03-13 | 2019-04-22 | ClinicalTrials.gov |
| NCT03498625 | Crohn's Disease Endoscopic REmission Definition in an Objective Way | Na | CD | Completed | 2018-03-13 | 2021-12-31 | ClinicalTrials.gov |
| NCT03487900 | Is the Endoscopic Remission Evaluation, Using the CREDO 1 Index / Score in CD P… | Na | CD | Unknown | 2018-03-13 | 2023-12-31 | ClinicalTrials.gov |
| NCT03498625 | Crohn's Disease Endoscopic REmission Definition in an Objective Way | Na | CD | Completed | 2018-03-13 | 2021-12-31 | ClinicalTrials.gov |
| NCT03498625 | Crohn's Disease Endoscopic REmission Definition in an Objective Way | Na | CD | Completed | 2018-03-13 | 2021-12-31 | ClinicalTrials.gov |
| NCT03487900 | Is the Endoscopic Remission Evaluation, Using the CREDO 1 Index / Score in CD P… | Na | CD | Unknown | 2018-03-13 | 2023-12-31 | ClinicalTrials.gov |
| NCT03498625 | Crohn's Disease Endoscopic REmission Definition in an Objective Way | Na | CD | Completed | 2018-03-13 | 2021-12-31 | ClinicalTrials.gov |
| NCT03415035 | Study Venetoclax Effectiveness and Real-Life Treatment Management in Participan… | — | Cancer - Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2018-03-09 | 2026-06-01 | ClinicalTrials.gov |
| NCT03415035 | Study Venetoclax Effectiveness and Real-Life Treatment Management in Participan… | — | Cancer - Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2018-03-09 | 2026-06-01 | ClinicalTrials.gov |
| NCT03415035 | Study Venetoclax Effectiveness and Real-Life Treatment Management in Participan… | — | Cancer - Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2018-03-09 | 2026-06-01 | ClinicalTrials.gov |
| NCT03415035 | Study Venetoclax Effectiveness and Real-Life Treatment Management in Participan… | — | Cancer - Chronic Lymphocytic Leukemia | Active_Not_Recruiting | 2018-03-09 | 2026-06-01 | ClinicalTrials.gov |
| NCT03398148 | A Multicenter, Randomized, Double-Blind, Placebo Controlled Induction Study to … | Phase2 | Ulcerative Colitis (UC) | Completed | 2018-03-07 | 2023-05-11 | ClinicalTrials.gov |
| NCT03398148 | A Multicenter, Randomized, Double-Blind, Placebo Controlled Induction Study to … | Phase2 | Ulcerative Colitis (UC) | Completed | 2018-03-07 | 2023-05-11 | ClinicalTrials.gov |
| NCT03398148 | A Multicenter, Randomized, Double-Blind, Placebo Controlled Induction Study to … | Phase2 | Ulcerative Colitis (UC) | Completed | 2018-03-07 | 2023-05-11 | ClinicalTrials.gov |
| NCT03398148 | A Multicenter, Randomized, Double-Blind, Placebo Controlled Induction Study to … | Phase2 | Ulcerative Colitis (UC) | Completed | 2018-03-07 | 2023-05-11 | ClinicalTrials.gov |
| NCT03249311 | Levomilnacipran in Healthy Males | Phase4 | None (i.e. Healthy Volunteers) | Unknown | 2018-03-02 | 2022-05-01 | ClinicalTrials.gov |
| NCT03249311 | Levomilnacipran in Healthy Males | Phase4 | None (i.e. Healthy Volunteers) | Unknown | 2018-03-02 | 2022-05-01 | ClinicalTrials.gov |
| NCT03249311 | Levomilnacipran in Healthy Males | Phase4 | None (i.e. Healthy Volunteers) | Unknown | 2018-03-02 | 2022-05-01 | ClinicalTrials.gov |
| NCT03249311 | Levomilnacipran in Healthy Males | Phase4 | None (i.e. Healthy Volunteers) | Unknown | 2018-03-02 | 2022-05-01 | ClinicalTrials.gov |
| NCT03441581 | Eluxadoline Bile Acid Malabsorption (BAM) Study | Phase4 | Irritable Bowel Syndrome With Diarrhea | Completed | 2018-02-23 | 2020-04-28 | ClinicalTrials.gov |
| NCT03441581 | Eluxadoline Bile Acid Malabsorption (BAM) Study | Phase4 | Irritable Bowel Syndrome With Diarrhea | Completed | 2018-02-23 | 2020-04-28 | ClinicalTrials.gov |
| NCT03441581 | Eluxadoline Bile Acid Malabsorption (BAM) Study | Phase4 | Irritable Bowel Syndrome With Diarrhea | Completed | 2018-02-23 | 2020-04-28 | ClinicalTrials.gov |
| NCT03441581 | Eluxadoline Bile Acid Malabsorption (BAM) Study | Phase4 | Irritable Bowel Syndrome With Diarrhea | Completed | 2018-02-23 | 2020-04-28 | ClinicalTrials.gov |
| NCT03426345 | Study to Evaluate the Safety and Efficacy of Relamorelin in Participants With D… | Phase3 | Gastroparesis | Terminated | 2018-02-16 | 2020-07-16 | ClinicalTrials.gov |
| NCT03426345 | Study to Evaluate the Safety and Efficacy of Relamorelin in Participants With D… | Phase3 | Gastroparesis | Terminated | 2018-02-16 | 2020-07-16 | ClinicalTrials.gov |
| NCT03426345 | Study to Evaluate the Safety and Efficacy of Relamorelin in Participants With D… | Phase3 | Gastroparesis | Terminated | 2018-02-16 | 2020-07-16 | ClinicalTrials.gov |
| NCT03426345 | Study to Evaluate the Safety and Efficacy of Relamorelin in Participants With D… | Phase3 | Gastroparesis | Terminated | 2018-02-16 | 2020-07-16 | ClinicalTrials.gov |
| NCT03097835 | Evaluation of Skin Quality Improvement | Phase2 | Skin Quality | Completed | 2018-02-12 | 2018-07-26 | ClinicalTrials.gov |
| NCT03097835 | Evaluation of Skin Quality Improvement | Phase2 | Skin Quality | Completed | 2018-02-12 | 2018-07-26 | ClinicalTrials.gov |
| NCT03097835 | Evaluation of Skin Quality Improvement | Phase2 | Skin Quality | Completed | 2018-02-12 | 2018-07-26 | ClinicalTrials.gov |
| NCT03097835 | Evaluation of Skin Quality Improvement | Phase2 | Skin Quality | Completed | 2018-02-12 | 2018-07-26 | ClinicalTrials.gov |
| NCT03438266 | A Study of the Safety and Effectiveness of JUVÉDERM VOLUMA® XC Injectable Gel f… | Na | Age-related Volume Deficit in the Mid-face | Completed | 2018-02-05 | 2018-08-02 | ClinicalTrials.gov |
| NCT03438266 | A Study of the Safety and Effectiveness of JUVÉDERM VOLUMA® XC Injectable Gel f… | Na | Age-related Volume Deficit in the Mid-face | Completed | 2018-02-05 | 2018-08-02 | ClinicalTrials.gov |
| NCT03438266 | A Study of the Safety and Effectiveness of JUVÉDERM VOLUMA® XC Injectable Gel f… | Na | Age-related Volume Deficit in the Mid-face | Completed | 2018-02-05 | 2018-08-02 | ClinicalTrials.gov |
| NCT03438266 | A Study of the Safety and Effectiveness of JUVÉDERM VOLUMA® XC Injectable Gel f… | Na | Age-related Volume Deficit in the Mid-face | Completed | 2018-02-05 | 2018-08-02 | ClinicalTrials.gov |
| NCT03430986 | Safety and Effectiveness of JUVÉDERM® VOLUMA® With Lidocaine for Improvement of… | Na | Nose Enhancement | Completed | 2018-02-02 | 2019-12-04 | ClinicalTrials.gov |
| NCT03430986 | Safety and Effectiveness of JUVÉDERM® VOLUMA® With Lidocaine for Improvement of… | Na | Nose Enhancement | Completed | 2018-02-02 | 2019-12-04 | ClinicalTrials.gov |
| NCT03425253 | Sequential Treatment With BELKYRA® Then Juvéderm® VOLUMA™ With Lidocaine for Ov… | Phase4 | Contour | Completed | 2018-02-02 | 2019-12-05 | ClinicalTrials.gov |
| NCT03425253 | Sequential Treatment With BELKYRA® Then Juvéderm® VOLUMA™ With Lidocaine for Ov… | Phase4 | Contour | Completed | 2018-02-02 | 2019-12-05 | ClinicalTrials.gov |
| NCT03425253 | Sequential Treatment With BELKYRA® Then Juvéderm® VOLUMA™ With Lidocaine for Ov… | Phase4 | Contour | Completed | 2018-02-02 | 2019-12-05 | ClinicalTrials.gov |
| NCT03425253 | Sequential Treatment With BELKYRA® Then Juvéderm® VOLUMA™ With Lidocaine for Ov… | Phase4 | Contour | Completed | 2018-02-02 | 2019-12-05 | ClinicalTrials.gov |
| NCT03430986 | Safety and Effectiveness of JUVÉDERM® VOLUMA® With Lidocaine for Improvement of… | Na | Nose Enhancement | Completed | 2018-02-02 | 2019-12-04 | ClinicalTrials.gov |
| NCT03430986 | Safety and Effectiveness of JUVÉDERM® VOLUMA® With Lidocaine for Improvement of… | Na | Nose Enhancement | Completed | 2018-02-02 | 2019-12-04 | ClinicalTrials.gov |
| NCT03211390 | Using Telemedicine to Improve Spasticity Diagnosis Rates | — | Spasticity, Muscle | Completed | 2018-01-30 | 2018-08-01 | ClinicalTrials.gov |
| NCT03211390 | Using Telemedicine to Improve Spasticity Diagnosis Rates | — | Spasticity, Muscle | Completed | 2018-01-30 | 2018-08-01 | ClinicalTrials.gov |
| NCT03211390 | Using Telemedicine to Improve Spasticity Diagnosis Rates | — | Spasticity, Muscle | Completed | 2018-01-30 | 2018-08-01 | ClinicalTrials.gov |
| NCT03250988 | Prevalence of Comorbid Spasticity and Urinary Incontinence in Residents of a Lo… | — | Spasticity, Muscle | Completed | 2018-01-30 | 2018-08-01 | ClinicalTrials.gov |
| NCT03211390 | Using Telemedicine to Improve Spasticity Diagnosis Rates | — | Spasticity, Muscle | Completed | 2018-01-30 | 2018-08-01 | ClinicalTrials.gov |
| NCT03250988 | Prevalence of Comorbid Spasticity and Urinary Incontinence in Residents of a Lo… | — | Spasticity, Muscle | Completed | 2018-01-30 | 2018-08-01 | ClinicalTrials.gov |
| NCT03250988 | Prevalence of Comorbid Spasticity and Urinary Incontinence in Residents of a Lo… | — | Spasticity, Muscle | Completed | 2018-01-30 | 2018-08-01 | ClinicalTrials.gov |
| NCT03250988 | Prevalence of Comorbid Spasticity and Urinary Incontinence in Residents of a Lo… | — | Spasticity, Muscle | Completed | 2018-01-30 | 2018-08-01 | ClinicalTrials.gov |
| NCT03418545 | A Safety and Effectiveness of VOLBELLA XC Hyaluronic Acid (HA) Injectable Gel t… | Phase3 | Infraorbital Hollowing | Completed | 2018-01-26 | 2019-08-22 | ClinicalTrials.gov |
| NCT03418545 | A Safety and Effectiveness of VOLBELLA XC Hyaluronic Acid (HA) Injectable Gel t… | Phase3 | Infraorbital Hollowing | Completed | 2018-01-26 | 2019-08-22 | ClinicalTrials.gov |
| NCT03418545 | A Safety and Effectiveness of VOLBELLA XC Hyaluronic Acid (HA) Injectable Gel t… | Phase3 | Infraorbital Hollowing | Completed | 2018-01-26 | 2019-08-22 | ClinicalTrials.gov |
| NCT03418545 | A Safety and Effectiveness of VOLBELLA XC Hyaluronic Acid (HA) Injectable Gel t… | Phase3 | Infraorbital Hollowing | Completed | 2018-01-26 | 2019-08-22 | ClinicalTrials.gov |
| NCT03339102 | Post-marketing Surveillance Study of Adalimumab (Humira®) for Non-infectious In… | — | Non-infectious Intermediate, Posterior and Panuveitis | Completed | 2018-01-25 | 2020-07-16 | ClinicalTrials.gov |
| NCT03339102 | Post-marketing Surveillance Study of Adalimumab (Humira®) for Non-infectious In… | — | Non-infectious Intermediate, Posterior and Panuveitis | Completed | 2018-01-25 | 2020-07-16 | ClinicalTrials.gov |
| NCT03339102 | Post-marketing Surveillance Study of Adalimumab (Humira®) for Non-infectious In… | — | Non-infectious Intermediate, Posterior and Panuveitis | Completed | 2018-01-25 | 2020-07-16 | ClinicalTrials.gov |
| NCT03339102 | Post-marketing Surveillance Study of Adalimumab (Humira®) for Non-infectious In… | — | Non-infectious Intermediate, Posterior and Panuveitis | Completed | 2018-01-25 | 2020-07-16 | ClinicalTrials.gov |
| NCT03391765 | An Extension Study of ABBV-8E12 in Progressive Supranuclear Palsy (PSP) | Phase2 | Progressive Supranuclear Palsy (PSP) | Terminated | 2018-01-24 | 2019-12-13 | ClinicalTrials.gov |
| NCT03391765 | An Extension Study of ABBV-8E12 in Progressive Supranuclear Palsy (PSP) | Phase2 | Progressive Supranuclear Palsy (PSP) | Terminated | 2018-01-24 | 2019-12-13 | ClinicalTrials.gov |
| NCT03391765 | An Extension Study of ABBV-8E12 in Progressive Supranuclear Palsy (PSP) | Phase2 | Progressive Supranuclear Palsy (PSP) | Terminated | 2018-01-24 | 2019-12-13 | ClinicalTrials.gov |
| NCT03420781 | A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis Study 03 | Phase3 | Gastroparesis | Terminated | 2018-01-24 | 2020-10-30 | ClinicalTrials.gov |
| NCT03420781 | A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis Study 03 | Phase3 | Gastroparesis | Terminated | 2018-01-24 | 2020-10-30 | ClinicalTrials.gov |
| NCT03391765 | An Extension Study of ABBV-8E12 in Progressive Supranuclear Palsy (PSP) | Phase2 | Progressive Supranuclear Palsy (PSP) | Terminated | 2018-01-24 | 2019-12-13 | ClinicalTrials.gov |
| NCT03420781 | A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis Study 03 | Phase3 | Gastroparesis | Terminated | 2018-01-24 | 2020-10-30 | ClinicalTrials.gov |
| NCT03420781 | A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis Study 03 | Phase3 | Gastroparesis | Terminated | 2018-01-24 | 2020-10-30 | ClinicalTrials.gov |
| NCT03364725 | Toward Elimination of Hepatitis C Virus (HCV): A Pilot Study | Phase4 | Hepatitis C | Unknown | 2018-01-15 | 2019-03-01 | ClinicalTrials.gov |
| NCT03193359 | Open Label Study of BOTOX® (Botulinum Toxin Type A) as Headache Prophylaxis in … | Phase3 | Migraine Disorders | Withdrawn | 2018-01-15 | 2021-09-09 | ClinicalTrials.gov |
| NCT03364725 | Toward Elimination of Hepatitis C Virus (HCV): A Pilot Study | Phase4 | Hepatitis C | Unknown | 2018-01-15 | 2019-03-01 | ClinicalTrials.gov |
| NCT03364725 | Toward Elimination of Hepatitis C Virus (HCV): A Pilot Study | Phase4 | Hepatitis C | Unknown | 2018-01-15 | 2019-03-01 | ClinicalTrials.gov |
| NCT03193359 | Open Label Study of BOTOX® (Botulinum Toxin Type A) as Headache Prophylaxis in … | Phase3 | Migraine Disorders | Withdrawn | 2018-01-15 | 2021-09-09 | ClinicalTrials.gov |
| NCT03193359 | Open Label Study of BOTOX® (Botulinum Toxin Type A) as Headache Prophylaxis in … | Phase3 | Migraine Disorders | Withdrawn | 2018-01-15 | 2021-09-09 | ClinicalTrials.gov |
| NCT03193359 | Open Label Study of BOTOX® (Botulinum Toxin Type A) as Headache Prophylaxis in … | Phase3 | Migraine Disorders | Withdrawn | 2018-01-15 | 2021-09-09 | ClinicalTrials.gov |
| NCT03364725 | Toward Elimination of Hepatitis C Virus (HCV): A Pilot Study | Phase4 | Hepatitis C | Unknown | 2018-01-15 | 2019-03-01 | ClinicalTrials.gov |
| NCT03310190 | Study to Describe the Management and the Use of Healthcare Resources in Patient… | — | Chronic Lymphocytic Leukemia | Completed | 2018-01-10 | 2022-04-30 | ClinicalTrials.gov |
| NCT03310190 | Study to Describe the Management and the Use of Healthcare Resources in Patient… | — | Chronic Lymphocytic Leukemia | Completed | 2018-01-10 | 2022-04-30 | ClinicalTrials.gov |
| NCT03310190 | Study to Describe the Management and the Use of Healthcare Resources in Patient… | — | Chronic Lymphocytic Leukemia | Completed | 2018-01-10 | 2022-04-30 | ClinicalTrials.gov |
| NCT03310190 | Study to Describe the Management and the Use of Healthcare Resources in Patient… | — | Chronic Lymphocytic Leukemia | Completed | 2018-01-10 | 2022-04-30 | ClinicalTrials.gov |
| NCT03316794 | A Study of SC-005 in Subjects With Triple Negative Breast Cancer (TNBC) | Phase1 | Breast Cancer | Terminated | 2018-01-04 | 2018-10-05 | ClinicalTrials.gov |
| NCT03544593 | The Volumetric Analysis of Fat Grafting | Na | Autologous Fat Grafting | Unknown | 2018-01-04 | 2019-03-01 | ClinicalTrials.gov |
| NCT03544593 | The Volumetric Analysis of Fat Grafting | Na | Autologous Fat Grafting | Unknown | 2018-01-04 | 2019-03-01 | ClinicalTrials.gov |
| NCT03316794 | A Study of SC-005 in Subjects With Triple Negative Breast Cancer (TNBC) | Phase1 | Breast Cancer | Terminated | 2018-01-04 | 2018-10-05 | ClinicalTrials.gov |
| NCT03316794 | A Study of SC-005 in Subjects With Triple Negative Breast Cancer (TNBC) | Phase1 | Breast Cancer | Terminated | 2018-01-04 | 2018-10-05 | ClinicalTrials.gov |
| NCT03544593 | The Volumetric Analysis of Fat Grafting | Na | Autologous Fat Grafting | Unknown | 2018-01-04 | 2019-03-01 | ClinicalTrials.gov |
| NCT03544593 | The Volumetric Analysis of Fat Grafting | Na | Autologous Fat Grafting | Unknown | 2018-01-04 | 2019-03-01 | ClinicalTrials.gov |
| NCT03316794 | A Study of SC-005 in Subjects With Triple Negative Breast Cancer (TNBC) | Phase1 | Breast Cancer | Terminated | 2018-01-04 | 2018-10-05 | ClinicalTrials.gov |
| NCT02955212 | A Study With Upadacitinib (ABT-494) in Subjects From China and Selected Countri… | Phase3 | Rheumatoid Arthritis (RA) | Completed | 2018-01-03 | 2020-09-03 | ClinicalTrials.gov |
| NCT02955212 | A Study With Upadacitinib (ABT-494) in Subjects From China and Selected Countri… | Phase3 | Rheumatoid Arthritis (RA) | Completed | 2018-01-03 | 2020-09-03 | ClinicalTrials.gov |
| NCT02955212 | A Study With Upadacitinib (ABT-494) in Subjects From China and Selected Countri… | Phase3 | Rheumatoid Arthritis (RA) | Completed | 2018-01-03 | 2020-09-03 | ClinicalTrials.gov |
| NCT02955212 | A Study With Upadacitinib (ABT-494) in Subjects From China and Selected Countri… | Phase3 | Rheumatoid Arthritis (RA) | Completed | 2018-01-03 | 2020-09-03 | ClinicalTrials.gov |
| NCT03386513 | Study of IMGN632 in Patients With Untreated BPDCN and Relapsed/Refractory BPDCN | Phase1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | Active_Not_Recruiting | 2018-01-02 | 2026-12-30 | ClinicalTrials.gov |
| NCT03386513 | Study of IMGN632 in Patients With Untreated BPDCN and Relapsed/Refractory BPDCN | Phase1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | Active_Not_Recruiting | 2018-01-02 | 2026-12-30 | ClinicalTrials.gov |
| NCT03386513 | Study of IMGN632 in Patients With Untreated BPDCN and Relapsed/Refractory BPDCN | Phase1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | Active_Not_Recruiting | 2018-01-02 | 2026-12-30 | ClinicalTrials.gov |
| NCT03386513 | Study of IMGN632 in Patients With Untreated BPDCN and Relapsed/Refractory BPDCN | Phase1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | Active_Not_Recruiting | 2018-01-02 | 2026-12-30 | ClinicalTrials.gov |
| NCT03549416 | BioDay Registry: Data Collection Regarding the Use of New Systemic Treatment Op… | — | Atopic Dermatitis | Recruiting | 2018-01-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT03549416 | BioDay Registry: Data Collection Regarding the Use of New Systemic Treatment Op… | — | Atopic Dermatitis | Recruiting | 2018-01-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT03549416 | BioDay Registry: Data Collection Regarding the Use of New Systemic Treatment Op… | — | Atopic Dermatitis | Recruiting | 2018-01-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT03549416 | BioDay Registry: Data Collection Regarding the Use of New Systemic Treatment Op… | — | Atopic Dermatitis | Recruiting | 2018-01-01 | 2028-12-31 | ClinicalTrials.gov |
| NCT03343067 | A Study to Evaluate Safety and Efficacy of Elagolix in Participants With Endome… | Phase3 | Endometriosis | Terminated | 2017-12-27 | 2018-10-23 | ClinicalTrials.gov |
| NCT03341871 | Glecaprevir/Pibrentasvir Drug Use Results Survey in Patients Infected With Hepa… | — | Hepatitis C Virus (HCV) | Completed | 2017-12-27 | 2020-09-15 | ClinicalTrials.gov |
| NCT03343067 | A Study to Evaluate Safety and Efficacy of Elagolix in Participants With Endome… | Phase3 | Endometriosis | Terminated | 2017-12-27 | 2018-10-23 | ClinicalTrials.gov |
| NCT03343067 | A Study to Evaluate Safety and Efficacy of Elagolix in Participants With Endome… | Phase3 | Endometriosis | Terminated | 2017-12-27 | 2018-10-23 | ClinicalTrials.gov |
| NCT03341871 | Glecaprevir/Pibrentasvir Drug Use Results Survey in Patients Infected With Hepa… | — | Hepatitis C Virus (HCV) | Completed | 2017-12-27 | 2020-09-15 | ClinicalTrials.gov |
| NCT03343067 | A Study to Evaluate Safety and Efficacy of Elagolix in Participants With Endome… | Phase3 | Endometriosis | Terminated | 2017-12-27 | 2018-10-23 | ClinicalTrials.gov |
| NCT03341871 | Glecaprevir/Pibrentasvir Drug Use Results Survey in Patients Infected With Hepa… | — | Hepatitis C Virus (HCV) | Completed | 2017-12-27 | 2020-09-15 | ClinicalTrials.gov |
| NCT03341871 | Glecaprevir/Pibrentasvir Drug Use Results Survey in Patients Infected With Hepa… | — | Hepatitis C Virus (HCV) | Completed | 2017-12-27 | 2020-09-15 | ClinicalTrials.gov |
| NCT03104413 | A Study to Assess the Efficacy and Safety of Risankizumab in Participants With … | Phase3 | Crohn's Disease | Completed | 2017-12-18 | 2021-05-19 | ClinicalTrials.gov |
| NCT03104413 | A Study to Assess the Efficacy and Safety of Risankizumab in Participants With … | Phase3 | Crohn's Disease | Completed | 2017-12-18 | 2021-05-19 | ClinicalTrials.gov |
| NCT03104413 | A Study to Assess the Efficacy and Safety of Risankizumab in Participants With … | Phase3 | Crohn's Disease | Completed | 2017-12-18 | 2021-05-19 | ClinicalTrials.gov |
| NCT03104413 | A Study to Assess the Efficacy and Safety of Risankizumab in Participants With … | Phase3 | Crohn's Disease | Completed | 2017-12-18 | 2021-05-19 | ClinicalTrials.gov |
| NCT03352453 | A Study of Rapastinel for Rapid Treatment of Depression and Suicidality in Majo… | Phase2 | Depressive Disorder, Major | Terminated | 2017-12-15 | 2019-06-21 | ClinicalTrials.gov |
| NCT03352453 | A Study of Rapastinel for Rapid Treatment of Depression and Suicidality in Majo… | Phase2 | Depressive Disorder, Major | Terminated | 2017-12-15 | 2019-06-21 | ClinicalTrials.gov |
| NCT03352453 | A Study of Rapastinel for Rapid Treatment of Depression and Suicidality in Majo… | Phase2 | Depressive Disorder, Major | Terminated | 2017-12-15 | 2019-06-21 | ClinicalTrials.gov |
| NCT03352453 | A Study of Rapastinel for Rapid Treatment of Depression and Suicidality in Majo… | Phase2 | Depressive Disorder, Major | Terminated | 2017-12-15 | 2019-06-21 | ClinicalTrials.gov |
| NCT03362879 | COmedication Study Assessing Mono- and cOmbination Therapy With Levodopa-carbid… | — | Parkinson's Disease (PD) | Completed | 2017-12-14 | 2018-12-17 | ClinicalTrials.gov |
| NCT03362879 | COmedication Study Assessing Mono- and cOmbination Therapy With Levodopa-carbid… | — | Parkinson's Disease (PD) | Completed | 2017-12-14 | 2018-12-17 | ClinicalTrials.gov |
| NCT03362879 | COmedication Study Assessing Mono- and cOmbination Therapy With Levodopa-carbid… | — | Parkinson's Disease (PD) | Completed | 2017-12-14 | 2018-12-17 | ClinicalTrials.gov |
| NCT03362879 | COmedication Study Assessing Mono- and cOmbination Therapy With Levodopa-carbid… | — | Parkinson's Disease (PD) | Completed | 2017-12-14 | 2018-12-17 | ClinicalTrials.gov |
| NCT03258814 | A Post-Marketing-Observational Study (PMOS) to Determine the Effectiveness of C… | — | Axial Spondyloarthritis | Terminated | 2017-12-08 | 2018-09-14 | ClinicalTrials.gov |
| NCT03258814 | A Post-Marketing-Observational Study (PMOS) to Determine the Effectiveness of C… | — | Axial Spondyloarthritis | Terminated | 2017-12-08 | 2018-09-14 | ClinicalTrials.gov |
| NCT03258814 | A Post-Marketing-Observational Study (PMOS) to Determine the Effectiveness of C… | — | Axial Spondyloarthritis | Terminated | 2017-12-08 | 2018-09-14 | ClinicalTrials.gov |
| NCT03258814 | A Post-Marketing-Observational Study (PMOS) to Determine the Effectiveness of C… | — | Axial Spondyloarthritis | Terminated | 2017-12-08 | 2018-09-14 | ClinicalTrials.gov |
| NCT03345849 | A Study of the Efficacy and Safety of Upadacitinib in Participants With Moderat… | Phase3 | Crohn's Disease | Completed | 2017-12-07 | 2022-01-13 | ClinicalTrials.gov |
| NCT03345849 | A Study of the Efficacy and Safety of Upadacitinib in Participants With Moderat… | Phase3 | Crohn's Disease | Completed | 2017-12-07 | 2022-01-13 | ClinicalTrials.gov |
| NCT03345849 | A Study of the Efficacy and Safety of Upadacitinib in Participants With Moderat… | Phase3 | Crohn's Disease | Completed | 2017-12-07 | 2022-01-13 | ClinicalTrials.gov |
| NCT03345849 | A Study of the Efficacy and Safety of Upadacitinib in Participants With Moderat… | Phase3 | Crohn's Disease | Completed | 2017-12-07 | 2022-01-13 | ClinicalTrials.gov |
| NCT03342144 | Study of the Use of Venetoclax in Participants With Chronic Lymphocytic Leukemi… | — | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2017-12-04 | 2030-12-01 | ClinicalTrials.gov |
| NCT03342144 | Study of the Use of Venetoclax in Participants With Chronic Lymphocytic Leukemi… | — | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2017-12-04 | 2030-12-01 | ClinicalTrials.gov |
| NCT03342144 | Study of the Use of Venetoclax in Participants With Chronic Lymphocytic Leukemi… | — | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2017-12-04 | 2030-12-01 | ClinicalTrials.gov |
| NCT03342144 | Study of the Use of Venetoclax in Participants With Chronic Lymphocytic Leukemi… | — | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2017-12-04 | 2030-12-01 | ClinicalTrials.gov |
| NCT03345836 | A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants Wi… | Phase3 | Crohn's Disease | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03379428 | Trial of Ibrutinib Plus Trastuzumab in HER2-amplified Metastatic Breast Cancer | Phase1 | Breast Neoplasms | Active_Not_Recruiting | 2017-11-29 | 2025-01-01 | ClinicalTrials.gov |
| NCT03345836 | A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants Wi… | Phase3 | Crohn's Disease | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03345836 | A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants Wi… | Phase3 | Crohn's Disease | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03379428 | Trial of Ibrutinib Plus Trastuzumab in HER2-amplified Metastatic Breast Cancer | Phase1 | Breast Neoplasms | Active_Not_Recruiting | 2017-11-29 | 2025-01-01 | ClinicalTrials.gov |
| NCT03345836 | A Study of the Efficacy and Safety of Upadacitinib (ABT-494) in Participants Wi… | Phase3 | Crohn's Disease | Completed | 2017-11-29 | 2021-08-11 | ClinicalTrials.gov |
| NCT03379428 | Trial of Ibrutinib Plus Trastuzumab in HER2-amplified Metastatic Breast Cancer | Phase1 | Breast Neoplasms | Active_Not_Recruiting | 2017-11-29 | 2025-01-01 | ClinicalTrials.gov |
| NCT03379428 | Trial of Ibrutinib Plus Trastuzumab in HER2-amplified Metastatic Breast Cancer | Phase1 | Breast Neoplasms | Active_Not_Recruiting | 2017-11-29 | 2025-01-01 | ClinicalTrials.gov |
| NCT03335852 | Safety and Pharmacokinetics of Abicipar Pegol Intravitreal Injections in Japane… | Phase1 | Macular Degeneration | Completed | 2017-11-28 | 2018-10-08 | ClinicalTrials.gov |
| NCT03335852 | Safety and Pharmacokinetics of Abicipar Pegol Intravitreal Injections in Japane… | Phase1 | Macular Degeneration | Completed | 2017-11-28 | 2018-10-08 | ClinicalTrials.gov |
| NCT03335852 | Safety and Pharmacokinetics of Abicipar Pegol Intravitreal Injections in Japane… | Phase1 | Macular Degeneration | Completed | 2017-11-28 | 2018-10-08 | ClinicalTrials.gov |
| NCT03335852 | Safety and Pharmacokinetics of Abicipar Pegol Intravitreal Injections in Japane… | Phase1 | Macular Degeneration | Completed | 2017-11-28 | 2018-10-08 | ClinicalTrials.gov |
| NCT03181126 | A Study of Venetoclax in Combination With Navitoclax and Chemotherapy in Subjec… | Phase1 | Acute Lymphoblastic Leukemia (ALL) | Completed | 2017-11-27 | 2020-11-14 | ClinicalTrials.gov |
| NCT03181126 | A Study of Venetoclax in Combination With Navitoclax and Chemotherapy in Subjec… | Phase1 | Acute Lymphoblastic Leukemia (ALL) | Completed | 2017-11-27 | 2020-11-14 | ClinicalTrials.gov |
| NCT03181126 | A Study of Venetoclax in Combination With Navitoclax and Chemotherapy in Subjec… | Phase1 | Acute Lymphoblastic Leukemia (ALL) | Completed | 2017-11-27 | 2020-11-14 | ClinicalTrials.gov |
| NCT03181126 | A Study of Venetoclax in Combination With Navitoclax and Chemotherapy in Subjec… | Phase1 | Acute Lymphoblastic Leukemia (ALL) | Completed | 2017-11-27 | 2020-11-14 | ClinicalTrials.gov |
| NCT03223012 | Impact of AbbVie Care Patient Support Program on Clinical, Health Economic and … | — | Crohn's Disease | Completed | 2017-11-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT03223012 | Impact of AbbVie Care Patient Support Program on Clinical, Health Economic and … | — | Crohn's Disease | Completed | 2017-11-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT03339128 | Study to Explore the Therapeutic Effect of Eluxadoline in Treating Irritable Bo… | Phase2 | Irritable Bowel Syndrome | Recruiting | 2017-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03339128 | Study to Explore the Therapeutic Effect of Eluxadoline in Treating Irritable Bo… | Phase2 | Irritable Bowel Syndrome | Recruiting | 2017-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03223012 | Impact of AbbVie Care Patient Support Program on Clinical, Health Economic and … | — | Crohn's Disease | Completed | 2017-11-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT03339128 | Study to Explore the Therapeutic Effect of Eluxadoline in Treating Irritable Bo… | Phase2 | Irritable Bowel Syndrome | Recruiting | 2017-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03223012 | Impact of AbbVie Care Patient Support Program on Clinical, Health Economic and … | — | Crohn's Disease | Completed | 2017-11-15 | 2019-02-28 | ClinicalTrials.gov |
| NCT03339128 | Study to Explore the Therapeutic Effect of Eluxadoline in Treating Irritable Bo… | Phase2 | Irritable Bowel Syndrome | Recruiting | 2017-11-15 | 2026-12-01 | ClinicalTrials.gov |
| NCT03303599 | Study of the Effectiveness and Clinical Practice Use of Glecaprevir Plus Pibren… | — | Hepatitis C | Completed | 2017-11-13 | 2020-01-24 | ClinicalTrials.gov |
| NCT03303599 | Study of the Effectiveness and Clinical Practice Use of Glecaprevir Plus Pibren… | — | Hepatitis C | Completed | 2017-11-13 | 2020-01-24 | ClinicalTrials.gov |
| NCT03303599 | Study of the Effectiveness and Clinical Practice Use of Glecaprevir Plus Pibren… | — | Hepatitis C | Completed | 2017-11-13 | 2020-01-24 | ClinicalTrials.gov |
| NCT03303599 | Study of the Effectiveness and Clinical Practice Use of Glecaprevir Plus Pibren… | — | Hepatitis C | Completed | 2017-11-13 | 2020-01-24 | ClinicalTrials.gov |
| NCT03332342 | Closed Eye Neutrophils in Dry Eye Disease | Na | Dry Eye | Completed | 2017-11-08 | 2019-05-14 | ClinicalTrials.gov |
| NCT03236857 | A Study of the Safety and Pharmacokinetics of Venetoclax in Pediatric and Young… | Phase1 | Malignancies | Completed | 2017-11-08 | 2023-04-19 | ClinicalTrials.gov |
| NCT03332342 | Closed Eye Neutrophils in Dry Eye Disease | Na | Dry Eye | Completed | 2017-11-08 | 2019-05-14 | ClinicalTrials.gov |
| NCT03332342 | Closed Eye Neutrophils in Dry Eye Disease | Na | Dry Eye | Completed | 2017-11-08 | 2019-05-14 | ClinicalTrials.gov |
| NCT03332342 | Closed Eye Neutrophils in Dry Eye Disease | Na | Dry Eye | Completed | 2017-11-08 | 2019-05-14 | ClinicalTrials.gov |
| NCT03236857 | A Study of the Safety and Pharmacokinetics of Venetoclax in Pediatric and Young… | Phase1 | Malignancies | Completed | 2017-11-08 | 2023-04-19 | ClinicalTrials.gov |
| NCT03236857 | A Study of the Safety and Pharmacokinetics of Venetoclax in Pediatric and Young… | Phase1 | Malignancies | Completed | 2017-11-08 | 2023-04-19 | ClinicalTrials.gov |
| NCT03236857 | A Study of the Safety and Pharmacokinetics of Venetoclax in Pediatric and Young… | Phase1 | Malignancies | Completed | 2017-11-08 | 2023-04-19 | ClinicalTrials.gov |
| NCT03311477 | A Study to Evaluate the Safety and Pharmacokinetics ABBV-399 in Japanese Partic… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-11-06 | 2019-03-04 | ClinicalTrials.gov |
| NCT03311477 | A Study to Evaluate the Safety and Pharmacokinetics ABBV-399 in Japanese Partic… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-11-06 | 2019-03-04 | ClinicalTrials.gov |
| NCT03311477 | A Study to Evaluate the Safety and Pharmacokinetics ABBV-399 in Japanese Partic… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-11-06 | 2019-03-04 | ClinicalTrials.gov |
| NCT03311477 | A Study to Evaluate the Safety and Pharmacokinetics ABBV-399 in Japanese Partic… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-11-06 | 2019-03-04 | ClinicalTrials.gov |
| NCT03222609 | A Study Evaluating Tolerability and Efficacy of Navitoclax Alone or in Combinat… | Phase2 | Myelofibrosis (MF) | Completed | 2017-10-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT03222609 | A Study Evaluating Tolerability and Efficacy of Navitoclax Alone or in Combinat… | Phase2 | Myelofibrosis (MF) | Completed | 2017-10-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT03222609 | A Study Evaluating Tolerability and Efficacy of Navitoclax Alone or in Combinat… | Phase2 | Myelofibrosis (MF) | Completed | 2017-10-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT03222609 | A Study Evaluating Tolerability and Efficacy of Navitoclax Alone or in Combinat… | Phase2 | Myelofibrosis (MF) | Completed | 2017-10-31 | 2025-01-29 | ClinicalTrials.gov |
| NCT03319901 | Venetoclax and Chemotherapy as Frontline Therapy in Older Patients and Patients… | Phase1 | Leukemia | Active_Not_Recruiting | 2017-10-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT03319901 | Venetoclax and Chemotherapy as Frontline Therapy in Older Patients and Patients… | Phase1 | Leukemia | Active_Not_Recruiting | 2017-10-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT03319901 | Venetoclax and Chemotherapy as Frontline Therapy in Older Patients and Patients… | Phase1 | Leukemia | Active_Not_Recruiting | 2017-10-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT03319901 | Venetoclax and Chemotherapy as Frontline Therapy in Older Patients and Patients… | Phase1 | Leukemia | Active_Not_Recruiting | 2017-10-30 | 2028-05-30 | ClinicalTrials.gov |
| NCT03311464 | A Study Assessing the Efficacy and Safety of Adalimumab in Active Ulcer(s) of P… | Phase3 | Pyoderma Gangrenosum | Completed | 2017-10-27 | 2020-04-21 | ClinicalTrials.gov |
| NCT03311464 | A Study Assessing the Efficacy and Safety of Adalimumab in Active Ulcer(s) of P… | Phase3 | Pyoderma Gangrenosum | Completed | 2017-10-27 | 2020-04-21 | ClinicalTrials.gov |
| NCT03311464 | A Study Assessing the Efficacy and Safety of Adalimumab in Active Ulcer(s) of P… | Phase3 | Pyoderma Gangrenosum | Completed | 2017-10-27 | 2020-04-21 | ClinicalTrials.gov |
| NCT03311464 | A Study Assessing the Efficacy and Safety of Adalimumab in Active Ulcer(s) of P… | Phase3 | Pyoderma Gangrenosum | Completed | 2017-10-27 | 2020-04-21 | ClinicalTrials.gov |
| NCT03178487 | A Study Evaluating the Safety and Efficacy of Upadacitinib in Adults With Activ… | Phase2 | Ankylosing Spondylitis (AS) | Completed | 2017-10-24 | 2022-02-17 | ClinicalTrials.gov |
| NCT03178487 | A Study Evaluating the Safety and Efficacy of Upadacitinib in Adults With Activ… | Phase2 | Ankylosing Spondylitis (AS) | Completed | 2017-10-24 | 2022-02-17 | ClinicalTrials.gov |
| NCT03178487 | A Study Evaluating the Safety and Efficacy of Upadacitinib in Adults With Activ… | Phase2 | Ankylosing Spondylitis (AS) | Completed | 2017-10-24 | 2022-02-17 | ClinicalTrials.gov |
| NCT03178487 | A Study Evaluating the Safety and Efficacy of Upadacitinib in Adults With Activ… | Phase2 | Ankylosing Spondylitis (AS) | Completed | 2017-10-24 | 2022-02-17 | ClinicalTrials.gov |
| NCT03003338 | MHH-HCV-NPM-Neuropsychiatric Manifestations of HCV-infection During and After T… | Phase4 | Hepatitis C, Chronic | Terminated | 2017-10-24 | 2018-10-22 | ClinicalTrials.gov |
| NCT03003338 | MHH-HCV-NPM-Neuropsychiatric Manifestations of HCV-infection During and After T… | Phase4 | Hepatitis C, Chronic | Terminated | 2017-10-24 | 2018-10-22 | ClinicalTrials.gov |
| NCT03003338 | MHH-HCV-NPM-Neuropsychiatric Manifestations of HCV-infection During and After T… | Phase4 | Hepatitis C, Chronic | Terminated | 2017-10-24 | 2018-10-22 | ClinicalTrials.gov |
| NCT03003338 | MHH-HCV-NPM-Neuropsychiatric Manifestations of HCV-infection During and After T… | Phase4 | Hepatitis C, Chronic | Terminated | 2017-10-24 | 2018-10-22 | ClinicalTrials.gov |
| NCT05305222 | A Study in Healthy Japanese and Caucasian Subjects to Assess the Pharmacokineti… | Phase1 | Healthy Volunteers | Completed | 2017-10-23 | 2018-06-15 | ClinicalTrials.gov |
| NCT05305222 | A Study in Healthy Japanese and Caucasian Subjects to Assess the Pharmacokineti… | Phase1 | Healthy Volunteers | Completed | 2017-10-23 | 2018-06-15 | ClinicalTrials.gov |
| NCT05305222 | A Study in Healthy Japanese and Caucasian Subjects to Assess the Pharmacokineti… | Phase1 | Healthy Volunteers | Completed | 2017-10-23 | 2018-06-15 | ClinicalTrials.gov |
| NCT05305222 | A Study in Healthy Japanese and Caucasian Subjects to Assess the Pharmacokineti… | Phase1 | Healthy Volunteers | Completed | 2017-10-23 | 2018-06-15 | ClinicalTrials.gov |
| NCT03274999 | Clinical Study to Evaluate Tear Characteristics Following Acute TrueTear™ Use | Na | Dry Eye Syndromes | Terminated | 2017-10-18 | 2017-11-09 | ClinicalTrials.gov |
| NCT03274999 | Clinical Study to Evaluate Tear Characteristics Following Acute TrueTear™ Use | Na | Dry Eye Syndromes | Terminated | 2017-10-18 | 2017-11-09 | ClinicalTrials.gov |
| NCT03274999 | Clinical Study to Evaluate Tear Characteristics Following Acute TrueTear™ Use | Na | Dry Eye Syndromes | Terminated | 2017-10-18 | 2017-11-09 | ClinicalTrials.gov |
| NCT03274999 | Clinical Study to Evaluate Tear Characteristics Following Acute TrueTear™ Use | Na | Dry Eye Syndromes | Terminated | 2017-10-18 | 2017-11-09 | ClinicalTrials.gov |
| NCT02966756 | A Study of Venetoclax in Participants With Relapsed or Refractory Chronic Lymph… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2017-10-12 | 2029-05-01 | ClinicalTrials.gov |
| NCT02966756 | A Study of Venetoclax in Participants With Relapsed or Refractory Chronic Lymph… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2017-10-12 | 2029-05-01 | ClinicalTrials.gov |
| NCT02966756 | A Study of Venetoclax in Participants With Relapsed or Refractory Chronic Lymph… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2017-10-12 | 2029-05-01 | ClinicalTrials.gov |
| NCT02966756 | A Study of Venetoclax in Participants With Relapsed or Refractory Chronic Lymph… | Phase2 | Chronic Lymphocytic Leukemia (CLL) | Recruiting | 2017-10-12 | 2029-05-01 | ClinicalTrials.gov |
| NCT03234712 | A Study Evaluating the Safety, Pharmacokinetics, and Anti-tumor Activity of ABB… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-10-10 | 2021-04-14 | ClinicalTrials.gov |
| NCT03234712 | A Study Evaluating the Safety, Pharmacokinetics, and Anti-tumor Activity of ABB… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-10-10 | 2021-04-14 | ClinicalTrials.gov |
| NCT03234712 | A Study Evaluating the Safety, Pharmacokinetics, and Anti-tumor Activity of ABB… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-10-10 | 2021-04-14 | ClinicalTrials.gov |
| NCT03234712 | A Study Evaluating the Safety, Pharmacokinetics, and Anti-tumor Activity of ABB… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-10-10 | 2021-04-14 | ClinicalTrials.gov |
| NCT03220841 | Stricture Definition and Treatment (STRIDENT) Drug Therapy Study | Phase4 | Crohn Disease | Unknown | 2017-10-09 | 2021-09-01 | ClinicalTrials.gov |
| NCT03220841 | Stricture Definition and Treatment (STRIDENT) Drug Therapy Study | Phase4 | Crohn Disease | Unknown | 2017-10-09 | 2021-09-01 | ClinicalTrials.gov |
| NCT03220841 | Stricture Definition and Treatment (STRIDENT) Drug Therapy Study | Phase4 | Crohn Disease | Unknown | 2017-10-09 | 2021-09-01 | ClinicalTrials.gov |
| NCT03220841 | Stricture Definition and Treatment (STRIDENT) Drug Therapy Study | Phase4 | Crohn Disease | Unknown | 2017-10-09 | 2021-09-01 | ClinicalTrials.gov |
| NCT03301649 | Clinical Endpoint Study of Ivermectin 0.5% Lotion | Phase3 | Head Lice | Completed | 2017-10-07 | 2018-03-12 | ClinicalTrials.gov |
| NCT03301649 | Clinical Endpoint Study of Ivermectin 0.5% Lotion | Phase3 | Head Lice | Completed | 2017-10-07 | 2018-03-12 | ClinicalTrials.gov |
| NCT03301649 | Clinical Endpoint Study of Ivermectin 0.5% Lotion | Phase3 | Head Lice | Completed | 2017-10-07 | 2018-03-12 | ClinicalTrials.gov |
| NCT03301649 | Clinical Endpoint Study of Ivermectin 0.5% Lotion | Phase3 | Head Lice | Completed | 2017-10-07 | 2018-03-12 | ClinicalTrials.gov |
| NCT03222583 | A Study to Evaluate the Efficacy and Safety of Glecaprevir/Pibrentasvir (ABT-49… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-10-04 | 2019-02-15 | ClinicalTrials.gov |
| NCT03222583 | A Study to Evaluate the Efficacy and Safety of Glecaprevir/Pibrentasvir (ABT-49… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-10-04 | 2019-02-15 | ClinicalTrials.gov |
| NCT03222583 | A Study to Evaluate the Efficacy and Safety of Glecaprevir/Pibrentasvir (ABT-49… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-10-04 | 2019-02-15 | ClinicalTrials.gov |
| NCT03222583 | A Study to Evaluate the Efficacy and Safety of Glecaprevir/Pibrentasvir (ABT-49… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-10-04 | 2019-02-15 | ClinicalTrials.gov |
| NCT03373162 | Functional Effects of Botox on the Brain Using MRS and fMRI | Phase4 | Healthy | Completed | 2017-09-30 | 2018-03-16 | ClinicalTrials.gov |
| NCT03373162 | Functional Effects of Botox on the Brain Using MRS and fMRI | Phase4 | Healthy | Completed | 2017-09-30 | 2018-03-16 | ClinicalTrials.gov |
| NCT03373162 | Functional Effects of Botox on the Brain Using MRS and fMRI | Phase4 | Healthy | Completed | 2017-09-30 | 2018-03-16 | ClinicalTrials.gov |
| NCT03373162 | Functional Effects of Botox on the Brain Using MRS and fMRI | Phase4 | Healthy | Completed | 2017-09-30 | 2018-03-16 | ClinicalTrials.gov |
| NCT03285308 | A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis 01 | Phase3 | Gastroparesis | Terminated | 2017-09-29 | 2020-07-08 | ClinicalTrials.gov |
| NCT03235349 | Efficacy and Safety of Glecaprevir/Pibrentasvir (ABT-493/ABT-530) in Treatment-… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-09-29 | 2019-02-25 | ClinicalTrials.gov |
| NCT03235349 | Efficacy and Safety of Glecaprevir/Pibrentasvir (ABT-493/ABT-530) in Treatment-… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-09-29 | 2019-02-25 | ClinicalTrials.gov |
| NCT03235349 | Efficacy and Safety of Glecaprevir/Pibrentasvir (ABT-493/ABT-530) in Treatment-… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-09-29 | 2019-02-25 | ClinicalTrials.gov |
| NCT03235349 | Efficacy and Safety of Glecaprevir/Pibrentasvir (ABT-493/ABT-530) in Treatment-… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-09-29 | 2019-02-25 | ClinicalTrials.gov |
| NCT03285308 | A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis 01 | Phase3 | Gastroparesis | Terminated | 2017-09-29 | 2020-07-08 | ClinicalTrials.gov |
| NCT03285308 | A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis 01 | Phase3 | Gastroparesis | Terminated | 2017-09-29 | 2020-07-08 | ClinicalTrials.gov |
| NCT03285308 | A Safety and Efficacy Study of Relamorelin in Diabetic Gastroparesis 01 | Phase3 | Gastroparesis | Terminated | 2017-09-29 | 2020-07-08 | ClinicalTrials.gov |
| NCT03017014 | A Study to Assess Safety and Effectiveness of Adalimumab for Treating Children … | — | Crohn's Disease | Terminated | 2017-09-26 | 2019-10-14 | ClinicalTrials.gov |
| NCT03017014 | A Study to Assess Safety and Effectiveness of Adalimumab for Treating Children … | — | Crohn's Disease | Terminated | 2017-09-26 | 2019-10-14 | ClinicalTrials.gov |
| NCT03017014 | A Study to Assess Safety and Effectiveness of Adalimumab for Treating Children … | — | Crohn's Disease | Terminated | 2017-09-26 | 2019-10-14 | ClinicalTrials.gov |
| NCT03017014 | A Study to Assess Safety and Effectiveness of Adalimumab for Treating Children … | — | Crohn's Disease | Terminated | 2017-09-26 | 2019-10-14 | ClinicalTrials.gov |
| NCT03302559 | Study to Assess the Cosmetic Changes in the Facial Skin After Use of a Topical … | Na | Skin Care | Completed | 2017-09-18 | 2018-04-30 | ClinicalTrials.gov |
| NCT03302559 | Study to Assess the Cosmetic Changes in the Facial Skin After Use of a Topical … | Na | Skin Care | Completed | 2017-09-18 | 2018-04-30 | ClinicalTrials.gov |
| NCT03302559 | Study to Assess the Cosmetic Changes in the Facial Skin After Use of a Topical … | Na | Skin Care | Completed | 2017-09-18 | 2018-04-30 | ClinicalTrials.gov |
| NCT03302559 | Study to Assess the Cosmetic Changes in the Facial Skin After Use of a Topical … | Na | Skin Care | Completed | 2017-09-18 | 2018-04-30 | ClinicalTrials.gov |
| NCT03253185 | A Study of SC-007 in Subjects With Advanced Cancer | Phase1 | Colorectal Cancer (CRC) | Terminated | 2017-09-13 | 2018-04-02 | ClinicalTrials.gov |
| NCT03271489 | Long-Term Safety Study of Elagolix in Combination With Estradiol/Norethindrone … | Phase3 | Heavy Menstrual Bleeding | Completed | 2017-09-13 | 2024-06-28 | ClinicalTrials.gov |
| NCT03253185 | A Study of SC-007 in Subjects With Advanced Cancer | Phase1 | Colorectal Cancer (CRC) | Terminated | 2017-09-13 | 2018-04-02 | ClinicalTrials.gov |
| NCT03253185 | A Study of SC-007 in Subjects With Advanced Cancer | Phase1 | Colorectal Cancer (CRC) | Terminated | 2017-09-13 | 2018-04-02 | ClinicalTrials.gov |
| NCT03253185 | A Study of SC-007 in Subjects With Advanced Cancer | Phase1 | Colorectal Cancer (CRC) | Terminated | 2017-09-13 | 2018-04-02 | ClinicalTrials.gov |
| NCT03271489 | Long-Term Safety Study of Elagolix in Combination With Estradiol/Norethindrone … | Phase3 | Heavy Menstrual Bleeding | Completed | 2017-09-13 | 2024-06-28 | ClinicalTrials.gov |
| NCT03271489 | Long-Term Safety Study of Elagolix in Combination With Estradiol/Norethindrone … | Phase3 | Heavy Menstrual Bleeding | Completed | 2017-09-13 | 2024-06-28 | ClinicalTrials.gov |
| NCT03271489 | Long-Term Safety Study of Elagolix in Combination With Estradiol/Norethindrone … | Phase3 | Heavy Menstrual Bleeding | Completed | 2017-09-13 | 2024-06-28 | ClinicalTrials.gov |
| NCT05283694 | A Study to Evaluate the Bioavailability of Risankizumab Following Subcutaneous … | Phase1 | Healthy Volunteers | Completed | 2017-09-11 | 2018-06-12 | ClinicalTrials.gov |
| NCT05283694 | A Study to Evaluate the Bioavailability of Risankizumab Following Subcutaneous … | Phase1 | Healthy Volunteers | Completed | 2017-09-11 | 2018-06-12 | ClinicalTrials.gov |
| NCT05283694 | A Study to Evaluate the Bioavailability of Risankizumab Following Subcutaneous … | Phase1 | Healthy Volunteers | Completed | 2017-09-11 | 2018-06-12 | ClinicalTrials.gov |
| NCT05283694 | A Study to Evaluate the Bioavailability of Risankizumab Following Subcutaneous … | Phase1 | Healthy Volunteers | Completed | 2017-09-11 | 2018-06-12 | ClinicalTrials.gov |
| NCT03236870 | A Study to Evaluate the Effectiveness and Patient-Reported Outcome of Adalimuma… | — | Psoriasis | Completed | 2017-09-08 | 2020-08-25 | ClinicalTrials.gov |
| NCT03236870 | A Study to Evaluate the Effectiveness and Patient-Reported Outcome of Adalimuma… | — | Psoriasis | Completed | 2017-09-08 | 2020-08-25 | ClinicalTrials.gov |
| NCT03236870 | A Study to Evaluate the Effectiveness and Patient-Reported Outcome of Adalimuma… | — | Psoriasis | Completed | 2017-09-08 | 2020-08-25 | ClinicalTrials.gov |
| NCT03236870 | A Study to Evaluate the Effectiveness and Patient-Reported Outcome of Adalimuma… | — | Psoriasis | Completed | 2017-09-08 | 2020-08-25 | ClinicalTrials.gov |
| NCT02951117 | A Study of Venetoclax and ABBV-838 Combination Therapy With Dexamethasone in Pa… | Phase1 | Multiple Myeloma | Withdrawn | 2017-08-31 | 2021-04-28 | ClinicalTrials.gov |
| NCT02951117 | A Study of Venetoclax and ABBV-838 Combination Therapy With Dexamethasone in Pa… | Phase1 | Multiple Myeloma | Withdrawn | 2017-08-31 | 2021-04-28 | ClinicalTrials.gov |
| NCT02951117 | A Study of Venetoclax and ABBV-838 Combination Therapy With Dexamethasone in Pa… | Phase1 | Multiple Myeloma | Withdrawn | 2017-08-31 | 2021-04-28 | ClinicalTrials.gov |
| NCT02951117 | A Study of Venetoclax and ABBV-838 Combination Therapy With Dexamethasone in Pa… | Phase1 | Multiple Myeloma | Withdrawn | 2017-08-31 | 2021-04-28 | ClinicalTrials.gov |
| NCT03155113 | Role of the Host Immunity in the Non-response to Direct Anti-viral Agent (DAA) … | Na | Chronic Hepatitis C | Completed | 2017-08-30 | 2019-12-31 | ClinicalTrials.gov |
| NCT03155113 | Role of the Host Immunity in the Non-response to Direct Anti-viral Agent (DAA) … | Na | Chronic Hepatitis C | Completed | 2017-08-30 | 2019-12-31 | ClinicalTrials.gov |
| NCT03155113 | Role of the Host Immunity in the Non-response to Direct Anti-viral Agent (DAA) … | Na | Chronic Hepatitis C | Completed | 2017-08-30 | 2019-12-31 | ClinicalTrials.gov |
| NCT03155113 | Role of the Host Immunity in the Non-response to Direct Anti-viral Agent (DAA) … | Na | Chronic Hepatitis C | Completed | 2017-08-30 | 2019-12-31 | ClinicalTrials.gov |
| NCT03255382 | A Study to Assess the Efficacy of Risankizumab Compared to FUMADERM® in Subject… | Phase3 | Psoriasis | Completed | 2017-08-22 | 2018-07-06 | ClinicalTrials.gov |
| NCT03255382 | A Study to Assess the Efficacy of Risankizumab Compared to FUMADERM® in Subject… | Phase3 | Psoriasis | Completed | 2017-08-22 | 2018-07-06 | ClinicalTrials.gov |
| NCT03255382 | A Study to Assess the Efficacy of Risankizumab Compared to FUMADERM® in Subject… | Phase3 | Psoriasis | Completed | 2017-08-22 | 2018-07-06 | ClinicalTrials.gov |
| NCT03255382 | A Study to Assess the Efficacy of Risankizumab Compared to FUMADERM® in Subject… | Phase3 | Psoriasis | Completed | 2017-08-22 | 2018-07-06 | ClinicalTrials.gov |
| NCT03201718 | A Study of Viekira/Exviera for Korean Hepatitis C Patients According to the Sta… | — | Hepatitis C Virus (HCV) | Completed | 2017-08-17 | 2019-10-11 | ClinicalTrials.gov |
| NCT03194269 | Long Term Prospective Uncontrolled Study Of Earfold™ For The Treatment Of Promi… | Phase4 | Prominent Ears | Completed | 2017-08-17 | 2021-09-07 | ClinicalTrials.gov |
| NCT03201718 | A Study of Viekira/Exviera for Korean Hepatitis C Patients According to the Sta… | — | Hepatitis C Virus (HCV) | Completed | 2017-08-17 | 2019-10-11 | ClinicalTrials.gov |
| NCT03201718 | A Study of Viekira/Exviera for Korean Hepatitis C Patients According to the Sta… | — | Hepatitis C Virus (HCV) | Completed | 2017-08-17 | 2019-10-11 | ClinicalTrials.gov |
| NCT03194269 | Long Term Prospective Uncontrolled Study Of Earfold™ For The Treatment Of Promi… | Phase4 | Prominent Ears | Completed | 2017-08-17 | 2021-09-07 | ClinicalTrials.gov |
| NCT03194269 | Long Term Prospective Uncontrolled Study Of Earfold™ For The Treatment Of Promi… | Phase4 | Prominent Ears | Completed | 2017-08-17 | 2021-09-07 | ClinicalTrials.gov |
| NCT03201718 | A Study of Viekira/Exviera for Korean Hepatitis C Patients According to the Sta… | — | Hepatitis C Virus (HCV) | Completed | 2017-08-17 | 2019-10-11 | ClinicalTrials.gov |
| NCT03194269 | Long Term Prospective Uncontrolled Study Of Earfold™ For The Treatment Of Promi… | Phase4 | Prominent Ears | Completed | 2017-08-17 | 2021-09-07 | ClinicalTrials.gov |
| NCT03048721 | Skin Tape Harvesting for Transcriptomics Analysis | Na | Psoriasis | Completed | 2017-08-14 | 2018-09-24 | ClinicalTrials.gov |
| NCT03048721 | Skin Tape Harvesting for Transcriptomics Analysis | Na | Psoriasis | Completed | 2017-08-14 | 2018-09-24 | ClinicalTrials.gov |
| NCT03048721 | Skin Tape Harvesting for Transcriptomics Analysis | Na | Psoriasis | Completed | 2017-08-14 | 2018-09-24 | ClinicalTrials.gov |
| NCT03048721 | Skin Tape Harvesting for Transcriptomics Analysis | Na | Psoriasis | Completed | 2017-08-14 | 2018-09-24 | ClinicalTrials.gov |
| NCT03212521 | Efficacy and Safety of 8-weeks of Glecaprevir/Pibrentasvir in Treatment-Naïve A… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-08-07 | 2018-08-13 | ClinicalTrials.gov |
| NCT03212521 | Efficacy and Safety of 8-weeks of Glecaprevir/Pibrentasvir in Treatment-Naïve A… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-08-07 | 2018-08-13 | ClinicalTrials.gov |
| NCT03212521 | Efficacy and Safety of 8-weeks of Glecaprevir/Pibrentasvir in Treatment-Naïve A… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-08-07 | 2018-08-13 | ClinicalTrials.gov |
| NCT03212521 | Efficacy and Safety of 8-weeks of Glecaprevir/Pibrentasvir in Treatment-Naïve A… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-08-07 | 2018-08-13 | ClinicalTrials.gov |
| NCT03226769 | Safety and Efficacy of TrueTear™ for the Treatment of Meibomian Gland Disease | Na | Meibomian Glands | Completed | 2017-07-26 | 2017-12-12 | ClinicalTrials.gov |
| NCT03226769 | Safety and Efficacy of TrueTear™ for the Treatment of Meibomian Gland Disease | Na | Meibomian Glands | Completed | 2017-07-26 | 2017-12-12 | ClinicalTrials.gov |
| NCT03226769 | Safety and Efficacy of TrueTear™ for the Treatment of Meibomian Gland Disease | Na | Meibomian Glands | Completed | 2017-07-26 | 2017-12-12 | ClinicalTrials.gov |
| NCT03226769 | Safety and Efficacy of TrueTear™ for the Treatment of Meibomian Gland Disease | Na | Meibomian Glands | Completed | 2017-07-26 | 2017-12-12 | ClinicalTrials.gov |
| NCT03233438 | Development of a New Critical Pathway for Treatment of Acute Bacterial Skin and… | Phase4 | Bacterial Infections | Completed | 2017-07-24 | 2018-10-30 | ClinicalTrials.gov |
| NCT03233438 | Development of a New Critical Pathway for Treatment of Acute Bacterial Skin and… | Phase4 | Bacterial Infections | Completed | 2017-07-24 | 2018-10-30 | ClinicalTrials.gov |
| NCT03233438 | Development of a New Critical Pathway for Treatment of Acute Bacterial Skin and… | Phase4 | Bacterial Infections | Completed | 2017-07-24 | 2018-10-30 | ClinicalTrials.gov |
| NCT03233438 | Development of a New Critical Pathway for Treatment of Acute Bacterial Skin and… | Phase4 | Bacterial Infections | Completed | 2017-07-24 | 2018-10-30 | ClinicalTrials.gov |
| NCT03213457 | A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Participant… | Phase3 | Endometriosis | Completed | 2017-07-07 | 2023-12-06 | ClinicalTrials.gov |
| NCT03213457 | A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Participant… | Phase3 | Endometriosis | Completed | 2017-07-07 | 2023-12-06 | ClinicalTrials.gov |
| NCT03213457 | A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Participant… | Phase3 | Endometriosis | Completed | 2017-07-07 | 2023-12-06 | ClinicalTrials.gov |
| NCT03213457 | A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Participant… | Phase3 | Endometriosis | Completed | 2017-07-07 | 2023-12-06 | ClinicalTrials.gov |
| NCT03193346 | BOTOX® (Botulinum Toxin Type A) as Headache Prophylaxis in Chinese Participants… | Phase3 | Migraine Disorders | Withdrawn | 2017-07-03 | 2021-03-25 | ClinicalTrials.gov |
| NCT03193346 | BOTOX® (Botulinum Toxin Type A) as Headache Prophylaxis in Chinese Participants… | Phase3 | Migraine Disorders | Withdrawn | 2017-07-03 | 2021-03-25 | ClinicalTrials.gov |
| NCT03145909 | A Study Evaluating the Safety, Pharmacokinetics and Anti-Tumor Activity of ABBV… | Phase1 | Advanced Solid Tumors Cancer | Terminated | 2017-07-03 | 2018-11-27 | ClinicalTrials.gov |
| NCT03208673 | Optive Brand For Day And Night Dry Eye Management | Na | Dry Eye | Completed | 2017-07-03 | 2017-09-06 | ClinicalTrials.gov |
| NCT03145909 | A Study Evaluating the Safety, Pharmacokinetics and Anti-Tumor Activity of ABBV… | Phase1 | Advanced Solid Tumors Cancer | Terminated | 2017-07-03 | 2018-11-27 | ClinicalTrials.gov |
| NCT03208673 | Optive Brand For Day And Night Dry Eye Management | Na | Dry Eye | Completed | 2017-07-03 | 2017-09-06 | ClinicalTrials.gov |
| NCT03193346 | BOTOX® (Botulinum Toxin Type A) as Headache Prophylaxis in Chinese Participants… | Phase3 | Migraine Disorders | Withdrawn | 2017-07-03 | 2021-03-25 | ClinicalTrials.gov |
| NCT03145909 | A Study Evaluating the Safety, Pharmacokinetics and Anti-Tumor Activity of ABBV… | Phase1 | Advanced Solid Tumors Cancer | Terminated | 2017-07-03 | 2018-11-27 | ClinicalTrials.gov |
| NCT03145909 | A Study Evaluating the Safety, Pharmacokinetics and Anti-Tumor Activity of ABBV… | Phase1 | Advanced Solid Tumors Cancer | Terminated | 2017-07-03 | 2018-11-27 | ClinicalTrials.gov |
| NCT03208673 | Optive Brand For Day And Night Dry Eye Management | Na | Dry Eye | Completed | 2017-07-03 | 2017-09-06 | ClinicalTrials.gov |
| NCT03193346 | BOTOX® (Botulinum Toxin Type A) as Headache Prophylaxis in Chinese Participants… | Phase3 | Migraine Disorders | Withdrawn | 2017-07-03 | 2021-03-25 | ClinicalTrials.gov |
| NCT03208673 | Optive Brand For Day And Night Dry Eye Management | Na | Dry Eye | Completed | 2017-07-03 | 2017-09-06 | ClinicalTrials.gov |
| NCT03050905 | Proof of Concept Study To Evaluate the Efficacy and Justification Of OBV/PTV/r … | Phase4 | HCV Coinfection | Completed | 2017-06-22 | 2018-11-28 | ClinicalTrials.gov |
| NCT03050905 | Proof of Concept Study To Evaluate the Efficacy and Justification Of OBV/PTV/r … | Phase4 | HCV Coinfection | Completed | 2017-06-22 | 2018-11-28 | ClinicalTrials.gov |
| NCT03050905 | Proof of Concept Study To Evaluate the Efficacy and Justification Of OBV/PTV/r … | Phase4 | HCV Coinfection | Completed | 2017-06-22 | 2018-11-28 | ClinicalTrials.gov |
| NCT03050905 | Proof of Concept Study To Evaluate the Efficacy and Justification Of OBV/PTV/r … | Phase4 | HCV Coinfection | Completed | 2017-06-22 | 2018-11-28 | ClinicalTrials.gov |
| NCT03063398 | Post Acute Pancreatitis Pancreatic Exocrine Insufficiency | — | Acute Pancreatitis | Completed | 2017-06-21 | 2024-06-30 | ClinicalTrials.gov |
| NCT03063398 | Post Acute Pancreatitis Pancreatic Exocrine Insufficiency | — | Acute Pancreatitis | Completed | 2017-06-21 | 2024-06-30 | ClinicalTrials.gov |
| NCT03063398 | Post Acute Pancreatitis Pancreatic Exocrine Insufficiency | — | Acute Pancreatitis | Completed | 2017-06-21 | 2024-06-30 | ClinicalTrials.gov |
| NCT03063398 | Post Acute Pancreatitis Pancreatic Exocrine Insufficiency | — | Acute Pancreatitis | Completed | 2017-06-21 | 2024-06-30 | ClinicalTrials.gov |
| NCT03155243 | Impact of Humira® Therapy on Ocular Inflammation, Selected Health Care Resource… | — | Uveitis | Completed | 2017-06-20 | 2020-02-24 | ClinicalTrials.gov |
| NCT03155243 | Impact of Humira® Therapy on Ocular Inflammation, Selected Health Care Resource… | — | Uveitis | Completed | 2017-06-20 | 2020-02-24 | ClinicalTrials.gov |
| NCT03155243 | Impact of Humira® Therapy on Ocular Inflammation, Selected Health Care Resource… | — | Uveitis | Completed | 2017-06-20 | 2020-02-24 | ClinicalTrials.gov |
| NCT03155243 | Impact of Humira® Therapy on Ocular Inflammation, Selected Health Care Resource… | — | Uveitis | Completed | 2017-06-20 | 2020-02-24 | ClinicalTrials.gov |
| NCT03138408 | SC-004 Alone or With ABBV-181 in Subjects With Epithelial Ovarian, Fallopian Tu… | Phase1 | Cancer | Terminated | 2017-06-14 | 2019-05-02 | ClinicalTrials.gov |
| NCT03138408 | SC-004 Alone or With ABBV-181 in Subjects With Epithelial Ovarian, Fallopian Tu… | Phase1 | Cancer | Terminated | 2017-06-14 | 2019-05-02 | ClinicalTrials.gov |
| NCT03138408 | SC-004 Alone or With ABBV-181 in Subjects With Epithelial Ovarian, Fallopian Tu… | Phase1 | Cancer | Terminated | 2017-06-14 | 2019-05-02 | ClinicalTrials.gov |
| NCT03138408 | SC-004 Alone or With ABBV-181 in Subjects With Epithelial Ovarian, Fallopian Tu… | Phase1 | Cancer | Terminated | 2017-06-14 | 2019-05-02 | ClinicalTrials.gov |
| NCT03347747 | Facial Asymmetrical Clinical Evaluation Study | — | Loss of Facial Adipose Tissue | Unknown | 2017-06-09 | 2018-07-31 | ClinicalTrials.gov |
| NCT03347747 | Facial Asymmetrical Clinical Evaluation Study | — | Loss of Facial Adipose Tissue | Unknown | 2017-06-09 | 2018-07-31 | ClinicalTrials.gov |
| NCT03347747 | Facial Asymmetrical Clinical Evaluation Study | — | Loss of Facial Adipose Tissue | Unknown | 2017-06-09 | 2018-07-31 | ClinicalTrials.gov |
| NCT03347747 | Facial Asymmetrical Clinical Evaluation Study | — | Loss of Facial Adipose Tissue | Unknown | 2017-06-09 | 2018-07-31 | ClinicalTrials.gov |
| NCT03061188 | Phase I/Ib Study of Nivolumab & Veliparib in Patients With Advanced Solid Tumor… | Phase1 | Advanced Solid Neoplasm | Completed | 2017-05-23 | 2020-08-04 | ClinicalTrials.gov |
| NCT03069352 | A Study of Venetoclax in Combination With Low Dose Cytarabine Versus Low Dose C… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2017-05-23 | 2025-08-21 | ClinicalTrials.gov |
| NCT03061188 | Phase I/Ib Study of Nivolumab & Veliparib in Patients With Advanced Solid Tumor… | Phase1 | Advanced Solid Neoplasm | Completed | 2017-05-23 | 2020-08-04 | ClinicalTrials.gov |
| NCT03061188 | Phase I/Ib Study of Nivolumab & Veliparib in Patients With Advanced Solid Tumor… | Phase1 | Advanced Solid Neoplasm | Completed | 2017-05-23 | 2020-08-04 | ClinicalTrials.gov |
| NCT03061188 | Phase I/Ib Study of Nivolumab & Veliparib in Patients With Advanced Solid Tumor… | Phase1 | Advanced Solid Neoplasm | Completed | 2017-05-23 | 2020-08-04 | ClinicalTrials.gov |
| NCT03069352 | A Study of Venetoclax in Combination With Low Dose Cytarabine Versus Low Dose C… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2017-05-23 | 2025-08-21 | ClinicalTrials.gov |
| NCT03069352 | A Study of Venetoclax in Combination With Low Dose Cytarabine Versus Low Dose C… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2017-05-23 | 2025-08-21 | ClinicalTrials.gov |
| NCT03069352 | A Study of Venetoclax in Combination With Low Dose Cytarabine Versus Low Dose C… | Phase3 | Acute Myeloid Leukemia (AML) | Completed | 2017-05-23 | 2025-08-21 | ClinicalTrials.gov |
| NCT03033498 | A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutane… | Phase1 | Parkinson's Disease (PD) | Completed | 2017-05-17 | 2019-06-08 | ClinicalTrials.gov |
| NCT03033498 | A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutane… | Phase1 | Parkinson's Disease (PD) | Completed | 2017-05-17 | 2019-06-08 | ClinicalTrials.gov |
| NCT03033498 | A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutane… | Phase1 | Parkinson's Disease (PD) | Completed | 2017-05-17 | 2019-06-08 | ClinicalTrials.gov |
| NCT03033498 | A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Subcutane… | Phase1 | Parkinson's Disease (PD) | Completed | 2017-05-17 | 2019-06-08 | ClinicalTrials.gov |
| NCT03091439 | Safety and Efficacy of Dalbavancin Versus Active Comparator in Adult Patients W… | Phase2 | Osteomyelitis | Terminated | 2017-05-15 | 2017-08-31 | ClinicalTrials.gov |
| NCT03091439 | Safety and Efficacy of Dalbavancin Versus Active Comparator in Adult Patients W… | Phase2 | Osteomyelitis | Terminated | 2017-05-15 | 2017-08-31 | ClinicalTrials.gov |
| NCT03091439 | Safety and Efficacy of Dalbavancin Versus Active Comparator in Adult Patients W… | Phase2 | Osteomyelitis | Terminated | 2017-05-15 | 2017-08-31 | ClinicalTrials.gov |
| NCT03091439 | Safety and Efficacy of Dalbavancin Versus Active Comparator in Adult Patients W… | Phase2 | Osteomyelitis | Terminated | 2017-05-15 | 2017-08-31 | ClinicalTrials.gov |
| NCT03148756 | Efficacy and Safety of Dalbavancin Compared to Standard of Care Antibiotic Ther… | Phase2 | Endocarditis | Terminated | 2017-05-12 | 2017-08-04 | ClinicalTrials.gov |
| NCT03148756 | Efficacy and Safety of Dalbavancin Compared to Standard of Care Antibiotic Ther… | Phase2 | Endocarditis | Terminated | 2017-05-12 | 2017-08-04 | ClinicalTrials.gov |
| NCT03148756 | Efficacy and Safety of Dalbavancin Compared to Standard of Care Antibiotic Ther… | Phase2 | Endocarditis | Terminated | 2017-05-12 | 2017-08-04 | ClinicalTrials.gov |
| NCT03148756 | Efficacy and Safety of Dalbavancin Compared to Standard of Care Antibiotic Ther… | Phase2 | Endocarditis | Terminated | 2017-05-12 | 2017-08-04 | ClinicalTrials.gov |
| NCT03105128 | A Study of the Efficacy and Safety of Risankizumab in Participants With Moderat… | Phase3 | Crohn's Disease | Completed | 2017-05-10 | 2021-04-14 | ClinicalTrials.gov |
| NCT03105128 | A Study of the Efficacy and Safety of Risankizumab in Participants With Moderat… | Phase3 | Crohn's Disease | Completed | 2017-05-10 | 2021-04-14 | ClinicalTrials.gov |
| NCT03105128 | A Study of the Efficacy and Safety of Risankizumab in Participants With Moderat… | Phase3 | Crohn's Disease | Completed | 2017-05-10 | 2021-04-14 | ClinicalTrials.gov |
| NCT03105128 | A Study of the Efficacy and Safety of Risankizumab in Participants With Moderat… | Phase3 | Crohn's Disease | Completed | 2017-05-10 | 2021-04-14 | ClinicalTrials.gov |
| NCT03145948 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-553 i… | Phase1 | Psoriasis | Terminated | 2017-05-09 | 2017-08-16 | ClinicalTrials.gov |
| NCT03086343 | A Phase 3 Study to Compare Upadacitinib to Abatacept in Subjects With Rheumatoi… | Phase3 | Rheumatoid Arthritis (RA) | Completed | 2017-05-09 | 2023-06-06 | ClinicalTrials.gov |
| NCT03086343 | A Phase 3 Study to Compare Upadacitinib to Abatacept in Subjects With Rheumatoi… | Phase3 | Rheumatoid Arthritis (RA) | Completed | 2017-05-09 | 2023-06-06 | ClinicalTrials.gov |
| NCT03086343 | A Phase 3 Study to Compare Upadacitinib to Abatacept in Subjects With Rheumatoi… | Phase3 | Rheumatoid Arthritis (RA) | Completed | 2017-05-09 | 2023-06-06 | ClinicalTrials.gov |
| NCT03086343 | A Phase 3 Study to Compare Upadacitinib to Abatacept in Subjects With Rheumatoi… | Phase3 | Rheumatoid Arthritis (RA) | Completed | 2017-05-09 | 2023-06-06 | ClinicalTrials.gov |
| NCT03145948 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-553 i… | Phase1 | Psoriasis | Terminated | 2017-05-09 | 2017-08-16 | ClinicalTrials.gov |
| NCT03145948 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-553 i… | Phase1 | Psoriasis | Terminated | 2017-05-09 | 2017-08-16 | ClinicalTrials.gov |
| NCT03145948 | A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of ABBV-553 i… | Phase1 | Psoriasis | Terminated | 2017-05-09 | 2017-08-16 | ClinicalTrials.gov |
| NCT03104374 | A Study Comparing Upadacitinib (ABT-494) to Placebo in Participants With Active… | Phase3 | Psoriatic Arthritis | Completed | 2017-05-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT03187873 | Chamas for Change Validation | Na | Pregnancy Related | Unknown | 2017-05-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03104374 | A Study Comparing Upadacitinib (ABT-494) to Placebo in Participants With Active… | Phase3 | Psoriatic Arthritis | Completed | 2017-05-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT03187873 | Chamas for Change Validation | Na | Pregnancy Related | Unknown | 2017-05-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03104374 | A Study Comparing Upadacitinib (ABT-494) to Placebo in Participants With Active… | Phase3 | Psoriatic Arthritis | Completed | 2017-05-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT03187873 | Chamas for Change Validation | Na | Pregnancy Related | Unknown | 2017-05-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03104374 | A Study Comparing Upadacitinib (ABT-494) to Placebo in Participants With Active… | Phase3 | Psoriatic Arthritis | Completed | 2017-05-01 | 2024-09-30 | ClinicalTrials.gov |
| NCT03187873 | Chamas for Change Validation | Na | Pregnancy Related | Unknown | 2017-05-01 | 2018-12-01 | ClinicalTrials.gov |
| NCT03086239 | A Study on the Safety and Tolerability of Rovalpituzumab Tesirine in Japanese P… | Phase1 | Small Cell Lung Cancer | Completed | 2017-04-28 | 2018-08-20 | ClinicalTrials.gov |
| NCT03089944 | A Study of Glecaprevir (GLE)/Pibrentasvir (PIB) in Treatment-Naive Adults With … | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-04-28 | 2019-11-08 | ClinicalTrials.gov |
| NCT03086239 | A Study on the Safety and Tolerability of Rovalpituzumab Tesirine in Japanese P… | Phase1 | Small Cell Lung Cancer | Completed | 2017-04-28 | 2018-08-20 | ClinicalTrials.gov |
| NCT03089944 | A Study of Glecaprevir (GLE)/Pibrentasvir (PIB) in Treatment-Naive Adults With … | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-04-28 | 2019-11-08 | ClinicalTrials.gov |
| NCT03086239 | A Study on the Safety and Tolerability of Rovalpituzumab Tesirine in Japanese P… | Phase1 | Small Cell Lung Cancer | Completed | 2017-04-28 | 2018-08-20 | ClinicalTrials.gov |
| NCT03089944 | A Study of Glecaprevir (GLE)/Pibrentasvir (PIB) in Treatment-Naive Adults With … | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-04-28 | 2019-11-08 | ClinicalTrials.gov |
| NCT03089944 | A Study of Glecaprevir (GLE)/Pibrentasvir (PIB) in Treatment-Naive Adults With … | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-04-28 | 2019-11-08 | ClinicalTrials.gov |
| NCT03086239 | A Study on the Safety and Tolerability of Rovalpituzumab Tesirine in Japanese P… | Phase1 | Small Cell Lung Cancer | Completed | 2017-04-28 | 2018-08-20 | ClinicalTrials.gov |
| NCT03104400 | A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Partic… | Phase3 | Psoriatic Arthritis | Completed | 2017-04-27 | 2024-09-09 | ClinicalTrials.gov |
| NCT03104400 | A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Partic… | Phase3 | Psoriatic Arthritis | Completed | 2017-04-27 | 2024-09-09 | ClinicalTrials.gov |
| NCT03104400 | A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Partic… | Phase3 | Psoriatic Arthritis | Completed | 2017-04-27 | 2024-09-09 | ClinicalTrials.gov |
| NCT03104400 | A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Partic… | Phase3 | Psoriatic Arthritis | Completed | 2017-04-27 | 2024-09-09 | ClinicalTrials.gov |
| NCT03166618 | Safety and Effectiveness of JUVÉDERM VOLUMA® XC Injectable Gel for Correction o… | Na | Temple Hollowing | Terminated | 2017-04-24 | 2017-07-21 | ClinicalTrials.gov |
| NCT03166618 | Safety and Effectiveness of JUVÉDERM VOLUMA® XC Injectable Gel for Correction o… | Na | Temple Hollowing | Terminated | 2017-04-24 | 2017-07-21 | ClinicalTrials.gov |
| NCT03166618 | Safety and Effectiveness of JUVÉDERM VOLUMA® XC Injectable Gel for Correction o… | Na | Temple Hollowing | Terminated | 2017-04-24 | 2017-07-21 | ClinicalTrials.gov |
| NCT03166618 | Safety and Effectiveness of JUVÉDERM VOLUMA® XC Injectable Gel for Correction o… | Na | Temple Hollowing | Terminated | 2017-04-24 | 2017-07-21 | ClinicalTrials.gov |
| NCT03092375 | Multi-Center, Randomized, Open-Label Study of G/P +/- RBV for NS5A + SOF Previo… | Phase3 | Hepatitis C | Completed | 2017-04-20 | 2020-02-06 | ClinicalTrials.gov |
| NCT03092375 | Multi-Center, Randomized, Open-Label Study of G/P +/- RBV for NS5A + SOF Previo… | Phase3 | Hepatitis C | Completed | 2017-04-20 | 2020-02-06 | ClinicalTrials.gov |
| NCT03092375 | Multi-Center, Randomized, Open-Label Study of G/P +/- RBV for NS5A + SOF Previo… | Phase3 | Hepatitis C | Completed | 2017-04-20 | 2020-02-06 | ClinicalTrials.gov |
| NCT03092375 | Multi-Center, Randomized, Open-Label Study of G/P +/- RBV for NS5A + SOF Previo… | Phase3 | Hepatitis C | Completed | 2017-04-20 | 2020-02-06 | ClinicalTrials.gov |
| NCT02881567 | Efficacy and Safety of Daclizumab in Participants With RRMS Switching From Nata… | Phase3 | Relapsing-Remitting Multiple Sclerosis (RRMS) | Terminated | 2017-04-18 | 2018-09-12 | ClinicalTrials.gov |
| NCT02881567 | Efficacy and Safety of Daclizumab in Participants With RRMS Switching From Nata… | Phase3 | Relapsing-Remitting Multiple Sclerosis (RRMS) | Terminated | 2017-04-18 | 2018-09-12 | ClinicalTrials.gov |
| NCT02881567 | Efficacy and Safety of Daclizumab in Participants With RRMS Switching From Nata… | Phase3 | Relapsing-Remitting Multiple Sclerosis (RRMS) | Terminated | 2017-04-18 | 2018-09-12 | ClinicalTrials.gov |
| NCT02881567 | Efficacy and Safety of Daclizumab in Participants With RRMS Switching From Nata… | Phase3 | Relapsing-Remitting Multiple Sclerosis (RRMS) | Terminated | 2017-04-18 | 2018-09-12 | ClinicalTrials.gov |
| NCT03061812 | Study Comparing Rovalpituzumab Tesirine Versus Topotecan in Subjects With Advan… | Phase3 | Small Cell Lung Cancer | Completed | 2017-04-11 | 2020-02-12 | ClinicalTrials.gov |
| NCT03061812 | Study Comparing Rovalpituzumab Tesirine Versus Topotecan in Subjects With Advan… | Phase3 | Small Cell Lung Cancer | Completed | 2017-04-11 | 2020-02-12 | ClinicalTrials.gov |
| NCT03061812 | Study Comparing Rovalpituzumab Tesirine Versus Topotecan in Subjects With Advan… | Phase3 | Small Cell Lung Cancer | Completed | 2017-04-11 | 2020-02-12 | ClinicalTrials.gov |
| NCT03061812 | Study Comparing Rovalpituzumab Tesirine Versus Topotecan in Subjects With Advan… | Phase3 | Small Cell Lung Cancer | Completed | 2017-04-11 | 2020-02-12 | ClinicalTrials.gov |
| NCT03217734 | MAP Study: Methotrexate and Adalimumab in Psoriasis | Phase2 | Psoriasis | Completed | 2017-04-10 | 2018-12-31 | ClinicalTrials.gov |
| NCT03217734 | MAP Study: Methotrexate and Adalimumab in Psoriasis | Phase2 | Psoriasis | Completed | 2017-04-10 | 2018-12-31 | ClinicalTrials.gov |
| NCT03217734 | MAP Study: Methotrexate and Adalimumab in Psoriasis | Phase2 | Psoriasis | Completed | 2017-04-10 | 2018-12-31 | ClinicalTrials.gov |
| NCT03217734 | MAP Study: Methotrexate and Adalimumab in Psoriasis | Phase2 | Psoriasis | Completed | 2017-04-10 | 2018-12-31 | ClinicalTrials.gov |
| NCT03099083 | Real-World Outcome of Psoriasis Subjects in Korea on Adalimumab | — | Psoriasis | Completed | 2017-03-31 | 2019-04-05 | ClinicalTrials.gov |
| NCT03099083 | Real-World Outcome of Psoriasis Subjects in Korea on Adalimumab | — | Psoriasis | Completed | 2017-03-31 | 2019-04-05 | ClinicalTrials.gov |
| NCT03099083 | Real-World Outcome of Psoriasis Subjects in Korea on Adalimumab | — | Psoriasis | Completed | 2017-03-31 | 2019-04-05 | ClinicalTrials.gov |
| NCT03099083 | Real-World Outcome of Psoriasis Subjects in Korea on Adalimumab | — | Psoriasis | Completed | 2017-03-31 | 2019-04-05 | ClinicalTrials.gov |
| NCT02814916 | Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infect… | Phase3 | Methicillin-Resistant Staphylococcus Aureus | Completed | 2017-03-30 | 2024-01-01 | ClinicalTrials.gov |
| NCT03026166 | A Study of Rovalpituzumab Tesirine Administered in Combination With Nivolumab a… | Phase1 | Small Cell Lung Cancer | Terminated | 2017-03-30 | 2019-07-03 | ClinicalTrials.gov |
| NCT02814916 | Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infect… | Phase3 | Methicillin-Resistant Staphylococcus Aureus | Completed | 2017-03-30 | 2024-01-01 | ClinicalTrials.gov |
| NCT03026166 | A Study of Rovalpituzumab Tesirine Administered in Combination With Nivolumab a… | Phase1 | Small Cell Lung Cancer | Terminated | 2017-03-30 | 2019-07-03 | ClinicalTrials.gov |
| NCT03026166 | A Study of Rovalpituzumab Tesirine Administered in Combination With Nivolumab a… | Phase1 | Small Cell Lung Cancer | Terminated | 2017-03-30 | 2019-07-03 | ClinicalTrials.gov |
| NCT02814916 | Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infect… | Phase3 | Methicillin-Resistant Staphylococcus Aureus | Completed | 2017-03-30 | 2024-01-01 | ClinicalTrials.gov |
| NCT03026166 | A Study of Rovalpituzumab Tesirine Administered in Combination With Nivolumab a… | Phase1 | Small Cell Lung Cancer | Terminated | 2017-03-30 | 2019-07-03 | ClinicalTrials.gov |
| NCT02814916 | Dalbavancin for the Treatment of Acute Bacterial Skin and Skin Structure Infect… | Phase3 | Methicillin-Resistant Staphylococcus Aureus | Completed | 2017-03-30 | 2024-01-01 | ClinicalTrials.gov |
| NCT03069365 | A Study to Evaluate the Efficacy and Safety of Glecaprevir/Pibrentasvir in Adul… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-03-28 | 2018-06-05 | ClinicalTrials.gov |
| NCT03069365 | A Study to Evaluate the Efficacy and Safety of Glecaprevir/Pibrentasvir in Adul… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-03-28 | 2018-06-05 | ClinicalTrials.gov |
| NCT03069365 | A Study to Evaluate the Efficacy and Safety of Glecaprevir/Pibrentasvir in Adul… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-03-28 | 2018-06-05 | ClinicalTrials.gov |
| NCT03069365 | A Study to Evaluate the Efficacy and Safety of Glecaprevir/Pibrentasvir in Adul… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-03-28 | 2018-06-05 | ClinicalTrials.gov |
| NCT03097029 | Use of Pancreatic Enzymes in Short Bowel Syndrome | Phase2 | Short Bowel Syndrome | Completed | 2017-03-24 | 2019-02-01 | ClinicalTrials.gov |
| NCT03097029 | Use of Pancreatic Enzymes in Short Bowel Syndrome | Phase2 | Short Bowel Syndrome | Completed | 2017-03-24 | 2019-02-01 | ClinicalTrials.gov |
| NCT03097029 | Use of Pancreatic Enzymes in Short Bowel Syndrome | Phase2 | Short Bowel Syndrome | Completed | 2017-03-24 | 2019-02-01 | ClinicalTrials.gov |
| NCT03097029 | Use of Pancreatic Enzymes in Short Bowel Syndrome | Phase2 | Short Bowel Syndrome | Completed | 2017-03-24 | 2019-02-01 | ClinicalTrials.gov |
| NCT03071757 | A Study of the Safety, Tolerability and Pharmacokinetics of ABBV-368 as a Singl… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-03-21 | 2022-04-13 | ClinicalTrials.gov |
| NCT03071757 | A Study of the Safety, Tolerability and Pharmacokinetics of ABBV-368 as a Singl… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-03-21 | 2022-04-13 | ClinicalTrials.gov |
| NCT03071757 | A Study of the Safety, Tolerability and Pharmacokinetics of ABBV-368 as a Singl… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-03-21 | 2022-04-13 | ClinicalTrials.gov |
| NCT03071757 | A Study of the Safety, Tolerability and Pharmacokinetics of ABBV-368 as a Singl… | Phase1 | Advanced Solid Tumors Cancer | Completed | 2017-03-21 | 2022-04-13 | ClinicalTrials.gov |
| NCT03067129 | A Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Glecaprevir/P… | Phase2 | Hepatitis C Virus (HCV) | Completed | 2017-03-20 | 2022-09-12 | ClinicalTrials.gov |
| NCT03082209 | A Study of the Safety and Tolerability of ABBV-621 in Participants With Previou… | Phase1 | Advanced Solid Tumors | Completed | 2017-03-20 | 2022-01-21 | ClinicalTrials.gov |
| NCT03053180 | Real World Evidence of the Effectiveness of Paritaprevir/Ritonavir (r) - Ombita… | — | Chronic Hepatitis C | Completed | 2017-03-20 | 2017-12-18 | ClinicalTrials.gov |
| NCT03082209 | A Study of the Safety and Tolerability of ABBV-621 in Participants With Previou… | Phase1 | Advanced Solid Tumors | Completed | 2017-03-20 | 2022-01-21 | ClinicalTrials.gov |
| NCT03067129 | A Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Glecaprevir/P… | Phase2 | Hepatitis C Virus (HCV) | Completed | 2017-03-20 | 2022-09-12 | ClinicalTrials.gov |
| NCT03067129 | A Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Glecaprevir/P… | Phase2 | Hepatitis C Virus (HCV) | Completed | 2017-03-20 | 2022-09-12 | ClinicalTrials.gov |
| NCT03053180 | Real World Evidence of the Effectiveness of Paritaprevir/Ritonavir (r) - Ombita… | — | Chronic Hepatitis C | Completed | 2017-03-20 | 2017-12-18 | ClinicalTrials.gov |
| NCT03053180 | Real World Evidence of the Effectiveness of Paritaprevir/Ritonavir (r) - Ombita… | — | Chronic Hepatitis C | Completed | 2017-03-20 | 2017-12-18 | ClinicalTrials.gov |
| NCT03082209 | A Study of the Safety and Tolerability of ABBV-621 in Participants With Previou… | Phase1 | Advanced Solid Tumors | Completed | 2017-03-20 | 2022-01-21 | ClinicalTrials.gov |
| NCT03053180 | Real World Evidence of the Effectiveness of Paritaprevir/Ritonavir (r) - Ombita… | — | Chronic Hepatitis C | Completed | 2017-03-20 | 2017-12-18 | ClinicalTrials.gov |
| NCT03067129 | A Study to Evaluate the Pharmacokinetics, Safety, and Efficacy of Glecaprevir/P… | Phase2 | Hepatitis C Virus (HCV) | Completed | 2017-03-20 | 2022-09-12 | ClinicalTrials.gov |
| NCT03082209 | A Study of the Safety and Tolerability of ABBV-621 in Participants With Previou… | Phase1 | Advanced Solid Tumors | Completed | 2017-03-20 | 2022-01-21 | ClinicalTrials.gov |
| NCT02874066 | PrOD for Non-Cirrhotic Patients With HCV-1b Receiving Hemodialysis | Phase4 | Hepatitis Viruses | Completed | 2017-03-13 | 2018-12-25 | ClinicalTrials.gov |
| NCT02874066 | PrOD for Non-Cirrhotic Patients With HCV-1b Receiving Hemodialysis | Phase4 | Hepatitis Viruses | Completed | 2017-03-13 | 2018-12-25 | ClinicalTrials.gov |
| NCT02874066 | PrOD for Non-Cirrhotic Patients With HCV-1b Receiving Hemodialysis | Phase4 | Hepatitis Viruses | Completed | 2017-03-13 | 2018-12-25 | ClinicalTrials.gov |
| NCT02874066 | PrOD for Non-Cirrhotic Patients With HCV-1b Receiving Hemodialysis | Phase4 | Hepatitis Viruses | Completed | 2017-03-13 | 2018-12-25 | ClinicalTrials.gov |
| NCT03001115 | Post-Marketing Surveillance of Adalimumab in Korean Hidradenitis Suppurativa Su… | — | Hidradenitis Suppurativa (HS) | Completed | 2017-03-10 | 2019-07-31 | ClinicalTrials.gov |
| NCT03001115 | Post-Marketing Surveillance of Adalimumab in Korean Hidradenitis Suppurativa Su… | — | Hidradenitis Suppurativa (HS) | Completed | 2017-03-10 | 2019-07-31 | ClinicalTrials.gov |
| NCT03001115 | Post-Marketing Surveillance of Adalimumab in Korean Hidradenitis Suppurativa Su… | — | Hidradenitis Suppurativa (HS) | Completed | 2017-03-10 | 2019-07-31 | ClinicalTrials.gov |
| NCT03001115 | Post-Marketing Surveillance of Adalimumab in Korean Hidradenitis Suppurativa Su… | — | Hidradenitis Suppurativa (HS) | Completed | 2017-03-10 | 2019-07-31 | ClinicalTrials.gov |
| NCT03035279 | A Study of SC-006 and in Combination With ABBV-181 in Subjects With Advanced Co… | Phase1 | Colorectal Cancer | Terminated | 2017-03-08 | 2019-03-28 | ClinicalTrials.gov |
| NCT03035279 | A Study of SC-006 and in Combination With ABBV-181 in Subjects With Advanced Co… | Phase1 | Colorectal Cancer | Terminated | 2017-03-08 | 2019-03-28 | ClinicalTrials.gov |
| NCT03035279 | A Study of SC-006 and in Combination With ABBV-181 in Subjects With Advanced Co… | Phase1 | Colorectal Cancer | Terminated | 2017-03-08 | 2019-03-28 | ClinicalTrials.gov |
| NCT03035279 | A Study of SC-006 and in Combination With ABBV-181 in Subjects With Advanced Co… | Phase1 | Colorectal Cancer | Terminated | 2017-03-08 | 2019-03-28 | ClinicalTrials.gov |
| NCT02966782 | A Study Evaluating Venetoclax Alone and in Combination With Azacitidine in Part… | Phase1 | Myelodysplastic Syndromes (MDS) | Completed | 2017-03-07 | 2023-04-05 | ClinicalTrials.gov |
| NCT02966782 | A Study Evaluating Venetoclax Alone and in Combination With Azacitidine in Part… | Phase1 | Myelodysplastic Syndromes (MDS) | Completed | 2017-03-07 | 2023-04-05 | ClinicalTrials.gov |
| NCT02966782 | A Study Evaluating Venetoclax Alone and in Combination With Azacitidine in Part… | Phase1 | Myelodysplastic Syndromes (MDS) | Completed | 2017-03-07 | 2023-04-05 | ClinicalTrials.gov |
| NCT02966782 | A Study Evaluating Venetoclax Alone and in Combination With Azacitidine in Part… | Phase1 | Myelodysplastic Syndromes (MDS) | Completed | 2017-03-07 | 2023-04-05 | ClinicalTrials.gov |
| NCT03002818 | Quality of Life Measurement in Treatment Naïve Patients With Hepatitis C Virus … | — | Chronic Hepatitis C Virus (HCV) | Completed | 2017-03-01 | 2018-04-25 | ClinicalTrials.gov |
| NCT03002818 | Quality of Life Measurement in Treatment Naïve Patients With Hepatitis C Virus … | — | Chronic Hepatitis C Virus (HCV) | Completed | 2017-03-01 | 2018-04-25 | ClinicalTrials.gov |
| NCT03002818 | Quality of Life Measurement in Treatment Naïve Patients With Hepatitis C Virus … | — | Chronic Hepatitis C Virus (HCV) | Completed | 2017-03-01 | 2018-04-25 | ClinicalTrials.gov |
| NCT03002818 | Quality of Life Measurement in Treatment Naïve Patients With Hepatitis C Virus … | — | Chronic Hepatitis C Virus (HCV) | Completed | 2017-03-01 | 2018-04-25 | ClinicalTrials.gov |
| NCT02956382 | Ibrutinib and Venetoclax in Relapsed and Refractory Follicular Lymphoma | Phase1 | Refractory Follicular Lymphoma | Completed | 2017-03-01 | 2024-03-07 | ClinicalTrials.gov |
| NCT02956382 | Ibrutinib and Venetoclax in Relapsed and Refractory Follicular Lymphoma | Phase1 | Refractory Follicular Lymphoma | Completed | 2017-03-01 | 2024-03-07 | ClinicalTrials.gov |
| NCT04196647 | Guideline for Hometitration With Duodopa for Parkinson Patients | — | Parkinson Disease | Completed | 2017-03-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT04196647 | Guideline for Hometitration With Duodopa for Parkinson Patients | — | Parkinson Disease | Completed | 2017-03-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT04196647 | Guideline for Hometitration With Duodopa for Parkinson Patients | — | Parkinson Disease | Completed | 2017-03-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT04196647 | Guideline for Hometitration With Duodopa for Parkinson Patients | — | Parkinson Disease | Completed | 2017-03-01 | 2022-06-30 | ClinicalTrials.gov |
| NCT02956382 | Ibrutinib and Venetoclax in Relapsed and Refractory Follicular Lymphoma | Phase1 | Refractory Follicular Lymphoma | Completed | 2017-03-01 | 2024-03-07 | ClinicalTrials.gov |
| NCT02956382 | Ibrutinib and Venetoclax in Relapsed and Refractory Follicular Lymphoma | Phase1 | Refractory Follicular Lymphoma | Completed | 2017-03-01 | 2024-03-07 | ClinicalTrials.gov |
| NCT03047395 | A Study to Assess the Safety and Efficacy of Risankizumab for Maintenance in Mo… | Phase3 | Psoriasis | Completed | 2017-02-27 | 2023-11-29 | ClinicalTrials.gov |
| NCT03047395 | A Study to Assess the Safety and Efficacy of Risankizumab for Maintenance in Mo… | Phase3 | Psoriasis | Completed | 2017-02-27 | 2023-11-29 | ClinicalTrials.gov |
| NCT03047395 | A Study to Assess the Safety and Efficacy of Risankizumab for Maintenance in Mo… | Phase3 | Psoriasis | Completed | 2017-02-27 | 2023-11-29 | ClinicalTrials.gov |
| NCT03047395 | A Study to Assess the Safety and Efficacy of Risankizumab for Maintenance in Mo… | Phase3 | Psoriasis | Completed | 2017-02-27 | 2023-11-29 | ClinicalTrials.gov |
| NCT02851069 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2017-02-23 | 2018-08-30 | ClinicalTrials.gov |
| NCT02851069 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2017-02-23 | 2018-08-30 | ClinicalTrials.gov |
| NCT02851069 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2017-02-23 | 2018-08-30 | ClinicalTrials.gov |
| NCT02851069 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2017-02-23 | 2018-08-30 | ClinicalTrials.gov |
| NCT02988960 | A Study of ABBV-927 and ABBV-181, an Immunotherapy, in Participants With Advanc… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2017-02-22 | 2026-09-01 | ClinicalTrials.gov |
| NCT02988960 | A Study of ABBV-927 and ABBV-181, an Immunotherapy, in Participants With Advanc… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2017-02-22 | 2026-09-01 | ClinicalTrials.gov |
| NCT02988960 | A Study of ABBV-927 and ABBV-181, an Immunotherapy, in Participants With Advanc… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2017-02-22 | 2026-09-01 | ClinicalTrials.gov |
| NCT02988960 | A Study of ABBV-927 and ABBV-181, an Immunotherapy, in Participants With Advanc… | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2017-02-22 | 2026-09-01 | ClinicalTrials.gov |
| NCT02799381 | A Study Comparing Efficacy of Levodopa-Carbidopa Intestinal Gel/Carbidopa-Levod… | Phase3 | Parkinson's Disease (PD) | Completed | 2017-02-09 | 2019-09-19 | ClinicalTrials.gov |
| NCT02799381 | A Study Comparing Efficacy of Levodopa-Carbidopa Intestinal Gel/Carbidopa-Levod… | Phase3 | Parkinson's Disease (PD) | Completed | 2017-02-09 | 2019-09-19 | ClinicalTrials.gov |
| NCT02799381 | A Study Comparing Efficacy of Levodopa-Carbidopa Intestinal Gel/Carbidopa-Levod… | Phase3 | Parkinson's Disease (PD) | Completed | 2017-02-09 | 2019-09-19 | ClinicalTrials.gov |
| NCT02799381 | A Study Comparing Efficacy of Levodopa-Carbidopa Intestinal Gel/Carbidopa-Levod… | Phase3 | Parkinson's Disease (PD) | Completed | 2017-02-09 | 2019-09-19 | ClinicalTrials.gov |
| NCT04619303 | Intravitreal Dexamethasone vs Bevacizumab in Aboriginal People With DMO | Phase4 | Diabetic Macular Edema | Completed | 2017-02-07 | 2020-02-14 | ClinicalTrials.gov |
| NCT03180593 | Efficacy and Safety of Valsartan and Nebivolol/Valsartan in Hypertensive Patien… | Phase4 | Hypertension Complicated | Completed | 2017-02-07 | 2018-01-25 | ClinicalTrials.gov |
| NCT03033511 | A Study of Rovalpituzumab Tesirine as Maintenance Therapy Following First- Line… | Phase3 | Small Cell Lung Cancer | Terminated | 2017-02-07 | 2019-11-20 | ClinicalTrials.gov |
| NCT03180593 | Efficacy and Safety of Valsartan and Nebivolol/Valsartan in Hypertensive Patien… | Phase4 | Hypertension Complicated | Completed | 2017-02-07 | 2018-01-25 | ClinicalTrials.gov |
| NCT03180593 | Efficacy and Safety of Valsartan and Nebivolol/Valsartan in Hypertensive Patien… | Phase4 | Hypertension Complicated | Completed | 2017-02-07 | 2018-01-25 | ClinicalTrials.gov |
| NCT04619303 | Intravitreal Dexamethasone vs Bevacizumab in Aboriginal People With DMO | Phase4 | Diabetic Macular Edema | Completed | 2017-02-07 | 2020-02-14 | ClinicalTrials.gov |
| NCT03033511 | A Study of Rovalpituzumab Tesirine as Maintenance Therapy Following First- Line… | Phase3 | Small Cell Lung Cancer | Terminated | 2017-02-07 | 2019-11-20 | ClinicalTrials.gov |
| NCT03033511 | A Study of Rovalpituzumab Tesirine as Maintenance Therapy Following First- Line… | Phase3 | Small Cell Lung Cancer | Terminated | 2017-02-07 | 2019-11-20 | ClinicalTrials.gov |
| NCT04619303 | Intravitreal Dexamethasone vs Bevacizumab in Aboriginal People With DMO | Phase4 | Diabetic Macular Edema | Completed | 2017-02-07 | 2020-02-14 | ClinicalTrials.gov |
| NCT03180593 | Efficacy and Safety of Valsartan and Nebivolol/Valsartan in Hypertensive Patien… | Phase4 | Hypertension Complicated | Completed | 2017-02-07 | 2018-01-25 | ClinicalTrials.gov |
| NCT03033511 | A Study of Rovalpituzumab Tesirine as Maintenance Therapy Following First- Line… | Phase3 | Small Cell Lung Cancer | Terminated | 2017-02-07 | 2019-11-20 | ClinicalTrials.gov |
| NCT04619303 | Intravitreal Dexamethasone vs Bevacizumab in Aboriginal People With DMO | Phase4 | Diabetic Macular Edema | Completed | 2017-02-07 | 2020-02-14 | ClinicalTrials.gov |
| NCT02993523 | A Study of Venetoclax in Combination With Azacitidine Versus Azacitidine in Tre… | Phase3 | Acute Myeloid Leukemia (AML) | Active_Not_Recruiting | 2017-02-02 | 2026-06-15 | ClinicalTrials.gov |
| NCT02993523 | A Study of Venetoclax in Combination With Azacitidine Versus Azacitidine in Tre… | Phase3 | Acute Myeloid Leukemia (AML) | Active_Not_Recruiting | 2017-02-02 | 2026-06-15 | ClinicalTrials.gov |
| NCT02993523 | A Study of Venetoclax in Combination With Azacitidine Versus Azacitidine in Tre… | Phase3 | Acute Myeloid Leukemia (AML) | Active_Not_Recruiting | 2017-02-02 | 2026-06-15 | ClinicalTrials.gov |
| NCT02993523 | A Study of Venetoclax in Combination With Azacitidine Versus Azacitidine in Tre… | Phase3 | Acute Myeloid Leukemia (AML) | Active_Not_Recruiting | 2017-02-02 | 2026-06-15 | ClinicalTrials.gov |
| NCT02946034 | Viekira Pak or Mavyret Treatment for Patient With Chronic Kidney Disease and He… | Phase4 | Chronic Kidney Disease | Completed | 2017-02-01 | 2020-09-16 | ClinicalTrials.gov |
| NCT02946034 | Viekira Pak or Mavyret Treatment for Patient With Chronic Kidney Disease and He… | Phase4 | Chronic Kidney Disease | Completed | 2017-02-01 | 2020-09-16 | ClinicalTrials.gov |
| NCT02946034 | Viekira Pak or Mavyret Treatment for Patient With Chronic Kidney Disease and He… | Phase4 | Chronic Kidney Disease | Completed | 2017-02-01 | 2020-09-16 | ClinicalTrials.gov |
| NCT02946034 | Viekira Pak or Mavyret Treatment for Patient With Chronic Kidney Disease and He… | Phase4 | Chronic Kidney Disease | Completed | 2017-02-01 | 2020-09-16 | ClinicalTrials.gov |
| NCT03006068 | A Study to Evaluate the Long-Term Safety and Efficacy of Upadacitinib (ABT-494)… | Phase3 | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2017-01-31 | 2027-07-01 | ClinicalTrials.gov |
| NCT03006068 | A Study to Evaluate the Long-Term Safety and Efficacy of Upadacitinib (ABT-494)… | Phase3 | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2017-01-31 | 2027-07-01 | ClinicalTrials.gov |
| NCT03006068 | A Study to Evaluate the Long-Term Safety and Efficacy of Upadacitinib (ABT-494)… | Phase3 | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2017-01-31 | 2027-07-01 | ClinicalTrials.gov |
| NCT03006068 | A Study to Evaluate the Long-Term Safety and Efficacy of Upadacitinib (ABT-494)… | Phase3 | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2017-01-31 | 2027-07-01 | ClinicalTrials.gov |
| NCT03022045 | A Study to Assess Efficacy and Safety of Two Different Dose Regimens of Risanki… | Phase3 | Psoriasis | Completed | 2017-01-26 | 2020-11-19 | ClinicalTrials.gov |
| NCT02880956 | A Study to Evaluate the Efficacy and Safety of ABBV-8E12 in Participants With E… | Phase2 | Alzheimer's Disease | Completed | 2017-01-26 | 2021-07-28 | ClinicalTrials.gov |
| NCT03022045 | A Study to Assess Efficacy and Safety of Two Different Dose Regimens of Risanki… | Phase3 | Psoriasis | Completed | 2017-01-26 | 2020-11-19 | ClinicalTrials.gov |
| NCT02880956 | A Study to Evaluate the Efficacy and Safety of ABBV-8E12 in Participants With E… | Phase2 | Alzheimer's Disease | Completed | 2017-01-26 | 2021-07-28 | ClinicalTrials.gov |
| NCT02880956 | A Study to Evaluate the Efficacy and Safety of ABBV-8E12 in Participants With E… | Phase2 | Alzheimer's Disease | Completed | 2017-01-26 | 2021-07-28 | ClinicalTrials.gov |
| NCT03022045 | A Study to Assess Efficacy and Safety of Two Different Dose Regimens of Risanki… | Phase3 | Psoriasis | Completed | 2017-01-26 | 2020-11-19 | ClinicalTrials.gov |
| NCT03022045 | A Study to Assess Efficacy and Safety of Two Different Dose Regimens of Risanki… | Phase3 | Psoriasis | Completed | 2017-01-26 | 2020-11-19 | ClinicalTrials.gov |
| NCT02880956 | A Study to Evaluate the Efficacy and Safety of ABBV-8E12 in Participants With E… | Phase2 | Alzheimer's Disease | Completed | 2017-01-26 | 2021-07-28 | ClinicalTrials.gov |
| NCT02951975 | Ozurdex® in Patients With Non-infectious Uveitis Affecting the Posterior Segmen… | — | Non-infectious Uveitis | Terminated | 2017-01-25 | 2018-12-19 | ClinicalTrials.gov |
| NCT02951975 | Ozurdex® in Patients With Non-infectious Uveitis Affecting the Posterior Segmen… | — | Non-infectious Uveitis | Terminated | 2017-01-25 | 2018-12-19 | ClinicalTrials.gov |
| NCT02966795 | A Study of of Glecaprevir/Pibrentasvir in Adults With Chronic Hepatitis C Virus… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-01-25 | 2018-08-29 | ClinicalTrials.gov |
| NCT02966795 | A Study of of Glecaprevir/Pibrentasvir in Adults With Chronic Hepatitis C Virus… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-01-25 | 2018-08-29 | ClinicalTrials.gov |
| NCT02951975 | Ozurdex® in Patients With Non-infectious Uveitis Affecting the Posterior Segmen… | — | Non-infectious Uveitis | Terminated | 2017-01-25 | 2018-12-19 | ClinicalTrials.gov |
| NCT02966795 | A Study of of Glecaprevir/Pibrentasvir in Adults With Chronic Hepatitis C Virus… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-01-25 | 2018-08-29 | ClinicalTrials.gov |
| NCT02966795 | A Study of of Glecaprevir/Pibrentasvir in Adults With Chronic Hepatitis C Virus… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2017-01-25 | 2018-08-29 | ClinicalTrials.gov |
| NCT02951975 | Ozurdex® in Patients With Non-infectious Uveitis Affecting the Posterior Segmen… | — | Non-infectious Uveitis | Terminated | 2017-01-25 | 2018-12-19 | ClinicalTrials.gov |
| NCT02899052 | Study of Venetoclax in Combination With Carfilzomib and Dexamethasone in Partic… | Phase2 | Multiple Myeloma | Active_Not_Recruiting | 2017-01-19 | 2027-06-01 | ClinicalTrials.gov |
| NCT02899052 | Study of Venetoclax in Combination With Carfilzomib and Dexamethasone in Partic… | Phase2 | Multiple Myeloma | Active_Not_Recruiting | 2017-01-19 | 2027-06-01 | ClinicalTrials.gov |
| NCT02899052 | Study of Venetoclax in Combination With Carfilzomib and Dexamethasone in Partic… | Phase2 | Multiple Myeloma | Active_Not_Recruiting | 2017-01-19 | 2027-06-01 | ClinicalTrials.gov |
| NCT02899052 | Study of Venetoclax in Combination With Carfilzomib and Dexamethasone in Partic… | Phase2 | Multiple Myeloma | Active_Not_Recruiting | 2017-01-19 | 2027-06-01 | ClinicalTrials.gov |
| NCT03261102 | TDM Guided Early Optimization of ADAL in Crohn's Disease | Na | Crohn Disease | Active_Not_Recruiting | 2017-01-17 | 2025-06-01 | ClinicalTrials.gov |
| NCT03261102 | TDM Guided Early Optimization of ADAL in Crohn's Disease | Na | Crohn Disease | Active_Not_Recruiting | 2017-01-17 | 2025-06-01 | ClinicalTrials.gov |
| NCT03261102 | TDM Guided Early Optimization of ADAL in Crohn's Disease | Na | Crohn Disease | Active_Not_Recruiting | 2017-01-17 | 2025-06-01 | ClinicalTrials.gov |
| NCT03261102 | TDM Guided Early Optimization of ADAL in Crohn's Disease | Na | Crohn Disease | Active_Not_Recruiting | 2017-01-17 | 2025-06-01 | ClinicalTrials.gov |
| NCT02495168 | Randomized, Placebo-Controlled, Multidose, Study Comparing Generic Budesonide/F… | Phase3 | Asthma | Completed | 2017-01-13 | 2018-05-31 | ClinicalTrials.gov |
| NCT02495168 | Randomized, Placebo-Controlled, Multidose, Study Comparing Generic Budesonide/F… | Phase3 | Asthma | Completed | 2017-01-13 | 2018-05-31 | ClinicalTrials.gov |
| NCT02495168 | Randomized, Placebo-Controlled, Multidose, Study Comparing Generic Budesonide/F… | Phase3 | Asthma | Completed | 2017-01-13 | 2018-05-31 | ClinicalTrials.gov |
| NCT02495168 | Randomized, Placebo-Controlled, Multidose, Study Comparing Generic Budesonide/F… | Phase3 | Asthma | Completed | 2017-01-13 | 2018-05-31 | ClinicalTrials.gov |
| NCT02942290 | A Study Evaluating Venetoclax in Combination With Azacitidine in Participants W… | Phase1 | Myelodysplastic Syndromes (MDS) | Active_Not_Recruiting | 2017-01-12 | 2027-01-01 | ClinicalTrials.gov |
| NCT02942290 | A Study Evaluating Venetoclax in Combination With Azacitidine in Participants W… | Phase1 | Myelodysplastic Syndromes (MDS) | Active_Not_Recruiting | 2017-01-12 | 2027-01-01 | ClinicalTrials.gov |
| NCT02942290 | A Study Evaluating Venetoclax in Combination With Azacitidine in Participants W… | Phase1 | Myelodysplastic Syndromes (MDS) | Active_Not_Recruiting | 2017-01-12 | 2027-01-01 | ClinicalTrials.gov |
| NCT02942290 | A Study Evaluating Venetoclax in Combination With Azacitidine in Participants W… | Phase1 | Myelodysplastic Syndromes (MDS) | Active_Not_Recruiting | 2017-01-12 | 2027-01-01 | ClinicalTrials.gov |
| NCT03254121 | Genome Studies of Hepatocellular Carcinoma Developed in Hepatitis C Patients Wi… | — | Hepatocellular Carcinoma | Completed | 2017-01-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT04358991 | Pharmacokinetics of Ceftazidime-avibactam Among Critically-ill Patients Receivi… | — | Bacterial Infections | Completed | 2017-01-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT04358991 | Pharmacokinetics of Ceftazidime-avibactam Among Critically-ill Patients Receivi… | — | Bacterial Infections | Completed | 2017-01-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT03254121 | Genome Studies of Hepatocellular Carcinoma Developed in Hepatitis C Patients Wi… | — | Hepatocellular Carcinoma | Completed | 2017-01-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT04358991 | Pharmacokinetics of Ceftazidime-avibactam Among Critically-ill Patients Receivi… | — | Bacterial Infections | Completed | 2017-01-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT03254121 | Genome Studies of Hepatocellular Carcinoma Developed in Hepatitis C Patients Wi… | — | Hepatocellular Carcinoma | Completed | 2017-01-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT03254121 | Genome Studies of Hepatocellular Carcinoma Developed in Hepatitis C Patients Wi… | — | Hepatocellular Carcinoma | Completed | 2017-01-01 | 2020-09-01 | ClinicalTrials.gov |
| NCT04358991 | Pharmacokinetics of Ceftazidime-avibactam Among Critically-ill Patients Receivi… | — | Bacterial Infections | Completed | 2017-01-01 | 2019-12-31 | ClinicalTrials.gov |
| NCT02944396 | Study of Veliparib in Combination With Nivolumab and Platinum Doublet Chemother… | Phase1 | Non-Small Cell Lung Cancer | Completed | 2016-12-23 | 2019-10-02 | ClinicalTrials.gov |
| NCT02944396 | Study of Veliparib in Combination With Nivolumab and Platinum Doublet Chemother… | Phase1 | Non-Small Cell Lung Cancer | Completed | 2016-12-23 | 2019-10-02 | ClinicalTrials.gov |
| NCT02944396 | Study of Veliparib in Combination With Nivolumab and Platinum Doublet Chemother… | Phase1 | Non-Small Cell Lung Cancer | Completed | 2016-12-23 | 2019-10-02 | ClinicalTrials.gov |
| NCT02944396 | Study of Veliparib in Combination With Nivolumab and Platinum Doublet Chemother… | Phase1 | Non-Small Cell Lung Cancer | Completed | 2016-12-23 | 2019-10-02 | ClinicalTrials.gov |
| NCT02988674 | A Study to Assess Retention Rate, Persistence and Adherence in Population of Sp… | — | Spondylarthritis | Completed | 2016-12-22 | 2019-10-16 | ClinicalTrials.gov |
| NCT02988674 | A Study to Assess Retention Rate, Persistence and Adherence in Population of Sp… | — | Spondylarthritis | Completed | 2016-12-22 | 2019-10-16 | ClinicalTrials.gov |
| NCT02988674 | A Study to Assess Retention Rate, Persistence and Adherence in Population of Sp… | — | Spondylarthritis | Completed | 2016-12-22 | 2019-10-16 | ClinicalTrials.gov |
| NCT02988674 | A Study to Assess Retention Rate, Persistence and Adherence in Population of Sp… | — | Spondylarthritis | Completed | 2016-12-22 | 2019-10-16 | ClinicalTrials.gov |
| NCT02896985 | Observational Study Evaluating the Effectiveness of Drug Concentration to Predi… | — | Crohn's Disease | Completed | 2016-12-16 | 2020-03-11 | ClinicalTrials.gov |
| NCT02896985 | Observational Study Evaluating the Effectiveness of Drug Concentration to Predi… | — | Crohn's Disease | Completed | 2016-12-16 | 2020-03-11 | ClinicalTrials.gov |
| NCT02896985 | Observational Study Evaluating the Effectiveness of Drug Concentration to Predi… | — | Crohn's Disease | Completed | 2016-12-16 | 2020-03-11 | ClinicalTrials.gov |
| NCT02896985 | Observational Study Evaluating the Effectiveness of Drug Concentration to Predi… | — | Crohn's Disease | Completed | 2016-12-16 | 2020-03-11 | ClinicalTrials.gov |
| NCT02986373 | A Study to Investigate Safety With Risankizumab in Psoriatic Arthritis Subjects… | Phase2 | Psoriatic Arthritis | Completed | 2016-12-15 | 2018-07-30 | ClinicalTrials.gov |
| NCT02986373 | A Study to Investigate Safety With Risankizumab in Psoriatic Arthritis Subjects… | Phase2 | Psoriatic Arthritis | Completed | 2016-12-15 | 2018-07-30 | ClinicalTrials.gov |
| NCT02986373 | A Study to Investigate Safety With Risankizumab in Psoriatic Arthritis Subjects… | Phase2 | Psoriatic Arthritis | Completed | 2016-12-15 | 2018-07-30 | ClinicalTrials.gov |
| NCT02986373 | A Study to Investigate Safety With Risankizumab in Psoriatic Arthritis Subjects… | Phase2 | Psoriatic Arthritis | Completed | 2016-12-15 | 2018-07-30 | ClinicalTrials.gov |
| NCT03000257 | A Study of Budigalimab (ABBV-181) in Participants With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2016-12-14 | 2022-03-29 | ClinicalTrials.gov |
| NCT03000257 | A Study of Budigalimab (ABBV-181) in Participants With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2016-12-14 | 2022-03-29 | ClinicalTrials.gov |
| NCT03000257 | A Study of Budigalimab (ABBV-181) in Participants With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2016-12-14 | 2022-03-29 | ClinicalTrials.gov |
| NCT03000257 | A Study of Budigalimab (ABBV-181) in Participants With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2016-12-14 | 2022-03-29 | ClinicalTrials.gov |
| NCT02977507 | Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topica… | Na | Melasma | Completed | 2016-12-13 | 2017-10-09 | ClinicalTrials.gov |
| NCT02980731 | A Study Evaluating the Impact of Venetoclax on the Quality of Life for Subjects… | Phase3 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2016-12-13 | 2021-12-29 | ClinicalTrials.gov |
| NCT02965846 | Topical Ophthalmic AGN-195263 for the Treatment of Evaporative Dry Eye | Phase3 | Dry Eye Syndromes | Terminated | 2016-12-13 | 2017-06-13 | ClinicalTrials.gov |
| NCT02950051 | Standard Chemoimmunotherapy (FCR/BR) Versus Rituximab + Venetoclax (RVe) Versus… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2016-12-13 | 2024-02-29 | ClinicalTrials.gov |
| NCT02965846 | Topical Ophthalmic AGN-195263 for the Treatment of Evaporative Dry Eye | Phase3 | Dry Eye Syndromes | Terminated | 2016-12-13 | 2017-06-13 | ClinicalTrials.gov |
| NCT02950051 | Standard Chemoimmunotherapy (FCR/BR) Versus Rituximab + Venetoclax (RVe) Versus… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2016-12-13 | 2024-02-29 | ClinicalTrials.gov |
| NCT02950051 | Standard Chemoimmunotherapy (FCR/BR) Versus Rituximab + Venetoclax (RVe) Versus… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2016-12-13 | 2024-02-29 | ClinicalTrials.gov |
| NCT02980731 | A Study Evaluating the Impact of Venetoclax on the Quality of Life for Subjects… | Phase3 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2016-12-13 | 2021-12-29 | ClinicalTrials.gov |
| NCT02980731 | A Study Evaluating the Impact of Venetoclax on the Quality of Life for Subjects… | Phase3 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2016-12-13 | 2021-12-29 | ClinicalTrials.gov |
| NCT02977507 | Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topica… | Na | Melasma | Completed | 2016-12-13 | 2017-10-09 | ClinicalTrials.gov |
| NCT02977507 | Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topica… | Na | Melasma | Completed | 2016-12-13 | 2017-10-09 | ClinicalTrials.gov |
| NCT02950051 | Standard Chemoimmunotherapy (FCR/BR) Versus Rituximab + Venetoclax (RVe) Versus… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2016-12-13 | 2024-02-29 | ClinicalTrials.gov |
| NCT02965846 | Topical Ophthalmic AGN-195263 for the Treatment of Evaporative Dry Eye | Phase3 | Dry Eye Syndromes | Terminated | 2016-12-13 | 2017-06-13 | ClinicalTrials.gov |
| NCT02977507 | Split-face Study Comparing the Cosmetic Efficacy and Tolerability of Two Topica… | Na | Melasma | Completed | 2016-12-13 | 2017-10-09 | ClinicalTrials.gov |
| NCT02965846 | Topical Ophthalmic AGN-195263 for the Treatment of Evaporative Dry Eye | Phase3 | Dry Eye Syndromes | Terminated | 2016-12-13 | 2017-06-13 | ClinicalTrials.gov |
| NCT02980731 | A Study Evaluating the Impact of Venetoclax on the Quality of Life for Subjects… | Phase3 | Chronic Lymphocytic Leukemia (CLL) | Completed | 2016-12-13 | 2021-12-29 | ClinicalTrials.gov |
| NCT02985879 | A Study to Assess Efficacy, Safety, Tolerability, and Pharmacokinetics of ABBV-… | Phase2 | Progressive Supranuclear Palsy | Terminated | 2016-12-12 | 2019-11-20 | ClinicalTrials.gov |
| NCT02985879 | A Study to Assess Efficacy, Safety, Tolerability, and Pharmacokinetics of ABBV-… | Phase2 | Progressive Supranuclear Palsy | Terminated | 2016-12-12 | 2019-11-20 | ClinicalTrials.gov |
| NCT03052764 | Evaluation of an Alternative Injection Paradigm for OnabotulinumtoxinA (BOTOX®)… | Phase4 | Urinary Bladder, Overactive | Completed | 2016-12-12 | 2018-12-10 | ClinicalTrials.gov |
| NCT02985879 | A Study to Assess Efficacy, Safety, Tolerability, and Pharmacokinetics of ABBV-… | Phase2 | Progressive Supranuclear Palsy | Terminated | 2016-12-12 | 2019-11-20 | ClinicalTrials.gov |
| NCT03052764 | Evaluation of an Alternative Injection Paradigm for OnabotulinumtoxinA (BOTOX®)… | Phase4 | Urinary Bladder, Overactive | Completed | 2016-12-12 | 2018-12-10 | ClinicalTrials.gov |
| NCT03052764 | Evaluation of an Alternative Injection Paradigm for OnabotulinumtoxinA (BOTOX®)… | Phase4 | Urinary Bladder, Overactive | Completed | 2016-12-12 | 2018-12-10 | ClinicalTrials.gov |
| NCT02985879 | A Study to Assess Efficacy, Safety, Tolerability, and Pharmacokinetics of ABBV-… | Phase2 | Progressive Supranuclear Palsy | Terminated | 2016-12-12 | 2019-11-20 | ClinicalTrials.gov |
| NCT03052764 | Evaluation of an Alternative Injection Paradigm for OnabotulinumtoxinA (BOTOX®)… | Phase4 | Urinary Bladder, Overactive | Completed | 2016-12-12 | 2018-12-10 | ClinicalTrials.gov |
| NCT03000075 | BI 655066 (Risankizumab) Compared to Placebo in Japanese Patients With Moderate… | Phase2 | Psoriasis | Completed | 2016-12-02 | 2018-06-20 | ClinicalTrials.gov |
| NCT03000075 | BI 655066 (Risankizumab) Compared to Placebo in Japanese Patients With Moderate… | Phase2 | Psoriasis | Completed | 2016-12-02 | 2018-06-20 | ClinicalTrials.gov |
| NCT03000075 | BI 655066 (Risankizumab) Compared to Placebo in Japanese Patients With Moderate… | Phase2 | Psoriasis | Completed | 2016-12-02 | 2018-06-20 | ClinicalTrials.gov |
| NCT03000075 | BI 655066 (Risankizumab) Compared to Placebo in Japanese Patients With Moderate… | Phase2 | Psoriasis | Completed | 2016-12-02 | 2018-06-20 | ClinicalTrials.gov |
| NCT02939989 | Efficacy and Safety of Glecaprevir (ABT-493)/Pibrentasvir (ABT 530) (GLE/PIB) i… | Phase3 | Hepatitis C Virus Infection | Completed | 2016-11-21 | 2021-07-30 | ClinicalTrials.gov |
| NCT02939989 | Efficacy and Safety of Glecaprevir (ABT-493)/Pibrentasvir (ABT 530) (GLE/PIB) i… | Phase3 | Hepatitis C Virus Infection | Completed | 2016-11-21 | 2021-07-30 | ClinicalTrials.gov |
| NCT02939989 | Efficacy and Safety of Glecaprevir (ABT-493)/Pibrentasvir (ABT 530) (GLE/PIB) i… | Phase3 | Hepatitis C Virus Infection | Completed | 2016-11-21 | 2021-07-30 | ClinicalTrials.gov |
| NCT02939989 | Efficacy and Safety of Glecaprevir (ABT-493)/Pibrentasvir (ABT 530) (GLE/PIB) i… | Phase3 | Hepatitis C Virus Infection | Completed | 2016-11-21 | 2021-07-30 | ClinicalTrials.gov |
| NCT02955251 | A Study of ABBV-428, an Immunotherapy, in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors Cancer | Completed | 2016-11-18 | 2019-10-29 | ClinicalTrials.gov |
| NCT02955251 | A Study of ABBV-428, an Immunotherapy, in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors Cancer | Completed | 2016-11-18 | 2019-10-29 | ClinicalTrials.gov |
| NCT02955251 | A Study of ABBV-428, an Immunotherapy, in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors Cancer | Completed | 2016-11-18 | 2019-10-29 | ClinicalTrials.gov |
| NCT02955251 | A Study of ABBV-428, an Immunotherapy, in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors Cancer | Completed | 2016-11-18 | 2019-10-29 | ClinicalTrials.gov |
| NCT02916017 | HUMIRA® Long-term Treatment in Patients With Non-infectious Intermediate-, Post… | — | Uveitis | Completed | 2016-11-15 | 2020-10-14 | ClinicalTrials.gov |
| NCT02916017 | HUMIRA® Long-term Treatment in Patients With Non-infectious Intermediate-, Post… | — | Uveitis | Completed | 2016-11-15 | 2020-10-14 | ClinicalTrials.gov |
| NCT02916017 | HUMIRA® Long-term Treatment in Patients With Non-infectious Intermediate-, Post… | — | Uveitis | Completed | 2016-11-15 | 2020-10-14 | ClinicalTrials.gov |
| NCT02916017 | HUMIRA® Long-term Treatment in Patients With Non-infectious Intermediate-, Post… | — | Uveitis | Completed | 2016-11-15 | 2020-10-14 | ClinicalTrials.gov |
| NCT02951988 | A Study of Rapastinel as Adjunctive Therapy in the Prevention of Relapse in Pat… | Phase3 | Depressive Disorder, Major | Completed | 2016-11-13 | 2019-02-22 | ClinicalTrials.gov |
| NCT02951988 | A Study of Rapastinel as Adjunctive Therapy in the Prevention of Relapse in Pat… | Phase3 | Depressive Disorder, Major | Completed | 2016-11-13 | 2019-02-22 | ClinicalTrials.gov |
| NCT02951988 | A Study of Rapastinel as Adjunctive Therapy in the Prevention of Relapse in Pat… | Phase3 | Depressive Disorder, Major | Completed | 2016-11-13 | 2019-02-22 | ClinicalTrials.gov |
| NCT02951988 | A Study of Rapastinel as Adjunctive Therapy in the Prevention of Relapse in Pat… | Phase3 | Depressive Disorder, Major | Completed | 2016-11-13 | 2019-02-22 | ClinicalTrials.gov |
| NCT02968173 | A Study to Assess the Safety and Effectiveness of Palivizumab Administered to C… | Phase3 | Respiratory Syncytial Virus (RSV) | Completed | 2016-11-09 | 2017-07-13 | ClinicalTrials.gov |
| NCT02968173 | A Study to Assess the Safety and Effectiveness of Palivizumab Administered to C… | Phase3 | Respiratory Syncytial Virus (RSV) | Completed | 2016-11-09 | 2017-07-13 | ClinicalTrials.gov |
| NCT02968173 | A Study to Assess the Safety and Effectiveness of Palivizumab Administered to C… | Phase3 | Respiratory Syncytial Virus (RSV) | Completed | 2016-11-09 | 2017-07-13 | ClinicalTrials.gov |
| NCT02968173 | A Study to Assess the Safety and Effectiveness of Palivizumab Administered to C… | Phase3 | Respiratory Syncytial Virus (RSV) | Completed | 2016-11-09 | 2017-07-13 | ClinicalTrials.gov |
| NCT02943577 | A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-M… | Phase3 | Depressive Disorder, Major | Completed | 2016-11-02 | 2018-11-21 | ClinicalTrials.gov |
| NCT02943577 | A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-M… | Phase3 | Depressive Disorder, Major | Completed | 2016-11-02 | 2018-11-21 | ClinicalTrials.gov |
| NCT02943577 | A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-M… | Phase3 | Depressive Disorder, Major | Completed | 2016-11-02 | 2018-11-21 | ClinicalTrials.gov |
| NCT02943577 | A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-M… | Phase3 | Depressive Disorder, Major | Completed | 2016-11-02 | 2018-11-21 | ClinicalTrials.gov |
| NCT02910921 | Individualized Prediction of Migraine Attacks Using a Mobile Phone App and Fitb… | — | Migraine Disorders | Completed | 2016-11-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02910921 | Individualized Prediction of Migraine Attacks Using a Mobile Phone App and Fitb… | — | Migraine Disorders | Completed | 2016-11-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02910921 | Individualized Prediction of Migraine Attacks Using a Mobile Phone App and Fitb… | — | Migraine Disorders | Completed | 2016-11-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02910921 | Individualized Prediction of Migraine Attacks Using a Mobile Phone App and Fitb… | — | Migraine Disorders | Completed | 2016-11-01 | 2018-07-31 | ClinicalTrials.gov |
| NCT02830776 | Topical Bimatoprost for Chemical Blepharoplasty | Early_Phase1 | Dermatochalasis | Completed | 2016-11-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT02830776 | Topical Bimatoprost for Chemical Blepharoplasty | Early_Phase1 | Dermatochalasis | Completed | 2016-11-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT02830776 | Topical Bimatoprost for Chemical Blepharoplasty | Early_Phase1 | Dermatochalasis | Completed | 2016-11-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT02830776 | Topical Bimatoprost for Chemical Blepharoplasty | Early_Phase1 | Dermatochalasis | Completed | 2016-11-01 | 2017-06-30 | ClinicalTrials.gov |
| NCT02959970 | Safety and Efficacy Trial of ACZONE (Dapsone) Gel, 7.5% in 9 to 11 Year-Old Pat… | Phase4 | Acne Vulgaris | Completed | 2016-10-31 | 2018-03-09 | ClinicalTrials.gov |
| NCT02959970 | Safety and Efficacy Trial of ACZONE (Dapsone) Gel, 7.5% in 9 to 11 Year-Old Pat… | Phase4 | Acne Vulgaris | Completed | 2016-10-31 | 2018-03-09 | ClinicalTrials.gov |
| NCT02959970 | Safety and Efficacy Trial of ACZONE (Dapsone) Gel, 7.5% in 9 to 11 Year-Old Pat… | Phase4 | Acne Vulgaris | Completed | 2016-10-31 | 2018-03-09 | ClinicalTrials.gov |
| NCT02959970 | Safety and Efficacy Trial of ACZONE (Dapsone) Gel, 7.5% in 9 to 11 Year-Old Pat… | Phase4 | Acne Vulgaris | Completed | 2016-10-31 | 2018-03-09 | ClinicalTrials.gov |
| NCT02945228 | Drug Use-Results Survey in Participants Infected With Hepatitis C Virus Genotyp… | — | Chronic Hepatitis C Virus | Completed | 2016-10-26 | 2019-07-26 | ClinicalTrials.gov |
| NCT02945228 | Drug Use-Results Survey in Participants Infected With Hepatitis C Virus Genotyp… | — | Chronic Hepatitis C Virus | Completed | 2016-10-26 | 2019-07-26 | ClinicalTrials.gov |
| NCT02945228 | Drug Use-Results Survey in Participants Infected With Hepatitis C Virus Genotyp… | — | Chronic Hepatitis C Virus | Completed | 2016-10-26 | 2019-07-26 | ClinicalTrials.gov |
| NCT02945228 | Drug Use-Results Survey in Participants Infected With Hepatitis C Virus Genotyp… | — | Chronic Hepatitis C Virus | Completed | 2016-10-26 | 2019-07-26 | ClinicalTrials.gov |
| NCT02925117 | A Study to Evaluate ABT-494 (Upadacitinib) in Adults With Moderate to Severe At… | Phase2 | Atopic Dermatitis | Completed | 2016-10-25 | 2019-01-31 | ClinicalTrials.gov |
| NCT02925117 | A Study to Evaluate ABT-494 (Upadacitinib) in Adults With Moderate to Severe At… | Phase2 | Atopic Dermatitis | Completed | 2016-10-25 | 2019-01-31 | ClinicalTrials.gov |
| NCT02959983 | Efficacy of Eluxadoline in the Treatment of Irritable Bowel Syndrome With Diarr… | Phase4 | Irritable Bowel Syndrome With Diarrhea | Completed | 2016-10-25 | 2018-01-22 | ClinicalTrials.gov |
| NCT02925117 | A Study to Evaluate ABT-494 (Upadacitinib) in Adults With Moderate to Severe At… | Phase2 | Atopic Dermatitis | Completed | 2016-10-25 | 2019-01-31 | ClinicalTrials.gov |
| NCT02959983 | Efficacy of Eluxadoline in the Treatment of Irritable Bowel Syndrome With Diarr… | Phase4 | Irritable Bowel Syndrome With Diarrhea | Completed | 2016-10-25 | 2018-01-22 | ClinicalTrials.gov |
| NCT02925117 | A Study to Evaluate ABT-494 (Upadacitinib) in Adults With Moderate to Severe At… | Phase2 | Atopic Dermatitis | Completed | 2016-10-25 | 2019-01-31 | ClinicalTrials.gov |
| NCT02959983 | Efficacy of Eluxadoline in the Treatment of Irritable Bowel Syndrome With Diarr… | Phase4 | Irritable Bowel Syndrome With Diarrhea | Completed | 2016-10-25 | 2018-01-22 | ClinicalTrials.gov |
| NCT02959983 | Efficacy of Eluxadoline in the Treatment of Irritable Bowel Syndrome With Diarr… | Phase4 | Irritable Bowel Syndrome With Diarrhea | Completed | 2016-10-25 | 2018-01-22 | ClinicalTrials.gov |
| NCT02601885 | A Multiple Dose Study of ABT-555 in Subjects With Relapsing Forms of Multiple S… | Phase1 | Multiple Sclerosis | Completed | 2016-10-18 | 2018-04-20 | ClinicalTrials.gov |
| NCT02601885 | A Multiple Dose Study of ABT-555 in Subjects With Relapsing Forms of Multiple S… | Phase1 | Multiple Sclerosis | Completed | 2016-10-18 | 2018-04-20 | ClinicalTrials.gov |
| NCT02601885 | A Multiple Dose Study of ABT-555 in Subjects With Relapsing Forms of Multiple S… | Phase1 | Multiple Sclerosis | Completed | 2016-10-18 | 2018-04-20 | ClinicalTrials.gov |
| NCT02601885 | A Multiple Dose Study of ABT-555 in Subjects With Relapsing Forms of Multiple S… | Phase1 | Multiple Sclerosis | Completed | 2016-10-18 | 2018-04-20 | ClinicalTrials.gov |
| NCT02932943 | A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-M… | Phase3 | Depressive Disorder, Major | Completed | 2016-10-15 | 2018-11-08 | ClinicalTrials.gov |
| NCT02932943 | A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-M… | Phase3 | Depressive Disorder, Major | Completed | 2016-10-15 | 2018-11-08 | ClinicalTrials.gov |
| NCT02932943 | A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-M… | Phase3 | Depressive Disorder, Major | Completed | 2016-10-15 | 2018-11-08 | ClinicalTrials.gov |
| NCT02932943 | A Study of Rapastinel as Adjunctive Therapy in Major Depressive Disorder (RAP-M… | Phase3 | Depressive Disorder, Major | Completed | 2016-10-15 | 2018-11-08 | ClinicalTrials.gov |
| NCT02849704 | Fat Malabsorption in Chronic Pancreatitis | Phase2 | Chronic Pancreatitis | Completed | 2016-10-13 | 2017-11-01 | ClinicalTrials.gov |
| NCT02849704 | Fat Malabsorption in Chronic Pancreatitis | Phase2 | Chronic Pancreatitis | Completed | 2016-10-13 | 2017-11-01 | ClinicalTrials.gov |
| NCT02849704 | Fat Malabsorption in Chronic Pancreatitis | Phase2 | Chronic Pancreatitis | Completed | 2016-10-13 | 2017-11-01 | ClinicalTrials.gov |
| NCT02849704 | Fat Malabsorption in Chronic Pancreatitis | Phase2 | Chronic Pancreatitis | Completed | 2016-10-13 | 2017-11-01 | ClinicalTrials.gov |
| NCT02819999 | A Study of Rovalpituzumab Tesirine (SC16LD6.5) in the Frontline Treatment of Pa… | Phase1 | Small Cell Lung Cancer | Terminated | 2016-10-01 | 2019-05-31 | ClinicalTrials.gov |
| NCT02819999 | A Study of Rovalpituzumab Tesirine (SC16LD6.5) in the Frontline Treatment of Pa… | Phase1 | Small Cell Lung Cancer | Terminated | 2016-10-01 | 2019-05-31 | ClinicalTrials.gov |
| NCT02819999 | A Study of Rovalpituzumab Tesirine (SC16LD6.5) in the Frontline Treatment of Pa… | Phase1 | Small Cell Lung Cancer | Terminated | 2016-10-01 | 2019-05-31 | ClinicalTrials.gov |
| NCT02819999 | A Study of Rovalpituzumab Tesirine (SC16LD6.5) in the Frontline Treatment of Pa… | Phase1 | Small Cell Lung Cancer | Terminated | 2016-10-01 | 2019-05-31 | ClinicalTrials.gov |
| NCT02860065 | CPC-201 Alzheimer's Disease Type Dementia: PET Study | Phase2 | Alzheimer's Disease | Withdrawn | 2016-09-30 | 2017-06-30 | ClinicalTrials.gov |
| NCT02860065 | CPC-201 Alzheimer's Disease Type Dementia: PET Study | Phase2 | Alzheimer's Disease | Withdrawn | 2016-09-30 | 2017-06-30 | ClinicalTrials.gov |
| NCT02860065 | CPC-201 Alzheimer's Disease Type Dementia: PET Study | Phase2 | Alzheimer's Disease | Withdrawn | 2016-09-30 | 2017-06-30 | ClinicalTrials.gov |
| NCT02860065 | CPC-201 Alzheimer's Disease Type Dementia: PET Study | Phase2 | Alzheimer's Disease | Withdrawn | 2016-09-30 | 2017-06-30 | ClinicalTrials.gov |
| NCT02819635 | A Study to Evaluate the Safety and Efficacy of Upadacitinib (ABT-494) for Induc… | Phase2 | Ulcerative Colitis (UC) | Completed | 2016-09-26 | 2021-12-13 | ClinicalTrials.gov |
| NCT02819635 | A Study to Evaluate the Safety and Efficacy of Upadacitinib (ABT-494) for Induc… | Phase2 | Ulcerative Colitis (UC) | Completed | 2016-09-26 | 2021-12-13 | ClinicalTrials.gov |
| NCT02819635 | A Study to Evaluate the Safety and Efficacy of Upadacitinib (ABT-494) for Induc… | Phase2 | Ulcerative Colitis (UC) | Completed | 2016-09-26 | 2021-12-13 | ClinicalTrials.gov |
| NCT02819635 | A Study to Evaluate the Safety and Efficacy of Upadacitinib (ABT-494) for Induc… | Phase2 | Ulcerative Colitis (UC) | Completed | 2016-09-26 | 2021-12-13 | ClinicalTrials.gov |
| NCT02709889 | Rovalpituzumab Tesirine in Delta-Like Protein 3-Expressing Advanced Solid Tumors | Phase1 | Malignant Melanoma | Terminated | 2016-09-23 | 2019-08-27 | ClinicalTrials.gov |
| NCT02709889 | Rovalpituzumab Tesirine in Delta-Like Protein 3-Expressing Advanced Solid Tumors | Phase1 | Malignant Melanoma | Terminated | 2016-09-23 | 2019-08-27 | ClinicalTrials.gov |
| NCT02709889 | Rovalpituzumab Tesirine in Delta-Like Protein 3-Expressing Advanced Solid Tumors | Phase1 | Malignant Melanoma | Terminated | 2016-09-23 | 2019-08-27 | ClinicalTrials.gov |
| NCT02709889 | Rovalpituzumab Tesirine in Delta-Like Protein 3-Expressing Advanced Solid Tumors | Phase1 | Malignant Melanoma | Terminated | 2016-09-23 | 2019-08-27 | ClinicalTrials.gov |
| NCT02896920 | Canadian Humira Post Marketing Observational Epidemiological Study : Assessing … | — | Hidradenitis Suppurativa (HS) | Completed | 2016-09-20 | 2019-04-29 | ClinicalTrials.gov |
| NCT02896920 | Canadian Humira Post Marketing Observational Epidemiological Study : Assessing … | — | Hidradenitis Suppurativa (HS) | Completed | 2016-09-20 | 2019-04-29 | ClinicalTrials.gov |
| NCT02896920 | Canadian Humira Post Marketing Observational Epidemiological Study : Assessing … | — | Hidradenitis Suppurativa (HS) | Completed | 2016-09-20 | 2019-04-29 | ClinicalTrials.gov |
| NCT02896920 | Canadian Humira Post Marketing Observational Epidemiological Study : Assessing … | — | Hidradenitis Suppurativa (HS) | Completed | 2016-09-20 | 2019-04-29 | ClinicalTrials.gov |
| NCT02871440 | A Two Comparator, Controlled Phase 3 Study in Patients With and Without Evapora… | Phase3 | Dry Eye Syndromes | Completed | 2016-09-19 | 2017-09-18 | ClinicalTrials.gov |
| NCT02871440 | A Two Comparator, Controlled Phase 3 Study in Patients With and Without Evapora… | Phase3 | Dry Eye Syndromes | Completed | 2016-09-19 | 2017-09-18 | ClinicalTrials.gov |
| NCT02871440 | A Two Comparator, Controlled Phase 3 Study in Patients With and Without Evapora… | Phase3 | Dry Eye Syndromes | Completed | 2016-09-19 | 2017-09-18 | ClinicalTrials.gov |
| NCT02871440 | A Two Comparator, Controlled Phase 3 Study in Patients With and Without Evapora… | Phase3 | Dry Eye Syndromes | Completed | 2016-09-19 | 2017-09-18 | ClinicalTrials.gov |
| NCT02772601 | This Study Tests the Effect of Risankizumab on the Metabolism in the Liver of F… | Phase1 | Psoriasis | Completed | 2016-09-15 | 2017-09-22 | ClinicalTrials.gov |
| NCT02772601 | This Study Tests the Effect of Risankizumab on the Metabolism in the Liver of F… | Phase1 | Psoriasis | Completed | 2016-09-15 | 2017-09-22 | ClinicalTrials.gov |
| NCT02772601 | This Study Tests the Effect of Risankizumab on the Metabolism in the Liver of F… | Phase1 | Psoriasis | Completed | 2016-09-15 | 2017-09-22 | ClinicalTrials.gov |
| NCT02772601 | This Study Tests the Effect of Risankizumab on the Metabolism in the Liver of F… | Phase1 | Psoriasis | Completed | 2016-09-15 | 2017-09-22 | ClinicalTrials.gov |
| NCT02925494 | An Extension Study to Evaluate the Efficacy and Safety of Elagolix in Premenopa… | Phase3 | Uterine Fibroids | Completed | 2016-09-14 | 2019-03-22 | ClinicalTrials.gov |
| NCT02925494 | An Extension Study to Evaluate the Efficacy and Safety of Elagolix in Premenopa… | Phase3 | Uterine Fibroids | Completed | 2016-09-14 | 2019-03-22 | ClinicalTrials.gov |
| NCT02925494 | An Extension Study to Evaluate the Efficacy and Safety of Elagolix in Premenopa… | Phase3 | Uterine Fibroids | Completed | 2016-09-14 | 2019-03-22 | ClinicalTrials.gov |
| NCT02925494 | An Extension Study to Evaluate the Efficacy and Safety of Elagolix in Premenopa… | Phase3 | Uterine Fibroids | Completed | 2016-09-14 | 2019-03-22 | ClinicalTrials.gov |
| NCT02873221 | An Extension Study to Evaluate the Long-Term Safety and Tolerability of Ubrogep… | Phase3 | Migraine, With or Without Aura | Completed | 2016-09-13 | 2018-08-02 | ClinicalTrials.gov |
| NCT02873221 | An Extension Study to Evaluate the Long-Term Safety and Tolerability of Ubrogep… | Phase3 | Migraine, With or Without Aura | Completed | 2016-09-13 | 2018-08-02 | ClinicalTrials.gov |
| NCT02873221 | An Extension Study to Evaluate the Long-Term Safety and Tolerability of Ubrogep… | Phase3 | Migraine, With or Without Aura | Completed | 2016-09-13 | 2018-08-02 | ClinicalTrials.gov |
| NCT02873221 | An Extension Study to Evaluate the Long-Term Safety and Tolerability of Ubrogep… | Phase3 | Migraine, With or Without Aura | Completed | 2016-09-13 | 2018-08-02 | ClinicalTrials.gov |
| NCT02897115 | A Study Treating Participants With Early Axial Spondyloarthritis (axSpA) Taking… | Phase4 | Axial Spondyloarthritis | Terminated | 2016-09-12 | 2017-12-21 | ClinicalTrials.gov |
| NCT02897115 | A Study Treating Participants With Early Axial Spondyloarthritis (axSpA) Taking… | Phase4 | Axial Spondyloarthritis | Terminated | 2016-09-12 | 2017-12-21 | ClinicalTrials.gov |
| NCT02906488 | Special Drug Use-results Survey of Duodopa Enteral Solution in Patients With Pa… | — | Parkinson's Disease | Completed | 2016-09-12 | 2025-07-24 | ClinicalTrials.gov |
| NCT02897115 | A Study Treating Participants With Early Axial Spondyloarthritis (axSpA) Taking… | Phase4 | Axial Spondyloarthritis | Terminated | 2016-09-12 | 2017-12-21 | ClinicalTrials.gov |
| NCT02897115 | A Study Treating Participants With Early Axial Spondyloarthritis (axSpA) Taking… | Phase4 | Axial Spondyloarthritis | Terminated | 2016-09-12 | 2017-12-21 | ClinicalTrials.gov |
| NCT02906488 | Special Drug Use-results Survey of Duodopa Enteral Solution in Patients With Pa… | — | Parkinson's Disease | Completed | 2016-09-12 | 2025-07-24 | ClinicalTrials.gov |
| NCT02906488 | Special Drug Use-results Survey of Duodopa Enteral Solution in Patients With Pa… | — | Parkinson's Disease | Completed | 2016-09-12 | 2025-07-24 | ClinicalTrials.gov |
| NCT02906488 | Special Drug Use-results Survey of Duodopa Enteral Solution in Patients With Pa… | — | Parkinson's Disease | Completed | 2016-09-12 | 2025-07-24 | ClinicalTrials.gov |
| NCT02848326 | Efficacy, Safety, and Tolerability of Multiple Dosing Regimens of Oral Atogepan… | Phase2 | Migraine, With or Without Aura | Completed | 2016-09-06 | 2018-04-23 | ClinicalTrials.gov |
| NCT02848326 | Efficacy, Safety, and Tolerability of Multiple Dosing Regimens of Oral Atogepan… | Phase2 | Migraine, With or Without Aura | Completed | 2016-09-06 | 2018-04-23 | ClinicalTrials.gov |
| NCT02904902 | Open-label Study of Adalimumab in Japanese Subjects With Hidradenitis Suppurati… | Phase3 | Hidradenitis Suppurativa | Completed | 2016-09-06 | 2019-05-30 | ClinicalTrials.gov |
| NCT02904902 | Open-label Study of Adalimumab in Japanese Subjects With Hidradenitis Suppurati… | Phase3 | Hidradenitis Suppurativa | Completed | 2016-09-06 | 2019-05-30 | ClinicalTrials.gov |
| NCT02904902 | Open-label Study of Adalimumab in Japanese Subjects With Hidradenitis Suppurati… | Phase3 | Hidradenitis Suppurativa | Completed | 2016-09-06 | 2019-05-30 | ClinicalTrials.gov |
| NCT02848326 | Efficacy, Safety, and Tolerability of Multiple Dosing Regimens of Oral Atogepan… | Phase2 | Migraine, With or Without Aura | Completed | 2016-09-06 | 2018-04-23 | ClinicalTrials.gov |
| NCT02848326 | Efficacy, Safety, and Tolerability of Multiple Dosing Regimens of Oral Atogepan… | Phase2 | Migraine, With or Without Aura | Completed | 2016-09-06 | 2018-04-23 | ClinicalTrials.gov |
| NCT02904902 | Open-label Study of Adalimumab in Japanese Subjects With Hidradenitis Suppurati… | Phase3 | Hidradenitis Suppurativa | Completed | 2016-09-06 | 2019-05-30 | ClinicalTrials.gov |
| NCT02758665 | Trial of Ibrutinib Plus Venetoclax Plus Obinutuzumab in Patients With CLL | Phase2 | Leukemia, Lymphocytic, Chronic | Completed | 2016-09-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02806362 | Study of Ombitasvir/Paritaprevir/Ritonavir in Japanese Adults With Genotype 1b … | Phase3 | Chronic Hepatitis C Virus | Withdrawn | 2016-09-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02806362 | Study of Ombitasvir/Paritaprevir/Ritonavir in Japanese Adults With Genotype 1b … | Phase3 | Chronic Hepatitis C Virus | Withdrawn | 2016-09-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02758665 | Trial of Ibrutinib Plus Venetoclax Plus Obinutuzumab in Patients With CLL | Phase2 | Leukemia, Lymphocytic, Chronic | Completed | 2016-09-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02758665 | Trial of Ibrutinib Plus Venetoclax Plus Obinutuzumab in Patients With CLL | Phase2 | Leukemia, Lymphocytic, Chronic | Completed | 2016-09-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02806362 | Study of Ombitasvir/Paritaprevir/Ritonavir in Japanese Adults With Genotype 1b … | Phase3 | Chronic Hepatitis C Virus | Withdrawn | 2016-09-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02806362 | Study of Ombitasvir/Paritaprevir/Ritonavir in Japanese Adults With Genotype 1b … | Phase3 | Chronic Hepatitis C Virus | Withdrawn | 2016-09-01 | 2018-08-01 | ClinicalTrials.gov |
| NCT02758665 | Trial of Ibrutinib Plus Venetoclax Plus Obinutuzumab in Patients With CLL | Phase2 | Leukemia, Lymphocytic, Chronic | Completed | 2016-09-01 | 2022-03-01 | ClinicalTrials.gov |
| NCT02867709 | Efficacy, Safety, and Tolerability of Oral Ubrogepant in the Acute Treatment of… | Phase3 | Migraine, With or Without Aura | Completed | 2016-08-26 | 2018-02-26 | ClinicalTrials.gov |
| NCT02867709 | Efficacy, Safety, and Tolerability of Oral Ubrogepant in the Acute Treatment of… | Phase3 | Migraine, With or Without Aura | Completed | 2016-08-26 | 2018-02-26 | ClinicalTrials.gov |
| NCT02867709 | Efficacy, Safety, and Tolerability of Oral Ubrogepant in the Acute Treatment of… | Phase3 | Migraine, With or Without Aura | Completed | 2016-08-26 | 2018-02-26 | ClinicalTrials.gov |
| NCT02867709 | Efficacy, Safety, and Tolerability of Oral Ubrogepant in the Acute Treatment of… | Phase3 | Migraine, With or Without Aura | Completed | 2016-08-26 | 2018-02-26 | ClinicalTrials.gov |
| NCT03200912 | An Equivalence Study of Generic Ingenol Mebutate Gel 0.015% and Picato Gel 0.01… | Phase3 | ACTINIC KERATOSIS | Completed | 2016-08-19 | 2017-03-22 | ClinicalTrials.gov |
| NCT03200912 | An Equivalence Study of Generic Ingenol Mebutate Gel 0.015% and Picato Gel 0.01… | Phase3 | ACTINIC KERATOSIS | Completed | 2016-08-19 | 2017-03-22 | ClinicalTrials.gov |
| NCT03200912 | An Equivalence Study of Generic Ingenol Mebutate Gel 0.015% and Picato Gel 0.01… | Phase3 | ACTINIC KERATOSIS | Completed | 2016-08-19 | 2017-03-22 | ClinicalTrials.gov |
| NCT03200912 | An Equivalence Study of Generic Ingenol Mebutate Gel 0.015% and Picato Gel 0.01… | Phase3 | ACTINIC KERATOSIS | Completed | 2016-08-19 | 2017-03-22 | ClinicalTrials.gov |
| NCT02726581 | An Investigational Immuno-therapy Study of Nivolumab, Pomalidomide and Dexameth… | Phase3 | Multiple Myeloma | Completed | 2016-08-10 | 2022-03-09 | ClinicalTrials.gov |
| NCT02726581 | An Investigational Immuno-therapy Study of Nivolumab, Pomalidomide and Dexameth… | Phase3 | Multiple Myeloma | Completed | 2016-08-10 | 2022-03-09 | ClinicalTrials.gov |
| NCT02726581 | An Investigational Immuno-therapy Study of Nivolumab, Pomalidomide and Dexameth… | Phase3 | Multiple Myeloma | Completed | 2016-08-10 | 2022-03-09 | ClinicalTrials.gov |
| NCT02726581 | An Investigational Immuno-therapy Study of Nivolumab, Pomalidomide and Dexameth… | Phase3 | Multiple Myeloma | Completed | 2016-08-10 | 2022-03-09 | ClinicalTrials.gov |
| NCT02478320 | Phase II Study of Ilorasertib (ABT348) in Patients With CDKN2A Deficient Solid … | Phase2 | Advanced Cancers | Terminated | 2016-08-05 | 2022-05-12 | ClinicalTrials.gov |
| NCT02478320 | Phase II Study of Ilorasertib (ABT348) in Patients With CDKN2A Deficient Solid … | Phase2 | Advanced Cancers | Terminated | 2016-08-05 | 2022-05-12 | ClinicalTrials.gov |
| NCT02814175 | A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness o… | Phase4 | Psoriatic Arthritis | Completed | 2016-08-05 | 2020-03-19 | ClinicalTrials.gov |
| NCT02478320 | Phase II Study of Ilorasertib (ABT348) in Patients With CDKN2A Deficient Solid … | Phase2 | Advanced Cancers | Terminated | 2016-08-05 | 2022-05-12 | ClinicalTrials.gov |
| NCT02814175 | A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness o… | Phase4 | Psoriatic Arthritis | Completed | 2016-08-05 | 2020-03-19 | ClinicalTrials.gov |
| NCT02814175 | A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness o… | Phase4 | Psoriatic Arthritis | Completed | 2016-08-05 | 2020-03-19 | ClinicalTrials.gov |
| NCT02814175 | A Study of Subjects With Psoriatic Arthritis to Investigate the Effectiveness o… | Phase4 | Psoriatic Arthritis | Completed | 2016-08-05 | 2020-03-19 | ClinicalTrials.gov |
| NCT02478320 | Phase II Study of Ilorasertib (ABT348) in Patients With CDKN2A Deficient Solid … | Phase2 | Advanced Cancers | Terminated | 2016-08-05 | 2022-05-12 | ClinicalTrials.gov |
| NCT04084145 | National Unified Renal Translation Research Enterprise - Chronic Kidney Disease | — | Chronic Kidney Diseases | Active_Not_Recruiting | 2016-07-27 | 2032-12-31 | ClinicalTrials.gov |
| NCT04084145 | National Unified Renal Translation Research Enterprise - Chronic Kidney Disease | — | Chronic Kidney Diseases | Active_Not_Recruiting | 2016-07-27 | 2032-12-31 | ClinicalTrials.gov |
| NCT04084145 | National Unified Renal Translation Research Enterprise - Chronic Kidney Disease | — | Chronic Kidney Diseases | Active_Not_Recruiting | 2016-07-27 | 2032-12-31 | ClinicalTrials.gov |
| NCT04084145 | National Unified Renal Translation Research Enterprise - Chronic Kidney Disease | — | Chronic Kidney Diseases | Active_Not_Recruiting | 2016-07-27 | 2032-12-31 | ClinicalTrials.gov |
| NCT02828020 | Efficacy, Safety, and Tolerability Study of Oral Ubrogepant in the Acute Treatm… | Phase3 | Migraine, With or Without Aura | Completed | 2016-07-22 | 2017-12-14 | ClinicalTrials.gov |
| NCT02828020 | Efficacy, Safety, and Tolerability Study of Oral Ubrogepant in the Acute Treatm… | Phase3 | Migraine, With or Without Aura | Completed | 2016-07-22 | 2017-12-14 | ClinicalTrials.gov |
| NCT02828020 | Efficacy, Safety, and Tolerability Study of Oral Ubrogepant in the Acute Treatm… | Phase3 | Migraine, With or Without Aura | Completed | 2016-07-22 | 2017-12-14 | ClinicalTrials.gov |
| NCT02828020 | Efficacy, Safety, and Tolerability Study of Oral Ubrogepant in the Acute Treatm… | Phase3 | Migraine, With or Without Aura | Completed | 2016-07-22 | 2017-12-14 | ClinicalTrials.gov |
| NCT03287791 | A Study to Evaluate Safety and Equivalence of Generic Azelaic Acid Foam and Fin… | Phase3 | Rosacea | Completed | 2016-07-19 | 2017-06-22 | ClinicalTrials.gov |
| NCT03287791 | A Study to Evaluate Safety and Equivalence of Generic Azelaic Acid Foam and Fin… | Phase3 | Rosacea | Completed | 2016-07-19 | 2017-06-22 | ClinicalTrials.gov |
| NCT03287791 | A Study to Evaluate Safety and Equivalence of Generic Azelaic Acid Foam and Fin… | Phase3 | Rosacea | Completed | 2016-07-19 | 2017-06-22 | ClinicalTrials.gov |
| NCT03287791 | A Study to Evaluate Safety and Equivalence of Generic Azelaic Acid Foam and Fin… | Phase3 | Rosacea | Completed | 2016-07-19 | 2017-06-22 | ClinicalTrials.gov |
| NCT02808975 | Safety and Efficacy of Adalimumab (Humira) for Hidradenitis Suppurativa (HS) Pe… | Phase4 | Hidradenitis Suppurativa (HS) | Completed | 2016-07-18 | 2019-10-16 | ClinicalTrials.gov |
| NCT02808975 | Safety and Efficacy of Adalimumab (Humira) for Hidradenitis Suppurativa (HS) Pe… | Phase4 | Hidradenitis Suppurativa (HS) | Completed | 2016-07-18 | 2019-10-16 | ClinicalTrials.gov |
| NCT02808975 | Safety and Efficacy of Adalimumab (Humira) for Hidradenitis Suppurativa (HS) Pe… | Phase4 | Hidradenitis Suppurativa (HS) | Completed | 2016-07-18 | 2019-10-16 | ClinicalTrials.gov |
| NCT02808975 | Safety and Efficacy of Adalimumab (Humira) for Hidradenitis Suppurativa (HS) Pe… | Phase4 | Hidradenitis Suppurativa (HS) | Completed | 2016-07-18 | 2019-10-16 | ClinicalTrials.gov |
| NCT02719613 | Continuing Treatment for Participants Who Have Participated in a Prior Protocol… | Phase2 | Multiple Myeloma | Completed | 2016-07-15 | 2026-02-23 | ClinicalTrials.gov |
| NCT02719613 | Continuing Treatment for Participants Who Have Participated in a Prior Protocol… | Phase2 | Multiple Myeloma | Completed | 2016-07-15 | 2026-02-23 | ClinicalTrials.gov |
| NCT02719613 | Continuing Treatment for Participants Who Have Participated in a Prior Protocol… | Phase2 | Multiple Myeloma | Completed | 2016-07-15 | 2026-02-23 | ClinicalTrials.gov |
| NCT02719613 | Continuing Treatment for Participants Who Have Participated in a Prior Protocol… | Phase2 | Multiple Myeloma | Completed | 2016-07-15 | 2026-02-23 | ClinicalTrials.gov |
| NCT02807402 | Effectiveness of Paritaprevir/Ritonavir, Ombitasvir, + Dasabuvir, ± Ribavirin i… | — | Chronic Hepatitis C | Completed | 2016-07-14 | 2017-08-04 | ClinicalTrials.gov |
| NCT02807402 | Effectiveness of Paritaprevir/Ritonavir, Ombitasvir, + Dasabuvir, ± Ribavirin i… | — | Chronic Hepatitis C | Completed | 2016-07-14 | 2017-08-04 | ClinicalTrials.gov |
| NCT02807402 | Effectiveness of Paritaprevir/Ritonavir, Ombitasvir, + Dasabuvir, ± Ribavirin i… | — | Chronic Hepatitis C | Completed | 2016-07-14 | 2017-08-04 | ClinicalTrials.gov |
| NCT02807402 | Effectiveness of Paritaprevir/Ritonavir, Ombitasvir, + Dasabuvir, ± Ribavirin i… | — | Chronic Hepatitis C | Completed | 2016-07-14 | 2017-08-04 | ClinicalTrials.gov |
| NCT02755597 | A Study Evaluating Venetoclax (ABT-199) in Multiple Myeloma Subjects Who Are Re… | Phase3 | Relapsed/Refractory Multiple Myeloma | Completed | 2016-07-11 | 2022-08-15 | ClinicalTrials.gov |
| NCT02755597 | A Study Evaluating Venetoclax (ABT-199) in Multiple Myeloma Subjects Who Are Re… | Phase3 | Relapsed/Refractory Multiple Myeloma | Completed | 2016-07-11 | 2022-08-15 | ClinicalTrials.gov |
| NCT02755597 | A Study Evaluating Venetoclax (ABT-199) in Multiple Myeloma Subjects Who Are Re… | Phase3 | Relapsed/Refractory Multiple Myeloma | Completed | 2016-07-11 | 2022-08-15 | ClinicalTrials.gov |
| NCT02755597 | A Study Evaluating Venetoclax (ABT-199) in Multiple Myeloma Subjects Who Are Re… | Phase3 | Relapsed/Refractory Multiple Myeloma | Completed | 2016-07-11 | 2022-08-15 | ClinicalTrials.gov |
| NCT02803138 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-07-07 | 2018-10-21 | ClinicalTrials.gov |
| NCT02803138 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-07-07 | 2018-10-21 | ClinicalTrials.gov |
| NCT02803138 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-07-07 | 2018-10-21 | ClinicalTrials.gov |
| NCT02803138 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-07-07 | 2018-10-21 | ClinicalTrials.gov |
| NCT02863705 | Efficacy and Safety of COMBIGAN® in Korean Patients With Primary Open Angle Gla… | Phase4 | Glaucoma, Open-Angle | Completed | 2016-07-05 | 2018-07-25 | ClinicalTrials.gov |
| NCT02863705 | Efficacy and Safety of COMBIGAN® in Korean Patients With Primary Open Angle Gla… | Phase4 | Glaucoma, Open-Angle | Completed | 2016-07-05 | 2018-07-25 | ClinicalTrials.gov |
| NCT02863705 | Efficacy and Safety of COMBIGAN® in Korean Patients With Primary Open Angle Gla… | Phase4 | Glaucoma, Open-Angle | Completed | 2016-07-05 | 2018-07-25 | ClinicalTrials.gov |
| NCT02863705 | Efficacy and Safety of COMBIGAN® in Korean Patients With Primary Open Angle Gla… | Phase4 | Glaucoma, Open-Angle | Completed | 2016-07-05 | 2018-07-25 | ClinicalTrials.gov |
| NCT02786576 | Effectiveness of Adalimumab in Moderate to Severe HidrAdenitis SuppuRativa Pati… | — | Hidradenitis Suppurativa | Completed | 2016-07-05 | 2019-01-07 | ClinicalTrials.gov |
| NCT02786576 | Effectiveness of Adalimumab in Moderate to Severe HidrAdenitis SuppuRativa Pati… | — | Hidradenitis Suppurativa | Completed | 2016-07-05 | 2019-01-07 | ClinicalTrials.gov |
| NCT02786576 | Effectiveness of Adalimumab in Moderate to Severe HidrAdenitis SuppuRativa Pati… | — | Hidradenitis Suppurativa | Completed | 2016-07-05 | 2019-01-07 | ClinicalTrials.gov |
| NCT02786576 | Effectiveness of Adalimumab in Moderate to Severe HidrAdenitis SuppuRativa Pati… | — | Hidradenitis Suppurativa | Completed | 2016-07-05 | 2019-01-07 | ClinicalTrials.gov |
| NCT02640833 | A Study of Duvelisib and Venetoclax in Subjects With Relapsed or Refractory Chr… | Phase1 | Chronic Lymphocytic Leukemia | Withdrawn | 2016-07-01 | 2021-02-01 | ClinicalTrials.gov |
| NCT02848300 | Local Pharmacokinetics and Tolerability of Bimatoprost Applied to the Scalp of … | Phase1 | Androgenetic Alopecia | Completed | 2016-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02848300 | Local Pharmacokinetics and Tolerability of Bimatoprost Applied to the Scalp of … | Phase1 | Androgenetic Alopecia | Completed | 2016-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02640833 | A Study of Duvelisib and Venetoclax in Subjects With Relapsed or Refractory Chr… | Phase1 | Chronic Lymphocytic Leukemia | Withdrawn | 2016-07-01 | 2021-02-01 | ClinicalTrials.gov |
| NCT02640833 | A Study of Duvelisib and Venetoclax in Subjects With Relapsed or Refractory Chr… | Phase1 | Chronic Lymphocytic Leukemia | Withdrawn | 2016-07-01 | 2021-02-01 | ClinicalTrials.gov |
| NCT02848300 | Local Pharmacokinetics and Tolerability of Bimatoprost Applied to the Scalp of … | Phase1 | Androgenetic Alopecia | Completed | 2016-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02640833 | A Study of Duvelisib and Venetoclax in Subjects With Relapsed or Refractory Chr… | Phase1 | Chronic Lymphocytic Leukemia | Withdrawn | 2016-07-01 | 2021-02-01 | ClinicalTrials.gov |
| NCT02848300 | Local Pharmacokinetics and Tolerability of Bimatoprost Applied to the Scalp of … | Phase1 | Androgenetic Alopecia | Completed | 2016-07-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02555982 | Evaluation of Botulinum Toxin Injection Efficacy in the Treatment of Head Essen… | Phase3 | Essential Head Tremor | Completed | 2016-06-27 | 2022-09-01 | ClinicalTrials.gov |
| NCT02555982 | Evaluation of Botulinum Toxin Injection Efficacy in the Treatment of Head Essen… | Phase3 | Essential Head Tremor | Completed | 2016-06-27 | 2022-09-01 | ClinicalTrials.gov |
| NCT02555982 | Evaluation of Botulinum Toxin Injection Efficacy in the Treatment of Head Essen… | Phase3 | Essential Head Tremor | Completed | 2016-06-27 | 2022-09-01 | ClinicalTrials.gov |
| NCT02555982 | Evaluation of Botulinum Toxin Injection Efficacy in the Treatment of Head Essen… | Phase3 | Essential Head Tremor | Completed | 2016-06-27 | 2022-09-01 | ClinicalTrials.gov |
| NCT02756611 | A Study to Evaluate the Efficacy of Venetoclax Monotherapy in Relapsed/Refracto… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2016-06-22 | 2022-03-11 | ClinicalTrials.gov |
| NCT02756611 | A Study to Evaluate the Efficacy of Venetoclax Monotherapy in Relapsed/Refracto… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2016-06-22 | 2022-03-11 | ClinicalTrials.gov |
| NCT02756611 | A Study to Evaluate the Efficacy of Venetoclax Monotherapy in Relapsed/Refracto… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2016-06-22 | 2022-03-11 | ClinicalTrials.gov |
| NCT02756611 | A Study to Evaluate the Efficacy of Venetoclax Monotherapy in Relapsed/Refracto… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2016-06-22 | 2022-03-11 | ClinicalTrials.gov |
| NCT02713295 | A Study to Provide Real-world Evidence on the Treatment Goal Achievement Rate, … | — | Moderate to Severe Plaque Psoriasis | Completed | 2016-06-16 | 2019-04-19 | ClinicalTrials.gov |
| NCT02713295 | A Study to Provide Real-world Evidence on the Treatment Goal Achievement Rate, … | — | Moderate to Severe Plaque Psoriasis | Completed | 2016-06-16 | 2019-04-19 | ClinicalTrials.gov |
| NCT02713295 | A Study to Provide Real-world Evidence on the Treatment Goal Achievement Rate, … | — | Moderate to Severe Plaque Psoriasis | Completed | 2016-06-16 | 2019-04-19 | ClinicalTrials.gov |
| NCT02713295 | A Study to Provide Real-world Evidence on the Treatment Goal Achievement Rate, … | — | Moderate to Severe Plaque Psoriasis | Completed | 2016-06-16 | 2019-04-19 | ClinicalTrials.gov |
| NCT02840461 | Clinical Endpoint Study of Ivermectin 1% Cream | Phase3 | Moderate to Severe Papulopustular Rosacea | Completed | 2016-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02786537 | Study of Oral Treatments for Hepatitis C | Phase4 | Chronic Hepatitis C | Completed | 2016-06-01 | 2020-09-02 | ClinicalTrials.gov |
| NCT02634008 | Treatment of Recently Acquired Hepatitis C With the 3D Regimen or G/P | Phase3 | Hepatitis C, Acute | Completed | 2016-06-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT02634008 | Treatment of Recently Acquired Hepatitis C With the 3D Regimen or G/P | Phase3 | Hepatitis C, Acute | Completed | 2016-06-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT02840461 | Clinical Endpoint Study of Ivermectin 1% Cream | Phase3 | Moderate to Severe Papulopustular Rosacea | Completed | 2016-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02840461 | Clinical Endpoint Study of Ivermectin 1% Cream | Phase3 | Moderate to Severe Papulopustular Rosacea | Completed | 2016-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02786537 | Study of Oral Treatments for Hepatitis C | Phase4 | Chronic Hepatitis C | Completed | 2016-06-01 | 2020-09-02 | ClinicalTrials.gov |
| NCT02786537 | Study of Oral Treatments for Hepatitis C | Phase4 | Chronic Hepatitis C | Completed | 2016-06-01 | 2020-09-02 | ClinicalTrials.gov |
| NCT02786537 | Study of Oral Treatments for Hepatitis C | Phase4 | Chronic Hepatitis C | Completed | 2016-06-01 | 2020-09-02 | ClinicalTrials.gov |
| NCT02634008 | Treatment of Recently Acquired Hepatitis C With the 3D Regimen or G/P | Phase3 | Hepatitis C, Acute | Completed | 2016-06-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT02634008 | Treatment of Recently Acquired Hepatitis C With the 3D Regimen or G/P | Phase3 | Hepatitis C, Acute | Completed | 2016-06-01 | 2021-04-30 | ClinicalTrials.gov |
| NCT02840461 | Clinical Endpoint Study of Ivermectin 1% Cream | Phase3 | Moderate to Severe Papulopustular Rosacea | Completed | 2016-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02780115 | A Safety, Efficacy and Pharmacokinetic Study of AGN-199201 and AGN-190584 in Pa… | Phase2 | Presbyopia | Completed | 2016-05-26 | 2017-10-31 | ClinicalTrials.gov |
| NCT02780115 | A Safety, Efficacy and Pharmacokinetic Study of AGN-199201 and AGN-190584 in Pa… | Phase2 | Presbyopia | Completed | 2016-05-26 | 2017-10-31 | ClinicalTrials.gov |
| NCT02780115 | A Safety, Efficacy and Pharmacokinetic Study of AGN-199201 and AGN-190584 in Pa… | Phase2 | Presbyopia | Completed | 2016-05-26 | 2017-10-31 | ClinicalTrials.gov |
| NCT02780115 | A Safety, Efficacy and Pharmacokinetic Study of AGN-199201 and AGN-190584 in Pa… | Phase2 | Presbyopia | Completed | 2016-05-26 | 2017-10-31 | ClinicalTrials.gov |
| NCT02798315 | Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patie… | — | Chronic Hepatitis C | Completed | 2016-05-25 | 2017-06-12 | ClinicalTrials.gov |
| NCT02798315 | Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patie… | — | Chronic Hepatitis C | Completed | 2016-05-25 | 2017-06-12 | ClinicalTrials.gov |
| NCT02798315 | Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patie… | — | Chronic Hepatitis C | Completed | 2016-05-25 | 2017-06-12 | ClinicalTrials.gov |
| NCT02798315 | Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patie… | — | Chronic Hepatitis C | Completed | 2016-05-25 | 2017-06-12 | ClinicalTrials.gov |
| NCT02782663 | A Study to Evaluate the Long-Term Efficacy, Safety, and Tolerability of Repeate… | Phase2 | Crohn's Disease (CD) | Completed | 2016-05-18 | 2025-07-18 | ClinicalTrials.gov |
| NCT02782663 | A Study to Evaluate the Long-Term Efficacy, Safety, and Tolerability of Repeate… | Phase2 | Crohn's Disease (CD) | Completed | 2016-05-18 | 2025-07-18 | ClinicalTrials.gov |
| NCT02782663 | A Study to Evaluate the Long-Term Efficacy, Safety, and Tolerability of Repeate… | Phase2 | Crohn's Disease (CD) | Completed | 2016-05-18 | 2025-07-18 | ClinicalTrials.gov |
| NCT03294538 | Study to Evaluate Equivalence of Estradiol Vaginal Cream 0.01% to Estrace® Crea… | Phase3 | Atrophic Vaginitis | Completed | 2016-05-18 | 2017-02-15 | ClinicalTrials.gov |
| NCT03294538 | Study to Evaluate Equivalence of Estradiol Vaginal Cream 0.01% to Estrace® Crea… | Phase3 | Atrophic Vaginitis | Completed | 2016-05-18 | 2017-02-15 | ClinicalTrials.gov |
| NCT02782663 | A Study to Evaluate the Long-Term Efficacy, Safety, and Tolerability of Repeate… | Phase2 | Crohn's Disease (CD) | Completed | 2016-05-18 | 2025-07-18 | ClinicalTrials.gov |
| NCT03294538 | Study to Evaluate Equivalence of Estradiol Vaginal Cream 0.01% to Estrace® Crea… | Phase3 | Atrophic Vaginitis | Completed | 2016-05-18 | 2017-02-15 | ClinicalTrials.gov |
| NCT03294538 | Study to Evaluate Equivalence of Estradiol Vaginal Cream 0.01% to Estrace® Crea… | Phase3 | Atrophic Vaginitis | Completed | 2016-05-18 | 2017-02-15 | ClinicalTrials.gov |
| NCT02738138 | A Study to Evaluate the Efficacy and Safety of Experimental Drugs ABT- 493/ABT-… | Phase3 | Hepatitis C Virus Infection | Completed | 2016-05-17 | 2017-06-07 | ClinicalTrials.gov |
| NCT02738138 | A Study to Evaluate the Efficacy and Safety of Experimental Drugs ABT- 493/ABT-… | Phase3 | Hepatitis C Virus Infection | Completed | 2016-05-17 | 2017-06-07 | ClinicalTrials.gov |
| NCT02738138 | A Study to Evaluate the Efficacy and Safety of Experimental Drugs ABT- 493/ABT-… | Phase3 | Hepatitis C Virus Infection | Completed | 2016-05-17 | 2017-06-07 | ClinicalTrials.gov |
| NCT02738138 | A Study to Evaluate the Efficacy and Safety of Experimental Drugs ABT- 493/ABT-… | Phase3 | Hepatitis C Virus Infection | Completed | 2016-05-17 | 2017-06-07 | ClinicalTrials.gov |
| NCT02677324 | Study of ABT-199 (GDC-199) In Patients With Relapsed Or Refractory Waldenström … | Phase2 | Waldenstrom Macroglobulinemia | Completed | 2016-05-09 | 2022-02-07 | ClinicalTrials.gov |
| NCT02677324 | Study of ABT-199 (GDC-199) In Patients With Relapsed Or Refractory Waldenström … | Phase2 | Waldenstrom Macroglobulinemia | Completed | 2016-05-09 | 2022-02-07 | ClinicalTrials.gov |
| NCT02677324 | Study of ABT-199 (GDC-199) In Patients With Relapsed Or Refractory Waldenström … | Phase2 | Waldenstrom Macroglobulinemia | Completed | 2016-05-09 | 2022-02-07 | ClinicalTrials.gov |
| NCT02677324 | Study of ABT-199 (GDC-199) In Patients With Relapsed Or Refractory Waldenström … | Phase2 | Waldenstrom Macroglobulinemia | Completed | 2016-05-09 | 2022-02-07 | ClinicalTrials.gov |
| NCT02750384 | Bioavailability and Effect of Food on DSM265 Granules in Healthy Adult Subjects | Phase1 | Healthy Volunteers | Terminated | 2016-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02750384 | Bioavailability and Effect of Food on DSM265 Granules in Healthy Adult Subjects | Phase1 | Healthy Volunteers | Terminated | 2016-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02750384 | Bioavailability and Effect of Food on DSM265 Granules in Healthy Adult Subjects | Phase1 | Healthy Volunteers | Terminated | 2016-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02668640 | Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in China | — | Rheumatoid Arthritis | Completed | 2016-05-01 | 2018-08-13 | ClinicalTrials.gov |
| NCT02668640 | Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in China | — | Rheumatoid Arthritis | Completed | 2016-05-01 | 2018-08-13 | ClinicalTrials.gov |
| NCT02668640 | Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in China | — | Rheumatoid Arthritis | Completed | 2016-05-01 | 2018-08-13 | ClinicalTrials.gov |
| NCT02668640 | Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in China | — | Rheumatoid Arthritis | Completed | 2016-05-01 | 2018-08-13 | ClinicalTrials.gov |
| NCT02750384 | Bioavailability and Effect of Food on DSM265 Granules in Healthy Adult Subjects | Phase1 | Healthy Volunteers | Terminated | 2016-05-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02738125 | Assessing Effectiveness of Adalimumab for Treating Ulcerative Colitis in Real L… | — | Ulcerative Colitis (UC) | Completed | 2016-04-29 | 2023-12-15 | ClinicalTrials.gov |
| NCT02738125 | Assessing Effectiveness of Adalimumab for Treating Ulcerative Colitis in Real L… | — | Ulcerative Colitis (UC) | Completed | 2016-04-29 | 2023-12-15 | ClinicalTrials.gov |
| NCT02738125 | Assessing Effectiveness of Adalimumab for Treating Ulcerative Colitis in Real L… | — | Ulcerative Colitis (UC) | Completed | 2016-04-29 | 2023-12-15 | ClinicalTrials.gov |
| NCT02595528 | A Study of the Concurrent Use of AGN-190584 and AGN-199201 in Participants With… | Phase2 | Presbyopia | Completed | 2016-04-29 | 2017-10-18 | ClinicalTrials.gov |
| NCT02595528 | A Study of the Concurrent Use of AGN-190584 and AGN-199201 in Participants With… | Phase2 | Presbyopia | Completed | 2016-04-29 | 2017-10-18 | ClinicalTrials.gov |
| NCT02595528 | A Study of the Concurrent Use of AGN-190584 and AGN-199201 in Participants With… | Phase2 | Presbyopia | Completed | 2016-04-29 | 2017-10-18 | ClinicalTrials.gov |
| NCT02738125 | Assessing Effectiveness of Adalimumab for Treating Ulcerative Colitis in Real L… | — | Ulcerative Colitis (UC) | Completed | 2016-04-29 | 2023-12-15 | ClinicalTrials.gov |
| NCT02595528 | A Study of the Concurrent Use of AGN-190584 and AGN-199201 in Participants With… | Phase2 | Presbyopia | Completed | 2016-04-29 | 2017-10-18 | ClinicalTrials.gov |
| NCT02692703 | A Study to Evaluate the Safety and Efficacy of ABT-493/ABT-530 in Adult Post-Li… | Phase3 | Chronic Hepatitis C | Completed | 2016-04-22 | 2017-06-29 | ClinicalTrials.gov |
| NCT02692703 | A Study to Evaluate the Safety and Efficacy of ABT-493/ABT-530 in Adult Post-Li… | Phase3 | Chronic Hepatitis C | Completed | 2016-04-22 | 2017-06-29 | ClinicalTrials.gov |
| NCT02692703 | A Study to Evaluate the Safety and Efficacy of ABT-493/ABT-530 in Adult Post-Li… | Phase3 | Chronic Hepatitis C | Completed | 2016-04-22 | 2017-06-29 | ClinicalTrials.gov |
| NCT02692703 | A Study to Evaluate the Safety and Efficacy of ABT-493/ABT-530 in Adult Post-Li… | Phase3 | Chronic Hepatitis C | Completed | 2016-04-22 | 2017-06-29 | ClinicalTrials.gov |
| NCT02669940 | Observational, Multi-Center Study of the Real World Evidence of the Effectivene… | — | Chronic Hepatitis C | Completed | 2016-04-15 | 2017-07-04 | ClinicalTrials.gov |
| NCT02669940 | Observational, Multi-Center Study of the Real World Evidence of the Effectivene… | — | Chronic Hepatitis C | Completed | 2016-04-15 | 2017-07-04 | ClinicalTrials.gov |
| NCT02669940 | Observational, Multi-Center Study of the Real World Evidence of the Effectivene… | — | Chronic Hepatitis C | Completed | 2016-04-15 | 2017-07-04 | ClinicalTrials.gov |
| NCT02669940 | Observational, Multi-Center Study of the Real World Evidence of the Effectivene… | — | Chronic Hepatitis C | Completed | 2016-04-15 | 2017-07-04 | ClinicalTrials.gov |
| NCT02723084 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adul… | Phase3 | Chronic Hepatitis C Virus | Completed | 2016-04-08 | 2017-03-24 | ClinicalTrials.gov |
| NCT02723084 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adul… | Phase3 | Chronic Hepatitis C Virus | Completed | 2016-04-08 | 2017-03-24 | ClinicalTrials.gov |
| NCT02723084 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adul… | Phase3 | Chronic Hepatitis C Virus | Completed | 2016-04-08 | 2017-03-24 | ClinicalTrials.gov |
| NCT02723084 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adul… | Phase3 | Chronic Hepatitis C Virus | Completed | 2016-04-08 | 2017-03-24 | ClinicalTrials.gov |
| NCT02750800 | Post-marketing Observational Study to Evaluate the Incremental Impact of AbbVie… | — | Rheumatoid Arthritis | Completed | 2016-04-07 | 2018-04-03 | ClinicalTrials.gov |
| NCT02750800 | Post-marketing Observational Study to Evaluate the Incremental Impact of AbbVie… | — | Rheumatoid Arthritis | Completed | 2016-04-07 | 2018-04-03 | ClinicalTrials.gov |
| NCT02750800 | Post-marketing Observational Study to Evaluate the Incremental Impact of AbbVie… | — | Rheumatoid Arthritis | Completed | 2016-04-07 | 2018-04-03 | ClinicalTrials.gov |
| NCT02739828 | Post Marketing Observational Study (PMOS) to Assess Quality of Life in Swedish … | — | Hidradenitis Suppurativa | Completed | 2016-04-07 | 2018-03-28 | ClinicalTrials.gov |
| NCT02739828 | Post Marketing Observational Study (PMOS) to Assess Quality of Life in Swedish … | — | Hidradenitis Suppurativa | Completed | 2016-04-07 | 2018-03-28 | ClinicalTrials.gov |
| NCT02750800 | Post-marketing Observational Study to Evaluate the Incremental Impact of AbbVie… | — | Rheumatoid Arthritis | Completed | 2016-04-07 | 2018-04-03 | ClinicalTrials.gov |
| NCT02739828 | Post Marketing Observational Study (PMOS) to Assess Quality of Life in Swedish … | — | Hidradenitis Suppurativa | Completed | 2016-04-07 | 2018-03-28 | ClinicalTrials.gov |
| NCT02739828 | Post Marketing Observational Study (PMOS) to Assess Quality of Life in Swedish … | — | Hidradenitis Suppurativa | Completed | 2016-04-07 | 2018-03-28 | ClinicalTrials.gov |
| NCT02725866 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-04-05 | 2017-10-31 | ClinicalTrials.gov |
| NCT02725866 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-04-05 | 2017-10-31 | ClinicalTrials.gov |
| NCT02725866 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-04-05 | 2017-10-31 | ClinicalTrials.gov |
| NCT02725866 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-04-05 | 2017-10-31 | ClinicalTrials.gov |
| NCT02719171 | BI 655066/ABBV-066/Risankizumab Compared to Placebo in Patients With Active Pso… | Phase2 | Arthritis, Psoriatic | Completed | 2016-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02719171 | BI 655066/ABBV-066/Risankizumab Compared to Placebo in Patients With Active Pso… | Phase2 | Arthritis, Psoriatic | Completed | 2016-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02688790 | Study Evaluate the PK Profile of Dalbavancin in Infants and Neonates Patients W… | Phase1 | Bacterial Infections | Terminated | 2016-04-01 | 2019-04-03 | ClinicalTrials.gov |
| NCT02719171 | BI 655066/ABBV-066/Risankizumab Compared to Placebo in Patients With Active Pso… | Phase2 | Arthritis, Psoriatic | Completed | 2016-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02719171 | BI 655066/ABBV-066/Risankizumab Compared to Placebo in Patients With Active Pso… | Phase2 | Arthritis, Psoriatic | Completed | 2016-04-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02688790 | Study Evaluate the PK Profile of Dalbavancin in Infants and Neonates Patients W… | Phase1 | Bacterial Infections | Terminated | 2016-04-01 | 2019-04-03 | ClinicalTrials.gov |
| NCT03241563 | Subcutaneous Sodium Deoxycholate Injections With or Without Triamcinolone for R… | Phase4 | Fat Reduction | Completed | 2016-04-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT03241563 | Subcutaneous Sodium Deoxycholate Injections With or Without Triamcinolone for R… | Phase4 | Fat Reduction | Completed | 2016-04-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02688790 | Study Evaluate the PK Profile of Dalbavancin in Infants and Neonates Patients W… | Phase1 | Bacterial Infections | Terminated | 2016-04-01 | 2019-04-03 | ClinicalTrials.gov |
| NCT03241563 | Subcutaneous Sodium Deoxycholate Injections With or Without Triamcinolone for R… | Phase4 | Fat Reduction | Completed | 2016-04-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02688790 | Study Evaluate the PK Profile of Dalbavancin in Infants and Neonates Patients W… | Phase1 | Bacterial Infections | Terminated | 2016-04-01 | 2019-04-03 | ClinicalTrials.gov |
| NCT03241563 | Subcutaneous Sodium Deoxycholate Injections With or Without Triamcinolone for R… | Phase4 | Fat Reduction | Completed | 2016-04-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02706951 | A Study Comparing Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Mono… | Phase3 | Rheumatoid Arthritis | Completed | 2016-03-23 | 2022-08-10 | ClinicalTrials.gov |
| NCT02706951 | A Study Comparing Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Mono… | Phase3 | Rheumatoid Arthritis | Completed | 2016-03-23 | 2022-08-10 | ClinicalTrials.gov |
| NCT02706951 | A Study Comparing Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Mono… | Phase3 | Rheumatoid Arthritis | Completed | 2016-03-23 | 2022-08-10 | ClinicalTrials.gov |
| NCT02706951 | A Study Comparing Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Mono… | Phase3 | Rheumatoid Arthritis | Completed | 2016-03-23 | 2022-08-10 | ClinicalTrials.gov |
| NCT02720523 | A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid … | Phase2 | Rheumatoid Arthritis | Completed | 2016-03-22 | 2022-06-07 | ClinicalTrials.gov |
| NCT02720523 | A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid … | Phase2 | Rheumatoid Arthritis | Completed | 2016-03-22 | 2022-06-07 | ClinicalTrials.gov |
| NCT02720523 | A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid … | Phase2 | Rheumatoid Arthritis | Completed | 2016-03-22 | 2022-06-07 | ClinicalTrials.gov |
| NCT02720523 | A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid … | Phase2 | Rheumatoid Arthritis | Completed | 2016-03-22 | 2022-06-07 | ClinicalTrials.gov |
| NCT02654132 | An Investigational Immuno-therapy Trial of Pomalidomide and Low-dose Dexamethas… | Phase2 | Multiple Myeloma | Completed | 2016-03-18 | 2021-10-21 | ClinicalTrials.gov |
| NCT02654132 | An Investigational Immuno-therapy Trial of Pomalidomide and Low-dose Dexamethas… | Phase2 | Multiple Myeloma | Completed | 2016-03-18 | 2021-10-21 | ClinicalTrials.gov |
| NCT02654132 | An Investigational Immuno-therapy Trial of Pomalidomide and Low-dose Dexamethas… | Phase2 | Multiple Myeloma | Completed | 2016-03-18 | 2021-10-21 | ClinicalTrials.gov |
| NCT02654132 | An Investigational Immuno-therapy Trial of Pomalidomide and Low-dose Dexamethas… | Phase2 | Multiple Myeloma | Completed | 2016-03-18 | 2021-10-21 | ClinicalTrials.gov |
| NCT02706847 | A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid … | Phase3 | Rheumatoid Arthritis | Completed | 2016-03-15 | 2022-02-08 | ClinicalTrials.gov |
| NCT02706847 | A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid … | Phase3 | Rheumatoid Arthritis | Completed | 2016-03-15 | 2022-02-08 | ClinicalTrials.gov |
| NCT02706847 | A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid … | Phase3 | Rheumatoid Arthritis | Completed | 2016-03-15 | 2022-02-08 | ClinicalTrials.gov |
| NCT02706847 | A Study to Compare Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid … | Phase3 | Rheumatoid Arthritis | Completed | 2016-03-15 | 2022-02-08 | ClinicalTrials.gov |
| NCT03052231 | Interactive Mobile Health Information to Enhance Patient Care at a Cystic Fibro… | Na | Medication Adherence | Completed | 2016-03-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02676310 | Safety, Tolerability, and Pharmacokinetics of Bimatoprost in Men With Androgene… | Phase1 | Alopecia | Terminated | 2016-03-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02684357 | BI 655066 Versus Placebo & Active Comparator (Ustekinumab) in Patients With Mod… | Phase3 | Psoriasis | Completed | 2016-03-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02684357 | BI 655066 Versus Placebo & Active Comparator (Ustekinumab) in Patients With Mod… | Phase3 | Psoriasis | Completed | 2016-03-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT03052231 | Interactive Mobile Health Information to Enhance Patient Care at a Cystic Fibro… | Na | Medication Adherence | Completed | 2016-03-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02684357 | BI 655066 Versus Placebo & Active Comparator (Ustekinumab) in Patients With Mod… | Phase3 | Psoriasis | Completed | 2016-03-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02694523 | BI 655066/ABBV-066 (Risankizumab) Compared to Active Comparator (Adalimumab) in… | Phase3 | Psoriasis | Completed | 2016-03-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02676310 | Safety, Tolerability, and Pharmacokinetics of Bimatoprost in Men With Androgene… | Phase1 | Alopecia | Terminated | 2016-03-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02676310 | Safety, Tolerability, and Pharmacokinetics of Bimatoprost in Men With Androgene… | Phase1 | Alopecia | Terminated | 2016-03-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02694523 | BI 655066/ABBV-066 (Risankizumab) Compared to Active Comparator (Adalimumab) in… | Phase3 | Psoriasis | Completed | 2016-03-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02694523 | BI 655066/ABBV-066 (Risankizumab) Compared to Active Comparator (Adalimumab) in… | Phase3 | Psoriasis | Completed | 2016-03-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT03710252 | A Study to Investigate HCV Response Rates in Real World Patients: HEARTLAND Stu… | Phase4 | Chronic Hepatitis C | Completed | 2016-03-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02676310 | Safety, Tolerability, and Pharmacokinetics of Bimatoprost in Men With Androgene… | Phase1 | Alopecia | Terminated | 2016-03-01 | 2017-03-01 | ClinicalTrials.gov |
| NCT02684357 | BI 655066 Versus Placebo & Active Comparator (Ustekinumab) in Patients With Mod… | Phase3 | Psoriasis | Completed | 2016-03-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT03052231 | Interactive Mobile Health Information to Enhance Patient Care at a Cystic Fibro… | Na | Medication Adherence | Completed | 2016-03-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT03710252 | A Study to Investigate HCV Response Rates in Real World Patients: HEARTLAND Stu… | Phase4 | Chronic Hepatitis C | Completed | 2016-03-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT03052231 | Interactive Mobile Health Information to Enhance Patient Care at a Cystic Fibro… | Na | Medication Adherence | Completed | 2016-03-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT03710252 | A Study to Investigate HCV Response Rates in Real World Patients: HEARTLAND Stu… | Phase4 | Chronic Hepatitis C | Completed | 2016-03-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT03710252 | A Study to Investigate HCV Response Rates in Real World Patients: HEARTLAND Stu… | Phase4 | Chronic Hepatitis C | Completed | 2016-03-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02694523 | BI 655066/ABBV-066 (Risankizumab) Compared to Active Comparator (Adalimumab) in… | Phase3 | Psoriasis | Completed | 2016-03-01 | 2017-08-01 | ClinicalTrials.gov |
| NCT02672852 | BI 655066 / ABBV-066 (Risankizumab) in Moderate to Severe Plaque Psoriasis With… | Phase3 | Psoriasis | Completed | 2016-02-29 | 2018-07-26 | ClinicalTrials.gov |
| NCT02672852 | BI 655066 / ABBV-066 (Risankizumab) in Moderate to Severe Plaque Psoriasis With… | Phase3 | Psoriasis | Completed | 2016-02-29 | 2018-07-26 | ClinicalTrials.gov |
| NCT02672852 | BI 655066 / ABBV-066 (Risankizumab) in Moderate to Severe Plaque Psoriasis With… | Phase3 | Psoriasis | Completed | 2016-02-29 | 2018-07-26 | ClinicalTrials.gov |
| NCT02672852 | BI 655066 / ABBV-066 (Risankizumab) in Moderate to Severe Plaque Psoriasis With… | Phase3 | Psoriasis | Completed | 2016-02-29 | 2018-07-26 | ClinicalTrials.gov |
| NCT02636946 | A Comparison of Bimatoprost SR to Selective Laser Trabeculoplasty in Patients W… | Phase3 | Glaucoma | Completed | 2016-02-24 | 2021-01-26 | ClinicalTrials.gov |
| NCT02636946 | A Comparison of Bimatoprost SR to Selective Laser Trabeculoplasty in Patients W… | Phase3 | Glaucoma | Completed | 2016-02-24 | 2021-01-26 | ClinicalTrials.gov |
| NCT02636946 | A Comparison of Bimatoprost SR to Selective Laser Trabeculoplasty in Patients W… | Phase3 | Glaucoma | Completed | 2016-02-24 | 2021-01-26 | ClinicalTrials.gov |
| NCT02636946 | A Comparison of Bimatoprost SR to Selective Laser Trabeculoplasty in Patients W… | Phase3 | Glaucoma | Completed | 2016-02-24 | 2021-01-26 | ClinicalTrials.gov |
| NCT02706873 | A Study to Compare Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Mon… | Phase3 | Rheumatoid Arthritis | Completed | 2016-02-23 | 2022-11-10 | ClinicalTrials.gov |
| NCT02706873 | A Study to Compare Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Mon… | Phase3 | Rheumatoid Arthritis | Completed | 2016-02-23 | 2022-11-10 | ClinicalTrials.gov |
| NCT02706873 | A Study to Compare Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Mon… | Phase3 | Rheumatoid Arthritis | Completed | 2016-02-23 | 2022-11-10 | ClinicalTrials.gov |
| NCT02706873 | A Study to Compare Upadacitinib (ABT-494) Monotherapy to Methotrexate (MTX) Mon… | Phase3 | Rheumatoid Arthritis | Completed | 2016-02-23 | 2022-11-10 | ClinicalTrials.gov |
| NCT02707952 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adul… | Phase3 | Chronic Hepatitis C Virus | Completed | 2016-02-22 | 2017-02-09 | ClinicalTrials.gov |
| NCT02707952 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adul… | Phase3 | Chronic Hepatitis C Virus | Completed | 2016-02-22 | 2017-02-09 | ClinicalTrials.gov |
| NCT02707952 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adul… | Phase3 | Chronic Hepatitis C Virus | Completed | 2016-02-22 | 2017-02-09 | ClinicalTrials.gov |
| NCT02707952 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Japanese Adul… | Phase3 | Chronic Hepatitis C Virus | Completed | 2016-02-22 | 2017-02-09 | ClinicalTrials.gov |
| NCT02687828 | A Prospective, Mono-Country and Multi-center Study to Observe Safety and Effect… | — | Intestinal Behcet's Disease (BD) | Completed | 2016-02-18 | 2020-03-30 | ClinicalTrials.gov |
| NCT02687828 | A Prospective, Mono-Country and Multi-center Study to Observe Safety and Effect… | — | Intestinal Behcet's Disease (BD) | Completed | 2016-02-18 | 2020-03-30 | ClinicalTrials.gov |
| NCT02687828 | A Prospective, Mono-Country and Multi-center Study to Observe Safety and Effect… | — | Intestinal Behcet's Disease (BD) | Completed | 2016-02-18 | 2020-03-30 | ClinicalTrials.gov |
| NCT02687828 | A Prospective, Mono-Country and Multi-center Study to Observe Safety and Effect… | — | Intestinal Behcet's Disease (BD) | Completed | 2016-02-18 | 2020-03-30 | ClinicalTrials.gov |
| NCT02691494 | Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Ace… | Phase3 | Uterine Fibroids | Completed | 2016-02-03 | 2019-01-23 | ClinicalTrials.gov |
| NCT02691494 | Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Ace… | Phase3 | Uterine Fibroids | Completed | 2016-02-03 | 2019-01-23 | ClinicalTrials.gov |
| NCT02691494 | Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Ace… | Phase3 | Uterine Fibroids | Completed | 2016-02-03 | 2019-01-23 | ClinicalTrials.gov |
| NCT02691494 | Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Ace… | Phase3 | Uterine Fibroids | Completed | 2016-02-03 | 2019-01-23 | ClinicalTrials.gov |
| NCT02322723 | Real Life Evaluation of Rheumatoid Arthritis Patients in Israel Treated With HU… | — | Rheumatoid Arthritis | Withdrawn | 2016-02-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02639052 | Itch Relieving Effect of Botox: a Study in Healthy Subjects | Phase1 | Pruritus | Completed | 2016-02-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02684370 | BI 655066 (Risankizumab) Compared to Placebo and Active Comparator (Ustekinumab… | Phase3 | Psoriasis | Completed | 2016-02-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02673047 | Observational Study of Botulinum Toxin Type A in Patients With Urinary Incontin… | — | Urinary Bladder, Overactive | Completed | 2016-02-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02322723 | Real Life Evaluation of Rheumatoid Arthritis Patients in Israel Treated With HU… | — | Rheumatoid Arthritis | Withdrawn | 2016-02-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02684370 | BI 655066 (Risankizumab) Compared to Placebo and Active Comparator (Ustekinumab… | Phase3 | Psoriasis | Completed | 2016-02-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02673047 | Observational Study of Botulinum Toxin Type A in Patients With Urinary Incontin… | — | Urinary Bladder, Overactive | Completed | 2016-02-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02322723 | Real Life Evaluation of Rheumatoid Arthritis Patients in Israel Treated With HU… | — | Rheumatoid Arthritis | Withdrawn | 2016-02-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02684370 | BI 655066 (Risankizumab) Compared to Placebo and Active Comparator (Ustekinumab… | Phase3 | Psoriasis | Completed | 2016-02-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02639052 | Itch Relieving Effect of Botox: a Study in Healthy Subjects | Phase1 | Pruritus | Completed | 2016-02-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02322723 | Real Life Evaluation of Rheumatoid Arthritis Patients in Israel Treated With HU… | — | Rheumatoid Arthritis | Withdrawn | 2016-02-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT02639052 | Itch Relieving Effect of Botox: a Study in Healthy Subjects | Phase1 | Pruritus | Completed | 2016-02-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02673047 | Observational Study of Botulinum Toxin Type A in Patients With Urinary Incontin… | — | Urinary Bladder, Overactive | Completed | 2016-02-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02684370 | BI 655066 (Risankizumab) Compared to Placebo and Active Comparator (Ustekinumab… | Phase3 | Psoriasis | Completed | 2016-02-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02673047 | Observational Study of Botulinum Toxin Type A in Patients With Urinary Incontin… | — | Urinary Bladder, Overactive | Completed | 2016-02-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02639052 | Itch Relieving Effect of Botox: a Study in Healthy Subjects | Phase1 | Pruritus | Completed | 2016-02-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02674568 | Study of Rovalpituzumab Tesirine (SC16LD6.5) for Third-Line and Later Treatment… | Phase2 | Small Cell Lung Cancer | Completed | 2016-01-25 | 2018-10-19 | ClinicalTrials.gov |
| NCT02674568 | Study of Rovalpituzumab Tesirine (SC16LD6.5) for Third-Line and Later Treatment… | Phase2 | Small Cell Lung Cancer | Completed | 2016-01-25 | 2018-10-19 | ClinicalTrials.gov |
| NCT02558283 | A Safety and Efficacy Study of JUVÉDERM® VOLIFT® With Lidocaine and Restylane® … | Na | Nasolabial Fold | Completed | 2016-01-25 | 2017-06-19 | ClinicalTrials.gov |
| NCT02558283 | A Safety and Efficacy Study of JUVÉDERM® VOLIFT® With Lidocaine and Restylane® … | Na | Nasolabial Fold | Completed | 2016-01-25 | 2017-06-19 | ClinicalTrials.gov |
| NCT02558283 | A Safety and Efficacy Study of JUVÉDERM® VOLIFT® With Lidocaine and Restylane® … | Na | Nasolabial Fold | Completed | 2016-01-25 | 2017-06-19 | ClinicalTrials.gov |
| NCT02674568 | Study of Rovalpituzumab Tesirine (SC16LD6.5) for Third-Line and Later Treatment… | Phase2 | Small Cell Lung Cancer | Completed | 2016-01-25 | 2018-10-19 | ClinicalTrials.gov |
| NCT02674568 | Study of Rovalpituzumab Tesirine (SC16LD6.5) for Third-Line and Later Treatment… | Phase2 | Small Cell Lung Cancer | Completed | 2016-01-25 | 2018-10-19 | ClinicalTrials.gov |
| NCT02558283 | A Safety and Efficacy Study of JUVÉDERM® VOLIFT® With Lidocaine and Restylane® … | Na | Nasolabial Fold | Completed | 2016-01-25 | 2017-06-19 | ClinicalTrials.gov |
| NCT02817594 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-01-20 | 2018-03-07 | ClinicalTrials.gov |
| NCT02817594 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-01-20 | 2018-03-07 | ClinicalTrials.gov |
| NCT02817594 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-01-20 | 2018-03-07 | ClinicalTrials.gov |
| NCT02817594 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2016-01-20 | 2018-03-07 | ClinicalTrials.gov |
| NCT02581020 | The Durability of Response and Persistence of Resistance to AbbVie's 2 Direct-a… | — | Hepatitis C Virus | Completed | 2016-01-14 | 2020-12-08 | ClinicalTrials.gov |
| NCT02581020 | The Durability of Response and Persistence of Resistance to AbbVie's 2 Direct-a… | — | Hepatitis C Virus | Completed | 2016-01-14 | 2020-12-08 | ClinicalTrials.gov |
| NCT02581020 | The Durability of Response and Persistence of Resistance to AbbVie's 2 Direct-a… | — | Hepatitis C Virus | Completed | 2016-01-14 | 2020-12-08 | ClinicalTrials.gov |
| NCT02581020 | The Durability of Response and Persistence of Resistance to AbbVie's 2 Direct-a… | — | Hepatitis C Virus | Completed | 2016-01-14 | 2020-12-08 | ClinicalTrials.gov |
| NCT02121262 | A Safety and Efficacy Study of Dexamethasone Versus Laser Photocoagulation in P… | Phase3 | Macular Edema | Completed | 2016-01-08 | 2019-11-01 | ClinicalTrials.gov |
| NCT02121262 | A Safety and Efficacy Study of Dexamethasone Versus Laser Photocoagulation in P… | Phase3 | Macular Edema | Completed | 2016-01-08 | 2019-11-01 | ClinicalTrials.gov |
| NCT02121262 | A Safety and Efficacy Study of Dexamethasone Versus Laser Photocoagulation in P… | Phase3 | Macular Edema | Completed | 2016-01-08 | 2019-11-01 | ClinicalTrials.gov |
| NCT02121262 | A Safety and Efficacy Study of Dexamethasone Versus Laser Photocoagulation in P… | Phase3 | Macular Edema | Completed | 2016-01-08 | 2019-11-01 | ClinicalTrials.gov |
| NCT02498418 | Study Comparing Rifaximin With Xifaxan 200 mg in Traveler's Diarrhea | Phase3 | Diarrhea | Completed | 2016-01-06 | 2017-02-28 | ClinicalTrials.gov |
| NCT02498418 | Study Comparing Rifaximin With Xifaxan 200 mg in Traveler's Diarrhea | Phase3 | Diarrhea | Completed | 2016-01-06 | 2017-02-28 | ClinicalTrials.gov |
| NCT02498418 | Study Comparing Rifaximin With Xifaxan 200 mg in Traveler's Diarrhea | Phase3 | Diarrhea | Completed | 2016-01-06 | 2017-02-28 | ClinicalTrials.gov |
| NCT02498418 | Study Comparing Rifaximin With Xifaxan 200 mg in Traveler's Diarrhea | Phase3 | Diarrhea | Completed | 2016-01-06 | 2017-02-28 | ClinicalTrials.gov |
| NCT02629172 | Drug Use-results Survey in Patients Infected With Hepatitis C Virus Genotype 1 | — | Chronic Hepatitis C Virus | Completed | 2016-01-05 | 2019-02-28 | ClinicalTrials.gov |
| NCT02629172 | Drug Use-results Survey in Patients Infected With Hepatitis C Virus Genotype 1 | — | Chronic Hepatitis C Virus | Completed | 2016-01-05 | 2019-02-28 | ClinicalTrials.gov |
| NCT02629172 | Drug Use-results Survey in Patients Infected With Hepatitis C Virus Genotype 1 | — | Chronic Hepatitis C Virus | Completed | 2016-01-05 | 2019-02-28 | ClinicalTrials.gov |
| NCT02629172 | Drug Use-results Survey in Patients Infected With Hepatitis C Virus Genotype 1 | — | Chronic Hepatitis C Virus | Completed | 2016-01-05 | 2019-02-28 | ClinicalTrials.gov |
| NCT02611713 | Observational Study Evaluating Long-Term Effectiveness of Duodopa/Duopa in Pati… | — | Advanced Parkinson's Disease | Completed | 2016-01-04 | 2020-12-24 | ClinicalTrials.gov |
| NCT02611713 | Observational Study Evaluating Long-Term Effectiveness of Duodopa/Duopa in Pati… | — | Advanced Parkinson's Disease | Completed | 2016-01-04 | 2020-12-24 | ClinicalTrials.gov |
| NCT02611713 | Observational Study Evaluating Long-Term Effectiveness of Duodopa/Duopa in Pati… | — | Advanced Parkinson's Disease | Completed | 2016-01-04 | 2020-12-24 | ClinicalTrials.gov |
| NCT02611713 | Observational Study Evaluating Long-Term Effectiveness of Duodopa/Duopa in Pati… | — | Advanced Parkinson's Disease | Completed | 2016-01-04 | 2020-12-24 | ClinicalTrials.gov |
| NCT02634541 | Adalimumab in Alleviating Inflammation in Patients With Axial Spondyloarthritis | Phase4 | Ankylosing Spondyloarthritis | Unknown | 2016-01-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02634541 | Adalimumab in Alleviating Inflammation in Patients With Axial Spondyloarthritis | Phase4 | Ankylosing Spondyloarthritis | Unknown | 2016-01-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02634541 | Adalimumab in Alleviating Inflammation in Patients With Axial Spondyloarthritis | Phase4 | Ankylosing Spondyloarthritis | Unknown | 2016-01-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02634541 | Adalimumab in Alleviating Inflammation in Patients With Axial Spondyloarthritis | Phase4 | Ankylosing Spondyloarthritis | Unknown | 2016-01-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02654054 | Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Ace… | Phase3 | Uterine Fibroids | Completed | 2015-12-22 | 2018-12-12 | ClinicalTrials.gov |
| NCT02654054 | Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Ace… | Phase3 | Uterine Fibroids | Completed | 2015-12-22 | 2018-12-12 | ClinicalTrials.gov |
| NCT02654054 | Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Ace… | Phase3 | Uterine Fibroids | Completed | 2015-12-22 | 2018-12-12 | ClinicalTrials.gov |
| NCT02654054 | Efficacy and Safety of Elagolix in Combination With Estradiol/Norethindrone Ace… | Phase3 | Uterine Fibroids | Completed | 2015-12-22 | 2018-12-12 | ClinicalTrials.gov |
| NCT02581202 | The Effectiveness of Dual Therapy (Lopinavir/Ritonavir + LamivudinE) in Treatme… | — | HIV-1 Infection | Completed | 2015-12-21 | 2017-05-27 | ClinicalTrials.gov |
| NCT02581202 | The Effectiveness of Dual Therapy (Lopinavir/Ritonavir + LamivudinE) in Treatme… | — | HIV-1 Infection | Completed | 2015-12-21 | 2017-05-27 | ClinicalTrials.gov |
| NCT02581202 | The Effectiveness of Dual Therapy (Lopinavir/Ritonavir + LamivudinE) in Treatme… | — | HIV-1 Infection | Completed | 2015-12-21 | 2017-05-27 | ClinicalTrials.gov |
| NCT02581202 | The Effectiveness of Dual Therapy (Lopinavir/Ritonavir + LamivudinE) in Treatme… | — | HIV-1 Infection | Completed | 2015-12-21 | 2017-05-27 | ClinicalTrials.gov |
| NCT02675426 | A Study Comparing Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid A… | Phase3 | Rheumatoid Arthritis | Completed | 2015-12-17 | 2022-03-10 | ClinicalTrials.gov |
| NCT02675426 | A Study Comparing Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid A… | Phase3 | Rheumatoid Arthritis | Completed | 2015-12-17 | 2022-03-10 | ClinicalTrials.gov |
| NCT02675426 | A Study Comparing Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid A… | Phase3 | Rheumatoid Arthritis | Completed | 2015-12-17 | 2022-03-10 | ClinicalTrials.gov |
| NCT02675426 | A Study Comparing Upadacitinib (ABT-494) to Placebo in Adults With Rheumatoid A… | Phase3 | Rheumatoid Arthritis | Completed | 2015-12-17 | 2022-03-10 | ClinicalTrials.gov |
| NCT02618928 | The Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavi… | — | Chronic Hepatitis C | Completed | 2015-12-15 | 2018-03-29 | ClinicalTrials.gov |
| NCT02618928 | The Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavi… | — | Chronic Hepatitis C | Completed | 2015-12-15 | 2018-03-29 | ClinicalTrials.gov |
| NCT02618928 | The Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavi… | — | Chronic Hepatitis C | Completed | 2015-12-15 | 2018-03-29 | ClinicalTrials.gov |
| NCT02618928 | The Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavi… | — | Chronic Hepatitis C | Completed | 2015-12-15 | 2018-03-29 | ClinicalTrials.gov |
| NCT02556736 | AGN-151597 (Formerly RST-001) Phase I/II Trial for Advanced Retinitis Pigmentosa | Phase1 | Advanced Retinitis Pigmentosa | Completed | 2015-12-14 | 2024-10-21 | ClinicalTrials.gov |
| NCT02556736 | AGN-151597 (Formerly RST-001) Phase I/II Trial for Advanced Retinitis Pigmentosa | Phase1 | Advanced Retinitis Pigmentosa | Completed | 2015-12-14 | 2024-10-21 | ClinicalTrials.gov |
| NCT02556736 | AGN-151597 (Formerly RST-001) Phase I/II Trial for Advanced Retinitis Pigmentosa | Phase1 | Advanced Retinitis Pigmentosa | Completed | 2015-12-14 | 2024-10-21 | ClinicalTrials.gov |
| NCT02556736 | AGN-151597 (Formerly RST-001) Phase I/II Trial for Advanced Retinitis Pigmentosa | Phase1 | Advanced Retinitis Pigmentosa | Completed | 2015-12-14 | 2024-10-21 | ClinicalTrials.gov |
| NCT02642432 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With C… | Phase3 | Hepatitis C Virus Infection | Completed | 2015-12-07 | 2017-02-10 | ClinicalTrials.gov |
| NCT02642432 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With C… | Phase3 | Hepatitis C Virus Infection | Completed | 2015-12-07 | 2017-02-10 | ClinicalTrials.gov |
| NCT02642432 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With C… | Phase3 | Hepatitis C Virus Infection | Completed | 2015-12-07 | 2017-02-10 | ClinicalTrials.gov |
| NCT02642432 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With C… | Phase3 | Hepatitis C Virus Infection | Completed | 2015-12-07 | 2017-02-10 | ClinicalTrials.gov |
| NCT02615145 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2015-12-03 | 2018-03-26 | ClinicalTrials.gov |
| NCT02615145 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2015-12-03 | 2018-03-26 | ClinicalTrials.gov |
| NCT02615145 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2015-12-03 | 2018-03-26 | ClinicalTrials.gov |
| NCT02615145 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2015-12-03 | 2018-03-26 | ClinicalTrials.gov |
| NCT02573740 | Safety, Tolerability and the Effects on Cerebrospinal Fluid Spectrin Breakdown … | Phase1 | Alzheimer's Disease | Terminated | 2015-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02417077 | Perception of Facial Expression in Subjects With and Without Crow's Feet Lines | — | Healthy Volunteers | Completed | 2015-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02417077 | Perception of Facial Expression in Subjects With and Without Crow's Feet Lines | — | Healthy Volunteers | Completed | 2015-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02417077 | Perception of Facial Expression in Subjects With and Without Crow's Feet Lines | — | Healthy Volunteers | Completed | 2015-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02651194 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Renally Impai… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2015-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02640157 | A Study Comparing Efficacy and Safety of ABT-493/ABT-530 to Sofosbuvir Dosed Wi… | Phase3 | Chronic Hepatitis C | Completed | 2015-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02629159 | A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Adults… | Phase3 | Rheumatoid Arthritis | Active_Not_Recruiting | 2015-12-01 | 2027-09-30 | ClinicalTrials.gov |
| NCT02417077 | Perception of Facial Expression in Subjects With and Without Crow's Feet Lines | — | Healthy Volunteers | Completed | 2015-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02651194 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Renally Impai… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2015-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02640157 | A Study Comparing Efficacy and Safety of ABT-493/ABT-530 to Sofosbuvir Dosed Wi… | Phase3 | Chronic Hepatitis C | Completed | 2015-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02629159 | A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Adults… | Phase3 | Rheumatoid Arthritis | Active_Not_Recruiting | 2015-12-01 | 2027-09-30 | ClinicalTrials.gov |
| NCT02573740 | Safety, Tolerability and the Effects on Cerebrospinal Fluid Spectrin Breakdown … | Phase1 | Alzheimer's Disease | Terminated | 2015-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02629159 | A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Adults… | Phase3 | Rheumatoid Arthritis | Active_Not_Recruiting | 2015-12-01 | 2027-09-30 | ClinicalTrials.gov |
| NCT02640157 | A Study Comparing Efficacy and Safety of ABT-493/ABT-530 to Sofosbuvir Dosed Wi… | Phase3 | Chronic Hepatitis C | Completed | 2015-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02651194 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Renally Impai… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2015-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02573740 | Safety, Tolerability and the Effects on Cerebrospinal Fluid Spectrin Breakdown … | Phase1 | Alzheimer's Disease | Terminated | 2015-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02573740 | Safety, Tolerability and the Effects on Cerebrospinal Fluid Spectrin Breakdown … | Phase1 | Alzheimer's Disease | Terminated | 2015-12-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02629159 | A Study Comparing Upadacitinib (ABT-494) to Placebo and to Adalimumab in Adults… | Phase3 | Rheumatoid Arthritis | Active_Not_Recruiting | 2015-12-01 | 2027-09-30 | ClinicalTrials.gov |
| NCT02640157 | A Study Comparing Efficacy and Safety of ABT-493/ABT-530 to Sofosbuvir Dosed Wi… | Phase3 | Chronic Hepatitis C | Completed | 2015-12-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02651194 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Renally Impai… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2015-12-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02636608 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2015-11-27 | 2018-05-23 | ClinicalTrials.gov |
| NCT02636608 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2015-11-27 | 2018-05-23 | ClinicalTrials.gov |
| NCT02636608 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2015-11-27 | 2018-05-23 | ClinicalTrials.gov |
| NCT02636608 | Real World Evidence of the Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasa… | — | Chronic Hepatitis C | Completed | 2015-11-27 | 2018-05-23 | ClinicalTrials.gov |
| NCT02632175 | Long-term Safety and Efficacy Study of Adalimumab in Pediatric Subjects With Ul… | Phase3 | Ulcerative Colitis | Completed | 2015-11-26 | 2025-04-08 | ClinicalTrials.gov |
| NCT02632175 | Long-term Safety and Efficacy Study of Adalimumab in Pediatric Subjects With Ul… | Phase3 | Ulcerative Colitis | Completed | 2015-11-26 | 2025-04-08 | ClinicalTrials.gov |
| NCT02640547 | Real World Evidence of the Effectiveness of Paritaprevir/Ritonavir, Ombitasvir,… | — | Chronic Hepatitis C | Completed | 2015-11-26 | 2017-03-29 | ClinicalTrials.gov |
| NCT02632175 | Long-term Safety and Efficacy Study of Adalimumab in Pediatric Subjects With Ul… | Phase3 | Ulcerative Colitis | Completed | 2015-11-26 | 2025-04-08 | ClinicalTrials.gov |
| NCT02640547 | Real World Evidence of the Effectiveness of Paritaprevir/Ritonavir, Ombitasvir,… | — | Chronic Hepatitis C | Completed | 2015-11-26 | 2017-03-29 | ClinicalTrials.gov |
| NCT02640547 | Real World Evidence of the Effectiveness of Paritaprevir/Ritonavir, Ombitasvir,… | — | Chronic Hepatitis C | Completed | 2015-11-26 | 2017-03-29 | ClinicalTrials.gov |
| NCT02640547 | Real World Evidence of the Effectiveness of Paritaprevir/Ritonavir, Ombitasvir,… | — | Chronic Hepatitis C | Completed | 2015-11-26 | 2017-03-29 | ClinicalTrials.gov |
| NCT02632175 | Long-term Safety and Efficacy Study of Adalimumab in Pediatric Subjects With Ul… | Phase3 | Ulcerative Colitis | Completed | 2015-11-26 | 2025-04-08 | ClinicalTrials.gov |
| NCT02582632 | A Study to Evaluate Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir in Treatmen… | Phase3 | Hepatitis C Infection | Completed | 2015-11-24 | 2016-12-01 | ClinicalTrials.gov |
| NCT02582632 | A Study to Evaluate Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir in Treatmen… | Phase3 | Hepatitis C Infection | Completed | 2015-11-24 | 2016-12-01 | ClinicalTrials.gov |
| NCT02582632 | A Study to Evaluate Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir in Treatmen… | Phase3 | Hepatitis C Infection | Completed | 2015-11-24 | 2016-12-01 | ClinicalTrials.gov |
| NCT02582632 | A Study to Evaluate Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir in Treatmen… | Phase3 | Hepatitis C Infection | Completed | 2015-11-24 | 2016-12-01 | ClinicalTrials.gov |
| NCT02627924 | Real-World Outcome of Rheumatoid Arthritis Patients in Korea on Adalimumab | — | Rheumatoid Arthritis | Completed | 2015-11-18 | 2017-12-28 | ClinicalTrials.gov |
| NCT02627924 | Real-World Outcome of Rheumatoid Arthritis Patients in Korea on Adalimumab | — | Rheumatoid Arthritis | Completed | 2015-11-18 | 2017-12-28 | ClinicalTrials.gov |
| NCT02627924 | Real-World Outcome of Rheumatoid Arthritis Patients in Korea on Adalimumab | — | Rheumatoid Arthritis | Completed | 2015-11-18 | 2017-12-28 | ClinicalTrials.gov |
| NCT02627924 | Real-World Outcome of Rheumatoid Arthritis Patients in Korea on Adalimumab | — | Rheumatoid Arthritis | Completed | 2015-11-18 | 2017-12-28 | ClinicalTrials.gov |
| NCT02571712 | Safety of GANFORT® Ophthalmic Solution in Chinese Patients With Open-angle Glau… | Phase4 | Glaucoma, Open-Angle | Completed | 2015-11-10 | 2018-06-21 | ClinicalTrials.gov |
| NCT02571712 | Safety of GANFORT® Ophthalmic Solution in Chinese Patients With Open-angle Glau… | Phase4 | Glaucoma, Open-Angle | Completed | 2015-11-10 | 2018-06-21 | ClinicalTrials.gov |
| NCT02571712 | Safety of GANFORT® Ophthalmic Solution in Chinese Patients With Open-angle Glau… | Phase4 | Glaucoma, Open-Angle | Completed | 2015-11-10 | 2018-06-21 | ClinicalTrials.gov |
| NCT02571712 | Safety of GANFORT® Ophthalmic Solution in Chinese Patients With Open-angle Glau… | Phase4 | Glaucoma, Open-Angle | Completed | 2015-11-10 | 2018-06-21 | ClinicalTrials.gov |
| NCT02582671 | The Effectiveness of ABT-450/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patien… | — | Chronic Hepatitis C | Completed | 2015-11-05 | 2017-11-29 | ClinicalTrials.gov |
| NCT02616380 | Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in Taiwan | — | Rheumatoid Arthritis | Completed | 2015-11-05 | 2017-11-23 | ClinicalTrials.gov |
| NCT02616380 | Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in Taiwan | — | Rheumatoid Arthritis | Completed | 2015-11-05 | 2017-11-23 | ClinicalTrials.gov |
| NCT02582671 | The Effectiveness of ABT-450/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patien… | — | Chronic Hepatitis C | Completed | 2015-11-05 | 2017-11-29 | ClinicalTrials.gov |
| NCT02616380 | Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in Taiwan | — | Rheumatoid Arthritis | Completed | 2015-11-05 | 2017-11-23 | ClinicalTrials.gov |
| NCT02582671 | The Effectiveness of ABT-450/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patien… | — | Chronic Hepatitis C | Completed | 2015-11-05 | 2017-11-29 | ClinicalTrials.gov |
| NCT02616380 | Real-World Outcome of Adalimumab on Rheumatoid Arthritis Patients in Taiwan | — | Rheumatoid Arthritis | Completed | 2015-11-05 | 2017-11-23 | ClinicalTrials.gov |
| NCT02582671 | The Effectiveness of ABT-450/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patien… | — | Chronic Hepatitis C | Completed | 2015-11-05 | 2017-11-29 | ClinicalTrials.gov |
| NCT02598570 | Study Evaluating Duvelisib in Japanese Subjects With Relapsed or Refractory Lym… | Phase1 | Lymphoma | Completed | 2015-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02636595 | The Efficacy and Safety of ABT-493/ABT-530 in Adults With Chronic Hepatitis C V… | Phase3 | Hepatitis C Virus | Completed | 2015-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02601287 | A Safety and Efficacy Study of Botulinum Toxin Type A (BOTOX®) to Treat Urinary… | Phase4 | Urinary Incontinence | Completed | 2015-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02651220 | Clinical End Point Study of Generic Adapalene and Benzoyl Peroxide Gel Versus E… | Phase3 | Acne | Completed | 2015-11-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02684084 | Combination OZURDEX® & LUCENTIS® vs. OZURDEX® Monotherapy in Incomplete-Respond… | Phase4 | Diabetic Macular Edema | Terminated | 2015-11-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02684084 | Combination OZURDEX® & LUCENTIS® vs. OZURDEX® Monotherapy in Incomplete-Respond… | Phase4 | Diabetic Macular Edema | Terminated | 2015-11-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02651220 | Clinical End Point Study of Generic Adapalene and Benzoyl Peroxide Gel Versus E… | Phase3 | Acne | Completed | 2015-11-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02601287 | A Safety and Efficacy Study of Botulinum Toxin Type A (BOTOX®) to Treat Urinary… | Phase4 | Urinary Incontinence | Completed | 2015-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02601287 | A Safety and Efficacy Study of Botulinum Toxin Type A (BOTOX®) to Treat Urinary… | Phase4 | Urinary Incontinence | Completed | 2015-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02651220 | Clinical End Point Study of Generic Adapalene and Benzoyl Peroxide Gel Versus E… | Phase3 | Acne | Completed | 2015-11-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02684084 | Combination OZURDEX® & LUCENTIS® vs. OZURDEX® Monotherapy in Incomplete-Respond… | Phase4 | Diabetic Macular Edema | Terminated | 2015-11-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02640482 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With C… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2015-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02636595 | The Efficacy and Safety of ABT-493/ABT-530 in Adults With Chronic Hepatitis C V… | Phase3 | Hepatitis C Virus | Completed | 2015-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02598570 | Study Evaluating Duvelisib in Japanese Subjects With Relapsed or Refractory Lym… | Phase1 | Lymphoma | Completed | 2015-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02601287 | A Safety and Efficacy Study of Botulinum Toxin Type A (BOTOX®) to Treat Urinary… | Phase4 | Urinary Incontinence | Completed | 2015-11-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02640482 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With C… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2015-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02636595 | The Efficacy and Safety of ABT-493/ABT-530 in Adults With Chronic Hepatitis C V… | Phase3 | Hepatitis C Virus | Completed | 2015-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02651220 | Clinical End Point Study of Generic Adapalene and Benzoyl Peroxide Gel Versus E… | Phase3 | Acne | Completed | 2015-11-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02598570 | Study Evaluating Duvelisib in Japanese Subjects With Relapsed or Refractory Lym… | Phase1 | Lymphoma | Completed | 2015-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02640482 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With C… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2015-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02636595 | The Efficacy and Safety of ABT-493/ABT-530 in Adults With Chronic Hepatitis C V… | Phase3 | Hepatitis C Virus | Completed | 2015-11-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02598570 | Study Evaluating Duvelisib in Japanese Subjects With Relapsed or Refractory Lym… | Phase1 | Lymphoma | Completed | 2015-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02684084 | Combination OZURDEX® & LUCENTIS® vs. OZURDEX® Monotherapy in Incomplete-Respond… | Phase4 | Diabetic Macular Edema | Terminated | 2015-11-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02640482 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Adults With C… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2015-11-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02609659 | Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With Low-Dose Ribavirin QD in S… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-10-28 | 2016-12-28 | ClinicalTrials.gov |
| NCT02486406 | A Study to Evaluate Treatment of Hepatitis C Virus Infection in Pediatric Subje… | Phase2 | Chronic Hepatitis C Infection | Completed | 2015-10-28 | 2020-11-19 | ClinicalTrials.gov |
| NCT02609659 | Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With Low-Dose Ribavirin QD in S… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-10-28 | 2016-12-28 | ClinicalTrials.gov |
| NCT02334683 | Compare Two Guidance Techniques for Botulinum Toxin Injections for the Treatmen… | Na | Spasticity | Completed | 2015-10-28 | 2020-03-03 | ClinicalTrials.gov |
| NCT02486406 | A Study to Evaluate Treatment of Hepatitis C Virus Infection in Pediatric Subje… | Phase2 | Chronic Hepatitis C Infection | Completed | 2015-10-28 | 2020-11-19 | ClinicalTrials.gov |
| NCT02334683 | Compare Two Guidance Techniques for Botulinum Toxin Injections for the Treatmen… | Na | Spasticity | Completed | 2015-10-28 | 2020-03-03 | ClinicalTrials.gov |
| NCT02486406 | A Study to Evaluate Treatment of Hepatitis C Virus Infection in Pediatric Subje… | Phase2 | Chronic Hepatitis C Infection | Completed | 2015-10-28 | 2020-11-19 | ClinicalTrials.gov |
| NCT02609659 | Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With Low-Dose Ribavirin QD in S… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-10-28 | 2016-12-28 | ClinicalTrials.gov |
| NCT02334683 | Compare Two Guidance Techniques for Botulinum Toxin Injections for the Treatmen… | Na | Spasticity | Completed | 2015-10-28 | 2020-03-03 | ClinicalTrials.gov |
| NCT02486406 | A Study to Evaluate Treatment of Hepatitis C Virus Infection in Pediatric Subje… | Phase2 | Chronic Hepatitis C Infection | Completed | 2015-10-28 | 2020-11-19 | ClinicalTrials.gov |
| NCT02609659 | Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With Low-Dose Ribavirin QD in S… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-10-28 | 2016-12-28 | ClinicalTrials.gov |
| NCT02334683 | Compare Two Guidance Techniques for Botulinum Toxin Injections for the Treatmen… | Na | Spasticity | Completed | 2015-10-28 | 2020-03-03 | ClinicalTrials.gov |
| NCT02549092 | A Study to Examine the Effect of Levodopa-Carbidopa Intestinal Gel (LCIG) Thera… | Phase3 | Advanced Parkinson's Disease | Completed | 2015-10-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT02549092 | A Study to Examine the Effect of Levodopa-Carbidopa Intestinal Gel (LCIG) Thera… | Phase3 | Advanced Parkinson's Disease | Completed | 2015-10-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT02549092 | A Study to Examine the Effect of Levodopa-Carbidopa Intestinal Gel (LCIG) Thera… | Phase3 | Advanced Parkinson's Disease | Completed | 2015-10-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT02549092 | A Study to Examine the Effect of Levodopa-Carbidopa Intestinal Gel (LCIG) Thera… | Phase3 | Advanced Parkinson's Disease | Completed | 2015-10-26 | 2022-11-18 | ClinicalTrials.gov |
| NCT02485600 | Observational Study Evaluating Long-term Health Outcomes of Canadian DUODOPA-tr… | — | Parkinson Disease (PD) | Completed | 2015-10-19 | 2020-02-26 | ClinicalTrials.gov |
| NCT02485600 | Observational Study Evaluating Long-term Health Outcomes of Canadian DUODOPA-tr… | — | Parkinson Disease (PD) | Completed | 2015-10-19 | 2020-02-26 | ClinicalTrials.gov |
| NCT02485600 | Observational Study Evaluating Long-term Health Outcomes of Canadian DUODOPA-tr… | — | Parkinson Disease (PD) | Completed | 2015-10-19 | 2020-02-26 | ClinicalTrials.gov |
| NCT02485600 | Observational Study Evaluating Long-term Health Outcomes of Canadian DUODOPA-tr… | — | Parkinson Disease (PD) | Completed | 2015-10-19 | 2020-02-26 | ClinicalTrials.gov |
| NCT02581189 | Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patie… | — | Chronic Hepatitis C | Completed | 2015-10-13 | 2017-12-20 | ClinicalTrials.gov |
| NCT02581189 | Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patie… | — | Chronic Hepatitis C | Completed | 2015-10-13 | 2017-12-20 | ClinicalTrials.gov |
| NCT02581189 | Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patie… | — | Chronic Hepatitis C | Completed | 2015-10-13 | 2017-12-20 | ClinicalTrials.gov |
| NCT02581189 | Effectiveness of Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patie… | — | Chronic Hepatitis C | Completed | 2015-10-13 | 2017-12-20 | ClinicalTrials.gov |
| NCT02581163 | Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavirin … | — | Chronic Hepatitis C, Genotype 1 or 4 | Completed | 2015-10-07 | 2018-02-12 | ClinicalTrials.gov |
| NCT02549196 | A Dose Titration Study of CPC-201 in Patients With Dementia of Alzheimer's Type | Phase2 | Dementia of Alzheimer's Type | Completed | 2015-10-07 | 2017-09-28 | ClinicalTrials.gov |
| NCT02581163 | Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavirin … | — | Chronic Hepatitis C, Genotype 1 or 4 | Completed | 2015-10-07 | 2018-02-12 | ClinicalTrials.gov |
| NCT02549196 | A Dose Titration Study of CPC-201 in Patients With Dementia of Alzheimer's Type | Phase2 | Dementia of Alzheimer's Type | Completed | 2015-10-07 | 2017-09-28 | ClinicalTrials.gov |
| NCT02549196 | A Dose Titration Study of CPC-201 in Patients With Dementia of Alzheimer's Type | Phase2 | Dementia of Alzheimer's Type | Completed | 2015-10-07 | 2017-09-28 | ClinicalTrials.gov |
| NCT02581163 | Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavirin … | — | Chronic Hepatitis C, Genotype 1 or 4 | Completed | 2015-10-07 | 2018-02-12 | ClinicalTrials.gov |
| NCT02549196 | A Dose Titration Study of CPC-201 in Patients With Dementia of Alzheimer's Type | Phase2 | Dementia of Alzheimer's Type | Completed | 2015-10-07 | 2017-09-28 | ClinicalTrials.gov |
| NCT02581163 | Effectiveness of Paritaprevir/Ritonavir - Ombitasvir, ± Dasabuvir, ± Ribavirin … | — | Chronic Hepatitis C, Genotype 1 or 4 | Completed | 2015-10-07 | 2018-02-12 | ClinicalTrials.gov |
| NCT02582658 | Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patients With Chronic … | — | Chronic Hepatitis C | Completed | 2015-10-06 | 2017-01-12 | ClinicalTrials.gov |
| NCT02582658 | Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patients With Chronic … | — | Chronic Hepatitis C | Completed | 2015-10-06 | 2017-01-12 | ClinicalTrials.gov |
| NCT02582658 | Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patients With Chronic … | — | Chronic Hepatitis C | Completed | 2015-10-06 | 2017-01-12 | ClinicalTrials.gov |
| NCT02582658 | Paritaprevir/r - Ombitasvir, ± Dasabuvir, ± Ribavirin in Patients With Chronic … | — | Chronic Hepatitis C | Completed | 2015-10-06 | 2017-01-12 | ClinicalTrials.gov |
| NCT02429895 | A Phase 2, Multicenter Open-Label Extension (OLE) Study With ABT-122 in Active … | Phase2 | Psoriatic Arthritis | Terminated | 2015-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02429895 | A Phase 2, Multicenter Open-Label Extension (OLE) Study With ABT-122 in Active … | Phase2 | Psoriatic Arthritis | Terminated | 2015-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02606630 | [11C]-PBR28 Positron Emission Tomography Study to Evaluate the Effect of ABT 55… | Phase1 | Multiple Sclerosis | Terminated | 2015-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02604017 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Subjects With… | Phase3 | Chronic Hepatitis C | Completed | 2015-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02606630 | [11C]-PBR28 Positron Emission Tomography Study to Evaluate the Effect of ABT 55… | Phase1 | Multiple Sclerosis | Terminated | 2015-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02429895 | A Phase 2, Multicenter Open-Label Extension (OLE) Study With ABT-122 in Active … | Phase2 | Psoriatic Arthritis | Terminated | 2015-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02606630 | [11C]-PBR28 Positron Emission Tomography Study to Evaluate the Effect of ABT 55… | Phase1 | Multiple Sclerosis | Terminated | 2015-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02429895 | A Phase 2, Multicenter Open-Label Extension (OLE) Study With ABT-122 in Active … | Phase2 | Psoriatic Arthritis | Terminated | 2015-10-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02604017 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Subjects With… | Phase3 | Chronic Hepatitis C | Completed | 2015-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02604017 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Subjects With… | Phase3 | Chronic Hepatitis C | Completed | 2015-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02604017 | A Study to Evaluate the Efficacy and Safety of ABT-493/ABT-530 in Subjects With… | Phase3 | Chronic Hepatitis C | Completed | 2015-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02606630 | [11C]-PBR28 Positron Emission Tomography Study to Evaluate the Effect of ABT 55… | Phase1 | Multiple Sclerosis | Terminated | 2015-10-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02487199 | Ombitasvir/Paritaprevir/Ritonavir With or Without Dasabuvir in Adults With Geno… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-09-30 | 2016-12-05 | ClinicalTrials.gov |
| NCT02487199 | Ombitasvir/Paritaprevir/Ritonavir With or Without Dasabuvir in Adults With Geno… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-09-30 | 2016-12-05 | ClinicalTrials.gov |
| NCT02487199 | Ombitasvir/Paritaprevir/Ritonavir With or Without Dasabuvir in Adults With Geno… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-09-30 | 2016-12-05 | ClinicalTrials.gov |
| NCT02487199 | Ombitasvir/Paritaprevir/Ritonavir With or Without Dasabuvir in Adults With Geno… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-09-30 | 2016-12-05 | ClinicalTrials.gov |
| NCT02533375 | Study to Investigate Efficacy and Safety of Adalimumab in Japanese Subjects Wit… | Phase3 | Generalized Pustular Psoriasis (GPP) | Completed | 2015-09-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT02533375 | Study to Investigate Efficacy and Safety of Adalimumab in Japanese Subjects Wit… | Phase3 | Generalized Pustular Psoriasis (GPP) | Completed | 2015-09-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT02533375 | Study to Investigate Efficacy and Safety of Adalimumab in Japanese Subjects Wit… | Phase3 | Generalized Pustular Psoriasis (GPP) | Completed | 2015-09-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT02533375 | Study to Investigate Efficacy and Safety of Adalimumab in Japanese Subjects Wit… | Phase3 | Generalized Pustular Psoriasis (GPP) | Completed | 2015-09-28 | 2017-07-20 | ClinicalTrials.gov |
| NCT02578238 | Post-Marketing Surveillance of Humira in Korean Pediatric Crohn's Disease (CD) … | — | Pediatric Crohn's Disease | Completed | 2015-09-24 | 2017-05-31 | ClinicalTrials.gov |
| NCT02578238 | Post-Marketing Surveillance of Humira in Korean Pediatric Crohn's Disease (CD) … | — | Pediatric Crohn's Disease | Completed | 2015-09-24 | 2017-05-31 | ClinicalTrials.gov |
| NCT02578238 | Post-Marketing Surveillance of Humira in Korean Pediatric Crohn's Disease (CD) … | — | Pediatric Crohn's Disease | Completed | 2015-09-24 | 2017-05-31 | ClinicalTrials.gov |
| NCT02578238 | Post-Marketing Surveillance of Humira in Korean Pediatric Crohn's Disease (CD) … | — | Pediatric Crohn's Disease | Completed | 2015-09-24 | 2017-05-31 | ClinicalTrials.gov |
| NCT02565758 | ABBV-085, an Antibody Drug Conjugate, in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2015-09-18 | 2019-03-25 | ClinicalTrials.gov |
| NCT02565758 | ABBV-085, an Antibody Drug Conjugate, in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2015-09-18 | 2019-03-25 | ClinicalTrials.gov |
| NCT02565758 | ABBV-085, an Antibody Drug Conjugate, in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2015-09-18 | 2019-03-25 | ClinicalTrials.gov |
| NCT02565758 | ABBV-085, an Antibody Drug Conjugate, in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2015-09-18 | 2019-03-25 | ClinicalTrials.gov |
| NCT02513459 | A Long Term Extension Trial of BI 655066/ABBV-066 (Risankizumab), in Patients W… | Phase2 | Crohn Disease | Completed | 2015-09-16 | 2019-06-19 | ClinicalTrials.gov |
| NCT02513459 | A Long Term Extension Trial of BI 655066/ABBV-066 (Risankizumab), in Patients W… | Phase2 | Crohn Disease | Completed | 2015-09-16 | 2019-06-19 | ClinicalTrials.gov |
| NCT02513459 | A Long Term Extension Trial of BI 655066/ABBV-066 (Risankizumab), in Patients W… | Phase2 | Crohn Disease | Completed | 2015-09-16 | 2019-06-19 | ClinicalTrials.gov |
| NCT02513459 | A Long Term Extension Trial of BI 655066/ABBV-066 (Risankizumab), in Patients W… | Phase2 | Crohn Disease | Completed | 2015-09-16 | 2019-06-19 | ClinicalTrials.gov |
| NCT02471105 | Investigation of IOP and Tolerability of Bimatoprost 0.01% and Tafluprost Unit … | Phase4 | Ocular Hypertension | Unknown | 2015-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02877069 | Safety and Effectiveness of VYC-12 Hyaluronic Acid Injectable Gel for Treatment… | Phase4 | Skin Roughness | Completed | 2015-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02471105 | Investigation of IOP and Tolerability of Bimatoprost 0.01% and Tafluprost Unit … | Phase4 | Ocular Hypertension | Unknown | 2015-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02534870 | Pharmacokinetics and Safety of the Co-administration of ABT-450/Ritonavir/ABT-2… | Phase1 | Healthy Volunteer | Completed | 2015-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02471105 | Investigation of IOP and Tolerability of Bimatoprost 0.01% and Tafluprost Unit … | Phase4 | Ocular Hypertension | Unknown | 2015-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02877069 | Safety and Effectiveness of VYC-12 Hyaluronic Acid Injectable Gel for Treatment… | Phase4 | Skin Roughness | Completed | 2015-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02877069 | Safety and Effectiveness of VYC-12 Hyaluronic Acid Injectable Gel for Treatment… | Phase4 | Skin Roughness | Completed | 2015-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02471105 | Investigation of IOP and Tolerability of Bimatoprost 0.01% and Tafluprost Unit … | Phase4 | Ocular Hypertension | Unknown | 2015-09-01 | 2017-12-01 | ClinicalTrials.gov |
| NCT02534870 | Pharmacokinetics and Safety of the Co-administration of ABT-450/Ritonavir/ABT-2… | Phase1 | Healthy Volunteer | Completed | 2015-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02792803 | A Comparison of Xalatan (Latanoprost) to Apo-latanoprost and Co-latanoprost in … | Phase4 | POAG | Unknown | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02792803 | A Comparison of Xalatan (Latanoprost) to Apo-latanoprost and Co-latanoprost in … | Phase4 | POAG | Unknown | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02792803 | A Comparison of Xalatan (Latanoprost) to Apo-latanoprost and Co-latanoprost in … | Phase4 | POAG | Unknown | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02792803 | A Comparison of Xalatan (Latanoprost) to Apo-latanoprost and Co-latanoprost in … | Phase4 | POAG | Unknown | 2015-09-01 | 2017-09-01 | ClinicalTrials.gov |
| NCT02534870 | Pharmacokinetics and Safety of the Co-administration of ABT-450/Ritonavir/ABT-2… | Phase1 | Healthy Volunteer | Completed | 2015-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02877069 | Safety and Effectiveness of VYC-12 Hyaluronic Acid Injectable Gel for Treatment… | Phase4 | Skin Roughness | Completed | 2015-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02534870 | Pharmacokinetics and Safety of the Co-administration of ABT-450/Ritonavir/ABT-2… | Phase1 | Healthy Volunteer | Completed | 2015-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02507687 | Comparison of Bimatoprost Sustained Release (SR) to Selective Laser Trabeculopl… | Phase3 | Glaucoma, Open-Angle | Completed | 2015-08-27 | 2023-05-31 | ClinicalTrials.gov |
| NCT02507687 | Comparison of Bimatoprost Sustained Release (SR) to Selective Laser Trabeculopl… | Phase3 | Glaucoma, Open-Angle | Completed | 2015-08-27 | 2023-05-31 | ClinicalTrials.gov |
| NCT02507687 | Comparison of Bimatoprost Sustained Release (SR) to Selective Laser Trabeculopl… | Phase3 | Glaucoma, Open-Angle | Completed | 2015-08-27 | 2023-05-31 | ClinicalTrials.gov |
| NCT02507687 | Comparison of Bimatoprost Sustained Release (SR) to Selective Laser Trabeculopl… | Phase3 | Glaucoma, Open-Angle | Completed | 2015-08-27 | 2023-05-31 | ClinicalTrials.gov |
| NCT02590263 | Study Evaluating ABT-414 in Japanese Subjects With Malignant Glioma | Phase1 | Malignant Glioma | Completed | 2015-08-24 | 2020-08-27 | ClinicalTrials.gov |
| NCT02590263 | Study Evaluating ABT-414 in Japanese Subjects With Malignant Glioma | Phase1 | Malignant Glioma | Completed | 2015-08-24 | 2020-08-27 | ClinicalTrials.gov |
| NCT02590263 | Study Evaluating ABT-414 in Japanese Subjects With Malignant Glioma | Phase1 | Malignant Glioma | Completed | 2015-08-24 | 2020-08-27 | ClinicalTrials.gov |
| NCT02590263 | Study Evaluating ABT-414 in Japanese Subjects With Malignant Glioma | Phase1 | Malignant Glioma | Completed | 2015-08-24 | 2020-08-27 | ClinicalTrials.gov |
| NCT02506179 | Impact of Adalimumab on Patient-reported Outcomes in Ulcerative Colitis | — | Ulcerative Colitis | Completed | 2015-08-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02506179 | Impact of Adalimumab on Patient-reported Outcomes in Ulcerative Colitis | — | Ulcerative Colitis | Completed | 2015-08-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02506179 | Impact of Adalimumab on Patient-reported Outcomes in Ulcerative Colitis | — | Ulcerative Colitis | Completed | 2015-08-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02506179 | Impact of Adalimumab on Patient-reported Outcomes in Ulcerative Colitis | — | Ulcerative Colitis | Completed | 2015-08-18 | 2020-02-10 | ClinicalTrials.gov |
| NCT02499783 | Study to Evaluate the Safety and Efficacy of Adalimumab in Chinese Subjects Wit… | Phase3 | Crohn's Disease | Completed | 2015-08-17 | 2017-12-15 | ClinicalTrials.gov |
| NCT02499783 | Study to Evaluate the Safety and Efficacy of Adalimumab in Chinese Subjects Wit… | Phase3 | Crohn's Disease | Completed | 2015-08-17 | 2017-12-15 | ClinicalTrials.gov |
| NCT02499783 | Study to Evaluate the Safety and Efficacy of Adalimumab in Chinese Subjects Wit… | Phase3 | Crohn's Disease | Completed | 2015-08-17 | 2017-12-15 | ClinicalTrials.gov |
| NCT02499783 | Study to Evaluate the Safety and Efficacy of Adalimumab in Chinese Subjects Wit… | Phase3 | Crohn's Disease | Completed | 2015-08-17 | 2017-12-15 | ClinicalTrials.gov |
| NCT02495857 | A Study of Hyaluronate Injectable Viscosupplement for Treatment of Osteoarthrit… | Na | Osteoarthritis | Completed | 2015-08-15 | 2016-12-05 | ClinicalTrials.gov |
| NCT02495857 | A Study of Hyaluronate Injectable Viscosupplement for Treatment of Osteoarthrit… | Na | Osteoarthritis | Completed | 2015-08-15 | 2016-12-05 | ClinicalTrials.gov |
| NCT02495857 | A Study of Hyaluronate Injectable Viscosupplement for Treatment of Osteoarthrit… | Na | Osteoarthritis | Completed | 2015-08-15 | 2016-12-05 | ClinicalTrials.gov |
| NCT02495857 | A Study of Hyaluronate Injectable Viscosupplement for Treatment of Osteoarthrit… | Na | Osteoarthritis | Completed | 2015-08-15 | 2016-12-05 | ClinicalTrials.gov |
| NCT02392026 | Safety and Tolerability of Metronidazole Gel 1.3% | Phase4 | Vaginosis, Bacterial | Completed | 2015-08-12 | 2016-10-05 | ClinicalTrials.gov |
| NCT02392026 | Safety and Tolerability of Metronidazole Gel 1.3% | Phase4 | Vaginosis, Bacterial | Completed | 2015-08-12 | 2016-10-05 | ClinicalTrials.gov |
| NCT02392026 | Safety and Tolerability of Metronidazole Gel 1.3% | Phase4 | Vaginosis, Bacterial | Completed | 2015-08-12 | 2016-10-05 | ClinicalTrials.gov |
| NCT02392026 | Safety and Tolerability of Metronidazole Gel 1.3% | Phase4 | Vaginosis, Bacterial | Completed | 2015-08-12 | 2016-10-05 | ClinicalTrials.gov |
| NCT03724292 | An Ascending Multiple Dose Study With VTP-43742 in Healthy Volunteers | Phase1 | Psoriasis | Completed | 2015-08-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02245958 | A Retrospective Chart Review of BOTOX® and Xeomin® for the Management of Cervic… | — | Cervical Dystonia | Completed | 2015-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02526641 | Macrophages, Portal Hypertension, and Liver Function During AbbVie Treatment of… | — | Hepatitis C | Completed | 2015-08-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT02557971 | Urinary Retention Rates in Clinical Practice After Treatment With Onabotulinumt… | — | Urinary Bladder, Overactive | Completed | 2015-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02555709 | An Ascending Multiple Dose Study With VTP-43742 in Healthy Volunteers and Psori… | Phase1 | Psoriasis | Completed | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02557971 | Urinary Retention Rates in Clinical Practice After Treatment With Onabotulinumt… | — | Urinary Bladder, Overactive | Completed | 2015-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02557971 | Urinary Retention Rates in Clinical Practice After Treatment With Onabotulinumt… | — | Urinary Bladder, Overactive | Completed | 2015-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02245958 | A Retrospective Chart Review of BOTOX® and Xeomin® for the Management of Cervic… | — | Cervical Dystonia | Completed | 2015-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02555709 | An Ascending Multiple Dose Study With VTP-43742 in Healthy Volunteers and Psori… | Phase1 | Psoriasis | Completed | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT03724292 | An Ascending Multiple Dose Study With VTP-43742 in Healthy Volunteers | Phase1 | Psoriasis | Completed | 2015-08-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT03724292 | An Ascending Multiple Dose Study With VTP-43742 in Healthy Volunteers | Phase1 | Psoriasis | Completed | 2015-08-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02555709 | An Ascending Multiple Dose Study With VTP-43742 in Healthy Volunteers and Psori… | Phase1 | Psoriasis | Completed | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02557971 | Urinary Retention Rates in Clinical Practice After Treatment With Onabotulinumt… | — | Urinary Bladder, Overactive | Completed | 2015-08-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02245958 | A Retrospective Chart Review of BOTOX® and Xeomin® for the Management of Cervic… | — | Cervical Dystonia | Completed | 2015-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02555709 | An Ascending Multiple Dose Study With VTP-43742 in Healthy Volunteers and Psori… | Phase1 | Psoriasis | Completed | 2015-08-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT03724292 | An Ascending Multiple Dose Study With VTP-43742 in Healthy Volunteers | Phase1 | Psoriasis | Completed | 2015-08-01 | 2016-03-08 | ClinicalTrials.gov |
| NCT02596217 | Safety, Tolerability and Pharmacokinetics of BI 655066/ABBV-066 (Risankizumab) … | Phase1 | Healthy | Completed | 2015-08-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02596217 | Safety, Tolerability and Pharmacokinetics of BI 655066/ABBV-066 (Risankizumab) … | Phase1 | Healthy | Completed | 2015-08-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02245958 | A Retrospective Chart Review of BOTOX® and Xeomin® for the Management of Cervic… | — | Cervical Dystonia | Completed | 2015-08-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02526641 | Macrophages, Portal Hypertension, and Liver Function During AbbVie Treatment of… | — | Hepatitis C | Completed | 2015-08-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT02596217 | Safety, Tolerability and Pharmacokinetics of BI 655066/ABBV-066 (Risankizumab) … | Phase1 | Healthy | Completed | 2015-08-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02596217 | Safety, Tolerability and Pharmacokinetics of BI 655066/ABBV-066 (Risankizumab) … | Phase1 | Healthy | Completed | 2015-08-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02526641 | Macrophages, Portal Hypertension, and Liver Function During AbbVie Treatment of… | — | Hepatitis C | Completed | 2015-08-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT02526641 | Macrophages, Portal Hypertension, and Liver Function During AbbVie Treatment of… | — | Hepatitis C | Completed | 2015-08-01 | 2020-11-01 | ClinicalTrials.gov |
| NCT02580578 | A Multicenter Prospective Non-Interventional Study Assessing the Management of … | — | Leiomyoma | Completed | 2015-07-31 | 2020-01-31 | ClinicalTrials.gov |
| NCT02580578 | A Multicenter Prospective Non-Interventional Study Assessing the Management of … | — | Leiomyoma | Completed | 2015-07-31 | 2020-01-31 | ClinicalTrials.gov |
| NCT02580578 | A Multicenter Prospective Non-Interventional Study Assessing the Management of … | — | Leiomyoma | Completed | 2015-07-31 | 2020-01-31 | ClinicalTrials.gov |
| NCT02580578 | A Multicenter Prospective Non-Interventional Study Assessing the Management of … | — | Leiomyoma | Completed | 2015-07-31 | 2020-01-31 | ClinicalTrials.gov |
| NCT02554981 | Evaluation of Maintaining Visual Performance in Participants Who Engage in Elec… | Phase4 | Dry Eye Syndromes | Completed | 2015-07-21 | 2016-03-24 | ClinicalTrials.gov |
| NCT02554981 | Evaluation of Maintaining Visual Performance in Participants Who Engage in Elec… | Phase4 | Dry Eye Syndromes | Completed | 2015-07-21 | 2016-03-24 | ClinicalTrials.gov |
| NCT02554981 | Evaluation of Maintaining Visual Performance in Participants Who Engage in Elec… | Phase4 | Dry Eye Syndromes | Completed | 2015-07-21 | 2016-03-24 | ClinicalTrials.gov |
| NCT02554981 | Evaluation of Maintaining Visual Performance in Participants Who Engage in Elec… | Phase4 | Dry Eye Syndromes | Completed | 2015-07-21 | 2016-03-24 | ClinicalTrials.gov |
| NCT02517528 | ABT-450/Ritonavir/ ABT-267 (ABT-450/r/ABT-267) and ABT-333 Co-Administered With… | Phase3 | Chronic Hepatitis C Virus (HCV) | Completed | 2015-07-20 | 2017-03-16 | ClinicalTrials.gov |
| NCT02517528 | ABT-450/Ritonavir/ ABT-267 (ABT-450/r/ABT-267) and ABT-333 Co-Administered With… | Phase3 | Chronic Hepatitis C Virus (HCV) | Completed | 2015-07-20 | 2017-03-16 | ClinicalTrials.gov |
| NCT02517528 | ABT-450/Ritonavir/ ABT-267 (ABT-450/r/ABT-267) and ABT-333 Co-Administered With… | Phase3 | Chronic Hepatitis C Virus (HCV) | Completed | 2015-07-20 | 2017-03-16 | ClinicalTrials.gov |
| NCT02517528 | ABT-450/Ritonavir/ ABT-267 (ABT-450/r/ABT-267) and ABT-333 Co-Administered With… | Phase3 | Chronic Hepatitis C Virus (HCV) | Completed | 2015-07-20 | 2017-03-16 | ClinicalTrials.gov |
| NCT02470585 | Veliparib With Carboplatin and Paclitaxel and as Continuation Maintenance Thera… | Phase3 | Ovarian Cancer | Terminated | 2015-07-14 | 2023-10-05 | ClinicalTrials.gov |
| NCT02470585 | Veliparib With Carboplatin and Paclitaxel and as Continuation Maintenance Thera… | Phase3 | Ovarian Cancer | Terminated | 2015-07-14 | 2023-10-05 | ClinicalTrials.gov |
| NCT02470585 | Veliparib With Carboplatin and Paclitaxel and as Continuation Maintenance Thera… | Phase3 | Ovarian Cancer | Terminated | 2015-07-14 | 2023-10-05 | ClinicalTrials.gov |
| NCT02470585 | Veliparib With Carboplatin and Paclitaxel and as Continuation Maintenance Thera… | Phase3 | Ovarian Cancer | Terminated | 2015-07-14 | 2023-10-05 | ClinicalTrials.gov |
| NCT02451839 | An ObserVatIonal STudy of the Effectiveness of AdaLimumab on Health and Disabil… | — | Crohn's Disease | Completed | 2015-07-06 | 2017-12-05 | ClinicalTrials.gov |
| NCT02451839 | An ObserVatIonal STudy of the Effectiveness of AdaLimumab on Health and Disabil… | — | Crohn's Disease | Completed | 2015-07-06 | 2017-12-05 | ClinicalTrials.gov |
| NCT02451839 | An ObserVatIonal STudy of the Effectiveness of AdaLimumab on Health and Disabil… | — | Crohn's Disease | Completed | 2015-07-06 | 2017-12-05 | ClinicalTrials.gov |
| NCT02451839 | An ObserVatIonal STudy of the Effectiveness of AdaLimumab on Health and Disabil… | — | Crohn's Disease | Completed | 2015-07-06 | 2017-12-05 | ClinicalTrials.gov |
| NCT02734173 | Pilot HCV Direct Acting Antiviral Therapy and Metabolism | Phase4 | Hepatitis C | Completed | 2015-07-01 | 2017-05-31 | ClinicalTrials.gov |
| NCT02483104 | Veliparib in Combination With Carboplatin And Weekly Paclitaxel in Japanese Sub… | Phase1 | Ovarian Cancer | Completed | 2015-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02531178 | A Study to Assess the Safety, Tolerability and Pharmacokinetics of Multiple Sub… | Phase1 | Rheumatoid Arthritis | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02162472 | Videocapillaroscopy Assessment During Systemic Agent Therapy in Psoriasis | — | Psoriasis | Completed | 2015-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02734173 | Pilot HCV Direct Acting Antiviral Therapy and Metabolism | Phase4 | Hepatitis C | Completed | 2015-07-01 | 2017-05-31 | ClinicalTrials.gov |
| NCT02162472 | Videocapillaroscopy Assessment During Systemic Agent Therapy in Psoriasis | — | Psoriasis | Completed | 2015-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02517515 | ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 in Treatment-Naïve an… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02504099 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/r With o… | Phase3 | Chronic Hepatitis C Infection | Terminated | 2015-07-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02531178 | A Study to Assess the Safety, Tolerability and Pharmacokinetics of Multiple Sub… | Phase1 | Rheumatoid Arthritis | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02517515 | ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 in Treatment-Naïve an… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02531178 | A Study to Assess the Safety, Tolerability and Pharmacokinetics of Multiple Sub… | Phase1 | Rheumatoid Arthritis | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02517515 | ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 in Treatment-Naïve an… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02734173 | Pilot HCV Direct Acting Antiviral Therapy and Metabolism | Phase4 | Hepatitis C | Completed | 2015-07-01 | 2017-05-31 | ClinicalTrials.gov |
| NCT02483104 | Veliparib in Combination With Carboplatin And Weekly Paclitaxel in Japanese Sub… | Phase1 | Ovarian Cancer | Completed | 2015-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02162472 | Videocapillaroscopy Assessment During Systemic Agent Therapy in Psoriasis | — | Psoriasis | Completed | 2015-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02504099 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/r With o… | Phase3 | Chronic Hepatitis C Infection | Terminated | 2015-07-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02162472 | Videocapillaroscopy Assessment During Systemic Agent Therapy in Psoriasis | — | Psoriasis | Completed | 2015-07-01 | 2021-12-31 | ClinicalTrials.gov |
| NCT02531178 | A Study to Assess the Safety, Tolerability and Pharmacokinetics of Multiple Sub… | Phase1 | Rheumatoid Arthritis | Completed | 2015-07-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02483104 | Veliparib in Combination With Carboplatin And Weekly Paclitaxel in Japanese Sub… | Phase1 | Ovarian Cancer | Completed | 2015-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02504099 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/r With o… | Phase3 | Chronic Hepatitis C Infection | Terminated | 2015-07-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02504099 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/r With o… | Phase3 | Chronic Hepatitis C Infection | Terminated | 2015-07-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02483104 | Veliparib in Combination With Carboplatin And Weekly Paclitaxel in Japanese Sub… | Phase1 | Ovarian Cancer | Completed | 2015-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02517515 | ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) and ABT-333 in Treatment-Naïve an… | Phase3 | Hepatitis C Virus (HCV) | Completed | 2015-07-01 | 2017-06-01 | ClinicalTrials.gov |
| NCT02734173 | Pilot HCV Direct Acting Antiviral Therapy and Metabolism | Phase4 | Hepatitis C | Completed | 2015-07-01 | 2017-05-31 | ClinicalTrials.gov |
| NCT02462486 | Safety and Efficacy of Abicipar Pegol in Participants With Neovascular Age-rela… | Phase3 | Macular Degeneration | Completed | 2015-06-25 | 2019-06-06 | ClinicalTrials.gov |
| NCT02462486 | Safety and Efficacy of Abicipar Pegol in Participants With Neovascular Age-rela… | Phase3 | Macular Degeneration | Completed | 2015-06-25 | 2019-06-06 | ClinicalTrials.gov |
| NCT02462486 | Safety and Efficacy of Abicipar Pegol in Participants With Neovascular Age-rela… | Phase3 | Macular Degeneration | Completed | 2015-06-25 | 2019-06-06 | ClinicalTrials.gov |
| NCT02462486 | Safety and Efficacy of Abicipar Pegol in Participants With Neovascular Age-rela… | Phase3 | Macular Degeneration | Completed | 2015-06-25 | 2019-06-06 | ClinicalTrials.gov |
| NCT02443298 | Efficacy and Safety of BI 655066/ABBV-066 (Risankizumab) in Patients With Sever… | Phase2 | Asthma | Completed | 2015-06-23 | 2018-02-02 | ClinicalTrials.gov |
| NCT02443298 | Efficacy and Safety of BI 655066/ABBV-066 (Risankizumab) in Patients With Sever… | Phase2 | Asthma | Completed | 2015-06-23 | 2018-02-02 | ClinicalTrials.gov |
| NCT02443298 | Efficacy and Safety of BI 655066/ABBV-066 (Risankizumab) in Patients With Sever… | Phase2 | Asthma | Completed | 2015-06-23 | 2018-02-02 | ClinicalTrials.gov |
| NCT02443298 | Efficacy and Safety of BI 655066/ABBV-066 (Risankizumab) in Patients With Sever… | Phase2 | Asthma | Completed | 2015-06-23 | 2018-02-02 | ClinicalTrials.gov |
| NCT02441283 | A Study to Assess Resistance and Durability of Response to ABT-493 and/or ABT-5… | Phase2 | Hepatitis C | Completed | 2015-06-22 | 2019-10-15 | ClinicalTrials.gov |
| NCT02441283 | A Study to Assess Resistance and Durability of Response to ABT-493 and/or ABT-5… | Phase2 | Hepatitis C | Completed | 2015-06-22 | 2019-10-15 | ClinicalTrials.gov |
| NCT02441283 | A Study to Assess Resistance and Durability of Response to ABT-493 and/or ABT-5… | Phase2 | Hepatitis C | Completed | 2015-06-22 | 2019-10-15 | ClinicalTrials.gov |
| NCT02441283 | A Study to Assess Resistance and Durability of Response to ABT-493 and/or ABT-5… | Phase2 | Hepatitis C | Completed | 2015-06-22 | 2019-10-15 | ClinicalTrials.gov |
| NCT02499263 | A Prospective Non-interventional Multicenter Study to Evaluate the Effectivenes… | — | Ulcerative Colitis | Completed | 2015-06-11 | 2018-09-17 | ClinicalTrials.gov |
| NCT02499263 | A Prospective Non-interventional Multicenter Study to Evaluate the Effectivenes… | — | Ulcerative Colitis | Completed | 2015-06-11 | 2018-09-17 | ClinicalTrials.gov |
| NCT02499263 | A Prospective Non-interventional Multicenter Study to Evaluate the Effectivenes… | — | Ulcerative Colitis | Completed | 2015-06-11 | 2018-09-17 | ClinicalTrials.gov |
| NCT02499263 | A Prospective Non-interventional Multicenter Study to Evaluate the Effectivenes… | — | Ulcerative Colitis | Completed | 2015-06-11 | 2018-09-17 | ClinicalTrials.gov |
| NCT02448043 | Cutaneous Prostaglandin Application: Nail Growth, Nail Brittleness, and Eye Pre… | Na | Nail Growth Cessation | Completed | 2015-06-04 | 2016-05-06 | ClinicalTrials.gov |
| NCT02448043 | Cutaneous Prostaglandin Application: Nail Growth, Nail Brittleness, and Eye Pre… | Na | Nail Growth Cessation | Completed | 2015-06-04 | 2016-05-06 | ClinicalTrials.gov |
| NCT02448043 | Cutaneous Prostaglandin Application: Nail Growth, Nail Brittleness, and Eye Pre… | Na | Nail Growth Cessation | Completed | 2015-06-04 | 2016-05-06 | ClinicalTrials.gov |
| NCT02448043 | Cutaneous Prostaglandin Application: Nail Growth, Nail Brittleness, and Eye Pre… | Na | Nail Growth Cessation | Completed | 2015-06-04 | 2016-05-06 | ClinicalTrials.gov |
| NCT02335905 | Ceftaroline for Treatment of Hematogenously Acquired Staphylococcus Aureus Oste… | Phase1 | Hematogenously Acquired Staphylococcus Aureus Osteomyelitis | Completed | 2015-06-03 | 2020-06-16 | ClinicalTrials.gov |
| NCT02335905 | Ceftaroline for Treatment of Hematogenously Acquired Staphylococcus Aureus Oste… | Phase1 | Hematogenously Acquired Staphylococcus Aureus Osteomyelitis | Completed | 2015-06-03 | 2020-06-16 | ClinicalTrials.gov |
| NCT02335905 | Ceftaroline for Treatment of Hematogenously Acquired Staphylococcus Aureus Oste… | Phase1 | Hematogenously Acquired Staphylococcus Aureus Osteomyelitis | Completed | 2015-06-03 | 2020-06-16 | ClinicalTrials.gov |
| NCT02335905 | Ceftaroline for Treatment of Hematogenously Acquired Staphylococcus Aureus Oste… | Phase1 | Hematogenously Acquired Staphylococcus Aureus Osteomyelitis | Completed | 2015-06-03 | 2020-06-16 | ClinicalTrials.gov |
| NCT02435914 | Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Su… | Phase2 | Dry Eye Syndromes | Completed | 2015-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02471651 | Dexamethasone Intravitreal Implant for the Treatment of Persistent Diabetic Mac… | Phase4 | Diabetic Macular Edema | Completed | 2015-06-01 | 2018-10-24 | ClinicalTrials.gov |
| NCT02420730 | Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Par… | Phase1 | Healthy Volunteers | Completed | 2015-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02435914 | Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Su… | Phase2 | Dry Eye Syndromes | Completed | 2015-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02435914 | Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Su… | Phase2 | Dry Eye Syndromes | Completed | 2015-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02476617 | Ombitasvir/ABT-450 (Paritaprevir)/Ritonavir With Dasabuvir and Ribavirin (RBV) … | Phase3 | Chronic Hepatitis C | Completed | 2015-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02471651 | Dexamethasone Intravitreal Implant for the Treatment of Persistent Diabetic Mac… | Phase4 | Diabetic Macular Edema | Completed | 2015-06-01 | 2018-10-24 | ClinicalTrials.gov |
| NCT02461745 | Real World Study: Genotype 1 Chronic Hepatitis C Virus Treatment and Evaluation… | Phase4 | Hepatitis C, Chronic | Completed | 2015-06-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02420730 | Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Par… | Phase1 | Healthy Volunteers | Completed | 2015-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02493855 | Ombitasvir/ABT-450/Ritonavir and Dasabuvir Therapy With Low Dose Ribavirin (RBV… | Phase2 | Chronic Hepatitis C | Completed | 2015-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02461745 | Real World Study: Genotype 1 Chronic Hepatitis C Virus Treatment and Evaluation… | Phase4 | Hepatitis C, Chronic | Completed | 2015-06-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02420730 | Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Par… | Phase1 | Healthy Volunteers | Completed | 2015-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02435914 | Safety, Efficacy, Tolerability and Pharmacokinetics of AGN-223575 Ophthalmic Su… | Phase2 | Dry Eye Syndromes | Completed | 2015-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02420730 | Safety, Tolerability and Systemic Pharmacokinetics of AGN-232411 in Healthy Par… | Phase1 | Healthy Volunteers | Completed | 2015-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02476617 | Ombitasvir/ABT-450 (Paritaprevir)/Ritonavir With Dasabuvir and Ribavirin (RBV) … | Phase3 | Chronic Hepatitis C | Completed | 2015-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02476617 | Ombitasvir/ABT-450 (Paritaprevir)/Ritonavir With Dasabuvir and Ribavirin (RBV) … | Phase3 | Chronic Hepatitis C | Completed | 2015-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02471651 | Dexamethasone Intravitreal Implant for the Treatment of Persistent Diabetic Mac… | Phase4 | Diabetic Macular Edema | Completed | 2015-06-01 | 2018-10-24 | ClinicalTrials.gov |
| NCT02493855 | Ombitasvir/ABT-450/Ritonavir and Dasabuvir Therapy With Low Dose Ribavirin (RBV… | Phase2 | Chronic Hepatitis C | Completed | 2015-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02476617 | Ombitasvir/ABT-450 (Paritaprevir)/Ritonavir With Dasabuvir and Ribavirin (RBV) … | Phase3 | Chronic Hepatitis C | Completed | 2015-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02493855 | Ombitasvir/ABT-450/Ritonavir and Dasabuvir Therapy With Low Dose Ribavirin (RBV… | Phase2 | Chronic Hepatitis C | Completed | 2015-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02461745 | Real World Study: Genotype 1 Chronic Hepatitis C Virus Treatment and Evaluation… | Phase4 | Hepatitis C, Chronic | Completed | 2015-06-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02471651 | Dexamethasone Intravitreal Implant for the Treatment of Persistent Diabetic Mac… | Phase4 | Diabetic Macular Edema | Completed | 2015-06-01 | 2018-10-24 | ClinicalTrials.gov |
| NCT02461745 | Real World Study: Genotype 1 Chronic Hepatitis C Virus Treatment and Evaluation… | Phase4 | Hepatitis C, Chronic | Completed | 2015-06-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02493855 | Ombitasvir/ABT-450/Ritonavir and Dasabuvir Therapy With Low Dose Ribavirin (RBV… | Phase2 | Chronic Hepatitis C | Completed | 2015-06-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02411110 | A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bla… | Phase2 | Cystitis, Interstitial | Completed | 2015-05-21 | 2017-01-09 | ClinicalTrials.gov |
| NCT02411110 | A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bla… | Phase2 | Cystitis, Interstitial | Completed | 2015-05-21 | 2017-01-09 | ClinicalTrials.gov |
| NCT02411110 | A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bla… | Phase2 | Cystitis, Interstitial | Completed | 2015-05-21 | 2017-01-09 | ClinicalTrials.gov |
| NCT02411110 | A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis/Bla… | Phase2 | Cystitis, Interstitial | Completed | 2015-05-21 | 2017-01-09 | ClinicalTrials.gov |
| NCT02442284 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C | Completed | 2015-05-13 | 2016-10-31 | ClinicalTrials.gov |
| NCT02442284 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C | Completed | 2015-05-13 | 2016-10-31 | ClinicalTrials.gov |
| NCT02442284 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C | Completed | 2015-05-13 | 2016-10-31 | ClinicalTrials.gov |
| NCT02442284 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C | Completed | 2015-05-13 | 2016-10-31 | ClinicalTrials.gov |
| NCT02462525 | Dose-Escalation Study of ABBV-838, an Antibody Drug Conjugate, in Subjects With… | Phase1 | Multiple Myeloma | Terminated | 2015-05-06 | 2017-12-06 | ClinicalTrials.gov |
| NCT02401503 | Sequential Regimen of Bendamustine-Debulking Followed by ABT-199 and GA101-Indu… | Phase2 | Chronic Lymphocytic Leucemia | Completed | 2015-05-06 | 2024-12-17 | ClinicalTrials.gov |
| NCT02401503 | Sequential Regimen of Bendamustine-Debulking Followed by ABT-199 and GA101-Indu… | Phase2 | Chronic Lymphocytic Leucemia | Completed | 2015-05-06 | 2024-12-17 | ClinicalTrials.gov |
| NCT02401503 | Sequential Regimen of Bendamustine-Debulking Followed by ABT-199 and GA101-Indu… | Phase2 | Chronic Lymphocytic Leucemia | Completed | 2015-05-06 | 2024-12-17 | ClinicalTrials.gov |
| NCT02401503 | Sequential Regimen of Bendamustine-Debulking Followed by ABT-199 and GA101-Indu… | Phase2 | Chronic Lymphocytic Leucemia | Completed | 2015-05-06 | 2024-12-17 | ClinicalTrials.gov |
| NCT02462525 | Dose-Escalation Study of ABBV-838, an Antibody Drug Conjugate, in Subjects With… | Phase1 | Multiple Myeloma | Terminated | 2015-05-06 | 2017-12-06 | ClinicalTrials.gov |
| NCT02462525 | Dose-Escalation Study of ABBV-838, an Antibody Drug Conjugate, in Subjects With… | Phase1 | Multiple Myeloma | Terminated | 2015-05-06 | 2017-12-06 | ClinicalTrials.gov |
| NCT02462525 | Dose-Escalation Study of ABBV-838, an Antibody Drug Conjugate, in Subjects With… | Phase1 | Multiple Myeloma | Terminated | 2015-05-06 | 2017-12-06 | ClinicalTrials.gov |
| NCT02255422 | RTA 408 Capsules in Patients With Mitochondrial Myopathy - MOTOR | Phase2 | MItochondrial Myopathies | Completed | 2015-05-05 | 2017-11-30 | ClinicalTrials.gov |
| NCT02255422 | RTA 408 Capsules in Patients With Mitochondrial Myopathy - MOTOR | Phase2 | MItochondrial Myopathies | Completed | 2015-05-05 | 2017-11-30 | ClinicalTrials.gov |
| NCT02255422 | RTA 408 Capsules in Patients With Mitochondrial Myopathy - MOTOR | Phase2 | MItochondrial Myopathies | Completed | 2015-05-05 | 2017-11-30 | ClinicalTrials.gov |
| NCT02255422 | RTA 408 Capsules in Patients With Mitochondrial Myopathy - MOTOR | Phase2 | MItochondrial Myopathies | Completed | 2015-05-05 | 2017-11-30 | ClinicalTrials.gov |
| NCT02475369 | Pancreatic Enzyme Supplementation for Celiac Disease | Phase4 | Celiac Disease | Terminated | 2015-05-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02616614 | Double-blind Placebo-controlled Trial of Generic Clindamycin/Benzoyl Peroxide G… | Phase3 | Acne Vulgaris | Completed | 2015-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02446314 | An Investigation Into the Effects of a Wild Blueberry Powder and a Wild Blueber… | Na | Cognitive Decline | Completed | 2015-05-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02475369 | Pancreatic Enzyme Supplementation for Celiac Disease | Phase4 | Celiac Disease | Terminated | 2015-05-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02616614 | Double-blind Placebo-controlled Trial of Generic Clindamycin/Benzoyl Peroxide G… | Phase3 | Acne Vulgaris | Completed | 2015-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02446314 | An Investigation Into the Effects of a Wild Blueberry Powder and a Wild Blueber… | Na | Cognitive Decline | Completed | 2015-05-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02446314 | An Investigation Into the Effects of a Wild Blueberry Powder and a Wild Blueber… | Na | Cognitive Decline | Completed | 2015-05-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02446314 | An Investigation Into the Effects of a Wild Blueberry Powder and a Wild Blueber… | Na | Cognitive Decline | Completed | 2015-05-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02616614 | Double-blind Placebo-controlled Trial of Generic Clindamycin/Benzoyl Peroxide G… | Phase3 | Acne Vulgaris | Completed | 2015-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02616614 | Double-blind Placebo-controlled Trial of Generic Clindamycin/Benzoyl Peroxide G… | Phase3 | Acne Vulgaris | Completed | 2015-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02475369 | Pancreatic Enzyme Supplementation for Celiac Disease | Phase4 | Celiac Disease | Terminated | 2015-05-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02475369 | Pancreatic Enzyme Supplementation for Celiac Disease | Phase4 | Celiac Disease | Terminated | 2015-05-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02412371 | A Study Evaluating the Efficacy and Tolerability of Veliparib in Combination Wi… | Phase1 | Non-small Cell Lung Cancer Stage III | Terminated | 2015-04-30 | 2019-08-05 | ClinicalTrials.gov |
| NCT02412371 | A Study Evaluating the Efficacy and Tolerability of Veliparib in Combination Wi… | Phase1 | Non-small Cell Lung Cancer Stage III | Terminated | 2015-04-30 | 2019-08-05 | ClinicalTrials.gov |
| NCT02412371 | A Study Evaluating the Efficacy and Tolerability of Veliparib in Combination Wi… | Phase1 | Non-small Cell Lung Cancer Stage III | Terminated | 2015-04-30 | 2019-08-05 | ClinicalTrials.gov |
| NCT02412371 | A Study Evaluating the Efficacy and Tolerability of Veliparib in Combination Wi… | Phase1 | Non-small Cell Lung Cancer Stage III | Terminated | 2015-04-30 | 2019-08-05 | ClinicalTrials.gov |
| NCT02349451 | A Phase 2 Study to Investigate the Safety, Tolerability and Efficacy of ABT-122… | Phase2 | Psoriatic Arthritis | Completed | 2015-04-28 | 2016-07-04 | ClinicalTrials.gov |
| NCT02349451 | A Phase 2 Study to Investigate the Safety, Tolerability and Efficacy of ABT-122… | Phase2 | Psoriatic Arthritis | Completed | 2015-04-28 | 2016-07-04 | ClinicalTrials.gov |
| NCT02349451 | A Phase 2 Study to Investigate the Safety, Tolerability and Efficacy of ABT-122… | Phase2 | Psoriatic Arthritis | Completed | 2015-04-28 | 2016-07-04 | ClinicalTrials.gov |
| NCT02349451 | A Phase 2 Study to Investigate the Safety, Tolerability and Efficacy of ABT-122… | Phase2 | Psoriatic Arthritis | Completed | 2015-04-28 | 2016-07-04 | ClinicalTrials.gov |
| NCT02442271 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs in Adul… | Phase3 | Chronic Hepatitis C Infection | Completed | 2015-04-27 | 2016-09-26 | ClinicalTrials.gov |
| NCT02442271 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs in Adul… | Phase3 | Chronic Hepatitis C Infection | Completed | 2015-04-27 | 2016-09-26 | ClinicalTrials.gov |
| NCT02442271 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs in Adul… | Phase3 | Chronic Hepatitis C Infection | Completed | 2015-04-27 | 2016-09-26 | ClinicalTrials.gov |
| NCT02442271 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs in Adul… | Phase3 | Chronic Hepatitis C Infection | Completed | 2015-04-27 | 2016-09-26 | ClinicalTrials.gov |
| NCT02381444 | Health Related Quality of Life in LCIG Patients and LCIG Eligible Patients Cont… | — | Parkinson's Disease (PD) | Completed | 2015-04-17 | 2020-01-07 | ClinicalTrials.gov |
| NCT02381444 | Health Related Quality of Life in LCIG Patients and LCIG Eligible Patients Cont… | — | Parkinson's Disease (PD) | Completed | 2015-04-17 | 2020-01-07 | ClinicalTrials.gov |
| NCT02381444 | Health Related Quality of Life in LCIG Patients and LCIG Eligible Patients Cont… | — | Parkinson's Disease (PD) | Completed | 2015-04-17 | 2020-01-07 | ClinicalTrials.gov |
| NCT02381444 | Health Related Quality of Life in LCIG Patients and LCIG Eligible Patients Cont… | — | Parkinson's Disease (PD) | Completed | 2015-04-17 | 2020-01-07 | ClinicalTrials.gov |
| NCT02395042 | A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis Wit… | Phase2 | Cystitis, Interstitial | Completed | 2015-04-15 | 2017-11-20 | ClinicalTrials.gov |
| NCT02395042 | A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis Wit… | Phase2 | Cystitis, Interstitial | Completed | 2015-04-15 | 2017-11-20 | ClinicalTrials.gov |
| NCT02395042 | A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis Wit… | Phase2 | Cystitis, Interstitial | Completed | 2015-04-15 | 2017-11-20 | ClinicalTrials.gov |
| NCT02395042 | A Safety and Efficacy Study of LiRIS® in Females With Interstitial Cystitis Wit… | Phase2 | Cystitis, Interstitial | Completed | 2015-04-15 | 2017-11-20 | ClinicalTrials.gov |
| NCT02391480 | A Study Evaluating the Safety and Pharmacokinetics of ABBV-075 in Subjects With… | Phase1 | Cancer | Completed | 2015-04-14 | 2019-07-05 | ClinicalTrials.gov |
| NCT02391480 | A Study Evaluating the Safety and Pharmacokinetics of ABBV-075 in Subjects With… | Phase1 | Cancer | Completed | 2015-04-14 | 2019-07-05 | ClinicalTrials.gov |
| NCT02391480 | A Study Evaluating the Safety and Pharmacokinetics of ABBV-075 in Subjects With… | Phase1 | Cancer | Completed | 2015-04-14 | 2019-07-05 | ClinicalTrials.gov |
| NCT02391480 | A Study Evaluating the Safety and Pharmacokinetics of ABBV-075 in Subjects With… | Phase1 | Cancer | Completed | 2015-04-14 | 2019-07-05 | ClinicalTrials.gov |
| NCT02118714 | Atrasentan Spermatogenesis and Testicular Function | Phase2 | Nephropathy | Completed | 2015-04-06 | 2018-07-16 | ClinicalTrials.gov |
| NCT02118714 | Atrasentan Spermatogenesis and Testicular Function | Phase2 | Nephropathy | Completed | 2015-04-06 | 2018-07-16 | ClinicalTrials.gov |
| NCT02118714 | Atrasentan Spermatogenesis and Testicular Function | Phase2 | Nephropathy | Completed | 2015-04-06 | 2018-07-16 | ClinicalTrials.gov |
| NCT02118714 | Atrasentan Spermatogenesis and Testicular Function | Phase2 | Nephropathy | Completed | 2015-04-06 | 2018-07-16 | ClinicalTrials.gov |
| NCT02419560 | Optimal Dose Finding Study ABT-199 and Ibrutinib in MCL | Phase1 | Lymphoma, Mantle-Cell | Completed | 2015-04-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02414633 | Special Investigation in Patients With Psoriatic Arthritis (PsA) (Working Produ… | — | Psoriatic Arthritis | Completed | 2015-04-01 | 2017-03-13 | ClinicalTrials.gov |
| NCT03288337 | Impact of Hidradenitis Suppurativa on Quality of Life Functions | — | Hidradenitis Suppurativa | Completed | 2015-04-01 | 2022-09-06 | ClinicalTrials.gov |
| NCT02446717 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of ABT-493 and A… | Phase2 | Chronic Hepatitis C | Completed | 2015-04-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02446717 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of ABT-493 and A… | Phase2 | Chronic Hepatitis C | Completed | 2015-04-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02433340 | Phase 2, Multicenter, Open-Label Extension Study With ABT-122 in Rheumatoid Art… | Phase2 | Rheumatoid Arthritis | Completed | 2015-04-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT03288337 | Impact of Hidradenitis Suppurativa on Quality of Life Functions | — | Hidradenitis Suppurativa | Completed | 2015-04-01 | 2022-09-06 | ClinicalTrials.gov |
| NCT02446717 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of ABT-493 and A… | Phase2 | Chronic Hepatitis C | Completed | 2015-04-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT03288337 | Impact of Hidradenitis Suppurativa on Quality of Life Functions | — | Hidradenitis Suppurativa | Completed | 2015-04-01 | 2022-09-06 | ClinicalTrials.gov |
| NCT02446717 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of ABT-493 and A… | Phase2 | Chronic Hepatitis C | Completed | 2015-04-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02419560 | Optimal Dose Finding Study ABT-199 and Ibrutinib in MCL | Phase1 | Lymphoma, Mantle-Cell | Completed | 2015-04-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02419560 | Optimal Dose Finding Study ABT-199 and Ibrutinib in MCL | Phase1 | Lymphoma, Mantle-Cell | Completed | 2015-04-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT02433340 | Phase 2, Multicenter, Open-Label Extension Study With ABT-122 in Rheumatoid Art… | Phase2 | Rheumatoid Arthritis | Completed | 2015-04-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02419560 | Optimal Dose Finding Study ABT-199 and Ibrutinib in MCL | Phase1 | Lymphoma, Mantle-Cell | Completed | 2015-04-01 | 2021-05-01 | ClinicalTrials.gov |
| NCT03288337 | Impact of Hidradenitis Suppurativa on Quality of Life Functions | — | Hidradenitis Suppurativa | Completed | 2015-04-01 | 2022-09-06 | ClinicalTrials.gov |
| NCT02414633 | Special Investigation in Patients With Psoriatic Arthritis (PsA) (Working Produ… | — | Psoriatic Arthritis | Completed | 2015-04-01 | 2017-03-13 | ClinicalTrials.gov |
| NCT02414633 | Special Investigation in Patients With Psoriatic Arthritis (PsA) (Working Produ… | — | Psoriatic Arthritis | Completed | 2015-04-01 | 2017-03-13 | ClinicalTrials.gov |
| NCT02433340 | Phase 2, Multicenter, Open-Label Extension Study With ABT-122 in Rheumatoid Art… | Phase2 | Rheumatoid Arthritis | Completed | 2015-04-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02433340 | Phase 2, Multicenter, Open-Label Extension Study With ABT-122 in Rheumatoid Art… | Phase2 | Rheumatoid Arthritis | Completed | 2015-04-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02414633 | Special Investigation in Patients With Psoriatic Arthritis (PsA) (Working Produ… | — | Psoriatic Arthritis | Completed | 2015-04-01 | 2017-03-13 | ClinicalTrials.gov |
| NCT02413346 | A Multi-Center Open-Label Evaluation of the Safety of Sarecycline Tablets in th… | Phase3 | Acne Vulgaris | Completed | 2015-03-20 | 2016-08-26 | ClinicalTrials.gov |
| NCT02413346 | A Multi-Center Open-Label Evaluation of the Safety of Sarecycline Tablets in th… | Phase3 | Acne Vulgaris | Completed | 2015-03-20 | 2016-08-26 | ClinicalTrials.gov |
| NCT02413346 | A Multi-Center Open-Label Evaluation of the Safety of Sarecycline Tablets in th… | Phase3 | Acne Vulgaris | Completed | 2015-03-20 | 2016-08-26 | ClinicalTrials.gov |
| NCT02413346 | A Multi-Center Open-Label Evaluation of the Safety of Sarecycline Tablets in th… | Phase3 | Acne Vulgaris | Completed | 2015-03-20 | 2016-08-26 | ClinicalTrials.gov |
| NCT02365649 | A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of ABT-494 fo… | Phase2 | Crohn's Disease | Completed | 2015-03-17 | 2017-08-03 | ClinicalTrials.gov |
| NCT02365649 | A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of ABT-494 fo… | Phase2 | Crohn's Disease | Completed | 2015-03-17 | 2017-08-03 | ClinicalTrials.gov |
| NCT02365649 | A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of ABT-494 fo… | Phase2 | Crohn's Disease | Completed | 2015-03-17 | 2017-08-03 | ClinicalTrials.gov |
| NCT02365649 | A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of ABT-494 fo… | Phase2 | Crohn's Disease | Completed | 2015-03-17 | 2017-08-03 | ClinicalTrials.gov |
| NCT02399345 | Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir Co-Administered With Sofosbuvir… | Phase3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | Completed | 2015-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02442258 | Pharmacokinetics and Safety of ABT-493 and ABT-530 in Subjects With Normal and … | Phase1 | Renal Impairment | Completed | 2015-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02399345 | Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir Co-Administered With Sofosbuvir… | Phase3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | Completed | 2015-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02471118 | Osteoarthritis of the Knee, Inflammation, and the Effect of Adalimumab (OKINADA) | Phase2 | Osteoarthritis, Knee | Completed | 2015-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02384538 | A Phase 2a Study Evaluating the Safety and Efficacy of ABT-981 in Patients With… | Phase2 | Erosive Hand Osteoarthritis | Completed | 2015-03-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02384538 | A Phase 2a Study Evaluating the Safety and Efficacy of ABT-981 in Patients With… | Phase2 | Erosive Hand Osteoarthritis | Completed | 2015-03-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02399345 | Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir Co-Administered With Sofosbuvir… | Phase3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | Completed | 2015-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02471118 | Osteoarthritis of the Knee, Inflammation, and the Effect of Adalimumab (OKINADA) | Phase2 | Osteoarthritis, Knee | Completed | 2015-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02442258 | Pharmacokinetics and Safety of ABT-493 and ABT-530 in Subjects With Normal and … | Phase1 | Renal Impairment | Completed | 2015-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02399345 | Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir Co-Administered With Sofosbuvir… | Phase3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | Completed | 2015-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02384538 | A Phase 2a Study Evaluating the Safety and Efficacy of ABT-981 in Patients With… | Phase2 | Erosive Hand Osteoarthritis | Completed | 2015-03-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02384538 | A Phase 2a Study Evaluating the Safety and Efficacy of ABT-981 in Patients With… | Phase2 | Erosive Hand Osteoarthritis | Completed | 2015-03-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02442258 | Pharmacokinetics and Safety of ABT-493 and ABT-530 in Subjects With Normal and … | Phase1 | Renal Impairment | Completed | 2015-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02442258 | Pharmacokinetics and Safety of ABT-493 and ABT-530 in Subjects With Normal and … | Phase1 | Renal Impairment | Completed | 2015-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02471118 | Osteoarthritis of the Knee, Inflammation, and the Effect of Adalimumab (OKINADA) | Phase2 | Osteoarthritis, Knee | Completed | 2015-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02471118 | Osteoarthritis of the Knee, Inflammation, and the Effect of Adalimumab (OKINADA) | Phase2 | Osteoarthritis, Knee | Completed | 2015-03-01 | 2021-03-01 | ClinicalTrials.gov |
| NCT02415959 | Efficacy and Safety Study of Creon IR in Subjects With Pancreatic Exocrine Insu… | Phase2 | Exocrine Pancreatic Insufficiency in Subjects With Cystic Fibrosis | Completed | 2015-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02559908 | A Study of Hyaluronic Acid Injectable Gel (VYC-25L) for Restoration and Creatio… | Na | Chin Retrusion | Completed | 2015-02-26 | 2017-12-01 | ClinicalTrials.gov |
| NCT02559908 | A Study of Hyaluronic Acid Injectable Gel (VYC-25L) for Restoration and Creatio… | Na | Chin Retrusion | Completed | 2015-02-26 | 2017-12-01 | ClinicalTrials.gov |
| NCT02559908 | A Study of Hyaluronic Acid Injectable Gel (VYC-25L) for Restoration and Creatio… | Na | Chin Retrusion | Completed | 2015-02-26 | 2017-12-01 | ClinicalTrials.gov |
| NCT02559908 | A Study of Hyaluronic Acid Injectable Gel (VYC-25L) for Restoration and Creatio… | Na | Chin Retrusion | Completed | 2015-02-26 | 2017-12-01 | ClinicalTrials.gov |
| NCT02272803 | Phase II Study of Lenalidomide/Dexamethasone With or Without Elotuzumab for New… | Phase2 | Multiple Myeloma | Completed | 2015-02-20 | 2021-07-21 | ClinicalTrials.gov |
| NCT02272803 | Phase II Study of Lenalidomide/Dexamethasone With or Without Elotuzumab for New… | Phase2 | Multiple Myeloma | Completed | 2015-02-20 | 2021-07-21 | ClinicalTrials.gov |
| NCT02272803 | Phase II Study of Lenalidomide/Dexamethasone With or Without Elotuzumab for New… | Phase2 | Multiple Myeloma | Completed | 2015-02-20 | 2021-07-21 | ClinicalTrials.gov |
| NCT02272803 | Phase II Study of Lenalidomide/Dexamethasone With or Without Elotuzumab for New… | Phase2 | Multiple Myeloma | Completed | 2015-02-20 | 2021-07-21 | ClinicalTrials.gov |
| NCT02343406 | Adult Study: ABT-414 Alone or ABT-414 Plus Temozolomide vs. Lomustine or Temozo… | Phase2 | Glioblastoma | Completed | 2015-02-17 | 2019-06-24 | ClinicalTrials.gov |
| NCT02343406 | Adult Study: ABT-414 Alone or ABT-414 Plus Temozolomide vs. Lomustine or Temozo… | Phase2 | Glioblastoma | Completed | 2015-02-17 | 2019-06-24 | ClinicalTrials.gov |
| NCT02343406 | Adult Study: ABT-414 Alone or ABT-414 Plus Temozolomide vs. Lomustine or Temozo… | Phase2 | Glioblastoma | Completed | 2015-02-17 | 2019-06-24 | ClinicalTrials.gov |
| NCT02343406 | Adult Study: ABT-414 Alone or ABT-414 Plus Temozolomide vs. Lomustine or Temozo… | Phase2 | Glioblastoma | Completed | 2015-02-17 | 2019-06-24 | ClinicalTrials.gov |
| NCT02356562 | A Study of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With or Without Sofo… | Phase2 | Chronic Hepatitis C Infection | Completed | 2015-02-03 | 2017-07-07 | ClinicalTrials.gov |
| NCT02356562 | A Study of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With or Without Sofo… | Phase2 | Chronic Hepatitis C Infection | Completed | 2015-02-03 | 2017-07-07 | ClinicalTrials.gov |
| NCT02356562 | A Study of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With or Without Sofo… | Phase2 | Chronic Hepatitis C Infection | Completed | 2015-02-03 | 2017-07-07 | ClinicalTrials.gov |
| NCT02356562 | A Study of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir With or Without Sofo… | Phase2 | Chronic Hepatitis C Infection | Completed | 2015-02-03 | 2017-07-07 | ClinicalTrials.gov |
| NCT02399657 | Effect of Dexamethasone Implant in Hard Exudate Complicated With Diabetic Macul… | Phase4 | Diabetes Mellitus | Unknown | 2015-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02366364 | Study of Safety, Tolerability and Pharmacokinetics of NRX-1074 in Normal Health… | Phase1 | Major Depressive Disorder | Completed | 2015-02-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02399657 | Effect of Dexamethasone Implant in Hard Exudate Complicated With Diabetic Macul… | Phase4 | Diabetes Mellitus | Unknown | 2015-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02366364 | Study of Safety, Tolerability and Pharmacokinetics of NRX-1074 in Normal Health… | Phase1 | Major Depressive Disorder | Completed | 2015-02-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02399657 | Effect of Dexamethasone Implant in Hard Exudate Complicated With Diabetic Macul… | Phase4 | Diabetes Mellitus | Unknown | 2015-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02791308 | Study of Equivalence of Generic Pimecrolimus Cream 1% and Elidel® 1% in Subject… | Phase3 | Atopic Dermatitis | Completed | 2015-02-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02791308 | Study of Equivalence of Generic Pimecrolimus Cream 1% and Elidel® 1% in Subject… | Phase3 | Atopic Dermatitis | Completed | 2015-02-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02399657 | Effect of Dexamethasone Implant in Hard Exudate Complicated With Diabetic Macul… | Phase4 | Diabetes Mellitus | Unknown | 2015-02-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT02366364 | Study of Safety, Tolerability and Pharmacokinetics of NRX-1074 in Normal Health… | Phase1 | Major Depressive Disorder | Completed | 2015-02-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02366364 | Study of Safety, Tolerability and Pharmacokinetics of NRX-1074 in Normal Health… | Phase1 | Major Depressive Disorder | Completed | 2015-02-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02791308 | Study of Equivalence of Generic Pimecrolimus Cream 1% and Elidel® 1% in Subject… | Phase3 | Atopic Dermatitis | Completed | 2015-02-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02791308 | Study of Equivalence of Generic Pimecrolimus Cream 1% and Elidel® 1% in Subject… | Phase3 | Atopic Dermatitis | Completed | 2015-02-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02255435 | A Study to Learn About the Effects and Safety of RTA 408 (Omaveloxolone) in Peo… | Phase2 | Friedreich Ataxia | Completed | 2015-01-31 | 2025-12-19 | ClinicalTrials.gov |
| NCT02255435 | A Study to Learn About the Effects and Safety of RTA 408 (Omaveloxolone) in Peo… | Phase2 | Friedreich Ataxia | Completed | 2015-01-31 | 2025-12-19 | ClinicalTrials.gov |
| NCT02255435 | A Study to Learn About the Effects and Safety of RTA 408 (Omaveloxolone) in Peo… | Phase2 | Friedreich Ataxia | Completed | 2015-01-31 | 2025-12-19 | ClinicalTrials.gov |
| NCT02255435 | A Study to Learn About the Effects and Safety of RTA 408 (Omaveloxolone) in Peo… | Phase2 | Friedreich Ataxia | Completed | 2015-01-31 | 2025-12-19 | ClinicalTrials.gov |
| NCT02357420 | Safety and Efficacy of Relamorelin Administered to Participants With Vomiting S… | Phase2 | Diabetes Mellitus | Completed | 2015-01-29 | 2016-06-09 | ClinicalTrials.gov |
| NCT02357420 | Safety and Efficacy of Relamorelin Administered to Participants With Vomiting S… | Phase2 | Diabetes Mellitus | Completed | 2015-01-29 | 2016-06-09 | ClinicalTrials.gov |
| NCT02357420 | Safety and Efficacy of Relamorelin Administered to Participants With Vomiting S… | Phase2 | Diabetes Mellitus | Completed | 2015-01-29 | 2016-06-09 | ClinicalTrials.gov |
| NCT02357420 | Safety and Efficacy of Relamorelin Administered to Participants With Vomiting S… | Phase2 | Diabetes Mellitus | Completed | 2015-01-29 | 2016-06-09 | ClinicalTrials.gov |
| NCT02362074 | Progress at Work - The Impact of Adalimumab on Work Related Productivity in Pat… | — | Rheumatoid Arthritis | Completed | 2015-01-21 | 2020-03-06 | ClinicalTrials.gov |
| NCT02362074 | Progress at Work - The Impact of Adalimumab on Work Related Productivity in Pat… | — | Rheumatoid Arthritis | Completed | 2015-01-21 | 2020-03-06 | ClinicalTrials.gov |
| NCT02362074 | Progress at Work - The Impact of Adalimumab on Work Related Productivity in Pat… | — | Rheumatoid Arthritis | Completed | 2015-01-21 | 2020-03-06 | ClinicalTrials.gov |
| NCT02362074 | Progress at Work - The Impact of Adalimumab on Work Related Productivity in Pat… | — | Rheumatoid Arthritis | Completed | 2015-01-21 | 2020-03-06 | ClinicalTrials.gov |
| NCT02213289 | PANGEA-IMBBP: Personalized Antibodies for Gastro-Esophageal Adenocarcinoma - A … | Phase2 | Adenocarcinoma | Completed | 2015-01-20 | 2020-08-20 | ClinicalTrials.gov |
| NCT02213289 | PANGEA-IMBBP: Personalized Antibodies for Gastro-Esophageal Adenocarcinoma - A … | Phase2 | Adenocarcinoma | Completed | 2015-01-20 | 2020-08-20 | ClinicalTrials.gov |
| NCT02213289 | PANGEA-IMBBP: Personalized Antibodies for Gastro-Esophageal Adenocarcinoma - A … | Phase2 | Adenocarcinoma | Completed | 2015-01-20 | 2020-08-20 | ClinicalTrials.gov |
| NCT02213289 | PANGEA-IMBBP: Personalized Antibodies for Gastro-Esophageal Adenocarcinoma - A … | Phase2 | Adenocarcinoma | Completed | 2015-01-20 | 2020-08-20 | ClinicalTrials.gov |
| NCT02365662 | A Study Evaluating Safety and Pharmacokinetics of ABBV-221 in Subjects With Adv… | Phase1 | Head and Neck Squamous Cell Carcinoma | Terminated | 2015-01-09 | 2018-03-15 | ClinicalTrials.gov |
| NCT02365662 | A Study Evaluating Safety and Pharmacokinetics of ABBV-221 in Subjects With Adv… | Phase1 | Head and Neck Squamous Cell Carcinoma | Terminated | 2015-01-09 | 2018-03-15 | ClinicalTrials.gov |
| NCT02365662 | A Study Evaluating Safety and Pharmacokinetics of ABBV-221 in Subjects With Adv… | Phase1 | Head and Neck Squamous Cell Carcinoma | Terminated | 2015-01-09 | 2018-03-15 | ClinicalTrials.gov |
| NCT02365662 | A Study Evaluating Safety and Pharmacokinetics of ABBV-221 in Subjects With Adv… | Phase1 | Head and Neck Squamous Cell Carcinoma | Terminated | 2015-01-09 | 2018-03-15 | ClinicalTrials.gov |
| NCT02434666 | Long Term Extension Safety Study in Patients With Dementia of the Alzheimer's T… | Phase2 | Dementia of the Alzheimer's Type | Completed | 2015-01-08 | 2016-11-22 | ClinicalTrials.gov |
| NCT02434666 | Long Term Extension Safety Study in Patients With Dementia of the Alzheimer's T… | Phase2 | Dementia of the Alzheimer's Type | Completed | 2015-01-08 | 2016-11-22 | ClinicalTrials.gov |
| NCT02434666 | Long Term Extension Safety Study in Patients With Dementia of the Alzheimer's T… | Phase2 | Dementia of the Alzheimer's Type | Completed | 2015-01-08 | 2016-11-22 | ClinicalTrials.gov |
| NCT02434666 | Long Term Extension Safety Study in Patients With Dementia of the Alzheimer's T… | Phase2 | Dementia of the Alzheimer's Type | Completed | 2015-01-08 | 2016-11-22 | ClinicalTrials.gov |
| NCT02198651 | A Phase 4 Trial Assessing the ImPact of Residual Inflammation Detected Via Imag… | Phase4 | Rheumatoid Arthritis | Completed | 2015-01-05 | 2018-08-08 | ClinicalTrials.gov |
| NCT02198651 | A Phase 4 Trial Assessing the ImPact of Residual Inflammation Detected Via Imag… | Phase4 | Rheumatoid Arthritis | Completed | 2015-01-05 | 2018-08-08 | ClinicalTrials.gov |
| NCT02198651 | A Phase 4 Trial Assessing the ImPact of Residual Inflammation Detected Via Imag… | Phase4 | Rheumatoid Arthritis | Completed | 2015-01-05 | 2018-08-08 | ClinicalTrials.gov |
| NCT02198651 | A Phase 4 Trial Assessing the ImPact of Residual Inflammation Detected Via Imag… | Phase4 | Rheumatoid Arthritis | Completed | 2015-01-05 | 2018-08-08 | ClinicalTrials.gov |
| NCT02573324 | A Study of ABT-414 in Participants With Newly Diagnosed Glioblastoma (GBM) With… | Phase3 | Glioblastoma | Completed | 2015-01-04 | 2022-04-04 | ClinicalTrials.gov |
| NCT02573324 | A Study of ABT-414 in Participants With Newly Diagnosed Glioblastoma (GBM) With… | Phase3 | Glioblastoma | Completed | 2015-01-04 | 2022-04-04 | ClinicalTrials.gov |
| NCT02573324 | A Study of ABT-414 in Participants With Newly Diagnosed Glioblastoma (GBM) With… | Phase3 | Glioblastoma | Completed | 2015-01-04 | 2022-04-04 | ClinicalTrials.gov |
| NCT02573324 | A Study of ABT-414 in Participants With Newly Diagnosed Glioblastoma (GBM) With… | Phase3 | Glioblastoma | Completed | 2015-01-04 | 2022-04-04 | ClinicalTrials.gov |
| NCT02165111 | Efficacy of Botulinum Toxin In Scleroderma-Associated Raynaud's Syndrome | Phase3 | Scleroderma | Completed | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02165111 | Efficacy of Botulinum Toxin In Scleroderma-Associated Raynaud's Syndrome | Phase3 | Scleroderma | Completed | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02165111 | Efficacy of Botulinum Toxin In Scleroderma-Associated Raynaud's Syndrome | Phase3 | Scleroderma | Completed | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02165111 | Efficacy of Botulinum Toxin In Scleroderma-Associated Raynaud's Syndrome | Phase3 | Scleroderma | Completed | 2015-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02242942 | Comparison of the Treatments of Obinutuzumab + Venetoclax Versus Obinutuzumab +… | Phase3 | Lymphocytic Leukemia, Chronic | Completed | 2014-12-31 | 2025-08-27 | ClinicalTrials.gov |
| NCT02242942 | Comparison of the Treatments of Obinutuzumab + Venetoclax Versus Obinutuzumab +… | Phase3 | Lymphocytic Leukemia, Chronic | Completed | 2014-12-31 | 2025-08-27 | ClinicalTrials.gov |
| NCT02333383 | Observe the Frequency of Extra-Axial Symptoms in Korean Ankylosing Spondylitis … | — | Ankylosing Spondylitis | Completed | 2014-12-31 | 2017-08-08 | ClinicalTrials.gov |
| NCT02242942 | Comparison of the Treatments of Obinutuzumab + Venetoclax Versus Obinutuzumab +… | Phase3 | Lymphocytic Leukemia, Chronic | Completed | 2014-12-31 | 2025-08-27 | ClinicalTrials.gov |
| NCT02242942 | Comparison of the Treatments of Obinutuzumab + Venetoclax Versus Obinutuzumab +… | Phase3 | Lymphocytic Leukemia, Chronic | Completed | 2014-12-31 | 2025-08-27 | ClinicalTrials.gov |
| NCT02333383 | Observe the Frequency of Extra-Axial Symptoms in Korean Ankylosing Spondylitis … | — | Ankylosing Spondylitis | Completed | 2014-12-31 | 2017-08-08 | ClinicalTrials.gov |
| NCT02287233 | A Study Evaluating Venetoclax in Combination With Low-Dose Cytarabine in Treatm… | Phase1 | Acute Myelogenous Leukemia | Completed | 2014-12-31 | 2021-08-10 | ClinicalTrials.gov |
| NCT02287233 | A Study Evaluating Venetoclax in Combination With Low-Dose Cytarabine in Treatm… | Phase1 | Acute Myelogenous Leukemia | Completed | 2014-12-31 | 2021-08-10 | ClinicalTrials.gov |
| NCT02287233 | A Study Evaluating Venetoclax in Combination With Low-Dose Cytarabine in Treatm… | Phase1 | Acute Myelogenous Leukemia | Completed | 2014-12-31 | 2021-08-10 | ClinicalTrials.gov |
| NCT02333383 | Observe the Frequency of Extra-Axial Symptoms in Korean Ankylosing Spondylitis … | — | Ankylosing Spondylitis | Completed | 2014-12-31 | 2017-08-08 | ClinicalTrials.gov |
| NCT02287233 | A Study Evaluating Venetoclax in Combination With Low-Dose Cytarabine in Treatm… | Phase1 | Acute Myelogenous Leukemia | Completed | 2014-12-31 | 2021-08-10 | ClinicalTrials.gov |
| NCT02333383 | Observe the Frequency of Extra-Axial Symptoms in Korean Ankylosing Spondylitis … | — | Ankylosing Spondylitis | Completed | 2014-12-31 | 2017-08-08 | ClinicalTrials.gov |
| NCT02292719 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/ABT-450/Ritonavir Wit… | Phase2 | Chronic Hepatitis C Virus Infection | Completed | 2014-12-19 | 2017-07-14 | ClinicalTrials.gov |
| NCT02292719 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/ABT-450/Ritonavir Wit… | Phase2 | Chronic Hepatitis C Virus Infection | Completed | 2014-12-19 | 2017-07-14 | ClinicalTrials.gov |
| NCT02292719 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/ABT-450/Ritonavir Wit… | Phase2 | Chronic Hepatitis C Virus Infection | Completed | 2014-12-19 | 2017-07-14 | ClinicalTrials.gov |
| NCT02292719 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/ABT-450/Ritonavir Wit… | Phase2 | Chronic Hepatitis C Virus Infection | Completed | 2014-12-19 | 2017-07-14 | ClinicalTrials.gov |
| NCT02320149 | Study to Evaluate Safety & Efficacy of Sarecycline in Treatment of Acne | Phase3 | Acne Vulgaris | Completed | 2014-12-18 | 2017-02-01 | ClinicalTrials.gov |
| NCT02320149 | Study to Evaluate Safety & Efficacy of Sarecycline in Treatment of Acne | Phase3 | Acne Vulgaris | Completed | 2014-12-18 | 2017-02-01 | ClinicalTrials.gov |
| NCT02320149 | Study to Evaluate Safety & Efficacy of Sarecycline in Treatment of Acne | Phase3 | Acne Vulgaris | Completed | 2014-12-18 | 2017-02-01 | ClinicalTrials.gov |
| NCT02320149 | Study to Evaluate Safety & Efficacy of Sarecycline in Treatment of Acne | Phase3 | Acne Vulgaris | Completed | 2014-12-18 | 2017-02-01 | ClinicalTrials.gov |
| NCT03341780 | Standard Amblyopia Therapy in Adult Amblyopes | — | Amblyopia | Completed | 2014-12-16 | 2016-10-24 | ClinicalTrials.gov |
| NCT03341780 | Standard Amblyopia Therapy in Adult Amblyopes | — | Amblyopia | Completed | 2014-12-16 | 2016-10-24 | ClinicalTrials.gov |
| NCT03341780 | Standard Amblyopia Therapy in Adult Amblyopes | — | Amblyopia | Completed | 2014-12-16 | 2016-10-24 | ClinicalTrials.gov |
| NCT03341780 | Standard Amblyopia Therapy in Adult Amblyopes | — | Amblyopia | Completed | 2014-12-16 | 2016-10-24 | ClinicalTrials.gov |
| NCT02250651 | Efficacy and Safety of Bimatoprost Sustained-Release (SR) in Patients With Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2014-12-15 | 2020-07-22 | ClinicalTrials.gov |
| NCT02250651 | Efficacy and Safety of Bimatoprost Sustained-Release (SR) in Patients With Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2014-12-15 | 2020-07-22 | ClinicalTrials.gov |
| NCT02247804 | Efficacy and Safety Study of Bimatoprost Sustained-Release (SR) in Participants… | Phase3 | Glaucoma, Open-Angle | Completed | 2014-12-15 | 2019-07-19 | ClinicalTrials.gov |
| NCT02250651 | Efficacy and Safety of Bimatoprost Sustained-Release (SR) in Patients With Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2014-12-15 | 2020-07-22 | ClinicalTrials.gov |
| NCT02247804 | Efficacy and Safety Study of Bimatoprost Sustained-Release (SR) in Participants… | Phase3 | Glaucoma, Open-Angle | Completed | 2014-12-15 | 2019-07-19 | ClinicalTrials.gov |
| NCT02247804 | Efficacy and Safety Study of Bimatoprost Sustained-Release (SR) in Participants… | Phase3 | Glaucoma, Open-Angle | Completed | 2014-12-15 | 2019-07-19 | ClinicalTrials.gov |
| NCT02250651 | Efficacy and Safety of Bimatoprost Sustained-Release (SR) in Patients With Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2014-12-15 | 2020-07-22 | ClinicalTrials.gov |
| NCT02247804 | Efficacy and Safety Study of Bimatoprost Sustained-Release (SR) in Participants… | Phase3 | Glaucoma, Open-Angle | Completed | 2014-12-15 | 2019-07-19 | ClinicalTrials.gov |
| NCT02505776 | Safety and Patient Satisfaction With GLASH VISTA™ (Bimatoprost 0.03%) in the Tr… | — | Eyelash Hypotrichosis | Completed | 2014-12-08 | 2018-05-21 | ClinicalTrials.gov |
| NCT02505776 | Safety and Patient Satisfaction With GLASH VISTA™ (Bimatoprost 0.03%) in the Tr… | — | Eyelash Hypotrichosis | Completed | 2014-12-08 | 2018-05-21 | ClinicalTrials.gov |
| NCT02505776 | Safety and Patient Satisfaction With GLASH VISTA™ (Bimatoprost 0.03%) in the Tr… | — | Eyelash Hypotrichosis | Completed | 2014-12-08 | 2018-05-21 | ClinicalTrials.gov |
| NCT02505776 | Safety and Patient Satisfaction With GLASH VISTA™ (Bimatoprost 0.03%) in the Tr… | — | Eyelash Hypotrichosis | Completed | 2014-12-08 | 2018-05-21 | ClinicalTrials.gov |
| NCT02305758 | Study Comparing Veliparib Plus FOLFIRI Versus Placebo Plus FOLFIRI With or With… | Phase2 | Untreated Metastatic Colorectal Cancer | Completed | 2014-12-02 | 2017-09-22 | ClinicalTrials.gov |
| NCT02305758 | Study Comparing Veliparib Plus FOLFIRI Versus Placebo Plus FOLFIRI With or With… | Phase2 | Untreated Metastatic Colorectal Cancer | Completed | 2014-12-02 | 2017-09-22 | ClinicalTrials.gov |
| NCT02305758 | Study Comparing Veliparib Plus FOLFIRI Versus Placebo Plus FOLFIRI With or With… | Phase2 | Untreated Metastatic Colorectal Cancer | Completed | 2014-12-02 | 2017-09-22 | ClinicalTrials.gov |
| NCT02305758 | Study Comparing Veliparib Plus FOLFIRI Versus Placebo Plus FOLFIRI With or With… | Phase2 | Untreated Metastatic Colorectal Cancer | Completed | 2014-12-02 | 2017-09-22 | ClinicalTrials.gov |
| NCT02539849 | Effect of Prebiotic FOS on Intestinal Abundance of Faecalibacterium Prausnitzii… | Na | Crohn Disease | Completed | 2014-12-01 | 2017-12-19 | ClinicalTrials.gov |
| NCT02455050 | A Study to Compare a New Eye Drop Formulation With Systane® Gel Drops and Gente… | Phase3 | Dry Eye Syndromes | Completed | 2014-12-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02539849 | Effect of Prebiotic FOS on Intestinal Abundance of Faecalibacterium Prausnitzii… | Na | Crohn Disease | Completed | 2014-12-01 | 2017-12-19 | ClinicalTrials.gov |
| NCT02330016 | Juvederm Voluma® XC for the Treatment of Hypoplastic Chin | Na | Mandibular Hypoplasia | Unknown | 2014-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02455050 | A Study to Compare a New Eye Drop Formulation With Systane® Gel Drops and Gente… | Phase3 | Dry Eye Syndromes | Completed | 2014-12-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02330016 | Juvederm Voluma® XC for the Treatment of Hypoplastic Chin | Na | Mandibular Hypoplasia | Unknown | 2014-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02187861 | A Study Evaluating the Safety and Efficacy of Venetoclax (GDC-0199) Plus Bendam… | Phase2 | Follicular Lymphoma | Completed | 2014-12-01 | 2018-03-16 | ClinicalTrials.gov |
| NCT02297100 | Intravesicular Onabotulinumtoxin A in Interstitial Cystitis | Phase4 | Interstitial Cystitis | Completed | 2014-12-01 | 2018-01-10 | ClinicalTrials.gov |
| NCT02455050 | A Study to Compare a New Eye Drop Formulation With Systane® Gel Drops and Gente… | Phase3 | Dry Eye Syndromes | Completed | 2014-12-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02297100 | Intravesicular Onabotulinumtoxin A in Interstitial Cystitis | Phase4 | Interstitial Cystitis | Completed | 2014-12-01 | 2018-01-10 | ClinicalTrials.gov |
| NCT02297100 | Intravesicular Onabotulinumtoxin A in Interstitial Cystitis | Phase4 | Interstitial Cystitis | Completed | 2014-12-01 | 2018-01-10 | ClinicalTrials.gov |
| NCT02330016 | Juvederm Voluma® XC for the Treatment of Hypoplastic Chin | Na | Mandibular Hypoplasia | Unknown | 2014-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02455050 | A Study to Compare a New Eye Drop Formulation With Systane® Gel Drops and Gente… | Phase3 | Dry Eye Syndromes | Completed | 2014-12-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02539849 | Effect of Prebiotic FOS on Intestinal Abundance of Faecalibacterium Prausnitzii… | Na | Crohn Disease | Completed | 2014-12-01 | 2017-12-19 | ClinicalTrials.gov |
| NCT02187861 | A Study Evaluating the Safety and Efficacy of Venetoclax (GDC-0199) Plus Bendam… | Phase2 | Follicular Lymphoma | Completed | 2014-12-01 | 2018-03-16 | ClinicalTrials.gov |
| NCT02297100 | Intravesicular Onabotulinumtoxin A in Interstitial Cystitis | Phase4 | Interstitial Cystitis | Completed | 2014-12-01 | 2018-01-10 | ClinicalTrials.gov |
| NCT02187861 | A Study Evaluating the Safety and Efficacy of Venetoclax (GDC-0199) Plus Bendam… | Phase2 | Follicular Lymphoma | Completed | 2014-12-01 | 2018-03-16 | ClinicalTrials.gov |
| NCT02187861 | A Study Evaluating the Safety and Efficacy of Venetoclax (GDC-0199) Plus Bendam… | Phase2 | Follicular Lymphoma | Completed | 2014-12-01 | 2018-03-16 | ClinicalTrials.gov |
| NCT02330016 | Juvederm Voluma® XC for the Treatment of Hypoplastic Chin | Na | Mandibular Hypoplasia | Unknown | 2014-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02539849 | Effect of Prebiotic FOS on Intestinal Abundance of Faecalibacterium Prausnitzii… | Na | Crohn Disease | Completed | 2014-12-01 | 2017-12-19 | ClinicalTrials.gov |
| NCT02219477 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C | Completed | 2014-11-24 | 2017-03-03 | ClinicalTrials.gov |
| NCT02219477 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C | Completed | 2014-11-24 | 2017-03-03 | ClinicalTrials.gov |
| NCT02219477 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C | Completed | 2014-11-24 | 2017-03-03 | ClinicalTrials.gov |
| NCT02219477 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C | Completed | 2014-11-24 | 2017-03-03 | ClinicalTrials.gov |
| NCT02203851 | Extension Trial Assessing the Safety and Efficacy of BI 655066/ABBV-066/Risanki… | Phase2 | Psoriasis | Completed | 2014-11-20 | 2018-09-04 | ClinicalTrials.gov |
| NCT02203851 | Extension Trial Assessing the Safety and Efficacy of BI 655066/ABBV-066/Risanki… | Phase2 | Psoriasis | Completed | 2014-11-20 | 2018-09-04 | ClinicalTrials.gov |
| NCT02203851 | Extension Trial Assessing the Safety and Efficacy of BI 655066/ABBV-066/Risanki… | Phase2 | Psoriasis | Completed | 2014-11-20 | 2018-09-04 | ClinicalTrials.gov |
| NCT02203851 | Extension Trial Assessing the Safety and Efficacy of BI 655066/ABBV-066/Risanki… | Phase2 | Psoriasis | Completed | 2014-11-20 | 2018-09-04 | ClinicalTrials.gov |
| NCT02313454 | Evaluation of the Safety and Effectiveness of the Oculeve Intranasal Lacrimal N… | Na | Dry Eye Syndromes | Completed | 2014-11-17 | 2015-04-08 | ClinicalTrials.gov |
| NCT02313454 | Evaluation of the Safety and Effectiveness of the Oculeve Intranasal Lacrimal N… | Na | Dry Eye Syndromes | Completed | 2014-11-17 | 2015-04-08 | ClinicalTrials.gov |
| NCT02313454 | Evaluation of the Safety and Effectiveness of the Oculeve Intranasal Lacrimal N… | Na | Dry Eye Syndromes | Completed | 2014-11-17 | 2015-04-08 | ClinicalTrials.gov |
| NCT02313454 | Evaluation of the Safety and Effectiveness of the Oculeve Intranasal Lacrimal N… | Na | Dry Eye Syndromes | Completed | 2014-11-17 | 2015-04-08 | ClinicalTrials.gov |
| NCT02247401 | Coadministration of ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) With Ribaviri… | Phase3 | HCV | Completed | 2014-11-04 | 2016-08-01 | ClinicalTrials.gov |
| NCT02247401 | Coadministration of ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) With Ribaviri… | Phase3 | HCV | Completed | 2014-11-04 | 2016-08-01 | ClinicalTrials.gov |
| NCT02247401 | Coadministration of ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) With Ribaviri… | Phase3 | HCV | Completed | 2014-11-04 | 2016-08-01 | ClinicalTrials.gov |
| NCT02247401 | Coadministration of ABT-450/Ritonavir/ABT-267 (ABT-450/r/ABT-267) With Ribaviri… | Phase3 | HCV | Completed | 2014-11-04 | 2016-08-01 | ClinicalTrials.gov |
| NCT02348476 | A Study of Simbrinza™ Therapy in Patients With Open-Angle Glaucoma or Ocular Hy… | — | Open-Angle Glaucoma | Completed | 2014-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02058836 | Botulinum Toxin for the Management of Chronic Orchialgia | Phase2 | Chronic Testicular Pain | Completed | 2014-11-01 | 2016-10-18 | ClinicalTrials.gov |
| NCT02348476 | A Study of Simbrinza™ Therapy in Patients With Open-Angle Glaucoma or Ocular Hy… | — | Open-Angle Glaucoma | Completed | 2014-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02348476 | A Study of Simbrinza™ Therapy in Patients With Open-Angle Glaucoma or Ocular Hy… | — | Open-Angle Glaucoma | Completed | 2014-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02058836 | Botulinum Toxin for the Management of Chronic Orchialgia | Phase2 | Chronic Testicular Pain | Completed | 2014-11-01 | 2016-10-18 | ClinicalTrials.gov |
| NCT02058836 | Botulinum Toxin for the Management of Chronic Orchialgia | Phase2 | Chronic Testicular Pain | Completed | 2014-11-01 | 2016-10-18 | ClinicalTrials.gov |
| NCT02348476 | A Study of Simbrinza™ Therapy in Patients With Open-Angle Glaucoma or Ocular Hy… | — | Open-Angle Glaucoma | Completed | 2014-11-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02058836 | Botulinum Toxin for the Management of Chronic Orchialgia | Phase2 | Chronic Testicular Pain | Completed | 2014-11-01 | 2016-10-18 | ClinicalTrials.gov |
| NCT02219490 | A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonav… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | Completed | 2014-10-30 | 2021-05-13 | ClinicalTrials.gov |
| NCT02219490 | A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonav… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | Completed | 2014-10-30 | 2021-05-13 | ClinicalTrials.gov |
| NCT02219490 | A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonav… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | Completed | 2014-10-30 | 2021-05-13 | ClinicalTrials.gov |
| NCT02219490 | A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonav… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | Completed | 2014-10-30 | 2021-05-13 | ClinicalTrials.gov |
| NCT02265237 | A Randomized, Open-Label Study to Evaluate the Safety and Efficacy of Ombitasvi… | Phase3 | Hepatitis C Virus | Completed | 2014-10-28 | 2017-04-07 | ClinicalTrials.gov |
| NCT02265237 | A Randomized, Open-Label Study to Evaluate the Safety and Efficacy of Ombitasvi… | Phase3 | Hepatitis C Virus | Completed | 2014-10-28 | 2017-04-07 | ClinicalTrials.gov |
| NCT02265237 | A Randomized, Open-Label Study to Evaluate the Safety and Efficacy of Ombitasvi… | Phase3 | Hepatitis C Virus | Completed | 2014-10-28 | 2017-04-07 | ClinicalTrials.gov |
| NCT02265237 | A Randomized, Open-Label Study to Evaluate the Safety and Efficacy of Ombitasvi… | Phase3 | Hepatitis C Virus | Completed | 2014-10-28 | 2017-04-07 | ClinicalTrials.gov |
| NCT02261493 | A Safety and Efficacy Study of OnabotulinumtoxinA in Upper Facial Rhytides | Phase3 | Facial Rhytides | Completed | 2014-10-27 | 2016-04-20 | ClinicalTrials.gov |
| NCT02261493 | A Safety and Efficacy Study of OnabotulinumtoxinA in Upper Facial Rhytides | Phase3 | Facial Rhytides | Completed | 2014-10-27 | 2016-04-20 | ClinicalTrials.gov |
| NCT02261493 | A Safety and Efficacy Study of OnabotulinumtoxinA in Upper Facial Rhytides | Phase3 | Facial Rhytides | Completed | 2014-10-27 | 2016-04-20 | ClinicalTrials.gov |
| NCT02261493 | A Safety and Efficacy Study of OnabotulinumtoxinA in Upper Facial Rhytides | Phase3 | Facial Rhytides | Completed | 2014-10-27 | 2016-04-20 | ClinicalTrials.gov |
| NCT02289690 | Dose Escalation and Double-blind Study of Veliparib in Combination With Carbopl… | Phase1 | Small Cell Lung Cancer | Completed | 2014-10-13 | 2019-04-17 | ClinicalTrials.gov |
| NCT02065557 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Ulcerative Colitis | Completed | 2014-10-13 | 2020-02-07 | ClinicalTrials.gov |
| NCT02065557 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Ulcerative Colitis | Completed | 2014-10-13 | 2020-02-07 | ClinicalTrials.gov |
| NCT02289690 | Dose Escalation and Double-blind Study of Veliparib in Combination With Carbopl… | Phase1 | Small Cell Lung Cancer | Completed | 2014-10-13 | 2019-04-17 | ClinicalTrials.gov |
| NCT02065557 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Ulcerative Colitis | Completed | 2014-10-13 | 2020-02-07 | ClinicalTrials.gov |
| NCT02289690 | Dose Escalation and Double-blind Study of Veliparib in Combination With Carbopl… | Phase1 | Small Cell Lung Cancer | Completed | 2014-10-13 | 2019-04-17 | ClinicalTrials.gov |
| NCT02289690 | Dose Escalation and Double-blind Study of Veliparib in Combination With Carbopl… | Phase1 | Small Cell Lung Cancer | Completed | 2014-10-13 | 2019-04-17 | ClinicalTrials.gov |
| NCT02065557 | Efficacy and Safety of Adalimumab in Pediatric Subjects With Moderate to Severe… | Phase3 | Ulcerative Colitis | Completed | 2014-10-13 | 2020-02-07 | ClinicalTrials.gov |
| NCT02203773 | Study of ABT-199 (GDC-0199) in Combination With Azacitidine or Decitabine (Chem… | Phase1 | Acute Myelogenous Leukemia | Terminated | 2014-10-06 | 2022-06-16 | ClinicalTrials.gov |
| NCT02203773 | Study of ABT-199 (GDC-0199) in Combination With Azacitidine or Decitabine (Chem… | Phase1 | Acute Myelogenous Leukemia | Terminated | 2014-10-06 | 2022-06-16 | ClinicalTrials.gov |
| NCT02203773 | Study of ABT-199 (GDC-0199) in Combination With Azacitidine or Decitabine (Chem… | Phase1 | Acute Myelogenous Leukemia | Terminated | 2014-10-06 | 2022-06-16 | ClinicalTrials.gov |
| NCT02203773 | Study of ABT-199 (GDC-0199) in Combination With Azacitidine or Decitabine (Chem… | Phase1 | Acute Myelogenous Leukemia | Terminated | 2014-10-06 | 2022-06-16 | ClinicalTrials.gov |
| NCT02230956 | BOTOX® Efficacy and Safety in the Treatment of Knee Osteoarthritis | Phase2 | Osteoarthritis | Completed | 2014-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02289729 | Patient- and Caregiver-reported Symptoms and Outcomes With Levodopa/Carbidopa I… | — | Parkinson's Disease | Completed | 2014-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02296905 | Pharmacokinetics and Safety of ABT-493 and/or ABT-530 in Subjects With Normal a… | Phase1 | Hepatic Impairment | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02070302 | BOTOX® (Onabotulinumtoxin A) Injection(s) as a Treatment for Carpal Tunnel Synd… | Phase2 | Carpal Tunnel Syndrome | Completed | 2014-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02070302 | BOTOX® (Onabotulinumtoxin A) Injection(s) as a Treatment for Carpal Tunnel Synd… | Phase2 | Carpal Tunnel Syndrome | Completed | 2014-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02282982 | Observational Program to Assess Respiratory Syncytial Virus (RSV) Hospitalizati… | — | Respiratory Syncytial Virus (RSV) | Completed | 2014-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02289729 | Patient- and Caregiver-reported Symptoms and Outcomes With Levodopa/Carbidopa I… | — | Parkinson's Disease | Completed | 2014-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02296905 | Pharmacokinetics and Safety of ABT-493 and/or ABT-530 in Subjects With Normal a… | Phase1 | Hepatic Impairment | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02305953 | Cytokines and Vascular Inflammation in Psoriasis | — | Vascular Inflammation | Completed | 2014-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02296905 | Pharmacokinetics and Safety of ABT-493 and/or ABT-530 in Subjects With Normal a… | Phase1 | Hepatic Impairment | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02230956 | BOTOX® Efficacy and Safety in the Treatment of Knee Osteoarthritis | Phase2 | Osteoarthritis | Completed | 2014-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02070302 | BOTOX® (Onabotulinumtoxin A) Injection(s) as a Treatment for Carpal Tunnel Synd… | Phase2 | Carpal Tunnel Syndrome | Completed | 2014-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02070302 | BOTOX® (Onabotulinumtoxin A) Injection(s) as a Treatment for Carpal Tunnel Synd… | Phase2 | Carpal Tunnel Syndrome | Completed | 2014-10-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02230956 | BOTOX® Efficacy and Safety in the Treatment of Knee Osteoarthritis | Phase2 | Osteoarthritis | Completed | 2014-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02305953 | Cytokines and Vascular Inflammation in Psoriasis | — | Vascular Inflammation | Completed | 2014-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02282982 | Observational Program to Assess Respiratory Syncytial Virus (RSV) Hospitalizati… | — | Respiratory Syncytial Virus (RSV) | Completed | 2014-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02289729 | Patient- and Caregiver-reported Symptoms and Outcomes With Levodopa/Carbidopa I… | — | Parkinson's Disease | Completed | 2014-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02282982 | Observational Program to Assess Respiratory Syncytial Virus (RSV) Hospitalizati… | — | Respiratory Syncytial Virus (RSV) | Completed | 2014-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02282982 | Observational Program to Assess Respiratory Syncytial Virus (RSV) Hospitalizati… | — | Respiratory Syncytial Virus (RSV) | Completed | 2014-10-01 | 2015-05-01 | ClinicalTrials.gov |
| NCT02230956 | BOTOX® Efficacy and Safety in the Treatment of Knee Osteoarthritis | Phase2 | Osteoarthritis | Completed | 2014-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02305953 | Cytokines and Vascular Inflammation in Psoriasis | — | Vascular Inflammation | Completed | 2014-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02289729 | Patient- and Caregiver-reported Symptoms and Outcomes With Levodopa/Carbidopa I… | — | Parkinson's Disease | Completed | 2014-10-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02296905 | Pharmacokinetics and Safety of ABT-493 and/or ABT-530 in Subjects With Normal a… | Phase1 | Hepatic Impairment | Completed | 2014-10-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02305953 | Cytokines and Vascular Inflammation in Psoriasis | — | Vascular Inflammation | Completed | 2014-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02264990 | Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Investigator's… | Phase3 | Non-squamous Non-small Cell Lung Cancer | Completed | 2014-09-30 | 2020-02-21 | ClinicalTrials.gov |
| NCT02264990 | Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Investigator's… | Phase3 | Non-squamous Non-small Cell Lung Cancer | Completed | 2014-09-30 | 2020-02-21 | ClinicalTrials.gov |
| NCT02264990 | Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Investigator's… | Phase3 | Non-squamous Non-small Cell Lung Cancer | Completed | 2014-09-30 | 2020-02-21 | ClinicalTrials.gov |
| NCT02264990 | Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Investigator's… | Phase3 | Non-squamous Non-small Cell Lung Cancer | Completed | 2014-09-30 | 2020-02-21 | ClinicalTrials.gov |
| NCT02207088 | Ombitasvir/ABT-450/Ritonavir and Dasabuvir With or Without Ribavirin in HCV Gen… | Phase3 | Chronic Hepatitis C | Completed | 2014-09-23 | 2016-12-06 | ClinicalTrials.gov |
| NCT02207088 | Ombitasvir/ABT-450/Ritonavir and Dasabuvir With or Without Ribavirin in HCV Gen… | Phase3 | Chronic Hepatitis C | Completed | 2014-09-23 | 2016-12-06 | ClinicalTrials.gov |
| NCT02207088 | Ombitasvir/ABT-450/Ritonavir and Dasabuvir With or Without Ribavirin in HCV Gen… | Phase3 | Chronic Hepatitis C | Completed | 2014-09-23 | 2016-12-06 | ClinicalTrials.gov |
| NCT02207088 | Ombitasvir/ABT-450/Ritonavir and Dasabuvir With or Without Ribavirin in HCV Gen… | Phase3 | Chronic Hepatitis C | Completed | 2014-09-23 | 2016-12-06 | ClinicalTrials.gov |
| NCT02265731 | Study Evaluating Venetoclax in Subjects With Hematological Malignancies | Phase1 | Non-Hodgkin Lymphoma (NHL) | Completed | 2014-09-22 | 2021-03-12 | ClinicalTrials.gov |
| NCT02265731 | Study Evaluating Venetoclax in Subjects With Hematological Malignancies | Phase1 | Non-Hodgkin Lymphoma (NHL) | Completed | 2014-09-22 | 2021-03-12 | ClinicalTrials.gov |
| NCT02265731 | Study Evaluating Venetoclax in Subjects With Hematological Malignancies | Phase1 | Non-Hodgkin Lymphoma (NHL) | Completed | 2014-09-22 | 2021-03-12 | ClinicalTrials.gov |
| NCT02265731 | Study Evaluating Venetoclax in Subjects With Hematological Malignancies | Phase1 | Non-Hodgkin Lymphoma (NHL) | Completed | 2014-09-22 | 2021-03-12 | ClinicalTrials.gov |
| NCT02243293 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-Administra… | Phase2 | Chronic Hepatitis C | Completed | 2014-09-19 | 2017-02-23 | ClinicalTrials.gov |
| NCT02243293 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-Administra… | Phase2 | Chronic Hepatitis C | Completed | 2014-09-19 | 2017-02-23 | ClinicalTrials.gov |
| NCT02243293 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-Administra… | Phase2 | Chronic Hepatitis C | Completed | 2014-09-19 | 2017-02-23 | ClinicalTrials.gov |
| NCT02243293 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-Administra… | Phase2 | Chronic Hepatitis C | Completed | 2014-09-19 | 2017-02-23 | ClinicalTrials.gov |
| NCT02141282 | A Phase 2 Open-Label Study of the Efficacy and Safety of ABT-199 (GDC-0199) in … | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2014-09-10 | 2021-12-22 | ClinicalTrials.gov |
| NCT02141282 | A Phase 2 Open-Label Study of the Efficacy and Safety of ABT-199 (GDC-0199) in … | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2014-09-10 | 2021-12-22 | ClinicalTrials.gov |
| NCT02141282 | A Phase 2 Open-Label Study of the Efficacy and Safety of ABT-199 (GDC-0199) in … | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2014-09-10 | 2021-12-22 | ClinicalTrials.gov |
| NCT02141282 | A Phase 2 Open-Label Study of the Efficacy and Safety of ABT-199 (GDC-0199) in … | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2014-09-10 | 2021-12-22 | ClinicalTrials.gov |
| NCT02192099 | Open Label Extension for GLYX13-C-202, NCT01684163 | Phase2 | Major Depressive Disorder | Terminated | 2014-09-08 | 2018-11-08 | ClinicalTrials.gov |
| NCT02192099 | Open Label Extension for GLYX13-C-202, NCT01684163 | Phase2 | Major Depressive Disorder | Terminated | 2014-09-08 | 2018-11-08 | ClinicalTrials.gov |
| NCT02192099 | Open Label Extension for GLYX13-C-202, NCT01684163 | Phase2 | Major Depressive Disorder | Terminated | 2014-09-08 | 2018-11-08 | ClinicalTrials.gov |
| NCT02192099 | Open Label Extension for GLYX13-C-202, NCT01684163 | Phase2 | Major Depressive Disorder | Terminated | 2014-09-08 | 2018-11-08 | ClinicalTrials.gov |
| NCT02158507 | Pilot Study of Veliparib (ABT-888) and Lapatinib (Tykerb) in Patients With Meta… | Na | Metastatic Triple Negative Breast Cancer | Completed | 2014-09-04 | 2021-07-22 | ClinicalTrials.gov |
| NCT02158507 | Pilot Study of Veliparib (ABT-888) and Lapatinib (Tykerb) in Patients With Meta… | Na | Metastatic Triple Negative Breast Cancer | Completed | 2014-09-04 | 2021-07-22 | ClinicalTrials.gov |
| NCT02158507 | Pilot Study of Veliparib (ABT-888) and Lapatinib (Tykerb) in Patients With Meta… | Na | Metastatic Triple Negative Breast Cancer | Completed | 2014-09-04 | 2021-07-22 | ClinicalTrials.gov |
| NCT02158507 | Pilot Study of Veliparib (ABT-888) and Lapatinib (Tykerb) in Patients With Meta… | Na | Metastatic Triple Negative Breast Cancer | Completed | 2014-09-04 | 2021-07-22 | ClinicalTrials.gov |
| NCT02220738 | Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ABT-957 in … | Phase1 | Alzheimer's Disease | Terminated | 2014-09-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02220738 | Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ABT-957 in … | Phase1 | Alzheimer's Disease | Terminated | 2014-09-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02216422 | A Study to Evaluate Chronic Hepatitis C Virus (HCV) Infection in Cirrhotic Adul… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2014-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02219503 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C Infection | Completed | 2014-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02181504 | A Study of Abicipar Pegol in Japanese Patients With Neovascular Age-related Mac… | Phase2 | Macular Degeneration | Completed | 2014-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02195687 | BOTOX® in the Treatment of Crow's Feet Lines in China | Phase3 | Lateral Canthal Lines | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02195687 | BOTOX® in the Treatment of Crow's Feet Lines in China | Phase3 | Lateral Canthal Lines | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02181504 | A Study of Abicipar Pegol in Japanese Patients With Neovascular Age-related Mac… | Phase2 | Macular Degeneration | Completed | 2014-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01920945 | OnabotulinumtoxinA for the Treatment of New Daily Persistent Headache: an Open … | Phase2 | New Daily Persistent Headache | Terminated | 2014-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02220738 | Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ABT-957 in … | Phase1 | Alzheimer's Disease | Terminated | 2014-09-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02219503 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C Infection | Completed | 2014-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02216422 | A Study to Evaluate Chronic Hepatitis C Virus (HCV) Infection in Cirrhotic Adul… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2014-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02095574 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes ABT-199 in A… | Phase1 | Relapsed/Refractory Non-Hodgkin's Lymphoma | Withdrawn | 2014-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02095574 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes ABT-199 in A… | Phase1 | Relapsed/Refractory Non-Hodgkin's Lymphoma | Withdrawn | 2014-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02216422 | A Study to Evaluate Chronic Hepatitis C Virus (HCV) Infection in Cirrhotic Adul… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2014-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02219503 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C Infection | Completed | 2014-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01920945 | OnabotulinumtoxinA for the Treatment of New Daily Persistent Headache: an Open … | Phase2 | New Daily Persistent Headache | Terminated | 2014-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT01920945 | OnabotulinumtoxinA for the Treatment of New Daily Persistent Headache: an Open … | Phase2 | New Daily Persistent Headache | Terminated | 2014-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02181504 | A Study of Abicipar Pegol in Japanese Patients With Neovascular Age-related Mac… | Phase2 | Macular Degeneration | Completed | 2014-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02181504 | A Study of Abicipar Pegol in Japanese Patients With Neovascular Age-related Mac… | Phase2 | Macular Degeneration | Completed | 2014-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02195687 | BOTOX® in the Treatment of Crow's Feet Lines in China | Phase3 | Lateral Canthal Lines | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02195687 | BOTOX® in the Treatment of Crow's Feet Lines in China | Phase3 | Lateral Canthal Lines | Completed | 2014-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02095574 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes ABT-199 in A… | Phase1 | Relapsed/Refractory Non-Hodgkin's Lymphoma | Withdrawn | 2014-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01920945 | OnabotulinumtoxinA for the Treatment of New Daily Persistent Headache: an Open … | Phase2 | New Daily Persistent Headache | Terminated | 2014-09-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT02220738 | Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ABT-957 in … | Phase1 | Alzheimer's Disease | Terminated | 2014-09-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02095574 | A Pharmacokinetic Study to Access How the Body Absorbs and Removes ABT-199 in A… | Phase1 | Relapsed/Refractory Non-Hodgkin's Lymphoma | Withdrawn | 2014-09-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02216422 | A Study to Evaluate Chronic Hepatitis C Virus (HCV) Infection in Cirrhotic Adul… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection | Completed | 2014-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02219503 | A Study to Evaluate the Safety and Efficacy of Ombitasvir/Paritaprevir/Ritonavi… | Phase3 | Chronic Hepatitis C Infection | Completed | 2014-09-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02130362 | A Non-Interventional Clinical Study to Evaluate Long-Term Safety and Effectiven… | — | Crohn's Disease | Active_Not_Recruiting | 2014-08-28 | 2030-11-01 | ClinicalTrials.gov |
| NCT02130362 | A Non-Interventional Clinical Study to Evaluate Long-Term Safety and Effectiven… | — | Crohn's Disease | Active_Not_Recruiting | 2014-08-28 | 2030-11-01 | ClinicalTrials.gov |
| NCT02130362 | A Non-Interventional Clinical Study to Evaluate Long-Term Safety and Effectiven… | — | Crohn's Disease | Active_Not_Recruiting | 2014-08-28 | 2030-11-01 | ClinicalTrials.gov |
| NCT02130362 | A Non-Interventional Clinical Study to Evaluate Long-Term Safety and Effectiven… | — | Crohn's Disease | Active_Not_Recruiting | 2014-08-28 | 2030-11-01 | ClinicalTrials.gov |
| NCT02185014 | Open Label Study to Evaluate Long Term Efficacy, Safety and Tolerability of Rep… | Phase3 | Crohn's Disease | Completed | 2014-08-12 | 2017-11-03 | ClinicalTrials.gov |
| NCT02185014 | Open Label Study to Evaluate Long Term Efficacy, Safety and Tolerability of Rep… | Phase3 | Crohn's Disease | Completed | 2014-08-12 | 2017-11-03 | ClinicalTrials.gov |
| NCT02185014 | Open Label Study to Evaluate Long Term Efficacy, Safety and Tolerability of Rep… | Phase3 | Crohn's Disease | Completed | 2014-08-12 | 2017-11-03 | ClinicalTrials.gov |
| NCT02185014 | Open Label Study to Evaluate Long Term Efficacy, Safety and Tolerability of Rep… | Phase3 | Crohn's Disease | Completed | 2014-08-12 | 2017-11-03 | ClinicalTrials.gov |
| NCT02191579 | Efficacy and Safety Study of BOTOX® Compared to Topiramate for the Prevention o… | Phase4 | Migraine Disorders | Completed | 2014-08-05 | 2017-09-01 | ClinicalTrials.gov |
| NCT02191579 | Efficacy and Safety Study of BOTOX® Compared to Topiramate for the Prevention o… | Phase4 | Migraine Disorders | Completed | 2014-08-05 | 2017-09-01 | ClinicalTrials.gov |
| NCT02196701 | Concomitant Longitudinal Evaluation of Adalimumab With Methotrexate in the Real… | Phase3 | Psoriasis | Completed | 2014-08-05 | 2017-03-17 | ClinicalTrials.gov |
| NCT02191579 | Efficacy and Safety Study of BOTOX® Compared to Topiramate for the Prevention o… | Phase4 | Migraine Disorders | Completed | 2014-08-05 | 2017-09-01 | ClinicalTrials.gov |
| NCT02191579 | Efficacy and Safety Study of BOTOX® Compared to Topiramate for the Prevention o… | Phase4 | Migraine Disorders | Completed | 2014-08-05 | 2017-09-01 | ClinicalTrials.gov |
| NCT02196701 | Concomitant Longitudinal Evaluation of Adalimumab With Methotrexate in the Real… | Phase3 | Psoriasis | Completed | 2014-08-05 | 2017-03-17 | ClinicalTrials.gov |
| NCT02196701 | Concomitant Longitudinal Evaluation of Adalimumab With Methotrexate in the Real… | Phase3 | Psoriasis | Completed | 2014-08-05 | 2017-03-17 | ClinicalTrials.gov |
| NCT02196701 | Concomitant Longitudinal Evaluation of Adalimumab With Methotrexate in the Real… | Phase3 | Psoriasis | Completed | 2014-08-05 | 2017-03-17 | ClinicalTrials.gov |
| NCT02293798 | Circumferential Periareolar Mastopexy Using SERI Surgical Scaffold | Na | Mastopexy | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02218034 | Safety, Tolerability and Pharmacokinetics of AGN-190168 in Subjects With Acne V… | Phase1 | Acne Vulgaris | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02173405 | Injection With OnabotulinumtoxinA (Botox) for the Treatment of Chronic Pelvic P… | Phase1 | Myofascial Pain Syndromes | Completed | 2014-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02167035 | Comparison of Combigan Two Times Daily (BID) Versus Simbrinza Three Times Daily… | Phase4 | Glaucoma | Completed | 2014-08-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02145689 | Long-Term Study of OnabotulinumtoxinA Treatment in Adult Patients With Upper Li… | Phase3 | Muscle Spasticity | Withdrawn | 2014-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02145689 | Long-Term Study of OnabotulinumtoxinA Treatment in Adult Patients With Upper Li… | Phase3 | Muscle Spasticity | Withdrawn | 2014-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02167035 | Comparison of Combigan Two Times Daily (BID) Versus Simbrinza Three Times Daily… | Phase4 | Glaucoma | Completed | 2014-08-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02173405 | Injection With OnabotulinumtoxinA (Botox) for the Treatment of Chronic Pelvic P… | Phase1 | Myofascial Pain Syndromes | Completed | 2014-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02218034 | Safety, Tolerability and Pharmacokinetics of AGN-190168 in Subjects With Acne V… | Phase1 | Acne Vulgaris | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02293798 | Circumferential Periareolar Mastopexy Using SERI Surgical Scaffold | Na | Mastopexy | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02243280 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-administra… | Phase2 | Chronic Hepatitis C | Completed | 2014-08-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02293798 | Circumferential Periareolar Mastopexy Using SERI Surgical Scaffold | Na | Mastopexy | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02218034 | Safety, Tolerability and Pharmacokinetics of AGN-190168 in Subjects With Acne V… | Phase1 | Acne Vulgaris | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02173405 | Injection With OnabotulinumtoxinA (Botox) for the Treatment of Chronic Pelvic P… | Phase1 | Myofascial Pain Syndromes | Completed | 2014-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02167035 | Comparison of Combigan Two Times Daily (BID) Versus Simbrinza Three Times Daily… | Phase4 | Glaucoma | Completed | 2014-08-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02243280 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-administra… | Phase2 | Chronic Hepatitis C | Completed | 2014-08-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02145689 | Long-Term Study of OnabotulinumtoxinA Treatment in Adult Patients With Upper Li… | Phase3 | Muscle Spasticity | Withdrawn | 2014-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02243280 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-administra… | Phase2 | Chronic Hepatitis C | Completed | 2014-08-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02293798 | Circumferential Periareolar Mastopexy Using SERI Surgical Scaffold | Na | Mastopexy | Completed | 2014-08-01 | 2016-06-01 | ClinicalTrials.gov |
| NCT02243280 | A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Co-administra… | Phase2 | Chronic Hepatitis C | Completed | 2014-08-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02218034 | Safety, Tolerability and Pharmacokinetics of AGN-190168 in Subjects With Acne V… | Phase1 | Acne Vulgaris | Completed | 2014-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02173405 | Injection With OnabotulinumtoxinA (Botox) for the Treatment of Chronic Pelvic P… | Phase1 | Myofascial Pain Syndromes | Completed | 2014-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02167035 | Comparison of Combigan Two Times Daily (BID) Versus Simbrinza Three Times Daily… | Phase4 | Glaucoma | Completed | 2014-08-01 | 2018-03-01 | ClinicalTrials.gov |
| NCT02145689 | Long-Term Study of OnabotulinumtoxinA Treatment in Adult Patients With Upper Li… | Phase3 | Muscle Spasticity | Withdrawn | 2014-08-01 | 2017-05-01 | ClinicalTrials.gov |
| NCT02185053 | A Phase II Study of CPC-201 to Treat Alzheimer's Disease Type Dementia | Phase2 | Alzheimer's Disease | Completed | 2014-07-31 | 2016-07-31 | ClinicalTrials.gov |
| NCT02185053 | A Phase II Study of CPC-201 to Treat Alzheimer's Disease Type Dementia | Phase2 | Alzheimer's Disease | Completed | 2014-07-31 | 2016-07-31 | ClinicalTrials.gov |
| NCT02185053 | A Phase II Study of CPC-201 to Treat Alzheimer's Disease Type Dementia | Phase2 | Alzheimer's Disease | Completed | 2014-07-31 | 2016-07-31 | ClinicalTrials.gov |
| NCT02185053 | A Phase II Study of CPC-201 to Treat Alzheimer's Disease Type Dementia | Phase2 | Alzheimer's Disease | Completed | 2014-07-31 | 2016-07-31 | ClinicalTrials.gov |
| NCT02188173 | An Observational Study of OZURDEX® in Diabetic Macular Edema (DME) | — | Macular Edema | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02092389 | Fecal Calprotectin Levels, Quality of Life, and Workability in Patients Sufferi… | — | Moderate to Severe Ulcerative Colitis | Terminated | 2014-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02210663 | A Phase 1 Study of Single Agent Veliparib in Japanese Subjects With Advanced So… | Phase1 | Advanced Solid Tumors | Completed | 2014-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02186119 | A Study of Abicipar Pegol in Patients With Diabetic Macular Edema | Phase2 | Macular Edema | Completed | 2014-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02181530 | Retrospective Data Collection Study in Patients With Macular Oedema Receiving O… | — | Macular Edema | Completed | 2014-07-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02181517 | A Study of Abicipar Pegol in Patients With Neovascular Age-related Macular Dege… | Phase2 | Macular Degeneration | Completed | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02289352 | Randomized, Double-blind, Multiple-site, Placebo-controlled, Parallel-design St… | Phase3 | Rosacea | Completed | 2014-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02289352 | Randomized, Double-blind, Multiple-site, Placebo-controlled, Parallel-design St… | Phase3 | Rosacea | Completed | 2014-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02141997 | A Study to Investigate the Safety and Efficacy of ABT-122 Given With Methotrexa… | Phase2 | Rheumatoid Arthritis | Completed | 2014-07-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02197806 | Safety and Efficacy of AGN-199201 and AGN-190584 in Patients With Presbyopia | Phase2 | Presbyopia | Completed | 2014-07-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02188173 | An Observational Study of OZURDEX® in Diabetic Macular Edema (DME) | — | Macular Edema | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02186119 | A Study of Abicipar Pegol in Patients With Diabetic Macular Edema | Phase2 | Macular Edema | Completed | 2014-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02092389 | Fecal Calprotectin Levels, Quality of Life, and Workability in Patients Sufferi… | — | Moderate to Severe Ulcerative Colitis | Terminated | 2014-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02197806 | Safety and Efficacy of AGN-199201 and AGN-190584 in Patients With Presbyopia | Phase2 | Presbyopia | Completed | 2014-07-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02181530 | Retrospective Data Collection Study in Patients With Macular Oedema Receiving O… | — | Macular Edema | Completed | 2014-07-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02210663 | A Phase 1 Study of Single Agent Veliparib in Japanese Subjects With Advanced So… | Phase1 | Advanced Solid Tumors | Completed | 2014-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02186119 | A Study of Abicipar Pegol in Patients With Diabetic Macular Edema | Phase2 | Macular Edema | Completed | 2014-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02181530 | Retrospective Data Collection Study in Patients With Macular Oedema Receiving O… | — | Macular Edema | Completed | 2014-07-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02181517 | A Study of Abicipar Pegol in Patients With Neovascular Age-related Macular Dege… | Phase2 | Macular Degeneration | Completed | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02181517 | A Study of Abicipar Pegol in Patients With Neovascular Age-related Macular Dege… | Phase2 | Macular Degeneration | Completed | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02092389 | Fecal Calprotectin Levels, Quality of Life, and Workability in Patients Sufferi… | — | Moderate to Severe Ulcerative Colitis | Terminated | 2014-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02141997 | A Study to Investigate the Safety and Efficacy of ABT-122 Given With Methotrexa… | Phase2 | Rheumatoid Arthritis | Completed | 2014-07-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02210663 | A Phase 1 Study of Single Agent Veliparib in Japanese Subjects With Advanced So… | Phase1 | Advanced Solid Tumors | Completed | 2014-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02141997 | A Study to Investigate the Safety and Efficacy of ABT-122 Given With Methotrexa… | Phase2 | Rheumatoid Arthritis | Completed | 2014-07-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02092389 | Fecal Calprotectin Levels, Quality of Life, and Workability in Patients Sufferi… | — | Moderate to Severe Ulcerative Colitis | Terminated | 2014-07-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02181517 | A Study of Abicipar Pegol in Patients With Neovascular Age-related Macular Dege… | Phase2 | Macular Degeneration | Completed | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02289352 | Randomized, Double-blind, Multiple-site, Placebo-controlled, Parallel-design St… | Phase3 | Rosacea | Completed | 2014-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02210663 | A Phase 1 Study of Single Agent Veliparib in Japanese Subjects With Advanced So… | Phase1 | Advanced Solid Tumors | Completed | 2014-07-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02181530 | Retrospective Data Collection Study in Patients With Macular Oedema Receiving O… | — | Macular Edema | Completed | 2014-07-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02141997 | A Study to Investigate the Safety and Efficacy of ABT-122 Given With Methotrexa… | Phase2 | Rheumatoid Arthritis | Completed | 2014-07-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT02186119 | A Study of Abicipar Pegol in Patients With Diabetic Macular Edema | Phase2 | Macular Edema | Completed | 2014-07-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02188173 | An Observational Study of OZURDEX® in Diabetic Macular Edema (DME) | — | Macular Edema | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02197806 | Safety and Efficacy of AGN-199201 and AGN-190584 in Patients With Presbyopia | Phase2 | Presbyopia | Completed | 2014-07-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02197806 | Safety and Efficacy of AGN-199201 and AGN-190584 in Patients With Presbyopia | Phase2 | Presbyopia | Completed | 2014-07-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT02188173 | An Observational Study of OZURDEX® in Diabetic Macular Edema (DME) | — | Macular Edema | Completed | 2014-07-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT02289352 | Randomized, Double-blind, Multiple-site, Placebo-controlled, Parallel-design St… | Phase3 | Rosacea | Completed | 2014-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02142959 | RTA 408 Lotion in Patients at Risk for Radiation Dermatitis - PRIMROSE | Phase2 | Breast Cancer | Completed | 2014-06-30 | 2015-04-30 | ClinicalTrials.gov |
| NCT02176356 | Patient Satisfaction Study of Combined Facial Treatment With BOTOX® Cosmetic, J… | Phase4 | Facial Rhytides | Completed | 2014-06-30 | 2015-05-03 | ClinicalTrials.gov |
| NCT02176356 | Patient Satisfaction Study of Combined Facial Treatment With BOTOX® Cosmetic, J… | Phase4 | Facial Rhytides | Completed | 2014-06-30 | 2015-05-03 | ClinicalTrials.gov |
| NCT02176356 | Patient Satisfaction Study of Combined Facial Treatment With BOTOX® Cosmetic, J… | Phase4 | Facial Rhytides | Completed | 2014-06-30 | 2015-05-03 | ClinicalTrials.gov |
| NCT02176356 | Patient Satisfaction Study of Combined Facial Treatment With BOTOX® Cosmetic, J… | Phase4 | Facial Rhytides | Completed | 2014-06-30 | 2015-05-03 | ClinicalTrials.gov |
| NCT02142959 | RTA 408 Lotion in Patients at Risk for Radiation Dermatitis - PRIMROSE | Phase2 | Breast Cancer | Completed | 2014-06-30 | 2015-04-30 | ClinicalTrials.gov |
| NCT02142959 | RTA 408 Lotion in Patients at Risk for Radiation Dermatitis - PRIMROSE | Phase2 | Breast Cancer | Completed | 2014-06-30 | 2015-04-30 | ClinicalTrials.gov |
| NCT02142959 | RTA 408 Lotion in Patients at Risk for Radiation Dermatitis - PRIMROSE | Phase2 | Breast Cancer | Completed | 2014-06-30 | 2015-04-30 | ClinicalTrials.gov |
| NCT02167945 | A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonav… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | Completed | 2014-06-12 | 2021-05-13 | ClinicalTrials.gov |
| NCT02167945 | A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonav… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | Completed | 2014-06-12 | 2021-05-13 | ClinicalTrials.gov |
| NCT02167945 | A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonav… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | Completed | 2014-06-12 | 2021-05-13 | ClinicalTrials.gov |
| NCT02167945 | A Study to Evaluate Long-term Outcomes Following Treatment With ABT-450/Ritonav… | Phase3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | Completed | 2014-06-12 | 2021-05-13 | ClinicalTrials.gov |
| NCT02161146 | AGN-229666 Ophthalmic Solution in Japanese Patients With Allergic Conjunctivitis | Phase3 | Conjunctivitis, Allergic | Completed | 2014-06-04 | 2014-12-20 | ClinicalTrials.gov |
| NCT02087904 | A Study Evaluating the Safety, Efficacy, and Pharmacodynamic Effects of ABT-981… | Phase2 | Knee Osteoarthritis | Completed | 2014-06-04 | 2016-12-13 | ClinicalTrials.gov |
| NCT02161146 | AGN-229666 Ophthalmic Solution in Japanese Patients With Allergic Conjunctivitis | Phase3 | Conjunctivitis, Allergic | Completed | 2014-06-04 | 2014-12-20 | ClinicalTrials.gov |
| NCT02087904 | A Study Evaluating the Safety, Efficacy, and Pharmacodynamic Effects of ABT-981… | Phase2 | Knee Osteoarthritis | Completed | 2014-06-04 | 2016-12-13 | ClinicalTrials.gov |
| NCT02087904 | A Study Evaluating the Safety, Efficacy, and Pharmacodynamic Effects of ABT-981… | Phase2 | Knee Osteoarthritis | Completed | 2014-06-04 | 2016-12-13 | ClinicalTrials.gov |
| NCT02161146 | AGN-229666 Ophthalmic Solution in Japanese Patients With Allergic Conjunctivitis | Phase3 | Conjunctivitis, Allergic | Completed | 2014-06-04 | 2014-12-20 | ClinicalTrials.gov |
| NCT02161146 | AGN-229666 Ophthalmic Solution in Japanese Patients With Allergic Conjunctivitis | Phase3 | Conjunctivitis, Allergic | Completed | 2014-06-04 | 2014-12-20 | ClinicalTrials.gov |
| NCT02087904 | A Study Evaluating the Safety, Efficacy, and Pharmacodynamic Effects of ABT-981… | Phase2 | Knee Osteoarthritis | Completed | 2014-06-04 | 2016-12-13 | ClinicalTrials.gov |
| NCT02267746 | A Study To Evaluate The Safety And Therapeutic Equivalence of Tazarotene Foam 0… | Phase3 | Acne Vulgaris | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02148718 | Rapidity of Response to Adalimumab Treatment in Patients With Crohn´s Disease | Phase4 | Moderate to Severe Crohn's Disease | Completed | 2014-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02267746 | A Study To Evaluate The Safety And Therapeutic Equivalence of Tazarotene Foam 0… | Phase3 | Acne Vulgaris | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02161159 | An Observational Study of BOTOX® for the Management of Urinary Incontinence in … | — | Urinary Incontinence | Completed | 2014-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02161159 | An Observational Study of BOTOX® for the Management of Urinary Incontinence in … | — | Urinary Incontinence | Completed | 2014-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02148718 | Rapidity of Response to Adalimumab Treatment in Patients With Crohn´s Disease | Phase4 | Moderate to Severe Crohn's Disease | Completed | 2014-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02148718 | Rapidity of Response to Adalimumab Treatment in Patients With Crohn´s Disease | Phase4 | Moderate to Severe Crohn's Disease | Completed | 2014-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02161159 | An Observational Study of BOTOX® for the Management of Urinary Incontinence in … | — | Urinary Incontinence | Completed | 2014-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02267746 | A Study To Evaluate The Safety And Therapeutic Equivalence of Tazarotene Foam 0… | Phase3 | Acne Vulgaris | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02161159 | An Observational Study of BOTOX® for the Management of Urinary Incontinence in … | — | Urinary Incontinence | Completed | 2014-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02148718 | Rapidity of Response to Adalimumab Treatment in Patients With Crohn´s Disease | Phase4 | Moderate to Severe Crohn's Disease | Completed | 2014-06-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02267746 | A Study To Evaluate The Safety And Therapeutic Equivalence of Tazarotene Foam 0… | Phase3 | Acne Vulgaris | Completed | 2014-06-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02128113 | RTA 408 Ophthalmic Suspension for the Prevention of Corneal Endothelial Cell Lo… | Phase2 | Corneal Endothelial Cell Loss | Completed | 2014-05-31 | 2015-04-30 | ClinicalTrials.gov |
| NCT02128113 | RTA 408 Ophthalmic Suspension for the Prevention of Corneal Endothelial Cell Lo… | Phase2 | Corneal Endothelial Cell Loss | Completed | 2014-05-31 | 2015-04-30 | ClinicalTrials.gov |
| NCT02128113 | RTA 408 Ophthalmic Suspension for the Prevention of Corneal Endothelial Cell Lo… | Phase2 | Corneal Endothelial Cell Loss | Completed | 2014-05-31 | 2015-04-30 | ClinicalTrials.gov |
| NCT02128113 | RTA 408 Ophthalmic Suspension for the Prevention of Corneal Endothelial Cell Lo… | Phase2 | Corneal Endothelial Cell Loss | Completed | 2014-05-31 | 2015-04-30 | ClinicalTrials.gov |
| NCT02143713 | Global Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Women… | Phase3 | Endometriosis | Completed | 2014-05-27 | 2017-05-23 | ClinicalTrials.gov |
| NCT02143713 | Global Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Women… | Phase3 | Endometriosis | Completed | 2014-05-27 | 2017-05-23 | ClinicalTrials.gov |
| NCT02143713 | Global Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Women… | Phase3 | Endometriosis | Completed | 2014-05-27 | 2017-05-23 | ClinicalTrials.gov |
| NCT02143713 | Global Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Women… | Phase3 | Endometriosis | Completed | 2014-05-27 | 2017-05-23 | ClinicalTrials.gov |
| NCT02097121 | OnabotulinumtoxinA for the Treatment of Urinary Incontinence Due to Overactive … | Phase3 | Urinary Incontinence | Terminated | 2014-05-23 | 2022-02-10 | ClinicalTrials.gov |
| NCT02097121 | OnabotulinumtoxinA for the Treatment of Urinary Incontinence Due to Overactive … | Phase3 | Urinary Incontinence | Terminated | 2014-05-23 | 2022-02-10 | ClinicalTrials.gov |
| NCT02097121 | OnabotulinumtoxinA for the Treatment of Urinary Incontinence Due to Overactive … | Phase3 | Urinary Incontinence | Terminated | 2014-05-23 | 2022-02-10 | ClinicalTrials.gov |
| NCT02097121 | OnabotulinumtoxinA for the Treatment of Urinary Incontinence Due to Overactive … | Phase3 | Urinary Incontinence | Terminated | 2014-05-23 | 2022-02-10 | ClinicalTrials.gov |
| NCT02176421 | A Prospective, Open Label Study Evaluating JUVÉDERM® VOLBELLA With Lidocaine Tr… | Na | Infra-orbital Skin Depressions | Completed | 2014-05-15 | 2015-07-03 | ClinicalTrials.gov |
| NCT02176421 | A Prospective, Open Label Study Evaluating JUVÉDERM® VOLBELLA With Lidocaine Tr… | Na | Infra-orbital Skin Depressions | Completed | 2014-05-15 | 2015-07-03 | ClinicalTrials.gov |
| NCT02176421 | A Prospective, Open Label Study Evaluating JUVÉDERM® VOLBELLA With Lidocaine Tr… | Na | Infra-orbital Skin Depressions | Completed | 2014-05-15 | 2015-07-03 | ClinicalTrials.gov |
| NCT02176421 | A Prospective, Open Label Study Evaluating JUVÉDERM® VOLBELLA With Lidocaine Tr… | Na | Infra-orbital Skin Depressions | Completed | 2014-05-15 | 2015-07-03 | ClinicalTrials.gov |
| NCT02087085 | A Safety and Efficacy Study of Brimonidine Intravitreal Implant in Geographic A… | Phase2 | Geographic Atrophy | Terminated | 2014-05-09 | 2018-03-30 | ClinicalTrials.gov |
| NCT02087085 | A Safety and Efficacy Study of Brimonidine Intravitreal Implant in Geographic A… | Phase2 | Geographic Atrophy | Terminated | 2014-05-09 | 2018-03-30 | ClinicalTrials.gov |
| NCT02087085 | A Safety and Efficacy Study of Brimonidine Intravitreal Implant in Geographic A… | Phase2 | Geographic Atrophy | Terminated | 2014-05-09 | 2018-03-30 | ClinicalTrials.gov |
| NCT02087085 | A Safety and Efficacy Study of Brimonidine Intravitreal Implant in Geographic A… | Phase2 | Geographic Atrophy | Terminated | 2014-05-09 | 2018-03-30 | ClinicalTrials.gov |
| NCT02155543 | A Safety, Tolerability, and Pharmacokinetics (PK) Study of AGN-223575 in Health… | Phase1 | Healthy Volunteers | Completed | 2014-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02324270 | Safety and Efficacy of Generic Diclofenac Epolamine Acute Pain Due to Minor Ank… | Phase3 | Ankle Sprain | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02065570 | Study to Evaluate Efficacy and Safety of Two Drug Regimens in Subjects With Mod… | Phase3 | Crohn's Disease | Completed | 2014-05-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT02097719 | Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travoprost 0… | Phase4 | Glaucoma | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02145650 | Spasticity Registry Evaluating Epidemiology, Treatment Patterns and Clinical Ne… | — | Muscle Spasticity | Withdrawn | 2014-05-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02324270 | Safety and Efficacy of Generic Diclofenac Epolamine Acute Pain Due to Minor Ank… | Phase3 | Ankle Sprain | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02131636 | Efficacy and Safety of AGN-199201 in Patients With Persistent Erythema Associat… | Phase3 | Erythema | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02065570 | Study to Evaluate Efficacy and Safety of Two Drug Regimens in Subjects With Mod… | Phase3 | Crohn's Disease | Completed | 2014-05-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT02132572 | Retrospective Study of Incidence and Etiology of Reoperation After Primary Augm… | — | Breast Implantation | Completed | 2014-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02155543 | A Safety, Tolerability, and Pharmacokinetics (PK) Study of AGN-223575 in Health… | Phase1 | Healthy Volunteers | Completed | 2014-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02131636 | Efficacy and Safety of AGN-199201 in Patients With Persistent Erythema Associat… | Phase3 | Erythema | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02065570 | Study to Evaluate Efficacy and Safety of Two Drug Regimens in Subjects With Mod… | Phase3 | Crohn's Disease | Completed | 2014-05-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT02132572 | Retrospective Study of Incidence and Etiology of Reoperation After Primary Augm… | — | Breast Implantation | Completed | 2014-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02097719 | Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travoprost 0… | Phase4 | Glaucoma | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02141984 | Surveillance of Humira in Korean JIA Patients | — | Polyarticular Juvenile Idiopathic Arthritis | Completed | 2014-05-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02155543 | A Safety, Tolerability, and Pharmacokinetics (PK) Study of AGN-223575 in Health… | Phase1 | Healthy Volunteers | Completed | 2014-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02141984 | Surveillance of Humira in Korean JIA Patients | — | Polyarticular Juvenile Idiopathic Arthritis | Completed | 2014-05-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02145676 | OnabotulinumtoxinA Treatment in Adult Patients With Upper Limb Spasticity | Phase3 | Muscle Spasticity | Terminated | 2014-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02141984 | Surveillance of Humira in Korean JIA Patients | — | Polyarticular Juvenile Idiopathic Arthritis | Completed | 2014-05-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02097719 | Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travoprost 0… | Phase4 | Glaucoma | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02145650 | Spasticity Registry Evaluating Epidemiology, Treatment Patterns and Clinical Ne… | — | Muscle Spasticity | Withdrawn | 2014-05-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02324270 | Safety and Efficacy of Generic Diclofenac Epolamine Acute Pain Due to Minor Ank… | Phase3 | Ankle Sprain | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02145676 | OnabotulinumtoxinA Treatment in Adult Patients With Upper Limb Spasticity | Phase3 | Muscle Spasticity | Terminated | 2014-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02324270 | Safety and Efficacy of Generic Diclofenac Epolamine Acute Pain Due to Minor Ank… | Phase3 | Ankle Sprain | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02132572 | Retrospective Study of Incidence and Etiology of Reoperation After Primary Augm… | — | Breast Implantation | Completed | 2014-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02132572 | Retrospective Study of Incidence and Etiology of Reoperation After Primary Augm… | — | Breast Implantation | Completed | 2014-05-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02145676 | OnabotulinumtoxinA Treatment in Adult Patients With Upper Limb Spasticity | Phase3 | Muscle Spasticity | Terminated | 2014-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02145676 | OnabotulinumtoxinA Treatment in Adult Patients With Upper Limb Spasticity | Phase3 | Muscle Spasticity | Terminated | 2014-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02155543 | A Safety, Tolerability, and Pharmacokinetics (PK) Study of AGN-223575 in Health… | Phase1 | Healthy Volunteers | Completed | 2014-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02131636 | Efficacy and Safety of AGN-199201 in Patients With Persistent Erythema Associat… | Phase3 | Erythema | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02065570 | Study to Evaluate Efficacy and Safety of Two Drug Regimens in Subjects With Mod… | Phase3 | Crohn's Disease | Completed | 2014-05-01 | 2020-01-30 | ClinicalTrials.gov |
| NCT02141984 | Surveillance of Humira in Korean JIA Patients | — | Polyarticular Juvenile Idiopathic Arthritis | Completed | 2014-05-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02097719 | Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travoprost 0… | Phase4 | Glaucoma | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02145650 | Spasticity Registry Evaluating Epidemiology, Treatment Patterns and Clinical Ne… | — | Muscle Spasticity | Withdrawn | 2014-05-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02131636 | Efficacy and Safety of AGN-199201 in Patients With Persistent Erythema Associat… | Phase3 | Erythema | Completed | 2014-05-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02145650 | Spasticity Registry Evaluating Epidemiology, Treatment Patterns and Clinical Ne… | — | Muscle Spasticity | Withdrawn | 2014-05-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02013791 | Phase 2 Study of a New Ophthalmic Formulation of Cyclosporine (Restasis® X) in … | Phase2 | Dry Eye Syndromes | Terminated | 2014-04-29 | 2017-04-12 | ClinicalTrials.gov |
| NCT02013791 | Phase 2 Study of a New Ophthalmic Formulation of Cyclosporine (Restasis® X) in … | Phase2 | Dry Eye Syndromes | Terminated | 2014-04-29 | 2017-04-12 | ClinicalTrials.gov |
| NCT02013791 | Phase 2 Study of a New Ophthalmic Formulation of Cyclosporine (Restasis® X) in … | Phase2 | Dry Eye Syndromes | Terminated | 2014-04-29 | 2017-04-12 | ClinicalTrials.gov |
| NCT02013791 | Phase 2 Study of a New Ophthalmic Formulation of Cyclosporine (Restasis® X) in … | Phase2 | Dry Eye Syndromes | Terminated | 2014-04-29 | 2017-04-12 | ClinicalTrials.gov |
| NCT02106546 | Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Placebo Plus C… | Phase3 | Squamous Non-Small Cell Lung Cancer | Completed | 2014-04-10 | 2019-11-20 | ClinicalTrials.gov |
| NCT02106546 | Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Placebo Plus C… | Phase3 | Squamous Non-Small Cell Lung Cancer | Completed | 2014-04-10 | 2019-11-20 | ClinicalTrials.gov |
| NCT02106546 | Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Placebo Plus C… | Phase3 | Squamous Non-Small Cell Lung Cancer | Completed | 2014-04-10 | 2019-11-20 | ClinicalTrials.gov |
| NCT02106546 | Study Comparing Veliparib Plus Carboplatin and Paclitaxel Versus Placebo Plus C… | Phase3 | Squamous Non-Small Cell Lung Cancer | Completed | 2014-04-10 | 2019-11-20 | ClinicalTrials.gov |
| NCT02163694 | A Phase 3 Randomized, Placebo-controlled Trial of Carboplatin and Paclitaxel Wi… | Phase3 | Metastatic Breast Cancer | Completed | 2014-04-08 | 2024-01-25 | ClinicalTrials.gov |
| NCT02163694 | A Phase 3 Randomized, Placebo-controlled Trial of Carboplatin and Paclitaxel Wi… | Phase3 | Metastatic Breast Cancer | Completed | 2014-04-08 | 2024-01-25 | ClinicalTrials.gov |
| NCT02163694 | A Phase 3 Randomized, Placebo-controlled Trial of Carboplatin and Paclitaxel Wi… | Phase3 | Metastatic Breast Cancer | Completed | 2014-04-08 | 2024-01-25 | ClinicalTrials.gov |
| NCT02163694 | A Phase 3 Randomized, Placebo-controlled Trial of Carboplatin and Paclitaxel Wi… | Phase3 | Metastatic Breast Cancer | Completed | 2014-04-08 | 2024-01-25 | ClinicalTrials.gov |
| NCT02121847 | Investigation of Maintaining Visual Performance Achieved With Cyclosporine Ther… | Phase4 | Dry Eye Syndromes | Completed | 2014-04-03 | 2014-09-23 | ClinicalTrials.gov |
| NCT02121847 | Investigation of Maintaining Visual Performance Achieved With Cyclosporine Ther… | Phase4 | Dry Eye Syndromes | Completed | 2014-04-03 | 2014-09-23 | ClinicalTrials.gov |
| NCT02121847 | Investigation of Maintaining Visual Performance Achieved With Cyclosporine Ther… | Phase4 | Dry Eye Syndromes | Completed | 2014-04-03 | 2014-09-23 | ClinicalTrials.gov |
| NCT02121847 | Investigation of Maintaining Visual Performance Achieved With Cyclosporine Ther… | Phase4 | Dry Eye Syndromes | Completed | 2014-04-03 | 2014-09-23 | ClinicalTrials.gov |
| NCT02032277 | A Study Evaluating Safety and Efficacy of the Addition of ABT-888 Plus Carbopla… | Phase3 | Triple Negative Breast Cancer | Completed | 2014-04-02 | 2020-11-12 | ClinicalTrials.gov |
| NCT02032277 | A Study Evaluating Safety and Efficacy of the Addition of ABT-888 Plus Carbopla… | Phase3 | Triple Negative Breast Cancer | Completed | 2014-04-02 | 2020-11-12 | ClinicalTrials.gov |
| NCT02032277 | A Study Evaluating Safety and Efficacy of the Addition of ABT-888 Plus Carbopla… | Phase3 | Triple Negative Breast Cancer | Completed | 2014-04-02 | 2020-11-12 | ClinicalTrials.gov |
| NCT02032277 | A Study Evaluating Safety and Efficacy of the Addition of ABT-888 Plus Carbopla… | Phase3 | Triple Negative Breast Cancer | Completed | 2014-04-02 | 2020-11-12 | ClinicalTrials.gov |
| NCT02037425 | Duration of Benefit for OnabotulinumtoxinA in Treatment of Chronic Migraine | Phase4 | Chronic Migraine | Completed | 2014-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02117752 | Dermal Tolerability of Dapsone Gel in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-04-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02037425 | Duration of Benefit for OnabotulinumtoxinA in Treatment of Chronic Migraine | Phase4 | Chronic Migraine | Completed | 2014-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02108483 | Phototoxicity Test of Dapsone Gel in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02095158 | A Long-Term Safety and Efficacy Study AGN-19920 in Patients With Persistent Ery… | Phase3 | Erythema | Completed | 2014-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02095158 | A Long-Term Safety and Efficacy Study AGN-19920 in Patients With Persistent Ery… | Phase3 | Erythema | Completed | 2014-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02117752 | Dermal Tolerability of Dapsone Gel in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-04-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01471054 | Dexamethasone Intravitreal Implant for Treatment of Macular Edema After Plaque … | Phase2 | Macular Edema | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01969682 | A Study to Assess the Effect of Rifampin on the Metabolism of ABT-199 | Phase1 | Non-Hodgkin's Lymphoma | Withdrawn | 2014-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02095158 | A Long-Term Safety and Efficacy Study AGN-19920 in Patients With Persistent Ery… | Phase3 | Erythema | Completed | 2014-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01471054 | Dexamethasone Intravitreal Implant for Treatment of Macular Edema After Plaque … | Phase2 | Macular Edema | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02037425 | Duration of Benefit for OnabotulinumtoxinA in Treatment of Chronic Migraine | Phase4 | Chronic Migraine | Completed | 2014-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01471054 | Dexamethasone Intravitreal Implant for Treatment of Macular Edema After Plaque … | Phase2 | Macular Edema | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02117752 | Dermal Tolerability of Dapsone Gel in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-04-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02117752 | Dermal Tolerability of Dapsone Gel in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-04-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02095158 | A Long-Term Safety and Efficacy Study AGN-19920 in Patients With Persistent Ery… | Phase3 | Erythema | Completed | 2014-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02108483 | Phototoxicity Test of Dapsone Gel in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01969682 | A Study to Assess the Effect of Rifampin on the Metabolism of ABT-199 | Phase1 | Non-Hodgkin's Lymphoma | Withdrawn | 2014-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02068222 | A Study to Evaluate the Safety and Antiviral Effect of ABT-450/Ritonavir and AB… | Phase2 | Chronic Hepatitis C | Completed | 2014-04-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02068222 | A Study to Evaluate the Safety and Antiviral Effect of ABT-450/Ritonavir and AB… | Phase2 | Chronic Hepatitis C | Completed | 2014-04-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02068222 | A Study to Evaluate the Safety and Antiviral Effect of ABT-450/Ritonavir and AB… | Phase2 | Chronic Hepatitis C | Completed | 2014-04-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01471054 | Dexamethasone Intravitreal Implant for Treatment of Macular Edema After Plaque … | Phase2 | Macular Edema | Terminated | 2014-04-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01969682 | A Study to Assess the Effect of Rifampin on the Metabolism of ABT-199 | Phase1 | Non-Hodgkin's Lymphoma | Withdrawn | 2014-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02068222 | A Study to Evaluate the Safety and Antiviral Effect of ABT-450/Ritonavir and AB… | Phase2 | Chronic Hepatitis C | Completed | 2014-04-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02108483 | Phototoxicity Test of Dapsone Gel in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01969682 | A Study to Assess the Effect of Rifampin on the Metabolism of ABT-199 | Phase1 | Non-Hodgkin's Lymphoma | Withdrawn | 2014-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02108483 | Phototoxicity Test of Dapsone Gel in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02037425 | Duration of Benefit for OnabotulinumtoxinA in Treatment of Chronic Migraine | Phase4 | Chronic Migraine | Completed | 2014-04-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02147197 | A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal … | Phase3 | Leiomyoma | Completed | 2014-03-31 | 2016-03-29 | ClinicalTrials.gov |
| NCT02087878 | A Blood and Tissue Sample Collection Study of Patients Who Have Inflammatory Bo… | — | Crohn's Disease | Withdrawn | 2014-03-31 | 2019-09-30 | ClinicalTrials.gov |
| NCT02087878 | A Blood and Tissue Sample Collection Study of Patients Who Have Inflammatory Bo… | — | Crohn's Disease | Withdrawn | 2014-03-31 | 2019-09-30 | ClinicalTrials.gov |
| NCT02147197 | A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal … | Phase3 | Leiomyoma | Completed | 2014-03-31 | 2016-03-29 | ClinicalTrials.gov |
| NCT02147197 | A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal … | Phase3 | Leiomyoma | Completed | 2014-03-31 | 2016-03-29 | ClinicalTrials.gov |
| NCT02087878 | A Blood and Tissue Sample Collection Study of Patients Who Have Inflammatory Bo… | — | Crohn's Disease | Withdrawn | 2014-03-31 | 2019-09-30 | ClinicalTrials.gov |
| NCT02147197 | A Study of the Efficacy and Safety of a 3-month Treatment Course of Ulipristal … | Phase3 | Leiomyoma | Completed | 2014-03-31 | 2016-03-29 | ClinicalTrials.gov |
| NCT02087878 | A Blood and Tissue Sample Collection Study of Patients Who Have Inflammatory Bo… | — | Crohn's Disease | Withdrawn | 2014-03-31 | 2019-09-30 | ClinicalTrials.gov |
| NCT02065622 | Study to Evaluate the Safety and Efficacy of Two Adalimumab Dosing Regimens in … | Phase3 | Ulcerative Colitis (UC) | Completed | 2014-03-27 | 2019-11-11 | ClinicalTrials.gov |
| NCT02065622 | Study to Evaluate the Safety and Efficacy of Two Adalimumab Dosing Regimens in … | Phase3 | Ulcerative Colitis (UC) | Completed | 2014-03-27 | 2019-11-11 | ClinicalTrials.gov |
| NCT02065622 | Study to Evaluate the Safety and Efficacy of Two Adalimumab Dosing Regimens in … | Phase3 | Ulcerative Colitis (UC) | Completed | 2014-03-27 | 2019-11-11 | ClinicalTrials.gov |
| NCT02065622 | Study to Evaluate the Safety and Efficacy of Two Adalimumab Dosing Regimens in … | Phase3 | Ulcerative Colitis (UC) | Completed | 2014-03-27 | 2019-11-11 | ClinicalTrials.gov |
| NCT02066389 | A Study Investigating the Efficacy and Safety of Upadacitinib (ABT-494) Given W… | Phase2 | Rheumatoid Arthritis | Completed | 2014-03-26 | 2015-07-02 | ClinicalTrials.gov |
| NCT02066389 | A Study Investigating the Efficacy and Safety of Upadacitinib (ABT-494) Given W… | Phase2 | Rheumatoid Arthritis | Completed | 2014-03-26 | 2015-07-02 | ClinicalTrials.gov |
| NCT02066389 | A Study Investigating the Efficacy and Safety of Upadacitinib (ABT-494) Given W… | Phase2 | Rheumatoid Arthritis | Completed | 2014-03-26 | 2015-07-02 | ClinicalTrials.gov |
| NCT02066389 | A Study Investigating the Efficacy and Safety of Upadacitinib (ABT-494) Given W… | Phase2 | Rheumatoid Arthritis | Completed | 2014-03-26 | 2015-07-02 | ClinicalTrials.gov |
| NCT02005471 | A Study to Evaluate the Benefit of Venetoclax Plus Rituximab Compared With Bend… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2014-03-17 | 2022-08-03 | ClinicalTrials.gov |
| NCT02005471 | A Study to Evaluate the Benefit of Venetoclax Plus Rituximab Compared With Bend… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2014-03-17 | 2022-08-03 | ClinicalTrials.gov |
| NCT02005471 | A Study to Evaluate the Benefit of Venetoclax Plus Rituximab Compared With Bend… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2014-03-17 | 2022-08-03 | ClinicalTrials.gov |
| NCT02005471 | A Study to Evaluate the Benefit of Venetoclax Plus Rituximab Compared With Bend… | Phase3 | Chronic Lymphocytic Leukemia | Completed | 2014-03-17 | 2022-08-03 | ClinicalTrials.gov |
| NCT02082249 | An Extension Study to Assess the Safety, Tolerability and Efficacy of ABT-SLV18… | Phase3 | Advanced Parkinson's Disease | Completed | 2014-03-10 | 2019-10-31 | ClinicalTrials.gov |
| NCT02082249 | An Extension Study to Assess the Safety, Tolerability and Efficacy of ABT-SLV18… | Phase3 | Advanced Parkinson's Disease | Completed | 2014-03-10 | 2019-10-31 | ClinicalTrials.gov |
| NCT02082249 | An Extension Study to Assess the Safety, Tolerability and Efficacy of ABT-SLV18… | Phase3 | Advanced Parkinson's Disease | Completed | 2014-03-10 | 2019-10-31 | ClinicalTrials.gov |
| NCT02082249 | An Extension Study to Assess the Safety, Tolerability and Efficacy of ABT-SLV18… | Phase3 | Advanced Parkinson's Disease | Completed | 2014-03-10 | 2019-10-31 | ClinicalTrials.gov |
| NCT02067793 | Study of Intravenous NRX-1074 in Patients With Major Depressive Disorder | Phase2 | Major Depressive Disorder | Completed | 2014-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02082197 | An Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men | Phase3 | Hypogonadism | Withdrawn | 2014-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02082262 | AGN-229666 Ophthalmic Solution for the Treatment of Seasonal or Perennial Aller… | Phase3 | Conjunctivitis, Allergic | Completed | 2014-03-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02199964 | The Effects of Cyclosporin A in a Low Humidity Environment, on the Ocular Surfa… | Na | Dry Eye | Terminated | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02082262 | AGN-229666 Ophthalmic Solution for the Treatment of Seasonal or Perennial Aller… | Phase3 | Conjunctivitis, Allergic | Completed | 2014-03-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT02199964 | The Effects of Cyclosporin A in a Low Humidity Environment, on the Ocular Surfa… | Na | Dry Eye | Terminated | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02199964 | The Effects of Cyclosporin A in a Low Humidity Environment, on the Ocular Surfa… | Na | Dry Eye | Terminated | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01946126 | A Retrospective Chart Review to Evaluate Diagnosis and Treatment of Chronic Mig… | — | Migraine Disorders | Completed | 2014-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02067793 | Study of Intravenous NRX-1074 in Patients With Major Depressive Disorder | Phase2 | Major Depressive Disorder | Completed | 2014-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02082197 | An Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men | Phase3 | Hypogonadism | Withdrawn | 2014-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01946126 | A Retrospective Chart Review to Evaluate Diagnosis and Treatment of Chronic Mig… | — | Migraine Disorders | Completed | 2014-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02199964 | The Effects of Cyclosporin A in a Low Humidity Environment, on the Ocular Surfa… | Na | Dry Eye | Terminated | 2014-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02082262 | AGN-229666 Ophthalmic Solution for the Treatment of Seasonal or Perennial Aller… | Phase3 | Conjunctivitis, Allergic | Completed | 2014-03-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01946126 | A Retrospective Chart Review to Evaluate Diagnosis and Treatment of Chronic Mig… | — | Migraine Disorders | Completed | 2014-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02067793 | Study of Intravenous NRX-1074 in Patients With Major Depressive Disorder | Phase2 | Major Depressive Disorder | Completed | 2014-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02082197 | An Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men | Phase3 | Hypogonadism | Withdrawn | 2014-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02067793 | Study of Intravenous NRX-1074 in Patients With Major Depressive Disorder | Phase2 | Major Depressive Disorder | Completed | 2014-03-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02082197 | An Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men | Phase3 | Hypogonadism | Withdrawn | 2014-03-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02082262 | AGN-229666 Ophthalmic Solution for the Treatment of Seasonal or Perennial Aller… | Phase3 | Conjunctivitis, Allergic | Completed | 2014-03-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01946126 | A Retrospective Chart Review to Evaluate Diagnosis and Treatment of Chronic Mig… | — | Migraine Disorders | Completed | 2014-03-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT02065375 | RTA 408 Ophthalmic Suspension for the Treatment of Ocular Inflammation and Pain… | Phase2 | Inflammation and Pain Following Ocular Surgery | Completed | 2014-02-28 | 2014-09-30 | ClinicalTrials.gov |
| NCT02065375 | RTA 408 Ophthalmic Suspension for the Treatment of Ocular Inflammation and Pain… | Phase2 | Inflammation and Pain Following Ocular Surgery | Completed | 2014-02-28 | 2014-09-30 | ClinicalTrials.gov |
| NCT02065375 | RTA 408 Ophthalmic Suspension for the Treatment of Ocular Inflammation and Pain… | Phase2 | Inflammation and Pain Following Ocular Surgery | Completed | 2014-02-28 | 2014-09-30 | ClinicalTrials.gov |
| NCT02065375 | RTA 408 Ophthalmic Suspension for the Treatment of Ocular Inflammation and Pain… | Phase2 | Inflammation and Pain Following Ocular Surgery | Completed | 2014-02-28 | 2014-09-30 | ClinicalTrials.gov |
| NCT01945866 | Phase II Combination Steroid and Anti-VEGF for Persistent DME | Phase2 | Diabetic Macular Edema | Completed | 2014-02-01 | 2017-06-05 | ClinicalTrials.gov |
| NCT02048605 | Training of Psychosocial Skills Based on Cognitive Behavioural Therapy for Pati… | Na | Parkinson's Disease | Completed | 2014-02-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02031276 | Efficacy, Safety and Pharmacokinetics of BI 655066/ABBV-066 (Risankizumab) in P… | Phase2 | Crohn Disease | Completed | 2014-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02010788 | Evaluation of Safety and Efficacy of Botulinum Toxin Type A (BOTOX®) to Treat U… | — | Urinary Incontinence | Completed | 2014-02-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02031276 | Efficacy, Safety and Pharmacokinetics of BI 655066/ABBV-066 (Risankizumab) in P… | Phase2 | Crohn Disease | Completed | 2014-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT01945866 | Phase II Combination Steroid and Anti-VEGF for Persistent DME | Phase2 | Diabetic Macular Edema | Completed | 2014-02-01 | 2017-06-05 | ClinicalTrials.gov |
| NCT01945866 | Phase II Combination Steroid and Anti-VEGF for Persistent DME | Phase2 | Diabetic Macular Edema | Completed | 2014-02-01 | 2017-06-05 | ClinicalTrials.gov |
| NCT02048605 | Training of Psychosocial Skills Based on Cognitive Behavioural Therapy for Pati… | Na | Parkinson's Disease | Completed | 2014-02-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02010788 | Evaluation of Safety and Efficacy of Botulinum Toxin Type A (BOTOX®) to Treat U… | — | Urinary Incontinence | Completed | 2014-02-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT01945866 | Phase II Combination Steroid and Anti-VEGF for Persistent DME | Phase2 | Diabetic Macular Edema | Completed | 2014-02-01 | 2017-06-05 | ClinicalTrials.gov |
| NCT02031276 | Efficacy, Safety and Pharmacokinetics of BI 655066/ABBV-066 (Risankizumab) in P… | Phase2 | Crohn Disease | Completed | 2014-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02031276 | Efficacy, Safety and Pharmacokinetics of BI 655066/ABBV-066 (Risankizumab) in P… | Phase2 | Crohn Disease | Completed | 2014-02-01 | 2016-11-01 | ClinicalTrials.gov |
| NCT02048605 | Training of Psychosocial Skills Based on Cognitive Behavioural Therapy for Pati… | Na | Parkinson's Disease | Completed | 2014-02-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02048605 | Training of Psychosocial Skills Based on Cognitive Behavioural Therapy for Pati… | Na | Parkinson's Disease | Completed | 2014-02-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT02010788 | Evaluation of Safety and Efficacy of Botulinum Toxin Type A (BOTOX®) to Treat U… | — | Urinary Incontinence | Completed | 2014-02-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02010788 | Evaluation of Safety and Efficacy of Botulinum Toxin Type A (BOTOX®) to Treat U… | — | Urinary Incontinence | Completed | 2014-02-01 | 2016-07-01 | ClinicalTrials.gov |
| NCT02047110 | BI 655066 (Risankizumab) Proof of Concept Dose Finding Study in Ankylosing Spon… | Phase2 | Ankylosing Spondylitis (AS) | Completed | 2014-01-28 | 2016-07-25 | ClinicalTrials.gov |
| NCT02072928 | Study of Botulinum Toxin Type A (BOTOX®) to Treat Urinary Incontinence From Neu… | — | Urinary Incontinence | Completed | 2014-01-28 | 2015-09-30 | ClinicalTrials.gov |
| NCT02047110 | BI 655066 (Risankizumab) Proof of Concept Dose Finding Study in Ankylosing Spon… | Phase2 | Ankylosing Spondylitis (AS) | Completed | 2014-01-28 | 2016-07-25 | ClinicalTrials.gov |
| NCT02072928 | Study of Botulinum Toxin Type A (BOTOX®) to Treat Urinary Incontinence From Neu… | — | Urinary Incontinence | Completed | 2014-01-28 | 2015-09-30 | ClinicalTrials.gov |
| NCT02047110 | BI 655066 (Risankizumab) Proof of Concept Dose Finding Study in Ankylosing Spon… | Phase2 | Ankylosing Spondylitis (AS) | Completed | 2014-01-28 | 2016-07-25 | ClinicalTrials.gov |
| NCT02072928 | Study of Botulinum Toxin Type A (BOTOX®) to Treat Urinary Incontinence From Neu… | — | Urinary Incontinence | Completed | 2014-01-28 | 2015-09-30 | ClinicalTrials.gov |
| NCT02047110 | BI 655066 (Risankizumab) Proof of Concept Dose Finding Study in Ankylosing Spon… | Phase2 | Ankylosing Spondylitis (AS) | Completed | 2014-01-28 | 2016-07-25 | ClinicalTrials.gov |
| NCT02072928 | Study of Botulinum Toxin Type A (BOTOX®) to Treat Urinary Incontinence From Neu… | — | Urinary Incontinence | Completed | 2014-01-28 | 2015-09-30 | ClinicalTrials.gov |
| NCT02049138 | An Open-label Extension Study Evaluating the Safety and Efficacy of Upadacitini… | Phase2 | Rheumatoid Arthritis | Completed | 2014-01-24 | 2021-07-29 | ClinicalTrials.gov |
| NCT02049138 | An Open-label Extension Study Evaluating the Safety and Efficacy of Upadacitini… | Phase2 | Rheumatoid Arthritis | Completed | 2014-01-24 | 2021-07-29 | ClinicalTrials.gov |
| NCT02049138 | An Open-label Extension Study Evaluating the Safety and Efficacy of Upadacitini… | Phase2 | Rheumatoid Arthritis | Completed | 2014-01-24 | 2021-07-29 | ClinicalTrials.gov |
| NCT02049138 | An Open-label Extension Study Evaluating the Safety and Efficacy of Upadacitini… | Phase2 | Rheumatoid Arthritis | Completed | 2014-01-24 | 2021-07-29 | ClinicalTrials.gov |
| NCT02010775 | Botulinum Toxin Type A (BOTOX®) Treatment of Masseter Muscle Hypertrophy | Phase2 | Masseter Muscle Hypertrophy | Completed | 2014-01-20 | 2017-11-29 | ClinicalTrials.gov |
| NCT02010775 | Botulinum Toxin Type A (BOTOX®) Treatment of Masseter Muscle Hypertrophy | Phase2 | Masseter Muscle Hypertrophy | Completed | 2014-01-20 | 2017-11-29 | ClinicalTrials.gov |
| NCT02010775 | Botulinum Toxin Type A (BOTOX®) Treatment of Masseter Muscle Hypertrophy | Phase2 | Masseter Muscle Hypertrophy | Completed | 2014-01-20 | 2017-11-29 | ClinicalTrials.gov |
| NCT02010775 | Botulinum Toxin Type A (BOTOX®) Treatment of Masseter Muscle Hypertrophy | Phase2 | Masseter Muscle Hypertrophy | Completed | 2014-01-20 | 2017-11-29 | ClinicalTrials.gov |
| NCT02099058 | A Study Evaluating the Safety, Pharmacokinetics (PK), and Preliminary Efficacy … | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2014-01-15 | 2026-08-01 | ClinicalTrials.gov |
| NCT02099058 | A Study Evaluating the Safety, Pharmacokinetics (PK), and Preliminary Efficacy … | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2014-01-15 | 2026-08-01 | ClinicalTrials.gov |
| NCT02099058 | A Study Evaluating the Safety, Pharmacokinetics (PK), and Preliminary Efficacy … | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2014-01-15 | 2026-08-01 | ClinicalTrials.gov |
| NCT02099058 | A Study Evaluating the Safety, Pharmacokinetics (PK), and Preliminary Efficacy … | Phase1 | Advanced Solid Tumors Cancer | Active_Not_Recruiting | 2014-01-15 | 2026-08-01 | ClinicalTrials.gov |
| NCT01671904 | A Study of Venetoclax in Combination With Bendamustine + Rituximab or Bendamust… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2014-01-13 | 2020-08-11 | ClinicalTrials.gov |
| NCT01671904 | A Study of Venetoclax in Combination With Bendamustine + Rituximab or Bendamust… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2014-01-13 | 2020-08-11 | ClinicalTrials.gov |
| NCT01671904 | A Study of Venetoclax in Combination With Bendamustine + Rituximab or Bendamust… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2014-01-13 | 2020-08-11 | ClinicalTrials.gov |
| NCT01671904 | A Study of Venetoclax in Combination With Bendamustine + Rituximab or Bendamust… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2014-01-13 | 2020-08-11 | ClinicalTrials.gov |
| NCT02028169 | To Observe the Impacts of Anti-Tumor Necrosis Factor (TNF) Effectiveness on Imp… | — | Psoriatic Arthritis | Completed | 2014-01-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02016482 | A Study to Evaluate the Safety and Efficacy of Adalimumab in Subjects With Chro… | Phase3 | Nail Psoriasis | Completed | 2014-01-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02049476 | Study of the Effectiveness of Ozurdex for the Control of Uveitis | Phase4 | Uveitis, Intermediate | Completed | 2014-01-01 | 2018-06-30 | ClinicalTrials.gov |
| NCT02036424 | Anti-Vascular Endothelial Growth Factor (Anti-VEGF) Alone Versus Ozurdex Given … | Phase4 | Diabetic Macular Edema | Completed | 2014-01-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02052362 | Bioavailability of ABT-450 and ABT-267 With Ritonavir | Phase1 | Absolute Bioavailability | Completed | 2014-01-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT02036424 | Anti-Vascular Endothelial Growth Factor (Anti-VEGF) Alone Versus Ozurdex Given … | Phase4 | Diabetic Macular Edema | Completed | 2014-01-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02036424 | Anti-Vascular Endothelial Growth Factor (Anti-VEGF) Alone Versus Ozurdex Given … | Phase4 | Diabetic Macular Edema | Completed | 2014-01-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT02052362 | Bioavailability of ABT-450 and ABT-267 With Ritonavir | Phase1 | Absolute Bioavailability | Completed | 2014-01-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT02028169 | To Observe the Impacts of Anti-Tumor Necrosis Factor (TNF) Effectiveness on Imp… | — | Psoriatic Arthritis | Completed | 2014-01-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02023112 | Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT- 267 (ABT-45… | Phase3 | Hepatitis C Virus | Completed | 2014-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01939977 | Efficacy and Safety of Paricalcitol in the Reduction of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism Due to Renal Causes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02210689 | A Multi-center, Double-blind, Randomized Study, Comparing Clindamycin Phosphate… | Phase3 | BACTERIAL VAGINOSIS | Completed | 2014-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02016482 | A Study to Evaluate the Safety and Efficacy of Adalimumab in Subjects With Chro… | Phase3 | Nail Psoriasis | Completed | 2014-01-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT01939977 | Efficacy and Safety of Paricalcitol in the Reduction of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism Due to Renal Causes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02049476 | Study of the Effectiveness of Ozurdex for the Control of Uveitis | Phase4 | Uveitis, Intermediate | Completed | 2014-01-01 | 2018-06-30 | ClinicalTrials.gov |
| NCT02210689 | A Multi-center, Double-blind, Randomized Study, Comparing Clindamycin Phosphate… | Phase3 | BACTERIAL VAGINOSIS | Completed | 2014-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01939977 | Efficacy and Safety of Paricalcitol in the Reduction of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism Due to Renal Causes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02016482 | A Study to Evaluate the Safety and Efficacy of Adalimumab in Subjects With Chro… | Phase3 | Nail Psoriasis | Completed | 2014-01-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02023112 | Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT- 267 (ABT-45… | Phase3 | Hepatitis C Virus | Completed | 2014-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02028169 | To Observe the Impacts of Anti-Tumor Necrosis Factor (TNF) Effectiveness on Imp… | — | Psoriatic Arthritis | Completed | 2014-01-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02049476 | Study of the Effectiveness of Ozurdex for the Control of Uveitis | Phase4 | Uveitis, Intermediate | Completed | 2014-01-01 | 2018-06-30 | ClinicalTrials.gov |
| NCT02052362 | Bioavailability of ABT-450 and ABT-267 With Ritonavir | Phase1 | Absolute Bioavailability | Completed | 2014-01-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT02028169 | To Observe the Impacts of Anti-Tumor Necrosis Factor (TNF) Effectiveness on Imp… | — | Psoriatic Arthritis | Completed | 2014-01-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02023112 | Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT- 267 (ABT-45… | Phase3 | Hepatitis C Virus | Completed | 2014-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02052362 | Bioavailability of ABT-450 and ABT-267 With Ritonavir | Phase1 | Absolute Bioavailability | Completed | 2014-01-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT02049476 | Study of the Effectiveness of Ozurdex for the Control of Uveitis | Phase4 | Uveitis, Intermediate | Completed | 2014-01-01 | 2018-06-30 | ClinicalTrials.gov |
| NCT02036424 | Anti-Vascular Endothelial Growth Factor (Anti-VEGF) Alone Versus Ozurdex Given … | Phase4 | Diabetic Macular Edema | Completed | 2014-01-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01939977 | Efficacy and Safety of Paricalcitol in the Reduction of Secondary Hyperparathyr… | Phase4 | Secondary Hyperparathyroidism Due to Renal Causes | Completed | 2014-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02210689 | A Multi-center, Double-blind, Randomized Study, Comparing Clindamycin Phosphate… | Phase3 | BACTERIAL VAGINOSIS | Completed | 2014-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02210689 | A Multi-center, Double-blind, Randomized Study, Comparing Clindamycin Phosphate… | Phase3 | BACTERIAL VAGINOSIS | Completed | 2014-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02016482 | A Study to Evaluate the Safety and Efficacy of Adalimumab in Subjects With Chro… | Phase3 | Nail Psoriasis | Completed | 2014-01-01 | 2016-04-01 | ClinicalTrials.gov |
| NCT02023112 | Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT- 267 (ABT-45… | Phase3 | Hepatitis C Virus | Completed | 2014-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02029716 | RTA 408 Lotion in Healthy Volunteers | Phase1 | Healthy | Completed | 2013-12-31 | 2014-04-01 | ClinicalTrials.gov |
| NCT02029729 | RTA 408 in the Treatment of Advanced Solid Tumors (NSCLC & Melanoma) - DISCOVER | Phase1 | Metastatic or Incurable Non-small Cell Lung Cancer | Completed | 2013-12-31 | 2015-10-01 | ClinicalTrials.gov |
| NCT02029716 | RTA 408 Lotion in Healthy Volunteers | Phase1 | Healthy | Completed | 2013-12-31 | 2014-04-01 | ClinicalTrials.gov |
| NCT02029729 | RTA 408 in the Treatment of Advanced Solid Tumors (NSCLC & Melanoma) - DISCOVER | Phase1 | Metastatic or Incurable Non-small Cell Lung Cancer | Completed | 2013-12-31 | 2015-10-01 | ClinicalTrials.gov |
| NCT02029729 | RTA 408 in the Treatment of Advanced Solid Tumors (NSCLC & Melanoma) - DISCOVER | Phase1 | Metastatic or Incurable Non-small Cell Lung Cancer | Completed | 2013-12-31 | 2015-10-01 | ClinicalTrials.gov |
| NCT02029729 | RTA 408 in the Treatment of Advanced Solid Tumors (NSCLC & Melanoma) - DISCOVER | Phase1 | Metastatic or Incurable Non-small Cell Lung Cancer | Completed | 2013-12-31 | 2015-10-01 | ClinicalTrials.gov |
| NCT02029716 | RTA 408 Lotion in Healthy Volunteers | Phase1 | Healthy | Completed | 2013-12-31 | 2014-04-01 | ClinicalTrials.gov |
| NCT02029716 | RTA 408 Lotion in Healthy Volunteers | Phase1 | Healthy | Completed | 2013-12-31 | 2014-04-01 | ClinicalTrials.gov |
| NCT01969695 | An Extension Study of ABT-199 in Subjects With Advanced Non-Hodgkin's Lymphoma | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2013-12-20 | 2019-12-16 | ClinicalTrials.gov |
| NCT01969695 | An Extension Study of ABT-199 in Subjects With Advanced Non-Hodgkin's Lymphoma | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2013-12-20 | 2019-12-16 | ClinicalTrials.gov |
| NCT01969695 | An Extension Study of ABT-199 in Subjects With Advanced Non-Hodgkin's Lymphoma | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2013-12-20 | 2019-12-16 | ClinicalTrials.gov |
| NCT01969695 | An Extension Study of ABT-199 in Subjects With Advanced Non-Hodgkin's Lymphoma | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2013-12-20 | 2019-12-16 | ClinicalTrials.gov |
| NCT02033551 | A Study Evaluating Veliparib as a Single Agent or in Combination With Chemother… | Phase1 | Breast Cancer | Completed | 2013-12-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01969669 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-199 | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2013-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02056184 | Targeted Ultrasound in Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2013-12-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02015793 | Study to Evaluate the Pharmacokinetics, Safety and Efficacy of Two Treatment Mo… | Phase2 | Crohn's Disease | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02032407 | A Study of Dapsone Gel in Females With Skin of Color and Acne Vulgaris | Phase4 | Acne Vulgaris | Completed | 2013-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02016690 | Synagis® Liquid 50mg, 100mg for Intramuscular Injection Special Investigation i… | — | Respiratory Syncytial Virus Infection | Completed | 2013-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02023099 | Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT-267 (ABT-450… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02032407 | A Study of Dapsone Gel in Females With Skin of Color and Acne Vulgaris | Phase4 | Acne Vulgaris | Completed | 2013-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02033551 | A Study Evaluating Veliparib as a Single Agent or in Combination With Chemother… | Phase1 | Breast Cancer | Completed | 2013-12-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02056184 | Targeted Ultrasound in Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2013-12-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02015793 | Study to Evaluate the Pharmacokinetics, Safety and Efficacy of Two Treatment Mo… | Phase2 | Crohn's Disease | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02056184 | Targeted Ultrasound in Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2013-12-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT02056184 | Targeted Ultrasound in Rheumatoid Arthritis | Phase4 | Rheumatoid Arthritis | Completed | 2013-12-01 | 2019-07-01 | ClinicalTrials.gov |
| NCT01969669 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-199 | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2013-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02023099 | Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT-267 (ABT-450… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02016690 | Synagis® Liquid 50mg, 100mg for Intramuscular Injection Special Investigation i… | — | Respiratory Syncytial Virus Infection | Completed | 2013-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02015793 | Study to Evaluate the Pharmacokinetics, Safety and Efficacy of Two Treatment Mo… | Phase2 | Crohn's Disease | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01969669 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-199 | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2013-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02023099 | Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT-267 (ABT-450… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02016690 | Synagis® Liquid 50mg, 100mg for Intramuscular Injection Special Investigation i… | — | Respiratory Syncytial Virus Infection | Completed | 2013-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02033551 | A Study Evaluating Veliparib as a Single Agent or in Combination With Chemother… | Phase1 | Breast Cancer | Completed | 2013-12-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02015793 | Study to Evaluate the Pharmacokinetics, Safety and Efficacy of Two Treatment Mo… | Phase2 | Crohn's Disease | Completed | 2013-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02016690 | Synagis® Liquid 50mg, 100mg for Intramuscular Injection Special Investigation i… | — | Respiratory Syncytial Virus Infection | Completed | 2013-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT02032407 | A Study of Dapsone Gel in Females With Skin of Color and Acne Vulgaris | Phase4 | Acne Vulgaris | Completed | 2013-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02033551 | A Study Evaluating Veliparib as a Single Agent or in Combination With Chemother… | Phase1 | Breast Cancer | Completed | 2013-12-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT02032407 | A Study of Dapsone Gel in Females With Skin of Color and Acne Vulgaris | Phase4 | Acne Vulgaris | Completed | 2013-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01969669 | A Study to Assess the Effect of Ketoconazole on the Metabolism of ABT-199 | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2013-12-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02023099 | Study to Evaluate the Efficacy and Safety of ABT-450/Ritonavir/ABT-267 (ABT-450… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT02055820 | A Study Evaluating the Safety, Efficacy and Pharmacokinetics of Venetoclax Comb… | Phase1 | Lymphoma, Non-Hodgkin | Completed | 2013-11-17 | 2019-06-28 | ClinicalTrials.gov |
| NCT02055820 | A Study Evaluating the Safety, Efficacy and Pharmacokinetics of Venetoclax Comb… | Phase1 | Lymphoma, Non-Hodgkin | Completed | 2013-11-17 | 2019-06-28 | ClinicalTrials.gov |
| NCT02055820 | A Study Evaluating the Safety, Efficacy and Pharmacokinetics of Venetoclax Comb… | Phase1 | Lymphoma, Non-Hodgkin | Completed | 2013-11-17 | 2019-06-28 | ClinicalTrials.gov |
| NCT02055820 | A Study Evaluating the Safety, Efficacy and Pharmacokinetics of Venetoclax Comb… | Phase1 | Lymphoma, Non-Hodgkin | Completed | 2013-11-17 | 2019-06-28 | ClinicalTrials.gov |
| NCT01966003 | Efficacy and Safety Study of ABP 215 Compared With Bevacizumab in Patients With… | Phase3 | Non-small Cell Lung Cancer Metastatic | Completed | 2013-11-11 | 2015-07-23 | ClinicalTrials.gov |
| NCT01966003 | Efficacy and Safety Study of ABP 215 Compared With Bevacizumab in Patients With… | Phase3 | Non-small Cell Lung Cancer Metastatic | Completed | 2013-11-11 | 2015-07-23 | ClinicalTrials.gov |
| NCT01966003 | Efficacy and Safety Study of ABP 215 Compared With Bevacizumab in Patients With… | Phase3 | Non-small Cell Lung Cancer Metastatic | Completed | 2013-11-11 | 2015-07-23 | ClinicalTrials.gov |
| NCT01966003 | Efficacy and Safety Study of ABP 215 Compared With Bevacizumab in Patients With… | Phase3 | Non-small Cell Lung Cancer Metastatic | Completed | 2013-11-11 | 2015-07-23 | ClinicalTrials.gov |
| NCT01974323 | Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris | Phase3 | Acne Vulgaris | Completed | 2013-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01974141 | A Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris | Phase3 | Acne Vulgaris | Completed | 2013-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02052349 | Bioavailability of ABT-333 Within the Gastrointestinal Tract in Healthy Subjects | Phase1 | Relative Bioavailability | Completed | 2013-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02052349 | Bioavailability of ABT-333 Within the Gastrointestinal Tract in Healthy Subjects | Phase1 | Relative Bioavailability | Completed | 2013-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02009631 | A Study to Evaluate the Effects of Veliparib on Heart Rhythms in Patients With … | Phase1 | Breast Cancer | Completed | 2013-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01995071 | A Study to Evaluate the Safety and Antiviral Effect of Multiple Doses of ABT-49… | Phase2 | Chronic Hepatitis C | Completed | 2013-11-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01994837 | A Phase 2 Study of ABT-199 in Subjects With Acute Myelogenous Leukemia (AML) | Phase2 | Acute Myelogenous Leukemia | Completed | 2013-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01994837 | A Phase 2 Study of ABT-199 in Subjects With Acute Myelogenous Leukemia (AML) | Phase2 | Acute Myelogenous Leukemia | Completed | 2013-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01995071 | A Study to Evaluate the Safety and Antiviral Effect of Multiple Doses of ABT-49… | Phase2 | Chronic Hepatitis C | Completed | 2013-11-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02009631 | A Study to Evaluate the Effects of Veliparib on Heart Rhythms in Patients With … | Phase1 | Breast Cancer | Completed | 2013-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02052349 | Bioavailability of ABT-333 Within the Gastrointestinal Tract in Healthy Subjects | Phase1 | Relative Bioavailability | Completed | 2013-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01974323 | Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris | Phase3 | Acne Vulgaris | Completed | 2013-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01974141 | A Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris | Phase3 | Acne Vulgaris | Completed | 2013-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01974141 | A Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris | Phase3 | Acne Vulgaris | Completed | 2013-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01974323 | Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris | Phase3 | Acne Vulgaris | Completed | 2013-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT02052349 | Bioavailability of ABT-333 Within the Gastrointestinal Tract in Healthy Subjects | Phase1 | Relative Bioavailability | Completed | 2013-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT02009631 | A Study to Evaluate the Effects of Veliparib on Heart Rhythms in Patients With … | Phase1 | Breast Cancer | Completed | 2013-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01995071 | A Study to Evaluate the Safety and Antiviral Effect of Multiple Doses of ABT-49… | Phase2 | Chronic Hepatitis C | Completed | 2013-11-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01994837 | A Phase 2 Study of ABT-199 in Subjects With Acute Myelogenous Leukemia (AML) | Phase2 | Acute Myelogenous Leukemia | Completed | 2013-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01994837 | A Phase 2 Study of ABT-199 in Subjects With Acute Myelogenous Leukemia (AML) | Phase2 | Acute Myelogenous Leukemia | Completed | 2013-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01995071 | A Study to Evaluate the Safety and Antiviral Effect of Multiple Doses of ABT-49… | Phase2 | Chronic Hepatitis C | Completed | 2013-11-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02009631 | A Study to Evaluate the Effects of Veliparib on Heart Rhythms in Patients With … | Phase1 | Breast Cancer | Completed | 2013-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01974141 | A Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris | Phase3 | Acne Vulgaris | Completed | 2013-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01974323 | Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris | Phase3 | Acne Vulgaris | Completed | 2013-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01976663 | A Safety and Effectiveness Study of JUVÉDERM VOLIFT® XC Versus Control for Mode… | Na | Moderate to Severe Nasolabial Folds | Completed | 2013-10-29 | 2015-10-26 | ClinicalTrials.gov |
| NCT01976663 | A Safety and Effectiveness Study of JUVÉDERM VOLIFT® XC Versus Control for Mode… | Na | Moderate to Severe Nasolabial Folds | Completed | 2013-10-29 | 2015-10-26 | ClinicalTrials.gov |
| NCT01976663 | A Safety and Effectiveness Study of JUVÉDERM VOLIFT® XC Versus Control for Mode… | Na | Moderate to Severe Nasolabial Folds | Completed | 2013-10-29 | 2015-10-26 | ClinicalTrials.gov |
| NCT01976663 | A Safety and Effectiveness Study of JUVÉDERM VOLIFT® XC Versus Control for Mode… | Na | Moderate to Severe Nasolabial Folds | Completed | 2013-10-29 | 2015-10-26 | ClinicalTrials.gov |
| NCT01945489 | OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With… | Phase4 | Overactive Bladder | Completed | 2013-10-28 | 2017-01-05 | ClinicalTrials.gov |
| NCT01945489 | OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With… | Phase4 | Overactive Bladder | Completed | 2013-10-28 | 2017-01-05 | ClinicalTrials.gov |
| NCT01945489 | OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With… | Phase4 | Overactive Bladder | Completed | 2013-10-28 | 2017-01-05 | ClinicalTrials.gov |
| NCT01945489 | OnabotulinumtoxinA (BOTOX®) Treatment for Urinary Incontinence in Patients With… | Phase4 | Overactive Bladder | Completed | 2013-10-28 | 2017-01-05 | ClinicalTrials.gov |
| NCT01970397 | JUVEDERM® Ultra XC vs. Belotero Balance® for Perioral Lines | Na | Patients With Moderate to Severe Perioral Lines | Completed | 2013-10-21 | 2014-08-04 | ClinicalTrials.gov |
| NCT01970397 | JUVEDERM® Ultra XC vs. Belotero Balance® for Perioral Lines | Na | Patients With Moderate to Severe Perioral Lines | Completed | 2013-10-21 | 2014-08-04 | ClinicalTrials.gov |
| NCT01970397 | JUVEDERM® Ultra XC vs. Belotero Balance® for Perioral Lines | Na | Patients With Moderate to Severe Perioral Lines | Completed | 2013-10-21 | 2014-08-04 | ClinicalTrials.gov |
| NCT01970397 | JUVEDERM® Ultra XC vs. Belotero Balance® for Perioral Lines | Na | Patients With Moderate to Severe Perioral Lines | Completed | 2013-10-21 | 2014-08-04 | ClinicalTrials.gov |
| NCT01930786 | An Adult Spasticity Registry of OnabotulinumtoxinA Treatment | — | Muscle Spasticity | Completed | 2013-10-16 | 2017-10-09 | ClinicalTrials.gov |
| NCT01930786 | An Adult Spasticity Registry of OnabotulinumtoxinA Treatment | — | Muscle Spasticity | Completed | 2013-10-16 | 2017-10-09 | ClinicalTrials.gov |
| NCT01930786 | An Adult Spasticity Registry of OnabotulinumtoxinA Treatment | — | Muscle Spasticity | Completed | 2013-10-16 | 2017-10-09 | ClinicalTrials.gov |
| NCT01930786 | An Adult Spasticity Registry of OnabotulinumtoxinA Treatment | — | Muscle Spasticity | Completed | 2013-10-16 | 2017-10-09 | ClinicalTrials.gov |
| NCT02120898 | A Study to Evaluate the Safety and Efficacy Imiquimod Cream, 2.5% in Participan… | Phase3 | Actinic Keratosis | Completed | 2013-10-10 | 2014-04-30 | ClinicalTrials.gov |
| NCT02120898 | A Study to Evaluate the Safety and Efficacy Imiquimod Cream, 2.5% in Participan… | Phase3 | Actinic Keratosis | Completed | 2013-10-10 | 2014-04-30 | ClinicalTrials.gov |
| NCT02120898 | A Study to Evaluate the Safety and Efficacy Imiquimod Cream, 2.5% in Participan… | Phase3 | Actinic Keratosis | Completed | 2013-10-10 | 2014-04-30 | ClinicalTrials.gov |
| NCT02120898 | A Study to Evaluate the Safety and Efficacy Imiquimod Cream, 2.5% in Participan… | Phase3 | Actinic Keratosis | Completed | 2013-10-10 | 2014-04-30 | ClinicalTrials.gov |
| NCT01908478 | Veliparib in Combination With Gemcitabine and Intensity Modulated Radiation The… | Phase1 | Pancreatic Cancer | Completed | 2013-10-02 | 2020-07-06 | ClinicalTrials.gov |
| NCT01908478 | Veliparib in Combination With Gemcitabine and Intensity Modulated Radiation The… | Phase1 | Pancreatic Cancer | Completed | 2013-10-02 | 2020-07-06 | ClinicalTrials.gov |
| NCT01908478 | Veliparib in Combination With Gemcitabine and Intensity Modulated Radiation The… | Phase1 | Pancreatic Cancer | Completed | 2013-10-02 | 2020-07-06 | ClinicalTrials.gov |
| NCT01908478 | Veliparib in Combination With Gemcitabine and Intensity Modulated Radiation The… | Phase1 | Pancreatic Cancer | Completed | 2013-10-02 | 2020-07-06 | ClinicalTrials.gov |
| NCT01999192 | Study to Investigate the Safety and Efficacy of Tregalizumab in Subjects (MTX-I… | Phase2 | Rheumatoid Arthritis | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01674413 | Calprotectin-Directed Humira® Maintenance Therapy (CADHUM) | Phase3 | Crohn's Disease | Withdrawn | 2013-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01999192 | Study to Investigate the Safety and Efficacy of Tregalizumab in Subjects (MTX-I… | Phase2 | Rheumatoid Arthritis | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01674413 | Calprotectin-Directed Humira® Maintenance Therapy (CADHUM) | Phase3 | Crohn's Disease | Withdrawn | 2013-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02138461 | Tolerability of Bimatoprost 0.01% vs Latanoprost Eye Drops | — | Glaucoma | Completed | 2013-10-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01999192 | Study to Investigate the Safety and Efficacy of Tregalizumab in Subjects (MTX-I… | Phase2 | Rheumatoid Arthritis | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02138461 | Tolerability of Bimatoprost 0.01% vs Latanoprost Eye Drops | — | Glaucoma | Completed | 2013-10-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01960855 | A Study Investigating the Efficacy and Safety of ABT-494 Given With Methotrexat… | Phase2 | Rheumatoid Arthritis | Completed | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01960842 | A Study to Assess the Efficacy, Safety and Tolerability of ABT-SLV187 Monothera… | Phase3 | Advanced Parkinson's Disease | Completed | 2013-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01929746 | Daclizumab Japanese PK Study | Phase1 | Healthy | Completed | 2013-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01929746 | Daclizumab Japanese PK Study | Phase1 | Healthy | Completed | 2013-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02016612 | Seri Surgical Scaffold Support of the Lower Pole of the Breast | Na | Recurrent Ptosis of the Breast | Completed | 2013-10-01 | 2016-11-30 | ClinicalTrials.gov |
| NCT01960842 | A Study to Assess the Efficacy, Safety and Tolerability of ABT-SLV187 Monothera… | Phase3 | Advanced Parkinson's Disease | Completed | 2013-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01960855 | A Study Investigating the Efficacy and Safety of ABT-494 Given With Methotrexat… | Phase2 | Rheumatoid Arthritis | Completed | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01999192 | Study to Investigate the Safety and Efficacy of Tregalizumab in Subjects (MTX-I… | Phase2 | Rheumatoid Arthritis | Terminated | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01674413 | Calprotectin-Directed Humira® Maintenance Therapy (CADHUM) | Phase3 | Crohn's Disease | Withdrawn | 2013-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01929746 | Daclizumab Japanese PK Study | Phase1 | Healthy | Completed | 2013-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT02138461 | Tolerability of Bimatoprost 0.01% vs Latanoprost Eye Drops | — | Glaucoma | Completed | 2013-10-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01960855 | A Study Investigating the Efficacy and Safety of ABT-494 Given With Methotrexat… | Phase2 | Rheumatoid Arthritis | Completed | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT02138461 | Tolerability of Bimatoprost 0.01% vs Latanoprost Eye Drops | — | Glaucoma | Completed | 2013-10-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01960842 | A Study to Assess the Efficacy, Safety and Tolerability of ABT-SLV187 Monothera… | Phase3 | Advanced Parkinson's Disease | Completed | 2013-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02016612 | Seri Surgical Scaffold Support of the Lower Pole of the Breast | Na | Recurrent Ptosis of the Breast | Completed | 2013-10-01 | 2016-11-30 | ClinicalTrials.gov |
| NCT02016612 | Seri Surgical Scaffold Support of the Lower Pole of the Breast | Na | Recurrent Ptosis of the Breast | Completed | 2013-10-01 | 2016-11-30 | ClinicalTrials.gov |
| NCT01674413 | Calprotectin-Directed Humira® Maintenance Therapy (CADHUM) | Phase3 | Crohn's Disease | Withdrawn | 2013-10-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT02016612 | Seri Surgical Scaffold Support of the Lower Pole of the Breast | Na | Recurrent Ptosis of the Breast | Completed | 2013-10-01 | 2016-11-30 | ClinicalTrials.gov |
| NCT01929746 | Daclizumab Japanese PK Study | Phase1 | Healthy | Completed | 2013-10-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01960842 | A Study to Assess the Efficacy, Safety and Tolerability of ABT-SLV187 Monothera… | Phase3 | Advanced Parkinson's Disease | Completed | 2013-10-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01960855 | A Study Investigating the Efficacy and Safety of ABT-494 Given With Methotrexat… | Phase2 | Rheumatoid Arthritis | Completed | 2013-10-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01960881 | Evaluation of Diet and Exercise in Prostate Cancer Patients | — | Prostate Cancer | Completed | 2013-09-19 | 2021-08-10 | ClinicalTrials.gov |
| NCT01960881 | Evaluation of Diet and Exercise in Prostate Cancer Patients | — | Prostate Cancer | Completed | 2013-09-19 | 2021-08-10 | ClinicalTrials.gov |
| NCT01960881 | Evaluation of Diet and Exercise in Prostate Cancer Patients | — | Prostate Cancer | Completed | 2013-09-19 | 2021-08-10 | ClinicalTrials.gov |
| NCT01960881 | Evaluation of Diet and Exercise in Prostate Cancer Patients | — | Prostate Cancer | Completed | 2013-09-19 | 2021-08-10 | ClinicalTrials.gov |
| NCT01931670 | A Global Phase 3 Study to Evaluate the Safety and Efficacy of Elagolix in Subje… | Phase3 | Endometriosis | Completed | 2013-09-09 | 2016-12-19 | ClinicalTrials.gov |
| NCT01931670 | A Global Phase 3 Study to Evaluate the Safety and Efficacy of Elagolix in Subje… | Phase3 | Endometriosis | Completed | 2013-09-09 | 2016-12-19 | ClinicalTrials.gov |
| NCT01931670 | A Global Phase 3 Study to Evaluate the Safety and Efficacy of Elagolix in Subje… | Phase3 | Endometriosis | Completed | 2013-09-09 | 2016-12-19 | ClinicalTrials.gov |
| NCT01931670 | A Global Phase 3 Study to Evaluate the Safety and Efficacy of Elagolix in Subje… | Phase3 | Endometriosis | Completed | 2013-09-09 | 2016-12-19 | ClinicalTrials.gov |
| NCT01564732 | Multicenter Prospective Randomized Controlled Trial of Plicated Laparoscopic Ad… | Na | Morbid Obesity | Terminated | 2013-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01564732 | Multicenter Prospective Randomized Controlled Trial of Plicated Laparoscopic Ad… | Na | Morbid Obesity | Terminated | 2013-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01958827 | A Study of Adalimumab After Dose Escalation in Japanese Subjects With Crohn's D… | Phase3 | Crohn's Disease | Completed | 2013-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01969162 | Tear Collection in Adult Volunteers | — | Healthy Volunteers | Completed | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01958827 | A Study of Adalimumab After Dose Escalation in Japanese Subjects With Crohn's D… | Phase3 | Crohn's Disease | Completed | 2013-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01956032 | Duodopa Home Titration Using Telemedicine: Evaluation of Use of Resources | — | Parkinson's Disease | Completed | 2013-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01969162 | Tear Collection in Adult Volunteers | — | Healthy Volunteers | Completed | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01969162 | Tear Collection in Adult Volunteers | — | Healthy Volunteers | Completed | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01958827 | A Study of Adalimumab After Dose Escalation in Japanese Subjects With Crohn's D… | Phase3 | Crohn's Disease | Completed | 2013-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01956032 | Duodopa Home Titration Using Telemedicine: Evaluation of Use of Resources | — | Parkinson's Disease | Completed | 2013-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT03079375 | The Pharmacist Follows You and Your Medication From Hospital to Your Daily Life… | Na | Cross-Sectional Study | Completed | 2013-09-01 | 2015-10-24 | ClinicalTrials.gov |
| NCT01969162 | Tear Collection in Adult Volunteers | — | Healthy Volunteers | Completed | 2013-09-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT03079375 | The Pharmacist Follows You and Your Medication From Hospital to Your Daily Life… | Na | Cross-Sectional Study | Completed | 2013-09-01 | 2015-10-24 | ClinicalTrials.gov |
| NCT01564732 | Multicenter Prospective Randomized Controlled Trial of Plicated Laparoscopic Ad… | Na | Morbid Obesity | Terminated | 2013-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01956032 | Duodopa Home Titration Using Telemedicine: Evaluation of Use of Resources | — | Parkinson's Disease | Completed | 2013-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01956032 | Duodopa Home Titration Using Telemedicine: Evaluation of Use of Resources | — | Parkinson's Disease | Completed | 2013-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01564732 | Multicenter Prospective Randomized Controlled Trial of Plicated Laparoscopic Ad… | Na | Morbid Obesity | Terminated | 2013-09-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT03079375 | The Pharmacist Follows You and Your Medication From Hospital to Your Daily Life… | Na | Cross-Sectional Study | Completed | 2013-09-01 | 2015-10-24 | ClinicalTrials.gov |
| NCT03079375 | The Pharmacist Follows You and Your Medication From Hospital to Your Daily Life… | Na | Cross-Sectional Study | Completed | 2013-09-01 | 2015-10-24 | ClinicalTrials.gov |
| NCT01958827 | A Study of Adalimumab After Dose Escalation in Japanese Subjects With Crohn's D… | Phase3 | Crohn's Disease | Completed | 2013-09-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01939197 | A Multipart, Open-label Study to Evaluate the Safety and Efficacy of ABT-450/r/… | Phase2 | Hepatitis C Virus Infection | Completed | 2013-08-30 | 2016-10-25 | ClinicalTrials.gov |
| NCT01939197 | A Multipart, Open-label Study to Evaluate the Safety and Efficacy of ABT-450/r/… | Phase2 | Hepatitis C Virus Infection | Completed | 2013-08-30 | 2016-10-25 | ClinicalTrials.gov |
| NCT01939197 | A Multipart, Open-label Study to Evaluate the Safety and Efficacy of ABT-450/r/… | Phase2 | Hepatitis C Virus Infection | Completed | 2013-08-30 | 2016-10-25 | ClinicalTrials.gov |
| NCT01939197 | A Multipart, Open-label Study to Evaluate the Safety and Efficacy of ABT-450/r/… | Phase2 | Hepatitis C Virus Infection | Completed | 2013-08-30 | 2016-10-25 | ClinicalTrials.gov |
| NCT01886690 | A Study to Compare the Safety and Efficacy of a New Eye Drop Formulation With R… | Phase3 | Bilateral LASIK Surgery | Completed | 2013-08-20 | 2014-08-18 | ClinicalTrials.gov |
| NCT01886690 | A Study to Compare the Safety and Efficacy of a New Eye Drop Formulation With R… | Phase3 | Bilateral LASIK Surgery | Completed | 2013-08-20 | 2014-08-18 | ClinicalTrials.gov |
| NCT01886690 | A Study to Compare the Safety and Efficacy of a New Eye Drop Formulation With R… | Phase3 | Bilateral LASIK Surgery | Completed | 2013-08-20 | 2014-08-18 | ClinicalTrials.gov |
| NCT01886690 | A Study to Compare the Safety and Efficacy of a New Eye Drop Formulation With R… | Phase3 | Bilateral LASIK Surgery | Completed | 2013-08-20 | 2014-08-18 | ClinicalTrials.gov |
| NCT01933919 | A Phase 3 Study of Fluvoxamine (SME3110) in Pediatric/Adolescent Patients With … | Phase3 | Obsessive Compulsive Disorder | Completed | 2013-08-14 | 2016-07-01 | ClinicalTrials.gov |
| NCT01933919 | A Phase 3 Study of Fluvoxamine (SME3110) in Pediatric/Adolescent Patients With … | Phase3 | Obsessive Compulsive Disorder | Completed | 2013-08-14 | 2016-07-01 | ClinicalTrials.gov |
| NCT01933919 | A Phase 3 Study of Fluvoxamine (SME3110) in Pediatric/Adolescent Patients With … | Phase3 | Obsessive Compulsive Disorder | Completed | 2013-08-14 | 2016-07-01 | ClinicalTrials.gov |
| NCT01933919 | A Phase 3 Study of Fluvoxamine (SME3110) in Pediatric/Adolescent Patients With … | Phase3 | Obsessive Compulsive Disorder | Completed | 2013-08-14 | 2016-07-01 | ClinicalTrials.gov |
| NCT01947816 | Special Investigation in Patients With Ulcerative Colitis | — | Ulcerative Colitis | Completed | 2013-08-09 | 2018-02-15 | ClinicalTrials.gov |
| NCT01947816 | Special Investigation in Patients With Ulcerative Colitis | — | Ulcerative Colitis | Completed | 2013-08-09 | 2018-02-15 | ClinicalTrials.gov |
| NCT01947816 | Special Investigation in Patients With Ulcerative Colitis | — | Ulcerative Colitis | Completed | 2013-08-09 | 2018-02-15 | ClinicalTrials.gov |
| NCT01947816 | Special Investigation in Patients With Ulcerative Colitis | — | Ulcerative Colitis | Completed | 2013-08-09 | 2018-02-15 | ClinicalTrials.gov |
| NCT01946074 | A Study of ABT-165 in Subjects With Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2013-08-08 | 2022-09-28 | ClinicalTrials.gov |
| NCT01946074 | A Study of ABT-165 in Subjects With Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2013-08-08 | 2022-09-28 | ClinicalTrials.gov |
| NCT01946074 | A Study of ABT-165 in Subjects With Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2013-08-08 | 2022-09-28 | ClinicalTrials.gov |
| NCT01946074 | A Study of ABT-165 in Subjects With Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2013-08-08 | 2022-09-28 | ClinicalTrials.gov |
| NCT01917006 | A Safety and Efficacy Study of OnabotulinumtoxinA in Premature Ejaculation | Phase2 | Premature Ejaculation | Terminated | 2013-08-07 | 2017-08-15 | ClinicalTrials.gov |
| NCT01917006 | A Safety and Efficacy Study of OnabotulinumtoxinA in Premature Ejaculation | Phase2 | Premature Ejaculation | Terminated | 2013-08-07 | 2017-08-15 | ClinicalTrials.gov |
| NCT01917006 | A Safety and Efficacy Study of OnabotulinumtoxinA in Premature Ejaculation | Phase2 | Premature Ejaculation | Terminated | 2013-08-07 | 2017-08-15 | ClinicalTrials.gov |
| NCT01917006 | A Safety and Efficacy Study of OnabotulinumtoxinA in Premature Ejaculation | Phase2 | Premature Ejaculation | Terminated | 2013-08-07 | 2017-08-15 | ClinicalTrials.gov |
| NCT01918371 | A Retrospective Study of Anti-Vascular Endothelial Growth Factor (VEGF) Injecti… | — | Retinal Vein Occlusion | Completed | 2013-08-02 | 2014-09-04 | ClinicalTrials.gov |
| NCT01918371 | A Retrospective Study of Anti-Vascular Endothelial Growth Factor (VEGF) Injecti… | — | Retinal Vein Occlusion | Completed | 2013-08-02 | 2014-09-04 | ClinicalTrials.gov |
| NCT01918371 | A Retrospective Study of Anti-Vascular Endothelial Growth Factor (VEGF) Injecti… | — | Retinal Vein Occlusion | Completed | 2013-08-02 | 2014-09-04 | ClinicalTrials.gov |
| NCT01918371 | A Retrospective Study of Anti-Vascular Endothelial Growth Factor (VEGF) Injecti… | — | Retinal Vein Occlusion | Completed | 2013-08-02 | 2014-09-04 | ClinicalTrials.gov |
| NCT01930799 | Bladder Management in Patients With Multiple Sclerosis: Optimizing Practice Pat… | Phase4 | Multiple Sclerosis | Completed | 2013-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01904721 | A Safety and Efficacy Study of Bimatoprost in Men With Androgenic Alopecia (AGA) | Phase2 | Alopecia | Completed | 2013-08-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01930799 | Bladder Management in Patients With Multiple Sclerosis: Optimizing Practice Pat… | Phase4 | Multiple Sclerosis | Completed | 2013-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01942226 | Investigation on Medical Management of Dry Eye Patients | — | Dry Eye Syndrome | Completed | 2013-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01904721 | A Safety and Efficacy Study of Bimatoprost in Men With Androgenic Alopecia (AGA) | Phase2 | Alopecia | Completed | 2013-08-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01942226 | Investigation on Medical Management of Dry Eye Patients | — | Dry Eye Syndrome | Completed | 2013-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01930799 | Bladder Management in Patients With Multiple Sclerosis: Optimizing Practice Pat… | Phase4 | Multiple Sclerosis | Completed | 2013-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01942226 | Investigation on Medical Management of Dry Eye Patients | — | Dry Eye Syndrome | Completed | 2013-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01904721 | A Safety and Efficacy Study of Bimatoprost in Men With Androgenic Alopecia (AGA) | Phase2 | Alopecia | Completed | 2013-08-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01930799 | Bladder Management in Patients With Multiple Sclerosis: Optimizing Practice Pat… | Phase4 | Multiple Sclerosis | Completed | 2013-08-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01858519 | Prevalence of Antibodies to Selected Porcine Viruses in Patients With Cystic Fi… | — | Cystic Fibrosis | Completed | 2013-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01858519 | Prevalence of Antibodies to Selected Porcine Viruses in Patients With Cystic Fi… | — | Cystic Fibrosis | Completed | 2013-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01904721 | A Safety and Efficacy Study of Bimatoprost in Men With Androgenic Alopecia (AGA) | Phase2 | Alopecia | Completed | 2013-08-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01942226 | Investigation on Medical Management of Dry Eye Patients | — | Dry Eye Syndrome | Completed | 2013-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01858519 | Prevalence of Antibodies to Selected Porcine Viruses in Patients With Cystic Fi… | — | Cystic Fibrosis | Completed | 2013-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01858519 | Prevalence of Antibodies to Selected Porcine Viruses in Patients With Cystic Fi… | — | Cystic Fibrosis | Completed | 2013-08-01 | 2016-09-01 | ClinicalTrials.gov |
| NCT01903720 | A Safety and Efficacy Study of OZURDEX® in Macular Edema Associated With Branch… | Phase4 | Macular Edema | Completed | 2013-07-16 | 2015-03-30 | ClinicalTrials.gov |
| NCT01903720 | A Safety and Efficacy Study of OZURDEX® in Macular Edema Associated With Branch… | Phase4 | Macular Edema | Completed | 2013-07-16 | 2015-03-30 | ClinicalTrials.gov |
| NCT01903720 | A Safety and Efficacy Study of OZURDEX® in Macular Edema Associated With Branch… | Phase4 | Macular Edema | Completed | 2013-07-16 | 2015-03-30 | ClinicalTrials.gov |
| NCT01903720 | A Safety and Efficacy Study of OZURDEX® in Macular Edema Associated With Branch… | Phase4 | Macular Edema | Completed | 2013-07-16 | 2015-03-30 | ClinicalTrials.gov |
| NCT01852045 | Study of OnabotulinumtoxinA (BOTOX®) for Urinary Incontinence Due to Neurogenic… | Phase3 | Urinary Incontinence | Completed | 2013-07-02 | 2018-10-11 | ClinicalTrials.gov |
| NCT01852045 | Study of OnabotulinumtoxinA (BOTOX®) for Urinary Incontinence Due to Neurogenic… | Phase3 | Urinary Incontinence | Completed | 2013-07-02 | 2018-10-11 | ClinicalTrials.gov |
| NCT01852045 | Study of OnabotulinumtoxinA (BOTOX®) for Urinary Incontinence Due to Neurogenic… | Phase3 | Urinary Incontinence | Completed | 2013-07-02 | 2018-10-11 | ClinicalTrials.gov |
| NCT01852045 | Study of OnabotulinumtoxinA (BOTOX®) for Urinary Incontinence Due to Neurogenic… | Phase3 | Urinary Incontinence | Completed | 2013-07-02 | 2018-10-11 | ClinicalTrials.gov |
| NCT01879683 | A Safety, Tolerability and Preliminary Efficacy Study of LiRIS® 400 mg in Women… | Phase1 | Chronic Interstitial Cystitis | Completed | 2013-07-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01893996 | Study of Adalimumab to Lower Cardiovascular Risk in RA Patients With Well Contr… | Phase4 | Rheumatoid Arthritis | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01908010 | Safety, Tolerability, and Pharmacokinetics of ABT-354 in Subjects With Mild-to-… | Phase1 | Alzheimer's Disease | Completed | 2013-07-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02120924 | A Study to Evaluate the Safety and Clinical Study of Azelaic Acid Gel 15% in Pa… | Phase3 | Rosacea | Completed | 2013-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01284166 | Safety and Efficacy of Triple Combination Therapy With Dorzolamide Hydrochlorid… | Phase3 | Glaucoma | Withdrawn | 2013-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01821573 | Study of the Effect of Botulinum Toxin Injection in Rectus Femoris and Triceps … | Phase3 | COMPARISON BETWEEN GROUP TREATED WITH BOTULINUM TOXIN AND PLACEBO | Completed | 2013-07-01 | 2019-05-23 | ClinicalTrials.gov |
| NCT01821573 | Study of the Effect of Botulinum Toxin Injection in Rectus Femoris and Triceps … | Phase3 | COMPARISON BETWEEN GROUP TREATED WITH BOTULINUM TOXIN AND PLACEBO | Completed | 2013-07-01 | 2019-05-23 | ClinicalTrials.gov |
| NCT01879683 | A Safety, Tolerability and Preliminary Efficacy Study of LiRIS® 400 mg in Women… | Phase1 | Chronic Interstitial Cystitis | Completed | 2013-07-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01853033 | A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple S… | Phase1 | Rheumatoid Arthritis | Completed | 2013-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02120924 | A Study to Evaluate the Safety and Clinical Study of Azelaic Acid Gel 15% in Pa… | Phase3 | Rosacea | Completed | 2013-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01879683 | A Safety, Tolerability and Preliminary Efficacy Study of LiRIS® 400 mg in Women… | Phase1 | Chronic Interstitial Cystitis | Completed | 2013-07-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01853033 | A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple S… | Phase1 | Rheumatoid Arthritis | Completed | 2013-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01853033 | A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple S… | Phase1 | Rheumatoid Arthritis | Completed | 2013-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01284166 | Safety and Efficacy of Triple Combination Therapy With Dorzolamide Hydrochlorid… | Phase3 | Glaucoma | Withdrawn | 2013-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01853033 | A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple S… | Phase1 | Rheumatoid Arthritis | Completed | 2013-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01284166 | Safety and Efficacy of Triple Combination Therapy With Dorzolamide Hydrochlorid… | Phase3 | Glaucoma | Withdrawn | 2013-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01893996 | Study of Adalimumab to Lower Cardiovascular Risk in RA Patients With Well Contr… | Phase4 | Rheumatoid Arthritis | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01893996 | Study of Adalimumab to Lower Cardiovascular Risk in RA Patients With Well Contr… | Phase4 | Rheumatoid Arthritis | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01908010 | Safety, Tolerability, and Pharmacokinetics of ABT-354 in Subjects With Mild-to-… | Phase1 | Alzheimer's Disease | Completed | 2013-07-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01908010 | Safety, Tolerability, and Pharmacokinetics of ABT-354 in Subjects With Mild-to-… | Phase1 | Alzheimer's Disease | Completed | 2013-07-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01879683 | A Safety, Tolerability and Preliminary Efficacy Study of LiRIS® 400 mg in Women… | Phase1 | Chronic Interstitial Cystitis | Completed | 2013-07-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01893996 | Study of Adalimumab to Lower Cardiovascular Risk in RA Patients With Well Contr… | Phase4 | Rheumatoid Arthritis | Completed | 2013-07-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT01908010 | Safety, Tolerability, and Pharmacokinetics of ABT-354 in Subjects With Mild-to-… | Phase1 | Alzheimer's Disease | Completed | 2013-07-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02120924 | A Study to Evaluate the Safety and Clinical Study of Azelaic Acid Gel 15% in Pa… | Phase3 | Rosacea | Completed | 2013-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT02120924 | A Study to Evaluate the Safety and Clinical Study of Azelaic Acid Gel 15% in Pa… | Phase3 | Rosacea | Completed | 2013-07-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01284166 | Safety and Efficacy of Triple Combination Therapy With Dorzolamide Hydrochlorid… | Phase3 | Glaucoma | Withdrawn | 2013-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01821573 | Study of the Effect of Botulinum Toxin Injection in Rectus Femoris and Triceps … | Phase3 | COMPARISON BETWEEN GROUP TREATED WITH BOTULINUM TOXIN AND PLACEBO | Completed | 2013-07-01 | 2019-05-23 | ClinicalTrials.gov |
| NCT01821573 | Study of the Effect of Botulinum Toxin Injection in Rectus Femoris and Triceps … | Phase3 | COMPARISON BETWEEN GROUP TREATED WITH BOTULINUM TOXIN AND PLACEBO | Completed | 2013-07-01 | 2019-05-23 | ClinicalTrials.gov |
| NCT01889186 | A Study of the Efficacy of ABT-199 in Subjects With Relapsed/Refractory or Prev… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2013-06-27 | 2020-12-15 | ClinicalTrials.gov |
| NCT01889186 | A Study of the Efficacy of ABT-199 in Subjects With Relapsed/Refractory or Prev… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2013-06-27 | 2020-12-15 | ClinicalTrials.gov |
| NCT01889186 | A Study of the Efficacy of ABT-199 in Subjects With Relapsed/Refractory or Prev… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2013-06-27 | 2020-12-15 | ClinicalTrials.gov |
| NCT01889186 | A Study of the Efficacy of ABT-199 in Subjects With Relapsed/Refractory or Prev… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2013-06-27 | 2020-12-15 | ClinicalTrials.gov |
| NCT01845818 | Study in Ankylosing Spondylitis (AS) and Psoriatic Arthritis (PsA) Patients to … | — | Ankylosing Spondylitis | Completed | 2013-06-05 | 2017-06-23 | ClinicalTrials.gov |
| NCT01845818 | Study in Ankylosing Spondylitis (AS) and Psoriatic Arthritis (PsA) Patients to … | — | Ankylosing Spondylitis | Completed | 2013-06-05 | 2017-06-23 | ClinicalTrials.gov |
| NCT01845818 | Study in Ankylosing Spondylitis (AS) and Psoriatic Arthritis (PsA) Patients to … | — | Ankylosing Spondylitis | Completed | 2013-06-05 | 2017-06-23 | ClinicalTrials.gov |
| NCT01845818 | Study in Ankylosing Spondylitis (AS) and Psoriatic Arthritis (PsA) Patients to … | — | Ankylosing Spondylitis | Completed | 2013-06-05 | 2017-06-23 | ClinicalTrials.gov |
| NCT01881126 | An Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travopros… | Phase4 | Glaucoma | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01863953 | A Safety and Efficacy Study of Fixed-Combination Bimatoprost and Brimonidine in… | Phase2 | Glaucoma | Completed | 2013-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01787669 | Trial of Switching Between Intravitreal Bevacizumab (Avastin®)& Intravitreal De… | Phase2 | Diabetes | Completed | 2013-06-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01828476 | Navitoclax and Abiraterone Acetate With or Without Hydroxychloroquine in Treati… | Phase2 | Prostate Cancer | Terminated | 2013-06-01 | 2016-03-03 | ClinicalTrials.gov |
| NCT01854528 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compare… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-06-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01828476 | Navitoclax and Abiraterone Acetate With or Without Hydroxychloroquine in Treati… | Phase2 | Prostate Cancer | Terminated | 2013-06-01 | 2016-03-03 | ClinicalTrials.gov |
| NCT01854528 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compare… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-06-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01854528 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compare… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-06-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01828476 | Navitoclax and Abiraterone Acetate With or Without Hydroxychloroquine in Treati… | Phase2 | Prostate Cancer | Terminated | 2013-06-01 | 2016-03-03 | ClinicalTrials.gov |
| NCT01882413 | A Study to Determine the Prevalence of Inflammatory Dry Eye Disease in Patients… | — | Dry Eye Syndromes | Completed | 2013-06-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01881126 | An Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travopros… | Phase4 | Glaucoma | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01863953 | A Safety and Efficacy Study of Fixed-Combination Bimatoprost and Brimonidine in… | Phase2 | Glaucoma | Completed | 2013-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01787669 | Trial of Switching Between Intravitreal Bevacizumab (Avastin®)& Intravitreal De… | Phase2 | Diabetes | Completed | 2013-06-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01828476 | Navitoclax and Abiraterone Acetate With or Without Hydroxychloroquine in Treati… | Phase2 | Prostate Cancer | Terminated | 2013-06-01 | 2016-03-03 | ClinicalTrials.gov |
| NCT01854528 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compare… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-06-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01787669 | Trial of Switching Between Intravitreal Bevacizumab (Avastin®)& Intravitreal De… | Phase2 | Diabetes | Completed | 2013-06-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01863953 | A Safety and Efficacy Study of Fixed-Combination Bimatoprost and Brimonidine in… | Phase2 | Glaucoma | Completed | 2013-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01881126 | An Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travopros… | Phase4 | Glaucoma | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01882413 | A Study to Determine the Prevalence of Inflammatory Dry Eye Disease in Patients… | — | Dry Eye Syndromes | Completed | 2013-06-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01787669 | Trial of Switching Between Intravitreal Bevacizumab (Avastin®)& Intravitreal De… | Phase2 | Diabetes | Completed | 2013-06-01 | 2017-10-01 | ClinicalTrials.gov |
| NCT01863953 | A Safety and Efficacy Study of Fixed-Combination Bimatoprost and Brimonidine in… | Phase2 | Glaucoma | Completed | 2013-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01881126 | An Efficacy and Safety Study of Bimatoprost 0.01% Alone Compared With Travopros… | Phase4 | Glaucoma | Completed | 2013-06-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01882413 | A Study to Determine the Prevalence of Inflammatory Dry Eye Disease in Patients… | — | Dry Eye Syndromes | Completed | 2013-06-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01882413 | A Study to Determine the Prevalence of Inflammatory Dry Eye Disease in Patients… | — | Dry Eye Syndromes | Completed | 2013-06-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01844388 | A Study to Compare a New Eye Drop Formulation With Refresh Contacts® | Phase3 | Contact Lens Lubrication | Completed | 2013-05-29 | 2013-12-02 | ClinicalTrials.gov |
| NCT01844388 | A Study to Compare a New Eye Drop Formulation With Refresh Contacts® | Phase3 | Contact Lens Lubrication | Completed | 2013-05-29 | 2013-12-02 | ClinicalTrials.gov |
| NCT01844388 | A Study to Compare a New Eye Drop Formulation With Refresh Contacts® | Phase3 | Contact Lens Lubrication | Completed | 2013-05-29 | 2013-12-02 | ClinicalTrials.gov |
| NCT01844388 | A Study to Compare a New Eye Drop Formulation With Refresh Contacts® | Phase3 | Contact Lens Lubrication | Completed | 2013-05-29 | 2013-12-02 | ClinicalTrials.gov |
| NCT01960790 | Special Investigation in Patients With Intestinal Behcet's Disease (All Case In… | — | Behcet's Disease | Completed | 2013-05-25 | 2017-05-15 | ClinicalTrials.gov |
| NCT01960790 | Special Investigation in Patients With Intestinal Behcet's Disease (All Case In… | — | Behcet's Disease | Completed | 2013-05-25 | 2017-05-15 | ClinicalTrials.gov |
| NCT01960790 | Special Investigation in Patients With Intestinal Behcet's Disease (All Case In… | — | Behcet's Disease | Completed | 2013-05-25 | 2017-05-15 | ClinicalTrials.gov |
| NCT01960790 | Special Investigation in Patients With Intestinal Behcet's Disease (All Case In… | — | Behcet's Disease | Completed | 2013-05-25 | 2017-05-15 | ClinicalTrials.gov |
| NCT01858532 | Study Of Diabetic Nephropathy With Atrasentan | Phase3 | Diabetic Nephropathy | Terminated | 2013-05-17 | 2018-03-29 | ClinicalTrials.gov |
| NCT01858532 | Study Of Diabetic Nephropathy With Atrasentan | Phase3 | Diabetic Nephropathy | Terminated | 2013-05-17 | 2018-03-29 | ClinicalTrials.gov |
| NCT01858532 | Study Of Diabetic Nephropathy With Atrasentan | Phase3 | Diabetic Nephropathy | Terminated | 2013-05-17 | 2018-03-29 | ClinicalTrials.gov |
| NCT01858532 | Study Of Diabetic Nephropathy With Atrasentan | Phase3 | Diabetic Nephropathy | Terminated | 2013-05-17 | 2018-03-29 | ClinicalTrials.gov |
| NCT01870440 | TAHOE: Intravitreal Dexamethasone Implant (Ozurdex) for Uveitic Macular Edema | Phase4 | Macular Edema | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01891487 | Safety and Efficacy of Bimatoprost 0.03% Solution for the Treatment of Thinning… | Phase4 | Hypotrichosis | Completed | 2013-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02035800 | Bone Resorption, Osteoclastogenesis and Adalimumab | Phase4 | RheumatoId Arthritis | Unknown | 2013-05-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT01870440 | TAHOE: Intravitreal Dexamethasone Implant (Ozurdex) for Uveitic Macular Edema | Phase4 | Macular Edema | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01854905 | An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusi… | — | Dry Eye Syndromes | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01891487 | Safety and Efficacy of Bimatoprost 0.03% Solution for the Treatment of Thinning… | Phase4 | Hypotrichosis | Completed | 2013-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT02035800 | Bone Resorption, Osteoclastogenesis and Adalimumab | Phase4 | RheumatoId Arthritis | Unknown | 2013-05-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT01897519 | A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prev… | Phase2 | Cardiothoracic Surgery | Terminated | 2013-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01814761 | A Study of Bimatoprost 0.01% in the Clinical Setting | — | Glaucoma, Primary Open Angle | Completed | 2013-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01814761 | A Study of Bimatoprost 0.01% in the Clinical Setting | — | Glaucoma, Primary Open Angle | Completed | 2013-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01749410 | A Retrospective Study to Evaluate the Effectiveness and Benefit of onabotulinum… | — | Chronic Migraine, Headaches | Completed | 2013-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01897519 | A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prev… | Phase2 | Cardiothoracic Surgery | Terminated | 2013-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01856556 | Safety and Pharmacokinetics of NRX-1074 in Normal Volunteers | Phase1 | Healthy | Completed | 2013-05-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01814761 | A Study of Bimatoprost 0.01% in the Clinical Setting | — | Glaucoma, Primary Open Angle | Completed | 2013-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01749410 | A Retrospective Study to Evaluate the Effectiveness and Benefit of onabotulinum… | — | Chronic Migraine, Headaches | Completed | 2013-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01897519 | A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prev… | Phase2 | Cardiothoracic Surgery | Terminated | 2013-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01749410 | A Retrospective Study to Evaluate the Effectiveness and Benefit of onabotulinum… | — | Chronic Migraine, Headaches | Completed | 2013-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01860846 | Anti-Tumor Necrosis Factor (TNF) Treatments, Work Productivity and Quality of L… | — | Crohn's Disease | Completed | 2013-05-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01854905 | An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusi… | — | Dry Eye Syndromes | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01897519 | A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prev… | Phase2 | Cardiothoracic Surgery | Terminated | 2013-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01854905 | An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusi… | — | Dry Eye Syndromes | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01856556 | Safety and Pharmacokinetics of NRX-1074 in Normal Volunteers | Phase1 | Healthy | Completed | 2013-05-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01749410 | A Retrospective Study to Evaluate the Effectiveness and Benefit of onabotulinum… | — | Chronic Migraine, Headaches | Completed | 2013-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01856556 | Safety and Pharmacokinetics of NRX-1074 in Normal Volunteers | Phase1 | Healthy | Completed | 2013-05-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01860846 | Anti-Tumor Necrosis Factor (TNF) Treatments, Work Productivity and Quality of L… | — | Crohn's Disease | Completed | 2013-05-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT02035800 | Bone Resorption, Osteoclastogenesis and Adalimumab | Phase4 | RheumatoId Arthritis | Unknown | 2013-05-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT02035800 | Bone Resorption, Osteoclastogenesis and Adalimumab | Phase4 | RheumatoId Arthritis | Unknown | 2013-05-01 | 2019-12-01 | ClinicalTrials.gov |
| NCT01854905 | An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusi… | — | Dry Eye Syndromes | Completed | 2013-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01891487 | Safety and Efficacy of Bimatoprost 0.03% Solution for the Treatment of Thinning… | Phase4 | Hypotrichosis | Completed | 2013-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01870440 | TAHOE: Intravitreal Dexamethasone Implant (Ozurdex) for Uveitic Macular Edema | Phase4 | Macular Edema | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01814761 | A Study of Bimatoprost 0.01% in the Clinical Setting | — | Glaucoma, Primary Open Angle | Completed | 2013-05-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01856556 | Safety and Pharmacokinetics of NRX-1074 in Normal Volunteers | Phase1 | Healthy | Completed | 2013-05-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01860846 | Anti-Tumor Necrosis Factor (TNF) Treatments, Work Productivity and Quality of L… | — | Crohn's Disease | Completed | 2013-05-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01860846 | Anti-Tumor Necrosis Factor (TNF) Treatments, Work Productivity and Quality of L… | — | Crohn's Disease | Completed | 2013-05-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01870440 | TAHOE: Intravitreal Dexamethasone Implant (Ozurdex) for Uveitic Macular Edema | Phase4 | Macular Edema | Completed | 2013-05-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01891487 | Safety and Efficacy of Bimatoprost 0.03% Solution for the Treatment of Thinning… | Phase4 | Hypotrichosis | Completed | 2013-05-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01901146 | Efficacy and Safety Study of ABP 980 Compared With Trastuzumab in Women With HE… | Phase3 | Breast Cancer | Completed | 2013-04-29 | 2017-01-27 | ClinicalTrials.gov |
| NCT01848561 | A Long-Term Registry of Humira® (Adalimumab) in Patients With Moderately to Sev… | — | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2013-04-29 | 2028-06-01 | ClinicalTrials.gov |
| NCT01901146 | Efficacy and Safety Study of ABP 980 Compared With Trastuzumab in Women With HE… | Phase3 | Breast Cancer | Completed | 2013-04-29 | 2017-01-27 | ClinicalTrials.gov |
| NCT01901146 | Efficacy and Safety Study of ABP 980 Compared With Trastuzumab in Women With HE… | Phase3 | Breast Cancer | Completed | 2013-04-29 | 2017-01-27 | ClinicalTrials.gov |
| NCT01901146 | Efficacy and Safety Study of ABP 980 Compared With Trastuzumab in Women With HE… | Phase3 | Breast Cancer | Completed | 2013-04-29 | 2017-01-27 | ClinicalTrials.gov |
| NCT01848561 | A Long-Term Registry of Humira® (Adalimumab) in Patients With Moderately to Sev… | — | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2013-04-29 | 2028-06-01 | ClinicalTrials.gov |
| NCT01848561 | A Long-Term Registry of Humira® (Adalimumab) in Patients With Moderately to Sev… | — | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2013-04-29 | 2028-06-01 | ClinicalTrials.gov |
| NCT01848561 | A Long-Term Registry of Humira® (Adalimumab) in Patients With Moderately to Sev… | — | Ulcerative Colitis (UC) | Active_Not_Recruiting | 2013-04-29 | 2028-06-01 | ClinicalTrials.gov |
| NCT01808118 | Continuing Versus Withdrawing Adalimumab in Maintaining Remission in Non-Radiog… | Phase3 | Axial Spondyloarthritis | Completed | 2013-04-16 | 2017-04-14 | ClinicalTrials.gov |
| NCT01808118 | Continuing Versus Withdrawing Adalimumab in Maintaining Remission in Non-Radiog… | Phase3 | Axial Spondyloarthritis | Completed | 2013-04-16 | 2017-04-14 | ClinicalTrials.gov |
| NCT01808118 | Continuing Versus Withdrawing Adalimumab in Maintaining Remission in Non-Radiog… | Phase3 | Axial Spondyloarthritis | Completed | 2013-04-16 | 2017-04-14 | ClinicalTrials.gov |
| NCT01808118 | Continuing Versus Withdrawing Adalimumab in Maintaining Remission in Non-Radiog… | Phase3 | Axial Spondyloarthritis | Completed | 2013-04-16 | 2017-04-14 | ClinicalTrials.gov |
| NCT01817530 | Safety and Efficacy in Premenopausal Women With Heavy Menstrual Bleeding (HMB) … | Phase2 | Heavy Uterine Bleeding | Completed | 2013-04-08 | 2015-12-01 | ClinicalTrials.gov |
| NCT01817530 | Safety and Efficacy in Premenopausal Women With Heavy Menstrual Bleeding (HMB) … | Phase2 | Heavy Uterine Bleeding | Completed | 2013-04-08 | 2015-12-01 | ClinicalTrials.gov |
| NCT01817530 | Safety and Efficacy in Premenopausal Women With Heavy Menstrual Bleeding (HMB) … | Phase2 | Heavy Uterine Bleeding | Completed | 2013-04-08 | 2015-12-01 | ClinicalTrials.gov |
| NCT01817530 | Safety and Efficacy in Premenopausal Women With Heavy Menstrual Bleeding (HMB) … | Phase2 | Heavy Uterine Bleeding | Completed | 2013-04-08 | 2015-12-01 | ClinicalTrials.gov |
| NCT01800695 | Evaluating the Safety and Pharmacokinetics of ABT-414 for Subjects With Gliobla… | Phase1 | Glioblastoma Multiforme | Completed | 2013-04-02 | 2017-06-19 | ClinicalTrials.gov |
| NCT01800695 | Evaluating the Safety and Pharmacokinetics of ABT-414 for Subjects With Gliobla… | Phase1 | Glioblastoma Multiforme | Completed | 2013-04-02 | 2017-06-19 | ClinicalTrials.gov |
| NCT01800695 | Evaluating the Safety and Pharmacokinetics of ABT-414 for Subjects With Gliobla… | Phase1 | Glioblastoma Multiforme | Completed | 2013-04-02 | 2017-06-19 | ClinicalTrials.gov |
| NCT01800695 | Evaluating the Safety and Pharmacokinetics of ABT-414 for Subjects With Gliobla… | Phase1 | Glioblastoma Multiforme | Completed | 2013-04-02 | 2017-06-19 | ClinicalTrials.gov |
| NCT01853085 | A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Swi… | — | Glaucoma, Primary Open Angle | Completed | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01853085 | A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Swi… | — | Glaucoma, Primary Open Angle | Completed | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01911845 | An Open-label, Single Arm, Phase 2 Study to Evaluate ABT-450/r/ABT-267 and ABT-… | Phase2 | Chronic Hepatitis C Infection | Completed | 2013-04-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01911845 | An Open-label, Single Arm, Phase 2 Study to Evaluate ABT-450/r/ABT-267 and ABT-… | Phase2 | Chronic Hepatitis C Infection | Completed | 2013-04-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01911845 | An Open-label, Single Arm, Phase 2 Study to Evaluate ABT-450/r/ABT-267 and ABT-… | Phase2 | Chronic Hepatitis C Infection | Completed | 2013-04-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01853085 | A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Swi… | — | Glaucoma, Primary Open Angle | Completed | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01866592 | Vascular Inflammation in Psoriasis - Extension Study | Phase4 | Psoriasis | Completed | 2013-04-01 | 2016-10-27 | ClinicalTrials.gov |
| NCT01826812 | Impairment of Reading Ability in Dry Eye Patients | — | Dry Eye Syndromes | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01833130 | Use of a Treatment Benefit Questionnaire in Patients With Chronic Migraine Trea… | Phase4 | Chronic Migraine | Completed | 2013-04-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01826812 | Impairment of Reading Ability in Dry Eye Patients | — | Dry Eye Syndromes | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01853085 | A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Swi… | — | Glaucoma, Primary Open Angle | Completed | 2013-04-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01833130 | Use of a Treatment Benefit Questionnaire in Patients With Chronic Migraine Trea… | Phase4 | Chronic Migraine | Completed | 2013-04-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01833130 | Use of a Treatment Benefit Questionnaire in Patients With Chronic Migraine Trea… | Phase4 | Chronic Migraine | Completed | 2013-04-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01866592 | Vascular Inflammation in Psoriasis - Extension Study | Phase4 | Psoriasis | Completed | 2013-04-01 | 2016-10-27 | ClinicalTrials.gov |
| NCT01833130 | Use of a Treatment Benefit Questionnaire in Patients With Chronic Migraine Trea… | Phase4 | Chronic Migraine | Completed | 2013-04-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01826812 | Impairment of Reading Ability in Dry Eye Patients | — | Dry Eye Syndromes | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01911845 | An Open-label, Single Arm, Phase 2 Study to Evaluate ABT-450/r/ABT-267 and ABT-… | Phase2 | Chronic Hepatitis C Infection | Completed | 2013-04-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01866592 | Vascular Inflammation in Psoriasis - Extension Study | Phase4 | Psoriasis | Completed | 2013-04-01 | 2016-10-27 | ClinicalTrials.gov |
| NCT01866592 | Vascular Inflammation in Psoriasis - Extension Study | Phase4 | Psoriasis | Completed | 2013-04-01 | 2016-10-27 | ClinicalTrials.gov |
| NCT01826812 | Impairment of Reading Ability in Dry Eye Patients | — | Dry Eye Syndromes | Completed | 2013-04-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01853306 | A Study to Evaluate the Safety, Pharmacokinetics and Oral Bio Availability of V… | Phase1 | Oncology | Completed | 2013-03-18 | 2017-06-29 | ClinicalTrials.gov |
| NCT01853306 | A Study to Evaluate the Safety, Pharmacokinetics and Oral Bio Availability of V… | Phase1 | Oncology | Completed | 2013-03-18 | 2017-06-29 | ClinicalTrials.gov |
| NCT01853306 | A Study to Evaluate the Safety, Pharmacokinetics and Oral Bio Availability of V… | Phase1 | Oncology | Completed | 2013-03-18 | 2017-06-29 | ClinicalTrials.gov |
| NCT01853306 | A Study to Evaluate the Safety, Pharmacokinetics and Oral Bio Availability of V… | Phase1 | Oncology | Completed | 2013-03-18 | 2017-06-29 | ClinicalTrials.gov |
| NCT01735214 | An Observational Study of Patients With Primary Open Angle Glaucoma (POAG) or O… | — | Glaucoma, Open-Angle | Completed | 2013-03-07 | 2014-04-10 | ClinicalTrials.gov |
| NCT01735214 | An Observational Study of Patients With Primary Open Angle Glaucoma (POAG) or O… | — | Glaucoma, Open-Angle | Completed | 2013-03-07 | 2014-04-10 | ClinicalTrials.gov |
| NCT01735214 | An Observational Study of Patients With Primary Open Angle Glaucoma (POAG) or O… | — | Glaucoma, Open-Angle | Completed | 2013-03-07 | 2014-04-10 | ClinicalTrials.gov |
| NCT01735214 | An Observational Study of Patients With Primary Open Angle Glaucoma (POAG) or O… | — | Glaucoma, Open-Angle | Completed | 2013-03-07 | 2014-04-10 | ClinicalTrials.gov |
| NCT01814670 | Treatment With Botulinum Toxin Type A (BOTOX®) in Chinese Patients With Moderat… | Phase4 | Glabellar Rhytides | Completed | 2013-03-06 | 2014-10-29 | ClinicalTrials.gov |
| NCT01814670 | Treatment With Botulinum Toxin Type A (BOTOX®) in Chinese Patients With Moderat… | Phase4 | Glabellar Rhytides | Completed | 2013-03-06 | 2014-10-29 | ClinicalTrials.gov |
| NCT01814670 | Treatment With Botulinum Toxin Type A (BOTOX®) in Chinese Patients With Moderat… | Phase4 | Glabellar Rhytides | Completed | 2013-03-06 | 2014-10-29 | ClinicalTrials.gov |
| NCT01814670 | Treatment With Botulinum Toxin Type A (BOTOX®) in Chinese Patients With Moderat… | Phase4 | Glabellar Rhytides | Completed | 2013-03-06 | 2014-10-29 | ClinicalTrials.gov |
| NCT01824303 | Safety, Tolerability and Efficacy Study of LiRIS® 400 mg in Women With Intersti… | Phase2 | Interstitial Cystitis | Terminated | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01834638 | Long-term Safety and Efficacy of ABT-126 in Subjects With Schizophrenia: An Ext… | Phase2 | Schizophrenia | Terminated | 2013-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01833533 | A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1a In… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-03-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01854697 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compare… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01736176 | A Study to Assess the Safety and Efficacy of Levodopa-carbidopa Intestinal Gel … | Phase3 | Advanced Parkinson's Disease | Completed | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01736176 | A Study to Assess the Safety and Efficacy of Levodopa-carbidopa Intestinal Gel … | Phase3 | Advanced Parkinson's Disease | Completed | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01824303 | Safety, Tolerability and Efficacy Study of LiRIS® 400 mg in Women With Intersti… | Phase2 | Interstitial Cystitis | Terminated | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT03088449 | Personalising Anti-TNF Therapy in Crohns Disease (PANTS) | — | Crohn Disease | Unknown | 2013-03-01 | 2019-07-30 | ClinicalTrials.gov |
| NCT01834638 | Long-term Safety and Efficacy of ABT-126 in Subjects With Schizophrenia: An Ext… | Phase2 | Schizophrenia | Terminated | 2013-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01821534 | Reliability of a Masseter Muscle Prominence Scale and Lower Facial Shape Classi… | — | Healthy Volunteers | Completed | 2013-03-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01833533 | A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1a In… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-03-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01736176 | A Study to Assess the Safety and Efficacy of Levodopa-carbidopa Intestinal Gel … | Phase3 | Advanced Parkinson's Disease | Completed | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01854697 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compare… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01785836 | An Extension Study to Assess the Safety, Tolerability, Efficacy, and Treatment … | Phase1 | Acne Vulgaris | Withdrawn | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01833533 | A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1a In… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-03-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01834638 | Long-term Safety and Efficacy of ABT-126 in Subjects With Schizophrenia: An Ext… | Phase2 | Schizophrenia | Terminated | 2013-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01834638 | Long-term Safety and Efficacy of ABT-126 in Subjects With Schizophrenia: An Ext… | Phase2 | Schizophrenia | Terminated | 2013-03-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01854697 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compare… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01833533 | A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1a In… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-03-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01767519 | A Study Evaluating the Efficacy and Safety of BOTOX® or Solifenacin in Patients… | Phase3 | Overactive Bladder | Completed | 2013-03-01 | 2015-03-18 | ClinicalTrials.gov |
| NCT03088449 | Personalising Anti-TNF Therapy in Crohns Disease (PANTS) | — | Crohn Disease | Unknown | 2013-03-01 | 2019-07-30 | ClinicalTrials.gov |
| NCT01767519 | A Study Evaluating the Efficacy and Safety of BOTOX® or Solifenacin in Patients… | Phase3 | Overactive Bladder | Completed | 2013-03-01 | 2015-03-18 | ClinicalTrials.gov |
| NCT03088449 | Personalising Anti-TNF Therapy in Crohns Disease (PANTS) | — | Crohn Disease | Unknown | 2013-03-01 | 2019-07-30 | ClinicalTrials.gov |
| NCT01767519 | A Study Evaluating the Efficacy and Safety of BOTOX® or Solifenacin in Patients… | Phase3 | Overactive Bladder | Completed | 2013-03-01 | 2015-03-18 | ClinicalTrials.gov |
| NCT01785836 | An Extension Study to Assess the Safety, Tolerability, Efficacy, and Treatment … | Phase1 | Acne Vulgaris | Withdrawn | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01821534 | Reliability of a Masseter Muscle Prominence Scale and Lower Facial Shape Classi… | — | Healthy Volunteers | Completed | 2013-03-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT03088449 | Personalising Anti-TNF Therapy in Crohns Disease (PANTS) | — | Crohn Disease | Unknown | 2013-03-01 | 2019-07-30 | ClinicalTrials.gov |
| NCT01785836 | An Extension Study to Assess the Safety, Tolerability, Efficacy, and Treatment … | Phase1 | Acne Vulgaris | Withdrawn | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01736176 | A Study to Assess the Safety and Efficacy of Levodopa-carbidopa Intestinal Gel … | Phase3 | Advanced Parkinson's Disease | Completed | 2013-03-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01767519 | A Study Evaluating the Efficacy and Safety of BOTOX® or Solifenacin in Patients… | Phase3 | Overactive Bladder | Completed | 2013-03-01 | 2015-03-18 | ClinicalTrials.gov |
| NCT01821534 | Reliability of a Masseter Muscle Prominence Scale and Lower Facial Shape Classi… | — | Healthy Volunteers | Completed | 2013-03-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01785836 | An Extension Study to Assess the Safety, Tolerability, Efficacy, and Treatment … | Phase1 | Acne Vulgaris | Withdrawn | 2013-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01821534 | Reliability of a Masseter Muscle Prominence Scale and Lower Facial Shape Classi… | — | Healthy Volunteers | Completed | 2013-03-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01824303 | Safety, Tolerability and Efficacy Study of LiRIS® 400 mg in Women With Intersti… | Phase2 | Interstitial Cystitis | Terminated | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01824303 | Safety, Tolerability and Efficacy Study of LiRIS® 400 mg in Women With Intersti… | Phase2 | Interstitial Cystitis | Terminated | 2013-03-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01854697 | A Study to Evaluate the Efficacy and Safety of Three Experimental Drugs Compare… | Phase3 | Chronic Hepatitis C Infection | Completed | 2013-03-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01782495 | A Study to Evaluate Chronic Hepatitis C Infection in Adult Transplant Recipients | Phase2 | Chronic Hepatitis C Infection | Completed | 2013-02-25 | 2017-07-13 | ClinicalTrials.gov |
| NCT01782495 | A Study to Evaluate Chronic Hepatitis C Infection in Adult Transplant Recipients | Phase2 | Chronic Hepatitis C Infection | Completed | 2013-02-25 | 2017-07-13 | ClinicalTrials.gov |
| NCT01782495 | A Study to Evaluate Chronic Hepatitis C Infection in Adult Transplant Recipients | Phase2 | Chronic Hepatitis C Infection | Completed | 2013-02-25 | 2017-07-13 | ClinicalTrials.gov |
| NCT01782495 | A Study to Evaluate Chronic Hepatitis C Infection in Adult Transplant Recipients | Phase2 | Chronic Hepatitis C Infection | Completed | 2013-02-25 | 2017-07-13 | ClinicalTrials.gov |
| NCT01641367 | A5288/MULTI-OCTAVE: Management Using Latest Technologies to Optimize Combinatio… | Phase4 | HIV-1 Infection | Completed | 2013-02-22 | 2018-12-31 | ClinicalTrials.gov |
| NCT01641367 | A5288/MULTI-OCTAVE: Management Using Latest Technologies to Optimize Combinatio… | Phase4 | HIV-1 Infection | Completed | 2013-02-22 | 2018-12-31 | ClinicalTrials.gov |
| NCT01641367 | A5288/MULTI-OCTAVE: Management Using Latest Technologies to Optimize Combinatio… | Phase4 | HIV-1 Infection | Completed | 2013-02-22 | 2018-12-31 | ClinicalTrials.gov |
| NCT01641367 | A5288/MULTI-OCTAVE: Management Using Latest Technologies to Optimize Combinatio… | Phase4 | HIV-1 Infection | Completed | 2013-02-22 | 2018-12-31 | ClinicalTrials.gov |
| NCT01797965 | Long-Term Extension Study in Participants With Multiple Sclerosis Who Have Comp… | Phase3 | Relapsing-Remitting Multiple Sclerosis | Terminated | 2013-02-15 | 2018-09-24 | ClinicalTrials.gov |
| NCT01797965 | Long-Term Extension Study in Participants With Multiple Sclerosis Who Have Comp… | Phase3 | Relapsing-Remitting Multiple Sclerosis | Terminated | 2013-02-15 | 2018-09-24 | ClinicalTrials.gov |
| NCT01797965 | Long-Term Extension Study in Participants With Multiple Sclerosis Who Have Comp… | Phase3 | Relapsing-Remitting Multiple Sclerosis | Terminated | 2013-02-15 | 2018-09-24 | ClinicalTrials.gov |
| NCT01797965 | Long-Term Extension Study in Participants With Multiple Sclerosis Who Have Comp… | Phase3 | Relapsing-Remitting Multiple Sclerosis | Terminated | 2013-02-15 | 2018-09-24 | ClinicalTrials.gov |
| NCT01768858 | Assessment of Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosing Spondylitis… | — | Rheumatoid Arthritis | Completed | 2013-02-05 | 2017-08-13 | ClinicalTrials.gov |
| NCT01768858 | Assessment of Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosing Spondylitis… | — | Rheumatoid Arthritis | Completed | 2013-02-05 | 2017-08-13 | ClinicalTrials.gov |
| NCT01768858 | Assessment of Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosing Spondylitis… | — | Rheumatoid Arthritis | Completed | 2013-02-05 | 2017-08-13 | ClinicalTrials.gov |
| NCT01768858 | Assessment of Rheumatoid Arthritis, Psoriatic Arthritis, Ankylosing Spondylitis… | — | Rheumatoid Arthritis | Completed | 2013-02-05 | 2017-08-13 | ClinicalTrials.gov |
| NCT01613014 | ABT-436 for Alcohol Dependence | Phase2 | Alcohol Dependence | Completed | 2013-02-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01850823 | Clinical Equivalence Study of Mometasone Nasal Spray | Phase3 | Seasonal Allergic Rhinitis | Completed | 2013-02-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01797094 | BOTOX® in the Treatment of Upper Facial Lines in Japan | Phase3 | Upper Facial Rhytides | Completed | 2013-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01804517 | Impact of a Nurse for Migraine Management: the IMPACT Project | — | Migraine Without Aura | Completed | 2013-02-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01613014 | ABT-436 for Alcohol Dependence | Phase2 | Alcohol Dependence | Completed | 2013-02-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01879449 | Prevalence of Spasticity in Veterans Living in a Long-term Care Facility | — | Spasticity | Completed | 2013-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01613014 | ABT-436 for Alcohol Dependence | Phase2 | Alcohol Dependence | Completed | 2013-02-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01797094 | BOTOX® in the Treatment of Upper Facial Lines in Japan | Phase3 | Upper Facial Rhytides | Completed | 2013-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01804517 | Impact of a Nurse for Migraine Management: the IMPACT Project | — | Migraine Without Aura | Completed | 2013-02-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01613014 | ABT-436 for Alcohol Dependence | Phase2 | Alcohol Dependence | Completed | 2013-02-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01747655 | A Post Marketing Observational Study of Activities of Daily Living in Advanced … | — | Parkinson's Disease | Completed | 2013-02-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01747655 | A Post Marketing Observational Study of Activities of Daily Living in Advanced … | — | Parkinson's Disease | Completed | 2013-02-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01747655 | A Post Marketing Observational Study of Activities of Daily Living in Advanced … | — | Parkinson's Disease | Completed | 2013-02-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01879449 | Prevalence of Spasticity in Veterans Living in a Long-term Care Facility | — | Spasticity | Completed | 2013-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01850823 | Clinical Equivalence Study of Mometasone Nasal Spray | Phase3 | Seasonal Allergic Rhinitis | Completed | 2013-02-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01879449 | Prevalence of Spasticity in Veterans Living in a Long-term Care Facility | — | Spasticity | Completed | 2013-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01850823 | Clinical Equivalence Study of Mometasone Nasal Spray | Phase3 | Seasonal Allergic Rhinitis | Completed | 2013-02-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01783730 | Assessment of the Safety of Adalimumab in Rheumatoid Arthritis Patients Showing… | — | Rheumatoid Arthritis | Completed | 2013-02-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01804517 | Impact of a Nurse for Migraine Management: the IMPACT Project | — | Migraine Without Aura | Completed | 2013-02-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01783730 | Assessment of the Safety of Adalimumab in Rheumatoid Arthritis Patients Showing… | — | Rheumatoid Arthritis | Completed | 2013-02-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01797094 | BOTOX® in the Treatment of Upper Facial Lines in Japan | Phase3 | Upper Facial Rhytides | Completed | 2013-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01747655 | A Post Marketing Observational Study of Activities of Daily Living in Advanced … | — | Parkinson's Disease | Completed | 2013-02-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01777165 | A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prev… | Phase2 | Acute Kidney Injury | Completed | 2013-02-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01804517 | Impact of a Nurse for Migraine Management: the IMPACT Project | — | Migraine Without Aura | Completed | 2013-02-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01850823 | Clinical Equivalence Study of Mometasone Nasal Spray | Phase3 | Seasonal Allergic Rhinitis | Completed | 2013-02-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01797094 | BOTOX® in the Treatment of Upper Facial Lines in Japan | Phase3 | Upper Facial Rhytides | Completed | 2013-02-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01783730 | Assessment of the Safety of Adalimumab in Rheumatoid Arthritis Patients Showing… | — | Rheumatoid Arthritis | Completed | 2013-02-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01777165 | A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prev… | Phase2 | Acute Kidney Injury | Completed | 2013-02-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01879449 | Prevalence of Spasticity in Veterans Living in a Long-term Care Facility | — | Spasticity | Completed | 2013-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01783730 | Assessment of the Safety of Adalimumab in Rheumatoid Arthritis Patients Showing… | — | Rheumatoid Arthritis | Completed | 2013-02-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01777165 | A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prev… | Phase2 | Acute Kidney Injury | Completed | 2013-02-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01777165 | A Safety and Efficacy Trial of Multiple Dosing Regimens of ABT-719 for the Prev… | Phase2 | Acute Kidney Injury | Completed | 2013-02-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01777620 | A Study of Subject Satisfaction With BOTOX® Cosmetic Treatment in Facial Rhytid… | Phase4 | Facial Rhytides | Completed | 2013-01-31 | 2013-07-31 | ClinicalTrials.gov |
| NCT01777620 | A Study of Subject Satisfaction With BOTOX® Cosmetic Treatment in Facial Rhytid… | Phase4 | Facial Rhytides | Completed | 2013-01-31 | 2013-07-31 | ClinicalTrials.gov |
| NCT01777620 | A Study of Subject Satisfaction With BOTOX® Cosmetic Treatment in Facial Rhytid… | Phase4 | Facial Rhytides | Completed | 2013-01-31 | 2013-07-31 | ClinicalTrials.gov |
| NCT01777620 | A Study of Subject Satisfaction With BOTOX® Cosmetic Treatment in Facial Rhytid… | Phase4 | Facial Rhytides | Completed | 2013-01-31 | 2013-07-31 | ClinicalTrials.gov |
| NCT01797081 | BOTOX® in the Treatment of Crow's Feet Lines in Japan | Phase3 | Lateral Canthus Rhytides | Completed | 2013-01-31 | 2014-07-07 | ClinicalTrials.gov |
| NCT01797081 | BOTOX® in the Treatment of Crow's Feet Lines in Japan | Phase3 | Lateral Canthus Rhytides | Completed | 2013-01-31 | 2014-07-07 | ClinicalTrials.gov |
| NCT01797081 | BOTOX® in the Treatment of Crow's Feet Lines in Japan | Phase3 | Lateral Canthus Rhytides | Completed | 2013-01-31 | 2014-07-07 | ClinicalTrials.gov |
| NCT01797081 | BOTOX® in the Treatment of Crow's Feet Lines in Japan | Phase3 | Lateral Canthus Rhytides | Completed | 2013-01-31 | 2014-07-07 | ClinicalTrials.gov |
| NCT01773122 | Safety, Tolerability, and Pharmacokinetics of Dapsone in Acne Vulgaris | Phase1 | Acne Vulgaris | Completed | 2013-01-21 | 2013-05-05 | ClinicalTrials.gov |
| NCT01773122 | Safety, Tolerability, and Pharmacokinetics of Dapsone in Acne Vulgaris | Phase1 | Acne Vulgaris | Completed | 2013-01-21 | 2013-05-05 | ClinicalTrials.gov |
| NCT01773122 | Safety, Tolerability, and Pharmacokinetics of Dapsone in Acne Vulgaris | Phase1 | Acne Vulgaris | Completed | 2013-01-21 | 2013-05-05 | ClinicalTrials.gov |
| NCT01773122 | Safety, Tolerability, and Pharmacokinetics of Dapsone in Acne Vulgaris | Phase1 | Acne Vulgaris | Completed | 2013-01-21 | 2013-05-05 | ClinicalTrials.gov |
| NCT01814774 | A Retrospective Chart Review of BOTOX® and Xeomin® for the Treatment of Cervica… | — | Cervical Dystonia | Completed | 2013-01-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01780636 | Ultrasound and EMG Guided Botox Injection for the Treatment of Non-Relaxing Pub… | Phase2 | Non-relaxing Puborectalis Syndrome | Terminated | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01678924 | A Safety and Efficacy Study of AGN-214868 in Patients With Postherpetic Neuralg… | Phase2 | Neuralgia, Postherpetic | Terminated | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01425320 | Pharmacokinetics Study of Dapsone-Adapalene Fixed Combination Gel in Acne | Phase1 | Acne Vulgaris | Withdrawn | 2013-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01781962 | A Study of Quantitative Assessments of Angle Width in Chinese Patients With Ope… | — | Open-angle Glaucoma | Terminated | 2013-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01425320 | Pharmacokinetics Study of Dapsone-Adapalene Fixed Combination Gel in Acne | Phase1 | Acne Vulgaris | Withdrawn | 2013-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01780636 | Ultrasound and EMG Guided Botox Injection for the Treatment of Non-Relaxing Pub… | Phase2 | Non-relaxing Puborectalis Syndrome | Terminated | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01781962 | A Study of Quantitative Assessments of Angle Width in Chinese Patients With Ope… | — | Open-angle Glaucoma | Terminated | 2013-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT02036541 | AqueSys XEN 45 Glaucoma Implant in Refractory Glaucoma | Na | Glaucoma | Completed | 2013-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01780636 | Ultrasound and EMG Guided Botox Injection for the Treatment of Non-Relaxing Pub… | Phase2 | Non-relaxing Puborectalis Syndrome | Terminated | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01781962 | A Study of Quantitative Assessments of Angle Width in Chinese Patients With Ope… | — | Open-angle Glaucoma | Terminated | 2013-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT02004067 | Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Dis… | Phase4 | Primary Sjogren Syndrome | Completed | 2013-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT02004067 | Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Dis… | Phase4 | Primary Sjogren Syndrome | Completed | 2013-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01759264 | An Observational Study of Fecal Calprotectin as Clinical Tool in Monitoring Mod… | — | Crohn's Disease | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT02004067 | Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Dis… | Phase4 | Primary Sjogren Syndrome | Completed | 2013-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01758289 | Post Marketing Observational Study on Paricalcitol IV Administered to Venezuela… | — | Chronic Kidney Disease Stage V | Terminated | 2013-01-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT02036541 | AqueSys XEN 45 Glaucoma Implant in Refractory Glaucoma | Na | Glaucoma | Completed | 2013-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01425320 | Pharmacokinetics Study of Dapsone-Adapalene Fixed Combination Gel in Acne | Phase1 | Acne Vulgaris | Withdrawn | 2013-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT02036541 | AqueSys XEN 45 Glaucoma Implant in Refractory Glaucoma | Na | Glaucoma | Completed | 2013-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01759264 | An Observational Study of Fecal Calprotectin as Clinical Tool in Monitoring Mod… | — | Crohn's Disease | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01814774 | A Retrospective Chart Review of BOTOX® and Xeomin® for the Treatment of Cervica… | — | Cervical Dystonia | Completed | 2013-01-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01678924 | A Safety and Efficacy Study of AGN-214868 in Patients With Postherpetic Neuralg… | Phase2 | Neuralgia, Postherpetic | Terminated | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01678924 | A Safety and Efficacy Study of AGN-214868 in Patients With Postherpetic Neuralg… | Phase2 | Neuralgia, Postherpetic | Terminated | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01780636 | Ultrasound and EMG Guided Botox Injection for the Treatment of Non-Relaxing Pub… | Phase2 | Non-relaxing Puborectalis Syndrome | Terminated | 2013-01-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01425320 | Pharmacokinetics Study of Dapsone-Adapalene Fixed Combination Gel in Acne | Phase1 | Acne Vulgaris | Withdrawn | 2013-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01781962 | A Study of Quantitative Assessments of Angle Width in Chinese Patients With Ope… | — | Open-angle Glaucoma | Terminated | 2013-01-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT02004067 | Safety Study of the Use of Topical Cyclosporine in the Treatment of Dry Eye Dis… | Phase4 | Primary Sjogren Syndrome | Completed | 2013-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01758289 | Post Marketing Observational Study on Paricalcitol IV Administered to Venezuela… | — | Chronic Kidney Disease Stage V | Terminated | 2013-01-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01814774 | A Retrospective Chart Review of BOTOX® and Xeomin® for the Treatment of Cervica… | — | Cervical Dystonia | Completed | 2013-01-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01814774 | A Retrospective Chart Review of BOTOX® and Xeomin® for the Treatment of Cervica… | — | Cervical Dystonia | Completed | 2013-01-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT02036541 | AqueSys XEN 45 Glaucoma Implant in Refractory Glaucoma | Na | Glaucoma | Completed | 2013-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01758289 | Post Marketing Observational Study on Paricalcitol IV Administered to Venezuela… | — | Chronic Kidney Disease Stage V | Terminated | 2013-01-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01759264 | An Observational Study of Fecal Calprotectin as Clinical Tool in Monitoring Mod… | — | Crohn's Disease | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01758289 | Post Marketing Observational Study on Paricalcitol IV Administered to Venezuela… | — | Chronic Kidney Disease Stage V | Terminated | 2013-01-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01759264 | An Observational Study of Fecal Calprotectin as Clinical Tool in Monitoring Mod… | — | Crohn's Disease | Completed | 2013-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01678924 | A Safety and Efficacy Study of AGN-214868 in Patients With Postherpetic Neuralg… | Phase2 | Neuralgia, Postherpetic | Terminated | 2013-01-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01760954 | Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Adults With … | Phase3 | Endometriosis | Completed | 2012-12-28 | 2016-04-15 | ClinicalTrials.gov |
| NCT01760954 | Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Adults With … | Phase3 | Endometriosis | Completed | 2012-12-28 | 2016-04-15 | ClinicalTrials.gov |
| NCT01760954 | Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Adults With … | Phase3 | Endometriosis | Completed | 2012-12-28 | 2016-04-15 | ClinicalTrials.gov |
| NCT01760954 | Study to Evaluate the Long-Term Safety and Efficacy of Elagolix in Adults With … | Phase3 | Endometriosis | Completed | 2012-12-28 | 2016-04-15 | ClinicalTrials.gov |
| NCT01609933 | A Study to Evaluate the Safety and Effect of Treatment With Experimental Antivi… | Phase2 | Chronic Hepatitis C | Completed | 2012-12-18 | 2017-05-03 | ClinicalTrials.gov |
| NCT01609933 | A Study to Evaluate the Safety and Effect of Treatment With Experimental Antivi… | Phase2 | Chronic Hepatitis C | Completed | 2012-12-18 | 2017-05-03 | ClinicalTrials.gov |
| NCT01609933 | A Study to Evaluate the Safety and Effect of Treatment With Experimental Antivi… | Phase2 | Chronic Hepatitis C | Completed | 2012-12-18 | 2017-05-03 | ClinicalTrials.gov |
| NCT01609933 | A Study to Evaluate the Safety and Effect of Treatment With Experimental Antivi… | Phase2 | Chronic Hepatitis C | Completed | 2012-12-18 | 2017-05-03 | ClinicalTrials.gov |
| NCT01785069 | Safety and Effectiveness of NATRELLE® 410 Highly Cohesive, Anatomically Shaped,… | Na | Breast Augmentation | Terminated | 2012-12-10 | 2015-11-30 | ClinicalTrials.gov |
| NCT01785069 | Safety and Effectiveness of NATRELLE® 410 Highly Cohesive, Anatomically Shaped,… | Na | Breast Augmentation | Terminated | 2012-12-10 | 2015-11-30 | ClinicalTrials.gov |
| NCT01785069 | Safety and Effectiveness of NATRELLE® 410 Highly Cohesive, Anatomically Shaped,… | Na | Breast Augmentation | Terminated | 2012-12-10 | 2015-11-30 | ClinicalTrials.gov |
| NCT01785069 | Safety and Effectiveness of NATRELLE® 410 Highly Cohesive, Anatomically Shaped,… | Na | Breast Augmentation | Terminated | 2012-12-10 | 2015-11-30 | ClinicalTrials.gov |
| NCT01744327 | TL1A Expression in Psoriatic Skin | — | Psoriasis | Unknown | 2012-12-01 | — | ClinicalTrials.gov |
| NCT01767116 | A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1b In… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01767116 | A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1b In… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01749631 | Investigation of the Effectiveness of Sevoflurane Anaesthesia in Difficult to I… | — | Intubation; Difficult | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01756235 | Physical Activity in Patients With Rheumatoid Arthritis Treated With Adalimumab… | — | Rheumatoid Arthritis | Completed | 2012-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01752855 | Study in Rheumatoid Arthritis for Subjects Who Completed Preceding Study M13-39… | Phase2 | Rheumatoid Arthritis | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01735201 | AGN-199201 for the Treatment of Erythema With Rosacea | Phase2 | Rosacea | Completed | 2012-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01749631 | Investigation of the Effectiveness of Sevoflurane Anaesthesia in Difficult to I… | — | Intubation; Difficult | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01754727 | Impact of Adalimumab (Humira®) Therapy on Selected Health Care Resource Utiliza… | — | Ankylosing Spondylitis | Completed | 2012-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01744327 | TL1A Expression in Psoriatic Skin | — | Psoriasis | Unknown | 2012-12-01 | — | ClinicalTrials.gov |
| NCT01767116 | A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1b In… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01735201 | AGN-199201 for the Treatment of Erythema With Rosacea | Phase2 | Rosacea | Completed | 2012-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01756235 | Physical Activity in Patients With Rheumatoid Arthritis Treated With Adalimumab… | — | Rheumatoid Arthritis | Completed | 2012-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01756235 | Physical Activity in Patients With Rheumatoid Arthritis Treated With Adalimumab… | — | Rheumatoid Arthritis | Completed | 2012-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01752855 | Study in Rheumatoid Arthritis for Subjects Who Completed Preceding Study M13-39… | Phase2 | Rheumatoid Arthritis | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01754727 | Impact of Adalimumab (Humira®) Therapy on Selected Health Care Resource Utiliza… | — | Ankylosing Spondylitis | Completed | 2012-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01749631 | Investigation of the Effectiveness of Sevoflurane Anaesthesia in Difficult to I… | — | Intubation; Difficult | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01735201 | AGN-199201 for the Treatment of Erythema With Rosacea | Phase2 | Rosacea | Completed | 2012-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01754727 | Impact of Adalimumab (Humira®) Therapy on Selected Health Care Resource Utiliza… | — | Ankylosing Spondylitis | Completed | 2012-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01735201 | AGN-199201 for the Treatment of Erythema With Rosacea | Phase2 | Rosacea | Completed | 2012-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01767116 | A Study to Evaluate Chronic Hepatitis C Infection in Adults With Genotype 1b In… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-12-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01756235 | Physical Activity in Patients With Rheumatoid Arthritis Treated With Adalimumab… | — | Rheumatoid Arthritis | Completed | 2012-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01754727 | Impact of Adalimumab (Humira®) Therapy on Selected Health Care Resource Utiliza… | — | Ankylosing Spondylitis | Completed | 2012-12-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01744327 | TL1A Expression in Psoriatic Skin | — | Psoriasis | Unknown | 2012-12-01 | — | ClinicalTrials.gov |
| NCT01749631 | Investigation of the Effectiveness of Sevoflurane Anaesthesia in Difficult to I… | — | Intubation; Difficult | Completed | 2012-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01752855 | Study in Rheumatoid Arthritis for Subjects Who Completed Preceding Study M13-39… | Phase2 | Rheumatoid Arthritis | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01752855 | Study in Rheumatoid Arthritis for Subjects Who Completed Preceding Study M13-39… | Phase2 | Rheumatoid Arthritis | Completed | 2012-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01744327 | TL1A Expression in Psoriatic Skin | — | Psoriasis | Unknown | 2012-12-01 | — | ClinicalTrials.gov |
| NCT01685892 | A Study of Venetoclax in Combination With Obinutuzumab in Participants With Chr… | Phase1 | Lymphocytic Leukemia, Chronic | Completed | 2012-11-29 | 2019-08-23 | ClinicalTrials.gov |
| NCT01685892 | A Study of Venetoclax in Combination With Obinutuzumab in Participants With Chr… | Phase1 | Lymphocytic Leukemia, Chronic | Completed | 2012-11-29 | 2019-08-23 | ClinicalTrials.gov |
| NCT01685892 | A Study of Venetoclax in Combination With Obinutuzumab in Participants With Chr… | Phase1 | Lymphocytic Leukemia, Chronic | Completed | 2012-11-29 | 2019-08-23 | ClinicalTrials.gov |
| NCT01685892 | A Study of Venetoclax in Combination With Obinutuzumab in Participants With Chr… | Phase1 | Lymphocytic Leukemia, Chronic | Completed | 2012-11-29 | 2019-08-23 | ClinicalTrials.gov |
| NCT01794507 | A Study Evaluating ABT-199 in Multiple Myeloma Subjects Who Are Receiving Borte… | Phase1 | Relapsed/Refractory Multiple Myeloma | Completed | 2012-11-19 | 2019-07-16 | ClinicalTrials.gov |
| NCT01794507 | A Study Evaluating ABT-199 in Multiple Myeloma Subjects Who Are Receiving Borte… | Phase1 | Relapsed/Refractory Multiple Myeloma | Completed | 2012-11-19 | 2019-07-16 | ClinicalTrials.gov |
| NCT01794507 | A Study Evaluating ABT-199 in Multiple Myeloma Subjects Who Are Receiving Borte… | Phase1 | Relapsed/Refractory Multiple Myeloma | Completed | 2012-11-19 | 2019-07-16 | ClinicalTrials.gov |
| NCT01794507 | A Study Evaluating ABT-199 in Multiple Myeloma Subjects Who Are Receiving Borte… | Phase1 | Relapsed/Refractory Multiple Myeloma | Completed | 2012-11-19 | 2019-07-16 | ClinicalTrials.gov |
| NCT01603641 | BOTOX® Open-Label Treatment in Pediatric Lower Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-11-05 | 2018-08-25 | ClinicalTrials.gov |
| NCT01603641 | BOTOX® Open-Label Treatment in Pediatric Lower Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-11-05 | 2018-08-25 | ClinicalTrials.gov |
| NCT01603641 | BOTOX® Open-Label Treatment in Pediatric Lower Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-11-05 | 2018-08-25 | ClinicalTrials.gov |
| NCT01603641 | BOTOX® Open-Label Treatment in Pediatric Lower Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-11-05 | 2018-08-25 | ClinicalTrials.gov |
| NCT02252744 | Prevalence of Dry Eye Disease in Patients Diagnosed With Rheumatoid Arthritis | — | Dry Eye Syndromes | Completed | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01716585 | A Study to Evaluate Chronic Hepatitis C Infection | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01684163 | Efficacy and Safety of GLYX-13 in Subjects With Inadequate/Partial Response to … | Phase2 | Major Depressive Disorder | Completed | 2012-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01732757 | A Study to Evaluate the Efficacy of Lastacaft® Compared to Pataday™ and Placebo… | Phase4 | Conjunctivitis, Allergic | Completed | 2012-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01716585 | A Study to Evaluate Chronic Hepatitis C Infection | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01684163 | Efficacy and Safety of GLYX-13 in Subjects With Inadequate/Partial Response to … | Phase2 | Major Depressive Disorder | Completed | 2012-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01716585 | A Study to Evaluate Chronic Hepatitis C Infection | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01741493 | A Study in Healthy Adults and Adult Subjects With Rheumatoid Arthritis to Evalu… | Phase1 | Rheumatoid Arthritis | Completed | 2012-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01749423 | A Retrospective Study to Evaluate the Effectiveness of onabotulinumtoxinA in Pr… | — | Chronic Migraine, Headache | Withdrawn | 2012-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01741493 | A Study in Healthy Adults and Adult Subjects With Rheumatoid Arthritis to Evalu… | Phase1 | Rheumatoid Arthritis | Completed | 2012-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01749423 | A Retrospective Study to Evaluate the Effectiveness of onabotulinumtoxinA in Pr… | — | Chronic Migraine, Headache | Withdrawn | 2012-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01698554 | Bimatoprost in the Treatment of Eyelash Hypotrichosis | Phase3 | Idiopathic Eyelash Hypotrichosis | Completed | 2012-11-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01715415 | A Study to Evaluate Chronic Hepatitis C Infection in Treatment Experienced Adul… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01673191 | A 3-Month Clinical Trial to Assess the Safety and Efficacy of the OZURDEX® Intr… | Phase2 | Macular Edema | Completed | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01760980 | Pivotal Bioequivalence Study of Exemestane 25 mg Tablets Under Fasting Conditio… | Phase1 | Healthy | Withdrawn | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01673191 | A 3-Month Clinical Trial to Assess the Safety and Efficacy of the OZURDEX® Intr… | Phase2 | Macular Edema | Completed | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01732757 | A Study to Evaluate the Efficacy of Lastacaft® Compared to Pataday™ and Placebo… | Phase4 | Conjunctivitis, Allergic | Completed | 2012-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01698554 | Bimatoprost in the Treatment of Eyelash Hypotrichosis | Phase3 | Idiopathic Eyelash Hypotrichosis | Completed | 2012-11-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01673191 | A 3-Month Clinical Trial to Assess the Safety and Efficacy of the OZURDEX® Intr… | Phase2 | Macular Edema | Completed | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01760980 | Pivotal Bioequivalence Study of Exemestane 25 mg Tablets Under Fasting Conditio… | Phase1 | Healthy | Withdrawn | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01698554 | Bimatoprost in the Treatment of Eyelash Hypotrichosis | Phase3 | Idiopathic Eyelash Hypotrichosis | Completed | 2012-11-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01673191 | A 3-Month Clinical Trial to Assess the Safety and Efficacy of the OZURDEX® Intr… | Phase2 | Macular Edema | Completed | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01684163 | Efficacy and Safety of GLYX-13 in Subjects With Inadequate/Partial Response to … | Phase2 | Major Depressive Disorder | Completed | 2012-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01964105 | 3D Breast Imaging for Cosmetic and Reconstructive Breast Surgery | Na | Hypomastia | Completed | 2012-11-01 | 2017-05-16 | ClinicalTrials.gov |
| NCT02252744 | Prevalence of Dry Eye Disease in Patients Diagnosed With Rheumatoid Arthritis | — | Dry Eye Syndromes | Completed | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT02252744 | Prevalence of Dry Eye Disease in Patients Diagnosed With Rheumatoid Arthritis | — | Dry Eye Syndromes | Completed | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01964105 | 3D Breast Imaging for Cosmetic and Reconstructive Breast Surgery | Na | Hypomastia | Completed | 2012-11-01 | 2017-05-16 | ClinicalTrials.gov |
| NCT01741493 | A Study in Healthy Adults and Adult Subjects With Rheumatoid Arthritis to Evalu… | Phase1 | Rheumatoid Arthritis | Completed | 2012-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01749423 | A Retrospective Study to Evaluate the Effectiveness of onabotulinumtoxinA in Pr… | — | Chronic Migraine, Headache | Withdrawn | 2012-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01732757 | A Study to Evaluate the Efficacy of Lastacaft® Compared to Pataday™ and Placebo… | Phase4 | Conjunctivitis, Allergic | Completed | 2012-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT02252744 | Prevalence of Dry Eye Disease in Patients Diagnosed With Rheumatoid Arthritis | — | Dry Eye Syndromes | Completed | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01760980 | Pivotal Bioequivalence Study of Exemestane 25 mg Tablets Under Fasting Conditio… | Phase1 | Healthy | Withdrawn | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01684163 | Efficacy and Safety of GLYX-13 in Subjects With Inadequate/Partial Response to … | Phase2 | Major Depressive Disorder | Completed | 2012-11-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01715415 | A Study to Evaluate Chronic Hepatitis C Infection in Treatment Experienced Adul… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01715415 | A Study to Evaluate Chronic Hepatitis C Infection in Treatment Experienced Adul… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01964105 | 3D Breast Imaging for Cosmetic and Reconstructive Breast Surgery | Na | Hypomastia | Completed | 2012-11-01 | 2017-05-16 | ClinicalTrials.gov |
| NCT01741493 | A Study in Healthy Adults and Adult Subjects With Rheumatoid Arthritis to Evalu… | Phase1 | Rheumatoid Arthritis | Completed | 2012-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01698554 | Bimatoprost in the Treatment of Eyelash Hypotrichosis | Phase3 | Idiopathic Eyelash Hypotrichosis | Completed | 2012-11-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01732757 | A Study to Evaluate the Efficacy of Lastacaft® Compared to Pataday™ and Placebo… | Phase4 | Conjunctivitis, Allergic | Completed | 2012-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01716585 | A Study to Evaluate Chronic Hepatitis C Infection | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01749423 | A Retrospective Study to Evaluate the Effectiveness of onabotulinumtoxinA in Pr… | — | Chronic Migraine, Headache | Withdrawn | 2012-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01760980 | Pivotal Bioequivalence Study of Exemestane 25 mg Tablets Under Fasting Conditio… | Phase1 | Healthy | Withdrawn | 2012-11-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01964105 | 3D Breast Imaging for Cosmetic and Reconstructive Breast Surgery | Na | Hypomastia | Completed | 2012-11-01 | 2017-05-16 | ClinicalTrials.gov |
| NCT01715415 | A Study to Evaluate Chronic Hepatitis C Infection in Treatment Experienced Adul… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01603615 | BOTOX® Open-Label Treatment in Pediatric Upper Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-10-30 | 2018-09-03 | ClinicalTrials.gov |
| NCT01603615 | BOTOX® Open-Label Treatment in Pediatric Upper Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-10-30 | 2018-09-03 | ClinicalTrials.gov |
| NCT01603615 | BOTOX® Open-Label Treatment in Pediatric Upper Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-10-30 | 2018-09-03 | ClinicalTrials.gov |
| NCT01603615 | BOTOX® Open-Label Treatment in Pediatric Upper Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-10-30 | 2018-09-03 | ClinicalTrials.gov |
| NCT01736189 | Assessment of Clinical Effectiveness and Safety of Adalimumab and High Dose Met… | — | Rheumatoid Arthritis | Completed | 2012-10-11 | 2018-04-16 | ClinicalTrials.gov |
| NCT01736189 | Assessment of Clinical Effectiveness and Safety of Adalimumab and High Dose Met… | — | Rheumatoid Arthritis | Completed | 2012-10-11 | 2018-04-16 | ClinicalTrials.gov |
| NCT01736189 | Assessment of Clinical Effectiveness and Safety of Adalimumab and High Dose Met… | — | Rheumatoid Arthritis | Completed | 2012-10-11 | 2018-04-16 | ClinicalTrials.gov |
| NCT01736189 | Assessment of Clinical Effectiveness and Safety of Adalimumab and High Dose Met… | — | Rheumatoid Arthritis | Completed | 2012-10-11 | 2018-04-16 | ClinicalTrials.gov |
| NCT01794520 | Study Evaluating ABT-199 in Participants With Relapsed or Refractory Multiple M… | Phase1 | Relapsed/Refractory Multiple Myeloma | Completed | 2012-10-10 | 2021-11-29 | ClinicalTrials.gov |
| NCT01794520 | Study Evaluating ABT-199 in Participants With Relapsed or Refractory Multiple M… | Phase1 | Relapsed/Refractory Multiple Myeloma | Completed | 2012-10-10 | 2021-11-29 | ClinicalTrials.gov |
| NCT01794520 | Study Evaluating ABT-199 in Participants With Relapsed or Refractory Multiple M… | Phase1 | Relapsed/Refractory Multiple Myeloma | Completed | 2012-10-10 | 2021-11-29 | ClinicalTrials.gov |
| NCT01794520 | Study Evaluating ABT-199 in Participants With Relapsed or Refractory Multiple M… | Phase1 | Relapsed/Refractory Multiple Myeloma | Completed | 2012-10-10 | 2021-11-29 | ClinicalTrials.gov |
| NCT01662492 | A Study Using Botulinum Toxin Type A as Headache Prophylaxis in Adolescents Wit… | Phase3 | Migraine Disorders | Completed | 2012-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01684436 | Safety and Efficacy of Punctal Plug Insertion in Patients With Dry Eye | Phase4 | Dry Eye | Completed | 2012-10-01 | 2013-07-31 | ClinicalTrials.gov |
| NCT01662492 | A Study Using Botulinum Toxin Type A as Headache Prophylaxis in Adolescents Wit… | Phase3 | Migraine Disorders | Completed | 2012-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01700387 | A Study to Evaluate the Tolerability of Botox and Topiramate or Botox and Place… | Phase4 | Chronic Migraine | Completed | 2012-10-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01701518 | A Pilot Study of the Effectiveness of Intra-operative Ozurdex® in Vitrectomy Su… | Na | Epiretinal Membrane | Unknown | 2012-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01741727 | A Study of ABT-414 in Subjects With Solid Tumors | Phase1 | Squamous Cell Tumors | Completed | 2012-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01741727 | A Study of ABT-414 in Subjects With Solid Tumors | Phase1 | Squamous Cell Tumors | Completed | 2012-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01684436 | Safety and Efficacy of Punctal Plug Insertion in Patients With Dry Eye | Phase4 | Dry Eye | Completed | 2012-10-01 | 2013-07-31 | ClinicalTrials.gov |
| NCT01701518 | A Pilot Study of the Effectiveness of Intra-operative Ozurdex® in Vitrectomy Su… | Na | Epiretinal Membrane | Unknown | 2012-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01741727 | A Study of ABT-414 in Subjects With Solid Tumors | Phase1 | Squamous Cell Tumors | Completed | 2012-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01754766 | AGN-229666 for the Treatment of Allergic Conjunctivitis | Phase2 | Allergic Conjunctivitis | Completed | 2012-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01700387 | A Study to Evaluate the Tolerability of Botox and Topiramate or Botox and Place… | Phase4 | Chronic Migraine | Completed | 2012-10-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01701518 | A Pilot Study of the Effectiveness of Intra-operative Ozurdex® in Vitrectomy Su… | Na | Epiretinal Membrane | Unknown | 2012-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01754766 | AGN-229666 for the Treatment of Allergic Conjunctivitis | Phase2 | Allergic Conjunctivitis | Completed | 2012-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01700387 | A Study to Evaluate the Tolerability of Botox and Topiramate or Botox and Place… | Phase4 | Chronic Migraine | Completed | 2012-10-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01754766 | AGN-229666 for the Treatment of Allergic Conjunctivitis | Phase2 | Allergic Conjunctivitis | Completed | 2012-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01741727 | A Study of ABT-414 in Subjects With Solid Tumors | Phase1 | Squamous Cell Tumors | Completed | 2012-10-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01684436 | Safety and Efficacy of Punctal Plug Insertion in Patients With Dry Eye | Phase4 | Dry Eye | Completed | 2012-10-01 | 2013-07-31 | ClinicalTrials.gov |
| NCT01754766 | AGN-229666 for the Treatment of Allergic Conjunctivitis | Phase2 | Allergic Conjunctivitis | Completed | 2012-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01662492 | A Study Using Botulinum Toxin Type A as Headache Prophylaxis in Adolescents Wit… | Phase3 | Migraine Disorders | Completed | 2012-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01701518 | A Pilot Study of the Effectiveness of Intra-operative Ozurdex® in Vitrectomy Su… | Na | Epiretinal Membrane | Unknown | 2012-10-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01700387 | A Study to Evaluate the Tolerability of Botox and Topiramate or Botox and Place… | Phase4 | Chronic Migraine | Completed | 2012-10-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01684436 | Safety and Efficacy of Punctal Plug Insertion in Patients With Dry Eye | Phase4 | Dry Eye | Completed | 2012-10-01 | 2013-07-31 | ClinicalTrials.gov |
| NCT01662492 | A Study Using Botulinum Toxin Type A as Headache Prophylaxis in Adolescents Wit… | Phase3 | Migraine Disorders | Completed | 2012-10-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01660802 | Safety and Efficacy Study of Dexamethasone in the Treatment of Patients With Ma… | Phase3 | Macular Edema | Completed | 2012-09-04 | 2014-05-20 | ClinicalTrials.gov |
| NCT01660802 | Safety and Efficacy Study of Dexamethasone in the Treatment of Patients With Ma… | Phase3 | Macular Edema | Completed | 2012-09-04 | 2014-05-20 | ClinicalTrials.gov |
| NCT01660802 | Safety and Efficacy Study of Dexamethasone in the Treatment of Patients With Ma… | Phase3 | Macular Edema | Completed | 2012-09-04 | 2014-05-20 | ClinicalTrials.gov |
| NCT01660802 | Safety and Efficacy Study of Dexamethasone in the Treatment of Patients With Ma… | Phase3 | Macular Edema | Completed | 2012-09-04 | 2014-05-20 | ClinicalTrials.gov |
| NCT01805323 | A Retrospective Chart Review of OZURDEX® in Patients With Macular Edema | — | Macular Edema | Completed | 2012-09-01 | 2013-04-15 | ClinicalTrials.gov |
| NCT01805323 | A Retrospective Chart Review of OZURDEX® in Patients With Macular Edema | — | Macular Edema | Completed | 2012-09-01 | 2013-04-15 | ClinicalTrials.gov |
| NCT01690195 | Safety and Tolerability Study Evaluating a New Treatment for Subjects With Mild… | Phase2 | Alzheimer's Disease | Terminated | 2012-09-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01711424 | An Observational Study of OPTIVE PLUS® for the Treatment of Dry Eye Disease | — | Dry Eye Syndromes | Completed | 2012-09-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01668511 | A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple S… | Phase1 | Osteoarthritis | Completed | 2012-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01690195 | Safety and Tolerability Study Evaluating a New Treatment for Subjects With Mild… | Phase2 | Alzheimer's Disease | Terminated | 2012-09-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01805323 | A Retrospective Chart Review of OZURDEX® in Patients With Macular Edema | — | Macular Edema | Completed | 2012-09-01 | 2013-04-15 | ClinicalTrials.gov |
| NCT01805323 | A Retrospective Chart Review of OZURDEX® in Patients With Macular Edema | — | Macular Edema | Completed | 2012-09-01 | 2013-04-15 | ClinicalTrials.gov |
| NCT01668511 | A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple S… | Phase1 | Osteoarthritis | Completed | 2012-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01711424 | An Observational Study of OPTIVE PLUS® for the Treatment of Dry Eye Disease | — | Dry Eye Syndromes | Completed | 2012-09-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01690195 | Safety and Tolerability Study Evaluating a New Treatment for Subjects With Mild… | Phase2 | Alzheimer's Disease | Terminated | 2012-09-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01711424 | An Observational Study of OPTIVE PLUS® for the Treatment of Dry Eye Disease | — | Dry Eye Syndromes | Completed | 2012-09-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01668511 | A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple S… | Phase1 | Osteoarthritis | Completed | 2012-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01711424 | An Observational Study of OPTIVE PLUS® for the Treatment of Dry Eye Disease | — | Dry Eye Syndromes | Completed | 2012-09-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01668511 | A Study to Evaluate the Safety, Tolerability and Pharmacokinetics of Multiple S… | Phase1 | Osteoarthritis | Completed | 2012-09-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01690195 | Safety and Tolerability Study Evaluating a New Treatment for Subjects With Mild… | Phase2 | Alzheimer's Disease | Terminated | 2012-09-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01633788 | A Study of AGN-195263 for the Treatment of Meibomian Gland Dysfunction | Phase2 | Meibomian Gland Dysfunction | Completed | 2012-08-22 | 2015-02-05 | ClinicalTrials.gov |
| NCT01633788 | A Study of AGN-195263 for the Treatment of Meibomian Gland Dysfunction | Phase2 | Meibomian Gland Dysfunction | Completed | 2012-08-22 | 2015-02-05 | ClinicalTrials.gov |
| NCT01633788 | A Study of AGN-195263 for the Treatment of Meibomian Gland Dysfunction | Phase2 | Meibomian Gland Dysfunction | Completed | 2012-08-22 | 2015-02-05 | ClinicalTrials.gov |
| NCT01633788 | A Study of AGN-195263 for the Treatment of Meibomian Gland Dysfunction | Phase2 | Meibomian Gland Dysfunction | Completed | 2012-08-22 | 2015-02-05 | ClinicalTrials.gov |
| NCT01679015 | Evaluating Patients With Eye Allergies and Determining if There Are Also Dry Ey… | — | Dry Eyes | Completed | 2012-08-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01670240 | Adalimumab in the Treatment of Chronic Pouchitis | Phase3 | Ulcerative Colitis | Completed | 2012-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01678755 | A Phase 2 Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in … | Phase2 | Schizophrenia | Completed | 2012-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01674725 | A Study to Evaluate the Safety and Effect of the Experimental Drugs ABT-450/Rit… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01685203 | A Study to Evaluate the Safety and Effect of Co-administration of ABT-450 With … | Phase2 | Hepatitis C, Chronic | Completed | 2012-08-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01679015 | Evaluating Patients With Eye Allergies and Determining if There Are Also Dry Ey… | — | Dry Eyes | Completed | 2012-08-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01657370 | A Pharmacokinetic Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-… | Phase2 | Migraine | Completed | 2012-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01657370 | A Pharmacokinetic Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-… | Phase2 | Migraine | Completed | 2012-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01591746 | Botulinum Toxin A (Botox) in Tissue Expander Breast Reconstruction | Phase3 | Breast Cancer | Completed | 2012-08-01 | 2017-07-18 | ClinicalTrials.gov |
| NCT01670240 | Adalimumab in the Treatment of Chronic Pouchitis | Phase3 | Ulcerative Colitis | Completed | 2012-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01674725 | A Study to Evaluate the Safety and Effect of the Experimental Drugs ABT-450/Rit… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01679015 | Evaluating Patients With Eye Allergies and Determining if There Are Also Dry Ey… | — | Dry Eyes | Completed | 2012-08-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01678755 | A Phase 2 Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in … | Phase2 | Schizophrenia | Completed | 2012-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01682460 | Pilot Study on the Use of Artificial Tears to Treat Dry Eye in Glaucoma Patients | Phase4 | Glaucoma | Completed | 2012-08-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01591746 | Botulinum Toxin A (Botox) in Tissue Expander Breast Reconstruction | Phase3 | Breast Cancer | Completed | 2012-08-01 | 2017-07-18 | ClinicalTrials.gov |
| NCT01591746 | Botulinum Toxin A (Botox) in Tissue Expander Breast Reconstruction | Phase3 | Breast Cancer | Completed | 2012-08-01 | 2017-07-18 | ClinicalTrials.gov |
| NCT01685203 | A Study to Evaluate the Safety and Effect of Co-administration of ABT-450 With … | Phase2 | Hepatitis C, Chronic | Completed | 2012-08-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01678755 | A Phase 2 Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in … | Phase2 | Schizophrenia | Completed | 2012-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01670240 | Adalimumab in the Treatment of Chronic Pouchitis | Phase3 | Ulcerative Colitis | Completed | 2012-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01685203 | A Study to Evaluate the Safety and Effect of Co-administration of ABT-450 With … | Phase2 | Hepatitis C, Chronic | Completed | 2012-08-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01674725 | A Study to Evaluate the Safety and Effect of the Experimental Drugs ABT-450/Rit… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01678755 | A Phase 2 Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in … | Phase2 | Schizophrenia | Completed | 2012-08-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01674725 | A Study to Evaluate the Safety and Effect of the Experimental Drugs ABT-450/Rit… | Phase3 | Chronic Hepatitis C Infection | Completed | 2012-08-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01685203 | A Study to Evaluate the Safety and Effect of Co-administration of ABT-450 With … | Phase2 | Hepatitis C, Chronic | Completed | 2012-08-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT01646073 | Safety and Efficacy Study of Adalimumab in the Treatment of Plaque Psoriasis | Phase3 | Plaque Psoriasis | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01670240 | Adalimumab in the Treatment of Chronic Pouchitis | Phase3 | Ulcerative Colitis | Completed | 2012-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01646073 | Safety and Efficacy Study of Adalimumab in the Treatment of Plaque Psoriasis | Phase3 | Plaque Psoriasis | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01646073 | Safety and Efficacy Study of Adalimumab in the Treatment of Plaque Psoriasis | Phase3 | Plaque Psoriasis | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01646073 | Safety and Efficacy Study of Adalimumab in the Treatment of Plaque Psoriasis | Phase3 | Plaque Psoriasis | Completed | 2012-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01591746 | Botulinum Toxin A (Botox) in Tissue Expander Breast Reconstruction | Phase3 | Breast Cancer | Completed | 2012-08-01 | 2017-07-18 | ClinicalTrials.gov |
| NCT01682460 | Pilot Study on the Use of Artificial Tears to Treat Dry Eye in Glaucoma Patients | Phase4 | Glaucoma | Completed | 2012-08-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01657370 | A Pharmacokinetic Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-… | Phase2 | Migraine | Completed | 2012-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01682460 | Pilot Study on the Use of Artificial Tears to Treat Dry Eye in Glaucoma Patients | Phase4 | Glaucoma | Completed | 2012-08-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01657370 | A Pharmacokinetic Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-… | Phase2 | Migraine | Completed | 2012-08-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01679015 | Evaluating Patients With Eye Allergies and Determining if There Are Also Dry Ey… | — | Dry Eyes | Completed | 2012-08-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01682460 | Pilot Study on the Use of Artificial Tears to Treat Dry Eye in Glaucoma Patients | Phase4 | Glaucoma | Completed | 2012-08-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01652157 | Long-term Study in US Cystic Fibrosis Patients Receiving Digestive Enzyme Suppl… | — | Fibrosing Colonopathy | Terminated | 2012-07-31 | 2020-04-08 | ClinicalTrials.gov |
| NCT01652157 | Long-term Study in US Cystic Fibrosis Patients Receiving Digestive Enzyme Suppl… | — | Fibrosing Colonopathy | Terminated | 2012-07-31 | 2020-04-08 | ClinicalTrials.gov |
| NCT01652157 | Long-term Study in US Cystic Fibrosis Patients Receiving Digestive Enzyme Suppl… | — | Fibrosing Colonopathy | Terminated | 2012-07-31 | 2020-04-08 | ClinicalTrials.gov |
| NCT01652157 | Long-term Study in US Cystic Fibrosis Patients Receiving Digestive Enzyme Suppl… | — | Fibrosing Colonopathy | Terminated | 2012-07-31 | 2020-04-08 | ClinicalTrials.gov |
| NCT01682616 | A Phase 1b Study Evaluating the Safety and Tolerability of ABT-199 in Combinati… | Phase1 | Small Lymphocytic Lymphoma | Completed | 2012-07-25 | 2022-06-23 | ClinicalTrials.gov |
| NCT01682616 | A Phase 1b Study Evaluating the Safety and Tolerability of ABT-199 in Combinati… | Phase1 | Small Lymphocytic Lymphoma | Completed | 2012-07-25 | 2022-06-23 | ClinicalTrials.gov |
| NCT01682616 | A Phase 1b Study Evaluating the Safety and Tolerability of ABT-199 in Combinati… | Phase1 | Small Lymphocytic Lymphoma | Completed | 2012-07-25 | 2022-06-23 | ClinicalTrials.gov |
| NCT01682616 | A Phase 1b Study Evaluating the Safety and Tolerability of ABT-199 in Combinati… | Phase1 | Small Lymphocytic Lymphoma | Completed | 2012-07-25 | 2022-06-23 | ClinicalTrials.gov |
| NCT01686581 | An Observational Study of BOTOX® as Headache Prophylaxis for Chronic Migraine | — | Migraine Disorders | Completed | 2012-07-23 | 2016-10-12 | ClinicalTrials.gov |
| NCT01686581 | An Observational Study of BOTOX® as Headache Prophylaxis for Chronic Migraine | — | Migraine Disorders | Completed | 2012-07-23 | 2016-10-12 | ClinicalTrials.gov |
| NCT01686581 | An Observational Study of BOTOX® as Headache Prophylaxis for Chronic Migraine | — | Migraine Disorders | Completed | 2012-07-23 | 2016-10-12 | ClinicalTrials.gov |
| NCT01686581 | An Observational Study of BOTOX® as Headache Prophylaxis for Chronic Migraine | — | Migraine Disorders | Completed | 2012-07-23 | 2016-10-12 | ClinicalTrials.gov |
| NCT01603602 | BOTOX® Treatment in Pediatric Upper Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-07-12 | 2017-07-06 | ClinicalTrials.gov |
| NCT01603602 | BOTOX® Treatment in Pediatric Upper Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-07-12 | 2017-07-06 | ClinicalTrials.gov |
| NCT01603602 | BOTOX® Treatment in Pediatric Upper Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-07-12 | 2017-07-06 | ClinicalTrials.gov |
| NCT01603602 | BOTOX® Treatment in Pediatric Upper Limb Spasticity | Phase3 | Pediatrics | Completed | 2012-07-12 | 2017-07-06 | ClinicalTrials.gov |
| NCT01655862 | A Prospective, Observational Study of Patients With Cervical Dystonia (Dystonie… | — | Torticollis | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01655862 | A Prospective, Observational Study of Patients With Cervical Dystonia (Dystonie… | — | Torticollis | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01613248 | A Dose-Finding Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-006) | Phase2 | Migraine | Completed | 2012-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01648530 | Chronic Migraine Epidemiology and Outcomes Study | — | Migraine Disorders | Completed | 2012-07-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01613248 | A Dose-Finding Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-006) | Phase2 | Migraine | Completed | 2012-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01613716 | Ozurdex for Diabetic Macular Edema Treated With Pars Plana vitrEctomy and Membr… | Phase4 | Diabetic Macular Edema | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01613716 | Ozurdex for Diabetic Macular Edema Treated With Pars Plana vitrEctomy and Membr… | Phase4 | Diabetic Macular Edema | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01892228 | Pilot Study of Immediate HIV Treatment in Guangxi, China | Na | HIV | Unknown | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01715857 | Clinical Practice of Inhalation Anesthesia With Sevoflurane in China | — | Anesthesia, General | Completed | 2012-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01648530 | Chronic Migraine Epidemiology and Outcomes Study | — | Migraine Disorders | Completed | 2012-07-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01892228 | Pilot Study of Immediate HIV Treatment in Guangxi, China | Na | HIV | Unknown | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01613716 | Ozurdex for Diabetic Macular Edema Treated With Pars Plana vitrEctomy and Membr… | Phase4 | Diabetic Macular Edema | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01613248 | A Dose-Finding Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-006) | Phase2 | Migraine | Completed | 2012-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01613716 | Ozurdex for Diabetic Macular Edema Treated With Pars Plana vitrEctomy and Membr… | Phase4 | Diabetic Macular Edema | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01613248 | A Dose-Finding Study of MK-1602 in the Treatment of Acute Migraine (MK-1602-006) | Phase2 | Migraine | Completed | 2012-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01672983 | A Study to Evaluate ABT-450 With Ritonavir (ABT-450/r) and ABT-267 in Japanese … | Phase2 | Chronic Hepatitis C Infection | Completed | 2012-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01617018 | Assessing the Long Term Effectiveness and Safety of Biotherapies in the Treatme… | — | Psoriasis | Completed | 2012-07-01 | 2021-09-05 | ClinicalTrials.gov |
| NCT01617018 | Assessing the Long Term Effectiveness and Safety of Biotherapies in the Treatme… | — | Psoriasis | Completed | 2012-07-01 | 2021-09-05 | ClinicalTrials.gov |
| NCT01672983 | A Study to Evaluate ABT-450 With Ritonavir (ABT-450/r) and ABT-267 in Japanese … | Phase2 | Chronic Hepatitis C Infection | Completed | 2012-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01892228 | Pilot Study of Immediate HIV Treatment in Guangxi, China | Na | HIV | Unknown | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01617018 | Assessing the Long Term Effectiveness and Safety of Biotherapies in the Treatme… | — | Psoriasis | Completed | 2012-07-01 | 2021-09-05 | ClinicalTrials.gov |
| NCT01892228 | Pilot Study of Immediate HIV Treatment in Guangxi, China | Na | HIV | Unknown | 2012-07-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01617018 | Assessing the Long Term Effectiveness and Safety of Biotherapies in the Treatme… | — | Psoriasis | Completed | 2012-07-01 | 2021-09-05 | ClinicalTrials.gov |
| NCT01655862 | A Prospective, Observational Study of Patients With Cervical Dystonia (Dystonie… | — | Torticollis | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01715857 | Clinical Practice of Inhalation Anesthesia With Sevoflurane in China | — | Anesthesia, General | Completed | 2012-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01672983 | A Study to Evaluate ABT-450 With Ritonavir (ABT-450/r) and ABT-267 in Japanese … | Phase2 | Chronic Hepatitis C Infection | Completed | 2012-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01648530 | Chronic Migraine Epidemiology and Outcomes Study | — | Migraine Disorders | Completed | 2012-07-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01715857 | Clinical Practice of Inhalation Anesthesia With Sevoflurane in China | — | Anesthesia, General | Completed | 2012-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01655862 | A Prospective, Observational Study of Patients With Cervical Dystonia (Dystonie… | — | Torticollis | Completed | 2012-07-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT01648530 | Chronic Migraine Epidemiology and Outcomes Study | — | Migraine Disorders | Completed | 2012-07-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01672983 | A Study to Evaluate ABT-450 With Ritonavir (ABT-450/r) and ABT-267 in Japanese … | Phase2 | Chronic Hepatitis C Infection | Completed | 2012-07-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01715857 | Clinical Practice of Inhalation Anesthesia With Sevoflurane in China | — | Anesthesia, General | Completed | 2012-07-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01628549 | Double-Blind, Placebo-Controlled Study to Evaluate 3 Doses of a Novel Tetracycl… | Phase2 | Acne Vulgaris | Completed | 2012-06-30 | 2013-01-31 | ClinicalTrials.gov |
| NCT01628549 | Double-Blind, Placebo-Controlled Study to Evaluate 3 Doses of a Novel Tetracycl… | Phase2 | Acne Vulgaris | Completed | 2012-06-30 | 2013-01-31 | ClinicalTrials.gov |
| NCT01628549 | Double-Blind, Placebo-Controlled Study to Evaluate 3 Doses of a Novel Tetracycl… | Phase2 | Acne Vulgaris | Completed | 2012-06-30 | 2013-01-31 | ClinicalTrials.gov |
| NCT01628549 | Double-Blind, Placebo-Controlled Study to Evaluate 3 Doses of a Novel Tetracycl… | Phase2 | Acne Vulgaris | Completed | 2012-06-30 | 2013-01-31 | ClinicalTrials.gov |
| NCT01639755 | European New Texture Implant Clinical Experience With Shaped Breast Implants | Phase4 | Breast Augmentation | Completed | 2012-06-18 | 2017-10-16 | ClinicalTrials.gov |
| NCT01639742 | European New Texture Implant Clinical Experience With Round Breast Implants | Na | Breast Augmentation | Completed | 2012-06-18 | 2017-10-12 | ClinicalTrials.gov |
| NCT01639755 | European New Texture Implant Clinical Experience With Shaped Breast Implants | Phase4 | Breast Augmentation | Completed | 2012-06-18 | 2017-10-16 | ClinicalTrials.gov |
| NCT01639742 | European New Texture Implant Clinical Experience With Round Breast Implants | Na | Breast Augmentation | Completed | 2012-06-18 | 2017-10-12 | ClinicalTrials.gov |
| NCT01639755 | European New Texture Implant Clinical Experience With Shaped Breast Implants | Phase4 | Breast Augmentation | Completed | 2012-06-18 | 2017-10-16 | ClinicalTrials.gov |
| NCT01639742 | European New Texture Implant Clinical Experience With Round Breast Implants | Na | Breast Augmentation | Completed | 2012-06-18 | 2017-10-12 | ClinicalTrials.gov |
| NCT01639742 | European New Texture Implant Clinical Experience With Round Breast Implants | Na | Breast Augmentation | Completed | 2012-06-18 | 2017-10-12 | ClinicalTrials.gov |
| NCT01639755 | European New Texture Implant Clinical Experience With Shaped Breast Implants | Phase4 | Breast Augmentation | Completed | 2012-06-18 | 2017-10-16 | ClinicalTrials.gov |
| NCT01600716 | Safety and Efficacy Study of OnabotulinumtoxinA for the Treatment of Urinary In… | Phase3 | Urinary Incontinence | Completed | 2012-06-13 | 2015-03-27 | ClinicalTrials.gov |
| NCT01600716 | Safety and Efficacy Study of OnabotulinumtoxinA for the Treatment of Urinary In… | Phase3 | Urinary Incontinence | Completed | 2012-06-13 | 2015-03-27 | ClinicalTrials.gov |
| NCT01600716 | Safety and Efficacy Study of OnabotulinumtoxinA for the Treatment of Urinary In… | Phase3 | Urinary Incontinence | Completed | 2012-06-13 | 2015-03-27 | ClinicalTrials.gov |
| NCT01600716 | Safety and Efficacy Study of OnabotulinumtoxinA for the Treatment of Urinary In… | Phase3 | Urinary Incontinence | Completed | 2012-06-13 | 2015-03-27 | ClinicalTrials.gov |
| NCT01557777 | Open-label Extension Study of Navitoclax in Subjects With Chronic Lymphocytic L… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2012-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01680497 | Post-Market Study of JUVÉDERM VOLIFT™ With Lidocaine for the Correction of Naso… | Na | Moderate to Severe Nasolabial Folds | Completed | 2012-06-01 | 2014-03-06 | ClinicalTrials.gov |
| NCT01589419 | A Clinical Study Conducted in Multiple Centers Evaluating Escalating Doses of V… | Phase1 | Locally Advanced Rectal Cancer | Completed | 2012-06-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01605942 | A Safety and Efficacy Study of a Dexamethasone Drug Delivery System for Postope… | Phase1 | Cataract | Terminated | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01557777 | Open-label Extension Study of Navitoclax in Subjects With Chronic Lymphocytic L… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2012-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01680497 | Post-Market Study of JUVÉDERM VOLIFT™ With Lidocaine for the Correction of Naso… | Na | Moderate to Severe Nasolabial Folds | Completed | 2012-06-01 | 2014-03-06 | ClinicalTrials.gov |
| NCT01557777 | Open-label Extension Study of Navitoclax in Subjects With Chronic Lymphocytic L… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2012-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01589419 | A Clinical Study Conducted in Multiple Centers Evaluating Escalating Doses of V… | Phase1 | Locally Advanced Rectal Cancer | Completed | 2012-06-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01712178 | A Study in Rheumatoid Arthritis (RA) Patients to Compare Two Formulations of Ad… | Phase2 | Rheumatoid Arthritis | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01712178 | A Study in Rheumatoid Arthritis (RA) Patients to Compare Two Formulations of Ad… | Phase2 | Rheumatoid Arthritis | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01600729 | Reliability of the Facial Wrinkle Scale in Japanese Subjects | — | Facial Rhytides | Completed | 2012-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01600729 | Reliability of the Facial Wrinkle Scale in Japanese Subjects | — | Facial Rhytides | Completed | 2012-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01557777 | Open-label Extension Study of Navitoclax in Subjects With Chronic Lymphocytic L… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2012-06-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01680497 | Post-Market Study of JUVÉDERM VOLIFT™ With Lidocaine for the Correction of Naso… | Na | Moderate to Severe Nasolabial Folds | Completed | 2012-06-01 | 2014-03-06 | ClinicalTrials.gov |
| NCT01605942 | A Safety and Efficacy Study of a Dexamethasone Drug Delivery System for Postope… | Phase1 | Cataract | Terminated | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01589419 | A Clinical Study Conducted in Multiple Centers Evaluating Escalating Doses of V… | Phase1 | Locally Advanced Rectal Cancer | Completed | 2012-06-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01605942 | A Safety and Efficacy Study of a Dexamethasone Drug Delivery System for Postope… | Phase1 | Cataract | Terminated | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01605942 | A Safety and Efficacy Study of a Dexamethasone Drug Delivery System for Postope… | Phase1 | Cataract | Terminated | 2012-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01680497 | Post-Market Study of JUVÉDERM VOLIFT™ With Lidocaine for the Correction of Naso… | Na | Moderate to Severe Nasolabial Folds | Completed | 2012-06-01 | 2014-03-06 | ClinicalTrials.gov |
| NCT01712178 | A Study in Rheumatoid Arthritis (RA) Patients to Compare Two Formulations of Ad… | Phase2 | Rheumatoid Arthritis | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01600729 | Reliability of the Facial Wrinkle Scale in Japanese Subjects | — | Facial Rhytides | Completed | 2012-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01600729 | Reliability of the Facial Wrinkle Scale in Japanese Subjects | — | Facial Rhytides | Completed | 2012-06-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01589419 | A Clinical Study Conducted in Multiple Centers Evaluating Escalating Doses of V… | Phase1 | Locally Advanced Rectal Cancer | Completed | 2012-06-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01712178 | A Study in Rheumatoid Arthritis (RA) Patients to Compare Two Formulations of Ad… | Phase2 | Rheumatoid Arthritis | Completed | 2012-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01620528 | A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Subjects Wi… | Phase3 | Endometriosis | Completed | 2012-05-22 | 2015-09-28 | ClinicalTrials.gov |
| NCT01620528 | A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Subjects Wi… | Phase3 | Endometriosis | Completed | 2012-05-22 | 2015-09-28 | ClinicalTrials.gov |
| NCT01620528 | A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Subjects Wi… | Phase3 | Endometriosis | Completed | 2012-05-22 | 2015-09-28 | ClinicalTrials.gov |
| NCT01620528 | A Clinical Study to Evaluate the Safety and Efficacy of Elagolix in Subjects Wi… | Phase3 | Endometriosis | Completed | 2012-05-22 | 2015-09-28 | ClinicalTrials.gov |
| NCT01594229 | A Study Evaluating the Safety and Pharmacokinetics of ABT-199 in Combination Wi… | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2012-05-21 | 2020-07-14 | ClinicalTrials.gov |
| NCT01594229 | A Study Evaluating the Safety and Pharmacokinetics of ABT-199 in Combination Wi… | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2012-05-21 | 2020-07-14 | ClinicalTrials.gov |
| NCT01594229 | A Study Evaluating the Safety and Pharmacokinetics of ABT-199 in Combination Wi… | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2012-05-21 | 2020-07-14 | ClinicalTrials.gov |
| NCT01594229 | A Study Evaluating the Safety and Pharmacokinetics of ABT-199 in Combination Wi… | Phase1 | Non-Hodgkin's Lymphoma | Completed | 2012-05-21 | 2020-07-14 | ClinicalTrials.gov |
| NCT01506947 | A Pilot Clinical Study Evaluating the Effect of Parathyroid Hormone (PTH) Lower… | Phase4 | Moderate to Severe Secondary Hyperparathyroidism | Completed | 2012-05-10 | 2016-04-07 | ClinicalTrials.gov |
| NCT01506947 | A Pilot Clinical Study Evaluating the Effect of Parathyroid Hormone (PTH) Lower… | Phase4 | Moderate to Severe Secondary Hyperparathyroidism | Completed | 2012-05-10 | 2016-04-07 | ClinicalTrials.gov |
| NCT01506947 | A Pilot Clinical Study Evaluating the Effect of Parathyroid Hormone (PTH) Lower… | Phase4 | Moderate to Severe Secondary Hyperparathyroidism | Completed | 2012-05-10 | 2016-04-07 | ClinicalTrials.gov |
| NCT01506947 | A Pilot Clinical Study Evaluating the Effect of Parathyroid Hormone (PTH) Lower… | Phase4 | Moderate to Severe Secondary Hyperparathyroidism | Completed | 2012-05-10 | 2016-04-07 | ClinicalTrials.gov |
| NCT01644396 | An Open-Label, Prospective Study to Assess the Safety and Effectiveness of Adal… | Phase4 | Moderate to Severe Plaque Psoriasis | Completed | 2012-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01589471 | The Value of Botox-A for Management of Low Anterior Resection Syndrome | Phase2 | Low Anterior Resection Syndrome | Completed | 2012-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01550965 | A Study to Evaluate the Impact of Adalimumab on Quality of Life, Health Care Ut… | Phase3 | Ulcerative Colitis | Completed | 2012-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01632150 | Safety Study of Elotuzumab in Combination With Thalidomide and Dexamethasone in… | Phase2 | Relapsed and/or Refractory Multiple Myeloma | Completed | 2012-05-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01589471 | The Value of Botox-A for Management of Low Anterior Resection Syndrome | Phase2 | Low Anterior Resection Syndrome | Completed | 2012-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01655680 | A Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in Schizoph… | Phase2 | Schizophrenia | Completed | 2012-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01636765 | Study of Inter- and Intra-rater Reliability of the Clinician Erythema Assessmen… | — | Erythema | Completed | 2012-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01617928 | A Study of Veliparib in Combination With Carboplatin and Paclitaxel in Japanese… | Phase1 | Solid Tumors | Completed | 2012-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01575054 | BOTOX® Treatment in Adult Patients With Post-Stroke Lower Limb Spasticity | Phase3 | Muscle Spasticity | Completed | 2012-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01575054 | BOTOX® Treatment in Adult Patients With Post-Stroke Lower Limb Spasticity | Phase3 | Muscle Spasticity | Completed | 2012-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01589471 | The Value of Botox-A for Management of Low Anterior Resection Syndrome | Phase2 | Low Anterior Resection Syndrome | Completed | 2012-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01575054 | BOTOX® Treatment in Adult Patients With Post-Stroke Lower Limb Spasticity | Phase3 | Muscle Spasticity | Completed | 2012-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01632150 | Safety Study of Elotuzumab in Combination With Thalidomide and Dexamethasone in… | Phase2 | Relapsed and/or Refractory Multiple Myeloma | Completed | 2012-05-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01655680 | A Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in Schizoph… | Phase2 | Schizophrenia | Completed | 2012-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01550965 | A Study to Evaluate the Impact of Adalimumab on Quality of Life, Health Care Ut… | Phase3 | Ulcerative Colitis | Completed | 2012-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01550965 | A Study to Evaluate the Impact of Adalimumab on Quality of Life, Health Care Ut… | Phase3 | Ulcerative Colitis | Completed | 2012-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01636765 | Study of Inter- and Intra-rater Reliability of the Clinician Erythema Assessmen… | — | Erythema | Completed | 2012-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01644396 | An Open-Label, Prospective Study to Assess the Safety and Effectiveness of Adal… | Phase4 | Moderate to Severe Plaque Psoriasis | Completed | 2012-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01646151 | A Study Comparing IOP-Lowering Treatments to Bimatoprost in Patients With Prima… | — | Glaucoma, Open-Angle | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01617928 | A Study of Veliparib in Combination With Carboplatin and Paclitaxel in Japanese… | Phase1 | Solid Tumors | Completed | 2012-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01550965 | A Study to Evaluate the Impact of Adalimumab on Quality of Life, Health Care Ut… | Phase3 | Ulcerative Colitis | Completed | 2012-05-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01646151 | A Study Comparing IOP-Lowering Treatments to Bimatoprost in Patients With Prima… | — | Glaucoma, Open-Angle | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01632150 | Safety Study of Elotuzumab in Combination With Thalidomide and Dexamethasone in… | Phase2 | Relapsed and/or Refractory Multiple Myeloma | Completed | 2012-05-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01655680 | A Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in Schizoph… | Phase2 | Schizophrenia | Completed | 2012-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01636765 | Study of Inter- and Intra-rater Reliability of the Clinician Erythema Assessmen… | — | Erythema | Completed | 2012-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01644396 | An Open-Label, Prospective Study to Assess the Safety and Effectiveness of Adal… | Phase4 | Moderate to Severe Plaque Psoriasis | Completed | 2012-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01636765 | Study of Inter- and Intra-rater Reliability of the Clinician Erythema Assessmen… | — | Erythema | Completed | 2012-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01646151 | A Study Comparing IOP-Lowering Treatments to Bimatoprost in Patients With Prima… | — | Glaucoma, Open-Angle | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01644396 | An Open-Label, Prospective Study to Assess the Safety and Effectiveness of Adal… | Phase4 | Moderate to Severe Plaque Psoriasis | Completed | 2012-05-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01617928 | A Study of Veliparib in Combination With Carboplatin and Paclitaxel in Japanese… | Phase1 | Solid Tumors | Completed | 2012-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01646151 | A Study Comparing IOP-Lowering Treatments to Bimatoprost in Patients With Prima… | — | Glaucoma, Open-Angle | Completed | 2012-05-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01575054 | BOTOX® Treatment in Adult Patients With Post-Stroke Lower Limb Spasticity | Phase3 | Muscle Spasticity | Completed | 2012-05-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01617928 | A Study of Veliparib in Combination With Carboplatin and Paclitaxel in Japanese… | Phase1 | Solid Tumors | Completed | 2012-05-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01589471 | The Value of Botox-A for Management of Low Anterior Resection Syndrome | Phase2 | Low Anterior Resection Syndrome | Completed | 2012-05-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01655680 | A Study to Evaluate ABT-126 for the Treatment of Cognitive Deficits in Schizoph… | Phase2 | Schizophrenia | Completed | 2012-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01632150 | Safety Study of Elotuzumab in Combination With Thalidomide and Dexamethasone in… | Phase2 | Relapsed and/or Refractory Multiple Myeloma | Completed | 2012-05-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01571557 | A Safety and Efficacy Study to Assess OZURDEX® in Patients With Macular Oedema … | — | Macular Edema | Completed | 2012-04-30 | 2014-06-30 | ClinicalTrials.gov |
| NCT01571557 | A Safety and Efficacy Study to Assess OZURDEX® in Patients With Macular Oedema … | — | Macular Edema | Completed | 2012-04-30 | 2014-06-30 | ClinicalTrials.gov |
| NCT01571557 | A Safety and Efficacy Study to Assess OZURDEX® in Patients With Macular Oedema … | — | Macular Edema | Completed | 2012-04-30 | 2014-06-30 | ClinicalTrials.gov |
| NCT01571557 | A Safety and Efficacy Study to Assess OZURDEX® in Patients With Macular Oedema … | — | Macular Edema | Completed | 2012-04-30 | 2014-06-30 | ClinicalTrials.gov |
| NCT01608672 | Long-Term Patient Satisfaction of Facial Aesthetic Treatment With BOTOX® | — | Glabellar Lines | Completed | 2012-04-01 | 2012-12-31 | ClinicalTrials.gov |
| NCT01577550 | Single Rising Dose Study of BI 655066 in Patients With Moderate and Severe Psor… | Phase1 | Psoriasis | Completed | 2012-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01608672 | Long-Term Patient Satisfaction of Facial Aesthetic Treatment With BOTOX® | — | Glabellar Lines | Completed | 2012-04-01 | 2012-12-31 | ClinicalTrials.gov |
| NCT01608672 | Long-Term Patient Satisfaction of Facial Aesthetic Treatment With BOTOX® | — | Glabellar Lines | Completed | 2012-04-01 | 2012-12-31 | ClinicalTrials.gov |
| NCT01589510 | A Study of Lumigan® 0.01% in Patients With Primary Open Angle Glaucoma (POAG) o… | — | Glaucoma, Open-Angle | Completed | 2012-04-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01589432 | A Randomized, Double-blind, Placebo- and Active-controlled Study of the Electri… | Phase2 | Diabetic Neuropathic Pain | Completed | 2012-04-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01579279 | A Study Comparing the Efficacy and Safety of ABT-652 to Placebo in Subjects Wit… | Phase2 | Diabetic Neuropathic Pain | Terminated | 2012-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01579084 | Safety and Tolerability of AGN-199201 in Patients With Erythema Associated With… | Phase1 | Rosacea | Completed | 2012-04-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01571232 | Ozurdex for Treatment of Recalcitrant Diabetic Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2012-04-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01579305 | Safety and Effectiveness of Juvéderm® Volbella With Lidocaine Versus Restylane-… | Na | Lip Volume Enhancement | Completed | 2012-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01589510 | A Study of Lumigan® 0.01% in Patients With Primary Open Angle Glaucoma (POAG) o… | — | Glaucoma, Open-Angle | Completed | 2012-04-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01579305 | Safety and Effectiveness of Juvéderm® Volbella With Lidocaine Versus Restylane-… | Na | Lip Volume Enhancement | Completed | 2012-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01589432 | A Randomized, Double-blind, Placebo- and Active-controlled Study of the Electri… | Phase2 | Diabetic Neuropathic Pain | Completed | 2012-04-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01579279 | A Study Comparing the Efficacy and Safety of ABT-652 to Placebo in Subjects Wit… | Phase2 | Diabetic Neuropathic Pain | Terminated | 2012-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01579084 | Safety and Tolerability of AGN-199201 in Patients With Erythema Associated With… | Phase1 | Rosacea | Completed | 2012-04-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01571232 | Ozurdex for Treatment of Recalcitrant Diabetic Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2012-04-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01577550 | Single Rising Dose Study of BI 655066 in Patients With Moderate and Severe Psor… | Phase1 | Psoriasis | Completed | 2012-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01635764 | Open-label Study of the Safety and Efficacy of Adalimumab in the Treatment of H… | Phase3 | Hidradenitis Suppurativa | Completed | 2012-04-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01635764 | Open-label Study of the Safety and Efficacy of Adalimumab in the Treatment of H… | Phase3 | Hidradenitis Suppurativa | Completed | 2012-04-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01579305 | Safety and Effectiveness of Juvéderm® Volbella With Lidocaine Versus Restylane-… | Na | Lip Volume Enhancement | Completed | 2012-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01571232 | Ozurdex for Treatment of Recalcitrant Diabetic Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2012-04-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01579084 | Safety and Tolerability of AGN-199201 in Patients With Erythema Associated With… | Phase1 | Rosacea | Completed | 2012-04-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01579279 | A Study Comparing the Efficacy and Safety of ABT-652 to Placebo in Subjects Wit… | Phase2 | Diabetic Neuropathic Pain | Terminated | 2012-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01589432 | A Randomized, Double-blind, Placebo- and Active-controlled Study of the Electri… | Phase2 | Diabetic Neuropathic Pain | Completed | 2012-04-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01589510 | A Study of Lumigan® 0.01% in Patients With Primary Open Angle Glaucoma (POAG) o… | — | Glaucoma, Open-Angle | Completed | 2012-04-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01608672 | Long-Term Patient Satisfaction of Facial Aesthetic Treatment With BOTOX® | — | Glabellar Lines | Completed | 2012-04-01 | 2012-12-31 | ClinicalTrials.gov |
| NCT01579305 | Safety and Effectiveness of Juvéderm® Volbella With Lidocaine Versus Restylane-… | Na | Lip Volume Enhancement | Completed | 2012-04-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01577550 | Single Rising Dose Study of BI 655066 in Patients With Moderate and Severe Psor… | Phase1 | Psoriasis | Completed | 2012-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01571232 | Ozurdex for Treatment of Recalcitrant Diabetic Macular Edema | Phase2 | Diabetic Macular Edema | Completed | 2012-04-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01577550 | Single Rising Dose Study of BI 655066 in Patients With Moderate and Severe Psor… | Phase1 | Psoriasis | Completed | 2012-04-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01589432 | A Randomized, Double-blind, Placebo- and Active-controlled Study of the Electri… | Phase2 | Diabetic Neuropathic Pain | Completed | 2012-04-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01579084 | Safety and Tolerability of AGN-199201 in Patients With Erythema Associated With… | Phase1 | Rosacea | Completed | 2012-04-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01635764 | Open-label Study of the Safety and Efficacy of Adalimumab in the Treatment of H… | Phase3 | Hidradenitis Suppurativa | Completed | 2012-04-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01589510 | A Study of Lumigan® 0.01% in Patients With Primary Open Angle Glaucoma (POAG) o… | — | Glaucoma, Open-Angle | Completed | 2012-04-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01635764 | Open-label Study of the Safety and Efficacy of Adalimumab in the Treatment of H… | Phase3 | Hidradenitis Suppurativa | Completed | 2012-04-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01579279 | A Study Comparing the Efficacy and Safety of ABT-652 to Placebo in Subjects Wit… | Phase2 | Diabetic Neuropathic Pain | Terminated | 2012-04-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01492400 | Safety and Efficacy Study of Dexamethasone Versus Ranibizumab in Patients With … | Phase2 | Macular Edema | Completed | 2012-03-09 | 2014-02-13 | ClinicalTrials.gov |
| NCT01492400 | Safety and Efficacy Study of Dexamethasone Versus Ranibizumab in Patients With … | Phase2 | Macular Edema | Completed | 2012-03-09 | 2014-02-13 | ClinicalTrials.gov |
| NCT01492400 | Safety and Efficacy Study of Dexamethasone Versus Ranibizumab in Patients With … | Phase2 | Macular Edema | Completed | 2012-03-09 | 2014-02-13 | ClinicalTrials.gov |
| NCT01492400 | Safety and Efficacy Study of Dexamethasone Versus Ranibizumab in Patients With … | Phase2 | Macular Edema | Completed | 2012-03-09 | 2014-02-13 | ClinicalTrials.gov |
| NCT01561313 | Crossover Study of Safety and Tolerability of Two Formulations of Adalimumab. | Phase2 | Rheumatoid Arthritis | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01561313 | Crossover Study of Safety and Tolerability of Two Formulations of Adalimumab. | Phase2 | Rheumatoid Arthritis | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01549834 | Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate A… | Phase2 | Alzheimer's Disease | Completed | 2012-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01549834 | Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate A… | Phase2 | Alzheimer's Disease | Completed | 2012-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01549834 | Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate A… | Phase2 | Alzheimer's Disease | Completed | 2012-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01561313 | Crossover Study of Safety and Tolerability of Two Formulations of Adalimumab. | Phase2 | Rheumatoid Arthritis | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01594970 | A Safety and Efficacy Study of Bimatoprost 0.01% in Primary Open-Angle Glaucoma… | Phase4 | Glaucoma, Open-Angle | Completed | 2012-03-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01594970 | A Safety and Efficacy Study of Bimatoprost 0.01% in Primary Open-Angle Glaucoma… | Phase4 | Glaucoma, Open-Angle | Completed | 2012-03-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01594970 | A Safety and Efficacy Study of Bimatoprost 0.01% in Primary Open-Angle Glaucoma… | Phase4 | Glaucoma, Open-Angle | Completed | 2012-03-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01561313 | Crossover Study of Safety and Tolerability of Two Formulations of Adalimumab. | Phase2 | Rheumatoid Arthritis | Completed | 2012-03-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01549834 | Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate A… | Phase2 | Alzheimer's Disease | Completed | 2012-03-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01594970 | A Safety and Efficacy Study of Bimatoprost 0.01% in Primary Open-Angle Glaucoma… | Phase4 | Glaucoma, Open-Angle | Completed | 2012-03-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT03682471 | Long-term 24-month Follow-up Study on Safety and Maintenance of Efficacy of ATX… | — | Subcutaneous Fat | Completed | 2012-02-14 | 2013-12-13 | ClinicalTrials.gov |
| NCT03682471 | Long-term 24-month Follow-up Study on Safety and Maintenance of Efficacy of ATX… | — | Subcutaneous Fat | Completed | 2012-02-14 | 2013-12-13 | ClinicalTrials.gov |
| NCT03682471 | Long-term 24-month Follow-up Study on Safety and Maintenance of Efficacy of ATX… | — | Subcutaneous Fat | Completed | 2012-02-14 | 2013-12-13 | ClinicalTrials.gov |
| NCT03682471 | Long-term 24-month Follow-up Study on Safety and Maintenance of Efficacy of ATX… | — | Subcutaneous Fat | Completed | 2012-02-14 | 2013-12-13 | ClinicalTrials.gov |
| NCT01560104 | A Clinical Study Conducted in Multiple Centers Comparing Veliparib in Combinati… | Phase2 | Non-Small -Cell Lung Cancer | Completed | 2012-02-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01527916 | Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate A… | Phase2 | Alzheimer's Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01543061 | Efficacy Study of a New Eyedrop on Silicone Hydrogel Contact Lens Wearers With … | Phase4 | Contact Lens Related Dry Eye Syndrome | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01559064 | The Volumizing Effect of Juvéderm VOLUMA® in the Mid-Face | — | Age-related Volume Deficit in the Mid-face | Completed | 2012-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01527916 | Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate A… | Phase2 | Alzheimer's Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01559064 | The Volumizing Effect of Juvéderm VOLUMA® in the Mid-Face | — | Age-related Volume Deficit in the Mid-face | Completed | 2012-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01543061 | Efficacy Study of a New Eyedrop on Silicone Hydrogel Contact Lens Wearers With … | Phase4 | Contact Lens Related Dry Eye Syndrome | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01540370 | Study Comparing Quantitative Assessments in Open-angle Glaucoma (OAG) and/or Oc… | — | Glaucoma, Open-Angle | Completed | 2012-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01540370 | Study Comparing Quantitative Assessments in Open-angle Glaucoma (OAG) and/or Oc… | — | Glaucoma, Open-Angle | Completed | 2012-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01559064 | The Volumizing Effect of Juvéderm VOLUMA® in the Mid-Face | — | Age-related Volume Deficit in the Mid-face | Completed | 2012-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01560104 | A Clinical Study Conducted in Multiple Centers Comparing Veliparib in Combinati… | Phase2 | Non-Small -Cell Lung Cancer | Completed | 2012-02-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01543061 | Efficacy Study of a New Eyedrop on Silicone Hydrogel Contact Lens Wearers With … | Phase4 | Contact Lens Related Dry Eye Syndrome | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01543061 | Efficacy Study of a New Eyedrop on Silicone Hydrogel Contact Lens Wearers With … | Phase4 | Contact Lens Related Dry Eye Syndrome | Completed | 2012-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01540370 | Study Comparing Quantitative Assessments in Open-angle Glaucoma (OAG) and/or Oc… | — | Glaucoma, Open-Angle | Completed | 2012-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01560104 | A Clinical Study Conducted in Multiple Centers Comparing Veliparib in Combinati… | Phase2 | Non-Small -Cell Lung Cancer | Completed | 2012-02-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01527916 | Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate A… | Phase2 | Alzheimer's Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01527916 | Evaluate the Efficacy and Safety of ABT-126 in Subjects With Mild to Moderate A… | Phase2 | Alzheimer's Disease | Completed | 2012-02-01 | 2013-11-01 | ClinicalTrials.gov |
| NCT01540370 | Study Comparing Quantitative Assessments in Open-angle Glaucoma (OAG) and/or Oc… | — | Glaucoma, Open-Angle | Completed | 2012-02-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01560104 | A Clinical Study Conducted in Multiple Centers Comparing Veliparib in Combinati… | Phase2 | Non-Small -Cell Lung Cancer | Completed | 2012-02-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01559064 | The Volumizing Effect of Juvéderm VOLUMA® in the Mid-Face | — | Age-related Volume Deficit in the Mid-face | Completed | 2012-02-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01506609 | Study Evaluating Efficacy And Tolerability Of Veliparib in Combination With Tem… | Phase2 | Metastatic Breast Cancer | Completed | 2012-01-23 | 2020-09-02 | ClinicalTrials.gov |
| NCT01506609 | Study Evaluating Efficacy And Tolerability Of Veliparib in Combination With Tem… | Phase2 | Metastatic Breast Cancer | Completed | 2012-01-23 | 2020-09-02 | ClinicalTrials.gov |
| NCT01506609 | Study Evaluating Efficacy And Tolerability Of Veliparib in Combination With Tem… | Phase2 | Metastatic Breast Cancer | Completed | 2012-01-23 | 2020-09-02 | ClinicalTrials.gov |
| NCT01506609 | Study Evaluating Efficacy And Tolerability Of Veliparib in Combination With Tem… | Phase2 | Metastatic Breast Cancer | Completed | 2012-01-23 | 2020-09-02 | ClinicalTrials.gov |
| NCT01393964 | Study of Elotuzumab in Combination With Lenalidomide and Dexamethasone in Subje… | Phase1 | Multiple Myeloma | Completed | 2012-01-06 | 2016-07-18 | ClinicalTrials.gov |
| NCT01393964 | Study of Elotuzumab in Combination With Lenalidomide and Dexamethasone in Subje… | Phase1 | Multiple Myeloma | Completed | 2012-01-06 | 2016-07-18 | ClinicalTrials.gov |
| NCT01393964 | Study of Elotuzumab in Combination With Lenalidomide and Dexamethasone in Subje… | Phase1 | Multiple Myeloma | Completed | 2012-01-06 | 2016-07-18 | ClinicalTrials.gov |
| NCT01393964 | Study of Elotuzumab in Combination With Lenalidomide and Dexamethasone in Subje… | Phase1 | Multiple Myeloma | Completed | 2012-01-06 | 2016-07-18 | ClinicalTrials.gov |
| NCT01469221 | Efficacy and Safety Study of Apaziquone vs. Placebo in Patients With Non-Muscle… | Phase3 | Bladder Cancer | Terminated | 2012-01-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02922192 | Incidence of Hospitalizations for Serious Infections in Patients Receiving Biol… | — | Rheumatoid Arthritis | Completed | 2012-01-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01537198 | Surveillance of Synagis in Korean Pediatric Patients | — | Respiratory Syncytial Virus Infection | Completed | 2012-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01502423 | A Crossover Study of the Safety and Tolerability of Two Formulations of Adalimu… | Phase2 | Rheumatoid Arthritis | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01502423 | A Crossover Study of the Safety and Tolerability of Two Formulations of Adalimu… | Phase2 | Rheumatoid Arthritis | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01537198 | Surveillance of Synagis in Korean Pediatric Patients | — | Respiratory Syncytial Virus Infection | Completed | 2012-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT02922192 | Incidence of Hospitalizations for Serious Infections in Patients Receiving Biol… | — | Rheumatoid Arthritis | Completed | 2012-01-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01537198 | Surveillance of Synagis in Korean Pediatric Patients | — | Respiratory Syncytial Virus Infection | Completed | 2012-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT02922192 | Incidence of Hospitalizations for Serious Infections in Patients Receiving Biol… | — | Rheumatoid Arthritis | Completed | 2012-01-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01469221 | Efficacy and Safety Study of Apaziquone vs. Placebo in Patients With Non-Muscle… | Phase3 | Bladder Cancer | Terminated | 2012-01-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01502423 | A Crossover Study of the Safety and Tolerability of Two Formulations of Adalimu… | Phase2 | Rheumatoid Arthritis | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01518257 | Safety and Efficacy Study of Botulinum Toxin Type A as Treatment for Osteoarthr… | Phase1 | Osteoarthritis | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01518257 | Safety and Efficacy Study of Botulinum Toxin Type A as Treatment for Osteoarthr… | Phase1 | Osteoarthritis | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01537198 | Surveillance of Synagis in Korean Pediatric Patients | — | Respiratory Syncytial Virus Infection | Completed | 2012-01-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01741142 | Efficacy and Safety Study of ABT-436 in Major Depressive Disorder | Phase2 | Major Depressive Disorder | Terminated | 2012-01-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01469221 | Efficacy and Safety Study of Apaziquone vs. Placebo in Patients With Non-Muscle… | Phase3 | Bladder Cancer | Terminated | 2012-01-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT01741142 | Efficacy and Safety Study of ABT-436 in Major Depressive Disorder | Phase2 | Major Depressive Disorder | Terminated | 2012-01-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01518257 | Safety and Efficacy Study of Botulinum Toxin Type A as Treatment for Osteoarthr… | Phase1 | Osteoarthritis | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01518257 | Safety and Efficacy Study of Botulinum Toxin Type A as Treatment for Osteoarthr… | Phase1 | Osteoarthritis | Completed | 2012-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01469221 | Efficacy and Safety Study of Apaziquone vs. Placebo in Patients With Non-Muscle… | Phase3 | Bladder Cancer | Terminated | 2012-01-01 | 2013-04-01 | ClinicalTrials.gov |
| NCT02922192 | Incidence of Hospitalizations for Serious Infections in Patients Receiving Biol… | — | Rheumatoid Arthritis | Completed | 2012-01-01 | 2020-06-01 | ClinicalTrials.gov |
| NCT01741142 | Efficacy and Safety Study of ABT-436 in Major Depressive Disorder | Phase2 | Major Depressive Disorder | Terminated | 2012-01-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01502423 | A Crossover Study of the Safety and Tolerability of Two Formulations of Adalimu… | Phase2 | Rheumatoid Arthritis | Completed | 2012-01-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01741142 | Efficacy and Safety Study of ABT-436 in Major Depressive Disorder | Phase2 | Major Depressive Disorder | Terminated | 2012-01-01 | 2015-08-01 | ClinicalTrials.gov |
| NCT01441973 | Biomarker Study of Elotuzumab in High Risk Smoldering Myeloma | Phase2 | Smoldering Multiple Myeloma | Completed | 2011-12-28 | 2017-01-17 | ClinicalTrials.gov |
| NCT01441973 | Biomarker Study of Elotuzumab in High Risk Smoldering Myeloma | Phase2 | Smoldering Multiple Myeloma | Completed | 2011-12-28 | 2017-01-17 | ClinicalTrials.gov |
| NCT01441973 | Biomarker Study of Elotuzumab in High Risk Smoldering Myeloma | Phase2 | Smoldering Multiple Myeloma | Completed | 2011-12-28 | 2017-01-17 | ClinicalTrials.gov |
| NCT01441973 | Biomarker Study of Elotuzumab in High Risk Smoldering Myeloma | Phase2 | Smoldering Multiple Myeloma | Completed | 2011-12-28 | 2017-01-17 | ClinicalTrials.gov |
| NCT01464333 | Special Investigation (Long-term Investigation) in Patients With Crohn's Disease | — | Crohn's Disease | Completed | 2011-12-16 | 2018-03-31 | ClinicalTrials.gov |
| NCT01464333 | Special Investigation (Long-term Investigation) in Patients With Crohn's Disease | — | Crohn's Disease | Completed | 2011-12-16 | 2018-03-31 | ClinicalTrials.gov |
| NCT01464333 | Special Investigation (Long-term Investigation) in Patients With Crohn's Disease | — | Crohn's Disease | Completed | 2011-12-16 | 2018-03-31 | ClinicalTrials.gov |
| NCT01464333 | Special Investigation (Long-term Investigation) in Patients With Crohn's Disease | — | Crohn's Disease | Completed | 2011-12-16 | 2018-03-31 | ClinicalTrials.gov |
| NCT01518270 | Epidemiologic Analysis of Change in Eyelash Characteristics With Age in Healthy… | — | Health | Completed | 2011-12-01 | 2011-12-16 | ClinicalTrials.gov |
| NCT01464021 | A Post-Marketing Observational Study to Evaluate the Effectiveness of Adalimuma… | — | Arthritis | Terminated | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01516892 | A Long-term Efficacy, Safety, and Tolerability Study of BOTOX® in Patients With… | Phase4 | Migraine Disorders | Completed | 2011-12-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01464021 | A Post-Marketing Observational Study to Evaluate the Effectiveness of Adalimuma… | — | Arthritis | Terminated | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01518270 | Epidemiologic Analysis of Change in Eyelash Characteristics With Age in Healthy… | — | Health | Completed | 2011-12-01 | 2011-12-16 | ClinicalTrials.gov |
| NCT01428115 | Reveal the Level of Anxiety in Patients With Crohn's Disease Receiving Adalimum… | — | Severe Crohn's Disease | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01428115 | Reveal the Level of Anxiety in Patients With Crohn's Disease Receiving Adalimum… | — | Severe Crohn's Disease | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01428115 | Reveal the Level of Anxiety in Patients With Crohn's Disease Receiving Adalimum… | — | Severe Crohn's Disease | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01464021 | A Post-Marketing Observational Study to Evaluate the Effectiveness of Adalimuma… | — | Arthritis | Terminated | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01464021 | A Post-Marketing Observational Study to Evaluate the Effectiveness of Adalimuma… | — | Arthritis | Terminated | 2011-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01518270 | Epidemiologic Analysis of Change in Eyelash Characteristics With Age in Healthy… | — | Health | Completed | 2011-12-01 | 2011-12-16 | ClinicalTrials.gov |
| NCT01516892 | A Long-term Efficacy, Safety, and Tolerability Study of BOTOX® in Patients With… | Phase4 | Migraine Disorders | Completed | 2011-12-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01518270 | Epidemiologic Analysis of Change in Eyelash Characteristics With Age in Healthy… | — | Health | Completed | 2011-12-01 | 2011-12-16 | ClinicalTrials.gov |
| NCT01428115 | Reveal the Level of Anxiety in Patients With Crohn's Disease Receiving Adalimum… | — | Severe Crohn's Disease | Completed | 2011-12-01 | 2013-10-01 | ClinicalTrials.gov |
| NCT01516892 | A Long-term Efficacy, Safety, and Tolerability Study of BOTOX® in Patients With… | Phase4 | Migraine Disorders | Completed | 2011-12-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01516892 | A Long-term Efficacy, Safety, and Tolerability Study of BOTOX® in Patients With… | Phase4 | Migraine Disorders | Completed | 2011-12-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01478048 | Study of Bortezomib and Dexamethasone With or Without Elotuzumab to Treat Relap… | Phase2 | Multiple Myeloma | Completed | 2011-11-30 | 2017-04-21 | ClinicalTrials.gov |
| NCT01478048 | Study of Bortezomib and Dexamethasone With or Without Elotuzumab to Treat Relap… | Phase2 | Multiple Myeloma | Completed | 2011-11-30 | 2017-04-21 | ClinicalTrials.gov |
| NCT01478048 | Study of Bortezomib and Dexamethasone With or Without Elotuzumab to Treat Relap… | Phase2 | Multiple Myeloma | Completed | 2011-11-30 | 2017-04-21 | ClinicalTrials.gov |
| NCT01478048 | Study of Bortezomib and Dexamethasone With or Without Elotuzumab to Treat Relap… | Phase2 | Multiple Myeloma | Completed | 2011-11-30 | 2017-04-21 | ClinicalTrials.gov |
| NCT01618266 | Study of Ozurdex® Treatment Practice in Patients With Macular Oedema Due to Ret… | — | Macular Edema | Completed | 2011-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01945892 | Dexamethasone-Implant for the Treatment of Macula Edema Due to Irvine Gass Synd… | — | Macular Edema | Completed | 2011-11-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01618266 | Study of Ozurdex® Treatment Practice in Patients With Macular Oedema Due to Ret… | — | Macular Edema | Completed | 2011-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01489904 | Application of Botulinum Toxin Type A in Salivary Glands in the Treatment of Dr… | Phase2 | Sialorrhea | Unknown | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01475253 | Double-Blind Placebo Controlled Study of Safety,Tolerability, and Efficacy of L… | Phase2 | Interstitial Cystitis | Terminated | 2011-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01618266 | Study of Ozurdex® Treatment Practice in Patients With Macular Oedema Due to Ret… | — | Macular Edema | Completed | 2011-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01475253 | Double-Blind Placebo Controlled Study of Safety,Tolerability, and Efficacy of L… | Phase2 | Interstitial Cystitis | Terminated | 2011-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01489904 | Application of Botulinum Toxin Type A in Salivary Glands in the Treatment of Dr… | Phase2 | Sialorrhea | Unknown | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01474876 | Multi-country Post-Marketing Observational Study on Maintenance of Effectivenes… | — | Ankylosing Spondylitis | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01945892 | Dexamethasone-Implant for the Treatment of Macula Edema Due to Irvine Gass Synd… | — | Macular Edema | Completed | 2011-11-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01474876 | Multi-country Post-Marketing Observational Study on Maintenance of Effectivenes… | — | Ankylosing Spondylitis | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01468207 | Efficacy and Safety Study of Adalimumab in Treatment of Hidradenitis Suppurativa | Phase3 | Hidradenitis Suppurativa (HS) | Completed | 2011-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01468233 | Efficacy and Safety Study of Adalimumab in the Treatment of Hidradenitis Suppur… | Phase3 | Hidradenitis Suppurativa (HS) | Completed | 2011-11-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01468207 | Efficacy and Safety Study of Adalimumab in Treatment of Hidradenitis Suppurativa | Phase3 | Hidradenitis Suppurativa (HS) | Completed | 2011-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01468233 | Efficacy and Safety Study of Adalimumab in the Treatment of Hidradenitis Suppur… | Phase3 | Hidradenitis Suppurativa (HS) | Completed | 2011-11-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01468233 | Efficacy and Safety Study of Adalimumab in the Treatment of Hidradenitis Suppur… | Phase3 | Hidradenitis Suppurativa (HS) | Completed | 2011-11-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01468207 | Efficacy and Safety Study of Adalimumab in Treatment of Hidradenitis Suppurativa | Phase3 | Hidradenitis Suppurativa (HS) | Completed | 2011-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01945892 | Dexamethasone-Implant for the Treatment of Macula Edema Due to Irvine Gass Synd… | — | Macular Edema | Completed | 2011-11-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01618266 | Study of Ozurdex® Treatment Practice in Patients With Macular Oedema Due to Ret… | — | Macular Edema | Completed | 2011-11-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01489904 | Application of Botulinum Toxin Type A in Salivary Glands in the Treatment of Dr… | Phase2 | Sialorrhea | Unknown | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01475253 | Double-Blind Placebo Controlled Study of Safety,Tolerability, and Efficacy of L… | Phase2 | Interstitial Cystitis | Terminated | 2011-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01474876 | Multi-country Post-Marketing Observational Study on Maintenance of Effectivenes… | — | Ankylosing Spondylitis | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01474876 | Multi-country Post-Marketing Observational Study on Maintenance of Effectivenes… | — | Ankylosing Spondylitis | Completed | 2011-11-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01468207 | Efficacy and Safety Study of Adalimumab in Treatment of Hidradenitis Suppurativa | Phase3 | Hidradenitis Suppurativa (HS) | Completed | 2011-11-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01468233 | Efficacy and Safety Study of Adalimumab in the Treatment of Hidradenitis Suppur… | Phase3 | Hidradenitis Suppurativa (HS) | Completed | 2011-11-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01475253 | Double-Blind Placebo Controlled Study of Safety,Tolerability, and Efficacy of L… | Phase2 | Interstitial Cystitis | Terminated | 2011-11-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01489904 | Application of Botulinum Toxin Type A in Salivary Glands in the Treatment of Dr… | Phase2 | Sialorrhea | Unknown | 2011-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01945892 | Dexamethasone-Implant for the Treatment of Macula Edema Due to Irvine Gass Synd… | — | Macular Edema | Completed | 2011-11-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01427751 | Safety and Efficacy Study of Ozurdex® Compared to Lucentis® in Patients With Br… | Phase4 | Retinal Vein Occlusion | Completed | 2011-10-11 | 2014-11-04 | ClinicalTrials.gov |
| NCT01427751 | Safety and Efficacy Study of Ozurdex® Compared to Lucentis® in Patients With Br… | Phase4 | Retinal Vein Occlusion | Completed | 2011-10-11 | 2014-11-04 | ClinicalTrials.gov |
| NCT01427751 | Safety and Efficacy Study of Ozurdex® Compared to Lucentis® in Patients With Br… | Phase4 | Retinal Vein Occlusion | Completed | 2011-10-11 | 2014-11-04 | ClinicalTrials.gov |
| NCT01427751 | Safety and Efficacy Study of Ozurdex® Compared to Lucentis® in Patients With Br… | Phase4 | Retinal Vein Occlusion | Completed | 2011-10-11 | 2014-11-04 | ClinicalTrials.gov |
| NCT01472016 | Study of ABT-700 in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2011-10-06 | 2017-04-27 | ClinicalTrials.gov |
| NCT01472016 | Study of ABT-700 in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2011-10-06 | 2017-04-27 | ClinicalTrials.gov |
| NCT01472016 | Study of ABT-700 in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2011-10-06 | 2017-04-27 | ClinicalTrials.gov |
| NCT01472016 | Study of ABT-700 in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2011-10-06 | 2017-04-27 | ClinicalTrials.gov |
| NCT01445626 | A Retrospective Data Collection Study in Patients Receiving Dexamethasone Intra… | — | Macular Edema | Completed | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01449682 | Efficacy of an Intravitreal DEX Implant in Retinal Vein Occlusion Following Tre… | Phase3 | Retinal Vein Occlusion | Completed | 2011-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01406119 | An Extension Study of ABT-806 in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2011-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01459588 | Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subject… | Phase3 | Dry Eye Syndromes | Completed | 2011-10-01 | 2012-02-15 | ClinicalTrials.gov |
| NCT01470118 | A Study to Evaluate the Duration of LASTACAFT® in Acute Allergic Conjunctivitis | Phase4 | Conjunctivitis, Allergic | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01464827 | ABT-450 With Ritonavir and ABT-267 and/or ABT-333 With and Without Ribavirin in… | Phase2 | Chronic Hepatitis C | Completed | 2011-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01459588 | Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subject… | Phase3 | Dry Eye Syndromes | Completed | 2011-10-01 | 2012-02-15 | ClinicalTrials.gov |
| NCT01470118 | A Study to Evaluate the Duration of LASTACAFT® in Acute Allergic Conjunctivitis | Phase4 | Conjunctivitis, Allergic | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01449682 | Efficacy of an Intravitreal DEX Implant in Retinal Vein Occlusion Following Tre… | Phase3 | Retinal Vein Occlusion | Completed | 2011-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01382212 | A Study to Evaluate the Safety of Paricalcitol Capsules in Pediatric Subjects A… | Phase3 | End-Stage Renal Disease | Completed | 2011-10-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01459588 | Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subject… | Phase3 | Dry Eye Syndromes | Completed | 2011-10-01 | 2012-02-15 | ClinicalTrials.gov |
| NCT01449682 | Efficacy of an Intravitreal DEX Implant in Retinal Vein Occlusion Following Tre… | Phase3 | Retinal Vein Occlusion | Completed | 2011-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01448525 | Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Promi… | Phase4 | Hypotrichosis | Completed | 2011-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01423539 | A Study of Navitoclax in Addition to Bendamustine and Rituximab in Patients Wit… | Phase2 | Diffuse Large B-Cell Lymphoma | Withdrawn | 2011-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01423539 | A Study of Navitoclax in Addition to Bendamustine and Rituximab in Patients Wit… | Phase2 | Diffuse Large B-Cell Lymphoma | Withdrawn | 2011-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01382212 | A Study to Evaluate the Safety of Paricalcitol Capsules in Pediatric Subjects A… | Phase3 | End-Stage Renal Disease | Completed | 2011-10-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01382212 | A Study to Evaluate the Safety of Paricalcitol Capsules in Pediatric Subjects A… | Phase3 | End-Stage Renal Disease | Completed | 2011-10-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01568008 | Observational Study of Lumigan® 0.01% for Treatment of Primary Open Angle Glauc… | — | Open-Angle Glaucoma | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01406119 | An Extension Study of ABT-806 in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2011-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01568008 | Observational Study of Lumigan® 0.01% for Treatment of Primary Open Angle Glauc… | — | Open-Angle Glaucoma | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01406119 | An Extension Study of ABT-806 in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2011-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01464827 | ABT-450 With Ritonavir and ABT-267 and/or ABT-333 With and Without Ribavirin in… | Phase2 | Chronic Hepatitis C | Completed | 2011-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01464827 | ABT-450 With Ritonavir and ABT-267 and/or ABT-333 With and Without Ribavirin in… | Phase2 | Chronic Hepatitis C | Completed | 2011-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01382212 | A Study to Evaluate the Safety of Paricalcitol Capsules in Pediatric Subjects A… | Phase3 | End-Stage Renal Disease | Completed | 2011-10-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT01464827 | ABT-450 With Ritonavir and ABT-267 and/or ABT-333 With and Without Ribavirin in… | Phase2 | Chronic Hepatitis C | Completed | 2011-10-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01406119 | An Extension Study of ABT-806 in Subjects With Advanced Solid Tumors | Phase1 | Advanced Solid Tumors | Completed | 2011-10-01 | 2017-01-01 | ClinicalTrials.gov |
| NCT01470118 | A Study to Evaluate the Duration of LASTACAFT® in Acute Allergic Conjunctivitis | Phase4 | Conjunctivitis, Allergic | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01568008 | Observational Study of Lumigan® 0.01% for Treatment of Primary Open Angle Glauc… | — | Open-Angle Glaucoma | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01470118 | A Study to Evaluate the Duration of LASTACAFT® in Acute Allergic Conjunctivitis | Phase4 | Conjunctivitis, Allergic | Completed | 2011-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01423539 | A Study of Navitoclax in Addition to Bendamustine and Rituximab in Patients Wit… | Phase2 | Diffuse Large B-Cell Lymphoma | Withdrawn | 2011-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01423539 | A Study of Navitoclax in Addition to Bendamustine and Rituximab in Patients Wit… | Phase2 | Diffuse Large B-Cell Lymphoma | Withdrawn | 2011-10-01 | 2014-02-01 | ClinicalTrials.gov |
| NCT01445626 | A Retrospective Data Collection Study in Patients Receiving Dexamethasone Intra… | — | Macular Edema | Completed | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01459588 | Safety, Efficacy, and Acceptability Study of an Eye Drop Formulation in Subject… | Phase3 | Dry Eye Syndromes | Completed | 2011-10-01 | 2012-02-15 | ClinicalTrials.gov |
| NCT01449682 | Efficacy of an Intravitreal DEX Implant in Retinal Vein Occlusion Following Tre… | Phase3 | Retinal Vein Occlusion | Completed | 2011-10-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01448525 | Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Promi… | Phase4 | Hypotrichosis | Completed | 2011-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01445626 | A Retrospective Data Collection Study in Patients Receiving Dexamethasone Intra… | — | Macular Edema | Completed | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01568008 | Observational Study of Lumigan® 0.01% for Treatment of Primary Open Angle Glauc… | — | Open-Angle Glaucoma | Completed | 2011-10-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01445626 | A Retrospective Data Collection Study in Patients Receiving Dexamethasone Intra… | — | Macular Edema | Completed | 2011-10-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01448525 | Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Promi… | Phase4 | Hypotrichosis | Completed | 2011-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01448525 | Study Assessing Patient Satisfaction With LATISSE® for Increasing Eyelash Promi… | Phase4 | Hypotrichosis | Completed | 2011-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01432379 | BOTOX® Prophylaxis in Patients With Chronic Migraine | — | Migraine Disorders | Completed | 2011-09-09 | 2015-05-12 | ClinicalTrials.gov |
| NCT01432379 | BOTOX® Prophylaxis in Patients With Chronic Migraine | — | Migraine Disorders | Completed | 2011-09-09 | 2015-05-12 | ClinicalTrials.gov |
| NCT01432379 | BOTOX® Prophylaxis in Patients With Chronic Migraine | — | Migraine Disorders | Completed | 2011-09-09 | 2015-05-12 | ClinicalTrials.gov |
| NCT01432379 | BOTOX® Prophylaxis in Patients With Chronic Migraine | — | Migraine Disorders | Completed | 2011-09-09 | 2015-05-12 | ClinicalTrials.gov |
| NCT01441635 | Safety and Efficacy of Elagolix in Pre-Menopausal Women With Heavy Uterine Blee… | Phase2 | Heavy Uterine Bleeding | Completed | 2011-09-08 | 2014-05-17 | ClinicalTrials.gov |
| NCT01441635 | Safety and Efficacy of Elagolix in Pre-Menopausal Women With Heavy Uterine Blee… | Phase2 | Heavy Uterine Bleeding | Completed | 2011-09-08 | 2014-05-17 | ClinicalTrials.gov |
| NCT01441635 | Safety and Efficacy of Elagolix in Pre-Menopausal Women With Heavy Uterine Blee… | Phase2 | Heavy Uterine Bleeding | Completed | 2011-09-08 | 2014-05-17 | ClinicalTrials.gov |
| NCT01441635 | Safety and Efficacy of Elagolix in Pre-Menopausal Women With Heavy Uterine Blee… | Phase2 | Heavy Uterine Bleeding | Completed | 2011-09-08 | 2014-05-17 | ClinicalTrials.gov |
| NCT01458535 | A Study to Evaluate Paritaprevir With Ritonavir (ABT-450/r) When Given Together… | Phase2 | Hepatitis C Virus | Completed | 2011-09-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01397409 | Evaluation of AGN-150998 in Exudative Age-related Macular Degeneration (AMD) | Phase2 | Age-related Macular Degeneration | Completed | 2011-09-01 | 2014-04-30 | ClinicalTrials.gov |
| NCT01458535 | A Study to Evaluate Paritaprevir With Ritonavir (ABT-450/r) When Given Together… | Phase2 | Hepatitis C Virus | Completed | 2011-09-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01441895 | Corneal Sensation and Incidence of Dry Eye Post Refractive Cataract Extraction … | — | Cataract | Unknown | 2011-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01397409 | Evaluation of AGN-150998 in Exudative Age-related Macular Degeneration (AMD) | Phase2 | Age-related Macular Degeneration | Completed | 2011-09-01 | 2014-04-30 | ClinicalTrials.gov |
| NCT03023748 | Intravenous Paricalcitol in Chronic Hemodialysis Patients | Phase4 | Endstage Renal Disease | Unknown | 2011-09-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT01441895 | Corneal Sensation and Incidence of Dry Eye Post Refractive Cataract Extraction … | — | Cataract | Unknown | 2011-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01397409 | Evaluation of AGN-150998 in Exudative Age-related Macular Degeneration (AMD) | Phase2 | Age-related Macular Degeneration | Completed | 2011-09-01 | 2014-04-30 | ClinicalTrials.gov |
| NCT01741246 | Neuroimaging Studies of Chronic Primary Headaches Using Positron Emission Tomog… | — | Migraine | Completed | 2011-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01741246 | Neuroimaging Studies of Chronic Primary Headaches Using Positron Emission Tomog… | — | Migraine | Completed | 2011-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01441895 | Corneal Sensation and Incidence of Dry Eye Post Refractive Cataract Extraction … | — | Cataract | Unknown | 2011-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT01426113 | A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paedia… | Phase3 | Glaucoma | Terminated | 2011-09-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01741246 | Neuroimaging Studies of Chronic Primary Headaches Using Positron Emission Tomog… | — | Migraine | Completed | 2011-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01397409 | Evaluation of AGN-150998 in Exudative Age-related Macular Degeneration (AMD) | Phase2 | Age-related Macular Degeneration | Completed | 2011-09-01 | 2014-04-30 | ClinicalTrials.gov |
| NCT01741246 | Neuroimaging Studies of Chronic Primary Headaches Using Positron Emission Tomog… | — | Migraine | Completed | 2011-09-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01458535 | A Study to Evaluate Paritaprevir With Ritonavir (ABT-450/r) When Given Together… | Phase2 | Hepatitis C Virus | Completed | 2011-09-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT03023748 | Intravenous Paricalcitol in Chronic Hemodialysis Patients | Phase4 | Endstage Renal Disease | Unknown | 2011-09-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT01458535 | A Study to Evaluate Paritaprevir With Ritonavir (ABT-450/r) When Given Together… | Phase2 | Hepatitis C Virus | Completed | 2011-09-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01426113 | A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paedia… | Phase3 | Glaucoma | Terminated | 2011-09-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01441895 | Corneal Sensation and Incidence of Dry Eye Post Refractive Cataract Extraction … | — | Cataract | Unknown | 2011-09-01 | 2016-12-01 | ClinicalTrials.gov |
| NCT03023748 | Intravenous Paricalcitol in Chronic Hemodialysis Patients | Phase4 | Endstage Renal Disease | Unknown | 2011-09-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT03023748 | Intravenous Paricalcitol in Chronic Hemodialysis Patients | Phase4 | Endstage Renal Disease | Unknown | 2011-09-01 | 2018-01-01 | ClinicalTrials.gov |
| NCT01426113 | A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paedia… | Phase3 | Glaucoma | Terminated | 2011-09-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01426113 | A Study of the Safety and Efficacy of Bimatoprost Ophthalmic Solution in Paedia… | Phase3 | Glaucoma | Terminated | 2011-09-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01387815 | Canadian Humira Post Marketing Observational Epidemiological Study: Assessing E… | — | Psoriasis | Completed | 2011-08-16 | 2018-06-29 | ClinicalTrials.gov |
| NCT01387815 | Canadian Humira Post Marketing Observational Epidemiological Study: Assessing E… | — | Psoriasis | Completed | 2011-08-16 | 2018-06-29 | ClinicalTrials.gov |
| NCT01387815 | Canadian Humira Post Marketing Observational Epidemiological Study: Assessing E… | — | Psoriasis | Completed | 2011-08-16 | 2018-06-29 | ClinicalTrials.gov |
| NCT01387815 | Canadian Humira Post Marketing Observational Epidemiological Study: Assessing E… | — | Psoriasis | Completed | 2011-08-16 | 2018-06-29 | ClinicalTrials.gov |
| NCT01335399 | Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to… | Phase3 | Multiple Myeloma | Completed | 2011-08-04 | 2021-09-03 | ClinicalTrials.gov |
| NCT01335399 | Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to… | Phase3 | Multiple Myeloma | Completed | 2011-08-04 | 2021-09-03 | ClinicalTrials.gov |
| NCT01335399 | Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to… | Phase3 | Multiple Myeloma | Completed | 2011-08-04 | 2021-09-03 | ClinicalTrials.gov |
| NCT01335399 | Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to… | Phase3 | Multiple Myeloma | Completed | 2011-08-04 | 2021-09-03 | ClinicalTrials.gov |
| NCT01424319 | Reducing Residual Albuminuria in Subjects With Diabetes and Nephropathy With At… | Phase2 | Chronic Kidney Disease | Completed | 2011-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01368042 | Quality of Life in Greek Hemodialysis Patients Receiving Zemplar Intravenous | — | Chronic Kidney Disease | Completed | 2011-08-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01401452 | Effectiveness of Adalimumab in Moderate to Severe Plaque Psoriasis Patients Wit… | — | Moderate to Severe Plaque Psoriasis | Completed | 2011-08-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01424319 | Reducing Residual Albuminuria in Subjects With Diabetes and Nephropathy With At… | Phase2 | Chronic Kidney Disease | Completed | 2011-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01390961 | Comparison of Tolerability Between Two Allergy Drops | Phase4 | Allergic Conjunctivitis | Unknown | 2011-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01410201 | Dexamethasone Intravitreal Implant After Vitrectomy For Epiretinal Membrane | Na | Epiretinal Membrane | Terminated | 2011-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01412086 | Inter-rater and Intra-rater Reliability of the Global Eyebrow Assessment Scale | — | Healthy Volunteers | Completed | 2011-08-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01401452 | Effectiveness of Adalimumab in Moderate to Severe Plaque Psoriasis Patients Wit… | — | Moderate to Severe Plaque Psoriasis | Completed | 2011-08-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01387789 | A Study of Rheumatoid Arthritis Patients on Adalimumab to Evaluate Quality of L… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01401452 | Effectiveness of Adalimumab in Moderate to Severe Plaque Psoriasis Patients Wit… | — | Moderate to Severe Plaque Psoriasis | Completed | 2011-08-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01424319 | Reducing Residual Albuminuria in Subjects With Diabetes and Nephropathy With At… | Phase2 | Chronic Kidney Disease | Completed | 2011-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01368042 | Quality of Life in Greek Hemodialysis Patients Receiving Zemplar Intravenous | — | Chronic Kidney Disease | Completed | 2011-08-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01466062 | Clinical Study of Palivizumab in Japanese Newborns, Infants and Young Children … | Phase3 | Respiratory Syncytial Virus Infection | Completed | 2011-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00706940 | Tear Dynamics After Restasis Treatment in Dry Eye Patients | — | Dry Eye | Completed | 2011-08-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT00706940 | Tear Dynamics After Restasis Treatment in Dry Eye Patients | — | Dry Eye | Completed | 2011-08-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01466062 | Clinical Study of Palivizumab in Japanese Newborns, Infants and Young Children … | Phase3 | Respiratory Syncytial Virus Infection | Completed | 2011-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01466062 | Clinical Study of Palivizumab in Japanese Newborns, Infants and Young Children … | Phase3 | Respiratory Syncytial Virus Infection | Completed | 2011-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01412086 | Inter-rater and Intra-rater Reliability of the Global Eyebrow Assessment Scale | — | Healthy Volunteers | Completed | 2011-08-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01410201 | Dexamethasone Intravitreal Implant After Vitrectomy For Epiretinal Membrane | Na | Epiretinal Membrane | Terminated | 2011-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00706940 | Tear Dynamics After Restasis Treatment in Dry Eye Patients | — | Dry Eye | Completed | 2011-08-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01390961 | Comparison of Tolerability Between Two Allergy Drops | Phase4 | Allergic Conjunctivitis | Unknown | 2011-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01387789 | A Study of Rheumatoid Arthritis Patients on Adalimumab to Evaluate Quality of L… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01368042 | Quality of Life in Greek Hemodialysis Patients Receiving Zemplar Intravenous | — | Chronic Kidney Disease | Completed | 2011-08-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00706940 | Tear Dynamics After Restasis Treatment in Dry Eye Patients | — | Dry Eye | Completed | 2011-08-01 | 2016-12-31 | ClinicalTrials.gov |
| NCT01424319 | Reducing Residual Albuminuria in Subjects With Diabetes and Nephropathy With At… | Phase2 | Chronic Kidney Disease | Completed | 2011-08-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT01412086 | Inter-rater and Intra-rater Reliability of the Global Eyebrow Assessment Scale | — | Healthy Volunteers | Completed | 2011-08-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01401452 | Effectiveness of Adalimumab in Moderate to Severe Plaque Psoriasis Patients Wit… | — | Moderate to Severe Plaque Psoriasis | Completed | 2011-08-01 | 2016-05-01 | ClinicalTrials.gov |
| NCT01368042 | Quality of Life in Greek Hemodialysis Patients Receiving Zemplar Intravenous | — | Chronic Kidney Disease | Completed | 2011-08-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01387789 | A Study of Rheumatoid Arthritis Patients on Adalimumab to Evaluate Quality of L… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01410201 | Dexamethasone Intravitreal Implant After Vitrectomy For Epiretinal Membrane | Na | Epiretinal Membrane | Terminated | 2011-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01390961 | Comparison of Tolerability Between Two Allergy Drops | Phase4 | Allergic Conjunctivitis | Unknown | 2011-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01466062 | Clinical Study of Palivizumab in Japanese Newborns, Infants and Young Children … | Phase3 | Respiratory Syncytial Virus Infection | Completed | 2011-08-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01412086 | Inter-rater and Intra-rater Reliability of the Global Eyebrow Assessment Scale | — | Healthy Volunteers | Completed | 2011-08-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01410201 | Dexamethasone Intravitreal Implant After Vitrectomy For Epiretinal Membrane | Na | Epiretinal Membrane | Terminated | 2011-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01390961 | Comparison of Tolerability Between Two Allergy Drops | Phase4 | Allergic Conjunctivitis | Unknown | 2011-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01387789 | A Study of Rheumatoid Arthritis Patients on Adalimumab to Evaluate Quality of L… | — | Rheumatoid Arthritis | Completed | 2011-08-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT01410565 | Efficacy and Safety of Multi-Instillations of Apaziquone in Patients With Non-M… | Phase3 | Bladder Cancer | Terminated | 2011-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01282203 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01401478 | Observational Program of Zemplar in Patients With End Stage Chronic Kidney Dise… | — | Secondary Hyperparathyroidism | Completed | 2011-07-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01412021 | Special Investigation (All Case Survey) in Patients With Juvenile Idiopathic Ar… | — | Arthritis, Juvenile Rheumatoid | Completed | 2011-07-01 | 2018-04-02 | ClinicalTrials.gov |
| NCT01149291 | A Study to Follow-up Patients With End Stage Renal Disease Undergoing Hemodialy… | — | Secondary Hyperparathyroidism | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01391286 | Safety and Efficacy Study of Bimatoprost in Japanese Patients With Chemotherapy… | Phase3 | Eyelash Hypotrichosis | Completed | 2011-07-01 | 2012-05-25 | ClinicalTrials.gov |
| NCT01391273 | Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypo… | Phase3 | Eyelash Hypotrichosis | Completed | 2011-07-01 | 2012-05-19 | ClinicalTrials.gov |
| NCT01411696 | Retrospective Study in Patients Receiving Two or More OZURDEX® Injections for R… | — | Retinal Vein Occlusion | Completed | 2011-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01384851 | Efficacy of the Chronic Application of Tear Formulations | Na | Dry Eye | Unknown | 2011-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01412021 | Special Investigation (All Case Survey) in Patients With Juvenile Idiopathic Ar… | — | Arthritis, Juvenile Rheumatoid | Completed | 2011-07-01 | 2018-04-02 | ClinicalTrials.gov |
| NCT01410565 | Efficacy and Safety of Multi-Instillations of Apaziquone in Patients With Non-M… | Phase3 | Bladder Cancer | Terminated | 2011-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01501799 | A Bioequivalence Study With Clinical Endpoints Comparing Adapalene and Benzoyl … | Na | Acne Vulgaris | Completed | 2011-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01384851 | Efficacy of the Chronic Application of Tear Formulations | Na | Dry Eye | Unknown | 2011-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01149291 | A Study to Follow-up Patients With End Stage Renal Disease Undergoing Hemodialy… | — | Secondary Hyperparathyroidism | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01149291 | A Study to Follow-up Patients With End Stage Renal Disease Undergoing Hemodialy… | — | Secondary Hyperparathyroidism | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01384851 | Efficacy of the Chronic Application of Tear Formulations | Na | Dry Eye | Unknown | 2011-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01401478 | Observational Program of Zemplar in Patients With End Stage Chronic Kidney Dise… | — | Secondary Hyperparathyroidism | Completed | 2011-07-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01282203 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01411696 | Retrospective Study in Patients Receiving Two or More OZURDEX® Injections for R… | — | Retinal Vein Occlusion | Completed | 2011-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01410565 | Efficacy and Safety of Multi-Instillations of Apaziquone in Patients With Non-M… | Phase3 | Bladder Cancer | Terminated | 2011-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01501799 | A Bioequivalence Study With Clinical Endpoints Comparing Adapalene and Benzoyl … | Na | Acne Vulgaris | Completed | 2011-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01384851 | Efficacy of the Chronic Application of Tear Formulations | Na | Dry Eye | Unknown | 2011-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01501799 | A Bioequivalence Study With Clinical Endpoints Comparing Adapalene and Benzoyl … | Na | Acne Vulgaris | Completed | 2011-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01391286 | Safety and Efficacy Study of Bimatoprost in Japanese Patients With Chemotherapy… | Phase3 | Eyelash Hypotrichosis | Completed | 2011-07-01 | 2012-05-25 | ClinicalTrials.gov |
| NCT02020512 | A Study of 0.03% Bimatoprost in the Treatment of Primary Open Angle Glaucoma an… | Phase4 | Glaucoma, Open-Angle | Completed | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01412021 | Special Investigation (All Case Survey) in Patients With Juvenile Idiopathic Ar… | — | Arthritis, Juvenile Rheumatoid | Completed | 2011-07-01 | 2018-04-02 | ClinicalTrials.gov |
| NCT01391273 | Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypo… | Phase3 | Eyelash Hypotrichosis | Completed | 2011-07-01 | 2012-05-19 | ClinicalTrials.gov |
| NCT01401478 | Observational Program of Zemplar in Patients With End Stage Chronic Kidney Dise… | — | Secondary Hyperparathyroidism | Completed | 2011-07-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01282203 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01411696 | Retrospective Study in Patients Receiving Two or More OZURDEX® Injections for R… | — | Retinal Vein Occlusion | Completed | 2011-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01410565 | Efficacy and Safety of Multi-Instillations of Apaziquone in Patients With Non-M… | Phase3 | Bladder Cancer | Terminated | 2011-07-01 | 2014-03-01 | ClinicalTrials.gov |
| NCT01391286 | Safety and Efficacy Study of Bimatoprost in Japanese Patients With Chemotherapy… | Phase3 | Eyelash Hypotrichosis | Completed | 2011-07-01 | 2012-05-25 | ClinicalTrials.gov |
| NCT01401478 | Observational Program of Zemplar in Patients With End Stage Chronic Kidney Dise… | — | Secondary Hyperparathyroidism | Completed | 2011-07-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01391286 | Safety and Efficacy Study of Bimatoprost in Japanese Patients With Chemotherapy… | Phase3 | Eyelash Hypotrichosis | Completed | 2011-07-01 | 2012-05-25 | ClinicalTrials.gov |
| NCT01149291 | A Study to Follow-up Patients With End Stage Renal Disease Undergoing Hemodialy… | — | Secondary Hyperparathyroidism | Completed | 2011-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01501799 | A Bioequivalence Study With Clinical Endpoints Comparing Adapalene and Benzoyl … | Na | Acne Vulgaris | Completed | 2011-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01282203 | Evaluation of Volatile Induction and Maintenance Anesthesia (VIMA) With Sevoran… | — | Anesthesia, General | Completed | 2011-07-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01391273 | Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypo… | Phase3 | Eyelash Hypotrichosis | Completed | 2011-07-01 | 2012-05-19 | ClinicalTrials.gov |
| NCT01412021 | Special Investigation (All Case Survey) in Patients With Juvenile Idiopathic Ar… | — | Arthritis, Juvenile Rheumatoid | Completed | 2011-07-01 | 2018-04-02 | ClinicalTrials.gov |
| NCT01411696 | Retrospective Study in Patients Receiving Two or More OZURDEX® Injections for R… | — | Retinal Vein Occlusion | Completed | 2011-07-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT02020512 | A Study of 0.03% Bimatoprost in the Treatment of Primary Open Angle Glaucoma an… | Phase4 | Glaucoma, Open-Angle | Completed | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT02020512 | A Study of 0.03% Bimatoprost in the Treatment of Primary Open Angle Glaucoma an… | Phase4 | Glaucoma, Open-Angle | Completed | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT02020512 | A Study of 0.03% Bimatoprost in the Treatment of Primary Open Angle Glaucoma an… | Phase4 | Glaucoma, Open-Angle | Completed | 2011-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT01391273 | Safety and Efficacy Study of Bimatoprost in Japanese Patients With Eyelash Hypo… | Phase3 | Eyelash Hypotrichosis | Completed | 2011-07-01 | 2012-05-19 | ClinicalTrials.gov |
| NCT01387802 | Canadian Humira Post Marketing Observational Epidemiological Study: Assessing E… | — | Ankylosing Spondylitis | Completed | 2011-06-29 | 2019-12-16 | ClinicalTrials.gov |
| NCT01387802 | Canadian Humira Post Marketing Observational Epidemiological Study: Assessing E… | — | Ankylosing Spondylitis | Completed | 2011-06-29 | 2019-12-16 | ClinicalTrials.gov |
| NCT01387802 | Canadian Humira Post Marketing Observational Epidemiological Study: Assessing E… | — | Ankylosing Spondylitis | Completed | 2011-06-29 | 2019-12-16 | ClinicalTrials.gov |
| NCT01387802 | Canadian Humira Post Marketing Observational Epidemiological Study: Assessing E… | — | Ankylosing Spondylitis | Completed | 2011-06-29 | 2019-12-16 | ClinicalTrials.gov |
| NCT01386684 | Real Life Evaluation of Lupron in the Management of Prostate Cancer: A Canadian… | — | Prostate Cancer | Completed | 2011-06-28 | 2016-09-08 | ClinicalTrials.gov |
| NCT01386684 | Real Life Evaluation of Lupron in the Management of Prostate Cancer: A Canadian… | — | Prostate Cancer | Completed | 2011-06-28 | 2016-09-08 | ClinicalTrials.gov |
| NCT01386684 | Real Life Evaluation of Lupron in the Management of Prostate Cancer: A Canadian… | — | Prostate Cancer | Completed | 2011-06-28 | 2016-09-08 | ClinicalTrials.gov |
| NCT01386684 | Real Life Evaluation of Lupron in the Management of Prostate Cancer: A Canadian… | — | Prostate Cancer | Completed | 2011-06-28 | 2016-09-08 | ClinicalTrials.gov |
| NCT01239797 | Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to… | Phase3 | Lymphoma | Completed | 2011-06-20 | 2021-04-21 | ClinicalTrials.gov |
| NCT01239797 | Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to… | Phase3 | Lymphoma | Completed | 2011-06-20 | 2021-04-21 | ClinicalTrials.gov |
| NCT01239797 | Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to… | Phase3 | Lymphoma | Completed | 2011-06-20 | 2021-04-21 | ClinicalTrials.gov |
| NCT01239797 | Phase III Study of Lenalidomide and Dexamethasone With or Without Elotuzumab to… | Phase3 | Lymphoma | Completed | 2011-06-20 | 2021-04-21 | ClinicalTrials.gov |
| NCT01391299 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Forehe… | Na | Facial Rhytides | Completed | 2011-06-01 | 2012-02-28 | ClinicalTrials.gov |
| NCT01325337 | Safety and Efficacy Study of Bimatoprost in the Treatment of Men With Androgeni… | Phase2 | Alopecia | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01346488 | Special Investigation in Patients With Rheumatoid Arthritis (Working Productivi… | — | Rheumatoid Arthritis | Completed | 2011-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01403038 | An Open-label Study of the Effects of Elagolix in Adult Premenopausal Females | Phase1 | Folliculogenesis | Completed | 2011-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01364922 | Phase 2 Chronic Low Back Pain Study | Phase2 | Chronic Low Back Pain | Completed | 2011-06-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01328158 | Drug Use Investigation of Kaletra Tablets (Once Daily Administration) on Patien… | — | Human Immunodeficiency Virus Infection | Completed | 2011-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01364922 | Phase 2 Chronic Low Back Pain Study | Phase2 | Chronic Low Back Pain | Completed | 2011-06-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01391312 | Patient Satisfaction Study of BOTOX® Cosmetic in the Treatment of Moderate to S… | Phase4 | Glabellar Frown Lines | Completed | 2011-06-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01325337 | Safety and Efficacy Study of Bimatoprost in the Treatment of Men With Androgeni… | Phase2 | Alopecia | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01325350 | Safety and Efficacy Study of Bimatoprost in the Treatment of Women With Female … | Phase2 | Alopecia | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01328158 | Drug Use Investigation of Kaletra Tablets (Once Daily Administration) on Patien… | — | Human Immunodeficiency Virus Infection | Completed | 2011-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01413893 | An Extension Study of Linifanib (ABT-869) in Subjects With Advanced or Metastat… | Phase1 | Advanced Solid Tumors | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01391299 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Forehe… | Na | Facial Rhytides | Completed | 2011-06-01 | 2012-02-28 | ClinicalTrials.gov |
| NCT01403038 | An Open-label Study of the Effects of Elagolix in Adult Premenopausal Females | Phase1 | Folliculogenesis | Completed | 2011-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01380704 | Safety and Pharmacodynamic Study of ABT-436 in Major Depressive Disorder | Phase1 | Major Depressive Disorder | Completed | 2011-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01325350 | Safety and Efficacy Study of Bimatoprost in the Treatment of Women With Female … | Phase2 | Alopecia | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01413893 | An Extension Study of Linifanib (ABT-869) in Subjects With Advanced or Metastat… | Phase1 | Advanced Solid Tumors | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01413893 | An Extension Study of Linifanib (ABT-869) in Subjects With Advanced or Metastat… | Phase1 | Advanced Solid Tumors | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01387074 | Observational Study of Botox® Treatment for Patients With Upper Limb Adult Spas… | — | Muscle Spasticity | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01383005 | Treatment Perception of QD (Once a Day) Dosed Kaletra (Tablets) | — | Human Immunodeficiency Virus Infection | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01380704 | Safety and Pharmacodynamic Study of ABT-436 in Major Depressive Disorder | Phase1 | Major Depressive Disorder | Completed | 2011-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01391312 | Patient Satisfaction Study of BOTOX® Cosmetic in the Treatment of Moderate to S… | Phase4 | Glabellar Frown Lines | Completed | 2011-06-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01364922 | Phase 2 Chronic Low Back Pain Study | Phase2 | Chronic Low Back Pain | Completed | 2011-06-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01413893 | An Extension Study of Linifanib (ABT-869) in Subjects With Advanced or Metastat… | Phase1 | Advanced Solid Tumors | Completed | 2011-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01328158 | Drug Use Investigation of Kaletra Tablets (Once Daily Administration) on Patien… | — | Human Immunodeficiency Virus Infection | Completed | 2011-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01328158 | Drug Use Investigation of Kaletra Tablets (Once Daily Administration) on Patien… | — | Human Immunodeficiency Virus Infection | Completed | 2011-06-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01325350 | Safety and Efficacy Study of Bimatoprost in the Treatment of Women With Female … | Phase2 | Alopecia | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01325337 | Safety and Efficacy Study of Bimatoprost in the Treatment of Men With Androgeni… | Phase2 | Alopecia | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01391299 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Forehe… | Na | Facial Rhytides | Completed | 2011-06-01 | 2012-02-28 | ClinicalTrials.gov |
| NCT01346488 | Special Investigation in Patients With Rheumatoid Arthritis (Working Productivi… | — | Rheumatoid Arthritis | Completed | 2011-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01380704 | Safety and Pharmacodynamic Study of ABT-436 in Major Depressive Disorder | Phase1 | Major Depressive Disorder | Completed | 2011-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01383005 | Treatment Perception of QD (Once a Day) Dosed Kaletra (Tablets) | — | Human Immunodeficiency Virus Infection | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01391299 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Forehe… | Na | Facial Rhytides | Completed | 2011-06-01 | 2012-02-28 | ClinicalTrials.gov |
| NCT01383005 | Treatment Perception of QD (Once a Day) Dosed Kaletra (Tablets) | — | Human Immunodeficiency Virus Infection | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01325337 | Safety and Efficacy Study of Bimatoprost in the Treatment of Men With Androgeni… | Phase2 | Alopecia | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01325350 | Safety and Efficacy Study of Bimatoprost in the Treatment of Women With Female … | Phase2 | Alopecia | Completed | 2011-06-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01380704 | Safety and Pharmacodynamic Study of ABT-436 in Major Depressive Disorder | Phase1 | Major Depressive Disorder | Completed | 2011-06-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01346488 | Special Investigation in Patients With Rheumatoid Arthritis (Working Productivi… | — | Rheumatoid Arthritis | Completed | 2011-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01364922 | Phase 2 Chronic Low Back Pain Study | Phase2 | Chronic Low Back Pain | Completed | 2011-06-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01391312 | Patient Satisfaction Study of BOTOX® Cosmetic in the Treatment of Moderate to S… | Phase4 | Glabellar Frown Lines | Completed | 2011-06-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01403038 | An Open-label Study of the Effects of Elagolix in Adult Premenopausal Females | Phase1 | Folliculogenesis | Completed | 2011-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01383005 | Treatment Perception of QD (Once a Day) Dosed Kaletra (Tablets) | — | Human Immunodeficiency Virus Infection | Completed | 2011-06-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01391312 | Patient Satisfaction Study of BOTOX® Cosmetic in the Treatment of Moderate to S… | Phase4 | Glabellar Frown Lines | Completed | 2011-06-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01387074 | Observational Study of Botox® Treatment for Patients With Upper Limb Adult Spas… | — | Muscle Spasticity | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01387074 | Observational Study of Botox® Treatment for Patients With Upper Limb Adult Spas… | — | Muscle Spasticity | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01387074 | Observational Study of Botox® Treatment for Patients With Upper Limb Adult Spas… | — | Muscle Spasticity | Completed | 2011-06-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01346488 | Special Investigation in Patients With Rheumatoid Arthritis (Working Productivi… | — | Rheumatoid Arthritis | Completed | 2011-06-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01403038 | An Open-label Study of the Effects of Elagolix in Adult Premenopausal Females | Phase1 | Folliculogenesis | Completed | 2011-06-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01298700 | Long-Term Safety of Bimatoprost Ophthalmic Solution in Patients With Glaucoma o… | Phase4 | Glaucoma | Completed | 2011-05-31 | 2016-12-06 | ClinicalTrials.gov |
| NCT01298700 | Long-Term Safety of Bimatoprost Ophthalmic Solution in Patients With Glaucoma o… | Phase4 | Glaucoma | Completed | 2011-05-31 | 2016-12-06 | ClinicalTrials.gov |
| NCT01298700 | Long-Term Safety of Bimatoprost Ophthalmic Solution in Patients With Glaucoma o… | Phase4 | Glaucoma | Completed | 2011-05-31 | 2016-12-06 | ClinicalTrials.gov |
| NCT01298700 | Long-Term Safety of Bimatoprost Ophthalmic Solution in Patients With Glaucoma o… | Phase4 | Glaucoma | Completed | 2011-05-31 | 2016-12-06 | ClinicalTrials.gov |
| NCT01328626 | A Phase 1 Study Evaluating the Safety and Pharmacokinetics of ABT-199 in Subjec… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2011-05-23 | 2020-05-08 | ClinicalTrials.gov |
| NCT01328626 | A Phase 1 Study Evaluating the Safety and Pharmacokinetics of ABT-199 in Subjec… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2011-05-23 | 2020-05-08 | ClinicalTrials.gov |
| NCT01328626 | A Phase 1 Study Evaluating the Safety and Pharmacokinetics of ABT-199 in Subjec… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2011-05-23 | 2020-05-08 | ClinicalTrials.gov |
| NCT01328626 | A Phase 1 Study Evaluating the Safety and Pharmacokinetics of ABT-199 in Subjec… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2011-05-23 | 2020-05-08 | ClinicalTrials.gov |
| NCT01192568 | Safety and Efficacy Evaluation of Oxybutynin Topical Gel In Children With Neuro… | Phase4 | Overactive Detrusor | Completed | 2011-05-17 | 2023-10-24 | ClinicalTrials.gov |
| NCT01192568 | Safety and Efficacy Evaluation of Oxybutynin Topical Gel In Children With Neuro… | Phase4 | Overactive Detrusor | Completed | 2011-05-17 | 2023-10-24 | ClinicalTrials.gov |
| NCT01192568 | Safety and Efficacy Evaluation of Oxybutynin Topical Gel In Children With Neuro… | Phase4 | Overactive Detrusor | Completed | 2011-05-17 | 2023-10-24 | ClinicalTrials.gov |
| NCT01192568 | Safety and Efficacy Evaluation of Oxybutynin Topical Gel In Children With Neuro… | Phase4 | Overactive Detrusor | Completed | 2011-05-17 | 2023-10-24 | ClinicalTrials.gov |
| NCT01339650 | Study of ABT-767 in Subjects With Breast Cancer 1 and Breast Cancer 2 (BRCA 1 a… | Phase1 | Fallopian Tube | Completed | 2011-05-06 | 2017-11-30 | ClinicalTrials.gov |
| NCT01339650 | Study of ABT-767 in Subjects With Breast Cancer 1 and Breast Cancer 2 (BRCA 1 a… | Phase1 | Fallopian Tube | Completed | 2011-05-06 | 2017-11-30 | ClinicalTrials.gov |
| NCT01339650 | Study of ABT-767 in Subjects With Breast Cancer 1 and Breast Cancer 2 (BRCA 1 a… | Phase1 | Fallopian Tube | Completed | 2011-05-06 | 2017-11-30 | ClinicalTrials.gov |
| NCT01339650 | Study of ABT-767 in Subjects With Breast Cancer 1 and Breast Cancer 2 (BRCA 1 a… | Phase1 | Fallopian Tube | Completed | 2011-05-06 | 2017-11-30 | ClinicalTrials.gov |
| NCT01294384 | Safety and Efficacy Study of New Eye Drop Formulations With Refresh Tears® in P… | Phase3 | Dry Eye Syndromes | Completed | 2011-05-01 | 2012-09-25 | ClinicalTrials.gov |
| NCT01328366 | Quality of Life and Psychosocial Factors Associated With Severe Psoriasis Follo… | — | Psoriasis | Completed | 2011-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01294384 | Safety and Efficacy Study of New Eye Drop Formulations With Refresh Tears® in P… | Phase3 | Dry Eye Syndromes | Completed | 2011-05-01 | 2012-09-25 | ClinicalTrials.gov |
| NCT01751373 | Assessment and Management of Post-Stroke Spasticity With Botulinum Toxin-A | Na | Stroke | Completed | 2011-05-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01341782 | Comparison of Efficacy and Safety of Paricalcitol Injection With Maxacalcitol I… | Phase3 | Secondary Hyperparathyroidism | Completed | 2011-05-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01224015 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's… | Phase3 | Facial Rhytides | Completed | 2011-05-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01341782 | Comparison of Efficacy and Safety of Paricalcitol Injection With Maxacalcitol I… | Phase3 | Secondary Hyperparathyroidism | Completed | 2011-05-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01328366 | Quality of Life and Psychosocial Factors Associated With Severe Psoriasis Follo… | — | Psoriasis | Completed | 2011-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01294384 | Safety and Efficacy Study of New Eye Drop Formulations With Refresh Tears® in P… | Phase3 | Dry Eye Syndromes | Completed | 2011-05-01 | 2012-09-25 | ClinicalTrials.gov |
| NCT01224015 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's… | Phase3 | Facial Rhytides | Completed | 2011-05-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01751373 | Assessment and Management of Post-Stroke Spasticity With Botulinum Toxin-A | Na | Stroke | Completed | 2011-05-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01224015 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's… | Phase3 | Facial Rhytides | Completed | 2011-05-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01751373 | Assessment and Management of Post-Stroke Spasticity With Botulinum Toxin-A | Na | Stroke | Completed | 2011-05-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01224015 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's… | Phase3 | Facial Rhytides | Completed | 2011-05-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01751373 | Assessment and Management of Post-Stroke Spasticity With Botulinum Toxin-A | Na | Stroke | Completed | 2011-05-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01294384 | Safety and Efficacy Study of New Eye Drop Formulations With Refresh Tears® in P… | Phase3 | Dry Eye Syndromes | Completed | 2011-05-01 | 2012-09-25 | ClinicalTrials.gov |
| NCT01341782 | Comparison of Efficacy and Safety of Paricalcitol Injection With Maxacalcitol I… | Phase3 | Secondary Hyperparathyroidism | Completed | 2011-05-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01328366 | Quality of Life and Psychosocial Factors Associated With Severe Psoriasis Follo… | — | Psoriasis | Completed | 2011-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01341782 | Comparison of Efficacy and Safety of Paricalcitol Injection With Maxacalcitol I… | Phase3 | Secondary Hyperparathyroidism | Completed | 2011-05-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01328366 | Quality of Life and Psychosocial Factors Associated With Severe Psoriasis Follo… | — | Psoriasis | Completed | 2011-05-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01291108 | Safety and Efficacy of AGN-210669 Ophthalmic Solution Compared With Bimatoprost… | Phase2 | Glaucoma, Open-Angle | Completed | 2011-04-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01333722 | Acute Pain Study Following Bunionectomy | Phase2 | Pain | Completed | 2011-04-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01608659 | An Observational Retrospective Study to Evaluate Treatment Patterns of Botulinu… | — | Facial Rhytides | Completed | 2011-04-01 | 2011-06-17 | ClinicalTrials.gov |
| NCT01608659 | An Observational Retrospective Study to Evaluate Treatment Patterns of Botulinu… | — | Facial Rhytides | Completed | 2011-04-01 | 2011-06-17 | ClinicalTrials.gov |
| NCT01346501 | Special Investigation in Patients With Rheumatoid Arthritis (HOPEFUL III Study)… | — | Rheumatoid Arthritis | Completed | 2011-04-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01333722 | Acute Pain Study Following Bunionectomy | Phase2 | Pain | Completed | 2011-04-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01333722 | Acute Pain Study Following Bunionectomy | Phase2 | Pain | Completed | 2011-04-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01608659 | An Observational Retrospective Study to Evaluate Treatment Patterns of Botulinu… | — | Facial Rhytides | Completed | 2011-04-01 | 2011-06-17 | ClinicalTrials.gov |
| NCT01346501 | Special Investigation in Patients With Rheumatoid Arthritis (HOPEFUL III Study)… | — | Rheumatoid Arthritis | Completed | 2011-04-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01316224 | Prevalence and Incidence of Articular Symptoms and Signs Related to Psoriatic A… | — | Psoriasis | Completed | 2011-04-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01291108 | Safety and Efficacy of AGN-210669 Ophthalmic Solution Compared With Bimatoprost… | Phase2 | Glaucoma, Open-Angle | Completed | 2011-04-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01346501 | Special Investigation in Patients With Rheumatoid Arthritis (HOPEFUL III Study)… | — | Rheumatoid Arthritis | Completed | 2011-04-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01316224 | Prevalence and Incidence of Articular Symptoms and Signs Related to Psoriatic A… | — | Psoriasis | Completed | 2011-04-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01608659 | An Observational Retrospective Study to Evaluate Treatment Patterns of Botulinu… | — | Facial Rhytides | Completed | 2011-04-01 | 2011-06-17 | ClinicalTrials.gov |
| NCT01333722 | Acute Pain Study Following Bunionectomy | Phase2 | Pain | Completed | 2011-04-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01291108 | Safety and Efficacy of AGN-210669 Ophthalmic Solution Compared With Bimatoprost… | Phase2 | Glaucoma, Open-Angle | Completed | 2011-04-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01291108 | Safety and Efficacy of AGN-210669 Ophthalmic Solution Compared With Bimatoprost… | Phase2 | Glaucoma, Open-Angle | Completed | 2011-04-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01346501 | Special Investigation in Patients With Rheumatoid Arthritis (HOPEFUL III Study)… | — | Rheumatoid Arthritis | Completed | 2011-04-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01316224 | Prevalence and Incidence of Articular Symptoms and Signs Related to Psoriatic A… | — | Psoriasis | Completed | 2011-04-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01316224 | Prevalence and Incidence of Articular Symptoms and Signs Related to Psoriatic A… | — | Psoriasis | Completed | 2011-04-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01335126 | Comparison of Tolerability and Clinical Performance of Two Emulsion-type Artifi… | Phase3 | Dry Eye | Unknown | 2011-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01320293 | Cardiovascular Effects in Psoriasis Patients Treated With Adalimumab. | Na | Psoriasis | Completed | 2011-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01314261 | Study of ABT-267 in Treatment Naive Hepatitis C Virus (HCV) Genotype 1 Infected… | Phase2 | Chronic Hepatitis C | Completed | 2011-03-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01321424 | Diurnal Variation in Tear Osmolarity | — | Dry Eye Disease | Completed | 2011-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01319318 | Observational Study of Ocular Inflammation in Patients Undergoing a Pars Plana … | — | Vitrectomy | Completed | 2011-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01744158 | Exploring Hypertonia in Children With Cerebral Palsy | — | Cerebral Palsy. | Unknown | 2011-03-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01387906 | Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosi… | Phase4 | Hypotrichosis | Completed | 2011-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01241240 | Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2011-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01314261 | Study of ABT-267 in Treatment Naive Hepatitis C Virus (HCV) Genotype 1 Infected… | Phase2 | Chronic Hepatitis C | Completed | 2011-03-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01241240 | Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2011-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01314261 | Study of ABT-267 in Treatment Naive Hepatitis C Virus (HCV) Genotype 1 Infected… | Phase2 | Chronic Hepatitis C | Completed | 2011-03-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01387906 | Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosi… | Phase4 | Hypotrichosis | Completed | 2011-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01241240 | Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2011-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01744158 | Exploring Hypertonia in Children With Cerebral Palsy | — | Cerebral Palsy. | Unknown | 2011-03-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01282372 | Greek Study on Work Productivity and Sleep in Patients With Rheumatic Diseases … | — | Rheumatoid Arthritis | Completed | 2011-03-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01387906 | Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosi… | Phase4 | Hypotrichosis | Completed | 2011-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01356758 | Cardiovascular Risk Assessment in Patients With Severe Psoriasis Treated With B… | — | Psoriasis | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01744158 | Exploring Hypertonia in Children With Cerebral Palsy | — | Cerebral Palsy. | Unknown | 2011-03-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01320293 | Cardiovascular Effects in Psoriasis Patients Treated With Adalimumab. | Na | Psoriasis | Completed | 2011-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01321424 | Diurnal Variation in Tear Osmolarity | — | Dry Eye Disease | Completed | 2011-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01356758 | Cardiovascular Risk Assessment in Patients With Severe Psoriasis Treated With B… | — | Psoriasis | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01339936 | Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of … | Phase2 | Dry Eye Syndrome | Completed | 2011-03-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01335126 | Comparison of Tolerability and Clinical Performance of Two Emulsion-type Artifi… | Phase3 | Dry Eye | Unknown | 2011-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01319318 | Observational Study of Ocular Inflammation in Patients Undergoing a Pars Plana … | — | Vitrectomy | Completed | 2011-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01321424 | Diurnal Variation in Tear Osmolarity | — | Dry Eye Disease | Completed | 2011-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01282372 | Greek Study on Work Productivity and Sleep in Patients With Rheumatic Diseases … | — | Rheumatoid Arthritis | Completed | 2011-03-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01319318 | Observational Study of Ocular Inflammation in Patients Undergoing a Pars Plana … | — | Vitrectomy | Completed | 2011-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01282372 | Greek Study on Work Productivity and Sleep in Patients With Rheumatic Diseases … | — | Rheumatoid Arthritis | Completed | 2011-03-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01320293 | Cardiovascular Effects in Psoriasis Patients Treated With Adalimumab. | Na | Psoriasis | Completed | 2011-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01319318 | Observational Study of Ocular Inflammation in Patients Undergoing a Pars Plana … | — | Vitrectomy | Completed | 2011-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01282372 | Greek Study on Work Productivity and Sleep in Patients With Rheumatic Diseases … | — | Rheumatoid Arthritis | Completed | 2011-03-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01321424 | Diurnal Variation in Tear Osmolarity | — | Dry Eye Disease | Completed | 2011-03-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT01241240 | Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2011-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01320293 | Cardiovascular Effects in Psoriasis Patients Treated With Adalimumab. | Na | Psoriasis | Completed | 2011-03-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT01339936 | Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of … | Phase2 | Dry Eye Syndrome | Completed | 2011-03-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01335126 | Comparison of Tolerability and Clinical Performance of Two Emulsion-type Artifi… | Phase3 | Dry Eye | Unknown | 2011-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01339936 | Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of … | Phase2 | Dry Eye Syndrome | Completed | 2011-03-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01356758 | Cardiovascular Risk Assessment in Patients With Severe Psoriasis Treated With B… | — | Psoriasis | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01744158 | Exploring Hypertonia in Children With Cerebral Palsy | — | Cerebral Palsy. | Unknown | 2011-03-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT01356758 | Cardiovascular Risk Assessment in Patients With Severe Psoriasis Treated With B… | — | Psoriasis | Completed | 2011-03-01 | 2015-11-01 | ClinicalTrials.gov |
| NCT01387906 | Latisse (Bimatoprost .03% Opthalmic Solution) for the Treatment of Hypotrichosi… | Phase4 | Hypotrichosis | Completed | 2011-03-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01339936 | Evaluation of the Effect of Repeated Usage on the Tear Film Characteristics of … | Phase2 | Dry Eye Syndrome | Completed | 2011-03-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01335126 | Comparison of Tolerability and Clinical Performance of Two Emulsion-type Artifi… | Phase3 | Dry Eye | Unknown | 2011-03-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01314261 | Study of ABT-267 in Treatment Naive Hepatitis C Virus (HCV) Genotype 1 Infected… | Phase2 | Chronic Hepatitis C | Completed | 2011-03-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01294371 | Observational Program to Assess Routine Use of Add-back Therapy in Patients Wit… | — | Genital Endometriosis | Completed | 2011-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01320735 | Observational Program to Assess Use of Intermittent Adjuvant Deprivation Therap… | — | Prostate Cancer | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01265992 | Study to Assess Patient Management Practices and Quality of Life With Paricalci… | — | Secondary Hyperparathyroidism | Completed | 2011-02-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01265992 | Study to Assess Patient Management Practices and Quality of Life With Paricalci… | — | Secondary Hyperparathyroidism | Completed | 2011-02-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01737853 | Comparison of Efficacy & Tolerability Between Ganfort vs Krytantek in Mexican P… | — | Glaucoma Primary Open Angle | Completed | 2011-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01502020 | A Bioequivalence Study With Clinical Endpoints Comparing Generic Imiquimod Crea… | Na | Actinic Keratoses | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01737853 | Comparison of Efficacy & Tolerability Between Ganfort vs Krytantek in Mexican P… | — | Glaucoma Primary Open Angle | Completed | 2011-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01294371 | Observational Program to Assess Routine Use of Add-back Therapy in Patients Wit… | — | Genital Endometriosis | Completed | 2011-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01320735 | Observational Program to Assess Use of Intermittent Adjuvant Deprivation Therap… | — | Prostate Cancer | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01502020 | A Bioequivalence Study With Clinical Endpoints Comparing Generic Imiquimod Crea… | Na | Actinic Keratoses | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01383681 | Retrospective Study of Patients With Spasticity in the Spanish Population | — | Muscle Spasticity | Completed | 2011-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01265992 | Study to Assess Patient Management Practices and Quality of Life With Paricalci… | — | Secondary Hyperparathyroidism | Completed | 2011-02-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01502020 | A Bioequivalence Study With Clinical Endpoints Comparing Generic Imiquimod Crea… | Na | Actinic Keratoses | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01383681 | Retrospective Study of Patients With Spasticity in the Spanish Population | — | Muscle Spasticity | Completed | 2011-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01320735 | Observational Program to Assess Use of Intermittent Adjuvant Deprivation Therap… | — | Prostate Cancer | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01294371 | Observational Program to Assess Routine Use of Add-back Therapy in Patients Wit… | — | Genital Endometriosis | Completed | 2011-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01737853 | Comparison of Efficacy & Tolerability Between Ganfort vs Krytantek in Mexican P… | — | Glaucoma Primary Open Angle | Completed | 2011-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01383681 | Retrospective Study of Patients With Spasticity in the Spanish Population | — | Muscle Spasticity | Completed | 2011-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01294371 | Observational Program to Assess Routine Use of Add-back Therapy in Patients Wit… | — | Genital Endometriosis | Completed | 2011-02-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01265992 | Study to Assess Patient Management Practices and Quality of Life With Paricalci… | — | Secondary Hyperparathyroidism | Completed | 2011-02-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01383681 | Retrospective Study of Patients With Spasticity in the Spanish Population | — | Muscle Spasticity | Completed | 2011-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01737853 | Comparison of Efficacy & Tolerability Between Ganfort vs Krytantek in Mexican P… | — | Glaucoma Primary Open Angle | Completed | 2011-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01320735 | Observational Program to Assess Use of Intermittent Adjuvant Deprivation Therap… | — | Prostate Cancer | Completed | 2011-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01502020 | A Bioequivalence Study With Clinical Endpoints Comparing Generic Imiquimod Crea… | Na | Actinic Keratoses | Completed | 2011-02-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01373424 | The Dystonia Coalition Natural History and Biospecimen Repository for Isolated … | — | Dystonia | Completed | 2011-01-01 | 2020-09-30 | ClinicalTrials.gov |
| NCT01217606 | Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2011-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01284478 | Ozurdex for Combined Pseudophakic Cystoid Macular Edema and Diabetic Macular Ed… | Phase2 | Pseudophakic Cystoid Macular Edema, | Completed | 2011-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01273597 | Observational Study to Evaluate the Time to Achieving the Maintenance Dose of Z… | — | Kidney Failure, Chronic | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01273519 | Assessment of Pain Management in Rheumatoid Arthritis, Psoriatic Arthritis and … | — | Rheumatoid Arthritis | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01272414 | Use of Botox in the Management of Thyroid Related Upper Eyelid Retraction | Phase4 | Graves Ophthalmopathy | Withdrawn | 2011-01-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01217606 | Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2011-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01373424 | The Dystonia Coalition Natural History and Biospecimen Repository for Isolated … | — | Dystonia | Completed | 2011-01-01 | 2020-09-30 | ClinicalTrials.gov |
| NCT02922179 | Descriptive Analysis of Long- and Intermediate-Acting Insulin in Adult Diabetics | — | Diabetes | Completed | 2011-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT01272414 | Use of Botox in the Management of Thyroid Related Upper Eyelid Retraction | Phase4 | Graves Ophthalmopathy | Withdrawn | 2011-01-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01273519 | Assessment of Pain Management in Rheumatoid Arthritis, Psoriatic Arthritis and … | — | Rheumatoid Arthritis | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01273597 | Observational Study to Evaluate the Time to Achieving the Maintenance Dose of Z… | — | Kidney Failure, Chronic | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01284478 | Ozurdex for Combined Pseudophakic Cystoid Macular Edema and Diabetic Macular Ed… | Phase2 | Pseudophakic Cystoid Macular Edema, | Completed | 2011-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01373424 | The Dystonia Coalition Natural History and Biospecimen Repository for Isolated … | — | Dystonia | Completed | 2011-01-01 | 2020-09-30 | ClinicalTrials.gov |
| NCT01217606 | Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2011-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01284478 | Ozurdex for Combined Pseudophakic Cystoid Macular Edema and Diabetic Macular Ed… | Phase2 | Pseudophakic Cystoid Macular Edema, | Completed | 2011-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01273597 | Observational Study to Evaluate the Time to Achieving the Maintenance Dose of Z… | — | Kidney Failure, Chronic | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01273519 | Assessment of Pain Management in Rheumatoid Arthritis, Psoriatic Arthritis and … | — | Rheumatoid Arthritis | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01272414 | Use of Botox in the Management of Thyroid Related Upper Eyelid Retraction | Phase4 | Graves Ophthalmopathy | Withdrawn | 2011-01-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT02922179 | Descriptive Analysis of Long- and Intermediate-Acting Insulin in Adult Diabetics | — | Diabetes | Completed | 2011-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT01217606 | Safety and Efficacy of Triple Combination Therapy in Patients With Primary Open… | Phase3 | Glaucoma, Open-Angle | Completed | 2011-01-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02922179 | Descriptive Analysis of Long- and Intermediate-Acting Insulin in Adult Diabetics | — | Diabetes | Completed | 2011-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT01272414 | Use of Botox in the Management of Thyroid Related Upper Eyelid Retraction | Phase4 | Graves Ophthalmopathy | Withdrawn | 2011-01-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01273519 | Assessment of Pain Management in Rheumatoid Arthritis, Psoriatic Arthritis and … | — | Rheumatoid Arthritis | Completed | 2011-01-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01273597 | Observational Study to Evaluate the Time to Achieving the Maintenance Dose of Z… | — | Kidney Failure, Chronic | Completed | 2011-01-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01284478 | Ozurdex for Combined Pseudophakic Cystoid Macular Edema and Diabetic Macular Ed… | Phase2 | Pseudophakic Cystoid Macular Edema, | Completed | 2011-01-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01373424 | The Dystonia Coalition Natural History and Biospecimen Repository for Isolated … | — | Dystonia | Completed | 2011-01-01 | 2020-09-30 | ClinicalTrials.gov |
| NCT02922179 | Descriptive Analysis of Long- and Intermediate-Acting Insulin in Adult Diabetics | — | Diabetes | Completed | 2011-01-01 | 2019-01-01 | ClinicalTrials.gov |
| NCT00534339 | EasyBand GOAL Trial | Na | Morbid Obesity | Withdrawn | 2010-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01229410 | Pharmacokinetics of the Brimonidine Tartrate Posterior Segment Delivery System … | Phase1 | Vitrectomy | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01229410 | Pharmacokinetics of the Brimonidine Tartrate Posterior Segment Delivery System … | Phase1 | Vitrectomy | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01252147 | Inter-rater and Intra-rater Reliability Study of the Global Eyelash Assessment … | — | Healthy Volunteers | Completed | 2010-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01258309 | Safety and Efficacy of Olopatadine Hydrochloride/Ketorolac Tromethamine Ophthal… | Phase3 | Rhinitis, Allergic, Seasonal | Completed | 2010-12-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01258309 | Safety and Efficacy of Olopatadine Hydrochloride/Ketorolac Tromethamine Ophthal… | Phase3 | Rhinitis, Allergic, Seasonal | Completed | 2010-12-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00534339 | EasyBand GOAL Trial | Na | Morbid Obesity | Withdrawn | 2010-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01252147 | Inter-rater and Intra-rater Reliability Study of the Global Eyelash Assessment … | — | Healthy Volunteers | Completed | 2010-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01252147 | Inter-rater and Intra-rater Reliability Study of the Global Eyelash Assessment … | — | Healthy Volunteers | Completed | 2010-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00534339 | EasyBand GOAL Trial | Na | Morbid Obesity | Withdrawn | 2010-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01258309 | Safety and Efficacy of Olopatadine Hydrochloride/Ketorolac Tromethamine Ophthal… | Phase3 | Rhinitis, Allergic, Seasonal | Completed | 2010-12-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01229410 | Pharmacokinetics of the Brimonidine Tartrate Posterior Segment Delivery System … | Phase1 | Vitrectomy | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01252147 | Inter-rater and Intra-rater Reliability Study of the Global Eyelash Assessment … | — | Healthy Volunteers | Completed | 2010-12-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00534339 | EasyBand GOAL Trial | Na | Morbid Obesity | Withdrawn | 2010-12-01 | 2016-02-01 | ClinicalTrials.gov |
| NCT01258309 | Safety and Efficacy of Olopatadine Hydrochloride/Ketorolac Tromethamine Ophthal… | Phase3 | Rhinitis, Allergic, Seasonal | Completed | 2010-12-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01229410 | Pharmacokinetics of the Brimonidine Tartrate Posterior Segment Delivery System … | Phase1 | Vitrectomy | Completed | 2010-12-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01148225 | A Study of the Long-term Safety and Efficacy of Adalimumab in Subjects With Int… | Phase3 | Uveitis | Completed | 2010-11-23 | 2018-05-21 | ClinicalTrials.gov |
| NCT01148225 | A Study of the Long-term Safety and Efficacy of Adalimumab in Subjects With Int… | Phase3 | Uveitis | Completed | 2010-11-23 | 2018-05-21 | ClinicalTrials.gov |
| NCT01148225 | A Study of the Long-term Safety and Efficacy of Adalimumab in Subjects With Int… | Phase3 | Uveitis | Completed | 2010-11-23 | 2018-05-21 | ClinicalTrials.gov |
| NCT01148225 | A Study of the Long-term Safety and Efficacy of Adalimumab in Subjects With Int… | Phase3 | Uveitis | Completed | 2010-11-23 | 2018-05-21 | ClinicalTrials.gov |
| NCT01623479 | An Observational Study of Patients Treated With Bimatoprost 0.03% (Latisse®) fo… | — | Eyelash Hypotrichosis | Completed | 2010-11-19 | 2011-09-01 | ClinicalTrials.gov |
| NCT01623479 | An Observational Study of Patients Treated With Bimatoprost 0.03% (Latisse®) fo… | — | Eyelash Hypotrichosis | Completed | 2010-11-19 | 2011-09-01 | ClinicalTrials.gov |
| NCT01623479 | An Observational Study of Patients Treated With Bimatoprost 0.03% (Latisse®) fo… | — | Eyelash Hypotrichosis | Completed | 2010-11-19 | 2011-09-01 | ClinicalTrials.gov |
| NCT01623479 | An Observational Study of Patients Treated With Bimatoprost 0.03% (Latisse®) fo… | — | Eyelash Hypotrichosis | Completed | 2010-11-19 | 2011-09-01 | ClinicalTrials.gov |
| NCT01323829 | EMG Guided Botulinum Toxin Type A Injections for Refractory High Tone Pelvic Fl… | Na | High Tone Pelvic Floor Dysfunction | Completed | 2010-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01319773 | Study of Two Formulations of Cyclosporine Ophthalmic Emulsion in Healthy Volunt… | Phase1 | Dry Eye Syndromes | Completed | 2010-11-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01298648 | Special Investigation in Patients With Crohn's Disease (All Patients Investigat… | — | Crohn's Disease | Completed | 2010-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01323829 | EMG Guided Botulinum Toxin Type A Injections for Refractory High Tone Pelvic Fl… | Na | High Tone Pelvic Floor Dysfunction | Completed | 2010-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01156532 | Clinical Effectiveness and Impact on Health-related Quality of Life in Peruvian… | — | Moderate to Severe Psoriasis | Terminated | 2010-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01156532 | Clinical Effectiveness and Impact on Health-related Quality of Life in Peruvian… | — | Moderate to Severe Psoriasis | Terminated | 2010-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01298648 | Special Investigation in Patients With Crohn's Disease (All Patients Investigat… | — | Crohn's Disease | Completed | 2010-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01262339 | BTX-A Treatment for Palmar Hyperhidrosis | Phase2 | Primary Focal Hyperhidrosis of the Hands | Terminated | 2010-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01323829 | EMG Guided Botulinum Toxin Type A Injections for Refractory High Tone Pelvic Fl… | Na | High Tone Pelvic Floor Dysfunction | Completed | 2010-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01319773 | Study of Two Formulations of Cyclosporine Ophthalmic Emulsion in Healthy Volunt… | Phase1 | Dry Eye Syndromes | Completed | 2010-11-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01319773 | Study of Two Formulations of Cyclosporine Ophthalmic Emulsion in Healthy Volunt… | Phase1 | Dry Eye Syndromes | Completed | 2010-11-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01156532 | Clinical Effectiveness and Impact on Health-related Quality of Life in Peruvian… | — | Moderate to Severe Psoriasis | Terminated | 2010-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01262339 | BTX-A Treatment for Palmar Hyperhidrosis | Phase2 | Primary Focal Hyperhidrosis of the Hands | Terminated | 2010-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01262339 | BTX-A Treatment for Palmar Hyperhidrosis | Phase2 | Primary Focal Hyperhidrosis of the Hands | Terminated | 2010-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01216943 | Safety and Efficacy of Triple Combination Therapy in Patients With Glaucoma or … | Phase3 | Glaucoma | Completed | 2010-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01298648 | Special Investigation in Patients With Crohn's Disease (All Patients Investigat… | — | Crohn's Disease | Completed | 2010-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01262339 | BTX-A Treatment for Palmar Hyperhidrosis | Phase2 | Primary Focal Hyperhidrosis of the Hands | Terminated | 2010-11-01 | 2012-11-01 | ClinicalTrials.gov |
| NCT01216943 | Safety and Efficacy of Triple Combination Therapy in Patients With Glaucoma or … | Phase3 | Glaucoma | Completed | 2010-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01216943 | Safety and Efficacy of Triple Combination Therapy in Patients With Glaucoma or … | Phase3 | Glaucoma | Completed | 2010-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01298648 | Special Investigation in Patients With Crohn's Disease (All Patients Investigat… | — | Crohn's Disease | Completed | 2010-11-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01323829 | EMG Guided Botulinum Toxin Type A Injections for Refractory High Tone Pelvic Fl… | Na | High Tone Pelvic Floor Dysfunction | Completed | 2010-11-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01319773 | Study of Two Formulations of Cyclosporine Ophthalmic Emulsion in Healthy Volunt… | Phase1 | Dry Eye Syndromes | Completed | 2010-11-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT01156532 | Clinical Effectiveness and Impact on Health-related Quality of Life in Peruvian… | — | Moderate to Severe Psoriasis | Terminated | 2010-11-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01216943 | Safety and Efficacy of Triple Combination Therapy in Patients With Glaucoma or … | Phase3 | Glaucoma | Completed | 2010-11-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01329380 | Special Investigation in Patients With Ankylosing Spondylitis (All Patients Inv… | — | Ankylosing Spondylitis | Completed | 2010-10-27 | 2017-12-28 | ClinicalTrials.gov |
| NCT01329380 | Special Investigation in Patients With Ankylosing Spondylitis (All Patients Inv… | — | Ankylosing Spondylitis | Completed | 2010-10-27 | 2017-12-28 | ClinicalTrials.gov |
| NCT01329380 | Special Investigation in Patients With Ankylosing Spondylitis (All Patients Inv… | — | Ankylosing Spondylitis | Completed | 2010-10-27 | 2017-12-28 | ClinicalTrials.gov |
| NCT01329380 | Special Investigation in Patients With Ankylosing Spondylitis (All Patients Inv… | — | Ankylosing Spondylitis | Completed | 2010-10-27 | 2017-12-28 | ClinicalTrials.gov |
| NCT01265823 | Immediate Response With Adalimumab and Its Impact on Quality of Life and Other … | Phase4 | Psoriasis | Completed | 2010-10-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01221298 | A Pilot Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiv… | Phase2 | Hepatitis C | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01221298 | A Pilot Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiv… | Phase2 | Hepatitis C | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01265823 | Immediate Response With Adalimumab and Its Impact on Quality of Life and Other … | Phase4 | Psoriasis | Completed | 2010-10-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01243671 | A Study of Adalimumab in Japanese Subjects With Intestinal Behçet's Disease | Phase3 | Intestinal Behçet's Disease | Completed | 2010-10-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01224782 | Evaluation of Treatment With Zemplar Capsules in the Therapy of Secondary Hyper… | — | Chronic Kidney Disease | Completed | 2010-10-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01265823 | Immediate Response With Adalimumab and Its Impact on Quality of Life and Other … | Phase4 | Psoriasis | Completed | 2010-10-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01243671 | A Study of Adalimumab in Japanese Subjects With Intestinal Behçet's Disease | Phase3 | Intestinal Behçet's Disease | Completed | 2010-10-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01224782 | Evaluation of Treatment With Zemplar Capsules in the Therapy of Secondary Hyper… | — | Chronic Kidney Disease | Completed | 2010-10-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01215786 | Safety and Pharmacodynamics Study of AGN-207281 Ophthalmic Solutions Compared W… | Phase1 | Glaucoma, Open-Angle | Completed | 2010-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01215786 | Safety and Pharmacodynamics Study of AGN-207281 Ophthalmic Solutions Compared W… | Phase1 | Glaucoma, Open-Angle | Completed | 2010-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01189279 | Safety and Pharmacokinetics Study of New Formulation of Bimatoprost in Patients… | Phase1 | Alopecia | Completed | 2010-10-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01177098 | Safety and Efficacy of a New Formulation of Bimatoprost/Timolol Ophthalmic Solu… | Phase3 | Glaucoma | Completed | 2010-10-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01221298 | A Pilot Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiv… | Phase2 | Hepatitis C | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01189279 | Safety and Pharmacokinetics Study of New Formulation of Bimatoprost in Patients… | Phase1 | Alopecia | Completed | 2010-10-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01177098 | Safety and Efficacy of a New Formulation of Bimatoprost/Timolol Ophthalmic Solu… | Phase3 | Glaucoma | Completed | 2010-10-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01189279 | Safety and Pharmacokinetics Study of New Formulation of Bimatoprost in Patients… | Phase1 | Alopecia | Completed | 2010-10-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01215786 | Safety and Pharmacodynamics Study of AGN-207281 Ophthalmic Solutions Compared W… | Phase1 | Glaucoma, Open-Angle | Completed | 2010-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01224782 | Evaluation of Treatment With Zemplar Capsules in the Therapy of Secondary Hyper… | — | Chronic Kidney Disease | Completed | 2010-10-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01243671 | A Study of Adalimumab in Japanese Subjects With Intestinal Behçet's Disease | Phase3 | Intestinal Behçet's Disease | Completed | 2010-10-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01221298 | A Pilot Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiv… | Phase2 | Hepatitis C | Completed | 2010-10-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT01177098 | Safety and Efficacy of a New Formulation of Bimatoprost/Timolol Ophthalmic Solu… | Phase3 | Glaucoma | Completed | 2010-10-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01189279 | Safety and Pharmacokinetics Study of New Formulation of Bimatoprost in Patients… | Phase1 | Alopecia | Completed | 2010-10-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01177098 | Safety and Efficacy of a New Formulation of Bimatoprost/Timolol Ophthalmic Solu… | Phase3 | Glaucoma | Completed | 2010-10-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01215786 | Safety and Pharmacodynamics Study of AGN-207281 Ophthalmic Solutions Compared W… | Phase1 | Glaucoma, Open-Angle | Completed | 2010-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01224782 | Evaluation of Treatment With Zemplar Capsules in the Therapy of Secondary Hyper… | — | Chronic Kidney Disease | Completed | 2010-10-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01243671 | A Study of Adalimumab in Japanese Subjects With Intestinal Behçet's Disease | Phase3 | Intestinal Behçet's Disease | Completed | 2010-10-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01265823 | Immediate Response With Adalimumab and Its Impact on Quality of Life and Other … | Phase4 | Psoriasis | Completed | 2010-10-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01157364 | Safety and Efficacy of a New Ophthalmic Formulation of Bimatoprost in Patients … | Phase1 | Open-Angle Glaucoma | Completed | 2010-09-23 | 2016-08-09 | ClinicalTrials.gov |
| NCT01157364 | Safety and Efficacy of a New Ophthalmic Formulation of Bimatoprost in Patients … | Phase1 | Open-Angle Glaucoma | Completed | 2010-09-23 | 2016-08-09 | ClinicalTrials.gov |
| NCT01157364 | Safety and Efficacy of a New Ophthalmic Formulation of Bimatoprost in Patients … | Phase1 | Open-Angle Glaucoma | Completed | 2010-09-23 | 2016-08-09 | ClinicalTrials.gov |
| NCT01157364 | Safety and Efficacy of a New Ophthalmic Formulation of Bimatoprost in Patients … | Phase1 | Open-Angle Glaucoma | Completed | 2010-09-23 | 2016-08-09 | ClinicalTrials.gov |
| NCT01162421 | A Canadian Study to Evaluate Early Use of Adalimumab After Methotrexate Failure… | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01189760 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's… | Phase3 | Facial Rhytides | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01225302 | A Study of Linifanib (ABT-869) in Combination With Carboplatin/Paclitaxel in Ja… | Phase1 | Non-Small Cell Lung Cancer | Completed | 2010-09-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01189760 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's… | Phase3 | Facial Rhytides | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01185288 | A Study to Determine the Effect of Methotrexate (MTX) Dose on Clinical Outcome … | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01166282 | A Study of the Efficacy and Safety of Adalimumab in Pediatric Subjects With Ent… | Phase3 | Enthesitis Related Arthritis (ERA) | Completed | 2010-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01185288 | A Study to Determine the Effect of Methotrexate (MTX) Dose on Clinical Outcome … | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01225302 | A Study of Linifanib (ABT-869) in Combination With Carboplatin/Paclitaxel in Ja… | Phase1 | Non-Small Cell Lung Cancer | Completed | 2010-09-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01162421 | A Canadian Study to Evaluate Early Use of Adalimumab After Methotrexate Failure… | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01225302 | A Study of Linifanib (ABT-869) in Combination With Carboplatin/Paclitaxel in Ja… | Phase1 | Non-Small Cell Lung Cancer | Completed | 2010-09-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01166282 | A Study of the Efficacy and Safety of Adalimumab in Pediatric Subjects With Ent… | Phase3 | Enthesitis Related Arthritis (ERA) | Completed | 2010-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01271452 | Safety and Efficacy of Two Types of Botulinum Toxin Type A For the Treatment of… | Phase4 | Glabellar Lines | Completed | 2010-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01166282 | A Study of the Efficacy and Safety of Adalimumab in Pediatric Subjects With Ent… | Phase3 | Enthesitis Related Arthritis (ERA) | Completed | 2010-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01202565 | Effectiveness of Adalimumab (HUMIRA®) in the Treatment of Scalp and Nail Affect… | — | Moderate to Severe Plaque Psoriasis | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01271452 | Safety and Efficacy of Two Types of Botulinum Toxin Type A For the Treatment of… | Phase4 | Glabellar Lines | Completed | 2010-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01202565 | Effectiveness of Adalimumab (HUMIRA®) in the Treatment of Scalp and Nail Affect… | — | Moderate to Severe Plaque Psoriasis | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01162421 | A Canadian Study to Evaluate Early Use of Adalimumab After Methotrexate Failure… | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01225302 | A Study of Linifanib (ABT-869) in Combination With Carboplatin/Paclitaxel in Ja… | Phase1 | Non-Small Cell Lung Cancer | Completed | 2010-09-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01166282 | A Study of the Efficacy and Safety of Adalimumab in Pediatric Subjects With Ent… | Phase3 | Enthesitis Related Arthritis (ERA) | Completed | 2010-09-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01271452 | Safety and Efficacy of Two Types of Botulinum Toxin Type A For the Treatment of… | Phase4 | Glabellar Lines | Completed | 2010-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01189760 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's… | Phase3 | Facial Rhytides | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01185288 | A Study to Determine the Effect of Methotrexate (MTX) Dose on Clinical Outcome … | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01202565 | Effectiveness of Adalimumab (HUMIRA®) in the Treatment of Scalp and Nail Affect… | — | Moderate to Severe Plaque Psoriasis | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01271452 | Safety and Efficacy of Two Types of Botulinum Toxin Type A For the Treatment of… | Phase4 | Glabellar Lines | Completed | 2010-09-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01189760 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Crow's… | Phase3 | Facial Rhytides | Completed | 2010-09-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01185288 | A Study to Determine the Effect of Methotrexate (MTX) Dose on Clinical Outcome … | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01202565 | Effectiveness of Adalimumab (HUMIRA®) in the Treatment of Scalp and Nail Affect… | — | Moderate to Severe Plaque Psoriasis | Completed | 2010-09-01 | 2013-07-01 | ClinicalTrials.gov |
| NCT01162421 | A Canadian Study to Evaluate Early Use of Adalimumab After Methotrexate Failure… | Phase4 | Rheumatoid Arthritis | Completed | 2010-09-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT01193231 | A 6 Month Study to Evaluate the Safety, Analgesic Efficacy of ACUVAIL™ (Ketorol… | — | Must be PRK Candidate | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01191723 | QT Intervals Study to Compare the Acute Effects of Orally Inhaled Dihydroergota… | Phase1 | Healthy | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01225341 | Botulinum Toxin A for Herpes Labialis | Na | Herpes Labialis | Terminated | 2010-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01087151 | A Study of ABT-263 in Combination With Dose-Intensive Rituximab, or Dose-Intens… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2010-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01225341 | Botulinum Toxin A for Herpes Labialis | Na | Herpes Labialis | Terminated | 2010-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01197495 | Safety and Effectiveness of Juvederm(R) Ultra XC Injectable Gel for Lip Augment… | Na | Lip Augmentation | Completed | 2010-08-01 | 2015-06-15 | ClinicalTrials.gov |
| NCT01193231 | A 6 Month Study to Evaluate the Safety, Analgesic Efficacy of ACUVAIL™ (Ketorol… | — | Must be PRK Candidate | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01191723 | QT Intervals Study to Compare the Acute Effects of Orally Inhaled Dihydroergota… | Phase1 | Healthy | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01122511 | Safety and Efficacy of Dexamethasone as Adjunctive Therapy to Ranibizumab in Su… | Phase2 | Subfoveal Choroidal Neovascularization | Terminated | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01087151 | A Study of ABT-263 in Combination With Dose-Intensive Rituximab, or Dose-Intens… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2010-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01176773 | Safety and Effectiveness of Juvéderm® Ultra Lip Injectable Gel for Lip Enhancem… | Na | Lip Enhancement | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01122511 | Safety and Efficacy of Dexamethasone as Adjunctive Therapy to Ranibizumab in Su… | Phase2 | Subfoveal Choroidal Neovascularization | Terminated | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01087151 | A Study of ABT-263 in Combination With Dose-Intensive Rituximab, or Dose-Intens… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2010-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01191723 | QT Intervals Study to Compare the Acute Effects of Orally Inhaled Dihydroergota… | Phase1 | Healthy | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01087151 | A Study of ABT-263 in Combination With Dose-Intensive Rituximab, or Dose-Intens… | Phase2 | Chronic Lymphocytic Leukemia | Completed | 2010-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01122511 | Safety and Efficacy of Dexamethasone as Adjunctive Therapy to Ranibizumab in Su… | Phase2 | Subfoveal Choroidal Neovascularization | Terminated | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01193231 | A 6 Month Study to Evaluate the Safety, Analgesic Efficacy of ACUVAIL™ (Ketorol… | — | Must be PRK Candidate | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01197495 | Safety and Effectiveness of Juvederm(R) Ultra XC Injectable Gel for Lip Augment… | Na | Lip Augmentation | Completed | 2010-08-01 | 2015-06-15 | ClinicalTrials.gov |
| NCT01191723 | QT Intervals Study to Compare the Acute Effects of Orally Inhaled Dihydroergota… | Phase1 | Healthy | Completed | 2010-08-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01193231 | A 6 Month Study to Evaluate the Safety, Analgesic Efficacy of ACUVAIL™ (Ketorol… | — | Must be PRK Candidate | Completed | 2010-08-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01197495 | Safety and Effectiveness of Juvederm(R) Ultra XC Injectable Gel for Lip Augment… | Na | Lip Augmentation | Completed | 2010-08-01 | 2015-06-15 | ClinicalTrials.gov |
| NCT01225341 | Botulinum Toxin A for Herpes Labialis | Na | Herpes Labialis | Terminated | 2010-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01176773 | Safety and Effectiveness of Juvéderm® Ultra Lip Injectable Gel for Lip Enhancem… | Na | Lip Enhancement | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01225341 | Botulinum Toxin A for Herpes Labialis | Na | Herpes Labialis | Terminated | 2010-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01176773 | Safety and Effectiveness of Juvéderm® Ultra Lip Injectable Gel for Lip Enhancem… | Na | Lip Enhancement | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01122511 | Safety and Efficacy of Dexamethasone as Adjunctive Therapy to Ranibizumab in Su… | Phase2 | Subfoveal Choroidal Neovascularization | Terminated | 2010-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01176773 | Safety and Effectiveness of Juvéderm® Ultra Lip Injectable Gel for Lip Enhancem… | Na | Lip Enhancement | Completed | 2010-08-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01197495 | Safety and Effectiveness of Juvederm(R) Ultra XC Injectable Gel for Lip Augment… | Na | Lip Augmentation | Completed | 2010-08-01 | 2015-06-15 | ClinicalTrials.gov |
| NCT01468558 | Pharmacokinetics & Tolerability Study of MAP0004 Co-administered With Ketoconaz… | Phase1 | Healthy | Completed | 2010-07-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01159743 | A Comparison of Body Fat Distribution in HIV-1 Infected Patients Receiving, Sin… | — | HIV Infection | Completed | 2010-07-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01468558 | Pharmacokinetics & Tolerability Study of MAP0004 Co-administered With Ketoconaz… | Phase1 | Healthy | Completed | 2010-07-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01468558 | Pharmacokinetics & Tolerability Study of MAP0004 Co-administered With Ketoconaz… | Phase1 | Healthy | Completed | 2010-07-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01468558 | Pharmacokinetics & Tolerability Study of MAP0004 Co-administered With Ketoconaz… | Phase1 | Healthy | Completed | 2010-07-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01159743 | A Comparison of Body Fat Distribution in HIV-1 Infected Patients Receiving, Sin… | — | HIV Infection | Completed | 2010-07-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01159743 | A Comparison of Body Fat Distribution in HIV-1 Infected Patients Receiving, Sin… | — | HIV Infection | Completed | 2010-07-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01159743 | A Comparison of Body Fat Distribution in HIV-1 Infected Patients Receiving, Sin… | — | HIV Infection | Completed | 2010-07-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01129531 | A Study of the Safety and Efficacy of AGN-214868 in Patients With Postherpetic … | Phase2 | Neuralgia, Postherpetic | Completed | 2010-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01134315 | Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to… | — | Secondary Hyperparathyroidism | Terminated | 2010-06-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01134315 | Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to… | — | Secondary Hyperparathyroidism | Terminated | 2010-06-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01129531 | A Study of the Safety and Efficacy of AGN-214868 in Patients With Postherpetic … | Phase2 | Neuralgia, Postherpetic | Completed | 2010-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01071096 | Calcitonin Gene-related Peptide Levels in Chronic Migraine | Phase4 | Chronic Migraine | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01071096 | Calcitonin Gene-related Peptide Levels in Chronic Migraine | Phase4 | Chronic Migraine | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01109056 | Safety and Efficacy of Cyclosporine Ophthalmic Emulsion in Patients With Primar… | Phase2 | Pterygium | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01109056 | Safety and Efficacy of Cyclosporine Ophthalmic Emulsion in Patients With Primar… | Phase2 | Pterygium | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01199224 | To Determine the Food Effect and Bioavailability of Three Formulations of Velip… | Phase1 | Solid Tumors | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01110499 | Safety and Efficacy of AGN-210961 Ophthalmic Solution Compared With Bimatoprost… | Phase2 | Ocular Hypertension | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01134315 | Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to… | — | Secondary Hyperparathyroidism | Terminated | 2010-06-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01243567 | Safety and Efficacy of Bimatoprost/Timolol Fixed Combination Versus Latanoprost… | Phase4 | Glaucoma, Open-Angle | Completed | 2010-06-01 | 2012-02-14 | ClinicalTrials.gov |
| NCT01199224 | To Determine the Food Effect and Bioavailability of Three Formulations of Velip… | Phase1 | Solid Tumors | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01109056 | Safety and Efficacy of Cyclosporine Ophthalmic Emulsion in Patients With Primar… | Phase2 | Pterygium | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01110499 | Safety and Efficacy of AGN-210961 Ophthalmic Solution Compared With Bimatoprost… | Phase2 | Ocular Hypertension | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01023841 | Safety and Efficacy of Bimatoprost Solution in Treating Eyelash Loss or Hypotri… | Phase4 | Eyelash Hypotrichosis | Completed | 2010-06-01 | 2012-11-30 | ClinicalTrials.gov |
| NCT01071096 | Calcitonin Gene-related Peptide Levels in Chronic Migraine | Phase4 | Chronic Migraine | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01243567 | Safety and Efficacy of Bimatoprost/Timolol Fixed Combination Versus Latanoprost… | Phase4 | Glaucoma, Open-Angle | Completed | 2010-06-01 | 2012-02-14 | ClinicalTrials.gov |
| NCT01023841 | Safety and Efficacy of Bimatoprost Solution in Treating Eyelash Loss or Hypotri… | Phase4 | Eyelash Hypotrichosis | Completed | 2010-06-01 | 2012-11-30 | ClinicalTrials.gov |
| NCT01243567 | Safety and Efficacy of Bimatoprost/Timolol Fixed Combination Versus Latanoprost… | Phase4 | Glaucoma, Open-Angle | Completed | 2010-06-01 | 2012-02-14 | ClinicalTrials.gov |
| NCT01129531 | A Study of the Safety and Efficacy of AGN-214868 in Patients With Postherpetic … | Phase2 | Neuralgia, Postherpetic | Completed | 2010-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01243567 | Safety and Efficacy of Bimatoprost/Timolol Fixed Combination Versus Latanoprost… | Phase4 | Glaucoma, Open-Angle | Completed | 2010-06-01 | 2012-02-14 | ClinicalTrials.gov |
| NCT01199224 | To Determine the Food Effect and Bioavailability of Three Formulations of Velip… | Phase1 | Solid Tumors | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01071096 | Calcitonin Gene-related Peptide Levels in Chronic Migraine | Phase4 | Chronic Migraine | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01023841 | Safety and Efficacy of Bimatoprost Solution in Treating Eyelash Loss or Hypotri… | Phase4 | Eyelash Hypotrichosis | Completed | 2010-06-01 | 2012-11-30 | ClinicalTrials.gov |
| NCT01134315 | Study to Evaluate Safety of Vitamin D Receptor Activators in Patients Ages 0 to… | — | Secondary Hyperparathyroidism | Terminated | 2010-06-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01129531 | A Study of the Safety and Efficacy of AGN-214868 in Patients With Postherpetic … | Phase2 | Neuralgia, Postherpetic | Completed | 2010-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01110499 | Safety and Efficacy of AGN-210961 Ophthalmic Solution Compared With Bimatoprost… | Phase2 | Ocular Hypertension | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01109056 | Safety and Efficacy of Cyclosporine Ophthalmic Emulsion in Patients With Primar… | Phase2 | Pterygium | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01199224 | To Determine the Food Effect and Bioavailability of Three Formulations of Velip… | Phase1 | Solid Tumors | Completed | 2010-06-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01023841 | Safety and Efficacy of Bimatoprost Solution in Treating Eyelash Loss or Hypotri… | Phase4 | Eyelash Hypotrichosis | Completed | 2010-06-01 | 2012-11-30 | ClinicalTrials.gov |
| NCT01110499 | Safety and Efficacy of AGN-210961 Ophthalmic Solution Compared With Bimatoprost… | Phase2 | Ocular Hypertension | Completed | 2010-06-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01177358 | Botox in the Healing of Surgical Wounds of the Neck | Phase2 | Scar | Completed | 2010-05-31 | 2016-05-05 | ClinicalTrials.gov |
| NCT01177358 | Botox in the Healing of Surgical Wounds of the Neck | Phase2 | Scar | Completed | 2010-05-31 | 2016-05-05 | ClinicalTrials.gov |
| NCT01177358 | Botox in the Healing of Surgical Wounds of the Neck | Phase2 | Scar | Completed | 2010-05-31 | 2016-05-05 | ClinicalTrials.gov |
| NCT01177358 | Botox in the Healing of Surgical Wounds of the Neck | Phase2 | Scar | Completed | 2010-05-31 | 2016-05-05 | ClinicalTrials.gov |
| NCT01628601 | GANfort® in Patients With Primary Open Angle Glaucoma or Ocular Hypertension Wh… | — | Glaucoma, Open-Angle | Completed | 2010-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01257906 | Bioequivalence Study Comparing Clindamycin Phosphate (1.2%) and Tretinoin (0.02… | Na | MILD TO SEVERE ACNE VULGARIS | Completed | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01163617 | The Usability and Injection Time of the Physiolis Syringe and Autoinjector in R… | Phase2 | Rheumatoid Arthritis | Completed | 2010-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01130298 | An Open-Label Study of Serum Testosterone Levels in Non-dosed Females After Sec… | Phase1 | Healthy | Completed | 2010-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01628601 | GANfort® in Patients With Primary Open Angle Glaucoma or Ocular Hypertension Wh… | — | Glaucoma, Open-Angle | Completed | 2010-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01628601 | GANfort® in Patients With Primary Open Angle Glaucoma or Ocular Hypertension Wh… | — | Glaucoma, Open-Angle | Completed | 2010-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01121133 | A Study to Assess the Effect of Rifampin on the Metabolism of Navitoclax | Phase1 | Lymphoma, Including Chronic Lymphocytic Leukemia | Completed | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01161771 | Effects of Cataract Extraction Surgery and Limbal Relaxing Incision on Corneal … | — | Dry Eye | Completed | 2010-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01257906 | Bioequivalence Study Comparing Clindamycin Phosphate (1.2%) and Tretinoin (0.02… | Na | MILD TO SEVERE ACNE VULGARIS | Completed | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01161771 | Effects of Cataract Extraction Surgery and Limbal Relaxing Incision on Corneal … | — | Dry Eye | Completed | 2010-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01099774 | Safety and Efficacy of Different Formulations of Bimatoprost Ophthalmic Solutio… | Phase3 | Glaucoma | Completed | 2010-05-01 | 2011-04-29 | ClinicalTrials.gov |
| NCT01064401 | Efficacy and Safety of BIIB019 (Daclizumab High Yield Process) Versus Interfero… | Phase3 | Relapsing-Remitting Multiple Sclerosis | Completed | 2010-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01121133 | A Study to Assess the Effect of Rifampin on the Metabolism of Navitoclax | Phase1 | Lymphoma, Including Chronic Lymphocytic Leukemia | Completed | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01130298 | An Open-Label Study of Serum Testosterone Levels in Non-dosed Females After Sec… | Phase1 | Healthy | Completed | 2010-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01133548 | Pharmacokinetic and Comparative Bioavailability Study of Testosterone Absorptio… | Phase1 | Hypogonadism | Completed | 2010-05-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01161771 | Effects of Cataract Extraction Surgery and Limbal Relaxing Incision on Corneal … | — | Dry Eye | Completed | 2010-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01161771 | Effects of Cataract Extraction Surgery and Limbal Relaxing Incision on Corneal … | — | Dry Eye | Completed | 2010-05-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01121133 | A Study to Assess the Effect of Rifampin on the Metabolism of Navitoclax | Phase1 | Lymphoma, Including Chronic Lymphocytic Leukemia | Completed | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01257906 | Bioequivalence Study Comparing Clindamycin Phosphate (1.2%) and Tretinoin (0.02… | Na | MILD TO SEVERE ACNE VULGARIS | Completed | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01064401 | Efficacy and Safety of BIIB019 (Daclizumab High Yield Process) Versus Interfero… | Phase3 | Relapsing-Remitting Multiple Sclerosis | Completed | 2010-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01163617 | The Usability and Injection Time of the Physiolis Syringe and Autoinjector in R… | Phase2 | Rheumatoid Arthritis | Completed | 2010-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01130298 | An Open-Label Study of Serum Testosterone Levels in Non-dosed Females After Sec… | Phase1 | Healthy | Completed | 2010-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01099774 | Safety and Efficacy of Different Formulations of Bimatoprost Ophthalmic Solutio… | Phase3 | Glaucoma | Completed | 2010-05-01 | 2011-04-29 | ClinicalTrials.gov |
| NCT01130298 | An Open-Label Study of Serum Testosterone Levels in Non-dosed Females After Sec… | Phase1 | Healthy | Completed | 2010-05-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01163617 | The Usability and Injection Time of the Physiolis Syringe and Autoinjector in R… | Phase2 | Rheumatoid Arthritis | Completed | 2010-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01133548 | Pharmacokinetic and Comparative Bioavailability Study of Testosterone Absorptio… | Phase1 | Hypogonadism | Completed | 2010-05-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01628601 | GANfort® in Patients With Primary Open Angle Glaucoma or Ocular Hypertension Wh… | — | Glaucoma, Open-Angle | Completed | 2010-05-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01099774 | Safety and Efficacy of Different Formulations of Bimatoprost Ophthalmic Solutio… | Phase3 | Glaucoma | Completed | 2010-05-01 | 2011-04-29 | ClinicalTrials.gov |
| NCT01121133 | A Study to Assess the Effect of Rifampin on the Metabolism of Navitoclax | Phase1 | Lymphoma, Including Chronic Lymphocytic Leukemia | Completed | 2010-05-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT01163617 | The Usability and Injection Time of the Physiolis Syringe and Autoinjector in R… | Phase2 | Rheumatoid Arthritis | Completed | 2010-05-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01099774 | Safety and Efficacy of Different Formulations of Bimatoprost Ophthalmic Solutio… | Phase3 | Glaucoma | Completed | 2010-05-01 | 2011-04-29 | ClinicalTrials.gov |
| NCT01133548 | Pharmacokinetic and Comparative Bioavailability Study of Testosterone Absorptio… | Phase1 | Hypogonadism | Completed | 2010-05-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01064401 | Efficacy and Safety of BIIB019 (Daclizumab High Yield Process) Versus Interfero… | Phase3 | Relapsing-Remitting Multiple Sclerosis | Completed | 2010-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01064401 | Efficacy and Safety of BIIB019 (Daclizumab High Yield Process) Versus Interfero… | Phase3 | Relapsing-Remitting Multiple Sclerosis | Completed | 2010-05-01 | 2014-07-01 | ClinicalTrials.gov |
| NCT01257906 | Bioequivalence Study Comparing Clindamycin Phosphate (1.2%) and Tretinoin (0.02… | Na | MILD TO SEVERE ACNE VULGARIS | Completed | 2010-05-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT01133548 | Pharmacokinetic and Comparative Bioavailability Study of Testosterone Absorptio… | Phase1 | Hypogonadism | Completed | 2010-05-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT02061683 | A Study of Bimatoprost in the Treatment of Primary Open Angle Glaucoma and Ocul… | Phase4 | Glaucoma, Open-Angle | Completed | 2010-04-19 | 2011-06-24 | ClinicalTrials.gov |
| NCT02061683 | A Study of Bimatoprost in the Treatment of Primary Open Angle Glaucoma and Ocul… | Phase4 | Glaucoma, Open-Angle | Completed | 2010-04-19 | 2011-06-24 | ClinicalTrials.gov |
| NCT02061683 | A Study of Bimatoprost in the Treatment of Primary Open Angle Glaucoma and Ocul… | Phase4 | Glaucoma, Open-Angle | Completed | 2010-04-19 | 2011-06-24 | ClinicalTrials.gov |
| NCT02061683 | A Study of Bimatoprost in the Treatment of Primary Open Angle Glaucoma and Ocul… | Phase4 | Glaucoma, Open-Angle | Completed | 2010-04-19 | 2011-06-24 | ClinicalTrials.gov |
| NCT01162668 | Assessment of Outcomes Following Bariatric Surgery for Mississippi State Employ… | — | Obesity | Completed | 2010-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01422161 | Study of Botulinum Toxin and Recovery of Hand Function After Stroke | Phase3 | Stroke With Hemiparesis | Completed | 2010-04-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01110473 | ABT-348 as Monotherapy and in Combination With Azacitidine to Treat Advanced He… | Phase1 | Acute Lymphoblastic Leukemia | Completed | 2010-04-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01484990 | A Pharmacokinetic Study of Levodopa and Carbidopa Intestinal Gel in Subjects Wi… | Phase1 | Parkinson Disease | Completed | 2010-04-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01110473 | ABT-348 as Monotherapy and in Combination With Azacitidine to Treat Advanced He… | Phase1 | Acute Lymphoblastic Leukemia | Completed | 2010-04-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01422161 | Study of Botulinum Toxin and Recovery of Hand Function After Stroke | Phase3 | Stroke With Hemiparesis | Completed | 2010-04-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01162668 | Assessment of Outcomes Following Bariatric Surgery for Mississippi State Employ… | — | Obesity | Completed | 2010-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01162668 | Assessment of Outcomes Following Bariatric Surgery for Mississippi State Employ… | — | Obesity | Completed | 2010-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01484990 | A Pharmacokinetic Study of Levodopa and Carbidopa Intestinal Gel in Subjects Wi… | Phase1 | Parkinson Disease | Completed | 2010-04-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01422161 | Study of Botulinum Toxin and Recovery of Hand Function After Stroke | Phase3 | Stroke With Hemiparesis | Completed | 2010-04-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01110473 | ABT-348 as Monotherapy and in Combination With Azacitidine to Treat Advanced He… | Phase1 | Acute Lymphoblastic Leukemia | Completed | 2010-04-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01484990 | A Pharmacokinetic Study of Levodopa and Carbidopa Intestinal Gel in Subjects Wi… | Phase1 | Parkinson Disease | Completed | 2010-04-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01162668 | Assessment of Outcomes Following Bariatric Surgery for Mississippi State Employ… | — | Obesity | Completed | 2010-04-01 | 2014-06-01 | ClinicalTrials.gov |
| NCT01422161 | Study of Botulinum Toxin and Recovery of Hand Function After Stroke | Phase3 | Stroke With Hemiparesis | Completed | 2010-04-01 | 2015-10-01 | ClinicalTrials.gov |
| NCT01484990 | A Pharmacokinetic Study of Levodopa and Carbidopa Intestinal Gel in Subjects Wi… | Phase1 | Parkinson Disease | Completed | 2010-04-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01110473 | ABT-348 as Monotherapy and in Combination With Azacitidine to Treat Advanced He… | Phase1 | Acute Lymphoblastic Leukemia | Completed | 2010-04-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01051349 | Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) … | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2010-03-31 | 2016-08-25 | ClinicalTrials.gov |
| NCT01051349 | Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) … | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2010-03-31 | 2016-08-25 | ClinicalTrials.gov |
| NCT01051349 | Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) … | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2010-03-31 | 2016-08-25 | ClinicalTrials.gov |
| NCT01051349 | Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) … | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2010-03-31 | 2016-08-25 | ClinicalTrials.gov |
| NCT01628588 | Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hyperten… | — | Glaucoma, Open-Angle | Completed | 2010-03-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01113957 | A Trial of ABT-888 in Combination With Temozolomide Versus Pegylated Liposomal … | Phase2 | Ovarian Cancer | Completed | 2010-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01064882 | Safety and Efficacy of Bimatoprost Ophthalmic Solution in Increasing Eyelash Pr… | Phase2 | Eyelash Hypotrichosis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01064882 | Safety and Efficacy of Bimatoprost Ophthalmic Solution in Increasing Eyelash Pr… | Phase2 | Eyelash Hypotrichosis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01064882 | Safety and Efficacy of Bimatoprost Ophthalmic Solution in Increasing Eyelash Pr… | Phase2 | Eyelash Hypotrichosis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01086761 | Study of MP0112 Intravitreal Injection in Patients With Wet Age Related Macular… | Phase1 | Wet Age-Related Macular Degeneration | Terminated | 2010-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01089062 | Pharmacodynamic Study to Compare Acute Effects of Dihydroergotamine Mesylate (D… | Phase1 | Healthy | Completed | 2010-03-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01123876 | Evaluating the Safety and Tolerability of the Poly-ADP Ribose (PARP) Inhibitor … | Phase1 | Gastric Cancer | Completed | 2010-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01163292 | Special Investigation (Follow-up Survey of the Study of Adalimumab (D2E7) for P… | — | Rheumatoid Arthritis | Completed | 2010-03-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01628588 | Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hyperten… | — | Glaucoma, Open-Angle | Completed | 2010-03-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01110486 | ABT-348 as Monotherapy or Combination With Carboplatin or Docetaxel to Treat Ad… | Phase1 | Advanced Solid Tumors | Completed | 2010-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01163292 | Special Investigation (Follow-up Survey of the Study of Adalimumab (D2E7) for P… | — | Rheumatoid Arthritis | Completed | 2010-03-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01074008 | A Randomized Study to Evaluate the Safety, Tolerability and Antiviral Activity … | Phase2 | Hepatitis C | Completed | 2010-03-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01074008 | A Randomized Study to Evaluate the Safety, Tolerability and Antiviral Activity … | Phase2 | Hepatitis C | Completed | 2010-03-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01086761 | Study of MP0112 Intravitreal Injection in Patients With Wet Age Related Macular… | Phase1 | Wet Age-Related Macular Degeneration | Terminated | 2010-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01113957 | A Trial of ABT-888 in Combination With Temozolomide Versus Pegylated Liposomal … | Phase2 | Ovarian Cancer | Completed | 2010-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01089062 | Pharmacodynamic Study to Compare Acute Effects of Dihydroergotamine Mesylate (D… | Phase1 | Healthy | Completed | 2010-03-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01095562 | Safety and Efficacy Study for Cognitive Deficits in Adult Subjects With Schizop… | Phase2 | Cognitive Deficits in Schizophrenia | Completed | 2010-03-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01095562 | Safety and Efficacy Study for Cognitive Deficits in Adult Subjects With Schizop… | Phase2 | Cognitive Deficits in Schizophrenia | Completed | 2010-03-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01113957 | A Trial of ABT-888 in Combination With Temozolomide Versus Pegylated Liposomal … | Phase2 | Ovarian Cancer | Completed | 2010-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01064882 | Safety and Efficacy of Bimatoprost Ophthalmic Solution in Increasing Eyelash Pr… | Phase2 | Eyelash Hypotrichosis | Completed | 2010-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT01074008 | A Randomized Study to Evaluate the Safety, Tolerability and Antiviral Activity … | Phase2 | Hepatitis C | Completed | 2010-03-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01110486 | ABT-348 as Monotherapy or Combination With Carboplatin or Docetaxel to Treat Ad… | Phase1 | Advanced Solid Tumors | Completed | 2010-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01123876 | Evaluating the Safety and Tolerability of the Poly-ADP Ribose (PARP) Inhibitor … | Phase1 | Gastric Cancer | Completed | 2010-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01628588 | Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hyperten… | — | Glaucoma, Open-Angle | Completed | 2010-03-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01628588 | Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocular Hyperten… | — | Glaucoma, Open-Angle | Completed | 2010-03-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01086761 | Study of MP0112 Intravitreal Injection in Patients With Wet Age Related Macular… | Phase1 | Wet Age-Related Macular Degeneration | Terminated | 2010-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01089062 | Pharmacodynamic Study to Compare Acute Effects of Dihydroergotamine Mesylate (D… | Phase1 | Healthy | Completed | 2010-03-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01074008 | A Randomized Study to Evaluate the Safety, Tolerability and Antiviral Activity … | Phase2 | Hepatitis C | Completed | 2010-03-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT01089062 | Pharmacodynamic Study to Compare Acute Effects of Dihydroergotamine Mesylate (D… | Phase1 | Healthy | Completed | 2010-03-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01110486 | ABT-348 as Monotherapy or Combination With Carboplatin or Docetaxel to Treat Ad… | Phase1 | Advanced Solid Tumors | Completed | 2010-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01123876 | Evaluating the Safety and Tolerability of the Poly-ADP Ribose (PARP) Inhibitor … | Phase1 | Gastric Cancer | Completed | 2010-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01163292 | Special Investigation (Follow-up Survey of the Study of Adalimumab (D2E7) for P… | — | Rheumatoid Arthritis | Completed | 2010-03-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01123876 | Evaluating the Safety and Tolerability of the Poly-ADP Ribose (PARP) Inhibitor … | Phase1 | Gastric Cancer | Completed | 2010-03-01 | 2015-01-01 | ClinicalTrials.gov |
| NCT01086761 | Study of MP0112 Intravitreal Injection in Patients With Wet Age Related Macular… | Phase1 | Wet Age-Related Macular Degeneration | Terminated | 2010-03-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01095562 | Safety and Efficacy Study for Cognitive Deficits in Adult Subjects With Schizop… | Phase2 | Cognitive Deficits in Schizophrenia | Completed | 2010-03-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01113957 | A Trial of ABT-888 in Combination With Temozolomide Versus Pegylated Liposomal … | Phase2 | Ovarian Cancer | Completed | 2010-03-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01163292 | Special Investigation (Follow-up Survey of the Study of Adalimumab (D2E7) for P… | — | Rheumatoid Arthritis | Completed | 2010-03-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT01095562 | Safety and Efficacy Study for Cognitive Deficits in Adult Subjects With Schizop… | Phase2 | Cognitive Deficits in Schizophrenia | Completed | 2010-03-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01110486 | ABT-348 as Monotherapy or Combination With Carboplatin or Docetaxel to Treat Ad… | Phase1 | Advanced Solid Tumors | Completed | 2010-03-01 | 2013-09-01 | ClinicalTrials.gov |
| NCT01020487 | Safety and Efficacy of Paricalcitol Capsules in Decreasing Serum Parathyroid Ho… | Phase3 | Chronic Kidney Disease Stage 3 and 4 | Completed | 2010-02-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01282411 | Anatomic Outcomes Following Ozurdex Injections | — | Retinal Vein Occlusions | Completed | 2010-02-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01042678 | Study of MP0112 Intravitreal Injection in Patients With Diabetic Macular Edema | Phase1 | Diabetic Macular Edema | Terminated | 2010-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01064830 | Topical Cyclosporine Suspension for the Treatment of Brittle Nails | Phase2 | Brittle Nail Syndrome | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT06585189 | CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS4] | — | Metastatic Non Small Cell Lung Cancer | Completed | 2010-02-01 | 2023-04-13 | ClinicalTrials.gov |
| NCT06607393 | CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS3] | — | Metastatic Nonsmall Cell Lung Cancer | Completed | 2010-02-01 | 2023-06-28 | ClinicalTrials.gov |
| NCT06607601 | CARE Initiative: Real-world Emulation of the PALOMA-2 Trial | — | Metastatic Breast Cancer | Completed | 2010-02-01 | 2023-07-20 | ClinicalTrials.gov |
| NCT01064856 | Study of Adalimumab in Participants With Peripheral Spondyloarthritis (SpA) | Phase3 | Peripheral Spondyloarthritis | Completed | 2010-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01068964 | Safety and Efficacy of Bimatoprost Timolol Ophthalmic Solution in Patients With… | Na | Open-angle Glaucoma | Completed | 2010-02-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01020487 | Safety and Efficacy of Paricalcitol Capsules in Decreasing Serum Parathyroid Ho… | Phase3 | Chronic Kidney Disease Stage 3 and 4 | Completed | 2010-02-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01632423 | A Study of Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocul… | — | Glaucoma, Open-Angle | Completed | 2010-02-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01632423 | A Study of Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocul… | — | Glaucoma, Open-Angle | Completed | 2010-02-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01076192 | Study of Adalimumab (HUMIRA®) in Patients With Moderate to Severe Psoriasis (PS… | — | Moderate-to-severe Chronic Plaque Psoriasis | Completed | 2010-02-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01282411 | Anatomic Outcomes Following Ozurdex Injections | — | Retinal Vein Occlusions | Completed | 2010-02-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01068964 | Safety and Efficacy of Bimatoprost Timolol Ophthalmic Solution in Patients With… | Na | Open-angle Glaucoma | Completed | 2010-02-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01282411 | Anatomic Outcomes Following Ozurdex Injections | — | Retinal Vein Occlusions | Completed | 2010-02-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01064830 | Topical Cyclosporine Suspension for the Treatment of Brittle Nails | Phase2 | Brittle Nail Syndrome | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01042678 | Study of MP0112 Intravitreal Injection in Patients With Diabetic Macular Edema | Phase1 | Diabetic Macular Edema | Terminated | 2010-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01282411 | Anatomic Outcomes Following Ozurdex Injections | — | Retinal Vein Occlusions | Completed | 2010-02-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00915525 | Long Term Follow-up Study of Safety and Efficacy of Botulinum Toxin Type A for … | Phase3 | Overactive Bladder | Completed | 2010-02-01 | 2014-08-05 | ClinicalTrials.gov |
| NCT01632423 | A Study of Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocul… | — | Glaucoma, Open-Angle | Completed | 2010-02-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01076192 | Study of Adalimumab (HUMIRA®) in Patients With Moderate to Severe Psoriasis (PS… | — | Moderate-to-severe Chronic Plaque Psoriasis | Completed | 2010-02-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01076192 | Study of Adalimumab (HUMIRA®) in Patients With Moderate to Severe Psoriasis (PS… | — | Moderate-to-severe Chronic Plaque Psoriasis | Completed | 2010-02-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT01068964 | Safety and Efficacy of Bimatoprost Timolol Ophthalmic Solution in Patients With… | Na | Open-angle Glaucoma | Completed | 2010-02-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01064830 | Topical Cyclosporine Suspension for the Treatment of Brittle Nails | Phase2 | Brittle Nail Syndrome | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01042678 | Study of MP0112 Intravitreal Injection in Patients With Diabetic Macular Edema | Phase1 | Diabetic Macular Edema | Terminated | 2010-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00915525 | Long Term Follow-up Study of Safety and Efficacy of Botulinum Toxin Type A for … | Phase3 | Overactive Bladder | Completed | 2010-02-01 | 2014-08-05 | ClinicalTrials.gov |
| NCT00915525 | Long Term Follow-up Study of Safety and Efficacy of Botulinum Toxin Type A for … | Phase3 | Overactive Bladder | Completed | 2010-02-01 | 2014-08-05 | ClinicalTrials.gov |
| NCT01020487 | Safety and Efficacy of Paricalcitol Capsules in Decreasing Serum Parathyroid Ho… | Phase3 | Chronic Kidney Disease Stage 3 and 4 | Completed | 2010-02-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00915525 | Long Term Follow-up Study of Safety and Efficacy of Botulinum Toxin Type A for … | Phase3 | Overactive Bladder | Completed | 2010-02-01 | 2014-08-05 | ClinicalTrials.gov |
| NCT01064856 | Study of Adalimumab in Participants With Peripheral Spondyloarthritis (SpA) | Phase3 | Peripheral Spondyloarthritis | Completed | 2010-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01064856 | Study of Adalimumab in Participants With Peripheral Spondyloarthritis (SpA) | Phase3 | Peripheral Spondyloarthritis | Completed | 2010-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT06607601 | CARE Initiative: Real-world Emulation of the PALOMA-2 Trial | — | Metastatic Breast Cancer | Completed | 2010-02-01 | 2023-07-20 | ClinicalTrials.gov |
| NCT06607393 | CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS3] | — | Metastatic Nonsmall Cell Lung Cancer | Completed | 2010-02-01 | 2023-06-28 | ClinicalTrials.gov |
| NCT06585189 | CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS4] | — | Metastatic Non Small Cell Lung Cancer | Completed | 2010-02-01 | 2023-04-13 | ClinicalTrials.gov |
| NCT06585189 | CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS4] | — | Metastatic Non Small Cell Lung Cancer | Completed | 2010-02-01 | 2023-04-13 | ClinicalTrials.gov |
| NCT06607393 | CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS3] | — | Metastatic Nonsmall Cell Lung Cancer | Completed | 2010-02-01 | 2023-06-28 | ClinicalTrials.gov |
| NCT06607601 | CARE Initiative: Real-world Emulation of the PALOMA-2 Trial | — | Metastatic Breast Cancer | Completed | 2010-02-01 | 2023-07-20 | ClinicalTrials.gov |
| NCT01064856 | Study of Adalimumab in Participants With Peripheral Spondyloarthritis (SpA) | Phase3 | Peripheral Spondyloarthritis | Completed | 2010-02-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01632423 | A Study of Lumigan® in Patients With Primary Open Angle Glaucoma (POAG) or Ocul… | — | Glaucoma, Open-Angle | Completed | 2010-02-01 | 2010-11-01 | ClinicalTrials.gov |
| NCT01020487 | Safety and Efficacy of Paricalcitol Capsules in Decreasing Serum Parathyroid Ho… | Phase3 | Chronic Kidney Disease Stage 3 and 4 | Completed | 2010-02-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01042678 | Study of MP0112 Intravitreal Injection in Patients With Diabetic Macular Edema | Phase1 | Diabetic Macular Edema | Terminated | 2010-02-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT01076192 | Study of Adalimumab (HUMIRA®) in Patients With Moderate to Severe Psoriasis (PS… | — | Moderate-to-severe Chronic Plaque Psoriasis | Completed | 2010-02-01 | 2014-09-01 | ClinicalTrials.gov |
| NCT06607601 | CARE Initiative: Real-world Emulation of the PALOMA-2 Trial | — | Metastatic Breast Cancer | Completed | 2010-02-01 | 2023-07-20 | ClinicalTrials.gov |
| NCT01064830 | Topical Cyclosporine Suspension for the Treatment of Brittle Nails | Phase2 | Brittle Nail Syndrome | Completed | 2010-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01068964 | Safety and Efficacy of Bimatoprost Timolol Ophthalmic Solution in Patients With… | Na | Open-angle Glaucoma | Completed | 2010-02-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT06607393 | CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS3] | — | Metastatic Nonsmall Cell Lung Cancer | Completed | 2010-02-01 | 2023-06-28 | ClinicalTrials.gov |
| NCT06585189 | CARE Initiative: Real-world Emulation of the KEYNOTE-189 Trial [DS4] | — | Metastatic Non Small Cell Lung Cancer | Completed | 2010-02-01 | 2023-04-13 | ClinicalTrials.gov |
| NCT01199965 | Pharmacokinetics & Tolerability Study of MAP0004 in Smoking and Non-Smoking Adu… | Phase1 | Healthy Subjects | Completed | 2010-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01255891 | Adjuvant Androgen Suppression Plus Radiation Therapy for High-Risk Localized Ad… | Phase2 | Adenocarcinoma of the Prostate | Completed | 2010-01-01 | 2023-09-01 | ClinicalTrials.gov |
| NCT01199965 | Pharmacokinetics & Tolerability Study of MAP0004 in Smoking and Non-Smoking Adu… | Phase1 | Healthy Subjects | Completed | 2010-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01063816 | A Study of ABT-888 in Combination With Carboplatin and Gemcitabine in Subjects … | Phase1 | Advanced Solid Tumors | Completed | 2010-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01063816 | A Study of ABT-888 in Combination With Carboplatin and Gemcitabine in Subjects … | Phase1 | Advanced Solid Tumors | Completed | 2010-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01063816 | A Study of ABT-888 in Combination With Carboplatin and Gemcitabine in Subjects … | Phase1 | Advanced Solid Tumors | Completed | 2010-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01255891 | Adjuvant Androgen Suppression Plus Radiation Therapy for High-Risk Localized Ad… | Phase2 | Adenocarcinoma of the Prostate | Completed | 2010-01-01 | 2023-09-01 | ClinicalTrials.gov |
| NCT01199965 | Pharmacokinetics & Tolerability Study of MAP0004 in Smoking and Non-Smoking Adu… | Phase1 | Healthy Subjects | Completed | 2010-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01199965 | Pharmacokinetics & Tolerability Study of MAP0004 in Smoking and Non-Smoking Adu… | Phase1 | Healthy Subjects | Completed | 2010-01-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01255891 | Adjuvant Androgen Suppression Plus Radiation Therapy for High-Risk Localized Ad… | Phase2 | Adenocarcinoma of the Prostate | Completed | 2010-01-01 | 2023-09-01 | ClinicalTrials.gov |
| NCT01255891 | Adjuvant Androgen Suppression Plus Radiation Therapy for High-Risk Localized Ad… | Phase2 | Adenocarcinoma of the Prostate | Completed | 2010-01-01 | 2023-09-01 | ClinicalTrials.gov |
| NCT01063816 | A Study of ABT-888 in Combination With Carboplatin and Gemcitabine in Subjects … | Phase1 | Advanced Solid Tumors | Completed | 2010-01-01 | 2016-08-01 | ClinicalTrials.gov |
| NCT01833741 | A Study of LUMIGAN® RC in the Clinical Setting | Phase4 | Glaucoma, Primary Open Angle | Completed | 2009-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01170884 | Comparing Safety and Efficacy of Combigan® and Lumigan® With Lumigan® Alone in … | Phase4 | Glaucoma | Completed | 2009-12-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01163318 | Special Investigation of Humira® (Adalimumab) on Long-term Treatment in Patient… | — | Rheumatoid Arthritis | Completed | 2009-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01170884 | Comparing Safety and Efficacy of Combigan® and Lumigan® With Lumigan® Alone in … | Phase4 | Glaucoma | Completed | 2009-12-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01833741 | A Study of LUMIGAN® RC in the Clinical Setting | Phase4 | Glaucoma, Primary Open Angle | Completed | 2009-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01170884 | Comparing Safety and Efficacy of Combigan® and Lumigan® With Lumigan® Alone in … | Phase4 | Glaucoma | Completed | 2009-12-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01170884 | Comparing Safety and Efficacy of Combigan® and Lumigan® With Lumigan® Alone in … | Phase4 | Glaucoma | Completed | 2009-12-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01018875 | Efficacy and Safety Study of ABT-288 in Subjects With Mild-to-Moderate Alzheime… | Phase2 | Alzheimer's Disease | Completed | 2009-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01163318 | Special Investigation of Humira® (Adalimumab) on Long-term Treatment in Patient… | — | Rheumatoid Arthritis | Completed | 2009-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01018875 | Efficacy and Safety Study of ABT-288 in Subjects With Mild-to-Moderate Alzheime… | Phase2 | Alzheimer's Disease | Completed | 2009-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01833741 | A Study of LUMIGAN® RC in the Clinical Setting | Phase4 | Glaucoma, Primary Open Angle | Completed | 2009-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01163318 | Special Investigation of Humira® (Adalimumab) on Long-term Treatment in Patient… | — | Rheumatoid Arthritis | Completed | 2009-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01018875 | Efficacy and Safety Study of ABT-288 in Subjects With Mild-to-Moderate Alzheime… | Phase2 | Alzheimer's Disease | Completed | 2009-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01018875 | Efficacy and Safety Study of ABT-288 in Subjects With Mild-to-Moderate Alzheime… | Phase2 | Alzheimer's Disease | Completed | 2009-12-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01833741 | A Study of LUMIGAN® RC in the Clinical Setting | Phase4 | Glaucoma, Primary Open Angle | Completed | 2009-12-01 | 2011-03-01 | ClinicalTrials.gov |
| NCT01163318 | Special Investigation of Humira® (Adalimumab) on Long-term Treatment in Patient… | — | Rheumatoid Arthritis | Completed | 2009-12-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00660673 | Open Label Continuation Treatment Study With Levodopa-Carbidopa Intestinal Gel … | Phase3 | Advanced Parkinson's Disease | Completed | 2009-11-13 | 2021-11-30 | ClinicalTrials.gov |
| NCT00660673 | Open Label Continuation Treatment Study With Levodopa-Carbidopa Intestinal Gel … | Phase3 | Advanced Parkinson's Disease | Completed | 2009-11-13 | 2021-11-30 | ClinicalTrials.gov |
| NCT00660673 | Open Label Continuation Treatment Study With Levodopa-Carbidopa Intestinal Gel … | Phase3 | Advanced Parkinson's Disease | Completed | 2009-11-13 | 2021-11-30 | ClinicalTrials.gov |
| NCT00660673 | Open Label Continuation Treatment Study With Levodopa-Carbidopa Intestinal Gel … | Phase3 | Advanced Parkinson's Disease | Completed | 2009-11-13 | 2021-11-30 | ClinicalTrials.gov |
| NCT01010282 | Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects | Na | Dry Eye Syndrome | Completed | 2009-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01010282 | Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects | Na | Dry Eye Syndrome | Completed | 2009-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01013077 | The Effect of a New Emulsion in Dry Eye Patients on Tear Layer Aberrometry, Con… | Na | Dry Eye Syndrome | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01151904 | Study of Brimonidine and Timolol Ophthalmic Solution With Latanoprost Compared … | Phase4 | Glaucoma, Angle-Closure | Terminated | 2009-11-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01026077 | The Savella Pregnancy Registry | — | Fibromyalgia | Terminated | 2009-11-01 | 2024-10-09 | ClinicalTrials.gov |
| NCT01151904 | Study of Brimonidine and Timolol Ophthalmic Solution With Latanoprost Compared … | Phase4 | Glaucoma, Angle-Closure | Terminated | 2009-11-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01026077 | The Savella Pregnancy Registry | — | Fibromyalgia | Terminated | 2009-11-01 | 2024-10-09 | ClinicalTrials.gov |
| NCT00987727 | Safety and Efficacy of Carboxymethylcellulose for Ocular Surface Integrity in S… | Phase4 | Dry Eye Syndromes | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00958035 | Study of Bimatoprost Solution in Increasing Eyelash Prominence in African Ameri… | Phase4 | Hypotrichosis | Completed | 2009-11-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01151904 | Study of Brimonidine and Timolol Ophthalmic Solution With Latanoprost Compared … | Phase4 | Glaucoma, Angle-Closure | Terminated | 2009-11-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT00987727 | Safety and Efficacy of Carboxymethylcellulose for Ocular Surface Integrity in S… | Phase4 | Dry Eye Syndromes | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01229423 | Safety and Efficacy of LATISSE® in the Augmentation of Eyelashes of Korean Subj… | Phase4 | Eyelash Hypotrichosis | Completed | 2009-11-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00868413 | Study of ABT-263 When Administered in Combination With Either Fludarabine/Cyclo… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2009-11-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01026077 | The Savella Pregnancy Registry | — | Fibromyalgia | Terminated | 2009-11-01 | 2024-10-09 | ClinicalTrials.gov |
| NCT01013077 | The Effect of a New Emulsion in Dry Eye Patients on Tear Layer Aberrometry, Con… | Na | Dry Eye Syndrome | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01010282 | Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects | Na | Dry Eye Syndrome | Completed | 2009-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01229423 | Safety and Efficacy of LATISSE® in the Augmentation of Eyelashes of Korean Subj… | Phase4 | Eyelash Hypotrichosis | Completed | 2009-11-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00958035 | Study of Bimatoprost Solution in Increasing Eyelash Prominence in African Ameri… | Phase4 | Hypotrichosis | Completed | 2009-11-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01026077 | The Savella Pregnancy Registry | — | Fibromyalgia | Terminated | 2009-11-01 | 2024-10-09 | ClinicalTrials.gov |
| NCT00868413 | Study of ABT-263 When Administered in Combination With Either Fludarabine/Cyclo… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2009-11-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00987727 | Safety and Efficacy of Carboxymethylcellulose for Ocular Surface Integrity in S… | Phase4 | Dry Eye Syndromes | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT00987727 | Safety and Efficacy of Carboxymethylcellulose for Ocular Surface Integrity in S… | Phase4 | Dry Eye Syndromes | Completed | 2009-11-01 | 2010-09-01 | ClinicalTrials.gov |
| NCT01151904 | Study of Brimonidine and Timolol Ophthalmic Solution With Latanoprost Compared … | Phase4 | Glaucoma, Angle-Closure | Terminated | 2009-11-01 | 2012-02-01 | ClinicalTrials.gov |
| NCT01013077 | The Effect of a New Emulsion in Dry Eye Patients on Tear Layer Aberrometry, Con… | Na | Dry Eye Syndrome | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00958035 | Study of Bimatoprost Solution in Increasing Eyelash Prominence in African Ameri… | Phase4 | Hypotrichosis | Completed | 2009-11-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT00868413 | Study of ABT-263 When Administered in Combination With Either Fludarabine/Cyclo… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2009-11-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01229423 | Safety and Efficacy of LATISSE® in the Augmentation of Eyelashes of Korean Subj… | Phase4 | Eyelash Hypotrichosis | Completed | 2009-11-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00958035 | Study of Bimatoprost Solution in Increasing Eyelash Prominence in African Ameri… | Phase4 | Hypotrichosis | Completed | 2009-11-01 | 2010-08-01 | ClinicalTrials.gov |
| NCT01229423 | Safety and Efficacy of LATISSE® in the Augmentation of Eyelashes of Korean Subj… | Phase4 | Eyelash Hypotrichosis | Completed | 2009-11-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00868413 | Study of ABT-263 When Administered in Combination With Either Fludarabine/Cyclo… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2009-11-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01010282 | Safety and Efficacy of Two Artificial Tears in Dry Eye Subjects | Na | Dry Eye Syndrome | Completed | 2009-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01013077 | The Effect of a New Emulsion in Dry Eye Patients on Tear Layer Aberrometry, Con… | Na | Dry Eye Syndrome | Completed | 2009-11-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00973973 | Efficacy and Safety Study of Elagolix in Women With Endometriosis | Phase2 | Endometriosis, Pain | Completed | 2009-10-12 | 2010-09-22 | ClinicalTrials.gov |
| NCT00973973 | Efficacy and Safety Study of Elagolix in Women With Endometriosis | Phase2 | Endometriosis, Pain | Completed | 2009-10-12 | 2010-09-22 | ClinicalTrials.gov |
| NCT00973973 | Efficacy and Safety Study of Elagolix in Women With Endometriosis | Phase2 | Endometriosis, Pain | Completed | 2009-10-12 | 2010-09-22 | ClinicalTrials.gov |
| NCT00973973 | Efficacy and Safety Study of Elagolix in Women With Endometriosis | Phase2 | Endometriosis, Pain | Completed | 2009-10-12 | 2010-09-22 | ClinicalTrials.gov |
| NCT01004042 | Quality of Life and Self-esteem After Botox® Injections in Depressed and Non-de… | Phase4 | Depression | Completed | 2009-10-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01083173 | Surveillance of Kaletra in Korean Patients | — | HIV-1 Infection | Completed | 2009-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00986401 | Safety and Tolerability of Trospium Chloride and Metformin Hydrochloride in Hea… | Phase1 | Healthy | Completed | 2009-10-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00878449 | A Study Evaluating the Safety of ABT-263 in Combination With Etoposide/Cisplati… | Phase1 | Solid Tumors | Completed | 2009-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01083173 | Surveillance of Kaletra in Korean Patients | — | HIV-1 Infection | Completed | 2009-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01083173 | Surveillance of Kaletra in Korean Patients | — | HIV-1 Infection | Completed | 2009-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT00986401 | Safety and Tolerability of Trospium Chloride and Metformin Hydrochloride in Hea… | Phase1 | Healthy | Completed | 2009-10-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00878449 | A Study Evaluating the Safety of ABT-263 in Combination With Etoposide/Cisplati… | Phase1 | Solid Tumors | Completed | 2009-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01083173 | Surveillance of Kaletra in Korean Patients | — | HIV-1 Infection | Completed | 2009-10-01 | 2014-10-01 | ClinicalTrials.gov |
| NCT01009073 | A Study Evaluating ABT-263 With Erlotinib, ABT-263 With Irinotecan, and ABT-263… | Phase1 | Solid Tumors | Completed | 2009-10-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00878449 | A Study Evaluating the Safety of ABT-263 in Combination With Etoposide/Cisplati… | Phase1 | Solid Tumors | Completed | 2009-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01009073 | A Study Evaluating ABT-263 With Erlotinib, ABT-263 With Irinotecan, and ABT-263… | Phase1 | Solid Tumors | Completed | 2009-10-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00986037 | Assessment of the Safety of ABT-308 in Healthy Volunteers and Subjects With Ast… | Phase1 | Asthma | Completed | 2009-10-01 | — | ClinicalTrials.gov |
| NCT00991458 | Study of Cyclosporine in Post-LASIK Patients | Phase2 | Laser In Situ Keratomileusis | Completed | 2009-10-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01021761 | A Comparison of Prostaglandin E2 (PGE2) Inhibition of Acuvail(Ketorolac 0.45%),… | Phase4 | Cataracts | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01004042 | Quality of Life and Self-esteem After Botox® Injections in Depressed and Non-de… | Phase4 | Depression | Completed | 2009-10-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01001806 | A Comparison of Peak Aqueous Penetration of Acuvail (Ketorolac 0.45%), Xibrom (… | Phase4 | Cataracts | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00991458 | Study of Cyclosporine in Post-LASIK Patients | Phase2 | Laser In Situ Keratomileusis | Completed | 2009-10-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00986401 | Safety and Tolerability of Trospium Chloride and Metformin Hydrochloride in Hea… | Phase1 | Healthy | Completed | 2009-10-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00986401 | Safety and Tolerability of Trospium Chloride and Metformin Hydrochloride in Hea… | Phase1 | Healthy | Completed | 2009-10-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00982566 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Subjects With C… | Phase1 | Lymphoid Malignancy | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00991458 | Study of Cyclosporine in Post-LASIK Patients | Phase2 | Laser In Situ Keratomileusis | Completed | 2009-10-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01001806 | A Comparison of Peak Aqueous Penetration of Acuvail (Ketorolac 0.45%), Xibrom (… | Phase4 | Cataracts | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01004042 | Quality of Life and Self-esteem After Botox® Injections in Depressed and Non-de… | Phase4 | Depression | Completed | 2009-10-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00878449 | A Study Evaluating the Safety of ABT-263 in Combination With Etoposide/Cisplati… | Phase1 | Solid Tumors | Completed | 2009-10-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01001806 | A Comparison of Peak Aqueous Penetration of Acuvail (Ketorolac 0.45%), Xibrom (… | Phase4 | Cataracts | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01021761 | A Comparison of Prostaglandin E2 (PGE2) Inhibition of Acuvail(Ketorolac 0.45%),… | Phase4 | Cataracts | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01021761 | A Comparison of Prostaglandin E2 (PGE2) Inhibition of Acuvail(Ketorolac 0.45%),… | Phase4 | Cataracts | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00982566 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Subjects With C… | Phase1 | Lymphoid Malignancy | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00986037 | Assessment of the Safety of ABT-308 in Healthy Volunteers and Subjects With Ast… | Phase1 | Asthma | Completed | 2009-10-01 | — | ClinicalTrials.gov |
| NCT01009073 | A Study Evaluating ABT-263 With Erlotinib, ABT-263 With Irinotecan, and ABT-263… | Phase1 | Solid Tumors | Completed | 2009-10-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT01001806 | A Comparison of Peak Aqueous Penetration of Acuvail (Ketorolac 0.45%), Xibrom (… | Phase4 | Cataracts | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT01009073 | A Study Evaluating ABT-263 With Erlotinib, ABT-263 With Irinotecan, and ABT-263… | Phase1 | Solid Tumors | Completed | 2009-10-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00982566 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Subjects With C… | Phase1 | Lymphoid Malignancy | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00986037 | Assessment of the Safety of ABT-308 in Healthy Volunteers and Subjects With Ast… | Phase1 | Asthma | Completed | 2009-10-01 | — | ClinicalTrials.gov |
| NCT00991458 | Study of Cyclosporine in Post-LASIK Patients | Phase2 | Laser In Situ Keratomileusis | Completed | 2009-10-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01004042 | Quality of Life and Self-esteem After Botox® Injections in Depressed and Non-de… | Phase4 | Depression | Completed | 2009-10-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01021761 | A Comparison of Prostaglandin E2 (PGE2) Inhibition of Acuvail(Ketorolac 0.45%),… | Phase4 | Cataracts | Completed | 2009-10-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00986037 | Assessment of the Safety of ABT-308 in Healthy Volunteers and Subjects With Ast… | Phase1 | Asthma | Completed | 2009-10-01 | — | ClinicalTrials.gov |
| NCT00982566 | Assess the Oral Bioavailability of a New ABT-263 Formulation in Subjects With C… | Phase1 | Lymphoid Malignancy | Completed | 2009-10-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00887757 | Safety Study of ABT-263 in Combination With Gemzar (Gemcitabine) in Subjects Wi… | Phase1 | Solid Tumors | Completed | 2009-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00995904 | Tolerability and PK of Submicron Budesonide in Children 4 to 11 Years Old With … | Phase2 | Asthma | Completed | 2009-09-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT00910845 | Study of Botulinum Toxin Type A for the Treatment of Patients With Idiopathic O… | Phase3 | Overactive Bladder | Completed | 2009-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00995904 | Tolerability and PK of Submicron Budesonide in Children 4 to 11 Years Old With … | Phase2 | Asthma | Completed | 2009-09-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01077128 | Greek Study of the Quality of Life in Patients With Psoriasis Treated With Adal… | — | Psoriasis | Completed | 2009-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00910845 | Study of Botulinum Toxin Type A for the Treatment of Patients With Idiopathic O… | Phase3 | Overactive Bladder | Completed | 2009-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00995904 | Tolerability and PK of Submicron Budesonide in Children 4 to 11 Years Old With … | Phase2 | Asthma | Completed | 2009-09-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01077128 | Greek Study of the Quality of Life in Patients With Psoriasis Treated With Adal… | — | Psoriasis | Completed | 2009-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00910845 | Study of Botulinum Toxin Type A for the Treatment of Patients With Idiopathic O… | Phase3 | Overactive Bladder | Completed | 2009-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01077128 | Greek Study of the Quality of Life in Patients With Psoriasis Treated With Adal… | — | Psoriasis | Completed | 2009-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00887757 | Safety Study of ABT-263 in Combination With Gemzar (Gemcitabine) in Subjects Wi… | Phase1 | Solid Tumors | Completed | 2009-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00995904 | Tolerability and PK of Submicron Budesonide in Children 4 to 11 Years Old With … | Phase2 | Asthma | Completed | 2009-09-01 | 2009-11-01 | ClinicalTrials.gov |
| NCT01077128 | Greek Study of the Quality of Life in Patients With Psoriasis Treated With Adal… | — | Psoriasis | Completed | 2009-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00910845 | Study of Botulinum Toxin Type A for the Treatment of Patients With Idiopathic O… | Phase3 | Overactive Bladder | Completed | 2009-09-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00887757 | Safety Study of ABT-263 in Combination With Gemzar (Gemcitabine) in Subjects Wi… | Phase1 | Solid Tumors | Completed | 2009-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00887757 | Safety Study of ABT-263 in Combination With Gemzar (Gemcitabine) in Subjects Wi… | Phase1 | Solid Tumors | Completed | 2009-09-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01976624 | Safety and Efficacy of Bimatoprost/Timolol (Ganfort®) Ophthalmic Solution in Ko… | — | Glaucoma, Open-Angle | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00907426 | Safety and Efficacy Study of Bimatoprost to Treat Hypotrichosis of the Eyelashe… | Phase3 | Hypotrichosis | Completed | 2009-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00894517 | A Study Evaluating the Effect of Botulinum Toxin Type A on Semen Quality in Pat… | Phase1 | Benign Prostatic Hyperplasia | Completed | 2009-08-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00932477 | Safety and Tolerability of Artificial Tears in Dry Eye Subjects | Na | Dry Eye Syndrome | Completed | 2009-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01976624 | Safety and Efficacy of Bimatoprost/Timolol (Ganfort®) Ophthalmic Solution in Ko… | — | Glaucoma, Open-Angle | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00894517 | A Study Evaluating the Effect of Botulinum Toxin Type A on Semen Quality in Pat… | Phase1 | Benign Prostatic Hyperplasia | Completed | 2009-08-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00894517 | A Study Evaluating the Effect of Botulinum Toxin Type A on Semen Quality in Pat… | Phase1 | Benign Prostatic Hyperplasia | Completed | 2009-08-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT01976624 | Safety and Efficacy of Bimatoprost/Timolol (Ganfort®) Ophthalmic Solution in Ko… | — | Glaucoma, Open-Angle | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00907426 | Safety and Efficacy Study of Bimatoprost to Treat Hypotrichosis of the Eyelashe… | Phase3 | Hypotrichosis | Completed | 2009-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00978042 | Safety and Effectiveness of Juvéderm® VOLUMA XC Injectable Gel for Cheek Augmen… | Na | Mid-facial Volume Deficit Related to Aging | Completed | 2009-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00932477 | Safety and Tolerability of Artificial Tears in Dry Eye Subjects | Na | Dry Eye Syndrome | Completed | 2009-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00907426 | Safety and Efficacy Study of Bimatoprost to Treat Hypotrichosis of the Eyelashe… | Phase3 | Hypotrichosis | Completed | 2009-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00894517 | A Study Evaluating the Effect of Botulinum Toxin Type A on Semen Quality in Pat… | Phase1 | Benign Prostatic Hyperplasia | Completed | 2009-08-01 | 2012-08-01 | ClinicalTrials.gov |
| NCT00932477 | Safety and Tolerability of Artificial Tears in Dry Eye Subjects | Na | Dry Eye Syndrome | Completed | 2009-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00932477 | Safety and Tolerability of Artificial Tears in Dry Eye Subjects | Na | Dry Eye Syndrome | Completed | 2009-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00978042 | Safety and Effectiveness of Juvéderm® VOLUMA XC Injectable Gel for Cheek Augmen… | Na | Mid-facial Volume Deficit Related to Aging | Completed | 2009-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00907426 | Safety and Efficacy Study of Bimatoprost to Treat Hypotrichosis of the Eyelashe… | Phase3 | Hypotrichosis | Completed | 2009-08-01 | 2011-05-01 | ClinicalTrials.gov |
| NCT00978042 | Safety and Effectiveness of Juvéderm® VOLUMA XC Injectable Gel for Cheek Augmen… | Na | Mid-facial Volume Deficit Related to Aging | Completed | 2009-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01976624 | Safety and Efficacy of Bimatoprost/Timolol (Ganfort®) Ophthalmic Solution in Ko… | — | Glaucoma, Open-Angle | Completed | 2009-08-01 | 2014-01-01 | ClinicalTrials.gov |
| NCT00978042 | Safety and Effectiveness of Juvéderm® VOLUMA XC Injectable Gel for Cheek Augmen… | Na | Mid-facial Volume Deficit Related to Aging | Completed | 2009-08-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT00788684 | Safety Study of ABT-263 in Combination With Rituximab in Lymphoid Cancers | Phase1 | CD20-Positive Lymphoid Malignancies | Completed | 2009-07-21 | 2025-02-07 | ClinicalTrials.gov |
| NCT00788684 | Safety Study of ABT-263 in Combination With Rituximab in Lymphoid Cancers | Phase1 | CD20-Positive Lymphoid Malignancies | Completed | 2009-07-21 | 2025-02-07 | ClinicalTrials.gov |
| NCT00788684 | Safety Study of ABT-263 in Combination With Rituximab in Lymphoid Cancers | Phase1 | CD20-Positive Lymphoid Malignancies | Completed | 2009-07-21 | 2025-02-07 | ClinicalTrials.gov |
| NCT00788684 | Safety Study of ABT-263 in Combination With Rituximab in Lymphoid Cancers | Phase1 | CD20-Positive Lymphoid Malignancies | Completed | 2009-07-21 | 2025-02-07 | ClinicalTrials.gov |
| NCT00939003 | Study of Adalimumab in Patients With Axial Spondyloarthritis | Phase3 | Axial Spondyloarthritis | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00891605 | Safety Study of ABT-263 in Combination With Paclitaxel in Subjects With Solid T… | Phase1 | Solid Tumors | Completed | 2009-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00932022 | Trospium Chloride XR in Obese Female Patients With Overactive Bladder | Phase4 | Obesity | Completed | 2009-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00932022 | Trospium Chloride XR in Obese Female Patients With Overactive Bladder | Phase4 | Obesity | Completed | 2009-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00891605 | Safety Study of ABT-263 in Combination With Paclitaxel in Subjects With Solid T… | Phase1 | Solid Tumors | Completed | 2009-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00932022 | Trospium Chloride XR in Obese Female Patients With Overactive Bladder | Phase4 | Obesity | Completed | 2009-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00939003 | Study of Adalimumab in Patients With Axial Spondyloarthritis | Phase3 | Axial Spondyloarthritis | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00932022 | Trospium Chloride XR in Obese Female Patients With Overactive Bladder | Phase4 | Obesity | Completed | 2009-07-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00986427 | Restasis for Treatment of Brittle Nails | Phase2 | Brittle Nails | Completed | 2009-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00986427 | Restasis for Treatment of Brittle Nails | Phase2 | Brittle Nails | Completed | 2009-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00891605 | Safety Study of ABT-263 in Combination With Paclitaxel in Subjects With Solid T… | Phase1 | Solid Tumors | Completed | 2009-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00986427 | Restasis for Treatment of Brittle Nails | Phase2 | Brittle Nails | Completed | 2009-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00939003 | Study of Adalimumab in Patients With Axial Spondyloarthritis | Phase3 | Axial Spondyloarthritis | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00986427 | Restasis for Treatment of Brittle Nails | Phase2 | Brittle Nails | Completed | 2009-07-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00939003 | Study of Adalimumab in Patients With Axial Spondyloarthritis | Phase3 | Axial Spondyloarthritis | Completed | 2009-07-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00891605 | Safety Study of ABT-263 in Combination With Paclitaxel in Subjects With Solid T… | Phase1 | Solid Tumors | Completed | 2009-07-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00935311 | Hydrocodone/Acetaminophen for Acute Pain Following Third Molar Tooth Extraction | Phase2 | Pain | Completed | 2009-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01629407 | A Study of the Rate of Progression of Glaucoma During a Follow-up Period of Two… | — | Glaucoma, Open-Angle | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT03064815 | The SpACE Study - Small Bowel Crohn's Disease and Spondyloarthropathies | Na | Spondyloarthropathy | Completed | 2009-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00920764 | A Study of Atrasentan on Reducing Albuminuria in Type 2 Diabetic Nephropathy Tr… | Phase2 | Chronic Kidney Disease | Completed | 2009-06-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00669474 | Unicentric Comparing Study of Suction Curettage With Standard BOTOX Injection i… | Phase4 | Essential Axillary Hyperhidrosis | Terminated | 2009-06-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00824811 | Topical Cyclosporine vs. Placebo for Epiphora Associated With Docetaxel | Phase2 | Epiphora | Withdrawn | 2009-06-01 | — | ClinicalTrials.gov |
| NCT01083186 | Paricalcitol Oral Therapy in Predialysis CKD Patients. The Greek Experience | — | Chronic Kidney Failure | Completed | 2009-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00938704 | Study to Compare the Efficacy and Safety of Two Non-Preserved Artificial Tears … | Phase4 | Dry Eye Syndromes | Completed | 2009-06-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT03064815 | The SpACE Study - Small Bowel Crohn's Disease and Spondyloarthropathies | Na | Spondyloarthropathy | Completed | 2009-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00935311 | Hydrocodone/Acetaminophen for Acute Pain Following Third Molar Tooth Extraction | Phase2 | Pain | Completed | 2009-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00938704 | Study to Compare the Efficacy and Safety of Two Non-Preserved Artificial Tears … | Phase4 | Dry Eye Syndromes | Completed | 2009-06-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00824811 | Topical Cyclosporine vs. Placebo for Epiphora Associated With Docetaxel | Phase2 | Epiphora | Withdrawn | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00669474 | Unicentric Comparing Study of Suction Curettage With Standard BOTOX Injection i… | Phase4 | Essential Axillary Hyperhidrosis | Terminated | 2009-06-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01083186 | Paricalcitol Oral Therapy in Predialysis CKD Patients. The Greek Experience | — | Chronic Kidney Failure | Completed | 2009-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00920764 | A Study of Atrasentan on Reducing Albuminuria in Type 2 Diabetic Nephropathy Tr… | Phase2 | Chronic Kidney Disease | Completed | 2009-06-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01629407 | A Study of the Rate of Progression of Glaucoma During a Follow-up Period of Two… | — | Glaucoma, Open-Angle | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT03064815 | The SpACE Study - Small Bowel Crohn's Disease and Spondyloarthropathies | Na | Spondyloarthropathy | Completed | 2009-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT03064815 | The SpACE Study - Small Bowel Crohn's Disease and Spondyloarthropathies | Na | Spondyloarthropathy | Completed | 2009-06-01 | 2016-03-01 | ClinicalTrials.gov |
| NCT00920764 | A Study of Atrasentan on Reducing Albuminuria in Type 2 Diabetic Nephropathy Tr… | Phase2 | Chronic Kidney Disease | Completed | 2009-06-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00920764 | A Study of Atrasentan on Reducing Albuminuria in Type 2 Diabetic Nephropathy Tr… | Phase2 | Chronic Kidney Disease | Completed | 2009-06-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00669474 | Unicentric Comparing Study of Suction Curettage With Standard BOTOX Injection i… | Phase4 | Essential Axillary Hyperhidrosis | Terminated | 2009-06-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00824811 | Topical Cyclosporine vs. Placebo for Epiphora Associated With Docetaxel | Phase2 | Epiphora | Withdrawn | 2009-06-01 | — | ClinicalTrials.gov |
| NCT00935311 | Hydrocodone/Acetaminophen for Acute Pain Following Third Molar Tooth Extraction | Phase2 | Pain | Completed | 2009-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00938704 | Study to Compare the Efficacy and Safety of Two Non-Preserved Artificial Tears … | Phase4 | Dry Eye Syndromes | Completed | 2009-06-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01629407 | A Study of the Rate of Progression of Glaucoma During a Follow-up Period of Two… | — | Glaucoma, Open-Angle | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT01083186 | Paricalcitol Oral Therapy in Predialysis CKD Patients. The Greek Experience | — | Chronic Kidney Failure | Completed | 2009-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00669474 | Unicentric Comparing Study of Suction Curettage With Standard BOTOX Injection i… | Phase4 | Essential Axillary Hyperhidrosis | Terminated | 2009-06-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT01629407 | A Study of the Rate of Progression of Glaucoma During a Follow-up Period of Two… | — | Glaucoma, Open-Angle | Completed | 2009-06-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00824811 | Topical Cyclosporine vs. Placebo for Epiphora Associated With Docetaxel | Phase2 | Epiphora | Withdrawn | 2009-06-01 | — | ClinicalTrials.gov |
| NCT01083186 | Paricalcitol Oral Therapy in Predialysis CKD Patients. The Greek Experience | — | Chronic Kidney Failure | Completed | 2009-06-01 | 2012-01-01 | ClinicalTrials.gov |
| NCT00938704 | Study to Compare the Efficacy and Safety of Two Non-Preserved Artificial Tears … | Phase4 | Dry Eye Syndromes | Completed | 2009-06-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00935311 | Hydrocodone/Acetaminophen for Acute Pain Following Third Molar Tooth Extraction | Phase2 | Pain | Completed | 2009-06-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00908544 | New Era Study: Treatment With Multi Drug Class (MDC) HAART in HIV Infected Pati… | Na | HIV Infections | Completed | 2009-05-15 | 2018-05-01 | ClinicalTrials.gov |
| NCT00908544 | New Era Study: Treatment With Multi Drug Class (MDC) HAART in HIV Infected Pati… | Na | HIV Infections | Completed | 2009-05-15 | 2018-05-01 | ClinicalTrials.gov |
| NCT00908544 | New Era Study: Treatment With Multi Drug Class (MDC) HAART in HIV Infected Pati… | Na | HIV Infections | Completed | 2009-05-15 | 2018-05-01 | ClinicalTrials.gov |
| NCT00908544 | New Era Study: Treatment With Multi Drug Class (MDC) HAART in HIV Infected Pati… | Na | HIV Infections | Completed | 2009-05-15 | 2018-05-01 | ClinicalTrials.gov |
| NCT00884585 | Efficacy and Safety Study of Cyclosporine 0.010% to Treat Atopic Keratoconjunct… | Phase3 | Atopic Conjunctivitis | Completed | 2009-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00884585 | Efficacy and Safety Study of Cyclosporine 0.010% to Treat Atopic Keratoconjunct… | Phase3 | Atopic Conjunctivitis | Completed | 2009-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00884585 | Efficacy and Safety Study of Cyclosporine 0.010% to Treat Atopic Keratoconjunct… | Phase3 | Atopic Conjunctivitis | Completed | 2009-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00884585 | Efficacy and Safety Study of Cyclosporine 0.010% to Treat Atopic Keratoconjunct… | Phase3 | Atopic Conjunctivitis | Completed | 2009-05-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT01078402 | EValuation of HumIRA® in Patients With Active Rheumatoid Arthritis, Psoriatic A… | — | Ankylosing Spondylitis (AS) | Completed | 2009-04-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00863551 | Sanctura Muscarinic Receptor Antagonist Resists Transport (SMART) Trial | Phase4 | Elderly | Completed | 2009-04-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00872196 | A Follow-up Study to Assess Resistance to ABT-072 in HCV-infected Subjects Admi… | Phase2 | Hepatitis C Virus Infection | Completed | 2009-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01078402 | EValuation of HumIRA® in Patients With Active Rheumatoid Arthritis, Psoriatic A… | — | Ankylosing Spondylitis (AS) | Completed | 2009-04-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00863551 | Sanctura Muscarinic Receptor Antagonist Resists Transport (SMART) Trial | Phase4 | Elderly | Completed | 2009-04-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01637246 | A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Who… | — | Glaucoma, Open-Angle | Completed | 2009-04-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01637246 | A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Who… | — | Glaucoma, Open-Angle | Completed | 2009-04-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00908050 | Study of the Safety and Efficacy of Botox in Bruxism | Phase4 | Bruxism | Completed | 2009-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01078402 | EValuation of HumIRA® in Patients With Active Rheumatoid Arthritis, Psoriatic A… | — | Ankylosing Spondylitis (AS) | Completed | 2009-04-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00948246 | European Union (EU) Post-Market Study on Easyband® | — | Morbid Obesity | Completed | 2009-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00908050 | Study of the Safety and Efficacy of Botox in Bruxism | Phase4 | Bruxism | Completed | 2009-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00872196 | A Follow-up Study to Assess Resistance to ABT-072 in HCV-infected Subjects Admi… | Phase2 | Hepatitis C Virus Infection | Completed | 2009-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01637246 | A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Who… | — | Glaucoma, Open-Angle | Completed | 2009-04-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00863551 | Sanctura Muscarinic Receptor Antagonist Resists Transport (SMART) Trial | Phase4 | Elderly | Completed | 2009-04-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00948246 | European Union (EU) Post-Market Study on Easyband® | — | Morbid Obesity | Completed | 2009-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00872196 | A Follow-up Study to Assess Resistance to ABT-072 in HCV-infected Subjects Admi… | Phase2 | Hepatitis C Virus Infection | Completed | 2009-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00863551 | Sanctura Muscarinic Receptor Antagonist Resists Transport (SMART) Trial | Phase4 | Elderly | Completed | 2009-04-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00872196 | A Follow-up Study to Assess Resistance to ABT-072 in HCV-infected Subjects Admi… | Phase2 | Hepatitis C Virus Infection | Completed | 2009-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00948246 | European Union (EU) Post-Market Study on Easyband® | — | Morbid Obesity | Completed | 2009-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01637246 | A Study of Patients With Primary Open Angle Glaucoma or Ocular Hypertension Who… | — | Glaucoma, Open-Angle | Completed | 2009-04-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT01078402 | EValuation of HumIRA® in Patients With Active Rheumatoid Arthritis, Psoriatic A… | — | Ankylosing Spondylitis (AS) | Completed | 2009-04-01 | 2011-11-01 | ClinicalTrials.gov |
| NCT00908050 | Study of the Safety and Efficacy of Botox in Bruxism | Phase4 | Bruxism | Completed | 2009-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00908050 | Study of the Safety and Efficacy of Botox in Bruxism | Phase4 | Bruxism | Completed | 2009-04-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00948246 | European Union (EU) Post-Market Study on Easyband® | — | Morbid Obesity | Completed | 2009-04-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00851890 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral A… | Phase2 | Chronic Hepatitis C Virus Infection | Completed | 2009-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00775437 | Active Juvenile Idiopathic Arthritis (JIA) Compassionate Use | Phase3 | Juvenile Idiopathic Arthritis | Completed | 2009-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00856414 | Patient Satisfaction With Treatment of BOTOX® Cosmetic for the Temporary Correc… | Phase4 | Skin Aging | Completed | 2009-03-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01095640 | Study Comparing 0.3% Adapalene Topical Gel to Differin® 0.3% Adapalene Topical … | Na | Acne Vulgaris | Completed | 2009-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01078155 | Evaluation of the Role of Adalimumab on Extraarticular Manifestation - Bone Met… | — | Rheumatoid Arthritis | Completed | 2009-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01078155 | Evaluation of the Role of Adalimumab on Extraarticular Manifestation - Bone Met… | — | Rheumatoid Arthritis | Completed | 2009-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00874887 | A Clinical Study to Evaluate if Benzalkonium Chloride (BAK) in a Quinolone Eyed… | Phase4 | Anti-biotic Resistance | Completed | 2009-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00775437 | Active Juvenile Idiopathic Arthritis (JIA) Compassionate Use | Phase3 | Juvenile Idiopathic Arthritis | Completed | 2009-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00851890 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral A… | Phase2 | Chronic Hepatitis C Virus Infection | Completed | 2009-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00874887 | A Clinical Study to Evaluate if Benzalkonium Chloride (BAK) in a Quinolone Eyed… | Phase4 | Anti-biotic Resistance | Completed | 2009-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT01078155 | Evaluation of the Role of Adalimumab on Extraarticular Manifestation - Bone Met… | — | Rheumatoid Arthritis | Completed | 2009-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT01095640 | Study Comparing 0.3% Adapalene Topical Gel to Differin® 0.3% Adapalene Topical … | Na | Acne Vulgaris | Completed | 2009-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00856414 | Patient Satisfaction With Treatment of BOTOX® Cosmetic for the Temporary Correc… | Phase4 | Skin Aging | Completed | 2009-03-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01095640 | Study Comparing 0.3% Adapalene Topical Gel to Differin® 0.3% Adapalene Topical … | Na | Acne Vulgaris | Completed | 2009-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01095640 | Study Comparing 0.3% Adapalene Topical Gel to Differin® 0.3% Adapalene Topical … | Na | Acne Vulgaris | Completed | 2009-03-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00856414 | Patient Satisfaction With Treatment of BOTOX® Cosmetic for the Temporary Correc… | Phase4 | Skin Aging | Completed | 2009-03-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00856414 | Patient Satisfaction With Treatment of BOTOX® Cosmetic for the Temporary Correc… | Phase4 | Skin Aging | Completed | 2009-03-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00874887 | A Clinical Study to Evaluate if Benzalkonium Chloride (BAK) in a Quinolone Eyed… | Phase4 | Anti-biotic Resistance | Completed | 2009-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00775437 | Active Juvenile Idiopathic Arthritis (JIA) Compassionate Use | Phase3 | Juvenile Idiopathic Arthritis | Completed | 2009-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00851890 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral A… | Phase2 | Chronic Hepatitis C Virus Infection | Completed | 2009-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT00851890 | A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Antiviral A… | Phase2 | Chronic Hepatitis C Virus Infection | Completed | 2009-03-01 | 2009-07-01 | ClinicalTrials.gov |
| NCT01078155 | Evaluation of the Role of Adalimumab on Extraarticular Manifestation - Bone Met… | — | Rheumatoid Arthritis | Completed | 2009-03-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00874887 | A Clinical Study to Evaluate if Benzalkonium Chloride (BAK) in a Quinolone Eyed… | Phase4 | Anti-biotic Resistance | Completed | 2009-03-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00775437 | Active Juvenile Idiopathic Arthritis (JIA) Compassionate Use | Phase3 | Juvenile Idiopathic Arthritis | Completed | 2009-03-01 | 2013-03-01 | ClinicalTrials.gov |
| NCT00870740 | Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) … | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2009-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00870740 | Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) … | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2009-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00809848 | Safety and Efficacy of AGN 210669 Ophthalmic Solution in Patients With Ocular H… | Phase1 | Ocular Hypertension | Completed | 2009-02-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00733187 | Pharmacokinetic Study To Evaluate Effect of Food and Diurnal Variation on ABT-8… | Phase1 | Advanced Solid Tumors | Completed | 2009-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00809848 | Safety and Efficacy of AGN 210669 Ophthalmic Solution in Patients With Ocular H… | Phase1 | Ocular Hypertension | Completed | 2009-02-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT01421719 | Safety and Efficacy of botulinumA Toxin (BotoxA) for Treatment of Neurogenic Bl… | Phase4 | Parkinson's Disease | Completed | 2009-02-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00853099 | A Study of Adalimumab in Japanese Subjects With Moderately to Severely Active U… | Phase3 | Ulcerative Colitis | Completed | 2009-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01421719 | Safety and Efficacy of botulinumA Toxin (BotoxA) for Treatment of Neurogenic Bl… | Phase4 | Parkinson's Disease | Completed | 2009-02-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00809848 | Safety and Efficacy of AGN 210669 Ophthalmic Solution in Patients With Ocular H… | Phase1 | Ocular Hypertension | Completed | 2009-02-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT00733187 | Pharmacokinetic Study To Evaluate Effect of Food and Diurnal Variation on ABT-8… | Phase1 | Advanced Solid Tumors | Completed | 2009-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00870740 | Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) … | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2009-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00733187 | Pharmacokinetic Study To Evaluate Effect of Food and Diurnal Variation on ABT-8… | Phase1 | Advanced Solid Tumors | Completed | 2009-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00853099 | A Study of Adalimumab in Japanese Subjects With Moderately to Severely Active U… | Phase3 | Ulcerative Colitis | Completed | 2009-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00850044 | Safety, Tolerability and PK Study of Single Doses of ABT-450 With and Without R… | Phase1 | HCV Infection | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00804908 | A Study Evaluating Efficacy of ABT-888 in Combination With Temozolomide in Meta… | Phase2 | Melanoma | Completed | 2009-02-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00804908 | A Study Evaluating Efficacy of ABT-888 in Combination With Temozolomide in Meta… | Phase2 | Melanoma | Completed | 2009-02-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00850044 | Safety, Tolerability and PK Study of Single Doses of ABT-450 With and Without R… | Phase1 | HCV Infection | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00870740 | Safety and Efficacy Extension Study of Daclizumab High Yield Process (DAC HYP) … | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2009-02-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00850044 | Safety, Tolerability and PK Study of Single Doses of ABT-450 With and Without R… | Phase1 | HCV Infection | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT01421719 | Safety and Efficacy of botulinumA Toxin (BotoxA) for Treatment of Neurogenic Bl… | Phase4 | Parkinson's Disease | Completed | 2009-02-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00853099 | A Study of Adalimumab in Japanese Subjects With Moderately to Severely Active U… | Phase3 | Ulcerative Colitis | Completed | 2009-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00804908 | A Study Evaluating Efficacy of ABT-888 in Combination With Temozolomide in Meta… | Phase2 | Melanoma | Completed | 2009-02-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00733187 | Pharmacokinetic Study To Evaluate Effect of Food and Diurnal Variation on ABT-8… | Phase1 | Advanced Solid Tumors | Completed | 2009-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01421719 | Safety and Efficacy of botulinumA Toxin (BotoxA) for Treatment of Neurogenic Bl… | Phase4 | Parkinson's Disease | Completed | 2009-02-01 | 2011-07-01 | ClinicalTrials.gov |
| NCT00850044 | Safety, Tolerability and PK Study of Single Doses of ABT-450 With and Without R… | Phase1 | HCV Infection | Completed | 2009-02-01 | — | ClinicalTrials.gov |
| NCT00804908 | A Study Evaluating Efficacy of ABT-888 in Combination With Temozolomide in Meta… | Phase2 | Melanoma | Completed | 2009-02-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00853099 | A Study of Adalimumab in Japanese Subjects With Moderately to Severely Active U… | Phase3 | Ulcerative Colitis | Completed | 2009-02-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00809848 | Safety and Efficacy of AGN 210669 Ophthalmic Solution in Patients With Ocular H… | Phase1 | Ocular Hypertension | Completed | 2009-02-01 | 2009-05-01 | ClinicalTrials.gov |
| NCT01076205 | Safety and Effect on Quality of Life/Work Productivity of Humira in Patients Wi… | — | Rheumatoid Arthritis | Completed | 2009-01-12 | 2017-09-14 | ClinicalTrials.gov |
| NCT01076205 | Safety and Effect on Quality of Life/Work Productivity of Humira in Patients Wi… | — | Rheumatoid Arthritis | Completed | 2009-01-12 | 2017-09-14 | ClinicalTrials.gov |
| NCT01076205 | Safety and Effect on Quality of Life/Work Productivity of Humira in Patients Wi… | — | Rheumatoid Arthritis | Completed | 2009-01-12 | 2017-09-14 | ClinicalTrials.gov |
| NCT01076205 | Safety and Effect on Quality of Life/Work Productivity of Humira in Patients Wi… | — | Rheumatoid Arthritis | Completed | 2009-01-12 | 2017-09-14 | ClinicalTrials.gov |
| NCT00357994 | Study of Efficacy, Safety and Tolerability of Levodopa-Carbidopa Intestinal Gel… | Phase3 | Advanced Parkinson's Disease | Completed | 2009-01-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01987765 | Safety and Efficacy of Relestat Ophthalmic Solution 0.05% for Allergic Conjunct… | — | Conjunctivitis, Allergic | Completed | 2009-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00945295 | Efficacy and Safety Study of Botulinum Neurotoxin A With Rehabilitation Versus … | Na | Upper Limb Spasticity | Completed | 2009-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00945295 | Efficacy and Safety Study of Botulinum Neurotoxin A With Rehabilitation Versus … | Na | Upper Limb Spasticity | Completed | 2009-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00799227 | Safety and Efficacy of a New Treatment in Vitrectomized Subjects With Diabetic … | Phase2 | Diabetic Macular Edema | Completed | 2009-01-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00808509 | A Pilot Study of the Feasibility of Discontinuation of Adalimumab in Stable Rhe… | Phase4 | Arthritis, Rheumatoid | Completed | 2009-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00816517 | Use of Botulinum Toxin to Treat Psoriasis | Phase1 | Psoriasis Vulgaris | Completed | 2009-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00822523 | Assessment of the Effect of Botulinum Toxin in Extensor Digitorum Brevis Via St… | Na | Muscle Strength | Completed | 2009-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00827255 | Physician's Evaluation of Cyclosporine Ophthalmic Emulsion 0.05% | — | Dry Eye Disease | Completed | 2009-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00836017 | CD-PROBE: Cervical Dystonia Patient Registry for the Observation of onabotulinu… | — | Cervical Dystonia | Completed | 2009-01-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00876447 | A Long-term Follow-up Study of Botulinum Toxin Type A in Patients With Overacti… | Phase3 | Overactive Bladder | Completed | 2009-01-01 | 2013-09-04 | ClinicalTrials.gov |
| NCT00900666 | Efficacy of Botulinum Toxin Injections in the Rectus Femoris to Treat Stiff Kne… | Na | Stiff Knee Gait | Terminated | 2009-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00945295 | Efficacy and Safety Study of Botulinum Neurotoxin A With Rehabilitation Versus … | Na | Upper Limb Spasticity | Completed | 2009-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01029535 | Safety and Efficacy of Juvederm® VOLUMA™ for Correction of Mid-face Volume Defi… | Na | Mid-face Volume Deficiency | Completed | 2009-01-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00900666 | Efficacy of Botulinum Toxin Injections in the Rectus Femoris to Treat Stiff Kne… | Na | Stiff Knee Gait | Terminated | 2009-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00357994 | Study of Efficacy, Safety and Tolerability of Levodopa-Carbidopa Intestinal Gel… | Phase3 | Advanced Parkinson's Disease | Completed | 2009-01-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01987765 | Safety and Efficacy of Relestat Ophthalmic Solution 0.05% for Allergic Conjunct… | — | Conjunctivitis, Allergic | Completed | 2009-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00876447 | A Long-term Follow-up Study of Botulinum Toxin Type A in Patients With Overacti… | Phase3 | Overactive Bladder | Completed | 2009-01-01 | 2013-09-04 | ClinicalTrials.gov |
| NCT00357994 | Study of Efficacy, Safety and Tolerability of Levodopa-Carbidopa Intestinal Gel… | Phase3 | Advanced Parkinson's Disease | Completed | 2009-01-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00799227 | Safety and Efficacy of a New Treatment in Vitrectomized Subjects With Diabetic … | Phase2 | Diabetic Macular Edema | Completed | 2009-01-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00808509 | A Pilot Study of the Feasibility of Discontinuation of Adalimumab in Stable Rhe… | Phase4 | Arthritis, Rheumatoid | Completed | 2009-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00816517 | Use of Botulinum Toxin to Treat Psoriasis | Phase1 | Psoriasis Vulgaris | Completed | 2009-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00822523 | Assessment of the Effect of Botulinum Toxin in Extensor Digitorum Brevis Via St… | Na | Muscle Strength | Completed | 2009-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00827255 | Physician's Evaluation of Cyclosporine Ophthalmic Emulsion 0.05% | — | Dry Eye Disease | Completed | 2009-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00836017 | CD-PROBE: Cervical Dystonia Patient Registry for the Observation of onabotulinu… | — | Cervical Dystonia | Completed | 2009-01-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT00836017 | CD-PROBE: Cervical Dystonia Patient Registry for the Observation of onabotulinu… | — | Cervical Dystonia | Completed | 2009-01-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01629433 | Onabotulinumtoxina Intradetrusorial Injections and NGF Expression | — | Overactive Detrusor | Completed | 2009-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00876447 | A Long-term Follow-up Study of Botulinum Toxin Type A in Patients With Overacti… | Phase3 | Overactive Bladder | Completed | 2009-01-01 | 2013-09-04 | ClinicalTrials.gov |
| NCT00827255 | Physician's Evaluation of Cyclosporine Ophthalmic Emulsion 0.05% | — | Dry Eye Disease | Completed | 2009-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00900666 | Efficacy of Botulinum Toxin Injections in the Rectus Femoris to Treat Stiff Kne… | Na | Stiff Knee Gait | Terminated | 2009-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00822523 | Assessment of the Effect of Botulinum Toxin in Extensor Digitorum Brevis Via St… | Na | Muscle Strength | Completed | 2009-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00816517 | Use of Botulinum Toxin to Treat Psoriasis | Phase1 | Psoriasis Vulgaris | Completed | 2009-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00808509 | A Pilot Study of the Feasibility of Discontinuation of Adalimumab in Stable Rhe… | Phase4 | Arthritis, Rheumatoid | Completed | 2009-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00799227 | Safety and Efficacy of a New Treatment in Vitrectomized Subjects With Diabetic … | Phase2 | Diabetic Macular Edema | Completed | 2009-01-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00945295 | Efficacy and Safety Study of Botulinum Neurotoxin A With Rehabilitation Versus … | Na | Upper Limb Spasticity | Completed | 2009-01-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01218737 | Non-Inferiority of Gatifloxacin/Prednisolone Association vs Isolated Administra… | Phase3 | Ocular Infection and Inflammation | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00876447 | A Long-term Follow-up Study of Botulinum Toxin Type A in Patients With Overacti… | Phase3 | Overactive Bladder | Completed | 2009-01-01 | 2013-09-04 | ClinicalTrials.gov |
| NCT01029535 | Safety and Efficacy of Juvederm® VOLUMA™ for Correction of Mid-face Volume Defi… | Na | Mid-face Volume Deficiency | Completed | 2009-01-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01987765 | Safety and Efficacy of Relestat Ophthalmic Solution 0.05% for Allergic Conjunct… | — | Conjunctivitis, Allergic | Completed | 2009-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01218737 | Non-Inferiority of Gatifloxacin/Prednisolone Association vs Isolated Administra… | Phase3 | Ocular Infection and Inflammation | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01218737 | Non-Inferiority of Gatifloxacin/Prednisolone Association vs Isolated Administra… | Phase3 | Ocular Infection and Inflammation | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00357994 | Study of Efficacy, Safety and Tolerability of Levodopa-Carbidopa Intestinal Gel… | Phase3 | Advanced Parkinson's Disease | Completed | 2009-01-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00900666 | Efficacy of Botulinum Toxin Injections in the Rectus Femoris to Treat Stiff Kne… | Na | Stiff Knee Gait | Terminated | 2009-01-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT01629433 | Onabotulinumtoxina Intradetrusorial Injections and NGF Expression | — | Overactive Detrusor | Completed | 2009-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00799227 | Safety and Efficacy of a New Treatment in Vitrectomized Subjects With Diabetic … | Phase2 | Diabetic Macular Edema | Completed | 2009-01-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00808509 | A Pilot Study of the Feasibility of Discontinuation of Adalimumab in Stable Rhe… | Phase4 | Arthritis, Rheumatoid | Completed | 2009-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00816517 | Use of Botulinum Toxin to Treat Psoriasis | Phase1 | Psoriasis Vulgaris | Completed | 2009-01-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00822523 | Assessment of the Effect of Botulinum Toxin in Extensor Digitorum Brevis Via St… | Na | Muscle Strength | Completed | 2009-01-01 | 2015-07-01 | ClinicalTrials.gov |
| NCT00827255 | Physician's Evaluation of Cyclosporine Ophthalmic Emulsion 0.05% | — | Dry Eye Disease | Completed | 2009-01-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00836017 | CD-PROBE: Cervical Dystonia Patient Registry for the Observation of onabotulinu… | — | Cervical Dystonia | Completed | 2009-01-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01629433 | Onabotulinumtoxina Intradetrusorial Injections and NGF Expression | — | Overactive Detrusor | Completed | 2009-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01029535 | Safety and Efficacy of Juvederm® VOLUMA™ for Correction of Mid-face Volume Defi… | Na | Mid-face Volume Deficiency | Completed | 2009-01-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01987765 | Safety and Efficacy of Relestat Ophthalmic Solution 0.05% for Allergic Conjunct… | — | Conjunctivitis, Allergic | Completed | 2009-01-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01218737 | Non-Inferiority of Gatifloxacin/Prednisolone Association vs Isolated Administra… | Phase3 | Ocular Infection and Inflammation | Completed | 2009-01-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT01029535 | Safety and Efficacy of Juvederm® VOLUMA™ for Correction of Mid-face Volume Defi… | Na | Mid-face Volume Deficiency | Completed | 2009-01-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01629433 | Onabotulinumtoxina Intradetrusorial Injections and NGF Expression | — | Overactive Detrusor | Completed | 2009-01-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT01073462 | Study to Evaluate the Effect of Intravenous (IV) Paricalcitol (Zemplar) on Card… | — | Secondary Hyperparathyroidism | Completed | 2008-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00667446 | Safety Extension Study Of Leuprolide Acetate (Lupron Depot) In The Treatment Of… | Phase3 | Precocious | Completed | 2008-12-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01073462 | Study to Evaluate the Effect of Intravenous (IV) Paricalcitol (Zemplar) on Card… | — | Secondary Hyperparathyroidism | Completed | 2008-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00834210 | Dapsone Gel 5% and Tazarotene Cream 0.1% Versus Tazarotene Cream 0.1% Monothera… | Phase4 | Acne Vulgaris | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT01073462 | Study to Evaluate the Effect of Intravenous (IV) Paricalcitol (Zemplar) on Card… | — | Secondary Hyperparathyroidism | Completed | 2008-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00835198 | Dapsone Gel 5% and Tretinoin Gel 0.025% Versus Tretinoin Gel 0.025% Monotherapy… | Phase4 | Acne Vulgaris | Completed | 2008-12-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00667446 | Safety Extension Study Of Leuprolide Acetate (Lupron Depot) In The Treatment Of… | Phase3 | Precocious | Completed | 2008-12-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00811850 | Comparing Effects of Two Fixed Combinations Ophthalmic Solutions on Ocular Bloo… | Phase4 | Glaucoma | Completed | 2008-12-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00811850 | Comparing Effects of Two Fixed Combinations Ophthalmic Solutions on Ocular Bloo… | Phase4 | Glaucoma | Completed | 2008-12-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01073462 | Study to Evaluate the Effect of Intravenous (IV) Paricalcitol (Zemplar) on Card… | — | Secondary Hyperparathyroidism | Completed | 2008-12-01 | 2013-06-01 | ClinicalTrials.gov |
| NCT00811850 | Comparing Effects of Two Fixed Combinations Ophthalmic Solutions on Ocular Bloo… | Phase4 | Glaucoma | Completed | 2008-12-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00835198 | Dapsone Gel 5% and Tretinoin Gel 0.025% Versus Tretinoin Gel 0.025% Monotherapy… | Phase4 | Acne Vulgaris | Completed | 2008-12-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00667446 | Safety Extension Study Of Leuprolide Acetate (Lupron Depot) In The Treatment Of… | Phase3 | Precocious | Completed | 2008-12-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00667446 | Safety Extension Study Of Leuprolide Acetate (Lupron Depot) In The Treatment Of… | Phase3 | Precocious | Completed | 2008-12-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT00834210 | Dapsone Gel 5% and Tazarotene Cream 0.1% Versus Tazarotene Cream 0.1% Monothera… | Phase4 | Acne Vulgaris | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00835198 | Dapsone Gel 5% and Tretinoin Gel 0.025% Versus Tretinoin Gel 0.025% Monotherapy… | Phase4 | Acne Vulgaris | Completed | 2008-12-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00834210 | Dapsone Gel 5% and Tazarotene Cream 0.1% Versus Tazarotene Cream 0.1% Monothera… | Phase4 | Acne Vulgaris | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00811850 | Comparing Effects of Two Fixed Combinations Ophthalmic Solutions on Ocular Bloo… | Phase4 | Glaucoma | Completed | 2008-12-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00834210 | Dapsone Gel 5% and Tazarotene Cream 0.1% Versus Tazarotene Cream 0.1% Monothera… | Phase4 | Acne Vulgaris | Completed | 2008-12-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00835198 | Dapsone Gel 5% and Tretinoin Gel 0.025% Versus Tretinoin Gel 0.025% Monotherapy… | Phase4 | Acne Vulgaris | Completed | 2008-12-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00797225 | Efficacy and Safety Study of Elagolix Versus Placebo or Leuprorelin Acetate in … | Phase2 | Endometriosis | Completed | 2008-11-26 | 2010-02-24 | ClinicalTrials.gov |
| NCT00797225 | Efficacy and Safety Study of Elagolix Versus Placebo or Leuprorelin Acetate in … | Phase2 | Endometriosis | Completed | 2008-11-26 | 2010-02-24 | ClinicalTrials.gov |
| NCT00797225 | Efficacy and Safety Study of Elagolix Versus Placebo or Leuprorelin Acetate in … | Phase2 | Endometriosis | Completed | 2008-11-26 | 2010-02-24 | ClinicalTrials.gov |
| NCT00797225 | Efficacy and Safety Study of Elagolix Versus Placebo or Leuprorelin Acetate in … | Phase2 | Endometriosis | Completed | 2008-11-26 | 2010-02-24 | ClinicalTrials.gov |
| NCT00888693 | A Multiple Dose Study of Safety, Tolerability, Pharmacokinetics, and Pharmacody… | Phase1 | Schizophrenia | Completed | 2008-11-01 | — | ClinicalTrials.gov |
| NCT00888693 | A Multiple Dose Study of Safety, Tolerability, Pharmacokinetics, and Pharmacody… | Phase1 | Schizophrenia | Completed | 2008-11-01 | — | ClinicalTrials.gov |
| NCT00850889 | Juvederm Ultra With Lidocaine Compared With Restylane for the Correction of Nas… | Phase4 | Nasolabial Folds | Completed | 2008-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00850889 | Juvederm Ultra With Lidocaine Compared With Restylane for the Correction of Nas… | Phase4 | Nasolabial Folds | Completed | 2008-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00850889 | Juvederm Ultra With Lidocaine Compared With Restylane for the Correction of Nas… | Phase4 | Nasolabial Folds | Completed | 2008-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00775411 | Safety and Efficacy of a New Therapy as Adjunctive Therapy to Anti-vascular End… | Phase2 | Choroidal Neovascularization | Completed | 2008-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00888693 | A Multiple Dose Study of Safety, Tolerability, Pharmacokinetics, and Pharmacody… | Phase1 | Schizophrenia | Completed | 2008-11-01 | — | ClinicalTrials.gov |
| NCT00791323 | Efficacy of Ketorolac 0.4% in Prostaglandin Suppression | Phase4 | Inflammation | Completed | 2008-11-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00791323 | Efficacy of Ketorolac 0.4% in Prostaglandin Suppression | Phase4 | Inflammation | Completed | 2008-11-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00775411 | Safety and Efficacy of a New Therapy as Adjunctive Therapy to Anti-vascular End… | Phase2 | Choroidal Neovascularization | Completed | 2008-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00791323 | Efficacy of Ketorolac 0.4% in Prostaglandin Suppression | Phase4 | Inflammation | Completed | 2008-11-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00888693 | A Multiple Dose Study of Safety, Tolerability, Pharmacokinetics, and Pharmacody… | Phase1 | Schizophrenia | Completed | 2008-11-01 | — | ClinicalTrials.gov |
| NCT00775411 | Safety and Efficacy of a New Therapy as Adjunctive Therapy to Anti-vascular End… | Phase2 | Choroidal Neovascularization | Completed | 2008-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00791323 | Efficacy of Ketorolac 0.4% in Prostaglandin Suppression | Phase4 | Inflammation | Completed | 2008-11-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00850889 | Juvederm Ultra With Lidocaine Compared With Restylane for the Correction of Nas… | Phase4 | Nasolabial Folds | Completed | 2008-11-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00775411 | Safety and Efficacy of a New Therapy as Adjunctive Therapy to Anti-vascular End… | Phase2 | Choroidal Neovascularization | Completed | 2008-11-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT02075697 | Spanish Registry of Systemic Treatments in Psoriasis | — | Psoriasis | Unknown | 2008-10-01 | 2025-10-01 | ClinicalTrials.gov |
| NCT00707889 | Phase 2 Study of ABT-869 in Combination With mFOLFOX6 Versus Bevacizumab in Com… | Phase2 | Advanced Colorectal Cancer | Completed | 2008-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT02075697 | Spanish Registry of Systemic Treatments in Psoriasis | — | Psoriasis | Unknown | 2008-10-01 | 2025-10-01 | ClinicalTrials.gov |
| NCT02075697 | Spanish Registry of Systemic Treatments in Psoriasis | — | Psoriasis | Unknown | 2008-10-01 | 2025-10-01 | ClinicalTrials.gov |
| NCT02075697 | Spanish Registry of Systemic Treatments in Psoriasis | — | Psoriasis | Unknown | 2008-10-01 | 2025-10-01 | ClinicalTrials.gov |
| NCT00707889 | Phase 2 Study of ABT-869 in Combination With mFOLFOX6 Versus Bevacizumab in Com… | Phase2 | Advanced Colorectal Cancer | Completed | 2008-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00707889 | Phase 2 Study of ABT-869 in Combination With mFOLFOX6 Versus Bevacizumab in Com… | Phase2 | Advanced Colorectal Cancer | Completed | 2008-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00707889 | Phase 2 Study of ABT-869 in Combination With mFOLFOX6 Versus Bevacizumab in Com… | Phase2 | Advanced Colorectal Cancer | Completed | 2008-10-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00799877 | Chronic Plaque Psoriasis (Ps) Registry | — | Chronic Plaque Psoriasis | Completed | 2008-09-26 | 2023-02-13 | ClinicalTrials.gov |
| NCT00799877 | Chronic Plaque Psoriasis (Ps) Registry | — | Chronic Plaque Psoriasis | Completed | 2008-09-26 | 2023-02-13 | ClinicalTrials.gov |
| NCT00799877 | Chronic Plaque Psoriasis (Ps) Registry | — | Chronic Plaque Psoriasis | Completed | 2008-09-26 | 2023-02-13 | ClinicalTrials.gov |
| NCT00799877 | Chronic Plaque Psoriasis (Ps) Registry | — | Chronic Plaque Psoriasis | Completed | 2008-09-26 | 2023-02-13 | ClinicalTrials.gov |
| NCT02029677 | Appetite Suppression / Hormone Study Control Group | — | Morbid Obesity | Active_Not_Recruiting | 2008-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT00763321 | Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate … | Phase3 | Chronic Low Back Pain | Completed | 2008-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00763321 | Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate … | Phase3 | Chronic Low Back Pain | Completed | 2008-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00761150 | Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate … | Phase3 | Chronic Low Back Pain | Completed | 2008-09-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00756678 | Efficacy and Acceptability of Two Lubricant Eye Drops | Phase4 | Dry Eye Syndromes | Completed | 2008-09-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01076179 | Kaletra in Combination With Antiretroviral Agents | — | Human Immunodeficiency Virus | Completed | 2008-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT02029677 | Appetite Suppression / Hormone Study Control Group | — | Morbid Obesity | Active_Not_Recruiting | 2008-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT00756678 | Efficacy and Acceptability of Two Lubricant Eye Drops | Phase4 | Dry Eye Syndromes | Completed | 2008-09-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT01076179 | Kaletra in Combination With Antiretroviral Agents | — | Human Immunodeficiency Virus | Completed | 2008-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00756678 | Efficacy and Acceptability of Two Lubricant Eye Drops | Phase4 | Dry Eye Syndromes | Completed | 2008-09-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT00761150 | Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate … | Phase3 | Chronic Low Back Pain | Completed | 2008-09-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00763321 | Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate … | Phase3 | Chronic Low Back Pain | Completed | 2008-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00718380 | A Phase 1 Study of ABT-869 in Subjects With Solid Tumors | Phase1 | Solid Tumor | Completed | 2008-09-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00718380 | A Phase 1 Study of ABT-869 in Subjects With Solid Tumors | Phase1 | Solid Tumor | Completed | 2008-09-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT02029677 | Appetite Suppression / Hormone Study Control Group | — | Morbid Obesity | Active_Not_Recruiting | 2008-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT00718380 | A Phase 1 Study of ABT-869 in Subjects With Solid Tumors | Phase1 | Solid Tumor | Completed | 2008-09-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00718380 | A Phase 1 Study of ABT-869 in Subjects With Solid Tumors | Phase1 | Solid Tumor | Completed | 2008-09-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00763321 | Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate … | Phase3 | Chronic Low Back Pain | Completed | 2008-09-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00761150 | Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate … | Phase3 | Chronic Low Back Pain | Completed | 2008-09-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00756678 | Efficacy and Acceptability of Two Lubricant Eye Drops | Phase4 | Dry Eye Syndromes | Completed | 2008-09-01 | 2009-08-01 | ClinicalTrials.gov |
| NCT02029677 | Appetite Suppression / Hormone Study Control Group | — | Morbid Obesity | Active_Not_Recruiting | 2008-09-01 | 2024-12-01 | ClinicalTrials.gov |
| NCT01076179 | Kaletra in Combination With Antiretroviral Agents | — | Human Immunodeficiency Virus | Completed | 2008-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT01076179 | Kaletra in Combination With Antiretroviral Agents | — | Human Immunodeficiency Virus | Completed | 2008-09-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00761150 | Study to Evaluate the Safety and Efficacy of ABT-712 in Subjects With Moderate … | Phase3 | Chronic Low Back Pain | Completed | 2008-09-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00850733 | 516-BOTOX Urinary Incontinence Detrusor | — | Urinary Incontinence | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00726882 | A Follow-up Assessment of Resistance to ABT-333 in Hepatitis C Virus (HCV)-Infe… | Phase2 | HCV Infection | Completed | 2008-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00726882 | A Follow-up Assessment of Resistance to ABT-333 in Hepatitis C Virus (HCV)-Infe… | Phase2 | HCV Infection | Completed | 2008-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00726882 | A Follow-up Assessment of Resistance to ABT-333 in Hepatitis C Virus (HCV)-Infe… | Phase2 | HCV Infection | Completed | 2008-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00742560 | A Phase 1b/2, Dose-Escalation Study of Elotuzumab (Humanized Anti-CS1 Monoclona… | Phase2 | Hematologic Cancer | Completed | 2008-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT00850733 | 516-BOTOX Urinary Incontinence Detrusor | — | Urinary Incontinence | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00742560 | A Phase 1b/2, Dose-Escalation Study of Elotuzumab (Humanized Anti-CS1 Monoclona… | Phase2 | Hematologic Cancer | Completed | 2008-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT00850733 | 516-BOTOX Urinary Incontinence Detrusor | — | Urinary Incontinence | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00742560 | A Phase 1b/2, Dose-Escalation Study of Elotuzumab (Humanized Anti-CS1 Monoclona… | Phase2 | Hematologic Cancer | Completed | 2008-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT00850733 | 516-BOTOX Urinary Incontinence Detrusor | — | Urinary Incontinence | Completed | 2008-08-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00726882 | A Follow-up Assessment of Resistance to ABT-333 in Hepatitis C Virus (HCV)-Infe… | Phase2 | HCV Infection | Completed | 2008-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00742560 | A Phase 1b/2, Dose-Escalation Study of Elotuzumab (Humanized Anti-CS1 Monoclona… | Phase2 | Hematologic Cancer | Completed | 2008-08-01 | 2016-10-01 | ClinicalTrials.gov |
| NCT00783510 | Juvenile Idiopathic Arthritis (JIA) Registry | — | Juvenile Idiopathic Arthritis | Completed | 2008-07-11 | 2024-02-01 | ClinicalTrials.gov |
| NCT00783510 | Juvenile Idiopathic Arthritis (JIA) Registry | — | Juvenile Idiopathic Arthritis | Completed | 2008-07-11 | 2024-02-01 | ClinicalTrials.gov |
| NCT00783510 | Juvenile Idiopathic Arthritis (JIA) Registry | — | Juvenile Idiopathic Arthritis | Completed | 2008-07-11 | 2024-02-01 | ClinicalTrials.gov |
| NCT00783510 | Juvenile Idiopathic Arthritis (JIA) Registry | — | Juvenile Idiopathic Arthritis | Completed | 2008-07-11 | 2024-02-01 | ClinicalTrials.gov |
| NCT00735449 | Comparing Efficacy and Safety of Combigan With Timolol Adjunctive to Xalatan in… | Phase4 | Glaucoma | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00710580 | Study Comparing the Efficacy and Safety of ABT-874 to Etanercept and Placebo in… | Phase3 | Moderate to Severe Plaque Psoriasis | Completed | 2008-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00735449 | Comparing Efficacy and Safety of Combigan With Timolol Adjunctive to Xalatan in… | Phase4 | Glaucoma | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00645177 | Phase 2 Study of ABT-869 in Combination With Paclitaxel Versus Paclitaxel Alone… | Phase2 | Metastatic Breast Cancer | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00661479 | An Exploratory Study to Evaluate the Safety of Brimonidine Intravitreal Implant… | Phase1 | Retinitis Pigmentosa | Completed | 2008-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00735449 | Comparing Efficacy and Safety of Combigan With Timolol Adjunctive to Xalatan in… | Phase4 | Glaucoma | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00623636 | Phase 3 Study of MAP0004 in Adult Migraineurs | Phase3 | Migraine Disorders | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00623636 | Phase 3 Study of MAP0004 in Adult Migraineurs | Phase3 | Migraine Disorders | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00623636 | Phase 3 Study of MAP0004 in Adult Migraineurs | Phase3 | Migraine Disorders | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00710580 | Study Comparing the Efficacy and Safety of ABT-874 to Etanercept and Placebo in… | Phase3 | Moderate to Severe Plaque Psoriasis | Completed | 2008-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00710580 | Study Comparing the Efficacy and Safety of ABT-874 to Etanercept and Placebo in… | Phase3 | Moderate to Severe Plaque Psoriasis | Completed | 2008-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00645177 | Phase 2 Study of ABT-869 in Combination With Paclitaxel Versus Paclitaxel Alone… | Phase2 | Metastatic Breast Cancer | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00735449 | Comparing Efficacy and Safety of Combigan With Timolol Adjunctive to Xalatan in… | Phase4 | Glaucoma | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00645177 | Phase 2 Study of ABT-869 in Combination With Paclitaxel Versus Paclitaxel Alone… | Phase2 | Metastatic Breast Cancer | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00710580 | Study Comparing the Efficacy and Safety of ABT-874 to Etanercept and Placebo in… | Phase3 | Moderate to Severe Plaque Psoriasis | Completed | 2008-07-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00661479 | An Exploratory Study to Evaluate the Safety of Brimonidine Intravitreal Implant… | Phase1 | Retinitis Pigmentosa | Completed | 2008-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00645177 | Phase 2 Study of ABT-869 in Combination With Paclitaxel Versus Paclitaxel Alone… | Phase2 | Metastatic Breast Cancer | Completed | 2008-07-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00661479 | An Exploratory Study to Evaluate the Safety of Brimonidine Intravitreal Implant… | Phase1 | Retinitis Pigmentosa | Completed | 2008-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00661479 | An Exploratory Study to Evaluate the Safety of Brimonidine Intravitreal Implant… | Phase1 | Retinitis Pigmentosa | Completed | 2008-07-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00623636 | Phase 3 Study of MAP0004 in Adult Migraineurs | Phase3 | Migraine Disorders | Completed | 2008-07-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00716534 | Study of Carboplatin/Paclitaxel in Combination With ABT-869 in Subjects With Ad… | Phase2 | Advanced or Metastatic Non-Small Cell Lung Cancer | Completed | 2008-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00716534 | Study of Carboplatin/Paclitaxel in Combination With ABT-869 in Subjects With Ad… | Phase2 | Advanced or Metastatic Non-Small Cell Lung Cancer | Completed | 2008-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00696904 | Study of ABT-333 in Both Healthy Volunteers and Hepatitis C Virus (HCV) + Genot… | Phase1 | HCV Infection | Completed | 2008-06-01 | — | ClinicalTrials.gov |
| NCT00696904 | Study of ABT-333 in Both Healthy Volunteers and Hepatitis C Virus (HCV) + Genot… | Phase1 | HCV Infection | Completed | 2008-06-01 | — | ClinicalTrials.gov |
| NCT00716534 | Study of Carboplatin/Paclitaxel in Combination With ABT-869 in Subjects With Ad… | Phase2 | Advanced or Metastatic Non-Small Cell Lung Cancer | Completed | 2008-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00696904 | Study of ABT-333 in Both Healthy Volunteers and Hepatitis C Virus (HCV) + Genot… | Phase1 | HCV Infection | Completed | 2008-06-01 | — | ClinicalTrials.gov |
| NCT00696904 | Study of ABT-333 in Both Healthy Volunteers and Hepatitis C Virus (HCV) + Genot… | Phase1 | HCV Infection | Completed | 2008-06-01 | — | ClinicalTrials.gov |
| NCT00716534 | Study of Carboplatin/Paclitaxel in Combination With ABT-869 in Subjects With Ad… | Phase2 | Advanced or Metastatic Non-Small Cell Lung Cancer | Completed | 2008-06-01 | 2012-04-01 | ClinicalTrials.gov |
| NCT00658619 | Safety and Efficacy of Brimonidine Intravitreal Implant in Patients With Geogra… | Phase2 | Macular Degeneration | Completed | 2008-05-01 | 2011-04-08 | ClinicalTrials.gov |
| NCT00686933 | Long Term Safety and Tolerability Study of ABT-089 in Adults With Attention-Def… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00686933 | Long Term Safety and Tolerability Study of ABT-089 in Adults With Attention-Def… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00686933 | Long Term Safety and Tolerability Study of ABT-089 in Adults With Attention-Def… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00658619 | Safety and Efficacy of Brimonidine Intravitreal Implant in Patients With Geogra… | Phase2 | Macular Degeneration | Completed | 2008-05-01 | 2011-04-08 | ClinicalTrials.gov |
| NCT00658619 | Safety and Efficacy of Brimonidine Intravitreal Implant in Patients With Geogra… | Phase2 | Macular Degeneration | Completed | 2008-05-01 | 2011-04-08 | ClinicalTrials.gov |
| NCT00686374 | Efficacy and Long Term Safety of Adalimumab in Pediatric Subjects Who Have Demo… | Phase3 | Crohn's Disease | Completed | 2008-05-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT00686374 | Efficacy and Long Term Safety of Adalimumab in Pediatric Subjects Who Have Demo… | Phase3 | Crohn's Disease | Completed | 2008-05-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT00686374 | Efficacy and Long Term Safety of Adalimumab in Pediatric Subjects Who Have Demo… | Phase3 | Crohn's Disease | Completed | 2008-05-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT00686933 | Long Term Safety and Tolerability Study of ABT-089 in Adults With Attention-Def… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-05-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00686374 | Efficacy and Long Term Safety of Adalimumab in Pediatric Subjects Who Have Demo… | Phase3 | Crohn's Disease | Completed | 2008-05-01 | 2017-04-04 | ClinicalTrials.gov |
| NCT00658619 | Safety and Efficacy of Brimonidine Intravitreal Implant in Patients With Geogra… | Phase2 | Macular Degeneration | Completed | 2008-05-01 | 2011-04-08 | ClinicalTrials.gov |
| NCT00773253 | Botox for Cervical Dystonia Following EMG Mapping | Phase4 | Cervical Dystonia | Completed | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00697697 | A Study of 2 Doses of MAP0010 in Asthmatic Children | Phase3 | Asthma | Terminated | 2008-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00773253 | Botox for Cervical Dystonia Following EMG Mapping | Phase4 | Cervical Dystonia | Completed | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00697697 | A Study of 2 Doses of MAP0010 in Asthmatic Children | Phase3 | Asthma | Terminated | 2008-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00697697 | A Study of 2 Doses of MAP0010 in Asthmatic Children | Phase3 | Asthma | Terminated | 2008-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00773253 | Botox for Cervical Dystonia Following EMG Mapping | Phase4 | Cervical Dystonia | Completed | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00697697 | A Study of 2 Doses of MAP0010 in Asthmatic Children | Phase3 | Asthma | Terminated | 2008-04-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00773253 | Botox for Cervical Dystonia Following EMG Mapping | Phase4 | Cervical Dystonia | Completed | 2008-04-01 | 2011-01-01 | ClinicalTrials.gov |
| NCT00533351 | Safety and Efficacy of AGN201781 in Neuropathic Pain | Phase2 | Neuralgia | Terminated | 2008-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00640185 | Safety, Tolerability and Efficacy Study of ABT-089 in Adults With Attention-Def… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-03-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT01083849 | Long-Term Therapy Outcomes When Treating Chronic Kidney Disease (CKD) Patients … | — | Kidney Insufficiency | Completed | 2008-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00640419 | Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/Hyp… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-03-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00691197 | Safety and Acceptability of Using a Rewetting Drop With Contact Lens Wear | Phase2 | Ametropia | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00533351 | Safety and Efficacy of AGN201781 in Neuropathic Pain | Phase2 | Neuralgia | Terminated | 2008-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00691197 | Safety and Acceptability of Using a Rewetting Drop With Contact Lens Wear | Phase2 | Ametropia | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00640419 | Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/Hyp… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-03-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00640185 | Safety, Tolerability and Efficacy Study of ABT-089 in Adults With Attention-Def… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-03-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00691197 | Safety and Acceptability of Using a Rewetting Drop With Contact Lens Wear | Phase2 | Ametropia | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00533351 | Safety and Efficacy of AGN201781 in Neuropathic Pain | Phase2 | Neuralgia | Terminated | 2008-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00640419 | Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/Hyp… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-03-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00640185 | Safety, Tolerability and Efficacy Study of ABT-089 in Adults With Attention-Def… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-03-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00640419 | Safety and Tolerability Study of ABT-089 in Children With Attention-Deficit/Hyp… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-03-01 | 2008-07-01 | ClinicalTrials.gov |
| NCT00640185 | Safety, Tolerability and Efficacy Study of ABT-089 in Adults With Attention-Def… | Phase2 | Attention-Deficit/Hyperactivity Disorder | Completed | 2008-03-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00533351 | Safety and Efficacy of AGN201781 in Neuropathic Pain | Phase2 | Neuralgia | Terminated | 2008-03-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00691197 | Safety and Acceptability of Using a Rewetting Drop With Contact Lens Wear | Phase2 | Ametropia | Completed | 2008-03-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT01083849 | Long-Term Therapy Outcomes When Treating Chronic Kidney Disease (CKD) Patients … | — | Kidney Insufficiency | Completed | 2008-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01083849 | Long-Term Therapy Outcomes When Treating Chronic Kidney Disease (CKD) Patients … | — | Kidney Insufficiency | Completed | 2008-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01083849 | Long-Term Therapy Outcomes When Treating Chronic Kidney Disease (CKD) Patients … | — | Kidney Insufficiency | Completed | 2008-03-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00619866 | An Efficacy and Safety Study of Elagolix (NBI-56418) in Women With Endometriosis | Phase2 | Endometriosis, Pain | Completed | 2008-02-19 | 2009-08-28 | ClinicalTrials.gov |
| NCT00619866 | An Efficacy and Safety Study of Elagolix (NBI-56418) in Women With Endometriosis | Phase2 | Endometriosis, Pain | Completed | 2008-02-19 | 2009-08-28 | ClinicalTrials.gov |
| NCT00619866 | An Efficacy and Safety Study of Elagolix (NBI-56418) in Women With Endometriosis | Phase2 | Endometriosis, Pain | Completed | 2008-02-19 | 2009-08-28 | ClinicalTrials.gov |
| NCT00619866 | An Efficacy and Safety Study of Elagolix (NBI-56418) in Women With Endometriosis | Phase2 | Endometriosis, Pain | Completed | 2008-02-19 | 2009-08-28 | ClinicalTrials.gov |
| NCT00390221 | Safety and Efficacy Study of Daclizumab High Yield Process (DAC HYP) to Treat R… | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2008-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00616772 | Safety and Efficacy Study Using ABT-335 (Investigational Drug) in Combination W… | Phase3 | Coronary Artery Disease | Completed | 2008-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00626002 | Open Label Continuation Study in Moderate to Severe Psoriasis | Phase3 | Moderate to Severe Plaque Psoriasis | Completed | 2008-02-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00626002 | Open Label Continuation Study in Moderate to Severe Psoriasis | Phase3 | Moderate to Severe Plaque Psoriasis | Completed | 2008-02-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00616772 | Safety and Efficacy Study Using ABT-335 (Investigational Drug) in Combination W… | Phase3 | Coronary Artery Disease | Completed | 2008-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00518089 | A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial C… | Phase3 | Bacterial Conjunctivitis | Completed | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00626002 | Open Label Continuation Study in Moderate to Severe Psoriasis | Phase3 | Moderate to Severe Plaque Psoriasis | Completed | 2008-02-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT00518089 | A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial C… | Phase3 | Bacterial Conjunctivitis | Completed | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00390221 | Safety and Efficacy Study of Daclizumab High Yield Process (DAC HYP) to Treat R… | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2008-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00497146 | The PRIMO Study: Paricalcitol Capsules Benefits Renal Failure Induced Cardiac M… | Phase3 | Chronic Kidney Disease | Completed | 2008-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00518089 | A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial C… | Phase3 | Bacterial Conjunctivitis | Completed | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00497146 | The PRIMO Study: Paricalcitol Capsules Benefits Renal Failure Induced Cardiac M… | Phase3 | Chronic Kidney Disease | Completed | 2008-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00390221 | Safety and Efficacy Study of Daclizumab High Yield Process (DAC HYP) to Treat R… | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2008-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00497146 | The PRIMO Study: Paricalcitol Capsules Benefits Renal Failure Induced Cardiac M… | Phase3 | Chronic Kidney Disease | Completed | 2008-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00497146 | The PRIMO Study: Paricalcitol Capsules Benefits Renal Failure Induced Cardiac M… | Phase3 | Chronic Kidney Disease | Completed | 2008-02-01 | 2012-03-01 | ClinicalTrials.gov |
| NCT00390221 | Safety and Efficacy Study of Daclizumab High Yield Process (DAC HYP) to Treat R… | Phase2 | Relapsing-Remitting Multiple Sclerosis | Completed | 2008-02-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00518089 | A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial C… | Phase3 | Bacterial Conjunctivitis | Completed | 2008-02-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00616772 | Safety and Efficacy Study Using ABT-335 (Investigational Drug) in Combination W… | Phase3 | Coronary Artery Disease | Completed | 2008-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00616772 | Safety and Efficacy Study Using ABT-335 (Investigational Drug) in Combination W… | Phase3 | Coronary Artery Disease | Completed | 2008-02-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00626002 | Open Label Continuation Study in Moderate to Severe Psoriasis | Phase3 | Moderate to Severe Plaque Psoriasis | Completed | 2008-02-01 | 2011-10-01 | ClinicalTrials.gov |
| NCT01077232 | Documentation of Humira in Psoriasis Patients in Routine Clinical Practice | — | Moderate to Severe Plaque Psoriasis | Completed | 2008-01-04 | 2019-06-30 | ClinicalTrials.gov |
| NCT01077232 | Documentation of Humira in Psoriasis Patients in Routine Clinical Practice | — | Moderate to Severe Plaque Psoriasis | Completed | 2008-01-04 | 2019-06-30 | ClinicalTrials.gov |
| NCT01077232 | Documentation of Humira in Psoriasis Patients in Routine Clinical Practice | — | Moderate to Severe Plaque Psoriasis | Completed | 2008-01-04 | 2019-06-30 | ClinicalTrials.gov |
| NCT01077232 | Documentation of Humira in Psoriasis Patients in Routine Clinical Practice | — | Moderate to Severe Plaque Psoriasis | Completed | 2008-01-04 | 2019-06-30 | ClinicalTrials.gov |
| NCT01848028 | PsoBest - The German Psoriasis Registry | — | Psoriasis | Recruiting | 2008-01-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01848028 | PsoBest - The German Psoriasis Registry | — | Psoriasis | Recruiting | 2008-01-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT01848028 | PsoBest - The German Psoriasis Registry | — | Psoriasis | Recruiting | 2008-01-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT00335153 | Levodopa-Carbidopa Intestinal Gel Open-Label Study in Advanced Parkinson's Dise… | Phase3 | Advanced Parkinson's Disease | Completed | 2008-01-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01848028 | PsoBest - The German Psoriasis Registry | — | Psoriasis | Recruiting | 2008-01-01 | 2032-12-01 | ClinicalTrials.gov |
| NCT00335153 | Levodopa-Carbidopa Intestinal Gel Open-Label Study in Advanced Parkinson's Dise… | Phase3 | Advanced Parkinson's Disease | Completed | 2008-01-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00335153 | Levodopa-Carbidopa Intestinal Gel Open-Label Study in Advanced Parkinson's Dise… | Phase3 | Advanced Parkinson's Disease | Completed | 2008-01-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00335153 | Levodopa-Carbidopa Intestinal Gel Open-Label Study in Advanced Parkinson's Dise… | Phase3 | Advanced Parkinson's Disease | Completed | 2008-01-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00621933 | Surveillance of Ocular Surface Flora (SURFACE) | — | Cataract | Completed | 2007-12-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00621933 | Surveillance of Ocular Surface Flora (SURFACE) | — | Cataract | Completed | 2007-12-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00541242 | Safety and Efficacy of Bimatoprost Compared With Latanoprost in Patients With G… | Phase4 | Ocular Hypertension | Completed | 2007-12-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00564681 | Study to Evaluate Safety, Efficacy of Botulinum Toxin Type A in Patients With C… | Phase2 | Cervical Dystonia | Completed | 2007-12-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00569192 | A Study of 2 Doses of MAP0010 and Placebo in Asthmatic Children | Phase3 | Asthma | Completed | 2007-12-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00575016 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase2 | Overactive Bladder | Terminated | 2007-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00611403 | Safety and Efficacy Study of Cyclosporine Ophthalmic Emulsion in Post-LASIK Pat… | Phase2 | Dry Eye Syndromes | Completed | 2007-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00621933 | Surveillance of Ocular Surface Flora (SURFACE) | — | Cataract | Completed | 2007-12-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00611403 | Safety and Efficacy Study of Cyclosporine Ophthalmic Emulsion in Post-LASIK Pat… | Phase2 | Dry Eye Syndromes | Completed | 2007-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00895063 | Effect of Vocal Exercise After Botulinum Toxin Injection for Spasmodic Dysphonia | Na | Spasmodic Dysphonia | Terminated | 2007-12-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00621933 | Surveillance of Ocular Surface Flora (SURFACE) | — | Cataract | Completed | 2007-12-01 | 2008-11-01 | ClinicalTrials.gov |
| NCT00611403 | Safety and Efficacy Study of Cyclosporine Ophthalmic Emulsion in Post-LASIK Pat… | Phase2 | Dry Eye Syndromes | Completed | 2007-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00575016 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase2 | Overactive Bladder | Terminated | 2007-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00569192 | A Study of 2 Doses of MAP0010 and Placebo in Asthmatic Children | Phase3 | Asthma | Completed | 2007-12-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00564681 | Study to Evaluate Safety, Efficacy of Botulinum Toxin Type A in Patients With C… | Phase2 | Cervical Dystonia | Completed | 2007-12-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00541242 | Safety and Efficacy of Bimatoprost Compared With Latanoprost in Patients With G… | Phase4 | Ocular Hypertension | Completed | 2007-12-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00654758 | A Phase 1b Study With Volociximab in Combination With Carboplatin and Paclitaxe… | Phase1 | Non-small Cell Lung Cancer | Completed | 2007-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00654758 | A Phase 1b Study With Volociximab in Combination With Carboplatin and Paclitaxe… | Phase1 | Non-small Cell Lung Cancer | Completed | 2007-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00895063 | Effect of Vocal Exercise After Botulinum Toxin Injection for Spasmodic Dysphonia | Na | Spasmodic Dysphonia | Terminated | 2007-12-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00895063 | Effect of Vocal Exercise After Botulinum Toxin Injection for Spasmodic Dysphonia | Na | Spasmodic Dysphonia | Terminated | 2007-12-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00575016 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase2 | Overactive Bladder | Terminated | 2007-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00569192 | A Study of 2 Doses of MAP0010 and Placebo in Asthmatic Children | Phase3 | Asthma | Completed | 2007-12-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00654758 | A Phase 1b Study With Volociximab in Combination With Carboplatin and Paclitaxe… | Phase1 | Non-small Cell Lung Cancer | Completed | 2007-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00564681 | Study to Evaluate Safety, Efficacy of Botulinum Toxin Type A in Patients With C… | Phase2 | Cervical Dystonia | Completed | 2007-12-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00895063 | Effect of Vocal Exercise After Botulinum Toxin Injection for Spasmodic Dysphonia | Na | Spasmodic Dysphonia | Terminated | 2007-12-01 | 2013-05-01 | ClinicalTrials.gov |
| NCT00654758 | A Phase 1b Study With Volociximab in Combination With Carboplatin and Paclitaxe… | Phase1 | Non-small Cell Lung Cancer | Completed | 2007-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00541242 | Safety and Efficacy of Bimatoprost Compared With Latanoprost in Patients With G… | Phase4 | Ocular Hypertension | Completed | 2007-12-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00611403 | Safety and Efficacy Study of Cyclosporine Ophthalmic Emulsion in Post-LASIK Pat… | Phase2 | Dry Eye Syndromes | Completed | 2007-12-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00575016 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase2 | Overactive Bladder | Terminated | 2007-12-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00569192 | A Study of 2 Doses of MAP0010 and Placebo in Asthmatic Children | Phase3 | Asthma | Completed | 2007-12-01 | 2009-01-01 | ClinicalTrials.gov |
| NCT00541242 | Safety and Efficacy of Bimatoprost Compared With Latanoprost in Patients With G… | Phase4 | Ocular Hypertension | Completed | 2007-12-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00564681 | Study to Evaluate Safety, Efficacy of Botulinum Toxin Type A in Patients With C… | Phase2 | Cervical Dystonia | Completed | 2007-12-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00573794 | Long-term Open-label Safety and Efficacy Study of Adalimumab in Subjects With U… | Phase3 | Ulcerative Colitis | Completed | 2007-11-28 | 2016-12-01 | ClinicalTrials.gov |
| NCT00573794 | Long-term Open-label Safety and Efficacy Study of Adalimumab in Subjects With U… | Phase3 | Ulcerative Colitis | Completed | 2007-11-28 | 2016-12-01 | ClinicalTrials.gov |
| NCT00573794 | Long-term Open-label Safety and Efficacy Study of Adalimumab in Subjects With U… | Phase3 | Ulcerative Colitis | Completed | 2007-11-28 | 2016-12-01 | ClinicalTrials.gov |
| NCT00573794 | Long-term Open-label Safety and Efficacy Study of Adalimumab in Subjects With U… | Phase3 | Ulcerative Colitis | Completed | 2007-11-28 | 2016-12-01 | ClinicalTrials.gov |
| NCT00538304 | A Study of the Safety and Efficacy of Bimatoprost in Patients With Glaucoma or … | Phase2 | Glaucoma | Completed | 2007-11-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00554970 | A Study of 2 Doses of MAP0010 in Adult Asthmatics | Phase2 | Asthma | Completed | 2007-11-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00538304 | A Study of the Safety and Efficacy of Bimatoprost in Patients With Glaucoma or … | Phase2 | Glaucoma | Completed | 2007-11-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00462449 | Efficacy of Functional Electrical Stimulation (FES) in Persons Receiving Botuli… | Na | Upper Extremity Spasticity | Completed | 2007-11-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00511706 | Safety and Efficacy of a New Treatment as Adjunctive Therapy to Anti-vascular E… | Phase2 | Choroidal Neovascularization | Completed | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00554970 | A Study of 2 Doses of MAP0010 in Adult Asthmatics | Phase2 | Asthma | Completed | 2007-11-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00462449 | Efficacy of Functional Electrical Stimulation (FES) in Persons Receiving Botuli… | Na | Upper Extremity Spasticity | Completed | 2007-11-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00554970 | A Study of 2 Doses of MAP0010 in Adult Asthmatics | Phase2 | Asthma | Completed | 2007-11-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00462449 | Efficacy of Functional Electrical Stimulation (FES) in Persons Receiving Botuli… | Na | Upper Extremity Spasticity | Completed | 2007-11-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00538304 | A Study of the Safety and Efficacy of Bimatoprost in Patients With Glaucoma or … | Phase2 | Glaucoma | Completed | 2007-11-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00462449 | Efficacy of Functional Electrical Stimulation (FES) in Persons Receiving Botuli… | Na | Upper Extremity Spasticity | Completed | 2007-11-01 | 2010-01-01 | ClinicalTrials.gov |
| NCT00538304 | A Study of the Safety and Efficacy of Bimatoprost in Patients With Glaucoma or … | Phase2 | Glaucoma | Completed | 2007-11-01 | 2008-05-01 | ClinicalTrials.gov |
| NCT00511706 | Safety and Efficacy of a New Treatment as Adjunctive Therapy to Anti-vascular E… | Phase2 | Choroidal Neovascularization | Completed | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00511706 | Safety and Efficacy of a New Treatment as Adjunctive Therapy to Anti-vascular E… | Phase2 | Choroidal Neovascularization | Completed | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00511706 | Safety and Efficacy of a New Treatment as Adjunctive Therapy to Anti-vascular E… | Phase2 | Choroidal Neovascularization | Completed | 2007-11-01 | 2009-03-01 | ClinicalTrials.gov |
| NCT00554970 | A Study of 2 Doses of MAP0010 in Adult Asthmatics | Phase2 | Asthma | Completed | 2007-11-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00524264 | A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With… | Phase3 | Cataract Extraction | Completed | 2007-10-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00549783 | BOTOX® Economic Spasticity Trial (BEST) | Phase4 | Muscle Spasticity | Completed | 2007-10-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00565201 | Evaluation of BOTOX® With Rehabilitation Therapy for the Treatment of Wrist and… | Early_Phase1 | Stroke | Completed | 2007-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00524264 | A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With… | Phase3 | Cataract Extraction | Completed | 2007-10-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00521456 | A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With… | Phase3 | Cataract Extraction | Completed | 2007-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00514852 | Safety and Efficacy of an Artificial Tear for the Treatment of Dry Eye | Na | Dry Eye Syndrome | Completed | 2007-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00514852 | Safety and Efficacy of an Artificial Tear for the Treatment of Dry Eye | Na | Dry Eye Syndrome | Completed | 2007-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00521456 | A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With… | Phase3 | Cataract Extraction | Completed | 2007-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00549783 | BOTOX® Economic Spasticity Trial (BEST) | Phase4 | Muscle Spasticity | Completed | 2007-10-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00549783 | BOTOX® Economic Spasticity Trial (BEST) | Phase4 | Muscle Spasticity | Completed | 2007-10-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00565201 | Evaluation of BOTOX® With Rehabilitation Therapy for the Treatment of Wrist and… | Early_Phase1 | Stroke | Completed | 2007-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00524264 | A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With… | Phase3 | Cataract Extraction | Completed | 2007-10-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00565201 | Evaluation of BOTOX® With Rehabilitation Therapy for the Treatment of Wrist and… | Early_Phase1 | Stroke | Completed | 2007-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00514852 | Safety and Efficacy of an Artificial Tear for the Treatment of Dry Eye | Na | Dry Eye Syndrome | Completed | 2007-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00521456 | A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With… | Phase3 | Cataract Extraction | Completed | 2007-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00524264 | A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With… | Phase3 | Cataract Extraction | Completed | 2007-10-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00565201 | Evaluation of BOTOX® With Rehabilitation Therapy for the Treatment of Wrist and… | Early_Phase1 | Stroke | Completed | 2007-10-01 | 2011-12-01 | ClinicalTrials.gov |
| NCT00514852 | Safety and Efficacy of an Artificial Tear for the Treatment of Dry Eye | Na | Dry Eye Syndrome | Completed | 2007-10-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00549783 | BOTOX® Economic Spasticity Trial (BEST) | Phase4 | Muscle Spasticity | Completed | 2007-10-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00521456 | A Study of Ketorolac for the Treatment of Inflammation and Pain Associated With… | Phase3 | Cataract Extraction | Completed | 2007-10-01 | 2008-03-01 | ClinicalTrials.gov |
| NCT00544713 | Evaluate the Safety and Efficacy of a New Artificial Tear for Use After LASIK S… | Na | Dry Eye Syndrome | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00539526 | Evaluation of Hyperemia With the Use of Ocular Prostaglandin Analogues | Phase4 | Open Angle Glaucoma | Completed | 2007-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00528541 | Comparison of Efficacy and Safety of Two Different Types of Botulinum Toxin Typ… | Phase4 | Spasmodic Torticollis | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00539526 | Evaluation of Hyperemia With the Use of Ocular Prostaglandin Analogues | Phase4 | Open Angle Glaucoma | Completed | 2007-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00544713 | Evaluate the Safety and Efficacy of a New Artificial Tear for Use After LASIK S… | Na | Dry Eye Syndrome | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00544713 | Evaluate the Safety and Efficacy of a New Artificial Tear for Use After LASIK S… | Na | Dry Eye Syndrome | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00528541 | Comparison of Efficacy and Safety of Two Different Types of Botulinum Toxin Typ… | Phase4 | Spasmodic Torticollis | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00539526 | Evaluation of Hyperemia With the Use of Ocular Prostaglandin Analogues | Phase4 | Open Angle Glaucoma | Completed | 2007-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00539526 | Evaluation of Hyperemia With the Use of Ocular Prostaglandin Analogues | Phase4 | Open Angle Glaucoma | Completed | 2007-09-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00528541 | Comparison of Efficacy and Safety of Two Different Types of Botulinum Toxin Typ… | Phase4 | Spasmodic Torticollis | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00544713 | Evaluate the Safety and Efficacy of a New Artificial Tear for Use After LASIK S… | Na | Dry Eye Syndrome | Completed | 2007-09-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00528541 | Comparison of Efficacy and Safety of Two Different Types of Botulinum Toxin Typ… | Phase4 | Spasmodic Torticollis | Completed | 2007-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00507936 | Safety and Efficacy Study in Subjects With Diabetic Neuropathic Pain | Phase2 | Diabetic Neuralgia | Completed | 2007-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00517790 | Study of ABT-869 in Subjects With Advanced Non-small Cell Lung Cancer (NSCLC) | Phase2 | Non-Small Cell Lung Cancer (NSCLC) | Completed | 2007-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00509873 | A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial C… | Phase3 | Bacterial Conjunctivitis | Completed | 2007-08-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00507936 | Safety and Efficacy Study in Subjects With Diabetic Neuropathic Pain | Phase2 | Diabetic Neuralgia | Completed | 2007-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00526617 | A Phase I Study of ABT-888 in Combination With Temozolomide in Cancer Patients | Phase1 | Non-hematologic Malignancies | Completed | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00526617 | A Phase I Study of ABT-888 in Combination With Temozolomide in Cancer Patients | Phase1 | Non-hematologic Malignancies | Completed | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00507936 | Safety and Efficacy Study in Subjects With Diabetic Neuropathic Pain | Phase2 | Diabetic Neuralgia | Completed | 2007-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00509873 | A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial C… | Phase3 | Bacterial Conjunctivitis | Completed | 2007-08-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00517790 | Study of ABT-869 in Subjects With Advanced Non-small Cell Lung Cancer (NSCLC) | Phase2 | Non-Small Cell Lung Cancer (NSCLC) | Completed | 2007-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00526617 | A Phase I Study of ABT-888 in Combination With Temozolomide in Cancer Patients | Phase1 | Non-hematologic Malignancies | Completed | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00517790 | Study of ABT-869 in Subjects With Advanced Non-small Cell Lung Cancer (NSCLC) | Phase2 | Non-Small Cell Lung Cancer (NSCLC) | Completed | 2007-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00509873 | A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial C… | Phase3 | Bacterial Conjunctivitis | Completed | 2007-08-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00526617 | A Phase I Study of ABT-888 in Combination With Temozolomide in Cancer Patients | Phase1 | Non-hematologic Malignancies | Completed | 2007-08-01 | — | ClinicalTrials.gov |
| NCT00517790 | Study of ABT-869 in Subjects With Advanced Non-small Cell Lung Cancer (NSCLC) | Phase2 | Non-Small Cell Lung Cancer (NSCLC) | Completed | 2007-08-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00509873 | A Study of the Safety and Efficacy of Gatifloxacin in Patients With Bacterial C… | Phase3 | Bacterial Conjunctivitis | Completed | 2007-08-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00507936 | Safety and Efficacy Study in Subjects With Diabetic Neuropathic Pain | Phase2 | Diabetic Neuralgia | Completed | 2007-08-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00481091 | A Study of ABT-263 in Participants With Relapsed or Refractory Chronic Lymphocy… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2007-07-25 | 2022-05-12 | ClinicalTrials.gov |
| NCT00481091 | A Study of ABT-263 in Participants With Relapsed or Refractory Chronic Lymphocy… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2007-07-25 | 2022-05-12 | ClinicalTrials.gov |
| NCT00481091 | A Study of ABT-263 in Participants With Relapsed or Refractory Chronic Lymphocy… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2007-07-25 | 2022-05-12 | ClinicalTrials.gov |
| NCT00481091 | A Study of ABT-263 in Participants With Relapsed or Refractory Chronic Lymphocy… | Phase1 | Chronic Lymphocytic Leukemia | Completed | 2007-07-25 | 2022-05-12 | ClinicalTrials.gov |
| NCT00635193 | Efficacy and Safety Study of M200(Volociximab in Combination With Liposomal Dox… | Phase1 | Ovarian Cancer, Primary Peritoneal Cancer | Completed | 2007-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00635193 | Efficacy and Safety Study of M200(Volociximab in Combination With Liposomal Dox… | Phase1 | Ovarian Cancer, Primary Peritoneal Cancer | Completed | 2007-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00635193 | Efficacy and Safety Study of M200(Volociximab in Combination With Liposomal Dox… | Phase1 | Ovarian Cancer, Primary Peritoneal Cancer | Completed | 2007-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00635193 | Efficacy and Safety Study of M200(Volociximab in Combination With Liposomal Dox… | Phase1 | Ovarian Cancer, Primary Peritoneal Cancer | Completed | 2007-07-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT00650156 | Pharmacokinetic and Safety Study With Adalimumab in Chinese Subjects With Mild … | Phase1 | Rheumatoid Arthritis | Completed | 2007-06-01 | — | ClinicalTrials.gov |
| NCT00439140 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Terminated | 2007-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00432341 | Efficacy and Safety of Two Different Botulinum Toxin Type A Treatments for Mode… | Phase4 | Spasmodic Torticollis | Terminated | 2007-06-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00650156 | Pharmacokinetic and Safety Study With Adalimumab in Chinese Subjects With Mild … | Phase1 | Rheumatoid Arthritis | Completed | 2007-06-01 | — | ClinicalTrials.gov |
| NCT00650156 | Pharmacokinetic and Safety Study With Adalimumab in Chinese Subjects With Mild … | Phase1 | Rheumatoid Arthritis | Completed | 2007-06-01 | — | ClinicalTrials.gov |
| NCT00439140 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Terminated | 2007-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00464438 | A Study to Evaluate the Safety and Efficacy of Gatifloxacin for the Treatment o… | Phase4 | Bacterial Conjunctivitis | Completed | 2007-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00486538 | Study of ABT-869 in Subjects With Advanced Renal Cell Carcinoma Who Have Previo… | Phase2 | Advanced Renal Cell Carcinoma | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00439140 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Terminated | 2007-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00432341 | Efficacy and Safety of Two Different Botulinum Toxin Type A Treatments for Mode… | Phase4 | Spasmodic Torticollis | Terminated | 2007-06-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00486538 | Study of ABT-869 in Subjects With Advanced Renal Cell Carcinoma Who Have Previo… | Phase2 | Advanced Renal Cell Carcinoma | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00704275 | Comparison of Efficacy, Safety and Anti-Inflammatory Effect Between Topical 0.0… | Phase4 | Dry Eye | Unknown | 2007-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00464438 | A Study to Evaluate the Safety and Efficacy of Gatifloxacin for the Treatment o… | Phase4 | Bacterial Conjunctivitis | Completed | 2007-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00650156 | Pharmacokinetic and Safety Study With Adalimumab in Chinese Subjects With Mild … | Phase1 | Rheumatoid Arthritis | Completed | 2007-06-01 | — | ClinicalTrials.gov |
| NCT00704275 | Comparison of Efficacy, Safety and Anti-Inflammatory Effect Between Topical 0.0… | Phase4 | Dry Eye | Unknown | 2007-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00486538 | Study of ABT-869 in Subjects With Advanced Renal Cell Carcinoma Who Have Previo… | Phase2 | Advanced Renal Cell Carcinoma | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00432341 | Efficacy and Safety of Two Different Botulinum Toxin Type A Treatments for Mode… | Phase4 | Spasmodic Torticollis | Terminated | 2007-06-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00464438 | A Study to Evaluate the Safety and Efficacy of Gatifloxacin for the Treatment o… | Phase4 | Bacterial Conjunctivitis | Completed | 2007-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00704275 | Comparison of Efficacy, Safety and Anti-Inflammatory Effect Between Topical 0.0… | Phase4 | Dry Eye | Unknown | 2007-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00704275 | Comparison of Efficacy, Safety and Anti-Inflammatory Effect Between Topical 0.0… | Phase4 | Dry Eye | Unknown | 2007-06-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00439140 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Terminated | 2007-06-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00432341 | Efficacy and Safety of Two Different Botulinum Toxin Type A Treatments for Mode… | Phase4 | Spasmodic Torticollis | Terminated | 2007-06-01 | 2009-06-01 | ClinicalTrials.gov |
| NCT00486538 | Study of ABT-869 in Subjects With Advanced Renal Cell Carcinoma Who Have Previo… | Phase2 | Advanced Renal Cell Carcinoma | Completed | 2007-06-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00464438 | A Study to Evaluate the Safety and Efficacy of Gatifloxacin for the Treatment o… | Phase4 | Bacterial Conjunctivitis | Completed | 2007-06-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00477802 | Botulinum Toxin Type A (Botox) in the Management of Levodopa-Induced Peak-Dose … | Phase4 | Parkinson Disease | Terminated | 2007-05-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01083680 | Effectiveness and Safety in Patients With Crohn´s Disease in Clinical Routine | — | Crohn's Disease | Completed | 2007-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00444886 | Treatment of Thoracic Outlet Syndrome (TOS) With Botox | Phase2 | Thoracic Outlet Syndrome | Completed | 2007-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00461292 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00464685 | Safety and Efficacy of a New Treatment in Combination With Laser for Diabetic M… | Phase2 | Diabetic Macular Edema | Completed | 2007-05-01 | 2010-02-08 | ClinicalTrials.gov |
| NCT00477802 | Botulinum Toxin Type A (Botox) in the Management of Levodopa-Induced Peak-Dose … | Phase4 | Parkinson Disease | Terminated | 2007-05-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00464685 | Safety and Efficacy of a New Treatment in Combination With Laser for Diabetic M… | Phase2 | Diabetic Macular Edema | Completed | 2007-05-01 | 2010-02-08 | ClinicalTrials.gov |
| NCT00461292 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00444886 | Treatment of Thoracic Outlet Syndrome (TOS) With Botox | Phase2 | Thoracic Outlet Syndrome | Completed | 2007-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT01083680 | Effectiveness and Safety in Patients With Crohn´s Disease in Clinical Routine | — | Crohn's Disease | Completed | 2007-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00444886 | Treatment of Thoracic Outlet Syndrome (TOS) With Botox | Phase2 | Thoracic Outlet Syndrome | Completed | 2007-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00461292 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00464685 | Safety and Efficacy of a New Treatment in Combination With Laser for Diabetic M… | Phase2 | Diabetic Macular Edema | Completed | 2007-05-01 | 2010-02-08 | ClinicalTrials.gov |
| NCT00477802 | Botulinum Toxin Type A (Botox) in the Management of Levodopa-Induced Peak-Dose … | Phase4 | Parkinson Disease | Terminated | 2007-05-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT01083680 | Effectiveness and Safety in Patients With Crohn´s Disease in Clinical Routine | — | Crohn's Disease | Completed | 2007-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT01083680 | Effectiveness and Safety in Patients With Crohn´s Disease in Clinical Routine | — | Crohn's Disease | Completed | 2007-05-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00444886 | Treatment of Thoracic Outlet Syndrome (TOS) With Botox | Phase2 | Thoracic Outlet Syndrome | Completed | 2007-05-01 | 2011-02-01 | ClinicalTrials.gov |
| NCT00461292 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Completed | 2007-05-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00464685 | Safety and Efficacy of a New Treatment in Combination With Laser for Diabetic M… | Phase2 | Diabetic Macular Edema | Completed | 2007-05-01 | 2010-02-08 | ClinicalTrials.gov |
| NCT00477802 | Botulinum Toxin Type A (Botox) in the Management of Levodopa-Induced Peak-Dose … | Phase4 | Parkinson Disease | Terminated | 2007-05-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00693420 | Safety and Efficacy of Bimatoprost Solution in Increasing Overall Eyelash Promi… | Phase3 | Eyelashes | Completed | 2007-04-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00864604 | Single Dose Two-Way Crossover Fed Bioequivalence Study of Nabumetone 750 mg Tab… | Phase1 | Healthy | Completed | 2007-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00864604 | Single Dose Two-Way Crossover Fed Bioequivalence Study of Nabumetone 750 mg Tab… | Phase1 | Healthy | Completed | 2007-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00445198 | A Phase 1/2a Study of ABT-263 in Subjects With Small Cell Lung Cancer (SCLC) or… | Phase1 | Small Cell Lung Cancer | Completed | 2007-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00693420 | Safety and Efficacy of Bimatoprost Solution in Increasing Overall Eyelash Promi… | Phase3 | Eyelashes | Completed | 2007-04-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00693420 | Safety and Efficacy of Bimatoprost Solution in Increasing Overall Eyelash Promi… | Phase3 | Eyelashes | Completed | 2007-04-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00445198 | A Phase 1/2a Study of ABT-263 in Subjects With Small Cell Lung Cancer (SCLC) or… | Phase1 | Small Cell Lung Cancer | Completed | 2007-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00864604 | Single Dose Two-Way Crossover Fed Bioequivalence Study of Nabumetone 750 mg Tab… | Phase1 | Healthy | Completed | 2007-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00693420 | Safety and Efficacy of Bimatoprost Solution in Increasing Overall Eyelash Promi… | Phase3 | Eyelashes | Completed | 2007-04-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00445198 | A Phase 1/2a Study of ABT-263 in Subjects With Small Cell Lung Cancer (SCLC) or… | Phase1 | Small Cell Lung Cancer | Completed | 2007-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00864604 | Single Dose Two-Way Crossover Fed Bioequivalence Study of Nabumetone 750 mg Tab… | Phase1 | Healthy | Completed | 2007-04-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00445198 | A Phase 1/2a Study of ABT-263 in Subjects With Small Cell Lung Cancer (SCLC) or… | Phase1 | Small Cell Lung Cancer | Completed | 2007-04-01 | 2010-12-01 | ClinicalTrials.gov |
| NCT00445705 | Safety and Efficacy of AGN 203818 for Pain Associated With Fibromyalgia Syndrome | Phase2 | Fibromyalgia | Terminated | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00621335 | A Investigator Masked Parallel Comparison of Tolerability of Combigan and Cosopt | — | Open Angle Glaucoma | Completed | 2007-03-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00621335 | A Investigator Masked Parallel Comparison of Tolerability of Combigan and Cosopt | — | Open Angle Glaucoma | Completed | 2007-03-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00445003 | Laser-Ranibizumab-Triamcinolone for Proliferative Diabetic Retinopathy | Phase3 | Proliferative Diabetic Retinopathy | Completed | 2007-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00621335 | A Investigator Masked Parallel Comparison of Tolerability of Combigan and Cosopt | — | Open Angle Glaucoma | Completed | 2007-03-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00441766 | Safety and Efficacy of Oral AGN 203818 for the Relief of Irritable Bowel Syndro… | Phase2 | Irritable Bowel Syndrome | Terminated | 2007-03-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00621335 | A Investigator Masked Parallel Comparison of Tolerability of Combigan and Cosopt | — | Open Angle Glaucoma | Completed | 2007-03-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00445705 | Safety and Efficacy of AGN 203818 for Pain Associated With Fibromyalgia Syndrome | Phase2 | Fibromyalgia | Terminated | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00445003 | Laser-Ranibizumab-Triamcinolone for Proliferative Diabetic Retinopathy | Phase3 | Proliferative Diabetic Retinopathy | Completed | 2007-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00441766 | Safety and Efficacy of Oral AGN 203818 for the Relief of Irritable Bowel Syndro… | Phase2 | Irritable Bowel Syndrome | Terminated | 2007-03-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00441766 | Safety and Efficacy of Oral AGN 203818 for the Relief of Irritable Bowel Syndro… | Phase2 | Irritable Bowel Syndrome | Terminated | 2007-03-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00445003 | Laser-Ranibizumab-Triamcinolone for Proliferative Diabetic Retinopathy | Phase3 | Proliferative Diabetic Retinopathy | Completed | 2007-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00441766 | Safety and Efficacy of Oral AGN 203818 for the Relief of Irritable Bowel Syndro… | Phase2 | Irritable Bowel Syndrome | Terminated | 2007-03-01 | 2008-02-01 | ClinicalTrials.gov |
| NCT00445003 | Laser-Ranibizumab-Triamcinolone for Proliferative Diabetic Retinopathy | Phase3 | Proliferative Diabetic Retinopathy | Completed | 2007-03-01 | 2010-07-01 | ClinicalTrials.gov |
| NCT00445705 | Safety and Efficacy of AGN 203818 for Pain Associated With Fibromyalgia Syndrome | Phase2 | Fibromyalgia | Terminated | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00445705 | Safety and Efficacy of AGN 203818 for Pain Associated With Fibromyalgia Syndrome | Phase2 | Fibromyalgia | Terminated | 2007-03-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00443391 | A Safety and Tolerability Study of ABT-089 in Adults With Attention Deficit-Hyp… | Phase2 | Attention Deficit Hyperactivity Disorder | Completed | 2007-02-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00443391 | A Safety and Tolerability Study of ABT-089 in Adults With Attention Deficit-Hyp… | Phase2 | Attention Deficit Hyperactivity Disorder | Completed | 2007-02-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00443391 | A Safety and Tolerability Study of ABT-089 in Adults With Attention Deficit-Hyp… | Phase2 | Attention Deficit Hyperactivity Disorder | Completed | 2007-02-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00443391 | A Safety and Tolerability Study of ABT-089 in Adults With Attention Deficit-Hyp… | Phase2 | Attention Deficit Hyperactivity Disorder | Completed | 2007-02-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00395057 | A Study Using Intravitreal Injections of a Small Interfering RNA in Patients Wi… | Phase2 | Choroid Neovascularization | Terminated | 2007-01-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00479596 | This is a Prospective, Randomized, Double-Blind Study Comparing Intravesical In… | Phase2 | Overactive Bladder | Unknown | 2007-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00479596 | This is a Prospective, Randomized, Double-Blind Study Comparing Intravesical In… | Phase2 | Overactive Bladder | Unknown | 2007-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00395057 | A Study Using Intravitreal Injections of a Small Interfering RNA in Patients Wi… | Phase2 | Choroid Neovascularization | Terminated | 2007-01-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00395057 | A Study Using Intravitreal Injections of a Small Interfering RNA in Patients Wi… | Phase2 | Choroid Neovascularization | Terminated | 2007-01-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT02012764 | The CCP Study: Coordinated Programme to Prevent Arthritis - Can We Identify Art… | — | Inflammatory Arthritis | Active_Not_Recruiting | 2007-01-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT02012764 | The CCP Study: Coordinated Programme to Prevent Arthritis - Can We Identify Art… | — | Inflammatory Arthritis | Active_Not_Recruiting | 2007-01-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT00479596 | This is a Prospective, Randomized, Double-Blind Study Comparing Intravesical In… | Phase2 | Overactive Bladder | Unknown | 2007-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT02012764 | The CCP Study: Coordinated Programme to Prevent Arthritis - Can We Identify Art… | — | Inflammatory Arthritis | Active_Not_Recruiting | 2007-01-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT02012764 | The CCP Study: Coordinated Programme to Prevent Arthritis - Can We Identify Art… | — | Inflammatory Arthritis | Active_Not_Recruiting | 2007-01-01 | 2026-06-30 | ClinicalTrials.gov |
| NCT00479596 | This is a Prospective, Randomized, Double-Blind Study Comparing Intravesical In… | Phase2 | Overactive Bladder | Unknown | 2007-01-01 | 2007-05-01 | ClinicalTrials.gov |
| NCT00395057 | A Study Using Intravitreal Injections of a Small Interfering RNA in Patients Wi… | Phase2 | Choroid Neovascularization | Terminated | 2007-01-01 | 2009-02-01 | ClinicalTrials.gov |
| NCT00437658 | Elagolix Versus Subcutaneous Depot Medroxyprogesterone Acetate for the Treatmen… | Phase2 | Endometriosis | Completed | 2006-12-11 | 2008-11-24 | ClinicalTrials.gov |
| NCT00437658 | Elagolix Versus Subcutaneous Depot Medroxyprogesterone Acetate for the Treatmen… | Phase2 | Endometriosis | Completed | 2006-12-11 | 2008-11-24 | ClinicalTrials.gov |
| NCT00437658 | Elagolix Versus Subcutaneous Depot Medroxyprogesterone Acetate for the Treatmen… | Phase2 | Endometriosis | Completed | 2006-12-11 | 2008-11-24 | ClinicalTrials.gov |
| NCT00437658 | Elagolix Versus Subcutaneous Depot Medroxyprogesterone Acetate for the Treatmen… | Phase2 | Endometriosis | Completed | 2006-12-11 | 2008-11-24 | ClinicalTrials.gov |
| NCT00864357 | A Relative Bioavailability Study of Oxycodone 5 mg / Ibuprofen 400 mg Tablets U… | Phase1 | Healthy | Completed | 2006-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00381719 | Safety and Efficacy of AGN 203818 in Patients With Painful Diabetic Peripheral … | Phase2 | Diabetic Neuropathy, Painful | Completed | 2006-10-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00380783 | Safety and Efficacy of AGN 203818 for Pain Associated With Painful Bladder Synd… | Phase2 | Cystitis, Interstitial | Terminated | 2006-10-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00380783 | Safety and Efficacy of AGN 203818 for Pain Associated With Painful Bladder Synd… | Phase2 | Cystitis, Interstitial | Terminated | 2006-10-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00380783 | Safety and Efficacy of AGN 203818 for Pain Associated With Painful Bladder Synd… | Phase2 | Cystitis, Interstitial | Terminated | 2006-10-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00381719 | Safety and Efficacy of AGN 203818 in Patients With Painful Diabetic Peripheral … | Phase2 | Diabetic Neuropathy, Painful | Completed | 2006-10-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00864526 | A Relative Bioavailability Study of Oxycodone 5 mg / Ibuprofen 400 mg Tablets U… | Phase1 | Healthy | Completed | 2006-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00864357 | A Relative Bioavailability Study of Oxycodone 5 mg / Ibuprofen 400 mg Tablets U… | Phase1 | Healthy | Completed | 2006-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00864526 | A Relative Bioavailability Study of Oxycodone 5 mg / Ibuprofen 400 mg Tablets U… | Phase1 | Healthy | Completed | 2006-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00864357 | A Relative Bioavailability Study of Oxycodone 5 mg / Ibuprofen 400 mg Tablets U… | Phase1 | Healthy | Completed | 2006-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00864526 | A Relative Bioavailability Study of Oxycodone 5 mg / Ibuprofen 400 mg Tablets U… | Phase1 | Healthy | Completed | 2006-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00380783 | Safety and Efficacy of AGN 203818 for Pain Associated With Painful Bladder Synd… | Phase2 | Cystitis, Interstitial | Terminated | 2006-10-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00381719 | Safety and Efficacy of AGN 203818 in Patients With Painful Diabetic Peripheral … | Phase2 | Diabetic Neuropathy, Painful | Completed | 2006-10-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00864526 | A Relative Bioavailability Study of Oxycodone 5 mg / Ibuprofen 400 mg Tablets U… | Phase1 | Healthy | Completed | 2006-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00864357 | A Relative Bioavailability Study of Oxycodone 5 mg / Ibuprofen 400 mg Tablets U… | Phase1 | Healthy | Completed | 2006-10-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00381719 | Safety and Efficacy of AGN 203818 in Patients With Painful Diabetic Peripheral … | Phase2 | Diabetic Neuropathy, Painful | Completed | 2006-10-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00864279 | A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Fasting … | Phase1 | Healthy | Completed | 2006-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00863902 | A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Non-fast… | Phase1 | Healthy | Completed | 2006-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00864279 | A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Fasting … | Phase1 | Healthy | Completed | 2006-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01097655 | Study on the Usage, Dosing, Tolerability, and Effectiveness of Kaletra Tablet | — | Human Immunodeficiency Virus | Completed | 2006-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00440011 | Bimatoprost 0.03% Versus Travoprost 0.004% in Patients Currently on Latanoprost… | Phase4 | Glaucoma | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00311376 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Completed | 2006-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00440011 | Bimatoprost 0.03% Versus Travoprost 0.004% in Patients Currently on Latanoprost… | Phase4 | Glaucoma | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00440011 | Bimatoprost 0.03% Versus Travoprost 0.004% in Patients Currently on Latanoprost… | Phase4 | Glaucoma | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00759902 | Comparison of Two KADIAN 10 mg Capsules to a KADIAN 20 mg Capsule Under Fasted … | Phase1 | Healthy | Completed | 2006-08-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT01097655 | Study on the Usage, Dosing, Tolerability, and Effectiveness of Kaletra Tablet | — | Human Immunodeficiency Virus | Completed | 2006-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00759915 | Comparison of Two KADIAN 10 mg Capsules to a KADIAN 20 mg Capsule Under Fed Con… | Phase1 | Healthy | Completed | 2006-08-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00759902 | Comparison of Two KADIAN 10 mg Capsules to a KADIAN 20 mg Capsule Under Fasted … | Phase1 | Healthy | Completed | 2006-08-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00440011 | Bimatoprost 0.03% Versus Travoprost 0.004% in Patients Currently on Latanoprost… | Phase4 | Glaucoma | Completed | 2006-08-01 | 2007-10-01 | ClinicalTrials.gov |
| NCT00759915 | Comparison of Two KADIAN 10 mg Capsules to a KADIAN 20 mg Capsule Under Fed Con… | Phase1 | Healthy | Completed | 2006-08-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00863902 | A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Non-fast… | Phase1 | Healthy | Completed | 2006-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00759902 | Comparison of Two KADIAN 10 mg Capsules to a KADIAN 20 mg Capsule Under Fasted … | Phase1 | Healthy | Completed | 2006-08-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00759915 | Comparison of Two KADIAN 10 mg Capsules to a KADIAN 20 mg Capsule Under Fed Con… | Phase1 | Healthy | Completed | 2006-08-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00863902 | A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Non-fast… | Phase1 | Healthy | Completed | 2006-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00864279 | A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Fasting … | Phase1 | Healthy | Completed | 2006-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01097655 | Study on the Usage, Dosing, Tolerability, and Effectiveness of Kaletra Tablet | — | Human Immunodeficiency Virus | Completed | 2006-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00864279 | A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Fasting … | Phase1 | Healthy | Completed | 2006-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00759902 | Comparison of Two KADIAN 10 mg Capsules to a KADIAN 20 mg Capsule Under Fasted … | Phase1 | Healthy | Completed | 2006-08-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00311376 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Completed | 2006-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01097655 | Study on the Usage, Dosing, Tolerability, and Effectiveness of Kaletra Tablet | — | Human Immunodeficiency Virus | Completed | 2006-08-01 | 2016-01-01 | ClinicalTrials.gov |
| NCT00759915 | Comparison of Two KADIAN 10 mg Capsules to a KADIAN 20 mg Capsule Under Fed Con… | Phase1 | Healthy | Completed | 2006-08-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00863902 | A Relative Bioavailability Study of Cetirizine HCl 10 mg Tablets Under Non-fast… | Phase1 | Healthy | Completed | 2006-08-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00311376 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Completed | 2006-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00311376 | Safety and Efficacy Study of Botulinum Toxin Type A for the Treatment of Neurog… | Phase3 | Overactive Bladder | Completed | 2006-08-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00697801 | Study of MAP0010 in Asthmatic Children and Adolescents | Phase2 | Asthma | Completed | 2006-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT01188057 | A Relative Bioavailability Study of 2 mg Alprazolam OD Tablets Under Non-Fastin… | Phase1 | Healthy | Completed | 2006-07-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00697801 | Study of MAP0010 in Asthmatic Children and Adolescents | Phase2 | Asthma | Completed | 2006-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT01188057 | A Relative Bioavailability Study of 2 mg Alprazolam OD Tablets Under Non-Fastin… | Phase1 | Healthy | Completed | 2006-07-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00761592 | Comparison of Two Botulinum Type A Products in the Treatment of Blepharospasm | Phase4 | Blepharospasm | Completed | 2006-07-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00440141 | Brimonidine 0.1% Versus Brinzolamide 1% as Adjunctive Therapy to Latanoprost 0.… | Phase4 | Glaucoma | Completed | 2006-07-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00761592 | Comparison of Two Botulinum Type A Products in the Treatment of Blepharospasm | Phase4 | Blepharospasm | Completed | 2006-07-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT01188057 | A Relative Bioavailability Study of 2 mg Alprazolam OD Tablets Under Non-Fastin… | Phase1 | Healthy | Completed | 2006-07-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00440141 | Brimonidine 0.1% Versus Brinzolamide 1% as Adjunctive Therapy to Latanoprost 0.… | Phase4 | Glaucoma | Completed | 2006-07-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT01188057 | A Relative Bioavailability Study of 2 mg Alprazolam OD Tablets Under Non-Fastin… | Phase1 | Healthy | Completed | 2006-07-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00440141 | Brimonidine 0.1% Versus Brinzolamide 1% as Adjunctive Therapy to Latanoprost 0.… | Phase4 | Glaucoma | Completed | 2006-07-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00440141 | Brimonidine 0.1% Versus Brinzolamide 1% as Adjunctive Therapy to Latanoprost 0.… | Phase4 | Glaucoma | Completed | 2006-07-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00761592 | Comparison of Two Botulinum Type A Products in the Treatment of Blepharospasm | Phase4 | Blepharospasm | Completed | 2006-07-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT00697801 | Study of MAP0010 in Asthmatic Children and Adolescents | Phase2 | Asthma | Completed | 2006-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00697801 | Study of MAP0010 in Asthmatic Children and Adolescents | Phase2 | Asthma | Completed | 2006-07-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00761592 | Comparison of Two Botulinum Type A Products in the Treatment of Blepharospasm | Phase4 | Blepharospasm | Completed | 2006-07-01 | 2008-01-01 | ClinicalTrials.gov |
| NCT01188031 | A Relative Bioavailability Study of 2 mg Alprazolam OD Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2006-06-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT01188031 | A Relative Bioavailability Study of 2 mg Alprazolam OD Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2006-06-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00343187 | A Phase II Study of ACZONE™ (Dapsone) Gel, 5% As a Treatment For Tarceva® (Erlo… | Phase2 | Rash | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00348335 | Efficacy of Topical Cyclosporin for Ocular Rosacea | Phase4 | Rosacea | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00347828 | Effectiveness Study of Zymar Versus Vigamox for Preoperative Sterilization of t… | Phase4 | Eye Infection | Unknown | 2006-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00336349 | A Study of Intra-dermal Injection of Botulinum Toxin Type A for the Diabetic Ne… | Na | Diabetes Mellitus | Completed | 2006-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00343187 | A Phase II Study of ACZONE™ (Dapsone) Gel, 5% As a Treatment For Tarceva® (Erlo… | Phase2 | Rash | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00336349 | A Study of Intra-dermal Injection of Botulinum Toxin Type A for the Diabetic Ne… | Na | Diabetes Mellitus | Completed | 2006-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01188031 | A Relative Bioavailability Study of 2 mg Alprazolam OD Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2006-06-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT01188031 | A Relative Bioavailability Study of 2 mg Alprazolam OD Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2006-06-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00348335 | Efficacy of Topical Cyclosporin for Ocular Rosacea | Phase4 | Rosacea | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00336349 | A Study of Intra-dermal Injection of Botulinum Toxin Type A for the Diabetic Ne… | Na | Diabetes Mellitus | Completed | 2006-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00343187 | A Phase II Study of ACZONE™ (Dapsone) Gel, 5% As a Treatment For Tarceva® (Erlo… | Phase2 | Rash | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00347828 | Effectiveness Study of Zymar Versus Vigamox for Preoperative Sterilization of t… | Phase4 | Eye Infection | Unknown | 2006-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00336349 | A Study of Intra-dermal Injection of Botulinum Toxin Type A for the Diabetic Ne… | Na | Diabetes Mellitus | Completed | 2006-06-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00343187 | A Phase II Study of ACZONE™ (Dapsone) Gel, 5% As a Treatment For Tarceva® (Erlo… | Phase2 | Rash | Terminated | 2006-06-01 | 2007-07-01 | ClinicalTrials.gov |
| NCT00347828 | Effectiveness Study of Zymar Versus Vigamox for Preoperative Sterilization of t… | Phase4 | Eye Infection | Unknown | 2006-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00348335 | Efficacy of Topical Cyclosporin for Ocular Rosacea | Phase4 | Rosacea | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00347828 | Effectiveness Study of Zymar Versus Vigamox for Preoperative Sterilization of t… | Phase4 | Eye Infection | Unknown | 2006-06-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00348335 | Efficacy of Topical Cyclosporin for Ocular Rosacea | Phase4 | Rosacea | Completed | 2006-06-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00768183 | Comparison of KADIAN 100 mg When Dosed With Alcohol Under Fasting and Fed Condi… | Phase1 | Healthy | Completed | 2006-05-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00442312 | Combigan Ophthalmic Solution(Brimonidine 0.2% and Timolol 0.5%)With Latanoprost… | Phase4 | Glaucoma | Unknown | 2006-05-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00333814 | A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Interm… | Phase2 | Intermediate Uveitis | Completed | 2006-05-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00333996 | A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Anteri… | Phase2 | Anterior Uveitis | Terminated | 2006-05-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00333814 | A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Interm… | Phase2 | Intermediate Uveitis | Completed | 2006-05-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00768183 | Comparison of KADIAN 100 mg When Dosed With Alcohol Under Fasting and Fed Condi… | Phase1 | Healthy | Completed | 2006-05-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00768183 | Comparison of KADIAN 100 mg When Dosed With Alcohol Under Fasting and Fed Condi… | Phase1 | Healthy | Completed | 2006-05-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00333996 | A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Anteri… | Phase2 | Anterior Uveitis | Terminated | 2006-05-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT01086033 | A 3-year Study Following up Patients With Moderate to Severe Rheumatoid Arthrit… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00333814 | A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Interm… | Phase2 | Intermediate Uveitis | Completed | 2006-05-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT00442312 | Combigan Ophthalmic Solution(Brimonidine 0.2% and Timolol 0.5%)With Latanoprost… | Phase4 | Glaucoma | Unknown | 2006-05-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT01086033 | A 3-year Study Following up Patients With Moderate to Severe Rheumatoid Arthrit… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00768183 | Comparison of KADIAN 100 mg When Dosed With Alcohol Under Fasting and Fed Condi… | Phase1 | Healthy | Completed | 2006-05-01 | 2006-07-01 | ClinicalTrials.gov |
| NCT00442312 | Combigan Ophthalmic Solution(Brimonidine 0.2% and Timolol 0.5%)With Latanoprost… | Phase4 | Glaucoma | Unknown | 2006-05-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00333996 | A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Anteri… | Phase2 | Anterior Uveitis | Terminated | 2006-05-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT00333996 | A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Anteri… | Phase2 | Anterior Uveitis | Terminated | 2006-05-01 | 2007-03-01 | ClinicalTrials.gov |
| NCT01086033 | A 3-year Study Following up Patients With Moderate to Severe Rheumatoid Arthrit… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00333814 | A Study of the Safety and Efficacy of a New Treatment for Non-Infectious Interm… | Phase2 | Intermediate Uveitis | Completed | 2006-05-01 | 2009-04-01 | ClinicalTrials.gov |
| NCT01086033 | A 3-year Study Following up Patients With Moderate to Severe Rheumatoid Arthrit… | — | Rheumatoid Arthritis | Completed | 2006-05-01 | 2012-07-01 | ClinicalTrials.gov |
| NCT00442312 | Combigan Ophthalmic Solution(Brimonidine 0.2% and Timolol 0.5%)With Latanoprost… | Phase4 | Glaucoma | Unknown | 2006-05-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00871364 | A Relative Bioavailability Study of 50 mg Venlafaxine Hydrochloride Tablets Und… | Phase1 | Healthy | Completed | 2006-04-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00325715 | AGN 201904 Versus Esomeprazole in the Prevention of Aspirin-induced Stomach or … | Phase1 | Peptic Ulcer | Completed | 2006-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00320281 | Investigating Botulinum Toxin A to Treat Acute Neck/Upper Shoulder Pain Followi… | Phase4 | Spinal Cord Injury | Completed | 2006-04-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00871364 | A Relative Bioavailability Study of 50 mg Venlafaxine Hydrochloride Tablets Und… | Phase1 | Healthy | Completed | 2006-04-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00325715 | AGN 201904 Versus Esomeprazole in the Prevention of Aspirin-induced Stomach or … | Phase1 | Peptic Ulcer | Completed | 2006-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00320281 | Investigating Botulinum Toxin A to Treat Acute Neck/Upper Shoulder Pain Followi… | Phase4 | Spinal Cord Injury | Completed | 2006-04-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00871364 | A Relative Bioavailability Study of 50 mg Venlafaxine Hydrochloride Tablets Und… | Phase1 | Healthy | Completed | 2006-04-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00325715 | AGN 201904 Versus Esomeprazole in the Prevention of Aspirin-induced Stomach or … | Phase1 | Peptic Ulcer | Completed | 2006-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00320281 | Investigating Botulinum Toxin A to Treat Acute Neck/Upper Shoulder Pain Followi… | Phase4 | Spinal Cord Injury | Completed | 2006-04-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00871364 | A Relative Bioavailability Study of 50 mg Venlafaxine Hydrochloride Tablets Und… | Phase1 | Healthy | Completed | 2006-04-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00325715 | AGN 201904 Versus Esomeprazole in the Prevention of Aspirin-induced Stomach or … | Phase1 | Peptic Ulcer | Completed | 2006-04-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00320281 | Investigating Botulinum Toxin A to Treat Acute Neck/Upper Shoulder Pain Followi… | Phase4 | Spinal Cord Injury | Completed | 2006-04-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00141518 | Long-term Study of Duodopa (Levodopa/Carbidopa) in Advanced Parkinson's: Health… | Phase4 | Advanced Idiopathic Parkinson's Disease | Completed | 2006-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00168428 | A Study Using Botulinum Toxin Type A as Headache Prophylaxis for Migraine Patie… | Phase3 | Migraine Disorders | Completed | 2006-03-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00168428 | A Study Using Botulinum Toxin Type A as Headache Prophylaxis for Migraine Patie… | Phase3 | Migraine Disorders | Completed | 2006-03-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00168428 | A Study Using Botulinum Toxin Type A as Headache Prophylaxis for Migraine Patie… | Phase3 | Migraine Disorders | Completed | 2006-03-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00865111 | A Relative Bioavailability Study of Bupropion Sustained Release 150 mg Tablets … | Phase1 | Healthy | Completed | 2006-03-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00865111 | A Relative Bioavailability Study of Bupropion Sustained Release 150 mg Tablets … | Phase1 | Healthy | Completed | 2006-03-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00141518 | Long-term Study of Duodopa (Levodopa/Carbidopa) in Advanced Parkinson's: Health… | Phase4 | Advanced Idiopathic Parkinson's Disease | Completed | 2006-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00168428 | A Study Using Botulinum Toxin Type A as Headache Prophylaxis for Migraine Patie… | Phase3 | Migraine Disorders | Completed | 2006-03-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00865111 | A Relative Bioavailability Study of Bupropion Sustained Release 150 mg Tablets … | Phase1 | Healthy | Completed | 2006-03-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00141518 | Long-term Study of Duodopa (Levodopa/Carbidopa) in Advanced Parkinson's: Health… | Phase4 | Advanced Idiopathic Parkinson's Disease | Completed | 2006-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT00865111 | A Relative Bioavailability Study of Bupropion Sustained Release 150 mg Tablets … | Phase1 | Healthy | Completed | 2006-03-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00141518 | Long-term Study of Duodopa (Levodopa/Carbidopa) in Advanced Parkinson's: Health… | Phase4 | Advanced Idiopathic Parkinson's Disease | Completed | 2006-03-01 | 2011-04-01 | ClinicalTrials.gov |
| NCT01079182 | Basic Documentation of Adalimumab (Humira) in Patients With Ankylosing Spondyli… | — | Ankylosing Spondylitis | Completed | 2006-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00863863 | A Relative Bioavailability Study of Griseofulvin 125 mg/5 mL Suspension Under N… | Phase1 | Healthy | Completed | 2006-01-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00347204 | Comparison of Acular LS Versus Nevanac for Pain Control in Eyes Undergoing PRK | Phase4 | Myopia | Completed | 2006-01-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT01079182 | Basic Documentation of Adalimumab (Humira) in Patients With Ankylosing Spondyli… | — | Ankylosing Spondylitis | Completed | 2006-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00863863 | A Relative Bioavailability Study of Griseofulvin 125 mg/5 mL Suspension Under N… | Phase1 | Healthy | Completed | 2006-01-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00529386 | Botox for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) | Phase1 | Prostatitis | Terminated | 2006-01-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00529386 | Botox for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) | Phase1 | Prostatitis | Terminated | 2006-01-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00863863 | A Relative Bioavailability Study of Griseofulvin 125 mg/5 mL Suspension Under N… | Phase1 | Healthy | Completed | 2006-01-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT01079182 | Basic Documentation of Adalimumab (Humira) in Patients With Ankylosing Spondyli… | — | Ankylosing Spondylitis | Completed | 2006-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00863863 | A Relative Bioavailability Study of Griseofulvin 125 mg/5 mL Suspension Under N… | Phase1 | Healthy | Completed | 2006-01-01 | 2006-01-01 | ClinicalTrials.gov |
| NCT00529386 | Botox for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) | Phase1 | Prostatitis | Terminated | 2006-01-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT01079182 | Basic Documentation of Adalimumab (Humira) in Patients With Ankylosing Spondyli… | — | Ankylosing Spondylitis | Completed | 2006-01-01 | 2014-05-01 | ClinicalTrials.gov |
| NCT00529386 | Botox for Chronic Prostatitis/Chronic Pelvic Pain Syndrome (CP/CPPS) | Phase1 | Prostatitis | Terminated | 2006-01-01 | 2009-12-01 | ClinicalTrials.gov |
| NCT00347204 | Comparison of Acular LS Versus Nevanac for Pain Control in Eyes Undergoing PRK | Phase4 | Myopia | Completed | 2006-01-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00347204 | Comparison of Acular LS Versus Nevanac for Pain Control in Eyes Undergoing PRK | Phase4 | Myopia | Completed | 2006-01-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00347204 | Comparison of Acular LS Versus Nevanac for Pain Control in Eyes Undergoing PRK | Phase4 | Myopia | Completed | 2006-01-01 | 2006-06-01 | ClinicalTrials.gov |
| NCT00284518 | Safety and Efficacy Study of Botulinum Toxin Type A to Treat Lower Urinary Symp… | Phase2 | Benign Prostatic Hyperplasia | Completed | 2005-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00627679 | Safety and Blood Level Study of Unit Dose Budesonide | Phase1 | Asthma | Completed | 2005-12-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00300443 | Safety and Efficacy Study of Bimatoprost in Patients With Glaucoma or Ocular Hy… | Phase2 | Ocular Hypertension | Completed | 2005-12-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00284518 | Safety and Efficacy Study of Botulinum Toxin Type A to Treat Lower Urinary Symp… | Phase2 | Benign Prostatic Hyperplasia | Completed | 2005-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00300443 | Safety and Efficacy Study of Bimatoprost in Patients With Glaucoma or Ocular Hy… | Phase2 | Ocular Hypertension | Completed | 2005-12-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00300443 | Safety and Efficacy Study of Bimatoprost in Patients With Glaucoma or Ocular Hy… | Phase2 | Ocular Hypertension | Completed | 2005-12-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00627679 | Safety and Blood Level Study of Unit Dose Budesonide | Phase1 | Asthma | Completed | 2005-12-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00284518 | Safety and Efficacy Study of Botulinum Toxin Type A to Treat Lower Urinary Symp… | Phase2 | Benign Prostatic Hyperplasia | Completed | 2005-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00627679 | Safety and Blood Level Study of Unit Dose Budesonide | Phase1 | Asthma | Completed | 2005-12-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00627679 | Safety and Blood Level Study of Unit Dose Budesonide | Phase1 | Asthma | Completed | 2005-12-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00284518 | Safety and Efficacy Study of Botulinum Toxin Type A to Treat Lower Urinary Symp… | Phase2 | Benign Prostatic Hyperplasia | Completed | 2005-12-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00300443 | Safety and Efficacy Study of Bimatoprost in Patients With Glaucoma or Ocular Hy… | Phase2 | Ocular Hypertension | Completed | 2005-12-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00243542 | Phase IV Study to Gather More Information About the Safety of ACZONE Gel, 5% in… | Phase4 | Acne Vulgaris | Completed | 2005-11-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00864500 | Pivotal Bioequivalence Study of Topically Delivered Clobetasol Propionate Lotio… | Phase1 | Healthy | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00292396 | Efficacy and Safety of ABT-874 in Subjects With Moderate to Severe Chronic Plaq… | Phase2 | Psoriasis | Completed | 2005-11-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00651612 | Study to Evaluate Safety of Brimonidine/Timolol Fixed Combination in Glaucoma o… | Phase3 | Glaucoma | Completed | 2005-11-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00249782 | A Phase II, Randomized Study of ACZONE™ (Dapsone) Gel, 5% for Papulopustular Ro… | Phase2 | Rosacea | Completed | 2005-11-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00864500 | Pivotal Bioequivalence Study of Topically Delivered Clobetasol Propionate Lotio… | Phase1 | Healthy | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00243542 | Phase IV Study to Gather More Information About the Safety of ACZONE Gel, 5% in… | Phase4 | Acne Vulgaris | Completed | 2005-11-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00243542 | Phase IV Study to Gather More Information About the Safety of ACZONE Gel, 5% in… | Phase4 | Acne Vulgaris | Completed | 2005-11-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00249782 | A Phase II, Randomized Study of ACZONE™ (Dapsone) Gel, 5% for Papulopustular Ro… | Phase2 | Rosacea | Completed | 2005-11-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00292396 | Efficacy and Safety of ABT-874 in Subjects With Moderate to Severe Chronic Plaq… | Phase2 | Psoriasis | Completed | 2005-11-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00292396 | Efficacy and Safety of ABT-874 in Subjects With Moderate to Severe Chronic Plaq… | Phase2 | Psoriasis | Completed | 2005-11-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00249782 | A Phase II, Randomized Study of ACZONE™ (Dapsone) Gel, 5% for Papulopustular Ro… | Phase2 | Rosacea | Completed | 2005-11-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00243542 | Phase IV Study to Gather More Information About the Safety of ACZONE Gel, 5% in… | Phase4 | Acne Vulgaris | Completed | 2005-11-01 | 2006-10-01 | ClinicalTrials.gov |
| NCT00651612 | Study to Evaluate Safety of Brimonidine/Timolol Fixed Combination in Glaucoma o… | Phase3 | Glaucoma | Completed | 2005-11-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00292396 | Efficacy and Safety of ABT-874 in Subjects With Moderate to Severe Chronic Plaq… | Phase2 | Psoriasis | Completed | 2005-11-01 | 2008-04-01 | ClinicalTrials.gov |
| NCT00864500 | Pivotal Bioequivalence Study of Topically Delivered Clobetasol Propionate Lotio… | Phase1 | Healthy | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00651612 | Study to Evaluate Safety of Brimonidine/Timolol Fixed Combination in Glaucoma o… | Phase3 | Glaucoma | Completed | 2005-11-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00249782 | A Phase II, Randomized Study of ACZONE™ (Dapsone) Gel, 5% for Papulopustular Ro… | Phase2 | Rosacea | Completed | 2005-11-01 | 2006-05-01 | ClinicalTrials.gov |
| NCT00651612 | Study to Evaluate Safety of Brimonidine/Timolol Fixed Combination in Glaucoma o… | Phase3 | Glaucoma | Completed | 2005-11-01 | 2007-01-01 | ClinicalTrials.gov |
| NCT00864500 | Pivotal Bioequivalence Study of Topically Delivered Clobetasol Propionate Lotio… | Phase1 | Healthy | Completed | 2005-11-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00864435 | A Relative Bioavailability Study of Carvedilol 12.5 mg Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2005-10-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00864240 | The Dose-response "Pilot" Study of Topically Delivered Clobetasol Propionate Lo… | Phase1 | Healthy | Completed | 2005-10-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00864240 | The Dose-response "Pilot" Study of Topically Delivered Clobetasol Propionate Lo… | Phase1 | Healthy | Completed | 2005-10-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00864240 | The Dose-response "Pilot" Study of Topically Delivered Clobetasol Propionate Lo… | Phase1 | Healthy | Completed | 2005-10-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00864435 | A Relative Bioavailability Study of Carvedilol 12.5 mg Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2005-10-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00864435 | A Relative Bioavailability Study of Carvedilol 12.5 mg Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2005-10-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00864240 | The Dose-response "Pilot" Study of Topically Delivered Clobetasol Propionate Lo… | Phase1 | Healthy | Completed | 2005-10-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00864435 | A Relative Bioavailability Study of Carvedilol 12.5 mg Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2005-10-01 | 2005-11-01 | ClinicalTrials.gov |
| NCT00865761 | A Relative Bioavailability Study of Alprazolam 3 mg ER Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2005-09-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00395759 | The Visual Effect of an Investigational Artificial Tear in the Tear Layer. | Na | Dry Eye Disease | Completed | 2005-09-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00865657 | A Relative Bioavailability Study of Alprazolam 3 mg Extended Release Tablets Un… | Phase1 | Healthy | Completed | 2005-09-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00865761 | A Relative Bioavailability Study of Alprazolam 3 mg ER Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2005-09-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00395759 | The Visual Effect of an Investigational Artificial Tear in the Tear Layer. | Na | Dry Eye Disease | Completed | 2005-09-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00243711 | A Multi-Center Randomized Study to Evaluate the Efficacy and Safety of an Inves… | Phase2 | Dry Eye | Completed | 2005-09-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00243711 | A Multi-Center Randomized Study to Evaluate the Efficacy and Safety of an Inves… | Phase2 | Dry Eye | Completed | 2005-09-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00865761 | A Relative Bioavailability Study of Alprazolam 3 mg ER Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2005-09-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00395759 | The Visual Effect of an Investigational Artificial Tear in the Tear Layer. | Na | Dry Eye Disease | Completed | 2005-09-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00865657 | A Relative Bioavailability Study of Alprazolam 3 mg Extended Release Tablets Un… | Phase1 | Healthy | Completed | 2005-09-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00865657 | A Relative Bioavailability Study of Alprazolam 3 mg Extended Release Tablets Un… | Phase1 | Healthy | Completed | 2005-09-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00865657 | A Relative Bioavailability Study of Alprazolam 3 mg Extended Release Tablets Un… | Phase1 | Healthy | Completed | 2005-09-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00243711 | A Multi-Center Randomized Study to Evaluate the Efficacy and Safety of an Inves… | Phase2 | Dry Eye | Completed | 2005-09-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00865761 | A Relative Bioavailability Study of Alprazolam 3 mg ER Tablets Under Fasting Co… | Phase1 | Healthy | Completed | 2005-09-01 | 2005-09-01 | ClinicalTrials.gov |
| NCT00395759 | The Visual Effect of an Investigational Artificial Tear in the Tear Layer. | Na | Dry Eye Disease | Completed | 2005-09-01 | 2007-09-01 | ClinicalTrials.gov |
| NCT00243711 | A Multi-Center Randomized Study to Evaluate the Efficacy and Safety of an Inves… | Phase2 | Dry Eye | Completed | 2005-09-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00168415 | A Study Using Botulinum Toxin Type A in Adolescents With Axillary Hyperhidrosis | Phase4 | Hyperhidrosis | Completed | 2005-08-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00168415 | A Study Using Botulinum Toxin Type A in Adolescents With Axillary Hyperhidrosis | Phase4 | Hyperhidrosis | Completed | 2005-08-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00168415 | A Study Using Botulinum Toxin Type A in Adolescents With Axillary Hyperhidrosis | Phase4 | Hyperhidrosis | Completed | 2005-08-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT01111240 | Efficacy and Safety of Humira® in Patients With Psoriatic Arthritis in Normal M… | — | Psoriatic Arthritis | Completed | 2005-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00648986 | Efficacy and Safety Study of Tazarotene (Tazorac) for the Treatment of Brittle … | Phase4 | Brittle Nails | Completed | 2005-08-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00648986 | Efficacy and Safety Study of Tazarotene (Tazorac) for the Treatment of Brittle … | Phase4 | Brittle Nails | Completed | 2005-08-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00648986 | Efficacy and Safety Study of Tazarotene (Tazorac) for the Treatment of Brittle … | Phase4 | Brittle Nails | Completed | 2005-08-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT01111240 | Efficacy and Safety of Humira® in Patients With Psoriatic Arthritis in Normal M… | — | Psoriatic Arthritis | Completed | 2005-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01111240 | Efficacy and Safety of Humira® in Patients With Psoriatic Arthritis in Normal M… | — | Psoriatic Arthritis | Completed | 2005-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT01111240 | Efficacy and Safety of Humira® in Patients With Psoriatic Arthritis in Normal M… | — | Psoriatic Arthritis | Completed | 2005-08-01 | 2013-12-01 | ClinicalTrials.gov |
| NCT00648986 | Efficacy and Safety Study of Tazarotene (Tazorac) for the Treatment of Brittle … | Phase4 | Brittle Nails | Completed | 2005-08-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00168415 | A Study Using Botulinum Toxin Type A in Adolescents With Axillary Hyperhidrosis | Phase4 | Hyperhidrosis | Completed | 2005-08-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT01117480 | Real Life Evaluation of Rheumatoid Arthritis in Canadians Taking HUMIRA | — | Moderate-to-severe Rheumatoid Arthritis | Completed | 2005-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00168454 | A Research Study for Patients With Overactive Bladder | Phase2 | Overactive Bladder | Completed | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT01117480 | Real Life Evaluation of Rheumatoid Arthritis in Canadians Taking HUMIRA | — | Moderate-to-severe Rheumatoid Arthritis | Completed | 2005-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01117480 | Real Life Evaluation of Rheumatoid Arthritis in Canadians Taking HUMIRA | — | Moderate-to-severe Rheumatoid Arthritis | Completed | 2005-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01117480 | Real Life Evaluation of Rheumatoid Arthritis in Canadians Taking HUMIRA | — | Moderate-to-severe Rheumatoid Arthritis | Completed | 2005-07-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT00865891 | A Relative Bioavailability Study of 60 mg Nifedipine Extended Release Tablets U… | Phase1 | Healthy | Completed | 2005-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00865891 | A Relative Bioavailability Study of 60 mg Nifedipine Extended Release Tablets U… | Phase1 | Healthy | Completed | 2005-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00865891 | A Relative Bioavailability Study of 60 mg Nifedipine Extended Release Tablets U… | Phase1 | Healthy | Completed | 2005-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00168454 | A Research Study for Patients With Overactive Bladder | Phase2 | Overactive Bladder | Completed | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00168454 | A Research Study for Patients With Overactive Bladder | Phase2 | Overactive Bladder | Completed | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00168454 | A Research Study for Patients With Overactive Bladder | Phase2 | Overactive Bladder | Completed | 2005-07-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00865891 | A Relative Bioavailability Study of 60 mg Nifedipine Extended Release Tablets U… | Phase1 | Healthy | Completed | 2005-07-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00496964 | Botox for Non-surgical Lateral Release in Patellofemoral Pain | Phase3 | Patellofemoral Pain Syndrome | Terminated | 2005-05-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00496964 | Botox for Non-surgical Lateral Release in Patellofemoral Pain | Phase3 | Patellofemoral Pain Syndrome | Terminated | 2005-05-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00168337 | A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2005-05-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00496964 | Botox for Non-surgical Lateral Release in Patellofemoral Pain | Phase3 | Patellofemoral Pain Syndrome | Terminated | 2005-05-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00864747 | A Relative Bioavailability Study of Propranolol HCl 160 mg Tablets Under Non-fa… | Phase1 | Healthy | Completed | 2005-05-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00864747 | A Relative Bioavailability Study of Propranolol HCl 160 mg Tablets Under Non-fa… | Phase1 | Healthy | Completed | 2005-05-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00822055 | Comparison of the Fixed Combinations of Brimonidine/Timolol and Dorzolamide/Tim… | Phase4 | Open-Angle Glaucoma | Completed | 2005-05-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00864747 | A Relative Bioavailability Study of Propranolol HCl 160 mg Tablets Under Non-fa… | Phase1 | Healthy | Completed | 2005-05-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00864617 | A Relative Bioavailability Study of 60 mg Nifedipine ER Tablets Under Non-fasti… | Phase1 | Healthy | Completed | 2005-05-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00168337 | A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2005-05-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00864617 | A Relative Bioavailability Study of 60 mg Nifedipine ER Tablets Under Non-fasti… | Phase1 | Healthy | Completed | 2005-05-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00864747 | A Relative Bioavailability Study of Propranolol HCl 160 mg Tablets Under Non-fa… | Phase1 | Healthy | Completed | 2005-05-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00822055 | Comparison of the Fixed Combinations of Brimonidine/Timolol and Dorzolamide/Tim… | Phase4 | Open-Angle Glaucoma | Completed | 2005-05-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00864617 | A Relative Bioavailability Study of 60 mg Nifedipine ER Tablets Under Non-fasti… | Phase1 | Healthy | Completed | 2005-05-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00168337 | A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2005-05-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00496964 | Botox for Non-surgical Lateral Release in Patellofemoral Pain | Phase3 | Patellofemoral Pain Syndrome | Terminated | 2005-05-01 | 2008-06-01 | ClinicalTrials.gov |
| NCT00168337 | A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2005-05-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT00822055 | Comparison of the Fixed Combinations of Brimonidine/Timolol and Dorzolamide/Tim… | Phase4 | Open-Angle Glaucoma | Completed | 2005-05-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00822055 | Comparison of the Fixed Combinations of Brimonidine/Timolol and Dorzolamide/Tim… | Phase4 | Open-Angle Glaucoma | Completed | 2005-05-01 | 2006-11-01 | ClinicalTrials.gov |
| NCT00864617 | A Relative Bioavailability Study of 60 mg Nifedipine ER Tablets Under Non-fasti… | Phase1 | Healthy | Completed | 2005-05-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00870571 | A Relative Bioavailability Study of Amlodipine Besylate 10 mg Tablets Tablets U… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00870142 | A Relative Bioavailability Study of Amlodipine Besylate 10 mg Tablets Under Fas… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00865215 | A Relative Bioavailability Study of Propranolol Hydrochloride 160 mg Tablets Un… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00865215 | A Relative Bioavailability Study of Propranolol Hydrochloride 160 mg Tablets Un… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00870571 | A Relative Bioavailability Study of Amlodipine Besylate 10 mg Tablets Tablets U… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00870142 | A Relative Bioavailability Study of Amlodipine Besylate 10 mg Tablets Under Fas… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00865215 | A Relative Bioavailability Study of Propranolol Hydrochloride 160 mg Tablets Un… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00870142 | A Relative Bioavailability Study of Amlodipine Besylate 10 mg Tablets Under Fas… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00870571 | A Relative Bioavailability Study of Amlodipine Besylate 10 mg Tablets Tablets U… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00865215 | A Relative Bioavailability Study of Propranolol Hydrochloride 160 mg Tablets Un… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-04-01 | ClinicalTrials.gov |
| NCT00870142 | A Relative Bioavailability Study of Amlodipine Besylate 10 mg Tablets Under Fas… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00870571 | A Relative Bioavailability Study of Amlodipine Besylate 10 mg Tablets Tablets U… | Phase1 | Healthy | Completed | 2005-04-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00856999 | Botox Cosmetic and the Young Patient With Glabellar Furrows | Phase4 | Glabellar Furrows | Completed | 2005-02-08 | 2010-11-17 | ClinicalTrials.gov |
| NCT00856999 | Botox Cosmetic and the Young Patient With Glabellar Furrows | Phase4 | Glabellar Furrows | Completed | 2005-02-08 | 2010-11-17 | ClinicalTrials.gov |
| NCT00856999 | Botox Cosmetic and the Young Patient With Glabellar Furrows | Phase4 | Glabellar Furrows | Completed | 2005-02-08 | 2010-11-17 | ClinicalTrials.gov |
| NCT00856999 | Botox Cosmetic and the Young Patient With Glabellar Furrows | Phase4 | Glabellar Furrows | Completed | 2005-02-08 | 2010-11-17 | ClinicalTrials.gov |
| NCT00352807 | Absorption of Brimonidine Ophthalmic Solution in the Aqueous Humor of Cataract … | Na | Cataract | Completed | 2005-02-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00151541 | A Phase 3 Study to Compare the Safety and Efficacy of 5% Dapsone Topical Gel, (… | Phase3 | Acne Vulgaris | Completed | 2005-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00168389 | A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2005-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00352807 | Absorption of Brimonidine Ophthalmic Solution in the Aqueous Humor of Cataract … | Na | Cataract | Completed | 2005-02-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00250952 | Study to Determine If the Volume Used to Dilute BOTOX Cosmetic™ for Injection A… | Na | Skin Wrinkling | Completed | 2005-02-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00168389 | A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2005-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00250952 | Study to Determine If the Volume Used to Dilute BOTOX Cosmetic™ for Injection A… | Na | Skin Wrinkling | Completed | 2005-02-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00168389 | A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2005-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00352807 | Absorption of Brimonidine Ophthalmic Solution in the Aqueous Humor of Cataract … | Na | Cataract | Completed | 2005-02-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00151541 | A Phase 3 Study to Compare the Safety and Efficacy of 5% Dapsone Topical Gel, (… | Phase3 | Acne Vulgaris | Completed | 2005-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00250952 | Study to Determine If the Volume Used to Dilute BOTOX Cosmetic™ for Injection A… | Na | Skin Wrinkling | Completed | 2005-02-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00352807 | Absorption of Brimonidine Ophthalmic Solution in the Aqueous Humor of Cataract … | Na | Cataract | Completed | 2005-02-01 | 2005-12-01 | ClinicalTrials.gov |
| NCT00250952 | Study to Determine If the Volume Used to Dilute BOTOX Cosmetic™ for Injection A… | Na | Skin Wrinkling | Completed | 2005-02-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00168389 | A Study of the Safety and Efficacy of a New Treatment for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2005-02-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT00151541 | A Phase 3 Study to Compare the Safety and Efficacy of 5% Dapsone Topical Gel, (… | Phase3 | Acne Vulgaris | Completed | 2005-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00151541 | A Phase 3 Study to Compare the Safety and Efficacy of 5% Dapsone Topical Gel, (… | Phase3 | Acne Vulgaris | Completed | 2005-02-01 | 2005-07-01 | ClinicalTrials.gov |
| NCT00822081 | Comparison of the Fixed Combinations of Brimonidine/Timolol and Dorzolamide/Tim… | Phase4 | Open-Angle Glaucoma | Completed | 2005-01-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00168363 | Safety and Efficacy of Brimonidine in Patients With Glaucoma or Ocular Hyperten… | Phase3 | Glaucoma | Completed | 2005-01-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00652496 | Safety and Efficacy Study of Different Formulations of Bimatoprost Once-Daily i… | Phase2 | Glaucoma | Completed | 2005-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00822081 | Comparison of the Fixed Combinations of Brimonidine/Timolol and Dorzolamide/Tim… | Phase4 | Open-Angle Glaucoma | Completed | 2005-01-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00652496 | Safety and Efficacy Study of Different Formulations of Bimatoprost Once-Daily i… | Phase2 | Glaucoma | Completed | 2005-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00822081 | Comparison of the Fixed Combinations of Brimonidine/Timolol and Dorzolamide/Tim… | Phase4 | Open-Angle Glaucoma | Completed | 2005-01-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00652496 | Safety and Efficacy Study of Different Formulations of Bimatoprost Once-Daily i… | Phase2 | Glaucoma | Completed | 2005-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00652496 | Safety and Efficacy Study of Different Formulations of Bimatoprost Once-Daily i… | Phase2 | Glaucoma | Completed | 2005-01-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00168363 | Safety and Efficacy of Brimonidine in Patients With Glaucoma or Ocular Hyperten… | Phase3 | Glaucoma | Completed | 2005-01-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00822081 | Comparison of the Fixed Combinations of Brimonidine/Timolol and Dorzolamide/Tim… | Phase4 | Open-Angle Glaucoma | Completed | 2005-01-01 | 2006-04-01 | ClinicalTrials.gov |
| NCT00168363 | Safety and Efficacy of Brimonidine in Patients With Glaucoma or Ocular Hyperten… | Phase3 | Glaucoma | Completed | 2005-01-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00168363 | Safety and Efficacy of Brimonidine in Patients With Glaucoma or Ocular Hyperten… | Phase3 | Glaucoma | Completed | 2005-01-01 | 2006-08-01 | ClinicalTrials.gov |
| NCT00168298 | A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulti… | Phase3 | Macular Edema | Completed | 2004-11-01 | 2008-09-05 | ClinicalTrials.gov |
| NCT01190748 | Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Do… | Phase1 | Healthy | Completed | 2004-11-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00871247 | A Relative Bioavailability Study of Finasteride 5 mg Tablets Under Fed Conditio… | Phase1 | Healthy | Completed | 2004-11-01 | 2004-11-01 | ClinicalTrials.gov |
| NCT00871247 | A Relative Bioavailability Study of Finasteride 5 mg Tablets Under Fed Conditio… | Phase1 | Healthy | Completed | 2004-11-01 | 2004-11-01 | ClinicalTrials.gov |
| NCT01190748 | Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Do… | Phase1 | Healthy | Completed | 2004-11-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT01190748 | Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Do… | Phase1 | Healthy | Completed | 2004-11-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00871247 | A Relative Bioavailability Study of Finasteride 5 mg Tablets Under Fed Conditio… | Phase1 | Healthy | Completed | 2004-11-01 | 2004-11-01 | ClinicalTrials.gov |
| NCT01190748 | Bioequivalence Study of Galantamine 4 mg Tablet and Reminyl Following a 4 mg Do… | Phase1 | Healthy | Completed | 2004-11-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00363714 | A Dose Escalation Trial of an Intravitreal Injection of Sirna-027 in Patients W… | Phase1 | Age-Related Macular Degeneration | Completed | 2004-11-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00168298 | A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulti… | Phase3 | Macular Edema | Completed | 2004-11-01 | 2008-09-05 | ClinicalTrials.gov |
| NCT00168298 | A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulti… | Phase3 | Macular Edema | Completed | 2004-11-01 | 2008-09-05 | ClinicalTrials.gov |
| NCT00363714 | A Dose Escalation Trial of an Intravitreal Injection of Sirna-027 in Patients W… | Phase1 | Age-Related Macular Degeneration | Completed | 2004-11-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00871247 | A Relative Bioavailability Study of Finasteride 5 mg Tablets Under Fed Conditio… | Phase1 | Healthy | Completed | 2004-11-01 | 2004-11-01 | ClinicalTrials.gov |
| NCT00168298 | A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulti… | Phase3 | Macular Edema | Completed | 2004-11-01 | 2008-09-05 | ClinicalTrials.gov |
| NCT00363714 | A Dose Escalation Trial of an Intravitreal Injection of Sirna-027 in Patients W… | Phase1 | Age-Related Macular Degeneration | Completed | 2004-11-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00363714 | A Dose Escalation Trial of an Intravitreal Injection of Sirna-027 in Patients W… | Phase1 | Age-Related Macular Degeneration | Completed | 2004-11-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00863915 | A Relative Bioavailability Study of Ramipril 10 mg Capsules Administered Orally… | Phase1 | Healthy | Completed | 2004-10-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00863915 | A Relative Bioavailability Study of Ramipril 10 mg Capsules Administered Orally… | Phase1 | Healthy | Completed | 2004-10-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00168324 | A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulti… | Phase3 | Macular Edema | Completed | 2004-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00168324 | A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulti… | Phase3 | Macular Edema | Completed | 2004-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00168324 | A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulti… | Phase3 | Macular Edema | Completed | 2004-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00863915 | A Relative Bioavailability Study of Ramipril 10 mg Capsules Administered Orally… | Phase1 | Healthy | Completed | 2004-10-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00863915 | A Relative Bioavailability Study of Ramipril 10 mg Capsules Administered Orally… | Phase1 | Healthy | Completed | 2004-10-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00168324 | A Study of the Safety and Efficacy of a New Treatment for Macular Edema Resulti… | Phase3 | Macular Edema | Completed | 2004-10-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00716742 | Safety and Efficacy Study of Bimatoprost, Latanoprost, and Travoprost in Patien… | — | Open-Angle Glaucoma | Completed | 2004-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00717418 | Efficacy Study of Cyclosporine Ophthalmic Emulsion in Patients With Dry Eye Dis… | — | Keratoconjunctivitis Sicca | Completed | 2004-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00864162 | A Relative Bioavailability Study of Ramipril 10 mg Capsules Under Fed Conditions | Phase1 | Healthy | Completed | 2004-09-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00114114 | Dose-Response of Gonadal Steroids and Bone Turnover in Older Men | Na | Healthy Volunteers | Completed | 2004-09-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT00865371 | A Relative Bioavailability Study of Bupropion Extended-Released 150 mg Tablets … | Phase1 | Healthy | Completed | 2004-09-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00114114 | Dose-Response of Gonadal Steroids and Bone Turnover in Older Men | Na | Healthy Volunteers | Completed | 2004-09-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT00716742 | Safety and Efficacy Study of Bimatoprost, Latanoprost, and Travoprost in Patien… | — | Open-Angle Glaucoma | Completed | 2004-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00865371 | A Relative Bioavailability Study of Bupropion Extended-Released 150 mg Tablets … | Phase1 | Healthy | Completed | 2004-09-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00864162 | A Relative Bioavailability Study of Ramipril 10 mg Capsules Under Fed Conditions | Phase1 | Healthy | Completed | 2004-09-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00717418 | Efficacy Study of Cyclosporine Ophthalmic Emulsion in Patients With Dry Eye Dis… | — | Keratoconjunctivitis Sicca | Completed | 2004-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00717418 | Efficacy Study of Cyclosporine Ophthalmic Emulsion in Patients With Dry Eye Dis… | — | Keratoconjunctivitis Sicca | Completed | 2004-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00716742 | Safety and Efficacy Study of Bimatoprost, Latanoprost, and Travoprost in Patien… | — | Open-Angle Glaucoma | Completed | 2004-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00716742 | Safety and Efficacy Study of Bimatoprost, Latanoprost, and Travoprost in Patien… | — | Open-Angle Glaucoma | Completed | 2004-09-01 | 2009-09-01 | ClinicalTrials.gov |
| NCT00717418 | Efficacy Study of Cyclosporine Ophthalmic Emulsion in Patients With Dry Eye Dis… | — | Keratoconjunctivitis Sicca | Completed | 2004-09-01 | 2008-08-01 | ClinicalTrials.gov |
| NCT00864162 | A Relative Bioavailability Study of Ramipril 10 mg Capsules Under Fed Conditions | Phase1 | Healthy | Completed | 2004-09-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00114114 | Dose-Response of Gonadal Steroids and Bone Turnover in Older Men | Na | Healthy Volunteers | Completed | 2004-09-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT00114114 | Dose-Response of Gonadal Steroids and Bone Turnover in Older Men | Na | Healthy Volunteers | Completed | 2004-09-01 | 2017-11-01 | ClinicalTrials.gov |
| NCT00865371 | A Relative Bioavailability Study of Bupropion Extended-Released 150 mg Tablets … | Phase1 | Healthy | Completed | 2004-09-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00865371 | A Relative Bioavailability Study of Bupropion Extended-Released 150 mg Tablets … | Phase1 | Healthy | Completed | 2004-09-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00864162 | A Relative Bioavailability Study of Ramipril 10 mg Capsules Under Fed Conditions | Phase1 | Healthy | Completed | 2004-09-01 | 2004-10-01 | ClinicalTrials.gov |
| NCT00864344 | A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Fasting… | Phase1 | Healthy | Completed | 2004-08-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00864019 | A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Non-fas… | Phase1 | Healthy | Completed | 2004-08-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00864019 | A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Non-fas… | Phase1 | Healthy | Completed | 2004-08-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00865410 | A Relative Bioavailability Study of Bupropion Extended-Released 150 mg Tablets … | Phase1 | Healthy | Completed | 2004-08-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00864019 | A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Non-fas… | Phase1 | Healthy | Completed | 2004-08-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00865410 | A Relative Bioavailability Study of Bupropion Extended-Released 150 mg Tablets … | Phase1 | Healthy | Completed | 2004-08-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00865410 | A Relative Bioavailability Study of Bupropion Extended-Released 150 mg Tablets … | Phase1 | Healthy | Completed | 2004-08-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00864019 | A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Non-fas… | Phase1 | Healthy | Completed | 2004-08-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00865410 | A Relative Bioavailability Study of Bupropion Extended-Released 150 mg Tablets … | Phase1 | Healthy | Completed | 2004-08-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00864344 | A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Fasting… | Phase1 | Healthy | Completed | 2004-08-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00864344 | A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Fasting… | Phase1 | Healthy | Completed | 2004-08-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00864344 | A Relative Bioavailability Study of Sertraline HCl 100 mg Tablets Under Fasting… | Phase1 | Healthy | Completed | 2004-08-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00865462 | A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fed Condi… | Phase1 | Healthy | Completed | 2004-07-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00367133 | Intravitreal Triamcinolone Acetonide Versus Laser for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2004-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00211718 | Intra-Articular Injection of Botulinum Toxin Type A for Shoulder Pain | Phase3 | Arthritis | Unknown | 2004-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00865462 | A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fed Condi… | Phase1 | Healthy | Completed | 2004-07-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00211718 | Intra-Articular Injection of Botulinum Toxin Type A for Shoulder Pain | Phase3 | Arthritis | Unknown | 2004-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00367133 | Intravitreal Triamcinolone Acetonide Versus Laser for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2004-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00211718 | Intra-Articular Injection of Botulinum Toxin Type A for Shoulder Pain | Phase3 | Arthritis | Unknown | 2004-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00367133 | Intravitreal Triamcinolone Acetonide Versus Laser for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2004-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00865462 | A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fed Condi… | Phase1 | Healthy | Completed | 2004-07-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00367133 | Intravitreal Triamcinolone Acetonide Versus Laser for Diabetic Macular Edema | Phase3 | Diabetic Macular Edema | Completed | 2004-07-01 | 2008-10-01 | ClinicalTrials.gov |
| NCT00865462 | A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fed Condi… | Phase1 | Healthy | Completed | 2004-07-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00211718 | Intra-Articular Injection of Botulinum Toxin Type A for Shoulder Pain | Phase3 | Arthritis | Unknown | 2004-07-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00168441 | A Study Evaluating Botulinum Toxin Type A in Subjects With Postherpetic Neuralg… | Phase2 | Postherpetic Neuralgia | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00211679 | Intra-articularInjection of Botulinum Toxin Type | Phase2 | Arthritis | Unknown | 2004-06-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00211679 | Intra-articularInjection of Botulinum Toxin Type | Phase2 | Arthritis | Unknown | 2004-06-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00168441 | A Study Evaluating Botulinum Toxin Type A in Subjects With Postherpetic Neuralg… | Phase2 | Postherpetic Neuralgia | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00863941 | A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fasting C… | Phase1 | Healthy | Completed | 2004-06-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00863941 | A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fasting C… | Phase1 | Healthy | Completed | 2004-06-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00211679 | Intra-articularInjection of Botulinum Toxin Type | Phase2 | Arthritis | Unknown | 2004-06-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00168441 | A Study Evaluating Botulinum Toxin Type A in Subjects With Postherpetic Neuralg… | Phase2 | Postherpetic Neuralgia | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00211679 | Intra-articularInjection of Botulinum Toxin Type | Phase2 | Arthritis | Unknown | 2004-06-01 | 2007-06-01 | ClinicalTrials.gov |
| NCT00863941 | A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fasting C… | Phase1 | Healthy | Completed | 2004-06-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00863941 | A Relative Bioavailability Study of Bupropion XL 150 mg Tablets Under Fasting C… | Phase1 | Healthy | Completed | 2004-06-01 | 2004-07-01 | ClinicalTrials.gov |
| NCT00168441 | A Study Evaluating Botulinum Toxin Type A in Subjects With Postherpetic Neuralg… | Phase2 | Postherpetic Neuralgia | Completed | 2004-06-01 | 2005-06-01 | ClinicalTrials.gov |
| NCT00782548 | Comparative Study to Evaluate KADIAN and Avinza in Healthy Adults | Phase4 | Healthy | Completed | 2004-05-01 | 2004-06-01 | ClinicalTrials.gov |
| NCT00782548 | Comparative Study to Evaluate KADIAN and Avinza in Healthy Adults | Phase4 | Healthy | Completed | 2004-05-01 | 2004-06-01 | ClinicalTrials.gov |
| NCT00782548 | Comparative Study to Evaluate KADIAN and Avinza in Healthy Adults | Phase4 | Healthy | Completed | 2004-05-01 | 2004-06-01 | ClinicalTrials.gov |
| NCT00782548 | Comparative Study to Evaluate KADIAN and Avinza in Healthy Adults | Phase4 | Healthy | Completed | 2004-05-01 | 2004-06-01 | ClinicalTrials.gov |
| NCT00850421 | Pilot Study of BOTOX for Migraine Headaches | Na | Migraine Headache | Terminated | 2004-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00850421 | Pilot Study of BOTOX for Migraine Headaches | Na | Migraine Headache | Terminated | 2004-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01077258 | Efficacy and Safety of Adalimumab in Patients With Rheumatoid Arthritis in Rout… | — | Rheumatoid Arthritis | Completed | 2004-04-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT01077258 | Efficacy and Safety of Adalimumab in Patients With Rheumatoid Arthritis in Rout… | — | Rheumatoid Arthritis | Completed | 2004-04-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00850421 | Pilot Study of BOTOX for Migraine Headaches | Na | Migraine Headache | Terminated | 2004-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01077258 | Efficacy and Safety of Adalimumab in Patients With Rheumatoid Arthritis in Rout… | — | Rheumatoid Arthritis | Completed | 2004-04-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00850421 | Pilot Study of BOTOX for Migraine Headaches | Na | Migraine Headache | Terminated | 2004-04-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT01077258 | Efficacy and Safety of Adalimumab in Patients With Rheumatoid Arthritis in Rout… | — | Rheumatoid Arthritis | Completed | 2004-04-01 | 2013-02-01 | ClinicalTrials.gov |
| NCT00651690 | Study of Responsiveness of Seven Functional Tasks in Patients With Poststroke U… | Phase2 | Stroke | Completed | 2004-03-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00580502 | Safety and Efficacy of Adjustable Gastric Band Operations for Patients With Bod… | Phase2 | Obesity | Completed | 2004-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00580502 | Safety and Efficacy of Adjustable Gastric Band Operations for Patients With Bod… | Phase2 | Obesity | Completed | 2004-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00651690 | Study of Responsiveness of Seven Functional Tasks in Patients With Poststroke U… | Phase2 | Stroke | Completed | 2004-03-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00405431 | Will Restasis Eye Drops Increase Your Chance of Having a Successful Surgery? | Na | Glaucoma | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00405431 | Will Restasis Eye Drops Increase Your Chance of Having a Successful Surgery? | Na | Glaucoma | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00580502 | Safety and Efficacy of Adjustable Gastric Band Operations for Patients With Bod… | Phase2 | Obesity | Completed | 2004-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00580502 | Safety and Efficacy of Adjustable Gastric Band Operations for Patients With Bod… | Phase2 | Obesity | Completed | 2004-03-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT00651690 | Study of Responsiveness of Seven Functional Tasks in Patients With Poststroke U… | Phase2 | Stroke | Completed | 2004-03-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00651690 | Study of Responsiveness of Seven Functional Tasks in Patients With Poststroke U… | Phase2 | Stroke | Completed | 2004-03-01 | 2005-05-01 | ClinicalTrials.gov |
| NCT00405431 | Will Restasis Eye Drops Increase Your Chance of Having a Successful Surgery? | Na | Glaucoma | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT00405431 | Will Restasis Eye Drops Increase Your Chance of Having a Successful Surgery? | Na | Glaucoma | Completed | 2004-03-01 | 2007-11-01 | ClinicalTrials.gov |
| NCT01075191 | Kaletra: Therapy With Double Protease Inhibitors | — | Human Immunodeficiency Virus | Completed | 2004-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01075191 | Kaletra: Therapy With Double Protease Inhibitors | — | Human Immunodeficiency Virus | Completed | 2004-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01075191 | Kaletra: Therapy With Double Protease Inhibitors | — | Human Immunodeficiency Virus | Completed | 2004-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01075191 | Kaletra: Therapy With Double Protease Inhibitors | — | Human Immunodeficiency Virus | Completed | 2004-01-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT00430196 | BOTOX® Versus Zanaflex® for the Treatment of Post-Stroke or Traumatic Brain Inj… | Phase4 | Upper Limb Spasticity | Completed | 2003-12-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00865267 | The Dose-response Study of Topically Delivered Halobetasol Propionate Ointment … | Phase1 | Healthy | Completed | 2003-12-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00430196 | BOTOX® Versus Zanaflex® for the Treatment of Post-Stroke or Traumatic Brain Inj… | Phase4 | Upper Limb Spasticity | Completed | 2003-12-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00430196 | BOTOX® Versus Zanaflex® for the Treatment of Post-Stroke or Traumatic Brain Inj… | Phase4 | Upper Limb Spasticity | Completed | 2003-12-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00865267 | The Dose-response Study of Topically Delivered Halobetasol Propionate Ointment … | Phase1 | Healthy | Completed | 2003-12-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00865267 | The Dose-response Study of Topically Delivered Halobetasol Propionate Ointment … | Phase1 | Healthy | Completed | 2003-12-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00865267 | The Dose-response Study of Topically Delivered Halobetasol Propionate Ointment … | Phase1 | Healthy | Completed | 2003-12-01 | 2003-12-01 | ClinicalTrials.gov |
| NCT00430196 | BOTOX® Versus Zanaflex® for the Treatment of Post-Stroke or Traumatic Brain Inj… | Phase4 | Upper Limb Spasticity | Completed | 2003-12-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT01129583 | Botulinum Toxin as a Novel Treatment for Prevention of Post-Traumatic Elbow Sti… | Na | Post Traumatic Stiffness | Completed | 2003-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00648999 | Safety and Efficacy of Kaletra in ARV Therapy Experienced Patients | Phase4 | Human Immunodeficiency Virus | Completed | 2003-11-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00648999 | Safety and Efficacy of Kaletra in ARV Therapy Experienced Patients | Phase4 | Human Immunodeficiency Virus | Completed | 2003-11-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00168480 | A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis | Phase4 | Hyperhidrosis | Completed | 2003-11-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00168480 | A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis | Phase4 | Hyperhidrosis | Completed | 2003-11-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00648999 | Safety and Efficacy of Kaletra in ARV Therapy Experienced Patients | Phase4 | Human Immunodeficiency Virus | Completed | 2003-11-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT01129583 | Botulinum Toxin as a Novel Treatment for Prevention of Post-Traumatic Elbow Sti… | Na | Post Traumatic Stiffness | Completed | 2003-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT01129583 | Botulinum Toxin as a Novel Treatment for Prevention of Post-Traumatic Elbow Sti… | Na | Post Traumatic Stiffness | Completed | 2003-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00168480 | A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis | Phase4 | Hyperhidrosis | Completed | 2003-11-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT01129583 | Botulinum Toxin as a Novel Treatment for Prevention of Post-Traumatic Elbow Sti… | Na | Post Traumatic Stiffness | Completed | 2003-11-01 | 2010-05-01 | ClinicalTrials.gov |
| NCT00648999 | Safety and Efficacy of Kaletra in ARV Therapy Experienced Patients | Phase4 | Human Immunodeficiency Virus | Completed | 2003-11-01 | 2006-12-01 | ClinicalTrials.gov |
| NCT00168480 | A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis | Phase4 | Hyperhidrosis | Completed | 2003-11-01 | 2007-04-01 | ClinicalTrials.gov |
| NCT00661089 | Randomized DB Controlled Trial of Botulinum Toxin A in Hemiplegic Shoulder Pain… | Na | Post-stroke Shoulder Pain and Spasticity | Completed | 2003-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00661089 | Randomized DB Controlled Trial of Botulinum Toxin A in Hemiplegic Shoulder Pain… | Na | Post-stroke Shoulder Pain and Spasticity | Completed | 2003-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00661089 | Randomized DB Controlled Trial of Botulinum Toxin A in Hemiplegic Shoulder Pain… | Na | Post-stroke Shoulder Pain and Spasticity | Completed | 2003-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00661089 | Randomized DB Controlled Trial of Botulinum Toxin A in Hemiplegic Shoulder Pain… | Na | Post-stroke Shoulder Pain and Spasticity | Completed | 2003-09-01 | 2010-02-01 | ClinicalTrials.gov |
| NCT00865852 | A Relative Bioavailability Study of Metformin HCl 750 mg ER Tablets Under Non-f… | Phase1 | Healthy | Completed | 2003-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865072 | A Relative Bioavailability Study of Metformin HCl 750 mg ER Tablets Under Fasti… | Phase1 | Healthy | Completed | 2003-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865852 | A Relative Bioavailability Study of Metformin HCl 750 mg ER Tablets Under Non-f… | Phase1 | Healthy | Completed | 2003-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865852 | A Relative Bioavailability Study of Metformin HCl 750 mg ER Tablets Under Non-f… | Phase1 | Healthy | Completed | 2003-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865072 | A Relative Bioavailability Study of Metformin HCl 750 mg ER Tablets Under Fasti… | Phase1 | Healthy | Completed | 2003-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865852 | A Relative Bioavailability Study of Metformin HCl 750 mg ER Tablets Under Non-f… | Phase1 | Healthy | Completed | 2003-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865072 | A Relative Bioavailability Study of Metformin HCl 750 mg ER Tablets Under Fasti… | Phase1 | Healthy | Completed | 2003-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865072 | A Relative Bioavailability Study of Metformin HCl 750 mg ER Tablets Under Fasti… | Phase1 | Healthy | Completed | 2003-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865943 | A Relative Bioavailability Study of Citalopram HBr 10 mg Tablets Under Fasting … | Phase1 | Healthy | Completed | 2003-07-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865943 | A Relative Bioavailability Study of Citalopram HBr 10 mg Tablets Under Fasting … | Phase1 | Healthy | Completed | 2003-07-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865943 | A Relative Bioavailability Study of Citalopram HBr 10 mg Tablets Under Fasting … | Phase1 | Healthy | Completed | 2003-07-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00865943 | A Relative Bioavailability Study of Citalopram HBr 10 mg Tablets Under Fasting … | Phase1 | Healthy | Completed | 2003-07-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00652106 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase3 | Glaucoma | Completed | 2003-06-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00241215 | Study to Evaluate the Efficacy of Botulinum Toxin Serotype A Injections for Cer… | Phase4 | Cervicobrachial Neuralgia | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00864890 | A Relative Bioavailability Study of Citalopram 40 mg Tablets Under Fed Conditio… | Phase1 | Healthy | Completed | 2003-06-01 | 2003-07-01 | ClinicalTrials.gov |
| NCT00865085 | A Relative Bioavailability Study of Citalopram 40 mg Tablets Under Fasting Cond… | Phase1 | Healthy | Completed | 2003-06-01 | 2003-07-01 | ClinicalTrials.gov |
| NCT00864890 | A Relative Bioavailability Study of Citalopram 40 mg Tablets Under Fed Conditio… | Phase1 | Healthy | Completed | 2003-06-01 | 2003-07-01 | ClinicalTrials.gov |
| NCT00865085 | A Relative Bioavailability Study of Citalopram 40 mg Tablets Under Fasting Cond… | Phase1 | Healthy | Completed | 2003-06-01 | 2003-07-01 | ClinicalTrials.gov |
| NCT00865085 | A Relative Bioavailability Study of Citalopram 40 mg Tablets Under Fasting Cond… | Phase1 | Healthy | Completed | 2003-06-01 | 2003-07-01 | ClinicalTrials.gov |
| NCT00864890 | A Relative Bioavailability Study of Citalopram 40 mg Tablets Under Fed Conditio… | Phase1 | Healthy | Completed | 2003-06-01 | 2003-07-01 | ClinicalTrials.gov |
| NCT00241215 | Study to Evaluate the Efficacy of Botulinum Toxin Serotype A Injections for Cer… | Phase4 | Cervicobrachial Neuralgia | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00241215 | Study to Evaluate the Efficacy of Botulinum Toxin Serotype A Injections for Cer… | Phase4 | Cervicobrachial Neuralgia | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00652106 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase3 | Glaucoma | Completed | 2003-06-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00864890 | A Relative Bioavailability Study of Citalopram 40 mg Tablets Under Fed Conditio… | Phase1 | Healthy | Completed | 2003-06-01 | 2003-07-01 | ClinicalTrials.gov |
| NCT00865085 | A Relative Bioavailability Study of Citalopram 40 mg Tablets Under Fasting Cond… | Phase1 | Healthy | Completed | 2003-06-01 | 2003-07-01 | ClinicalTrials.gov |
| NCT00241215 | Study to Evaluate the Efficacy of Botulinum Toxin Serotype A Injections for Cer… | Phase4 | Cervicobrachial Neuralgia | Completed | 2003-06-01 | — | ClinicalTrials.gov |
| NCT00652106 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase3 | Glaucoma | Completed | 2003-06-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00652106 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase3 | Glaucoma | Completed | 2003-06-01 | 2004-03-01 | ClinicalTrials.gov |
| NCT00332059 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00332059 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00332059 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00652483 | Safety and Efficacy Study of Brimonidine in Patients With Glaucoma or Ocular Hy… | Phase3 | Glaucoma | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00332059 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00652483 | Safety and Efficacy Study of Brimonidine in Patients With Glaucoma or Ocular Hy… | Phase3 | Glaucoma | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00652483 | Safety and Efficacy Study of Brimonidine in Patients With Glaucoma or Ocular Hy… | Phase3 | Glaucoma | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT00652483 | Safety and Efficacy Study of Brimonidine in Patients With Glaucoma or Ocular Hy… | Phase3 | Glaucoma | Completed | 2003-05-01 | 2004-09-01 | ClinicalTrials.gov |
| NCT01853605 | NATRELLE® 410 Full and Moderate Height/Projection Breast Implant Continued Acce… | Na | Breast Augmentation | Terminated | 2003-04-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01853605 | NATRELLE® 410 Full and Moderate Height/Projection Breast Implant Continued Acce… | Na | Breast Augmentation | Terminated | 2003-04-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00651729 | Safety Study of Botulinum Toxin Type A for the Treatment of Focal Upper Limb Po… | Phase2 | Stroke | Completed | 2003-04-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00651729 | Safety Study of Botulinum Toxin Type A for the Treatment of Focal Upper Limb Po… | Phase2 | Stroke | Completed | 2003-04-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00651729 | Safety Study of Botulinum Toxin Type A for the Treatment of Focal Upper Limb Po… | Phase2 | Stroke | Completed | 2003-04-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT00651729 | Safety Study of Botulinum Toxin Type A for the Treatment of Focal Upper Limb Po… | Phase2 | Stroke | Completed | 2003-04-01 | 2004-12-01 | ClinicalTrials.gov |
| NCT01853605 | NATRELLE® 410 Full and Moderate Height/Projection Breast Implant Continued Acce… | Na | Breast Augmentation | Terminated | 2003-04-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01853605 | NATRELLE® 410 Full and Moderate Height/Projection Breast Implant Continued Acce… | Na | Breast Augmentation | Terminated | 2003-04-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT00865241 | A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets… | Phase1 | Healthy | Completed | 2002-11-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00864734 | A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets… | Phase1 | Healthy | Completed | 2002-11-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00865241 | A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets… | Phase1 | Healthy | Completed | 2002-11-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00864734 | A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets… | Phase1 | Healthy | Completed | 2002-11-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00865241 | A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets… | Phase1 | Healthy | Completed | 2002-11-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00651859 | Safety and Efficacy Study of Bimatoprost in Ethnically Japanese Patients With O… | Phase2 | Glaucoma | Completed | 2002-11-01 | 2004-01-01 | ClinicalTrials.gov |
| NCT00651859 | Safety and Efficacy Study of Bimatoprost in Ethnically Japanese Patients With O… | Phase2 | Glaucoma | Completed | 2002-11-01 | 2004-01-01 | ClinicalTrials.gov |
| NCT00864734 | A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets… | Phase1 | Healthy | Completed | 2002-11-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00651859 | Safety and Efficacy Study of Bimatoprost in Ethnically Japanese Patients With O… | Phase2 | Glaucoma | Completed | 2002-11-01 | 2004-01-01 | ClinicalTrials.gov |
| NCT00864734 | A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets… | Phase1 | Healthy | Completed | 2002-11-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00651859 | Safety and Efficacy Study of Bimatoprost in Ethnically Japanese Patients With O… | Phase2 | Glaucoma | Completed | 2002-11-01 | 2004-01-01 | ClinicalTrials.gov |
| NCT00865241 | A Relative Bioavailability Study of Glyburide/Metformin HCl 5 mg/500 mg Tablets… | Phase1 | Healthy | Completed | 2002-11-01 | 2002-11-01 | ClinicalTrials.gov |
| NCT00199589 | Treatment of Spastic Equinovarus Foot After Stroke | Na | Spastic Equinovarus | Completed | 2002-10-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00199589 | Treatment of Spastic Equinovarus Foot After Stroke | Na | Spastic Equinovarus | Completed | 2002-10-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00199589 | Treatment of Spastic Equinovarus Foot After Stroke | Na | Spastic Equinovarus | Completed | 2002-10-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT00199589 | Treatment of Spastic Equinovarus Foot After Stroke | Na | Spastic Equinovarus | Completed | 2002-10-01 | 2007-12-01 | ClinicalTrials.gov |
| NCT01155193 | Prospective Study for the Use of Palivizumab (Synagis®) in High-risk Children i… | — | Respiratory Syncytial Virus Infections | Completed | 2002-09-01 | 2016-07-31 | ClinicalTrials.gov |
| NCT01155193 | Prospective Study for the Use of Palivizumab (Synagis®) in High-risk Children i… | — | Respiratory Syncytial Virus Infections | Completed | 2002-09-01 | 2016-07-31 | ClinicalTrials.gov |
| NCT01155193 | Prospective Study for the Use of Palivizumab (Synagis®) in High-risk Children i… | — | Respiratory Syncytial Virus Infections | Completed | 2002-09-01 | 2016-07-31 | ClinicalTrials.gov |
| NCT01155193 | Prospective Study for the Use of Palivizumab (Synagis®) in High-risk Children i… | — | Respiratory Syncytial Virus Infections | Completed | 2002-09-01 | 2016-07-31 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00179114 | Vanderbilt University Spasticity Management Program Evaluation Plan | Phase4 | Spasticity | Completed | 2002-08-01 | 2006-02-01 | ClinicalTrials.gov |
| NCT00487214 | Internet-based, Naturalistic Evaluation of Tolerability and Individual Patient … | — | Glaucoma, Open-Angle | Completed | 2002-06-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00487214 | Internet-based, Naturalistic Evaluation of Tolerability and Individual Patient … | — | Glaucoma, Open-Angle | Completed | 2002-06-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00487214 | Internet-based, Naturalistic Evaluation of Tolerability and Individual Patient … | — | Glaucoma, Open-Angle | Completed | 2002-06-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00487214 | Internet-based, Naturalistic Evaluation of Tolerability and Individual Patient … | — | Glaucoma, Open-Angle | Completed | 2002-06-01 | 2003-02-01 | ClinicalTrials.gov |
| NCT00865839 | A Relative Bioavailability Study of Metformin HCl 500 mg ER Tablets Under Fasti… | Phase1 | Healthy | Completed | 2002-03-01 | 2002-03-01 | ClinicalTrials.gov |
| NCT00145106 | Comparison of Tazarotene and Minocycline Therapies for Maintenance of Facial Ac… | Phase4 | Acne Vulgaris | Completed | 2002-03-01 | 2002-08-01 | ClinicalTrials.gov |
| NCT00865839 | A Relative Bioavailability Study of Metformin HCl 500 mg ER Tablets Under Fasti… | Phase1 | Healthy | Completed | 2002-03-01 | 2002-03-01 | ClinicalTrials.gov |
| NCT00865839 | A Relative Bioavailability Study of Metformin HCl 500 mg ER Tablets Under Fasti… | Phase1 | Healthy | Completed | 2002-03-01 | 2002-03-01 | ClinicalTrials.gov |
| NCT00145106 | Comparison of Tazarotene and Minocycline Therapies for Maintenance of Facial Ac… | Phase4 | Acne Vulgaris | Completed | 2002-03-01 | 2002-08-01 | ClinicalTrials.gov |
| NCT00865839 | A Relative Bioavailability Study of Metformin HCl 500 mg ER Tablets Under Fasti… | Phase1 | Healthy | Completed | 2002-03-01 | 2002-03-01 | ClinicalTrials.gov |
| NCT00145106 | Comparison of Tazarotene and Minocycline Therapies for Maintenance of Facial Ac… | Phase4 | Acne Vulgaris | Completed | 2002-03-01 | 2002-08-01 | ClinicalTrials.gov |
| NCT00145106 | Comparison of Tazarotene and Minocycline Therapies for Maintenance of Facial Ac… | Phase4 | Acne Vulgaris | Completed | 2002-03-01 | 2002-08-01 | ClinicalTrials.gov |
| NCT00168402 | A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis | Phase3 | Hyperhidrosis | Completed | 2002-02-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00168402 | A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis | Phase3 | Hyperhidrosis | Completed | 2002-02-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00168402 | A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis | Phase3 | Hyperhidrosis | Completed | 2002-02-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00168402 | A Study Using Botulinum Toxin Type A in Patients With Axillary Hyperhidrosis | Phase3 | Hyperhidrosis | Completed | 2002-02-01 | 2005-10-01 | ClinicalTrials.gov |
| NCT00178646 | Comparative Efficacy of Three Preparations of Botox-A in Treating Spasticity | Phase4 | Stroke | Completed | 2002-01-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00178646 | Comparative Efficacy of Three Preparations of Botox-A in Treating Spasticity | Phase4 | Stroke | Completed | 2002-01-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00178646 | Comparative Efficacy of Three Preparations of Botox-A in Treating Spasticity | Phase4 | Stroke | Completed | 2002-01-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00178646 | Comparative Efficacy of Three Preparations of Botox-A in Treating Spasticity | Phase4 | Stroke | Completed | 2002-01-01 | 2010-03-01 | ClinicalTrials.gov |
| NCT00035906 | Research Study in Patients With Persistent Macular Edema | Phase2 | Diabetes | Completed | 2001-10-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00035906 | Research Study in Patients With Persistent Macular Edema | Phase2 | Diabetes | Completed | 2001-10-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00035906 | Research Study in Patients With Persistent Macular Edema | Phase2 | Diabetes | Completed | 2001-10-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00035906 | Research Study in Patients With Persistent Macular Edema | Phase2 | Diabetes | Completed | 2001-10-01 | 2004-08-01 | ClinicalTrials.gov |
| NCT00865696 | A Relative Bioavailability Study of Mirtazapine 15 mg Tablets Under Fasting Con… | Phase1 | Healthy | Completed | 2001-09-01 | 2001-09-01 | ClinicalTrials.gov |
| NCT00865384 | A Relative Bioavailability Study of Mirtazapine 15 mg Tablets Under Non-fasting… | Phase1 | Healthy | Completed | 2001-09-01 | 2001-09-01 | ClinicalTrials.gov |
| NCT00865384 | A Relative Bioavailability Study of Mirtazapine 15 mg Tablets Under Non-fasting… | Phase1 | Healthy | Completed | 2001-09-01 | 2001-09-01 | ClinicalTrials.gov |
| NCT00865696 | A Relative Bioavailability Study of Mirtazapine 15 mg Tablets Under Fasting Con… | Phase1 | Healthy | Completed | 2001-09-01 | 2001-09-01 | ClinicalTrials.gov |
| NCT00865384 | A Relative Bioavailability Study of Mirtazapine 15 mg Tablets Under Non-fasting… | Phase1 | Healthy | Completed | 2001-09-01 | 2001-09-01 | ClinicalTrials.gov |
| NCT00865696 | A Relative Bioavailability Study of Mirtazapine 15 mg Tablets Under Fasting Con… | Phase1 | Healthy | Completed | 2001-09-01 | 2001-09-01 | ClinicalTrials.gov |
| NCT00865384 | A Relative Bioavailability Study of Mirtazapine 15 mg Tablets Under Non-fasting… | Phase1 | Healthy | Completed | 2001-09-01 | 2001-09-01 | ClinicalTrials.gov |
| NCT00865696 | A Relative Bioavailability Study of Mirtazapine 15 mg Tablets Under Fasting Con… | Phase1 | Healthy | Completed | 2001-09-01 | 2001-09-01 | ClinicalTrials.gov |
| NCT00332540 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2001-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00332072 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2001-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00332072 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2001-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00332540 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2001-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00332072 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2001-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00332072 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2001-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00332540 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2001-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00332540 | Safety and Efficacy Study of Bimatoprost/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 2001-08-01 | 2003-08-01 | ClinicalTrials.gov |
| NCT00025818 | Six Month Clinical Research Study for Patients With Moderate or Severe Dry Eye … | Phase3 | Keratoconjunctivitis Sicca | Completed | 2001-05-01 | 2003-03-01 | ClinicalTrials.gov |
| NCT00025818 | Six Month Clinical Research Study for Patients With Moderate or Severe Dry Eye … | Phase3 | Keratoconjunctivitis Sicca | Completed | 2001-05-01 | 2003-03-01 | ClinicalTrials.gov |
| NCT00025818 | Six Month Clinical Research Study for Patients With Moderate or Severe Dry Eye … | Phase3 | Keratoconjunctivitis Sicca | Completed | 2001-05-01 | 2003-03-01 | ClinicalTrials.gov |
| NCT00025818 | Six Month Clinical Research Study for Patients With Moderate or Severe Dry Eye … | Phase3 | Keratoconjunctivitis Sicca | Completed | 2001-05-01 | 2003-03-01 | ClinicalTrials.gov |
| NCT00865059 | A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Non-fasting… | Phase1 | Healthy | Completed | 2001-02-01 | 2001-03-01 | ClinicalTrials.gov |
| NCT00865423 | A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Fasting Con… | Phase1 | Healthy | Completed | 2001-02-01 | 2001-03-01 | ClinicalTrials.gov |
| NCT00690339 | Safety and Effectiveness of Style 410 Silicone-Filled Breast Implant Study | Na | Breast Augmentation | Completed | 2001-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00690339 | Safety and Effectiveness of Style 410 Silicone-Filled Breast Implant Study | Na | Breast Augmentation | Completed | 2001-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00865059 | A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Non-fasting… | Phase1 | Healthy | Completed | 2001-02-01 | 2001-03-01 | ClinicalTrials.gov |
| NCT00865423 | A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Fasting Con… | Phase1 | Healthy | Completed | 2001-02-01 | 2001-03-01 | ClinicalTrials.gov |
| NCT00865423 | A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Fasting Con… | Phase1 | Healthy | Completed | 2001-02-01 | 2001-03-01 | ClinicalTrials.gov |
| NCT00865423 | A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Fasting Con… | Phase1 | Healthy | Completed | 2001-02-01 | 2001-03-01 | ClinicalTrials.gov |
| NCT00690339 | Safety and Effectiveness of Style 410 Silicone-Filled Breast Implant Study | Na | Breast Augmentation | Completed | 2001-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00690339 | Safety and Effectiveness of Style 410 Silicone-Filled Breast Implant Study | Na | Breast Augmentation | Completed | 2001-02-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00865059 | A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Non-fasting… | Phase1 | Healthy | Completed | 2001-02-01 | 2001-03-01 | ClinicalTrials.gov |
| NCT00865059 | A Relative Bioavailability Study of Gabapentin Tablets 800 mg Under Non-fasting… | Phase1 | Healthy | Completed | 2001-02-01 | 2001-03-01 | ClinicalTrials.gov |
| NCT01277419 | German Spondyloarthritis Inception Cohort | — | Ankylosing Spondylitis (AS) / Radiographic Axial SpA (r-axSpA) | Recruiting | 2000-07-01 | 2030-07-01 | ClinicalTrials.gov |
| NCT01277419 | German Spondyloarthritis Inception Cohort | — | Ankylosing Spondylitis (AS) / Radiographic Axial SpA (r-axSpA) | Recruiting | 2000-07-01 | 2030-07-01 | ClinicalTrials.gov |
| NCT01277419 | German Spondyloarthritis Inception Cohort | — | Ankylosing Spondylitis (AS) / Radiographic Axial SpA (r-axSpA) | Recruiting | 2000-07-01 | 2030-07-01 | ClinicalTrials.gov |
| NCT01277419 | German Spondyloarthritis Inception Cohort | — | Ankylosing Spondylitis (AS) / Radiographic Axial SpA (r-axSpA) | Recruiting | 2000-07-01 | 2030-07-01 | ClinicalTrials.gov |
| NCT00168350 | Memantine in Patients With Chronic Glaucoma | Phase3 | Open-Angle Glaucoma | Completed | 2000-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00168350 | Memantine in Patients With Chronic Glaucoma | Phase3 | Open-Angle Glaucoma | Completed | 2000-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00168350 | Memantine in Patients With Chronic Glaucoma | Phase3 | Open-Angle Glaucoma | Completed | 2000-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00168350 | Memantine in Patients With Chronic Glaucoma | Phase3 | Open-Angle Glaucoma | Completed | 2000-03-01 | 2006-09-01 | ClinicalTrials.gov |
| NCT00332436 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 1999-12-01 | 2001-11-01 | ClinicalTrials.gov |
| NCT00332436 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 1999-12-01 | 2001-11-01 | ClinicalTrials.gov |
| NCT00332436 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 1999-12-01 | 2001-11-01 | ClinicalTrials.gov |
| NCT00332436 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase3 | Ocular Hypertension | Completed | 1999-12-01 | 2001-11-01 | ClinicalTrials.gov |
| NCT00332345 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase2 | Ocular Hypertension | Completed | 1999-07-01 | 1999-08-01 | ClinicalTrials.gov |
| NCT00332345 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase2 | Ocular Hypertension | Completed | 1999-07-01 | 1999-08-01 | ClinicalTrials.gov |
| NCT00332345 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase2 | Ocular Hypertension | Completed | 1999-07-01 | 1999-08-01 | ClinicalTrials.gov |
| NCT00332345 | Safety and Efficacy Study of Brimonidine/Timolol Fixed Combination in Patients … | Phase2 | Ocular Hypertension | Completed | 1999-07-01 | 1999-08-01 | ClinicalTrials.gov |
| NCT00864760 | A Relative Bioavailability Study of Gabapentin 800 mg Tablets Under Fasting Con… | Phase1 | Healthy | Completed | 1999-06-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT00864760 | A Relative Bioavailability Study of Gabapentin 800 mg Tablets Under Fasting Con… | Phase1 | Healthy | Completed | 1999-06-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT00864760 | A Relative Bioavailability Study of Gabapentin 800 mg Tablets Under Fasting Con… | Phase1 | Healthy | Completed | 1999-06-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT00864760 | A Relative Bioavailability Study of Gabapentin 800 mg Tablets Under Fasting Con… | Phase1 | Healthy | Completed | 1999-06-01 | 1999-06-01 | ClinicalTrials.gov |
| NCT00689871 | Safety and Effectiveness of Natrelle(TM) Cohesive Round Silicone-Filled Breast … | Na | Breast Augmentation | Completed | 1999-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00689871 | Safety and Effectiveness of Natrelle(TM) Cohesive Round Silicone-Filled Breast … | Na | Breast Augmentation | Completed | 1999-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00689871 | Safety and Effectiveness of Natrelle(TM) Cohesive Round Silicone-Filled Breast … | Na | Breast Augmentation | Completed | 1999-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00689871 | Safety and Effectiveness of Natrelle(TM) Cohesive Round Silicone-Filled Breast … | Na | Breast Augmentation | Completed | 1999-01-01 | 2011-08-01 | ClinicalTrials.gov |
| NCT00864058 | A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Fasting Co… | Phase1 | Healthy | Completed | 1998-01-01 | 1998-01-01 | ClinicalTrials.gov |
| NCT00864058 | A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Fasting Co… | Phase1 | Healthy | Completed | 1998-01-01 | 1998-01-01 | ClinicalTrials.gov |
| NCT00864058 | A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Fasting Co… | Phase1 | Healthy | Completed | 1998-01-01 | 1998-01-01 | ClinicalTrials.gov |
| NCT00864058 | A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Fasting Co… | Phase1 | Healthy | Completed | 1998-01-01 | 1998-01-01 | ClinicalTrials.gov |
| NCT00864305 | A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Non-fastin… | Phase1 | Healthy | Completed | 1997-12-01 | 1998-01-01 | ClinicalTrials.gov |
| NCT00691327 | Adjunct Study of Natrelle(TM) Cohesive Round Silicone-Filled Breast Implants | Na | Breast Reconstruction | Completed | 1997-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00691327 | Adjunct Study of Natrelle(TM) Cohesive Round Silicone-Filled Breast Implants | Na | Breast Reconstruction | Completed | 1997-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00691327 | Adjunct Study of Natrelle(TM) Cohesive Round Silicone-Filled Breast Implants | Na | Breast Reconstruction | Completed | 1997-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00864305 | A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Non-fastin… | Phase1 | Healthy | Completed | 1997-12-01 | 1998-01-01 | ClinicalTrials.gov |
| NCT00691327 | Adjunct Study of Natrelle(TM) Cohesive Round Silicone-Filled Breast Implants | Na | Breast Reconstruction | Completed | 1997-12-01 | 2012-12-01 | ClinicalTrials.gov |
| NCT00864305 | A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Non-fastin… | Phase1 | Healthy | Completed | 1997-12-01 | 1998-01-01 | ClinicalTrials.gov |
| NCT00864305 | A Relative Bioavailability Study of Gabapentin 400 mg Capsules Under Non-fastin… | Phase1 | Healthy | Completed | 1997-12-01 | 1998-01-01 | ClinicalTrials.gov |
| NCT00262626 | The Canadian Glaucoma Study | Na | Glaucoma | Terminated | 1995-02-01 | 1995-06-01 | ClinicalTrials.gov |
| NCT00262626 | The Canadian Glaucoma Study | Na | Glaucoma | Terminated | 1995-02-01 | 1995-06-01 | ClinicalTrials.gov |
| NCT00262626 | The Canadian Glaucoma Study | Na | Glaucoma | Terminated | 1995-02-01 | 1995-06-01 | ClinicalTrials.gov |
| NCT00262626 | The Canadian Glaucoma Study | Na | Glaucoma | Terminated | 1995-02-01 | 1995-06-01 | ClinicalTrials.gov |
| NCT00404989 | Antiretroviral Pregnancy Registry (APR): Multi-sponsor Registry to Detect Any M… | — | HIV Infections | Recruiting | 1989-01-01 | 2099-01-01 | ClinicalTrials.gov |
| NCT00404989 | Antiretroviral Pregnancy Registry (APR): Multi-sponsor Registry to Detect Any M… | — | HIV Infections | Recruiting | 1989-01-01 | 2099-01-01 | ClinicalTrials.gov |
| NCT00404989 | Antiretroviral Pregnancy Registry (APR): Multi-sponsor Registry to Detect Any M… | — | HIV Infections | Recruiting | 1989-01-01 | 2099-01-01 | ClinicalTrials.gov |
| NCT00404989 | Antiretroviral Pregnancy Registry (APR): Multi-sponsor Registry to Detect Any M… | — | HIV Infections | Recruiting | 1989-01-01 | 2099-01-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| ABBV-2001 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Iberdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Mezigdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Carfilzomib | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Lenalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Upadacitinib | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Oxaliplatin | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | ACTIVE_NOT_RECRUITING | NCT06628310 |
| Leucovorin | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | ACTIVE_NOT_RECRUITING | NCT06628310 |
| Fluorouracil | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | ACTIVE_NOT_RECRUITING | NCT06628310 |
| Budigalimab | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | ACTIVE_NOT_RECRUITING | NCT06628310 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | ACTIVE_NOT_RECRUITING | NCT06628310 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Upadacitinib | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Risankizumab | Other | Phase PHASE3 | Psoriatic Arthritis (PsA) | COMPLETED | NCT03671148 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis (PsA) | COMPLETED | NCT03671148 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Sitagliptin | Other | Phase PHASE1 | Healthy Volunteers | ACTIVE_NOT_RECRUITING | NCT07567781 |
| Pitavastatin | Other | Phase PHASE1 | Healthy Volunteers | ACTIVE_NOT_RECRUITING | NCT07567781 |
| Digoxin | Other | Phase PHASE1 | Healthy Volunteers | ACTIVE_NOT_RECRUITING | NCT07567781 |
| Metformin | Other | Phase PHASE1 | Healthy Volunteers | ACTIVE_NOT_RECRUITING | NCT07567781 |
| Midazolam | Other | Phase PHASE1 | Healthy Volunteers | ACTIVE_NOT_RECRUITING | NCT07567781 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | ACTIVE_NOT_RECRUITING | NCT07567781 |
| ABBV-8736 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07413133 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07600762 |
| Placebo for Atogepant | Other | Phase PHASE3 | Menstrual Migraine (MM) | ACTIVE_NOT_RECRUITING | NCT06806293 |
| Atogepant | Other | Phase PHASE3 | Menstrual Migraine (MM) | ACTIVE_NOT_RECRUITING | NCT06806293 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06417775 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Lutikizumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Thioguanine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Methotrexate | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Nelarabine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Mercaptopurine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Cytarabine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Cyclophosphamide | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Intrathecal triple therapy (methotrexate + hydrocortisone + cytarabine) | Drug | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Bortezomib | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Venetoclax | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Dasatinib | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Calaspargase pegol | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Daunorubicin | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Vincristine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Dexamethasone | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Upadacitinib | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Bevacizumab | Other | Phase PHASE1 | Ovarian Cancer | RECRUITING | NCT07278336 |
| ABBV-901 | Other | Phase PHASE1 | Ovarian Cancer | RECRUITING | NCT07278336 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Standard of Care | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT03891446 |
| Bimatoprost SR | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT03891446 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Bevacizumab | Other | Phase PHASE1 | Ovarian Cancer | RECRUITING | NCT07278336 |
| ABBV-901 | Other | Phase PHASE1 | Ovarian Cancer | RECRUITING | NCT07278336 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Osimertinib | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT07155187 |
| Standard of Care | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT07155187 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT07155187 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Aqueous PGE2 and inflammatory cytokines measurements | Other | Phase PHASE1 | Diabetic Retinopathy | COMPLETED | NCT04505566 |
| Placebo - Preservative-free artificial tears | Other | Phase PHASE1 | Diabetic Retinopathy | COMPLETED | NCT04505566 |
| Ketorolac 0.45% ophthalmic solution | Other | Phase PHASE1 | Diabetic Retinopathy | COMPLETED | NCT04505566 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT07136103 |
| ABBV-277 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT07136103 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-453 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Placebo for BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06137287 |
| BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06137287 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Ruxolitinib | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Questionnaire Administration | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Punch Biopsy | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Echocardiography Test | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Bone Marrow Aspiration | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Biospecimen Collection | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Azacitidine | Other | Phase PHASE1 | Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome | RECRUITING | NCT03874052 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Venetoclax | Other | Phase PHASE2 | Marginal Zone Lymphoma | ACTIVE_NOT_RECRUITING | NCT04416451 |
| Rituximab | Other | Phase PHASE2 | Marginal Zone Lymphoma | ACTIVE_NOT_RECRUITING | NCT04416451 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-453 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Placebo for Topiramate | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05748483 |
| Topiramate | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05748483 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05748483 |
| Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05748483 |
| Placebo | Other | Phase PHASE1 | JAK1 GOF | NOT_YET_RECRUITING | NCT07670156 |
| Upadacitinib | Other | Phase PHASE1 | JAK1 GOF | NOT_YET_RECRUITING | NCT07670156 |
| Ubrogepant | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07680686 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Non-Surgical Fat Reduction | COMPLETED | NCT07122583 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07466550 |
| Glecaprevir/pibrentasvir | Other | Phase PHASE1 | Hepatitis C | RECRUITING | NCT07040319 |
| Tagraxofusp | Other | Phase PHASE2 | Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) | RECRUITING | NCT07007052 |
| Venetoclax | Other | Phase PHASE2 | Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) | RECRUITING | NCT07007052 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | RECRUITING | NCT07607964 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| OnabotulinumtoxinA 145 UNT [Botox] | Other | Phase PHASE4 | Drug-resistant Focal Seizure | TERMINATED | NCT05605756 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06953934 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07673120 |
| ABBV-313 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07673120 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Upper Limb Essential Tremor | RECRUITING | NCT07673107 |
| AGN-151607-DP | Other | Phase PHASE2 | Upper Limb Essential Tremor | RECRUITING | NCT07673107 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| Placebo | Other | Phase PHASE1 | Moderate to Severe Glabellar Lines | COMPLETED | NCT06151561 |
| AGN-151586 | Other | Phase PHASE1 | Moderate to Severe Glabellar Lines | COMPLETED | NCT06151561 |
| IMGN853 | Other | Phase PHASE2 | Endometrial Cancer | RECRUITING | NCT03832361 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Placebo | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT06308198 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT06308198 |
| Placebo | Other | Phase PHASE1 | JAK1 GOF | NOT_YET_RECRUITING | NCT07670156 |
| Upadacitinib | Other | Phase PHASE1 | JAK1 GOF | NOT_YET_RECRUITING | NCT07670156 |
| ABBV-8736 | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Trosunilimab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Lutikizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Risankizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Placebo | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| BOTOX | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| AGN-151586 | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06673238 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06673238 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Bretisilocin | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07604558 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-453 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | RECRUITING | NCT07599670 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Cytarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Daunorubicin | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-453 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Lutikizumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | RECRUITING | NCT07607964 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Bevacizumab | Other | Phase PHASE1 | Ovarian Cancer | RECRUITING | NCT07278336 |
| ABBV-901 | Other | Phase PHASE1 | Ovarian Cancer | RECRUITING | NCT07278336 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| ABBV-932 | Other | Phase PHASE2 | Bipolar I or II Disorder | RECRUITING | NCT07220460 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| ABBV-547 Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07232004 |
| ABBV-547 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07232004 |
| Antidepressant Therapy (ADT) | Drug | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| Placebo for ABBV-932 | Other | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| ABBV-932 | Other | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03569293 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03569293 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Rituximab | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07231952 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07231952 |
| Pirtobrutinib | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07231952 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | RECRUITING | NCT07525206 |
| REFRESH OPTIVE UD | Other | Phase PHASE3 | Dry Eye Disease | ACTIVE_NOT_RECRUITING | NCT07284381 |
| ABBV-444 | Other | Phase PHASE3 | Dry Eye Disease | ACTIVE_NOT_RECRUITING | NCT07284381 |
| ABBV-969 | Other | Phase PHASE1 | Metastatic Castration-Resistant Prostate Cancer | ACTIVE_NOT_RECRUITING | NCT06318273 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT07502417 |
| Ethinyl Estradiol + Levonorgestrel | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT07502417 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07649954 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07649954 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | RECRUITING | NCT07607964 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT05216263 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| Epcoritamab | Other | Phase PHASE2 | Primary CNS Lymphoma (PCNSL) | RECRUITING | NCT06931652 |
| NX-13 Placebo | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| NX-13 750mg | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| NX-13 250mg | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| Paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) | TERMINATED | NCT04064827 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| SYFOVRE | Other | Phase PHASE1 | Geographic Atrophy | RECRUITING | NCT07160179 |
| ABBV-6628 | Other | Phase PHASE1 | Geographic Atrophy | RECRUITING | NCT07160179 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | RECRUITING | NCT07599670 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07587008 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Pivekimab Sunirine | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT07306832 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Combined Oral Contraceptive | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Placebo | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| Brimonidine tartrate ophthalmic solution eye drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Prednisolone acetate ophthalmic suspension 1% eye drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Lubricating Eye Drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Standard of care | Other | Approved | Stroke | NOT_YET_RECRUITING | NCT07639632 |
| Screener | Other | Approved | Stroke | NOT_YET_RECRUITING | NCT07639632 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05861427 |
| Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05861427 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | COMPLETED | NCT03573024 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | COMPLETED | NCT03573024 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Standard of care | Other | Approved | Stroke | NOT_YET_RECRUITING | NCT07639632 |
| Screener | Other | Approved | Stroke | NOT_YET_RECRUITING | NCT07639632 |
| Pancrelipase Capsules | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency | RECRUITING | NCT06477159 |
| Venetoclax Oral Tablet [Venclexta] | Other | Phase PHASE2 | Mantle Cell Lymphoma | TERMINATED | NCT05025423 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Glecaprevir/pibrentasvir | Other | Phase PHASE1 | Hepatitis C | RECRUITING | NCT07040319 |
| NB-UVB (narrow-band ultraviolet B) Phototherapy | Drug | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Placebo | Other | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Upadacitinib | Other | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | RECRUITING | NCT07607964 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | RECRUITING | NCT07490301 |
| Venetoclax Oral Tablet [Venclexta] | Other | Phase PHASE2 | Mantle Cell Lymphoma | TERMINATED | NCT05025423 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| ABBV-8736 | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Trosunilimab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Lutikizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Risankizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06849791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Cofetuzumab Pelidotin | Other | Phase PHASE1 | Cancer | TERMINATED | NCT04189614 |
| Positron Emission Tomography | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Ibrutinib | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Epcoritamab | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Computed Tomography | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Bone Marrow Aspiration | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Biospecimen Collection | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Olaparib | Other | Phase PHASE2 | Ovary Cancer | RECRUITING | NCT05887609 |
| Mirvetuximab Soravtansine-gynx | Other | Phase PHASE2 | Ovary Cancer | RECRUITING | NCT05887609 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Best Supportive Care (BSC) | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT07566130 |
| nacresertib | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT07566130 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Lutikizumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Rituximab | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07231952 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07231952 |
| Pirtobrutinib | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07231952 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Vedolizumab | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT06880744 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT06880744 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03607422 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03607422 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Lutikizumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Pivekimab Sunirine | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT07306832 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-453 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | RECRUITING | NCT07607964 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT06953934 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| ABBV-8736 | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Trosunilimab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Lutikizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Risankizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| ARTIA Reconstructive Tissue Matrix | Other | Phase PHASE3 | Breast Reconstruction | RECRUITING | NCT06575192 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| HArmonyCa Lidocaine Injectable Gel | Other | Phase PHASE3 | Mid Face Volume Deficit | COMPLETED | NCT05452070 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Standard Chemotherapy | Drug | Phase PHASE1 | Leukemia | ACTIVE_NOT_RECRUITING | NCT03319901 |
| Venetoclax | Other | Phase PHASE1 | Leukemia | ACTIVE_NOT_RECRUITING | NCT03319901 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04750226 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | RECRUITING | NCT07607964 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07570147 |
| ABBV-1451 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07570147 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| ABBV-8736 | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Trosunilimab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Lutikizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Risankizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Telisotuzumab Adizutecan | Other | Phase PHASE3 | Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06614192 |
| Vedolizumab | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT06880744 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT06880744 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Lutikizumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT06468228 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | NOT_YET_RECRUITING | NCT07607964 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | NOT_YET_RECRUITING | NCT07607964 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | NOT_YET_RECRUITING | NCT07607964 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | NOT_YET_RECRUITING | NCT07607964 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | NOT_YET_RECRUITING | NCT07607964 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | NOT_YET_RECRUITING | NCT07607964 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| ABBV-519 | Other | Phase PHASE1 | Systemic Lupus Erythematosus | NOT_YET_RECRUITING | NCT07607964 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04630652 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Nacresertib | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07600762 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian Cancer | RECRUITING | NCT06682988 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | ACTIVE_NOT_RECRUITING | NCT05094128 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05445778 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Bretisilocin | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07604558 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| KYBELLA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| SkinMedica Products | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| JUVÉDERM | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| Lumigan Vehicle | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Sham Administration | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Lumigan | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| AGN-193408 SR | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | NO_LONGER_AVAILABLE | NCT04278235 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Bretisilocin | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07604558 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| KYBELLA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| SkinMedica Products | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| JUVÉDERM | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| Lumigan Vehicle | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Sham Administration | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Lumigan | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| AGN-193408 SR | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | NO_LONGER_AVAILABLE | NCT04278235 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Bretisilocin | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07604558 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| KYBELLA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| SkinMedica Products | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| JUVÉDERM | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| Lumigan Vehicle | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Sham Administration | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Lumigan | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| AGN-193408 SR | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | NO_LONGER_AVAILABLE | NCT04278235 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Bretisilocin | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07604558 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| KYBELLA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| SkinMedica Products | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| JUVÉDERM | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| Lumigan Vehicle | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Sham Administration | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Lumigan | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| AGN-193408 SR | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | NO_LONGER_AVAILABLE | NCT04278235 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Bretisilocin | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07604558 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| KYBELLA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| SkinMedica Products | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| JUVÉDERM | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| Lumigan Vehicle | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Sham Administration | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Lumigan | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| AGN-193408 SR | Other | Phase PHASE1 | Open-angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT04499248 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | NO_LONGER_AVAILABLE | NCT04278235 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Nascertib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07600762 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | RECRUITING | NCT07592273 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | TERMINATED | NCT06773403 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Placebo for ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| ABBV-1758 | Other | Phase PHASE1 | Alzheimer's Disease | NOT_YET_RECRUITING | NCT07599670 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Bortezomib + Lenalidomide + Dexamethasone | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Isatuximab | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Etentamig | Other | Phase PHASE1 | Myeloma Multiple | NOT_YET_RECRUITING | NCT07600151 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07599761 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | COMPLETED | NCT05564650 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT06241313 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Artificial Tears | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Topical Steroid | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Sham | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Surabgene Lomparvovec | Other | Phase PHASE2 | Diabetic Retinopathy | NOT_YET_RECRUITING | NCT07592273 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Arthritis | UNKNOWN | NCT00211679 |
| intra-articular botulinum toxin type a | Other | Phase PHASE3 | Arthritis | UNKNOWN | NCT00211718 |
| Botox Cosmetic™ | Other | Approved | Skin Wrinkling | COMPLETED | NCT00250952 |
| Trabeculectomy | Other | Approved | Glaucoma | TERMINATED | NCT00262626 |
| Argon laser trabeculoplasty | Other | Approved | Glaucoma | TERMINATED | NCT00262626 |
| Intraocular pressure reduction | Other | Approved | Glaucoma | TERMINATED | NCT00262626 |
| Tazarotene 0.1% gel + placebo capsule, Oral minocycline (100 mg capsule) + vehicle gel, Tazarotene 0.1% gel + oral minocycline (100 mg capsule) | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00145106 |
| Nepafenac (Nevanac) | Other | Phase PHASE4 | Myopia | COMPLETED | NCT00347204 |
| ketorolac (Acular LS) | Other | Phase PHASE4 | Myopia | COMPLETED | NCT00347204 |
| Zanaflex® | Other | Phase PHASE4 | Upper Limb Spasticity | COMPLETED | NCT00430196 |
| BOTOX® | Other | Phase PHASE4 | Upper Limb Spasticity | COMPLETED | NCT00430196 |
| Combigan Ophthalmic Solutiom | Other | Phase PHASE4 | Glaucoma | UNKNOWN | NCT00442312 |
| Combigan Ophthalmic Solutiom | Other | Phase PHASE4 | Glaucoma | UNKNOWN | NCT00442312 |
| Combigan Ophthalmic Solutiom | Other | Phase PHASE4 | Glaucoma | UNKNOWN | NCT00442312 |
| Botox | Other | Phase PHASE2 | Overactive Bladder | UNKNOWN | NCT00479596 |
| Brimonidine Purite | Other | Approved | Cataract | COMPLETED | NCT00352807 |
| Optiva artificial tear by Allergan | Other | Approved | Dry Eye Disease | COMPLETED | NCT00395759 |
| latanoprost 0.005% eye drops and brinzolamide 1.0% eye drops | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00440141 |
| latanoprost 0.005% eye drops and brimonidine 0.1% eye drops | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00440141 |
| placebo capsule | Other | Phase PHASE2 | Diabetic Neuropathy, Painful | COMPLETED | NCT00381719 |
| AGN 203818 | Other | Phase PHASE2 | Diabetic Neuropathy, Painful | COMPLETED | NCT00381719 |
| placebo capsule | Other | Phase PHASE2 | Diabetic Neuropathy, Painful | COMPLETED | NCT00381719 |
| AGN 203818 | Other | Phase PHASE2 | Diabetic Neuropathy, Painful | COMPLETED | NCT00381719 |
| 0.05% cyclosporin eye drop | Other | Phase PHASE4 | Dry Eye | UNKNOWN | NCT00704275 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Upadacitinib Matching Placebo | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Upadacitinib 30mg Dose | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Upadacitinib Matching Placebo | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Upadacitinib 30mg Dose | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Upadacitinib Matching Placebo | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Upadacitinib 30mg Dose | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Upadacitinib Matching Placebo | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Upadacitinib 30mg Dose | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| adapalene 0.3% topical gel | Other | Approved | Acne Vulgaris | COMPLETED | NCT01095640 |
| adapalene 0.3% topical gel | Other | Approved | Acne Vulgaris | COMPLETED | NCT01095640 |
| adapalene 0.3% topical gel | Other | Approved | Acne Vulgaris | COMPLETED | NCT01095640 |
| Effexor® Tablets equivalent to 50 mg venlafaxine | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00871364 |
| VENLAFAXINE TABLETS 50 mg , single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00871364 |
| Proscar® 5 mg Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00871247 |
| Finasteride 5 mg Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00871247 |
| NorvasC® 10 mg Tablets | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00870571 |
| AMLODIPINE (as BESILATE) TABLETS 10 mg , single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00870571 |
| Norvasc® 10 mg Tablets | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00870142 |
| AMLODIPINE (as BESILATE) TABLETS 10 mg , single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00870142 |
| Wellbutrin XL® 150 mg Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865462 |
| Abrika Bupropion 150 mg XL Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865462 |
| Wellbutrin XL® 150 mg Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865462 |
| Abrika Bupropion 150 mg XL Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865462 |
| Wellbutrin XL® 150 mg Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865462 |
| Abrika Bupropion 150 mg XL Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865462 |
| Wellbutrin SR® 150 mg Extended-Release Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865410 |
| Abrika Bupropion 150 mg Extended-Released Tablet | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865410 |
| Wellbutrin SR® 150 mg Extended-Release Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865371 |
| Abrika Bupropion 150 mg Extended-Released Tablet | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865371 |
| Wellbutrin SR® 150 mg Sustained-Release Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865111 |
| Bupropion 150 mg Extended-Released Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865111 |
| Coreg® 12.5 mg Tablets , single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864435 |
| Carvedilol 12.5 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864435 |
| Zoloft® 100 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864344 |
| Sertraline HCl 100 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864344 |
| Zyrtec® 10 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864279 |
| Cetirizine Hydrochloride 10 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864279 |
| Atlace® 10 mg capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864162 |
| Ramipril10 mg Capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864162 |
| Zoloft® 100 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864019 |
| Sertraline HCl 100 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864019 |
| Atlace® 10 mg capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00863915 |
| Ramipril10 mg Capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00863915 |
| Zyrtec® 10 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00863902 |
| Cetirizine Hydrochloride 10 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00863902 |
| Grifulvin V® 125 mg/5 mL Suspension, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00863863 |
| Griseofulvin 125 mg/5 mL Suspension, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00863863 |
| Sham injection | Other | Phase PHASE2 | Intermediate Uveitis | COMPLETED | NCT00333814 |
| dexamethasone | Other | Phase PHASE2 | Intermediate Uveitis | COMPLETED | NCT00333814 |
| Dexamethasone | Other | Phase PHASE2 | Intermediate Uveitis | COMPLETED | NCT00333814 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Upadacitinib Matching Placebo | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Upadacitinib 30mg Dose | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Upadacitinib Matching Placebo | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Upadacitinib 30mg Dose | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07587008 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Upadacitinib Matching Placebo | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Upadacitinib 30mg Dose | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07587008 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Upadacitinib Matching Placebo | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Upadacitinib 30mg Dose | Other | Phase PHASE2 | EoE | NOT_YET_RECRUITING | NCT07588568 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07587008 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT02993523 |
| Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07587008 |
| Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07587008 |
| Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07587008 |
| Bimatoprost 0.03% ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.02% ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.015% formulation 2 ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.015% formulation 1 ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.01% ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.03% ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.02% ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.015% formulation 2 ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.015% formulation 1 ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Bimatoprost 0.01% ophthalmic solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00652496 |
| Brimonidine ophthalmic solution 0.2% | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00652483 |
| Brimonidine ophthalmic solution 0.1% | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00652483 |
| Brimonidine 0.2% ophthalmic solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00652106 |
| Concurrent brimonidine 0.2% and Timolol 0.5% ophthalmic solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00652106 |
| 0.2% brimonidine/0.5% timolol fixed combination ophthalmic solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00652106 |
| Bimatoprost Vehicle Ophthalmic Solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00651859 |
| Bimatoprost 0.03% Ophthalmic Solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00651859 |
| Bimatoprost 0.01% Ophthalmic Solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00651859 |
| Concurrent brimonidine 0.2% and 0.5% timolol | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00651612 |
| Brimonidine 0.2%/Timolol 0.5% Fixed Combination Ophthalmic Solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00651612 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Stroke | COMPLETED | NCT00651729 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Stroke | COMPLETED | NCT00651729 |
| Placebo | Other | Phase PHASE2 | Stroke | COMPLETED | NCT00651690 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Stroke | COMPLETED | NCT00651690 |
| Botulinum Toxin Type A | Other | Phase PHASE4 | Hyperhidrosis | COMPLETED | NCT00168480 |
| Botulinum Toxin Type A | Other | Phase PHASE4 | Hyperhidrosis | COMPLETED | NCT00168415 |
| Botulinic toxin (Botox) | Other | Approved | Spastic Equinovarus | COMPLETED | NCT00199589 |
| dorzolamide hcl 2%/timolol maleate 0.5% fixed combinatin as adjunctive to current prostaglandin therapy. | Drug | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822081 |
| brimonidine tartrate 0.2%/timolol maleate 0.5% fixed combination as adjunctive to current prostaglandin therapy. | Drug | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822081 |
| dorzolamide hcl 2%/ timolol maleate 0.5% fixed combination | Other | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822081 |
| brimonidine tartrate 0.2%/timolol maleate 0.5% fixed combination | Other | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822081 |
| dorzolamide hcl 2%/timolol maleate 0.5% fixed combinatin as adjunctive to current prostaglandin therapy. | Drug | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822081 |
| brimonidine tartrate 0.2%/timolol maleate 0.5% fixed combination as adjunctive to current prostaglandin therapy. | Drug | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822081 |
| dorzolamide hcl 2%/ timolol maleate 0.5% fixed combination | Other | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822081 |
| brimonidine tartrate 0.2%/timolol maleate 0.5% fixed combination | Other | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822081 |
| dorzolamide hcl 2%/timolol maleate 0.5% fixed combination as adjunctive to current prostaglandin therapy | Drug | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822055 |
| brimonidine tartrate 0.2%/timolol maleate 0.5% fixed combination as adjunctive to current prostaglandin therapy | Drug | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822055 |
| dorzolamide hcl 2%/timolol maleate 0.5% fixed combination | Other | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822055 |
| brimonidine tartrate 0.2%/timolol maleate 0.5% fixed combination | Other | Phase PHASE4 | Open-Angle Glaucoma | COMPLETED | NCT00822055 |
| Placebo | Other | Phase PHASE4 | Parkinson Disease | TERMINATED | NCT00477802 |
| Botulinum Toxin Type A | Other | Phase PHASE4 | Parkinson Disease | TERMINATED | NCT00477802 |
| ketorolac | Other | Phase PHASE3 | Cataract Extraction | COMPLETED | NCT00524264 |
| ketorolac eye drops | Other | Phase PHASE3 | Cataract Extraction | COMPLETED | NCT00521456 |
| Carboxymethylcellulose | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00514852 |
| Carboxymethylcellulose and Glycerin based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00514852 |
| CELEXATM 10 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865943 |
| Citalopram HBr eq. 10 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865943 |
| ADALAT® CC Extended Release Tablets 60 mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865891 |
| Nifedipine Extended Release tablets 60 mg, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865891 |
| GLUCOPHAGE® XR 750 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865852 |
| Metformin HCl 750 mg Extender Release tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865852 |
| GLUCOPHAGE® XR 750 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865852 |
| Metformin HCl 750 mg Extender Release tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865852 |
| CLUCOPHAGE® XR 500 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865839 |
| Metformin HCl 500 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865839 |
| XANAX XR® 3 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865761 |
| Alprazolam 3 mg Extended Release Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865761 |
| REMERON® 15 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865696 |
| Mirtazapine 15 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865696 |
| REMERON® 15 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865696 |
| Mirtazapine 15 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865696 |
| XANAX XR® 3 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865657 |
| Alprazolam 3 mg Extended Release Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865657 |
| NEURONTIN® 800 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865423 |
| Gabapentin 800 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865423 |
| REMERON® 15 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865384 |
| Mirtazapine 15 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865384 |
| Ultravate® 0.05% ointment, single exposure | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865267 |
| CLUCOVANCE® 5 mg/500 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865241 |
| Glyburide and Metformin Hydrochloride Tablets 5 mg/500 mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865241 |
| INDERAL® LA 160 mg Capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865215 |
| Propranolol Hydrochloride Extended Release Capsules 160 mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865215 |
| INDERAL® LA 160 mg Capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865215 |
| Propranolol Hydrochloride Extended Release Capsules 160 mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865215 |
| CelexaTM 40 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865085 |
| Citalopram HBr 40 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865085 |
| CelexaTM 40 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865085 |
| Citalopram HBr 40 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865085 |
| GLUCOPHAGE® XR 750 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865072 |
| Metformin HCl 750 mg Extender Release tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865072 |
| GLUCOPHAGE® XR 750 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865072 |
| Metformin HCl 750 mg Extender Release tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865072 |
| NEURONTIN® 800 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865059 |
| Gabapentin 800 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865059 |
| NEURONTIN® 800 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865059 |
| Gabapentin 800 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00865059 |
| CelexaTM 40 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864890 |
| Citalopram HBr 40 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864890 |
| CelexaTM 40 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864890 |
| Citalopram HBr 40 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864890 |
| NEURONTIN® 400 mg capsules, single dose (2 capsules) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864760 |
| Gabapentin 800 mg tablets, single dose (1 tablet) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864760 |
| INDERAL® LA 160 mg Capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864747 |
| Propranolol Hydrochloride Extended Release Capsules 160 mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864747 |
| CLUCOVANCE® 5 mg/500 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864734 |
| Glyburide and Metformin Hydrochloride Tablets 5 mg/500 mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864734 |
| CLUCOVANCE® 5 mg/500 mg Tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864734 |
| Glyburide and Metformin Hydrochloride Tablets 5 mg/500 mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864734 |
| ADALAT® CC Extended Release Tablets 60 mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864617 |
| Nifedipine Extended Release tablets 60 mg, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864617 |
| COMBONOX® tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864526 |
| Oxycodone HCl 5 mg / Ibuprofen 400 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864526 |
| COMBONOX® tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864357 |
| Oxycodone HCl 5 mg / Ibuprofen 400 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864357 |
| Gabapentin 400 mg capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864305 |
| NEURONTIN® 400 mg capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864305 |
| Gabapentin 400 mg capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864305 |
| Gabapentin 400 mg capsules, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864305 |
| NEURONTIN® 400 mg capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864305 |
| Gabapentin 400 mg capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864305 |
| NEURONTIN® 400 mg capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864058 |
| Gabapentin 400 mg capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864058 |
| KADIAN (morphine sulfate extended-release) capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00759915 |
| morphine sulfate extended-release capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00759915 |
| KADIAN (morphine sulfate extended-release) capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00759915 |
| morphine sulfate extended-release capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00759915 |
| KADIAN (morphine sulfate extended-release) capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00759902 |
| morphine sulfate extended-release capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00759902 |
| KADIAN (morphine sulfate extended-release) capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00759902 |
| morphine sulfate extended-release capsules | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00759902 |
| Wellbutrin XL® 150 mg Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00863941 |
| Abrika Bupropion 150 mg XL Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00863941 |
| NIRAVAM TM 2 mg orally disintegrating tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01188057 |
| ALPRAZOLAM ORALLY DISINTEGRATING TABLETS, 2.0 MG | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01188057 |
| NIRAVAM TM 2 mg orally disintegrating tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01188057 |
| ALPRAZOLAM ORALLY DISINTEGRATING TABLETS, 2.0 MG | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01188057 |
| NIRAVAM TM 2 mg orally disintegrating tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01188031 |
| ALPRAZOLAM ORALLY DISINTEGRATING TABLETS, 2.0 MG | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01188031 |
| memantine | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT00168350 |
| Vehicle Control | Other | Approved | MILD TO SEVERE ACNE VULGARIS | COMPLETED | NCT01257906 |
| ZIANA® | Other | Approved | MILD TO SEVERE ACNE VULGARIS | COMPLETED | NCT01257906 |
| CLIND PHOSPHATE (1.2%) AND TRETINOIN (0.025%) TOPICAL GEL | Other | Approved | MILD TO SEVERE ACNE VULGARIS | COMPLETED | NCT01257906 |
| Vehicle Control | Other | Approved | MILD TO SEVERE ACNE VULGARIS | COMPLETED | NCT01257906 |
| ZIANA® | Other | Approved | MILD TO SEVERE ACNE VULGARIS | COMPLETED | NCT01257906 |
| CLIND PHOSPHATE (1.2%) AND TRETINOIN (0.025%) TOPICAL GEL | Other | Approved | MILD TO SEVERE ACNE VULGARIS | COMPLETED | NCT01257906 |
| Botulinum Toxin Type A injection (BOTOX) | Other | Phase PHASE2 | Thoracic Outlet Syndrome | COMPLETED | NCT00444886 |
| Emulsion type artificial tear | Other | Phase PHASE3 | Dry Eye | UNKNOWN | NCT01335126 |
| ACZONE (dapsone) Gel, 5%, 1x/day (AM) + MetroGel (metronidazole gel), 1.0%, 1x/day (PM) | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| MetroGel® (metronidazole gel), 1.0% 1x/day | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| ACZONE (dapsone) Gel, 5%, 1x/day | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| ACZONE (dapsone) Gel, 5%, 2x/day | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| Vehicle control, 2x/day | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| ACZONE (dapsone) Gel, 5%, 1x/day (AM) + MetroGel (metronidazole gel), 1.0%, 1x/day (PM) | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| MetroGel® (metronidazole gel), 1.0% 1x/day | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| ACZONE (dapsone) Gel, 5%, 1x/day | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| ACZONE (dapsone) Gel, 5%, 2x/day | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| Vehicle control, 2x/day | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT00249782 |
| Carboxymethylcellulose sodium and Glycerin | Other | Phase PHASE2 | Dry Eye | COMPLETED | NCT00243711 |
| Vehicle | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00243542 |
| ACZONE Gel, 5% | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00243542 |
| Vehicle | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00243542 |
| ACZONE Gel, 5% | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00243542 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Postherpetic Neuralgia | COMPLETED | NCT00168441 |
| Botulinum Toxin Type A | Other | Phase PHASE3 | Hyperhidrosis | COMPLETED | NCT00168402 |
| Botulinum Toxin Type A | Other | Phase PHASE3 | Hyperhidrosis | COMPLETED | NCT00168402 |
| brimonidine | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00168363 |
| brimonidine | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT00168363 |
| Dapsone Topical Gel + vehicle control | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT00151541 |
| Dapsone Topical Gel + benzoyl peroxide gel 4% | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT00151541 |
| Dapsone Topical Gel + adapalene gel 0.1% | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT00151541 |
| Dapsone Topical Gel + vehicle control | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT00151541 |
| Dapsone Topical Gel + benzoyl peroxide gel 4% | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT00151541 |
| Dapsone Topical Gel + adapalene gel 0.1% | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT00151541 |
| DEX PS DDS® | Other | Phase PHASE2 | Diabetes | COMPLETED | NCT00035906 |
| Ophthalmic Emulsion | Other | Phase PHASE3 | Keratoconjunctivitis Sicca | COMPLETED | NCT00025818 |
| Refresh Contacts | Other | Approved | Dry Eye | UNKNOWN | NCT01384851 |
| Refresh Dry Eye Therapy | Drug | Approved | Dry Eye | UNKNOWN | NCT01384851 |
| Next Generation Emulsion | Other | Approved | Dry Eye | UNKNOWN | NCT01384851 |
| nepafenac | Other | Phase PHASE4 | Cataracts | COMPLETED | NCT01021761 |
| Bromfenac | Other | Phase PHASE4 | Cataracts | COMPLETED | NCT01021761 |
| Ketorolac Tromethamine | Other | Phase PHASE4 | Cataracts | COMPLETED | NCT01021761 |
| olopatadine hydrochloride 0.1% ophthalmic solution | Other | Phase PHASE3 | Rhinitis, Allergic, Seasonal | COMPLETED | NCT01258309 |
| olopatadine hydrochloride /ketorolac tromethamine fixed dose combination ophthalmic solution | Other | Phase PHASE3 | Rhinitis, Allergic, Seasonal | COMPLETED | NCT01258309 |
| olopatadine hydrochloride 0.1% ophthalmic solution | Other | Phase PHASE3 | Rhinitis, Allergic, Seasonal | COMPLETED | NCT01258309 |
| olopatadine hydrochloride /ketorolac tromethamine fixed dose combination ophthalmic solution | Other | Phase PHASE3 | Rhinitis, Allergic, Seasonal | COMPLETED | NCT01258309 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | TEMPORARILY_NOT_AVAILABLE | NCT04830202 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04379050 |
| Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | AVAILABLE | NCT04278235 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07587008 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Nab-Paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, budigalimab, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT03844048 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| AGN 203818 | Other | Phase PHASE2 | Cystitis, Interstitial | TERMINATED | NCT00380783 |
| Vehicle Control | Other | Phase PHASE2 | Rash | TERMINATED | NCT00343187 |
| ACZONE (dapsone) Gel, 5% | Other | Phase PHASE2 | Rash | TERMINATED | NCT00343187 |
| Dexamethasone | Other | Phase PHASE2 | Anterior Uveitis | TERMINATED | NCT00333996 |
| bimatoprost/timolol fixed combination | Other | Phase PHASE3 | Ocular Hypertension | COMPLETED | NCT00332540 |
| bimatoprost/timolol fixed combination | Other | Phase PHASE3 | Ocular Hypertension | COMPLETED | NCT00332540 |
| brimonidine/timolol fixed combination | Other | Phase PHASE3 | Ocular Hypertension | COMPLETED | NCT00332436 |
| brimonidine/timolol fixed combination | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT00332345 |
| bimatoprost/timolol fixed combination | Other | Phase PHASE3 | Ocular Hypertension | COMPLETED | NCT00332072 |
| bimatoprost/timolol fixed combination | Other | Phase PHASE3 | Ocular Hypertension | COMPLETED | NCT00332072 |
| bimatoprost/timolol fixed combination | Other | Phase PHASE3 | Ocular Hypertension | COMPLETED | NCT00332059 |
| bimatoprost | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT00300443 |
| bimatoprost | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT00300443 |
| esomeprazole | Other | Phase PHASE1 | Peptic Ulcer | COMPLETED | NCT00325715 |
| AGN 201904 | Other | Phase PHASE1 | Peptic Ulcer | COMPLETED | NCT00325715 |
| esomeprazole | Other | Phase PHASE1 | Peptic Ulcer | COMPLETED | NCT00325715 |
| AGN 201904 | Other | Phase PHASE1 | Peptic Ulcer | COMPLETED | NCT00325715 |
| alacaftadine and naphazoline HCl & pheniramine maleate | Other | Phase PHASE4 | Allergic Conjunctivitis | UNKNOWN | NCT01390961 |
| Botulinum Toxin Type A | Other | Approved | Diabetes Mellitus | COMPLETED | NCT00336349 |
| sodium hyaluronate 0.18% (VISMED® Multi) | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00987727 |
| carboxymethylcellulose 0.5% , glycerin 0.9% (OPTIVE® MD) | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00987727 |
| sodium hyaluronate 0.18% (VISMED® Multi) | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00987727 |
| carboxymethylcellulose 0.5% , glycerin 0.9% (OPTIVE® MD) | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00987727 |
| moxifloxacin 0.5% eye drops | Other | Phase PHASE4 | Bacterial Conjunctivitis | COMPLETED | NCT00464438 |
| gatifloxacin | Other | Phase PHASE4 | Bacterial Conjunctivitis | COMPLETED | NCT00464438 |
| Lubricating Eye Drop | Other | Phase PHASE4 | Inflammation | COMPLETED | NCT00791323 |
| Ketorolac 0.4% | Other | Phase PHASE4 | Inflammation | COMPLETED | NCT00791323 |
| Lubricating Eye Drop | Other | Phase PHASE4 | Inflammation | COMPLETED | NCT00791323 |
| Ketorolac 0.4% | Other | Phase PHASE4 | Inflammation | COMPLETED | NCT00791323 |
| nepafenac 0.1% | Other | Phase PHASE4 | Cataracts | COMPLETED | NCT01001806 |
| bromfenac 0.09% | Other | Phase PHASE4 | Cataracts | COMPLETED | NCT01001806 |
| Ketorolac Tromethamine 0.45% | Other | Phase PHASE4 | Cataracts | COMPLETED | NCT01001806 |
| latanoprost 0.005% eye drops | Other | Phase PHASE4 | Ocular Hypertension | COMPLETED | NCT00541242 |
| bimatoprost 0.03% eye drops | Other | Phase PHASE4 | Ocular Hypertension | COMPLETED | NCT00541242 |
| sodium hyaluronate 0.18% | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00938704 |
| carboxymethylcellulose 0.5% +glycerin 0.9% | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00938704 |
| sodium hyaluronate 0.18% | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00938704 |
| carboxymethylcellulose 0.5% +glycerin 0.9% | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00938704 |
| Tretinoin | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00835198 |
| Dapsone; Tretinoin | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00835198 |
| Tazarotene | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00834210 |
| Dapsone | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00834210 |
| Tazarotene | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00834210 |
| Dapsone | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT00834210 |
| Lubricating Eye Drops (blink® Tears) | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00756678 |
| Lubricant Eye Drops (Optive™) | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00756678 |
| Lubricating Eye Drops (blink® Tears) | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00756678 |
| Lubricant Eye Drops (Optive™) | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT00756678 |
| placebo eye drops | Other | Phase PHASE3 | Bacterial Conjunctivitis | COMPLETED | NCT00509873 |
| Gatifloxacin 0.5% eye drops | Other | Phase PHASE3 | Bacterial Conjunctivitis | COMPLETED | NCT00509873 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE2 | Eyelash Hypotrichosis | COMPLETED | NCT01064882 |
| bimatoprost ophthalmic solution 0.015% | Other | Phase PHASE2 | Eyelash Hypotrichosis | COMPLETED | NCT01064882 |
| bimatoprost ophthalmic solution 0.005% | Other | Phase PHASE2 | Eyelash Hypotrichosis | COMPLETED | NCT01064882 |
| Carboxymethylcellulose | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00544713 |
| Carboxymethylcellulose and Glycerin based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00544713 |
| Carboxymethylcellulose | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00544713 |
| Carboxymethylcellulose and Glycerin based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00544713 |
| botulinum toxin type A | Other | Phase PHASE4 | Spasmodic Torticollis | COMPLETED | NCT00528541 |
| botulinum toxin type A | Other | Phase PHASE4 | Spasmodic Torticollis | COMPLETED | NCT00528541 |
| botulinum toxin type A | Other | Phase PHASE4 | Spasmodic Torticollis | TERMINATED | NCT00432341 |
| Metformin hydrochloride (Glucophage®) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00986401 |
| Trospium Chloride (Sanctura XR®) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00986401 |
| gatifloxacin ophthalmic solution 0.3% | Other | Phase PHASE4 | Anti-biotic Resistance | COMPLETED | NCT00874887 |
| moxifloxacin 0.5% HCI ophthalmic solution | Other | Phase PHASE4 | Anti-biotic Resistance | COMPLETED | NCT00874887 |
| gatifloxacin ophthalmic solution 0.3% | Other | Phase PHASE4 | Anti-biotic Resistance | COMPLETED | NCT00874887 |
| moxifloxacin 0.5% HCI ophthalmic solution | Other | Phase PHASE4 | Anti-biotic Resistance | COMPLETED | NCT00874887 |
| Artificial Tears REFRESH ENDURA® | Other | Phase PHASE2 | Dry Eye Syndromes | COMPLETED | NCT00611403 |
| Cyclosporine Ophthalmic Emulsion 0.05% (RESTASIS®) | Other | Phase PHASE2 | Dry Eye Syndromes | COMPLETED | NCT00611403 |
| Placebo (Vehicle Gel) | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| EPIDUO | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| adapalene 0.1% and benzoyl peroxide 2.5% topical gel | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| Placebo (Vehicle Gel) | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| EPIDUO | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| adapalene 0.1% and benzoyl peroxide 2.5% topical gel | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| Placebo (Vehicle Gel) | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| EPIDUO | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| adapalene 0.1% and benzoyl peroxide 2.5% topical gel | Other | Approved | Acne Vulgaris | COMPLETED | NCT01501799 |
| Vehicle Cream | Other | Approved | Actinic Keratoses | COMPLETED | NCT01502020 |
| imiquimod cream, 3.75% | Other | Approved | Actinic Keratoses | COMPLETED | NCT01502020 |
| Vehicle Cream | Other | Approved | Actinic Keratoses | COMPLETED | NCT01502020 |
| imiquimod cream, 3.75% | Other | Approved | Actinic Keratoses | COMPLETED | NCT01502020 |
| Vehicle Cream | Other | Approved | Actinic Keratoses | COMPLETED | NCT01502020 |
| imiquimod cream, 3.75% | Other | Approved | Actinic Keratoses | COMPLETED | NCT01502020 |
| vehicle sterile solution (placebo) | Other | Phase PHASE4 | Hypotrichosis | COMPLETED | NCT00958035 |
| bimatoprost ophthalmic 0.03% solution | Other | Phase PHASE4 | Hypotrichosis | COMPLETED | NCT00958035 |
| bimatoprost 0.03%, latanoprost 0.005%, and travoprost 0.004% | Other | Preclinical | Open-Angle Glaucoma | COMPLETED | NCT00716742 |
| cyclosporine ophthalmic emulsion 0.05%, artificial tears | Other | Preclinical | Keratoconjunctivitis Sicca | COMPLETED | NCT00717418 |
| cyclosporine ophthalmic emulsion 0.05%, artificial tears | Other | Preclinical | Keratoconjunctivitis Sicca | COMPLETED | NCT00717418 |
| placebo | Other | Phase PHASE2 | Irritable Bowel Syndrome | TERMINATED | NCT00441766 |
| AGN 203818 | Other | Phase PHASE2 | Irritable Bowel Syndrome | TERMINATED | NCT00441766 |
| placebo | Other | Phase PHASE2 | Irritable Bowel Syndrome | TERMINATED | NCT00441766 |
| AGN 203818 | Other | Phase PHASE2 | Irritable Bowel Syndrome | TERMINATED | NCT00441766 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | TEMPORARILY_NOT_AVAILABLE | NCT04830202 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04379050 |
| Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Linaclotide | Other | Phase PHASE3 | Functional Constipation (FC) | COMPLETED | NCT05652205 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | AVAILABLE | NCT04278235 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07587008 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Nab-Paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, budigalimab, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT03844048 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| topical bimatoprost | Other | Phase PHASE4 | Hypotrichosis | COMPLETED | NCT01387906 |
| Vehicle | Other | Phase PHASE2 | Pterygium | COMPLETED | NCT01109056 |
| cyclosporine ophthalmic emulsion 0.05% | Other | Phase PHASE2 | Pterygium | COMPLETED | NCT01109056 |
| Cataract Surgery and Limbal relaxing incision | Procedure | Preclinical | Dry Eye | COMPLETED | NCT01161771 |
| Fluorometholone Eye Drops (FML Forte®) | Other | Phase PHASE2 | Epiphora | WITHDRAWN | NCT00824811 |
| Lubricant Eye Drops (Refresh Endura™) | Other | Phase PHASE2 | Epiphora | WITHDRAWN | NCT00824811 |
| Cyclosporine Eye Drops (Restasis) | Other | Phase PHASE2 | Epiphora | WITHDRAWN | NCT00824811 |
| Placebo | Other | Phase PHASE4 | Muscle Spasticity | COMPLETED | NCT00549783 |
| Botulinum Toxin Type A 900kD | Other | Phase PHASE4 | Muscle Spasticity | COMPLETED | NCT00549783 |
| Placebo | Other | Phase PHASE4 | Muscle Spasticity | COMPLETED | NCT00549783 |
| Botulinum Toxin Type A 900kD | Other | Phase PHASE4 | Muscle Spasticity | COMPLETED | NCT00549783 |
| ranibizumab | Other | Phase PHASE2 | Choroidal Neovascularization | COMPLETED | NCT00775411 |
| dexamethasone | Other | Phase PHASE2 | Choroidal Neovascularization | COMPLETED | NCT00775411 |
| sham | Other | Phase PHASE2 | Subfoveal Choroidal Neovascularization | TERMINATED | NCT01122511 |
| ranibizumab | Other | Phase PHASE2 | Subfoveal Choroidal Neovascularization | TERMINATED | NCT01122511 |
| 700 ug dexamethasone | Other | Phase PHASE2 | Subfoveal Choroidal Neovascularization | TERMINATED | NCT01122511 |
| Vehicle solution | Other | Phase PHASE3 | Hypotrichosis | COMPLETED | NCT00907426 |
| Bimatoprost 0.03% solution | Other | Phase PHASE3 | Hypotrichosis | COMPLETED | NCT00907426 |
| Any Fixed Combination Therapy | Drug | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01637246 |
| bimatoprost 0.01% | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01632423 |
| Fixed combination 0.3 mg bimatoprost and 5 mg timolol | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01628601 |
| bimatoprost 0.01% | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01628588 |
| normal saline (placebo) | Other | Phase PHASE4 | Glabellar Frown Lines | COMPLETED | NCT01391312 |
| botulinum toxin Type A | Other | Phase PHASE4 | Glabellar Frown Lines | COMPLETED | NCT01391312 |
| normal saline (placebo) | Other | Phase PHASE4 | Glabellar Frown Lines | COMPLETED | NCT01391312 |
| botulinum toxin Type A | Other | Phase PHASE4 | Glabellar Frown Lines | COMPLETED | NCT01391312 |
| No treatment | Drug | Preclinical | Healthy Volunteers | COMPLETED | NCT01252147 |
| Dexamethasone Implant | Other | Phase PHASE2 | Pseudophakic Cystoid Macular Edema, | COMPLETED | NCT01284478 |
| No Intervention | Other | Preclinical | Healthy Volunteers | COMPLETED | NCT01412086 |
| BOTULINUM NEUROTOXIN TYPE-A | Other | Phase PHASE2 | Sialorrhea | UNKNOWN | NCT01489904 |
| Cyclosporine 0.010% | Other | Phase PHASE3 | Atopic Conjunctivitis | COMPLETED | NCT00884585 |
| Cyclosporine Vehicle | Other | Phase PHASE3 | Atopic Conjunctivitis | COMPLETED | NCT00884585 |
| Cyclosporine 0.010% | Other | Phase PHASE3 | Atopic Conjunctivitis | COMPLETED | NCT00884585 |
| Cyclosporine Vehicle | Other | Phase PHASE3 | Atopic Conjunctivitis | COMPLETED | NCT00884585 |
| placebo | Other | Phase PHASE3 | Chronic Kidney Disease | COMPLETED | NCT00497146 |
| paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease | COMPLETED | NCT00497146 |
| fluorouracil | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| folinic acid | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| oxaliplatin | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| bevacizumab | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| ABT-869 | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| bimatoprost vehicle solution | Other | Phase PHASE4 | Hypotrichosis | COMPLETED | NCT01448525 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE4 | Hypotrichosis | COMPLETED | NCT01448525 |
| Refresh® Dry Eye therapy | Drug | Phase PHASE2 | Brittle Nails | COMPLETED | NCT00986427 |
| Restasis (cyclosporine ophthalmic emulsion) 0.05% | Other | Phase PHASE2 | Brittle Nails | COMPLETED | NCT00986427 |
| bimatoprost vehicle | Other | Phase PHASE2 | Glaucoma, Open-Angle | COMPLETED | NCT01291108 |
| bimatoprost | Other | Phase PHASE2 | Glaucoma, Open-Angle | COMPLETED | NCT01291108 |
| AGN-210669 | Other | Phase PHASE2 | Glaucoma, Open-Angle | COMPLETED | NCT01291108 |
| Ketoconazole | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01468558 |
| IV DHE | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01468558 |
| MAP0004 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01468558 |
| Ketoconazole | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01468558 |
| IV DHE | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01468558 |
| MAP0004 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01468558 |
| dextran 70 0.1%/hydroxypropyl methylcellulose 0.3% | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01732757 |
| Olopatadine 0.2% | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01732757 |
| Alcaftadine 0.25% | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01732757 |
| dextran 70 0.1%/hydroxypropyl methylcellulose 0.3% | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01732757 |
| Olopatadine 0.2% | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01732757 |
| Alcaftadine 0.25% | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01732757 |
| No Treatment | Drug | Preclinical | Dry Eye Syndromes | COMPLETED | NCT01854905 |
| OPTIVE PLUS® | Other | Preclinical | Dry Eye Syndromes | COMPLETED | NCT01711424 |
| Bimatoprost | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01646151 |
| Tear Sample Collection | Other | Preclinical | Healthy Volunteers | COMPLETED | NCT01969162 |
| Tear Sample Collection | Other | Preclinical | Healthy Volunteers | COMPLETED | NCT01969162 |
| botulinum toxin Type A (200U) | Other | Phase PHASE2 | Overactive Bladder | TERMINATED | NCT00575016 |
| botulinum toxin Type A (100U); botulinum toxin Type A (200U) | Other | Phase PHASE2 | Overactive Bladder | TERMINATED | NCT00575016 |
| botulinum toxin Type A (50U); botulinum toxin Type A (200U) | Other | Phase PHASE2 | Overactive Bladder | TERMINATED | NCT00575016 |
| Normal saline (Placebo); botulinum toxin Type A (200U) | Other | Phase PHASE2 | Overactive Bladder | TERMINATED | NCT00575016 |
| botulinum toxin Type A (200U) | Other | Phase PHASE2 | Overactive Bladder | TERMINATED | NCT00575016 |
| botulinum toxin Type A (100U); botulinum toxin Type A (200U) | Other | Phase PHASE2 | Overactive Bladder | TERMINATED | NCT00575016 |
| botulinum toxin Type A (50U); botulinum toxin Type A (200U) | Other | Phase PHASE2 | Overactive Bladder | TERMINATED | NCT00575016 |
| Normal saline (Placebo); botulinum toxin Type A (200U) | Other | Phase PHASE2 | Overactive Bladder | TERMINATED | NCT00575016 |
| Neurological Examination | Other | Preclinical | Spasticity, Muscle | COMPLETED | NCT03250988 |
| Belotero Balance® | Other | Approved | Patients With Moderate to Severe Perioral Lines | COMPLETED | NCT01970397 |
| JUVEDERM® Ultra XC | Other | Approved | Patients With Moderate to Severe Perioral Lines | COMPLETED | NCT01970397 |
| Belotero Balance® | Other | Approved | Patients With Moderate to Severe Perioral Lines | COMPLETED | NCT01970397 |
| JUVEDERM® Ultra XC | Other | Approved | Patients With Moderate to Severe Perioral Lines | COMPLETED | NCT01970397 |
| Punctal Plug | Other | Phase PHASE4 | Dry Eye | COMPLETED | NCT01684436 |
| Sham | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT01660802 |
| 700 μg Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT01660802 |
| botulinum toxin Type A | Other | Preclinical | Facial Rhytides | COMPLETED | NCT01608659 |
| Sham Injection | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168324 |
| 350 µg Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168324 |
| 700 µg Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168324 |
| Wild Blueberry extract 100mg | Other | Approved | Cognitive Decline | COMPLETED | NCT02446314 |
| Wild Blueberry Powder - 900 mg | Other | Approved | Cognitive Decline | COMPLETED | NCT02446314 |
| Wild Blueberry Powder - 450mg | Other | Approved | Cognitive Decline | COMPLETED | NCT02446314 |
| Placebo | Other | Approved | Cognitive Decline | COMPLETED | NCT02446314 |
| Wild Blueberry extract 100mg | Other | Approved | Cognitive Decline | COMPLETED | NCT02446314 |
| Wild Blueberry Powder - 900 mg | Other | Approved | Cognitive Decline | COMPLETED | NCT02446314 |
| Wild Blueberry Powder - 450mg | Other | Approved | Cognitive Decline | COMPLETED | NCT02446314 |
| Placebo | Other | Approved | Cognitive Decline | COMPLETED | NCT02446314 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03255382 |
| Fumaderm | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03255382 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | TEMPORARILY_NOT_AVAILABLE | NCT04830202 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | AVAILABLE | NCT04278235 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04379050 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Nab-Paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, budigalimab, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT03844048 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | TEMPORARILY_NOT_AVAILABLE | NCT04830202 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | AVAILABLE | NCT04278235 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04379050 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Nab-Paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, budigalimab, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT03844048 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| adapalene 0.3% gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01425320 |
| dapsone 5% gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01425320 |
| Fixed Combination dapsone/adapalene Formulation B Gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01425320 |
| Fixed Combination dapsone/adapalene Formulation A Gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01425320 |
| adapalene 0.3% gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01425320 |
| dapsone 5% gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01425320 |
| Fixed Combination dapsone/adapalene Formulation B Gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01425320 |
| Fixed Combination dapsone/adapalene Formulation A Gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01425320 |
| Krytantek | Other | Preclinical | Glaucoma Primary Open Angle | COMPLETED | NCT01737853 |
| Ganforti | Other | Preclinical | Glaucoma Primary Open Angle | COMPLETED | NCT01737853 |
| Krytantek | Other | Preclinical | Glaucoma Primary Open Angle | COMPLETED | NCT01737853 |
| Ganforti | Other | Preclinical | Glaucoma Primary Open Angle | COMPLETED | NCT01737853 |
| No intervention applicable | Other | Preclinical | Cerebral Palsy. | UNKNOWN | NCT01744158 |
| No intervention applicable | Other | Preclinical | Cerebral Palsy. | UNKNOWN | NCT01744158 |
| No intervention applicable | Other | Preclinical | Cerebral Palsy. | UNKNOWN | NCT01744158 |
| normal saline | Other | Phase PHASE2 | Benign Prostatic Hyperplasia | COMPLETED | NCT00284518 |
| botulinum toxin Type A | Other | Phase PHASE2 | Benign Prostatic Hyperplasia | COMPLETED | NCT00284518 |
| normal saline | Other | Phase PHASE2 | Benign Prostatic Hyperplasia | COMPLETED | NCT00284518 |
| botulinum toxin Type A | Other | Phase PHASE2 | Benign Prostatic Hyperplasia | COMPLETED | NCT00284518 |
| normal saline | Other | Phase PHASE2 | Benign Prostatic Hyperplasia | COMPLETED | NCT00284518 |
| botulinum toxin Type A | Other | Phase PHASE2 | Benign Prostatic Hyperplasia | COMPLETED | NCT00284518 |
| Lidocaine | Other | Phase PHASE2 | Diabetic Neuropathic Pain | COMPLETED | NCT01589432 |
| Placebo | Other | Phase PHASE2 | Diabetic Neuropathic Pain | COMPLETED | NCT01589432 |
| ABT-639 | Other | Phase PHASE2 | Diabetic Neuropathic Pain | COMPLETED | NCT01589432 |
| ABT-869 | Other | Phase PHASE2 | Advanced Renal Cell Carcinoma | COMPLETED | NCT00486538 |
| placebo | Other | Phase PHASE3 | Moderate to Severe Plaque Psoriasis | COMPLETED | NCT00710580 |
| etanercept | Other | Phase PHASE3 | Moderate to Severe Plaque Psoriasis | COMPLETED | NCT00710580 |
| ABT-874 | Other | Phase PHASE3 | Moderate to Severe Plaque Psoriasis | COMPLETED | NCT00710580 |
| placebo | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00640419 |
| ABT-089 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00640419 |
| Placebo | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00640185 |
| ABT-089 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00640185 |
| Liposomal Doxorubicin | Other | Phase PHASE1 | Ovarian Cancer, Primary Peritoneal Cancer | COMPLETED | NCT00635193 |
| M200 (Volociximab) | Other | Phase PHASE1 | Ovarian Cancer, Primary Peritoneal Cancer | COMPLETED | NCT00635193 |
| ABT-089 | Other | Phase PHASE2 | Attention Deficit Hyperactivity Disorder | COMPLETED | NCT00443391 |
| placebo | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00292396 |
| Anti IL-12 monoclonal antibody/ABT-874 | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT00292396 |
| placebo | Other | Phase PHASE4 | Obesity | COMPLETED | NCT00932022 |
| Trospium Chloride, Extended Release (XR) | Other | Phase PHASE4 | Obesity | COMPLETED | NCT00932022 |
| ABT-089 | Other | Phase PHASE2 | Attention-Deficit/Hyperactivity Disorder | COMPLETED | NCT00686933 |
| Duloxetine | Other | Phase PHASE2 | Diabetic Neuralgia | COMPLETED | NCT00507936 |
| placebo | Other | Phase PHASE2 | Diabetic Neuralgia | COMPLETED | NCT00507936 |
| ABT-894 | Other | Phase PHASE2 | Diabetic Neuralgia | COMPLETED | NCT00507936 |
| Placebo for ABT-869 | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT00645177 |
| paclitaxel | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT00645177 |
| ABT-869 | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT00645177 |
| ABT-874 | Other | Phase PHASE3 | Moderate to Severe Plaque Psoriasis | COMPLETED | NCT00626002 |
| ABT-874 | Other | Phase PHASE3 | Moderate to Severe Plaque Psoriasis | COMPLETED | NCT00626002 |
| ABT-874 | Other | Phase PHASE3 | Moderate to Severe Plaque Psoriasis | COMPLETED | NCT00626002 |
| latanoprost | Other | Phase PHASE4 | Glaucoma, Angle-Closure | TERMINATED | NCT01151904 |
| brimonidine 0.2%/timolol 0.5% fixed combination ophthalmic solution | Other | Phase PHASE4 | Glaucoma, Angle-Closure | TERMINATED | NCT01151904 |
| Saline | Other | Phase PHASE4 | Chronic Migraine | COMPLETED | NCT01071096 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Chronic Migraine | COMPLETED | NCT01071096 |
| dexamethasone intravitreal implant 0.7 mg | Other | Preclinical | Macular Edema | COMPLETED | NCT01445626 |
| dexamethasone intravitreal implant 0.7 mg | Other | Preclinical | Macular Edema | COMPLETED | NCT01445626 |
| dextran 70 0.1%/hydroxypropyl methylcellulose 0.3% | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01470118 |
| olopatadine 0.2% ophthalmic solution | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01470118 |
| alcaftadine 0.25% ophthalmic solution | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01470118 |
| dextran 70 0.1%/hydroxypropyl methylcellulose 0.3% | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01470118 |
| olopatadine 0.2% ophthalmic solution | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01470118 |
| alcaftadine 0.25% ophthalmic solution | Other | Phase PHASE4 | Conjunctivitis, Allergic | COMPLETED | NCT01470118 |
| Dapsone 5% Gel | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01785836 |
| Dapsone Formulation C | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01785836 |
| Dapsone Formulation B | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01785836 |
| Dapsone Formulation A | Other | Phase PHASE1 | Acne Vulgaris | WITHDRAWN | NCT01785836 |
| normal saline | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00910845 |
| onabotulinumtoxinA | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00910845 |
| Adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01265823 |
| lopinavir/ritonavir | Other | Phase PHASE4 | Human Immunodeficiency Virus | COMPLETED | NCT00648999 |
| lopinavir/ritonavir | Other | Phase PHASE4 | Human Immunodeficiency Virus | COMPLETED | NCT00648999 |
| bimatoprost/timolol fixed combination ophthalmic solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT01177098 |
| bimatoprost /timolol formulation A fixed combination ophthalmic solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT01177098 |
| bimatoprost/timolol fixed combination ophthalmic solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT01177098 |
| bimatoprost /timolol formulation A fixed combination ophthalmic solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT01177098 |
| ABT-072 | Other | Phase PHASE2 | Hepatitis C Virus Infection | COMPLETED | NCT00872196 |
| ABT-869 0.10 mg/kg | Other | Phase PHASE2 | Non-Small Cell Lung Cancer (NSCLC) | COMPLETED | NCT00517790 |
| ABT-869 .25 mg/kg | Other | Phase PHASE2 | Non-Small Cell Lung Cancer (NSCLC) | COMPLETED | NCT00517790 |
| dexamethasone intravitreal implant 0.7 mg | Other | Preclinical | Retinal Vein Occlusion | COMPLETED | NCT01411696 |
| Sham (no implant) | Other | Phase PHASE1 | Retinitis Pigmentosa | COMPLETED | NCT00661479 |
| 100 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Retinitis Pigmentosa | COMPLETED | NCT00661479 |
| 200 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Retinitis Pigmentosa | COMPLETED | NCT00661479 |
| 400 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Retinitis Pigmentosa | COMPLETED | NCT00661479 |
| Sham (no implant) | Other | Phase PHASE1 | Retinitis Pigmentosa | COMPLETED | NCT00661479 |
| 100 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Retinitis Pigmentosa | COMPLETED | NCT00661479 |
| 200 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Retinitis Pigmentosa | COMPLETED | NCT00661479 |
| 400 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Retinitis Pigmentosa | COMPLETED | NCT00661479 |
| Paclitaxel | Other | Phase PHASE2 | Advanced or Metastatic Non-Small Cell Lung Cancer | COMPLETED | NCT00716534 |
| Carboplatin | Other | Phase PHASE2 | Advanced or Metastatic Non-Small Cell Lung Cancer | COMPLETED | NCT00716534 |
| Placebo for ABT-869 | Other | Phase PHASE2 | Advanced or Metastatic Non-Small Cell Lung Cancer | COMPLETED | NCT00716534 |
| ABT-869 | Other | Phase PHASE2 | Advanced or Metastatic Non-Small Cell Lung Cancer | COMPLETED | NCT00716534 |
| fluorouracil | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| folinic acid | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| oxaliplatin | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| bevacizumab | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| ABT-869 | Other | Phase PHASE2 | Advanced Colorectal Cancer | COMPLETED | NCT00707889 |
| maxacalcitol placebo | Other | Phase PHASE3 | Secondary Hyperparathyroidism | COMPLETED | NCT01341782 |
| paricalcitol placebo | Other | Phase PHASE3 | Secondary Hyperparathyroidism | COMPLETED | NCT01341782 |
| maxacalcitol | Other | Phase PHASE3 | Secondary Hyperparathyroidism | COMPLETED | NCT01341782 |
| paricalcitol | Other | Phase PHASE3 | Secondary Hyperparathyroidism | COMPLETED | NCT01341782 |
| FCR | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT00868413 |
| ABT-263 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT00868413 |
| FCR | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT00868413 |
| ABT-263 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT00868413 |
| Palivizumab | Other | Phase PHASE3 | Respiratory Syncytial Virus Infection | COMPLETED | NCT01466062 |
| Standard of Care | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01629407 |
| Standard of Care | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01629407 |
| botulinum toxin A (BTX-A) | Other | Approved | Stiff Knee Gait | TERMINATED | NCT00900666 |
| placebo | Other | Approved | Stiff Knee Gait | TERMINATED | NCT00900666 |
| botulinum toxin A (BTX-A) | Other | Approved | Stiff Knee Gait | TERMINATED | NCT00900666 |
| placebo | Other | Approved | Stiff Knee Gait | TERMINATED | NCT00900666 |
| Pars Plana Vitrectomy | Other | Preclinical | Vitrectomy | COMPLETED | NCT01319318 |
| Placebo (Vehicle for Cyclosporine) | Other | Phase PHASE2 | Laser In Situ Keratomileusis | COMPLETED | NCT00991458 |
| Cyclosporine 0.005% eye drops | Other | Phase PHASE2 | Laser In Situ Keratomileusis | COMPLETED | NCT00991458 |
| Cyclosporine 0.010% eye drops | Other | Phase PHASE2 | Laser In Situ Keratomileusis | COMPLETED | NCT00991458 |
| Placebo (Vehicle for Cyclosporine) | Other | Phase PHASE2 | Laser In Situ Keratomileusis | COMPLETED | NCT00991458 |
| Cyclosporine 0.005% eye drops | Other | Phase PHASE2 | Laser In Situ Keratomileusis | COMPLETED | NCT00991458 |
| Cyclosporine 0.010% eye drops | Other | Phase PHASE2 | Laser In Situ Keratomileusis | COMPLETED | NCT00991458 |
| dorzolamide hydrochloride 2.0%/brimonidine tartrate 0.2%/timolol 0.5% ophthalmic solution | Other | Phase PHASE3 | Glaucoma | WITHDRAWN | NCT01284166 |
| 200 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Vitrectomy | COMPLETED | NCT01229410 |
| 400 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Vitrectomy | COMPLETED | NCT01229410 |
| 200 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Vitrectomy | COMPLETED | NCT01229410 |
| 400 µg Brimonidine Tartrate Implant | Other | Phase PHASE1 | Vitrectomy | COMPLETED | NCT01229410 |
| Calcitriol | Other | Preclinical | Secondary Hyperparathyroidism | TERMINATED | NCT01134315 |
| Paricalcitol | Other | Preclinical | Secondary Hyperparathyroidism | TERMINATED | NCT01134315 |
| Calcitriol | Other | Preclinical | Secondary Hyperparathyroidism | TERMINATED | NCT01134315 |
| Paricalcitol | Other | Preclinical | Secondary Hyperparathyroidism | TERMINATED | NCT01134315 |
| Calcitriol | Other | Preclinical | Secondary Hyperparathyroidism | TERMINATED | NCT01134315 |
| Paricalcitol | Other | Preclinical | Secondary Hyperparathyroidism | TERMINATED | NCT01134315 |
| Placebo and rehab | Other | Phase EARLY_PHASE1 | Stroke | COMPLETED | NCT00565201 |
| Botox and rehab | Other | Phase EARLY_PHASE1 | Stroke | COMPLETED | NCT00565201 |
| bimatoprost Formulation C | Other | Phase PHASE1 | Alopecia | COMPLETED | NCT01189279 |
| bimatoprost Formulation B | Other | Phase PHASE1 | Alopecia | COMPLETED | NCT01189279 |
| bimatoprost Formulation A | Other | Phase PHASE1 | Alopecia | COMPLETED | NCT01189279 |
| Ozurdex | Other | Preclinical | Macular Edema | COMPLETED | NCT01945892 |
| No Treatment | Drug | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01540370 |
| bimatoprost/brimonidine tartrate/timolol fixed combination ophthalmic solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT01216943 |
| Bimatoprost 0.01% ophthalmic solution | Other | Preclinical | Open-Angle Glaucoma | COMPLETED | NCT01568008 |
| Bimatoprost 0.01% | Other | Phase PHASE4 | Glaucoma, Primary Open Angle | COMPLETED | NCT01833741 |
| Duloxetine | Other | Phase PHASE2 | Diabetic Neuropathic Pain | TERMINATED | NCT01579279 |
| Placebo | Other | Phase PHASE2 | Diabetic Neuropathic Pain | TERMINATED | NCT01579279 |
| ABT-652 12 mg - 18 mg | Other | Phase PHASE2 | Diabetic Neuropathic Pain | TERMINATED | NCT01579279 |
| ABT-652 12 mg | Other | Phase PHASE2 | Diabetic Neuropathic Pain | TERMINATED | NCT01579279 |
| ABT-652 6 mg | Other | Phase PHASE2 | Diabetic Neuropathic Pain | TERMINATED | NCT01579279 |
| Blink Contacts® Eye Drops | Other | Phase PHASE4 | Contact Lens Related Dry Eye Syndrome | COMPLETED | NCT01543061 |
| No treatment | Drug | Phase PHASE4 | Contact Lens Related Dry Eye Syndrome | COMPLETED | NCT01543061 |
| OPTIVEtm Plus | Other | Phase PHASE4 | Contact Lens Related Dry Eye Syndrome | COMPLETED | NCT01543061 |
| No Intervention | Other | Preclinical | Facial Rhytides | COMPLETED | NCT01600729 |
| No Intervention | Other | Preclinical | Facial Rhytides | COMPLETED | NCT01600729 |
| Placebo (saline) | Other | Phase PHASE1 | Benign Prostatic Hyperplasia | COMPLETED | NCT00894517 |
| Botulinum Toxin Type A | Other | Phase PHASE1 | Benign Prostatic Hyperplasia | COMPLETED | NCT00894517 |
| Placebo (saline) | Other | Phase PHASE1 | Benign Prostatic Hyperplasia | COMPLETED | NCT00894517 |
| Botulinum Toxin Type A | Other | Phase PHASE1 | Benign Prostatic Hyperplasia | COMPLETED | NCT00894517 |
| Placebo (saline) | Other | Phase PHASE1 | Benign Prostatic Hyperplasia | COMPLETED | NCT00894517 |
| Botulinum Toxin Type A | Other | Phase PHASE1 | Benign Prostatic Hyperplasia | COMPLETED | NCT00894517 |
| Placebo | Other | Phase PHASE2 | Major Depressive Disorder | TERMINATED | NCT01741142 |
| Escitalopram | Other | Phase PHASE2 | Major Depressive Disorder | TERMINATED | NCT01741142 |
| ABT-436 | Other | Phase PHASE2 | Major Depressive Disorder | TERMINATED | NCT01741142 |
| AGN-210669 vehicle ophthalmic solution | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| AGN-210669 ophthalmic solution, 0.025% | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| AGN-210669 ophthalmic solution, 0.05% | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| AGN-210669 ophthalmic solution, 0.075% | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| AGN-210669 vehicle ophthalmic solution | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| AGN-210669 ophthalmic solution, 0.025% | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| AGN-210669 ophthalmic solution, 0.05% | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| AGN-210669 ophthalmic solution, 0.075% | Other | Phase PHASE1 | Ocular Hypertension | COMPLETED | NCT00809848 |
| vehicle sterile solution | Other | Phase PHASE3 | Eyelashes | COMPLETED | NCT00693420 |
| Bimatoprost 0.03% sterile solution | Other | Phase PHASE3 | Eyelashes | COMPLETED | NCT00693420 |
| vehicle sterile solution | Other | Phase PHASE3 | Eyelashes | COMPLETED | NCT00693420 |
| Bimatoprost 0.03% sterile solution | Other | Phase PHASE3 | Eyelashes | COMPLETED | NCT00693420 |
| Rehabilitation Therapy | Drug | Approved | Upper Limb Spasticity | COMPLETED | NCT00945295 |
| Botulinum toxin type A, BoNT-A | Other | Approved | Upper Limb Spasticity | COMPLETED | NCT00945295 |
| ABT-348 and docetaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01110486 |
| ABT-348 and carboplatin | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01110486 |
| ABT-348 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01110486 |
| Placebo | Other | Phase PHASE2 | Overactive Bladder | COMPLETED | NCT00168454 |
| botulinum toxin Type A | Other | Phase PHASE2 | Overactive Bladder | COMPLETED | NCT00168454 |
| No treatment | Drug | Preclinical | Muscle Spasticity | COMPLETED | NCT01383681 |
| Placebo to AGN-214868 | Other | Phase PHASE2 | Neuralgia, Postherpetic | COMPLETED | NCT01129531 |
| AGN-214868 | Other | Phase PHASE2 | Neuralgia, Postherpetic | COMPLETED | NCT01129531 |
| Placebo to AGN-214868 | Other | Phase PHASE2 | Neuralgia, Postherpetic | COMPLETED | NCT01129531 |
| AGN-214868 | Other | Phase PHASE2 | Neuralgia, Postherpetic | COMPLETED | NCT01129531 |
| placebo (saline) | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT00168428 |
| Botulinum Toxin Type A | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT00168428 |
| Botulinum Toxin Type A 150kDa | Other | Phase PHASE4 | Blepharospasm | COMPLETED | NCT00761592 |
| Botulinum Toxin Type A 900kDa | Other | Phase PHASE4 | Blepharospasm | COMPLETED | NCT00761592 |
| Botulinum Toxin Type A 150kDa | Other | Phase PHASE4 | Blepharospasm | COMPLETED | NCT00761592 |
| Botulinum Toxin Type A 900kDa | Other | Phase PHASE4 | Blepharospasm | COMPLETED | NCT00761592 |
| Carboxymethylcellulose sodium, glycerin and polysorbate 80 | Other | Phase PHASE2 | Dry Eye Syndrome | COMPLETED | NCT01339936 |
| Placebo | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01908010 |
| ABT-354 | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01908010 |
| Placebo | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01908010 |
| ABT-354 | Other | Phase PHASE1 | Alzheimer's Disease | COMPLETED | NCT01908010 |
| methotrexate | Other | Phase PHASE4 | Arthritis, Rheumatoid | COMPLETED | NCT00808509 |
| adalimumab | Other | Phase PHASE4 | Arthritis, Rheumatoid | COMPLETED | NCT00808509 |
| methotrexate | Other | Phase PHASE4 | Arthritis, Rheumatoid | COMPLETED | NCT00808509 |
| adalimumab | Other | Phase PHASE4 | Arthritis, Rheumatoid | COMPLETED | NCT00808509 |
| IV DHE | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT01199965 |
| MAP0004 | Other | Phase PHASE1 | Healthy Subjects | COMPLETED | NCT01199965 |
| Placebo Capsule | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01191723 |
| Moxifloxacin | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01191723 |
| Inhaler Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01191723 |
| MAP0004 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01191723 |
| Placebo Capsule | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01191723 |
| Moxifloxacin | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01191723 |
| Inhaler Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01191723 |
| MAP0004 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01191723 |
| IV Dihydroergotamine Mesylate (DHE) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| Placebo Inhaler | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| IV Placebo (Saline) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| MAP0004 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| IV Dihydroergotamine Mesylate (DHE) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| Placebo Inhaler | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| IV Placebo (Saline) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| MAP0004 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| IV Dihydroergotamine Mesylate (DHE) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| Placebo Inhaler | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| IV Placebo (Saline) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| MAP0004 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01089062 |
| 21ug MAP0020 | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00995904 |
| 42ug MAP0020 | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00995904 |
| 84ug MAP0020 | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00995904 |
| 21ug MAP0020 | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00995904 |
| 42ug MAP0020 | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00995904 |
| 84ug MAP0020 | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00995904 |
| Placebo | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00697801 |
| MAP0010 high dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00697801 |
| MAP0010 low dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00697801 |
| Placebo | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00697801 |
| MAP0010 high dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00697801 |
| MAP0010 low dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00697801 |
| 0.25mg MAP0010 | Other | Phase PHASE3 | Asthma | TERMINATED | NCT00697697 |
| 0.135mg MAP0010 | Other | Phase PHASE3 | Asthma | TERMINATED | NCT00697697 |
| 0.25mg MAP0010 | Other | Phase PHASE3 | Asthma | TERMINATED | NCT00697697 |
| 0.135mg MAP0010 | Other | Phase PHASE3 | Asthma | TERMINATED | NCT00697697 |
| 0.25mg MAP0010 | Other | Phase PHASE3 | Asthma | TERMINATED | NCT00697697 |
| 0.135mg MAP0010 | Other | Phase PHASE3 | Asthma | TERMINATED | NCT00697697 |
| Leuprolide Acetate 3 Month Depot | Other | Phase PHASE3 | Precocious | COMPLETED | NCT00667446 |
| MAP0010 high dose | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00627679 |
| MAP0010 intermediate dose | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00627679 |
| MAP0010 low dose | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00627679 |
| Budesonide Inhalation Suspension | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00627679 |
| MAP0010 high dose | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00627679 |
| MAP0010 intermediate dose | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00627679 |
| MAP0010 low dose | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00627679 |
| Budesonide Inhalation Suspension | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00627679 |
| Placebo | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT00623636 |
| MAP0004 | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT00623636 |
| Placebo | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT00623636 |
| MAP0004 | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT00623636 |
| Placebo | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT00623636 |
| MAP0004 | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT00623636 |
| Placebo | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00569192 |
| 0.25mg MAP0010 | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00569192 |
| 0.135mg MAP0010 | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00569192 |
| Placebo | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00569192 |
| 0.25mg MAP0010 | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00569192 |
| 0.135mg MAP0010 | Other | Phase PHASE3 | Asthma | COMPLETED | NCT00569192 |
| Budesonide inhalation suspension 0.5mg | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| Budesonide inhalation suspension 0.25mg | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| MAP0010 high dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| MAP0010 low dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| Budesonide inhalation suspension 0.5mg | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| Budesonide inhalation suspension 0.25mg | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| MAP0010 high dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| MAP0010 low dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| Budesonide inhalation suspension 0.5mg | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| Budesonide inhalation suspension 0.25mg | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| MAP0010 high dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| MAP0010 low dose | Other | Phase PHASE2 | Asthma | COMPLETED | NCT00554970 |
| Normal Saline (Placebo) | Other | Phase PHASE3 | Overactive Bladder | TERMINATED | NCT00439140 |
| botulinum toxin Type A | Other | Phase PHASE3 | Overactive Bladder | TERMINATED | NCT00439140 |
| Bimatoprost 0.01% | Other | Phase PHASE4 | Glaucoma, Open-Angle | COMPLETED | NCT01594970 |
| Placebo | Other | Phase PHASE2 | Chronic Low Back Pain | COMPLETED | NCT01364922 |
| hydrocodone/acetaminophen extended release | Other | Phase PHASE2 | Chronic Low Back Pain | COMPLETED | NCT01364922 |
| ABT-333 | Other | Phase PHASE1 | Relative Bioavailability | COMPLETED | NCT02052349 |
| ABT-333 | Other | Phase PHASE1 | Relative Bioavailability | COMPLETED | NCT02052349 |
| OnabotulinumtoxinA | Other | Preclinical | Chronic Migraine, Headache | WITHDRAWN | NCT01749423 |
| OnabotulinumtoxinA | Other | Preclinical | Chronic Migraine, Headache | WITHDRAWN | NCT01749423 |
| botulinum toxin Type A | Other | Preclinical | Muscle Spasticity | COMPLETED | NCT01387074 |
| vehicle of AGN-229666 | Other | Phase PHASE2 | Allergic Conjunctivitis | COMPLETED | NCT01754766 |
| AGN-229666 | Other | Phase PHASE2 | Allergic Conjunctivitis | COMPLETED | NCT01754766 |
| vehicle of AGN-229666 | Other | Phase PHASE2 | Allergic Conjunctivitis | COMPLETED | NCT01754766 |
| AGN-229666 | Other | Phase PHASE2 | Allergic Conjunctivitis | COMPLETED | NCT01754766 |
| Placebo | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00763321 |
| ABT-712 | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00763321 |
| Placebo | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00761150 |
| ABT-712 | Other | Phase PHASE3 | Chronic Low Back Pain | COMPLETED | NCT00761150 |
| ABT-450/r/ABT-267 | Other | Phase PHASE1 | Absolute Bioavailability | COMPLETED | NCT02052362 |
| ABT-450/r/ABT-267 | Other | Phase PHASE1 | Absolute Bioavailability | COMPLETED | NCT02052362 |
| Adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01561313 |
| Adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01502423 |
| Adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01502423 |
| onabotulinumtoxinA 24 U | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01224015 |
| onabotulinumtoxinA 44 U | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01224015 |
| normal saline | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01224015 |
| onabotulinumtoxinA 24 U | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01224015 |
| onabotulinumtoxinA 44 U | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01224015 |
| normal saline | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01224015 |
| Methotrexate | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01185288 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01185288 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT01333722 |
| Hydrocodone/Acetaminophen Extended Release | Other | Phase PHASE2 | Pain | COMPLETED | NCT01333722 |
| Placebo | Other | Phase PHASE2 | Pain | COMPLETED | NCT00935311 |
| Hydrocodone/Acetaminophen Immediate-release | Other | Phase PHASE2 | Pain | COMPLETED | NCT00935311 |
| ABT-712 Extended-release | Other | Phase PHASE2 | Pain | COMPLETED | NCT00935311 |
| minoxidil 2% solution | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325350 |
| bimatoprost vehicle solution | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325350 |
| bimatoprost Formulation C | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325350 |
| bimatoprost Formulation B | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325350 |
| bimatoprost Formulation A | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325350 |
| minoxidil 5% solution | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325337 |
| bimatoprost vehicle solution | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325337 |
| bimatoprost Formulation C | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325337 |
| bimatoprost Formulation B | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325337 |
| bimatoprost Formulation A | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01325337 |
| Relestat Ophthalmic Solution 0.05% | Other | Preclinical | Conjunctivitis, Allergic | COMPLETED | NCT01987765 |
| No Intervention | Other | Preclinical | Healthy Volunteers | COMPLETED | NCT01821534 |
| No Intervention | Other | Preclinical | Healthy Volunteers | COMPLETED | NCT01821534 |
| EMG Guidance of Injection | Other | Approved | High Tone Pelvic Floor Dysfunction | COMPLETED | NCT01323829 |
| EMG Guidance of Injection | Other | Approved | High Tone Pelvic Floor Dysfunction | COMPLETED | NCT01323829 |
| Rifampin | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | WITHDRAWN | NCT01969682 |
| ABT-199 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | WITHDRAWN | NCT01969682 |
| Rifampin | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | WITHDRAWN | NCT01969682 |
| ABT-199 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | WITHDRAWN | NCT01969682 |
| Rifampin | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | WITHDRAWN | NCT01969682 |
| ABT-199 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | WITHDRAWN | NCT01969682 |
| ABT-SLV176 | Other | Phase PHASE3 | Hypogonadism | WITHDRAWN | NCT02082197 |
| ABT-SLV176 | Other | Phase PHASE3 | Hypogonadism | WITHDRAWN | NCT02082197 |
| ABT-719 | Other | Phase PHASE2 | Cardiothoracic Surgery | TERMINATED | NCT01897519 |
| Placebo | Other | Phase PHASE2 | Cardiothoracic Surgery | TERMINATED | NCT01897519 |
| ABT-719 | Other | Phase PHASE2 | Cardiothoracic Surgery | TERMINATED | NCT01897519 |
| Placebo | Other | Phase PHASE2 | Cardiothoracic Surgery | TERMINATED | NCT01897519 |
| Adalimumab, new formulation | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01712178 |
| Adalimumab, current formulation | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01712178 |
| Adalimumab, new formulation | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01712178 |
| Adalimumab, current formulation | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01712178 |
| bimatoprost 0.01% ophthalmic solution | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01589510 |
| bimatoprost 0.01% ophthalmic solution | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01589510 |
| Functional Electrical Stimulation (FES) through the Ness H200 | Other | Approved | Upper Extremity Spasticity | COMPLETED | NCT00462449 |
| Tazorac | Other | Phase PHASE4 | Brittle Nails | COMPLETED | NCT00648986 |
| No Intervention | Other | Preclinical | Cervical Dystonia | COMPLETED | NCT01814774 |
| Navitoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia | COMPLETED | NCT01557777 |
| No Intervention | Other | Preclinical | Cervical Dystonia | COMPLETED | NCT00836017 |
| 0.03% Bimatoprost | Other | Phase PHASE4 | Glaucoma, Open-Angle | COMPLETED | NCT02020512 |
| No Treatment | Drug | Preclinical | Open-angle Glaucoma | TERMINATED | NCT01781962 |
| Sham | Other | Phase PHASE3 | Diabetic Macular Edema | COMPLETED | NCT00168389 |
| Dexamethasone | Other | Phase PHASE3 | Diabetic Macular Edema | COMPLETED | NCT00168389 |
| Sham | Other | Phase PHASE3 | Diabetic Macular Edema | COMPLETED | NCT00168337 |
| Dexamethasone | Other | Phase PHASE3 | Diabetic Macular Edema | COMPLETED | NCT00168337 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 7 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 6 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 5 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 4 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 3 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 2 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 1 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 7 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 6 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 5 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 4 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 3 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 2 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| AGN-210961 Formulation 1 | Other | Phase PHASE2 | Ocular Hypertension | COMPLETED | NCT01110499 |
| Normal Saline | Other | Phase PHASE1 | Osteoarthritis | COMPLETED | NCT01518257 |
| botulinum toxin Type A | Other | Phase PHASE1 | Osteoarthritis | COMPLETED | NCT01518257 |
| onabotulinumtoxinA | Other | Phase PHASE3 | Muscle Spasticity | WITHDRAWN | NCT02145689 |
| onabotulinumtoxinA | Other | Phase PHASE3 | Muscle Spasticity | WITHDRAWN | NCT02145689 |
| [14C]ABT-199 (GDC-0199) | Other | Phase PHASE1 | Relapsed/Refractory Non-Hodgkin's Lymphoma | WITHDRAWN | NCT02095574 |
| [14C]ABT-199 (GDC-0199) | Other | Phase PHASE1 | Relapsed/Refractory Non-Hodgkin's Lymphoma | WITHDRAWN | NCT02095574 |
| [14C]ABT-199 (GDC-0199) | Other | Phase PHASE1 | Relapsed/Refractory Non-Hodgkin's Lymphoma | WITHDRAWN | NCT02095574 |
| Open-label Adalimumab | Other | Phase PHASE3 | Axial Spondyloarthritis | COMPLETED | NCT00939003 |
| Placebo | Other | Phase PHASE3 | Axial Spondyloarthritis | COMPLETED | NCT00939003 |
| Adalimumab | Other | Phase PHASE3 | Axial Spondyloarthritis | COMPLETED | NCT00939003 |
| Fixed Combination 0.2% brimonidine tartrate/0.5% timolol ophthalmic solution | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT01241240 |
| bimatoprost/brimonidine tartrate/timolol ophthalmic solution (Triple Combination Therapy) | Drug | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT01241240 |
| Adalimumab | Other | Phase PHASE4 | Moderate to Severe Plaque Psoriasis | COMPLETED | NCT01644396 |
| Easyband (Telemetrically adjustable gastric banding device) | Device | Approved | Morbid Obesity | WITHDRAWN | NCT00534339 |
| Easyband (Telemetrically adjustable gastric banding device) | Device | Approved | Morbid Obesity | WITHDRAWN | NCT00534339 |
| Crosslinked hyaluronic acid gel (Juvéderm VOLUMA®) | Other | Preclinical | Age-related Volume Deficit in the Mid-face | COMPLETED | NCT01559064 |
| Crosslinked hyaluronic acid gel (Juvéderm VOLUMA®) | Other | Preclinical | Age-related Volume Deficit in the Mid-face | COMPLETED | NCT01559064 |
| Crosslinked hyaluronic acid gel (Juvéderm VOLUMA®) | Other | Preclinical | Age-related Volume Deficit in the Mid-face | COMPLETED | NCT01559064 |
| hyaluronic acid gel | Other | Approved | Lip Enhancement | COMPLETED | NCT01176773 |
| hyaluronic acid gel | Other | Approved | Lip Enhancement | COMPLETED | NCT01176773 |
| Easyband® | Other | Preclinical | Morbid Obesity | COMPLETED | NCT00948246 |
| Easyband® | Other | Preclinical | Morbid Obesity | COMPLETED | NCT00948246 |
| Easyband® | Other | Preclinical | Morbid Obesity | COMPLETED | NCT00948246 |
| Natrelle(TM) Silicone-Filled Breast Implants | Other | Approved | Breast Reconstruction | COMPLETED | NCT00691327 |
| Natrelle(TM) Silicone-Filled Breast Implants | Other | Approved | Breast Reconstruction | COMPLETED | NCT00691327 |
| Style 410 Silicone-Filled Breast Implants | Other | Approved | Breast Augmentation | COMPLETED | NCT00690339 |
| Style 410 Silicone-Filled Breast Implants | Other | Approved | Breast Augmentation | COMPLETED | NCT00690339 |
| Natrelle(TM) Silicone-Filled Breast Implants | Other | Approved | Breast Augmentation | COMPLETED | NCT00689871 |
| Natrelle(TM) Silicone-Filled Breast Implants | Other | Approved | Breast Augmentation | COMPLETED | NCT00689871 |
| Track B | Other | Phase PHASE4 | Hypotrichosis | COMPLETED | NCT01891487 |
| Track A | Other | Phase PHASE4 | Hypotrichosis | COMPLETED | NCT01891487 |
| Brimonidine Tartrate Ophthalmic Solution 0.2% | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT01863953 |
| Vehicle Ophthalmic Solution | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT01863953 |
| Bimatoprost Ophthalmic Solution 0.01% | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT01863953 |
| Fixed-Combination Bimatoprost/Brimonidine | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT01863953 |
| BTX-A | Other | Phase PHASE2 | Primary Focal Hyperhidrosis of the Hands | TERMINATED | NCT01262339 |
| No Treatment | Drug | Preclinical | Migraine Disorders | COMPLETED | NCT01648530 |
| botulinum toxin Type A (32U) | Other | Phase PHASE3 | Upper Facial Rhytides | COMPLETED | NCT01797094 |
| botulinum toxin Type A (44U) | Other | Phase PHASE3 | Upper Facial Rhytides | COMPLETED | NCT01797094 |
| vehicle of bimatoprost solution 0.03 % | Other | Phase PHASE3 | Idiopathic Eyelash Hypotrichosis | COMPLETED | NCT01698554 |
| vehicle of bimatoprost formulation A solution | Other | Phase PHASE3 | Idiopathic Eyelash Hypotrichosis | COMPLETED | NCT01698554 |
| bimatoprost solution 0.03 % | Other | Phase PHASE3 | Idiopathic Eyelash Hypotrichosis | COMPLETED | NCT01698554 |
| bimatoprost formulation A solution | Other | Phase PHASE3 | Idiopathic Eyelash Hypotrichosis | COMPLETED | NCT01698554 |
| Ozurdex Intravitreal Injection (0.7 mg) | Other | Phase PHASE4 | Macular Edema | COMPLETED | NCT01870440 |
| Ozurdex Intravitreal Injection (0.7 mg) | Other | Phase PHASE4 | Macular Edema | COMPLETED | NCT01870440 |
| LAP-BAND® Adjustable Gastric Band (LAGB®) | Other | Phase PHASE2 | Obesity | COMPLETED | NCT00580502 |
| Saline | Other | Approved | Post Traumatic Stiffness | COMPLETED | NCT01129583 |
| Botulinum Toxin Type A | Other | Approved | Post Traumatic Stiffness | COMPLETED | NCT01129583 |
| Saline | Other | Approved | Post Traumatic Stiffness | COMPLETED | NCT01129583 |
| Botulinum Toxin Type A | Other | Approved | Post Traumatic Stiffness | COMPLETED | NCT01129583 |
| Intravitreal dexamethasone 0.7mg implant | Other | Phase PHASE4 | Diabetes Mellitus | UNKNOWN | NCT02399657 |
| tazarotene cream 0.1% | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT02218034 |
| tazarotene gel 0.1% | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT02218034 |
| AGN-190168 Formulation 2 | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT02218034 |
| AGN-190168 Formulation 1 | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT02218034 |
| Standard Therapy | Drug | Approved | Stroke | COMPLETED | NCT01751373 |
| Optimal muscle activation therapy | Drug | Approved | Stroke | COMPLETED | NCT01751373 |
| No Intervention | Other | Preclinical | Macular Edema | COMPLETED | NCT02181530 |
| Saline injection | Other | Phase PHASE4 | Graves Ophthalmopathy | WITHDRAWN | NCT01272414 |
| Botulinum Toxin Type A | Other | Phase PHASE4 | Graves Ophthalmopathy | WITHDRAWN | NCT01272414 |
| Saline injection | Other | Phase PHASE4 | Graves Ophthalmopathy | WITHDRAWN | NCT01272414 |
| Botulinum Toxin Type A | Other | Phase PHASE4 | Graves Ophthalmopathy | WITHDRAWN | NCT01272414 |
| Treatment with Botox | Drug | Phase PHASE4 | Essential Axillary Hyperhidrosis | TERMINATED | NCT00669474 |
| Suction curettage | Other | Phase PHASE4 | Essential Axillary Hyperhidrosis | TERMINATED | NCT00669474 |
| Voluma XC | Other | Approved | Mandibular Hypoplasia | UNKNOWN | NCT02330016 |
| Placebo Drug Delivery System | Drug | Phase PHASE1 | Cataract | TERMINATED | NCT01605942 |
| Dexamethasone Drug Delivery System | Drug | Phase PHASE1 | Cataract | TERMINATED | NCT01605942 |
| sham procedure | Procedure | Phase PHASE2 | Macular Edema | COMPLETED | NCT02186119 |
| ranibizumab | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT02186119 |
| abicipar pegol | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT02186119 |
| Carboxymethylcellulose sodium | Other | Phase PHASE2 | Ametropia | COMPLETED | NCT00691197 |
| Carboxymethylcellulose sodium and Glycerin | Other | Phase PHASE2 | Ametropia | COMPLETED | NCT00691197 |
| Anatomically shaped silicone gel-filled breast implants | Other | Approved | Breast Augmentation | TERMINATED | NCT01853605 |
| AGN-207281 vehicle ophthalmic solution (Placebo) | Other | Phase PHASE1 | Glaucoma, Open-Angle | COMPLETED | NCT01215786 |
| timolol ophthalmic solution 0.5% | Other | Phase PHASE1 | Glaucoma, Open-Angle | COMPLETED | NCT01215786 |
| AGN-207281 ophthalmic solutions (0.1% and 0.3%); AGN-207281 vehicle ophthalmic solution (placebo) | Other | Phase PHASE1 | Glaucoma, Open-Angle | COMPLETED | NCT01215786 |
| AGN-207281 vehicle ophthalmic solution (Placebo) | Other | Phase PHASE1 | Glaucoma, Open-Angle | COMPLETED | NCT01215786 |
| timolol ophthalmic solution 0.5% | Other | Phase PHASE1 | Glaucoma, Open-Angle | COMPLETED | NCT01215786 |
| AGN-207281 ophthalmic solutions (0.1% and 0.3%); AGN-207281 vehicle ophthalmic solution (placebo) | Other | Phase PHASE1 | Glaucoma, Open-Angle | COMPLETED | NCT01215786 |
| Formulation 2: Carboxymethylcellulose sodium, glycerin, and Polysorbate 80 based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT01010282 |
| Formulation 1: Carboxymethylcellulose sodium, glycerin and Polysorbate 80, based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT01010282 |
| Glycerin and Polysorbate 80 based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT01010282 |
| Dapsone Gel | Other | Phase PHASE4 | Acne Vulgaris | COMPLETED | NCT02032407 |
| Glycerin and Polysorbate 80 based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00932477 |
| Formulation 2: Carboxymethylcellulose Sodium, Glycerin and Polysorbate 80, based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00932477 |
| Formulation 1: Carboxymethylcellulose Sodium, Glycerin and Polysorbate 80, based artificial tear | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT00932477 |
| cyclosporine ophthalmic emulsion Formulation A; cyclosporine ophthalmic emulsion Formulation B | Other | Phase PHASE1 | Dry Eye Syndromes | COMPLETED | NCT01319773 |
| cyclosporine ophthalmic emulsion Formulation B; cyclosporine ophthalmic emulsion 0.05% | Other | Phase PHASE1 | Dry Eye Syndromes | COMPLETED | NCT01319773 |
| cyclosporine ophthalmic emulsion Formulation A; cyclosporine ophthalmic emulsion 0.05% | Other | Phase PHASE1 | Dry Eye Syndromes | COMPLETED | NCT01319773 |
| cyclosporine ophthalmic emulsion Formulation B | Other | Phase PHASE1 | Dry Eye Syndromes | COMPLETED | NCT01319773 |
| cyclosporine ophthalmic emulsion Formulation A | Other | Phase PHASE1 | Dry Eye Syndromes | COMPLETED | NCT01319773 |
| AGN 203818 | Other | Phase PHASE2 | Fibromyalgia | TERMINATED | NCT00445705 |
| placebo | Other | Phase PHASE2 | Fibromyalgia | TERMINATED | NCT00445705 |
| Ranibizumab 500µg | Other | Phase PHASE2 | Choroid Neovascularization | TERMINATED | NCT00395057 |
| AGN 211745 | Other | Phase PHASE2 | Choroid Neovascularization | TERMINATED | NCT00395057 |
| onabotulinumtoxinA | Other | Preclinical | Chronic Migraine, Headaches | COMPLETED | NCT01749410 |
| No Intervention | Other | Preclinical | Open-Angle Glaucoma | COMPLETED | NCT02348476 |
| No Intervention | Other | Preclinical | Open-Angle Glaucoma | COMPLETED | NCT02348476 |
| Sham Cystoscopy Procedure | Procedure | Phase PHASE2 | Interstitial Cystitis | TERMINATED | NCT01475253 |
| LiRIS Placebo | Other | Phase PHASE2 | Interstitial Cystitis | TERMINATED | NCT01475253 |
| Lidocaine Releasing Intravesical System - LiRIS® | Other | Phase PHASE2 | Interstitial Cystitis | TERMINATED | NCT01475253 |
| bimatoprost/timolol | Other | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01976624 |
| bimatoprost vehicle | Other | Phase PHASE3 | Glaucoma | TERMINATED | NCT01426113 |
| timolol ophthalmic solution | Other | Phase PHASE3 | Glaucoma | TERMINATED | NCT01426113 |
| bimatoprost ophthalmic solution formulation A | Other | Phase PHASE3 | Glaucoma | TERMINATED | NCT01426113 |
| Normal saline (Placebo); botulinum toxin Type A (300U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00461292 |
| Normal saline (Placebo); botulinum toxin Type A (200U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00461292 |
| botulinum toxin Type A (300U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00461292 |
| botulinum toxin Type A (200U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00461292 |
| Normal saline (placebo) | Other | Phase PHASE4 | Chronic Migraine | COMPLETED | NCT01833130 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Chronic Migraine | COMPLETED | NCT01833130 |
| Bimatoprost 0.01% | Other | Preclinical | Glaucoma, Primary Open Angle | COMPLETED | NCT01814761 |
| No Intervention | Other | Preclinical | Muscle Spasticity | WITHDRAWN | NCT02145650 |
| No Intervention | Other | Preclinical | Muscle Spasticity | WITHDRAWN | NCT02145650 |
| Juvéderm® VOLUMA XC | Other | Approved | Mid-facial Volume Deficit Related to Aging | COMPLETED | NCT00978042 |
| Juvéderm® VOLUMA XC | Other | Approved | Mid-facial Volume Deficit Related to Aging | COMPLETED | NCT00978042 |
| hypromellose 0.3% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01881126 |
| timolol 0.5% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01881126 |
| travatan 0.004% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01881126 |
| bimatoprost 0.01% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01881126 |
| hypromellose 0.3% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01881126 |
| timolol 0.5% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01881126 |
| travatan 0.004% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01881126 |
| bimatoprost 0.01% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01881126 |
| Bevacizumab | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT02036424 |
| Ozurdex | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT02036424 |
| Bevacizumab | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT02036424 |
| Ozurdex | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT02036424 |
| AGN-199201 Vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02197806 |
| AGN-190584 | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02197806 |
| AGN-199201 | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02197806 |
| AGN-199201 Vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02197806 |
| AGN-190584 | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02197806 |
| AGN-199201 | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02197806 |
| No intervention | Other | Preclinical | Dry Eye Syndromes | COMPLETED | NCT01882413 |
| No intervention | Other | Preclinical | Dry Eye Syndromes | COMPLETED | NCT01882413 |
| Normal Saline (Placebo); botulinum toxin Type A (300U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00311376 |
| Normal Saline (Placebo); botulinum toxin Type A (200U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00311376 |
| botulinum toxin Type A (300U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00311376 |
| botulinum toxin Type A (200U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00311376 |
| Normal Saline (Placebo); botulinum toxin Type A (300U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00311376 |
| Normal Saline (Placebo); botulinum toxin Type A (200U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00311376 |
| botulinum toxin Type A (300U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00311376 |
| botulinum toxin Type A (200U) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00311376 |
| LiRIS® 400 mg | Other | Phase PHASE1 | Chronic Interstitial Cystitis | COMPLETED | NCT01879683 |
| LiRIS® 400 mg | Other | Phase PHASE1 | Chronic Interstitial Cystitis | COMPLETED | NCT01879683 |
| Ozurdex | Other | Approved | Epiretinal Membrane | UNKNOWN | NCT01701518 |
| Normal Saline | Other | Phase PHASE2 | Cervical Dystonia | COMPLETED | NCT00564681 |
| botulinum toxin type A Formulation 2 | Other | Phase PHASE2 | Cervical Dystonia | COMPLETED | NCT00564681 |
| botulinum toxin type A | Other | Phase PHASE2 | Cervical Dystonia | COMPLETED | NCT00564681 |
| No Intervention | Other | Preclinical | Cervical Dystonia | COMPLETED | NCT02245958 |
| hypromellose 0.3% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02097719 |
| timolol 0.5% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02097719 |
| travoprost 0.004% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02097719 |
| bimatoprost 0.01% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02097719 |
| hypromellose 0.3% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02097719 |
| timolol 0.5% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02097719 |
| travoprost 0.004% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02097719 |
| bimatoprost 0.01% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02097719 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01856556 |
| NRX-1074 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01856556 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01856556 |
| NRX-1074 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01856556 |
| LiRIS Placebo | Other | Phase PHASE2 | Interstitial Cystitis | TERMINATED | NCT01824303 |
| LiRIS 400 mg | Other | Phase PHASE2 | Interstitial Cystitis | TERMINATED | NCT01824303 |
| No intervention | Other | Preclinical | Dry Eye Syndromes | COMPLETED | NCT02252744 |
| NRX-1074 750 mg | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT02366364 |
| NRX-1074 500 mg | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT02366364 |
| NRX-1074 375 mg | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT02366364 |
| Placebo | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT02366364 |
| NRX-1074 750 mg | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT02366364 |
| NRX-1074 500 mg | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT02366364 |
| NRX-1074 375 mg | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT02366364 |
| Placebo | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT02366364 |
| placebo | Other | Phase PHASE2 | Neuralgia | TERMINATED | NCT00533351 |
| AGN201781 | Other | Phase PHASE2 | Neuralgia | TERMINATED | NCT00533351 |
| Trospium Chloride | Other | Phase PHASE4 | Elderly | COMPLETED | NCT00863551 |
| Vocal Exercise | Other | Approved | Spasmodic Dysphonia | TERMINATED | NCT00895063 |
| Cross-linked hyaluronic acid gel | Other | Approved | Mid-face Volume Deficiency | COMPLETED | NCT01029535 |
| Photographic Review | Other | Preclinical | Healthy Volunteers | COMPLETED | NCT02417077 |
| Normal Saline | Other | Phase PHASE3 | Lateral Canthal Lines | COMPLETED | NCT02195687 |
| botulinum toxin Type A | Other | Phase PHASE3 | Lateral Canthal Lines | COMPLETED | NCT02195687 |
| AGN-229666 | Other | Phase PHASE3 | Conjunctivitis, Allergic | COMPLETED | NCT02082262 |
| dexamethasone intravitreal implant | Other | Preclinical | Macular Edema | COMPLETED | NCT01618266 |
| dexamethasone intravitreal implant | Other | Preclinical | Macular Edema | COMPLETED | NCT01618266 |
| No Intervention | Other | Preclinical | Migraine Disorders | COMPLETED | NCT01946126 |
| No Intervention | Other | Preclinical | Migraine Disorders | COMPLETED | NCT01946126 |
| NRX-1074 10 mg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT02067793 |
| NRX-1074 5 mg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT02067793 |
| Placebo | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT02067793 |
| NRX-1074 1 mg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT02067793 |
| NRX-1074 10 mg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT02067793 |
| NRX-1074 5 mg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT02067793 |
| Placebo | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT02067793 |
| NRX-1074 1 mg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT02067793 |
| Placebo | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT01684163 |
| GLYX-13 10 mg/kg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT01684163 |
| GLYX-13 5 mg/kg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT01684163 |
| Placebo | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT01684163 |
| GLYX-13 10 mg/kg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT01684163 |
| GLYX-13 5 mg/kg | Other | Phase PHASE2 | Major Depressive Disorder | COMPLETED | NCT01684163 |
| Bimatoprost Vehicle | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01904721 |
| Bimatoprost Solution 2 | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01904721 |
| Bimatoprost Solution 1 | Other | Phase PHASE2 | Alopecia | COMPLETED | NCT01904721 |
| injection of botulinum toxin type A. | Other | Phase PHASE1 | Psoriasis Vulgaris | COMPLETED | NCT00816517 |
| AGN-223575 Vehicle | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02155543 |
| AGN-223575 Formulation C | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02155543 |
| AGN-223575 Formulation B | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02155543 |
| AGN-223575 Formulation A | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02155543 |
| botulinum toxin Type A | Other | Preclinical | Urinary Incontinence | COMPLETED | NCT02161159 |
| Tafluprost Unit Dose Preservative Free 15microgram/ml | Other | Phase PHASE4 | Ocular Hypertension | UNKNOWN | NCT02471105 |
| Preserved Bimatoprost 0.01% | Other | Phase PHASE4 | Ocular Hypertension | UNKNOWN | NCT02471105 |
| sham procedure | Procedure | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181517 |
| ranibizumab | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181517 |
| abicipar pegol | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181517 |
| Systematic Screening and Education Regimen | Other | Phase PHASE4 | Multiple Sclerosis | COMPLETED | NCT01930799 |
| Systematic Screening and Education Regimen | Other | Phase PHASE4 | Multiple Sclerosis | COMPLETED | NCT01930799 |
| dexamethasone 700 ㎍ intravitreal implant | Other | Preclinical | Macular Edema | COMPLETED | NCT02188173 |
| ABT-122 | Other | Phase PHASE2 | Psoriatic Arthritis | TERMINATED | NCT02429895 |
| Botulinum toxin serotype A | Other | Phase PHASE4 | Cervicobrachial Neuralgia | COMPLETED | NCT00241215 |
| Plicated-LAGB | Other | Approved | Morbid Obesity | TERMINATED | NCT01564732 |
| Standard-LAGB | Other | Approved | Morbid Obesity | TERMINATED | NCT01564732 |
| AGN-232411 Vehicle | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02420730 |
| AGN-232411 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02420730 |
| Botulinum Toxin Type A | Other | Phase PHASE4 | Urinary Incontinence | COMPLETED | NCT02601287 |
| Botulinum Toxin Type A | Other | Phase PHASE4 | Urinary Incontinence | COMPLETED | NCT02601287 |
| Dexamethasone Intravitreal Implant | Other | Approved | Epiretinal Membrane | TERMINATED | NCT01410201 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Chronic Migraine | COMPLETED | NCT02037425 |
| 4mg triamcinolone acetonide | Other | Phase PHASE3 | Diabetic Macular Edema | COMPLETED | NCT00367133 |
| 1mg triamcinolone acetonide | Other | Phase PHASE3 | Diabetic Macular Edema | COMPLETED | NCT00367133 |
| Standard of Care Group | Other | Phase PHASE3 | Diabetic Macular Edema | COMPLETED | NCT00367133 |
| onabotulinumtoxinA | Other | Preclinical | Urinary Bladder, Overactive | COMPLETED | NCT02557971 |
| BIOCELL™ Textured 410 Implant | Other | Preclinical | Breast Implantation | COMPLETED | NCT02132572 |
| botulinum toxin Type A | Other | Preclinical | Urinary Incontinence | COMPLETED | NCT02010788 |
| botulinum toxin Type A | Other | Preclinical | Urinary Incontinence | COMPLETED | NCT02010788 |
| Normal Saline | Other | Phase PHASE3 | Muscle Spasticity | COMPLETED | NCT01575054 |
| botulinum toxin Type A | Other | Phase PHASE3 | Muscle Spasticity | COMPLETED | NCT01575054 |
| VYC-12 HA injectable gel | Other | Phase PHASE4 | Skin Roughness | COMPLETED | NCT02877069 |
| botulinum toxin Type A | Other | Preclinical | Urinary Bladder, Overactive | COMPLETED | NCT02673047 |
| Bimatoprost 1% Formulation B | Other | Phase PHASE1 | Androgenetic Alopecia | COMPLETED | NCT02848300 |
| Bimatoprost 1% Formulation A | Other | Phase PHASE1 | Androgenetic Alopecia | COMPLETED | NCT02848300 |
| OnabotulinumtoxinA | Other | Phase PHASE2 | New Daily Persistent Headache | TERMINATED | NCT01920945 |
| OnabotulinumtoxinA | Other | Phase PHASE2 | New Daily Persistent Headache | TERMINATED | NCT01920945 |
| Endura (artificial tears) | Other | Approved | Glaucoma | COMPLETED | NCT00405431 |
| Restasis | Other | Approved | Glaucoma | COMPLETED | NCT00405431 |
| Ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C Virus | WITHDRAWN | NCT02806362 |
| Rescue medication | Drug | Phase PHASE2 | Migraine | COMPLETED | NCT01657370 |
| Placebo | Other | Phase PHASE2 | Migraine | COMPLETED | NCT01657370 |
| MK-1602 | Other | Phase PHASE2 | Migraine | COMPLETED | NCT01657370 |
| Placebo | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01410565 |
| Apaziquone | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01410565 |
| Placebo | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01410565 |
| Apaziquone | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01410565 |
| Placebo | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01410565 |
| Apaziquone | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01410565 |
| Fixed Combination 0.2% brimonidine tartrate/0.5% timolol ophthalmic solution | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT01217606 |
| bimatoprost/brimonidine tartrate/timolol ophthalmic solution (Triple Combination Therapy) | Drug | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT01217606 |
| sterile saline solution | Other | Phase PHASE3 | Scleroderma | COMPLETED | NCT02165111 |
| Onabotulinumtoxin A | Other | Phase PHASE3 | Scleroderma | COMPLETED | NCT02165111 |
| sterile saline solution | Other | Phase PHASE3 | Scleroderma | COMPLETED | NCT02165111 |
| Onabotulinumtoxin A | Other | Phase PHASE3 | Scleroderma | COMPLETED | NCT02165111 |
| Genteal® Lubricant Gel Drops | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02455050 |
| Systane® Gel Drops | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02455050 |
| Carboxymethylcellulose Sodium Based Eye Drops | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02455050 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Migraine Disorders | COMPLETED | NCT01516892 |
| Intravenous Paricalcitol | Other | Phase PHASE4 | Endstage Renal Disease | UNKNOWN | NCT03023748 |
| duvelisib | Other | Phase PHASE1 | Lymphoma | COMPLETED | NCT02598570 |
| duvelisib | Other | Phase PHASE1 | Lymphoma | COMPLETED | NCT02598570 |
| Cystoscopic injection of Botox into the urinary bladder | Other | Phase PHASE4 | Parkinson's Disease | COMPLETED | NCT01421719 |
| vehicle | Other | Phase PHASE2 | Brittle Nail Syndrome | COMPLETED | NCT01064830 |
| topical cyclosporine ophthalmic suspension 0.05% | Other | Phase PHASE2 | Brittle Nail Syndrome | COMPLETED | NCT01064830 |
| Bimatoprost | Other | Phase PHASE1 | Alopecia | TERMINATED | NCT02676310 |
| OnabotulinumtoxinA | Other | Preclinical | Torticollis | COMPLETED | NCT01655862 |
| OnabotulinumtoxinA | Other | Preclinical | Torticollis | COMPLETED | NCT01655862 |
| Steroid plus NSAID eye drop combination therapy | Drug | Phase PHASE2 | Macular Edema | COMPLETED | NCT01673191 |
| Dexamethasone intravitreal implant | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT01673191 |
| Steroid plus NSAID eye drop combination therapy | Drug | Phase PHASE2 | Macular Edema | COMPLETED | NCT01673191 |
| Dexamethasone intravitreal implant | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT01673191 |
| placebo (normal saline) | Other | Phase PHASE3 | Muscle Spasticity | TERMINATED | NCT02145676 |
| onabotulinumtoxinA | Other | Phase PHASE3 | Muscle Spasticity | TERMINATED | NCT02145676 |
| sham procedure | Procedure | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181504 |
| ranibizumab | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181504 |
| abicipar pegol | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181504 |
| sham procedure | Procedure | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181504 |
| ranibizumab | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181504 |
| abicipar pegol | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT02181504 |
| Saline | Other | Phase PHASE1 | Pruritus | COMPLETED | NCT02639052 |
| Botox | Other | Phase PHASE1 | Pruritus | COMPLETED | NCT02639052 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Adalimumab PRN | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Adalimumab PRN | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Adalimumab PRN | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | WITHDRAWN | NCT01674413 |
| Normal Saline | Other | Phase PHASE2 | Osteoarthritis | COMPLETED | NCT02230956 |
| onabotulinumtoxinA | Other | Phase PHASE2 | Osteoarthritis | COMPLETED | NCT02230956 |
| Normal Saline | Other | Phase PHASE2 | Osteoarthritis | COMPLETED | NCT02230956 |
| onabotulinumtoxinA | Other | Phase PHASE2 | Osteoarthritis | COMPLETED | NCT02230956 |
| Ozurdex | Other | Phase PHASE3 | Retinal Vein Occlusion | COMPLETED | NCT01449682 |
| Ozurdex | Other | Phase PHASE3 | Retinal Vein Occlusion | COMPLETED | NCT01449682 |
| Cyclosporine 0.05% Ophthalmic Emulsion | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT02554981 |
| AqueSys XEN 45 Glaucoma Implant | Other | Approved | Glaucoma | COMPLETED | NCT02036541 |
| Refresh Tears Lubricant Eye Drops (Allergan) | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01682460 |
| botulinum toxin Type A | Other | Phase PHASE3 | Migraine Disorders | WITHDRAWN | NCT03193359 |
| placebo (sodium chloride 0.9 mg) | Other | Phase PHASE3 | Migraine Disorders | WITHDRAWN | NCT03193346 |
| botulinum toxin Type A | Other | Phase PHASE3 | Migraine Disorders | WITHDRAWN | NCT03193346 |
| placebo (sodium chloride 0.9 mg) | Other | Phase PHASE3 | Migraine Disorders | WITHDRAWN | NCT03193346 |
| botulinum toxin Type A | Other | Phase PHASE3 | Migraine Disorders | WITHDRAWN | NCT03193346 |
| Normal Saline | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT02261493 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT02261493 |
| Co-Latanoprost | Other | Phase PHASE4 | POAG | UNKNOWN | NCT02792803 |
| Apo-Latanoprost | Other | Phase PHASE4 | POAG | UNKNOWN | NCT02792803 |
| Xalatan | Other | Phase PHASE4 | POAG | UNKNOWN | NCT02792803 |
| Co-Latanoprost | Other | Phase PHASE4 | POAG | UNKNOWN | NCT02792803 |
| Apo-Latanoprost | Other | Phase PHASE4 | POAG | UNKNOWN | NCT02792803 |
| Xalatan | Other | Phase PHASE4 | POAG | UNKNOWN | NCT02792803 |
| Triamcinolone | Other | Phase PHASE4 | Fat Reduction | COMPLETED | NCT03241563 |
| Sodium Deoxycholate | Other | Phase PHASE4 | Fat Reduction | COMPLETED | NCT03241563 |
| Positron emission tomography (PET) | Other | Phase PHASE2 | Alzheimer's Disease | WITHDRAWN | NCT02860065 |
| CPC-201 | Other | Phase PHASE2 | Alzheimer's Disease | WITHDRAWN | NCT02860065 |
| Positron emission tomography (PET) | Other | Phase PHASE2 | Alzheimer's Disease | WITHDRAWN | NCT02860065 |
| CPC-201 | Other | Phase PHASE2 | Alzheimer's Disease | WITHDRAWN | NCT02860065 |
| Positron emission tomography (PET) | Other | Phase PHASE2 | Alzheimer's Disease | WITHDRAWN | NCT02860065 |
| CPC-201 | Other | Phase PHASE2 | Alzheimer's Disease | WITHDRAWN | NCT02860065 |
| Restylane® | Other | Approved | Nasolabial Fold | COMPLETED | NCT02558283 |
| JUVÉDERM® VOLIFT® with Lidocaine | Other | Approved | Nasolabial Fold | COMPLETED | NCT02558283 |
| Placebo (Normal Saline) | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT01662492 |
| Botulinum toxin type A Dose 2 | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT01662492 |
| Botulinum toxin type A Dose 1 | Other | Phase PHASE3 | Migraine Disorders | COMPLETED | NCT01662492 |
| AGN-195263 Vehicle | Other | Phase PHASE2 | Meibomian Gland Dysfunction | COMPLETED | NCT01633788 |
| AGN-195263 0.01% | Other | Phase PHASE2 | Meibomian Gland Dysfunction | COMPLETED | NCT01633788 |
| AGN-195263 0.03% | Other | Phase PHASE2 | Meibomian Gland Dysfunction | COMPLETED | NCT01633788 |
| AGN-195263 0.1% | Other | Phase PHASE2 | Meibomian Gland Dysfunction | COMPLETED | NCT01633788 |
| ABT-493/ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02446717 |
| ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02446717 |
| ABT-493, ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02446717 |
| ABT-493/ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02446717 |
| ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02446717 |
| ABT-493, ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02446717 |
| CPC-201 | Other | Phase PHASE2 | Dementia of the Alzheimer's Type | COMPLETED | NCT02434666 |
| CPC-201 | Other | Phase PHASE2 | Dementia of the Alzheimer's Type | COMPLETED | NCT02434666 |
| Placebo | Other | Phase PHASE2 | Carpal Tunnel Syndrome | COMPLETED | NCT02070302 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Carpal Tunnel Syndrome | COMPLETED | NCT02070302 |
| Placebo | Other | Phase PHASE3 | Patellofemoral Pain Syndrome | TERMINATED | NCT00496964 |
| Botulinum toxin A + exercise | Other | Phase PHASE3 | Patellofemoral Pain Syndrome | TERMINATED | NCT00496964 |
| Normal saline | Other | Phase PHASE4 | Overactive Bladder | COMPLETED | NCT01945489 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Overactive Bladder | COMPLETED | NCT01945489 |
| amblyopia therapy | Drug | Preclinical | Amblyopia | COMPLETED | NCT03341780 |
| Study Photography + Personal & Medical History Collection | Other | Preclinical | Loss of Facial Adipose Tissue | UNKNOWN | NCT03347747 |
| Study Photography + Personal & Medical History Collection | Other | Preclinical | Loss of Facial Adipose Tissue | UNKNOWN | NCT03347747 |
| paclitaxel | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| carboplatin | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| veliparib | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| paclitaxel | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| carboplatin | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| veliparib | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| paclitaxel | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| carboplatin | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| veliparib | Other | Phase PHASE1 | Ovarian Cancer | COMPLETED | NCT02483104 |
| Veliparib | Other | Phase PHASE1 | Oncology | COMPLETED | NCT01853306 |
| Veliparib | Other | Phase PHASE1 | Oncology | COMPLETED | NCT01853306 |
| Whole Brain Radiation | Other | Phase PHASE1 | Glioblastoma Multiforme | COMPLETED | NCT01800695 |
| Temozolomide | Other | Phase PHASE1 | Glioblastoma Multiforme | COMPLETED | NCT01800695 |
| ABT-414 | Other | Phase PHASE1 | Glioblastoma Multiforme | COMPLETED | NCT01800695 |
| Levodopa-Carbidopa | Other | Phase PHASE1 | Parkinson Disease | COMPLETED | NCT01484990 |
| Levodopa-Carbidopa | Other | Phase PHASE1 | Parkinson Disease | COMPLETED | NCT01484990 |
| erlotinib | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01472016 |
| cetuximab | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01472016 |
| FOLFIRI | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01472016 |
| docetaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01472016 |
| ABT-700 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01472016 |
| linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01413893 |
| new texture shaped breast implants | Other | Phase PHASE4 | Breast Augmentation | COMPLETED | NCT01639755 |
| new texture shaped breast implants | Other | Phase PHASE4 | Breast Augmentation | COMPLETED | NCT01639755 |
| New texture round breast implants | Other | Approved | Breast Augmentation | COMPLETED | NCT01639742 |
| New texture round breast implants | Other | Approved | Breast Augmentation | COMPLETED | NCT01639742 |
| Hyaluronic Acid Injectable Gel | Other | Approved | Chin Retrusion | COMPLETED | NCT02559908 |
| Hyaluronic Acid Injectable Gel | Other | Approved | Chin Retrusion | COMPLETED | NCT02559908 |
| botulinum toxin Type A | Other | Preclinical | Urinary Incontinence | COMPLETED | NCT02072928 |
| Placebo | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01469221 |
| Apaziquone | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01469221 |
| Placebo | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01469221 |
| Apaziquone | Other | Phase PHASE3 | Bladder Cancer | TERMINATED | NCT01469221 |
| 3D Imaging | Other | Approved | Hypomastia | COMPLETED | NCT01964105 |
| LiRIS Placebo | Other | Phase PHASE2 | Cystitis, Interstitial | COMPLETED | NCT02411110 |
| LiRIS® | Other | Phase PHASE2 | Cystitis, Interstitial | COMPLETED | NCT02411110 |
| intra-rectal Botulinum toxin A injection | Other | Phase PHASE2 | Low Anterior Resection Syndrome | COMPLETED | NCT01589471 |
| Seri Surgical Scaffold | Other | Approved | Recurrent Ptosis of the Breast | COMPLETED | NCT02016612 |
| Seri Surgical Scaffold | Other | Approved | Recurrent Ptosis of the Breast | COMPLETED | NCT02016612 |
| Dry eye exam | Other | Preclinical | Dry Eye Syndromes | COMPLETED | NCT01826812 |
| 30 minutes sustained reading | Other | Preclinical | Dry Eye Syndromes | COMPLETED | NCT01826812 |
| Dry eye exam | Other | Preclinical | Dry Eye Syndromes | COMPLETED | NCT01826812 |
| 30 minutes sustained reading | Other | Preclinical | Dry Eye Syndromes | COMPLETED | NCT01826812 |
| Palivizumab | Other | Phase PHASE3 | Respiratory Syncytial Virus (RSV) | COMPLETED | NCT02968173 |
| Palivizumab | Other | Phase PHASE3 | Respiratory Syncytial Virus (RSV) | COMPLETED | NCT02968173 |
| Palivizumab | Other | Phase PHASE3 | Respiratory Syncytial Virus (RSV) | COMPLETED | NCT02968173 |
| Methotrexate | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02196701 |
| Adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02196701 |
| Methotrexate | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02196701 |
| Adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02196701 |
| isolated 0.3% gatifloxacin and 1.0% prednisolone acetate | Other | Phase PHASE3 | Ocular Infection and Inflammation | COMPLETED | NCT01218737 |
| 0.3% gatifloxacin and 1.0% prednisolone acetate association | Other | Phase PHASE3 | Ocular Infection and Inflammation | COMPLETED | NCT01218737 |
| Valsartan 80 mg | Other | Phase PHASE4 | Hypertension Complicated | COMPLETED | NCT03180593 |
| Valsartan 80 mg | Other | Phase PHASE4 | Hypertension Complicated | COMPLETED | NCT03180593 |
| Valsartan 80 mg | Other | Phase PHASE4 | Hypertension Complicated | COMPLETED | NCT03180593 |
| Cyclosporine New Ophthalmic Formulation | Other | Phase PHASE2 | Dry Eye Syndromes | TERMINATED | NCT02013791 |
| Sham | Other | Phase PHASE2 | Dry Eye Syndromes | TERMINATED | NCT02013791 |
| Vehicle | Other | Phase PHASE2 | Dry Eye Syndromes | TERMINATED | NCT02013791 |
| Cyclosporine New Ophthalmic Formulation | Other | Phase PHASE2 | Dry Eye Syndromes | TERMINATED | NCT02013791 |
| Sham | Other | Phase PHASE2 | Dry Eye Syndromes | TERMINATED | NCT02013791 |
| Vehicle | Other | Phase PHASE2 | Dry Eye Syndromes | TERMINATED | NCT02013791 |
| Ozurdex | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT01613716 |
| Revolve System | Other | Approved | Autologous Fat Grafting | UNKNOWN | NCT03544593 |
| Revolve System | Other | Approved | Autologous Fat Grafting | UNKNOWN | NCT03544593 |
| Pegylated Interferon alpha 2-a (PegIFN) | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01854697 |
| Telaprevir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01854697 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01854697 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01854697 |
| Telaprevir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01854528 |
| Pegylated Interferon a-2a (PegINF) | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01854528 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01854528 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01854528 |
| Topiramate | Other | Phase PHASE4 | Migraine Disorders | COMPLETED | NCT02191579 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Migraine Disorders | COMPLETED | NCT02191579 |
| bimatoprost 0.03% plus timolol 0.5% | Other | Phase PHASE4 | Glaucoma, Open-Angle | COMPLETED | NCT02571712 |
| Bimatoprost cutaneous solution 0.03% | Other | Preclinical | Eyelash Hypotrichosis | COMPLETED | NCT02505776 |
| Normal Saline (Placebo) | Other | Phase PHASE3 | Pediatrics | COMPLETED | NCT01603602 |
| botulinum toxin Type A | Other | Phase PHASE3 | Pediatrics | COMPLETED | NCT01603602 |
| Lucentis | Other | Phase PHASE4 | Diabetic Macular Edema | TERMINATED | NCT02684084 |
| Ozurdex | Other | Phase PHASE4 | Diabetic Macular Edema | TERMINATED | NCT02684084 |
| Sham (no implant) | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT00658619 |
| 200 µg Brimonidine Tartrate Implant | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT00658619 |
| 400 µg Brimonidine Tartrate Implant | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT00658619 |
| bimatoprost ophthalmic solution 0.01% | Other | Phase PHASE4 | Glaucoma, Open-Angle | COMPLETED | NCT02863705 |
| brimonidine tartrate/timolol malate Ophthalmic Solution | Other | Phase PHASE4 | Glaucoma, Open-Angle | COMPLETED | NCT02863705 |
| injections on posterior bladder wall excluding the trigone | Other | Phase PHASE4 | Interstitial Cystitis | COMPLETED | NCT02297100 |
| injections upper aspect of trigone of urinary bladder | Other | Phase PHASE4 | Interstitial Cystitis | COMPLETED | NCT02297100 |
| Onabotulinumtoxin A | Other | Phase PHASE4 | Interstitial Cystitis | COMPLETED | NCT02297100 |
| Normal saline injection | Other | Phase PHASE2 | Chronic Testicular Pain | COMPLETED | NCT02058836 |
| Botox Injection | Other | Phase PHASE2 | Chronic Testicular Pain | COMPLETED | NCT02058836 |
| Saline | Other | Approved | Muscle Strength | COMPLETED | NCT00822523 |
| Botulinum Toxin, Type A | Other | Approved | Muscle Strength | COMPLETED | NCT00822523 |
| Marvel AM | Other | Approved | Blue Light Damage | COMPLETED | NCT03594721 |
| Marvel AM | Other | Approved | Blue Light Damage | COMPLETED | NCT03594721 |
| bimatoprost 0.03% ophthalmic solution | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01298700 |
| bimatoprost 0.01% ophthalmic solution | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01298700 |
| Placebo | Other | Preclinical | Subcutaneous Fat | COMPLETED | NCT03682471 |
| Deoxycholic acid Injection | Other | Preclinical | Subcutaneous Fat | COMPLETED | NCT03682471 |
| Botox | Other | Phase PHASE2 | Hypertrophic Scar | UNKNOWN | NCT03631368 |
| Botox | Other | Phase PHASE2 | Hypertrophic Scar | UNKNOWN | NCT03631368 |
| Standard of Care | Other | Phase PHASE2 | Osteomyelitis | TERMINATED | NCT03091439 |
| Dalbavancin | Other | Phase PHASE2 | Osteomyelitis | TERMINATED | NCT03091439 |
| Standard of Care | Other | Phase PHASE2 | Osteomyelitis | TERMINATED | NCT03091439 |
| Dalbavancin | Other | Phase PHASE2 | Osteomyelitis | TERMINATED | NCT03091439 |
| Botulinum Toxin Type A | Other | Approved | Migraine Headache | TERMINATED | NCT00850421 |
| Botulinum Toxin Type A | Other | Approved | Migraine Headache | TERMINATED | NCT00850421 |
| LiRIS Placebo | Other | Phase PHASE2 | Cystitis, Interstitial | COMPLETED | NCT02395042 |
| LiRIS® | Other | Phase PHASE2 | Cystitis, Interstitial | COMPLETED | NCT02395042 |
| Teleneurological Examination | Other | Preclinical | Spasticity, Muscle | COMPLETED | NCT03211390 |
| Neurological Examination | Other | Preclinical | Spasticity, Muscle | COMPLETED | NCT03211390 |
| ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) | COMPLETED | NCT02517528 |
| ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) | COMPLETED | NCT02517528 |
| ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) | COMPLETED | NCT02517528 |
| Juvéderm® VOLUMA XC | Other | Approved | Temple Hollowing | TERMINATED | NCT03166618 |
| Normal Saline | Other | Phase PHASE2 | Premature Ejaculation | TERMINATED | NCT01917006 |
| OnabotulinumtoxinA | Other | Phase PHASE2 | Premature Ejaculation | TERMINATED | NCT01917006 |
| Simbrinza Three Times Daily (TID) | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02167035 |
| Combigan Two Times Daily (BID) | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT02167035 |
| VTP-43742 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03724292 |
| Placebo | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03724292 |
| VTP-43742 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03724292 |
| Placebo | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03724292 |
| VTP-43742 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03724292 |
| Placebo | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03724292 |
| Placebo 2 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02555709 |
| Placebo 1 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02555709 |
| VTP-43742 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02555709 |
| Placebo 2 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02555709 |
| Placebo 1 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02555709 |
| VTP-43742 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02555709 |
| Abicipar pegol | Other | Phase PHASE1 | Macular Degeneration | COMPLETED | NCT03335852 |
| botulinum toxin Type A | Other | Preclinical | Migraine Disorders | COMPLETED | NCT01686581 |
| Ozurdex (dexamethasone) | Other | Phase PHASE2 | Diabetes | COMPLETED | NCT01787669 |
| Avastin (Bevacizumab) | Other | Phase PHASE2 | Diabetes | COMPLETED | NCT01787669 |
| Vehicle | Other | Phase PHASE3 | Dry Eye Syndromes | TERMINATED | NCT02965846 |
| AGN-195263 | Other | Phase PHASE3 | Dry Eye Syndromes | TERMINATED | NCT02965846 |
| Placebo-matching Atogepant | Other | Phase PHASE2 | Migraine, With or Without Aura | COMPLETED | NCT02848326 |
| Atogepant | Other | Phase PHASE2 | Migraine, With or Without Aura | COMPLETED | NCT02848326 |
| SkinMedica Essential Defense Mineral Shield Broad Spectrum SPF 35 Sunscreen | Other | Approved | Melasma | COMPLETED | NCT02977507 |
| SkinMedica Rejuvenative Moisturizer | Other | Approved | Melasma | COMPLETED | NCT02977507 |
| SkinMedica Facial Cleanser | Other | Approved | Melasma | COMPLETED | NCT02977507 |
| 4% Hydroquinone Topical Cream | Other | Approved | Melasma | COMPLETED | NCT02977507 |
| Lytera 2.0 | Other | Approved | Melasma | COMPLETED | NCT02977507 |
| Placebo-matching Ubrogepant | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02828020 |
| Ubrogepant | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02828020 |
| Placebo-matching Ubrogepant | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02828020 |
| Ubrogepant | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02828020 |
| Rescue medication | Drug | Phase PHASE2 | Migraine | COMPLETED | NCT01613248 |
| Placebo-matching MK-1602 | Other | Phase PHASE2 | Migraine | COMPLETED | NCT01613248 |
| MK-1602 | Other | Phase PHASE2 | Migraine | COMPLETED | NCT01613248 |
| botulinum toxin Type A | Other | Preclinical | Migraine Disorders | COMPLETED | NCT01432379 |
| JUVÉDERM® VOLUMA® XC | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| JUVÉDERM® ULTRA PLUS XC | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| JUVÉDERM® ULTRA XC | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| JUVÉDERM® VOLUMA® XC | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| JUVÉDERM® ULTRA PLUS XC | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| JUVÉDERM® ULTRA XC | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT02176356 |
| A gel of hyaluronic acid (concentration of 20 mg/mL) | Other | Phase PHASE4 | Nasolabial Folds | COMPLETED | NCT00850889 |
| Hyaluronic acid gel (24 mg/mL) with 0.3% lidocaine | Other | Phase PHASE4 | Nasolabial Folds | COMPLETED | NCT00850889 |
| A gel of hyaluronic acid (concentration of 20 mg/mL) | Other | Phase PHASE4 | Nasolabial Folds | COMPLETED | NCT00850889 |
| Hyaluronic acid gel (24 mg/mL) with 0.3% lidocaine | Other | Phase PHASE4 | Nasolabial Folds | COMPLETED | NCT00850889 |
| A gel of hyaluronic acid (concentration of 20 mg/mL) | Other | Phase PHASE4 | Nasolabial Folds | COMPLETED | NCT00850889 |
| Hyaluronic acid gel (24 mg/mL) with 0.3% lidocaine | Other | Phase PHASE4 | Nasolabial Folds | COMPLETED | NCT00850889 |
| Restylane-L® | Other | Approved | Lip Volume Enhancement | COMPLETED | NCT01579305 |
| Juvéderm® Volbella with Lidocaine | Other | Approved | Lip Volume Enhancement | COMPLETED | NCT01579305 |
| Restylane-L® | Other | Approved | Lip Volume Enhancement | COMPLETED | NCT01579305 |
| Juvéderm® Volbella with Lidocaine | Other | Approved | Lip Volume Enhancement | COMPLETED | NCT01579305 |
| botulinum toxin type A | Other | Phase PHASE4 | Glabellar Lines | COMPLETED | NCT01271452 |
| bimatoprost 0.03% | Other | Phase PHASE4 | Eyelash Hypotrichosis | COMPLETED | NCT01229423 |
| botulinum toxin Type A | Other | Phase PHASE4 | Skin Aging | COMPLETED | NCT00856414 |
| on-label facial injection | Other | Approved | Facial Photodamage | COMPLETED | NCT03559972 |
| on-label facial injection | Other | Approved | Facial Photodamage | COMPLETED | NCT03559972 |
| onabotulinumtoxinA | Other | Preclinical | Muscle Spasticity | COMPLETED | NCT01930786 |
| Placebo | Other | Phase PHASE4 | Irritable Bowel Syndrome With Diarrhea | COMPLETED | NCT02959983 |
| Eluxadoline | Other | Phase PHASE4 | Irritable Bowel Syndrome With Diarrhea | COMPLETED | NCT02959983 |
| Placebo | Other | Phase PHASE4 | Irritable Bowel Syndrome With Diarrhea | COMPLETED | NCT02959983 |
| Eluxadoline | Other | Phase PHASE4 | Irritable Bowel Syndrome With Diarrhea | COMPLETED | NCT02959983 |
| Intravitreal anti-VEGF injection | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT02471651 |
| Dexamethasone intravitreal implant (0.7 mg) | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT02471651 |
| 0.9% saline solution | Other | Phase PHASE2 | Skin Quality | COMPLETED | NCT03097835 |
| Topical anesthesia | Other | Phase PHASE2 | Skin Quality | COMPLETED | NCT03097835 |
| Hyper-Diluted Botox | Other | Phase PHASE2 | Skin Quality | COMPLETED | NCT03097835 |
| Solifenacin | Other | Phase PHASE2 | Dementia of Alzheimer's Type | COMPLETED | NCT02549196 |
| Donepezil | Other | Phase PHASE2 | Dementia of Alzheimer's Type | COMPLETED | NCT02549196 |
| Solifenacin | Other | Phase PHASE2 | Dementia of Alzheimer's Type | COMPLETED | NCT02549196 |
| Donepezil | Other | Phase PHASE2 | Dementia of Alzheimer's Type | COMPLETED | NCT02549196 |
| Solifenacin | Other | Phase PHASE2 | Dementia of Alzheimer's Type | COMPLETED | NCT02549196 |
| Donepezil | Other | Phase PHASE2 | Dementia of Alzheimer's Type | COMPLETED | NCT02549196 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Paritaprevir/ritonavir/ombitasvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Paritaprevir/ritonavir/ombitasvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Paritaprevir/ritonavir/ombitasvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02725866 |
| Placebo-matching Ubrogepant | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02867709 |
| Ubrogepant | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02867709 |
| Botox | Other | Phase PHASE1 | Prostatitis | TERMINATED | NCT00529386 |
| Botox | Other | Phase PHASE1 | Prostatitis | TERMINATED | NCT00529386 |
| AGN-223575 vehicle ophthalmic solution | Other | Phase PHASE2 | Dry Eye Syndromes | COMPLETED | NCT02435914 |
| AGN-223575 ophthalmic solution | Other | Phase PHASE2 | Dry Eye Syndromes | COMPLETED | NCT02435914 |
| VOLBELLA® with lidocaine | Other | Approved | Infra-orbital Skin Depressions | COMPLETED | NCT02176421 |
| carboxymethylcellulose sodium based eye drops | Other | Phase PHASE3 | Bilateral LASIK Surgery | COMPLETED | NCT01886690 |
| carboxymethylcellulose sodium based new eye drop formulation | Other | Phase PHASE3 | Bilateral LASIK Surgery | COMPLETED | NCT01886690 |
| carboxymethylcellulose sodium based eye drop solution | Other | Phase PHASE3 | Contact Lens Lubrication | COMPLETED | NCT01844388 |
| carboxymethylcellulose based eye drop formula | Other | Phase PHASE3 | Contact Lens Lubrication | COMPLETED | NCT01844388 |
| Normal Saline | Other | Phase PHASE3 | Lateral Canthus Rhytides | COMPLETED | NCT01797081 |
| botulinum toxin Type A (12 U) | Other | Phase PHASE3 | Lateral Canthus Rhytides | COMPLETED | NCT01797081 |
| botulinum toxin Type A (24 U) | Other | Phase PHASE3 | Lateral Canthus Rhytides | COMPLETED | NCT01797081 |
| Crosslinked hyaluronic acid dermal filler | Other | Approved | Moderate to Severe Nasolabial Folds | COMPLETED | NCT01680497 |
| bimatoprost 0.03% | Other | Preclinical | Eyelash Hypotrichosis | COMPLETED | NCT01623479 |
| bimatoprost 0.03% | Other | Preclinical | Eyelash Hypotrichosis | COMPLETED | NCT01623479 |
| botulinum toxin Type A | Other | Preclinical | Glabellar Lines | COMPLETED | NCT01608672 |
| Carboxymethylcellulose Based Lubricant Eye Drops | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01459588 |
| Carboxymethylcellulose Based Preservative-Free Lubricant Eye Drops | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01459588 |
| Carboxymethylcellulose Based Eye Drop Formulation B | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01459588 |
| Carboxymethylcellulose Based Eye Drop Formulation A | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01459588 |
| Carboxymethylcellulose Based Lubricant Eye Drops | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01459588 |
| Carboxymethylcellulose Based Preservative-Free Lubricant Eye Drops | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01459588 |
| Carboxymethylcellulose Based Eye Drop Formulation B | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01459588 |
| Carboxymethylcellulose Based Eye Drop Formulation A | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01459588 |
| Sham Injection | Other | Phase PHASE2 | Age-related Macular Degeneration | COMPLETED | NCT01397409 |
| ranibizumab | Other | Phase PHASE2 | Age-related Macular Degeneration | COMPLETED | NCT01397409 |
| AGN-150998 | Other | Phase PHASE2 | Age-related Macular Degeneration | COMPLETED | NCT01397409 |
| carboxymethylcellulose sodium based Eye Drops | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01294384 |
| carboxymethylcellulose sodium based New Eye Drop Formulation 2 | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01294384 |
| carboxymethylcellulose sodium based New Eye Drop Formulation 1 | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT01294384 |
| hyaluronic acid gel | Other | Approved | Lip Augmentation | COMPLETED | NCT01197495 |
| hyaluronic acid gel | Other | Approved | Lip Augmentation | COMPLETED | NCT01197495 |
| normal saline | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01189760 |
| onabotulinumtoxinA 44 U | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01189760 |
| onabotulinumtoxinA 24 U | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01189760 |
| normal saline | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01189760 |
| onabotulinumtoxinA 44 U | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01189760 |
| onabotulinumtoxinA 24 U | Other | Phase PHASE3 | Facial Rhytides | COMPLETED | NCT01189760 |
| Olopatadine | Other | Phase PHASE3 | Conjunctivitis, Allergic | COMPLETED | NCT02161146 |
| Vehicle to AGN-229666 | Other | Phase PHASE3 | Conjunctivitis, Allergic | COMPLETED | NCT02161146 |
| AGN-229666 | Other | Phase PHASE3 | Conjunctivitis, Allergic | COMPLETED | NCT02161146 |
| dexamethasone implant | Other | Phase PHASE4 | Macular Edema | COMPLETED | NCT01903720 |
| dexamethasone implant | Other | Phase PHASE4 | Macular Edema | COMPLETED | NCT01903720 |
| botulinum toxin Type A | Other | Phase PHASE4 | Glabellar Rhytides | COMPLETED | NCT01814670 |
| Dexamethasone Intravitreal Implant | Other | Preclinical | Macular Edema | COMPLETED | NCT01805323 |
| Normal Saline | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT01777620 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT01777620 |
| Normal Saline | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT01777620 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Facial Rhytides | COMPLETED | NCT01777620 |
| botulinum toxin Type A | Other | Preclinical | Facial Rhytides | COMPLETED | NCT01608659 |
| ranibizumab | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT01492400 |
| dexamethasone Intravitreal Implant | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT01492400 |
| ranibizumab | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT01492400 |
| dexamethasone Intravitreal Implant | Other | Phase PHASE2 | Macular Edema | COMPLETED | NCT01492400 |
| Normal Saline | Other | Approved | Facial Rhytides | COMPLETED | NCT01391299 |
| botulinum toxin Type A | Other | Approved | Facial Rhytides | COMPLETED | NCT01391299 |
| Normal Saline | Other | Approved | Facial Rhytides | COMPLETED | NCT01391299 |
| botulinum toxin Type A | Other | Approved | Facial Rhytides | COMPLETED | NCT01391299 |
| Bimatoprost 0.03% Ophthalmic Solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT01099774 |
| Bimatoprost 0.03% Formulation B Ophthalmic Solution | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT01099774 |
| 0.03% Bimatoprost Ophthalmic Solution and 0.5% Timolol Ophthalmic Solution | Other | Approved | Open-angle Glaucoma | COMPLETED | NCT01068964 |
| 0.03% Bimatoprost/0.5% Timolol Ophthalmic Solution | Other | Approved | Open-angle Glaucoma | COMPLETED | NCT01068964 |
| Vehicle Sterile Solution | Other | Phase PHASE4 | Eyelash Hypotrichosis | COMPLETED | NCT01023841 |
| bimatoprost ophthalmic solution 0.03% | Other | Phase PHASE4 | Eyelash Hypotrichosis | COMPLETED | NCT01023841 |
| carboxymethylcellulose-based lubricant eye drops | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT02121847 |
| cyclosporine 0.05% ophthalmic emulsion | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT02121847 |
| carboxymethylcellulose-based lubricant eye drops | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT02121847 |
| cyclosporine 0.05% ophthalmic emulsion | Other | Phase PHASE4 | Dry Eye Syndromes | COMPLETED | NCT02121847 |
| Bimatoprost 0.03% | Other | Phase PHASE4 | Glaucoma, Open-Angle | COMPLETED | NCT02061683 |
| Anti-VEGF | Other | Preclinical | Retinal Vein Occlusion | COMPLETED | NCT01918371 |
| Prostaglandin Analogue -Containing IOP-Lowering Therapy | Drug | Preclinical | Glaucoma, Open-Angle | COMPLETED | NCT01735214 |
| ranibizumab | Other | Phase PHASE4 | Retinal Vein Occlusion | COMPLETED | NCT01427751 |
| dexamethasone intravitreal implant | Other | Phase PHASE4 | Retinal Vein Occlusion | COMPLETED | NCT01427751 |
| latanoprost 0.005% ophthalmic solution | Other | Phase PHASE4 | Glaucoma, Open-Angle | COMPLETED | NCT01243567 |
| bimatoprost 0.03%/timolol 0.5% combination ophthalmic solution | Other | Phase PHASE4 | Glaucoma, Open-Angle | COMPLETED | NCT01243567 |
| Bimatoprost Ophthalmic Solution | Other | Preclinical | Glaucoma, Primary Open Angle | COMPLETED | NCT01853085 |
| dexamethasone 700 ug intravitreal implant | Other | Preclinical | Macular Edema | COMPLETED | NCT01571557 |
| Sham | Other | Phase PHASE2 | Geographic Atrophy | TERMINATED | NCT02087085 |
| 400 µg Brimonidine Implant | Other | Phase PHASE2 | Geographic Atrophy | TERMINATED | NCT02087085 |
| Sham | Other | Phase PHASE2 | Geographic Atrophy | TERMINATED | NCT02087085 |
| 400 µg Brimonidine Implant | Other | Phase PHASE2 | Geographic Atrophy | TERMINATED | NCT02087085 |
| solifenacin placebo | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT01767519 |
| Botox placebo (normal saline) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT01767519 |
| solifenacin | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT01767519 |
| BOTOX® | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT01767519 |
| solifenacin placebo | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT01767519 |
| Botox placebo (normal saline) | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT01767519 |
| solifenacin | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT01767519 |
| BOTOX® | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT01767519 |
| Dexamethasone | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00799227 |
| Dexamethasone | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00799227 |
| latanoprost 0.005% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00735449 |
| timolol maleate 0.5% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00735449 |
| Fixed combination of brimonidine tartrate 0.2% timolol maleate 0.5% | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00735449 |
| placebo | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00538304 |
| bimatoprost eye drops | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00538304 |
| placebo | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00538304 |
| bimatoprost eye drops | Other | Phase PHASE2 | Glaucoma | COMPLETED | NCT00538304 |
| placebo eye drops | Other | Phase PHASE3 | Bacterial Conjunctivitis | COMPLETED | NCT00518089 |
| Gatifloxacin 0.5% eye drops | Other | Phase PHASE3 | Bacterial Conjunctivitis | COMPLETED | NCT00518089 |
| placebo eye drops | Other | Phase PHASE3 | Bacterial Conjunctivitis | COMPLETED | NCT00518089 |
| Gatifloxacin 0.5% eye drops | Other | Phase PHASE3 | Bacterial Conjunctivitis | COMPLETED | NCT00518089 |
| Sham Injection | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168324 |
| 350 µg Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168324 |
| 700 µg Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168324 |
| Sham Injection | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168298 |
| 350 µg Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168298 |
| 700 µg Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT00168298 |
| Dapsone 5% Gel | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT01773122 |
| Dapsone Formulation C | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT01773122 |
| Dapsone Formulation B | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT01773122 |
| Dapsone Formulation A | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT01773122 |
| Dapsone 5% Gel | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT01773122 |
| Dapsone Formulation C | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT01773122 |
| Dapsone Formulation B | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT01773122 |
| Dapsone Formulation A | Other | Phase PHASE1 | Acne Vulgaris | COMPLETED | NCT01773122 |
| bimatoprost 0.03% ophthalmic solution; hypromellose 0.2% eyedrops | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01170884 |
| fixed combination of brimonidine tartrate 0.2% timolol maleate 0.5% ophthalmic solution; bimatoprost 0.03% ophthalmic solution | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT01170884 |
| fixed combination of dorzolamide hydrochloride timolol maleate ophthalmic solution | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00811850 |
| fixed combination of brimonidine tartrate 0.2% timolol maleate 0.5% ophthalmic solution | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00811850 |
| latanoprost 0.005% eye drops | Other | Phase PHASE4 | Open Angle Glaucoma | COMPLETED | NCT00539526 |
| travoprost 0.004% | Other | Phase PHASE4 | Open Angle Glaucoma | COMPLETED | NCT00539526 |
| Bimatoprost 0.03% | Other | Phase PHASE4 | Open Angle Glaucoma | COMPLETED | NCT00539526 |
| Laser Photocoagulation | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00464685 |
| Sham injection | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00464685 |
| Dexamethasone | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00464685 |
| Laser Photocoagulation | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00464685 |
| Sham injection | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00464685 |
| Dexamethasone | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT00464685 |
| Cyclosporine Ophthalmic Emulsion 0.05% | Other | Preclinical | Dry Eye Disease | COMPLETED | NCT00827255 |
| sham | Other | Phase PHASE2 | Choroidal Neovascularization | COMPLETED | NCT00511706 |
| ranibizumab | Other | Phase PHASE2 | Choroidal Neovascularization | COMPLETED | NCT00511706 |
| dexamethasone | Other | Phase PHASE2 | Choroidal Neovascularization | COMPLETED | NCT00511706 |
| travoprost 0.004% eye drops | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00440011 |
| bimatoprost 0.03% eye drops | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00440011 |
| travoprost 0.004% eye drops | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00440011 |
| bimatoprost 0.03% eye drops | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT00440011 |
| Placebo | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT02147197 |
| Ulipristal acetate (UPA) | Other | Phase PHASE3 | Leiomyoma | COMPLETED | NCT02147197 |
| Placebo (Normal Saline) | Other | Phase PHASE3 | Urinary Incontinence | COMPLETED | NCT01600716 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Urinary Incontinence | COMPLETED | NCT01600716 |
| botulinum toxin Type A | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00915525 |
| No treatment | Drug | Preclinical | Health | COMPLETED | NCT01518270 |
| Botulinum Toxin Type A 200U | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00876447 |
| Botulinum Toxin Type A 300U | Other | Phase PHASE3 | Overactive Bladder | COMPLETED | NCT00876447 |
| Injectable sodium deoxycholate with Triamcinolone acetate | Other | Phase PHASE4 | Adiposity | COMPLETED | NCT03361176 |
| Injectable sodium deoxycholate | Other | Phase PHASE4 | Adiposity | COMPLETED | NCT03361176 |
| Control | Other | Approved | Moderate to Severe Nasolabial Folds | COMPLETED | NCT01976663 |
| JUVEDERM VOLIFT® XC | Other | Approved | Moderate to Severe Nasolabial Folds | COMPLETED | NCT01976663 |
| Placebo | Other | Phase PHASE1 | Human Abuse Potential | COMPLETED | NCT03799900 |
| Ketamine | Other | Phase PHASE1 | Human Abuse Potential | COMPLETED | NCT03799900 |
| Rapastinel | Other | Phase PHASE1 | Human Abuse Potential | COMPLETED | NCT03799900 |
| Placebo | Other | Phase PHASE1 | Human Abuse Potential | COMPLETED | NCT03799900 |
| Ketamine | Other | Phase PHASE1 | Human Abuse Potential | COMPLETED | NCT03799900 |
| Rapastinel | Other | Phase PHASE1 | Human Abuse Potential | COMPLETED | NCT03799900 |
| Eye wash | Other | Approved | Dry Eye | COMPLETED | NCT03332342 |
| Eye wash | Other | Approved | Dry Eye | COMPLETED | NCT03332342 |
| Normal saline | Other | Phase PHASE2 | Masseter Muscle Hypertrophy | COMPLETED | NCT02010775 |
| botulinum toxin Type A | Other | Phase PHASE2 | Masseter Muscle Hypertrophy | COMPLETED | NCT02010775 |
| injection of NaCl 0.9% | Other | Phase PHASE3 | COMPARISON BETWEEN GROUP TREATED WITH BOTULINUM TOXIN AND PLACEBO | COMPLETED | NCT01821573 |
| botulinum toxin type A | Other | Phase PHASE3 | COMPARISON BETWEEN GROUP TREATED WITH BOTULINUM TOXIN AND PLACEBO | COMPLETED | NCT01821573 |
| Skin Imaging | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Sunscreen | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Moisturizing lotion | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Facial cleanser | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Retinol Complex 0.5 | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Skin Imaging | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Sunscreen | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Moisturizing lotion | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Facial cleanser | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Retinol Complex 0.5 | Other | Approved | Skin Care | COMPLETED | NCT03302559 |
| Optive® Fusion + Optive® Gel Drop | Other | Approved | Dry Eye | COMPLETED | NCT03208673 |
| Placebo | Other | Phase PHASE3 | Stroke With Hemiparesis | COMPLETED | NCT01422161 |
| Botulinum Toxin commonly known as BOTOX® | Other | Phase PHASE3 | Stroke With Hemiparesis | COMPLETED | NCT01422161 |
| Dexamethasone pellet | Other | Phase PHASE4 | Uveitis, Intermediate | COMPLETED | NCT02049476 |
| Test product (B) Exemestane | Other | Phase PHASE1 | Healthy | WITHDRAWN | NCT01760980 |
| Reference product (A) Aromasin (Exemestane) | Other | Phase PHASE1 | Healthy | WITHDRAWN | NCT01760980 |
| bimatoprost vehicle solution | Other | Phase PHASE3 | Eyelash Hypotrichosis | COMPLETED | NCT01391286 |
| bimatoprost solution 0.03% | Other | Phase PHASE3 | Eyelash Hypotrichosis | COMPLETED | NCT01391286 |
| bimatoprost vehicle solution | Other | Phase PHASE3 | Eyelash Hypotrichosis | COMPLETED | NCT01391273 |
| bimatoprost solution 0.03% | Other | Phase PHASE3 | Eyelash Hypotrichosis | COMPLETED | NCT01391273 |
| bimatoprost vehicle solution | Other | Phase PHASE3 | Eyelash Hypotrichosis | COMPLETED | NCT01391273 |
| bimatoprost solution 0.03% | Other | Phase PHASE3 | Eyelash Hypotrichosis | COMPLETED | NCT01391273 |
| Clobex TM 0.05% Lotion, single exposure | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864500 |
| Clobetasol Propionate 0.05% lotion, single exposure | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864500 |
| Clobex TM (Clobetasol) 0.05% Lotion, single exposure | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864240 |
| Ketamine Matched Placebo | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Alprazolam Matched Placebo | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Rapastinel Matched Placebo | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Ketamine | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Alprazolam | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Rapastinel | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Ketamine Matched Placebo | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Alprazolam Matched Placebo | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Rapastinel Matched Placebo | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Ketamine | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Alprazolam | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Rapastinel | Other | Phase PHASE1 | Driving Performance | COMPLETED | NCT03814733 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | WITHDRAWN | NCT03855865 |
| Vortioxetine | Other | Phase PHASE3 | Depressive Disorder, Major | WITHDRAWN | NCT03855865 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | WITHDRAWN | NCT03855865 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | WITHDRAWN | NCT03855865 |
| Vortioxetine | Other | Phase PHASE3 | Depressive Disorder, Major | WITHDRAWN | NCT03855865 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | WITHDRAWN | NCT03855865 |
| Botox | Other | Phase PHASE4 | Glabellar Furrows | COMPLETED | NCT00856999 |
| Placebo | Other | Phase PHASE2 | Diabetes Mellitus | COMPLETED | NCT02357420 |
| Relamorelin | Other | Phase PHASE2 | Diabetes Mellitus | COMPLETED | NCT02357420 |
| Placebo | Other | Phase PHASE2 | Fecal Incontinence | WITHDRAWN | NCT03489265 |
| Eluxadoline 100 mg | Other | Phase PHASE2 | Fecal Incontinence | WITHDRAWN | NCT03489265 |
| Moisturizing Lotion | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Towel | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Sunscreen | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Cleanser | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Vehicle Foam | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Finacea® (Azelaic Acid) Foam | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Generic Azelaic Acid Foam | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Moisturizing Lotion | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Towel | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Sunscreen | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Cleanser | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Vehicle Foam | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Finacea® (Azelaic Acid) Foam | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| Generic Azelaic Acid Foam | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT03287791 |
| dexamethasone intravitreal implant | Other | Preclinical | Non-infectious Uveitis | TERMINATED | NCT02951975 |
| JUVÉDERM VOLUMA® XC injectable gel with needle | Other | Approved | Age-related Volume Deficit in the Mid-face | COMPLETED | NCT03438266 |
| JUVÉDERM VOLUMA® XC injectable gel with cannula | Other | Approved | Age-related Volume Deficit in the Mid-face | COMPLETED | NCT03438266 |
| Botulinum Toxin Type A | Other | Phase PHASE3 | Pediatrics | COMPLETED | NCT01603641 |
| Botulinum Toxin Type A | Other | Phase PHASE3 | Pediatrics | COMPLETED | NCT01603615 |
| Usual Care | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02873221 |
| Placebo-matching Ubrogepant | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02873221 |
| Ubrogepant | Other | Phase PHASE3 | Migraine, With or Without Aura | COMPLETED | NCT02873221 |
| Bevacizumab | Other | Phase PHASE2 | Macular Edema | TERMINATED | NCT01471054 |
| Ozurdex | Other | Phase PHASE2 | Macular Edema | TERMINATED | NCT01471054 |
| Bevacizumab | Other | Phase PHASE2 | Macular Edema | TERMINATED | NCT01471054 |
| Ozurdex | Other | Phase PHASE2 | Macular Edema | TERMINATED | NCT01471054 |
| silk surgical scaffold | Other | Approved | Mastopexy | COMPLETED | NCT02293798 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03255382 |
| Fumaderm | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03255382 |
| Placebo | Other | Phase PHASE3 | Breast Cancer | COMPLETED | NCT01591746 |
| Botulinum Toxin Type A | Other | Phase PHASE3 | Breast Cancer | COMPLETED | NCT01591746 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02932943 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02932943 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02932943 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02932943 |
| Facial Cleanser | Other | Preclinical | Skin Care | COMPLETED | NCT03767400 |
| Skin Imaging | Other | Preclinical | Skin Care | COMPLETED | NCT03767400 |
| Risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT02203851 |
| Risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT02203851 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02943577 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02943577 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02943577 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02943577 |
| Vehicle to AGN-199201 | Other | Phase PHASE3 | Erythema | COMPLETED | NCT02131636 |
| AGN-199201 | Other | Phase PHASE3 | Erythema | COMPLETED | NCT02131636 |
| Oxymetazoline HCL Cream 1.0% | Other | Phase PHASE3 | Erythema | COMPLETED | NCT02095158 |
| AGN-199201 Vehicle | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT01735201 |
| AGN-199201 Dose C | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT01735201 |
| AGN-199201 Dose B | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT01735201 |
| AGN-199201 Dose A | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT01735201 |
| AGN-199201 Vehicle | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT01735201 |
| AGN-199201 Dose C | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT01735201 |
| AGN-199201 Dose B | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT01735201 |
| AGN-199201 Dose A | Other | Phase PHASE2 | Rosacea | COMPLETED | NCT01735201 |
| No Intervention | Other | Preclinical | Erythema | COMPLETED | NCT01636765 |
| AGN-199201 Vehicle | Other | Phase PHASE1 | Rosacea | COMPLETED | NCT01579084 |
| AGN-199201 Formulation C | Other | Phase PHASE1 | Rosacea | COMPLETED | NCT01579084 |
| AGN-199201 Formulation B | Other | Phase PHASE1 | Rosacea | COMPLETED | NCT01579084 |
| AGN-199201 Formulation A | Other | Phase PHASE1 | Rosacea | COMPLETED | NCT01579084 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Urinary Incontinence | COMPLETED | NCT01852045 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Urinary Incontinence | COMPLETED | NCT01852045 |
| Rapastinel (225 mg/450 mg IV administration) | Other | Phase PHASE2 | Major Depressive Disorder | TERMINATED | NCT02192099 |
| Rapastinel (225 mg/450 mg IV administration) | Other | Phase PHASE2 | Major Depressive Disorder | TERMINATED | NCT02192099 |
| Placebo | Other | Phase PHASE3 | Asthma | COMPLETED | NCT02495168 |
| Symbicort® (Budesonide/Formoterol Fumarate Dihydrate) | Other | Phase PHASE3 | Asthma | COMPLETED | NCT02495168 |
| Generic Budesonide/Formoterol Fumarate Dihydrate | Other | Phase PHASE3 | Asthma | COMPLETED | NCT02495168 |
| Placebo | Other | Phase PHASE3 | Asthma | COMPLETED | NCT02495168 |
| Symbicort® (Budesonide/Formoterol Fumarate Dihydrate) | Other | Phase PHASE3 | Asthma | COMPLETED | NCT02495168 |
| Generic Budesonide/Formoterol Fumarate Dihydrate | Other | Phase PHASE3 | Asthma | COMPLETED | NCT02495168 |
| Venetoclax | Other | Phase PHASE1 | Cancer | COMPLETED | NCT02391480 |
| ABBV-075 | Other | Phase PHASE1 | Cancer | COMPLETED | NCT02391480 |
| Venetoclax | Other | Phase PHASE1 | Cancer | COMPLETED | NCT02391480 |
| ABBV-075 | Other | Phase PHASE1 | Cancer | COMPLETED | NCT02391480 |
| Venetoclax | Other | Phase PHASE1 | Cancer | COMPLETED | NCT02391480 |
| ABBV-075 | Other | Phase PHASE1 | Cancer | COMPLETED | NCT02391480 |
| extended intervention | Other | Approved | Cross-Sectional Study | COMPLETED | NCT03079375 |
| basic intervention | Other | Approved | Cross-Sectional Study | COMPLETED | NCT03079375 |
| extended intervention | Other | Approved | Cross-Sectional Study | COMPLETED | NCT03079375 |
| basic intervention | Other | Approved | Cross-Sectional Study | COMPLETED | NCT03079375 |
| extended intervention | Other | Approved | Cross-Sectional Study | COMPLETED | NCT03079375 |
| basic intervention | Other | Approved | Cross-Sectional Study | COMPLETED | NCT03079375 |
| Placebo Tablet | Other | Phase PHASE3 | Diarrhea | COMPLETED | NCT02498418 |
| Xifaxan® | Other | Phase PHASE3 | Diarrhea | COMPLETED | NCT02498418 |
| Rifaximin | Other | Phase PHASE3 | Diarrhea | COMPLETED | NCT02498418 |
| Vehicle Cream | Other | Phase PHASE3 | Actinic Keratosis | COMPLETED | NCT02120898 |
| Zyclara® | Other | Phase PHASE3 | Actinic Keratosis | COMPLETED | NCT02120898 |
| Imiquimod | Other | Phase PHASE3 | Actinic Keratosis | COMPLETED | NCT02120898 |
| Vehicle Cream | Other | Phase PHASE3 | Actinic Keratosis | COMPLETED | NCT02120898 |
| Zyclara® | Other | Phase PHASE3 | Actinic Keratosis | COMPLETED | NCT02120898 |
| Imiquimod | Other | Phase PHASE3 | Actinic Keratosis | COMPLETED | NCT02120898 |
| Placebo (saline) | Other | Phase PHASE4 | Urinary Bladder, Overactive | COMPLETED | NCT03052764 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Urinary Bladder, Overactive | COMPLETED | NCT03052764 |
| AGN-214868 Placebo (Vehicle) | Other | Phase PHASE2 | Neuralgia, Postherpetic | TERMINATED | NCT01678924 |
| AGN-214868 | Other | Phase PHASE2 | Neuralgia, Postherpetic | TERMINATED | NCT01678924 |
| AGN-214868 Placebo (Vehicle) | Other | Phase PHASE2 | Neuralgia, Postherpetic | TERMINATED | NCT01678924 |
| AGN-214868 | Other | Phase PHASE2 | Neuralgia, Postherpetic | TERMINATED | NCT01678924 |
| Nabumetone 750 mg tablets, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00864604 |
| Vehicle Foam | Other | Phase PHASE3 | ACTINIC KERATOSIS | COMPLETED | NCT03200912 |
| Generic Ingenol Mebutate | Other | Phase PHASE3 | ACTINIC KERATOSIS | COMPLETED | NCT03200912 |
| Ingenol Mebutate (Picato®) | Other | Phase PHASE3 | ACTINIC KERATOSIS | COMPLETED | NCT03200912 |
| placebo | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT02289352 |
| Brimonidine | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT02289352 |
| placebo | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT02289352 |
| Brimonidine | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT02289352 |
| Usual Care | Other | Phase PHASE4 | Bacterial Infections | COMPLETED | NCT03233438 |
| Dalbavancin | Other | Phase PHASE4 | Bacterial Infections | COMPLETED | NCT03233438 |
| OnabotulinumtoxinA 50 UNT [Botox Cosmetic] | Other | Phase PHASE4 | Aging | NOT_YET_RECRUITING | NCT04240535 |
| placebo | Other | Phase PHASE3 | BACTERIAL VAGINOSIS | COMPLETED | NCT02210689 |
| clindamycin phosphate vaginal cream 2% | Other | Phase PHASE3 | BACTERIAL VAGINOSIS | COMPLETED | NCT02210689 |
| placebo | Other | Phase PHASE3 | BACTERIAL VAGINOSIS | COMPLETED | NCT02210689 |
| clindamycin phosphate vaginal cream 2% | Other | Phase PHASE3 | BACTERIAL VAGINOSIS | COMPLETED | NCT02210689 |
| Intranasal Tear Neurostimulator | Other | Approved | Dry Eye Syndromes | COMPLETED | NCT02313454 |
| Intranasal Tear Neurostimulator | Other | Approved | Dry Eye Syndromes | COMPLETED | NCT02313454 |
| Endura, Refresh artificial tears | Other | Approved | Dry Eye | TERMINATED | NCT02199964 |
| Cyclosporin 0.05% emulsion | Other | Approved | Dry Eye | TERMINATED | NCT02199964 |
| No Intervention | Other | Preclinical | Leiomyoma | COMPLETED | NCT02580578 |
| No Intervention | Other | Preclinical | Leiomyoma | COMPLETED | NCT02580578 |
| Placebo-matching Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02951988 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02951988 |
| Placebo-matching Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02951988 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02951988 |
| Placebo-matching Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02951988 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | COMPLETED | NCT02951988 |
| Botulinum toxin A | Other | Phase PHASE4 | Cervical Dystonia | COMPLETED | NCT00773253 |
| bimatoprost 0.03% | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 10 µg generation 1 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 15 µg generation 1 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 6 µg generation 2 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 10 µg generation 2 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 15 µg generation 2 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 20 µg generation 2 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 0.03% | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 10 µg generation 1 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 15 µg generation 1 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 6 µg generation 2 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 10 µg generation 2 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 15 µg generation 2 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| bimatoprost 20 µg generation 2 | Other | Phase PHASE1 | Open-Angle Glaucoma | COMPLETED | NCT01157364 |
| Lytera | Other | Approved | Photoaging | COMPLETED | NCT03661697 |
| Basic Skin Care Regimen | Other | Approved | Photoaging | COMPLETED | NCT03661697 |
| Laser Therapy | Drug | Approved | Photoaging | COMPLETED | NCT03661697 |
| Lytera | Other | Approved | Photoaging | COMPLETED | NCT03661697 |
| Basic Skin Care Regimen | Other | Approved | Photoaging | COMPLETED | NCT03661697 |
| Laser Therapy | Drug | Approved | Photoaging | COMPLETED | NCT03661697 |
| Optive | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02871440 |
| Optive Advanced | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02871440 |
| Omega 3 | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02871440 |
| Optive | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02871440 |
| Optive Advanced | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02871440 |
| Omega 3 | Other | Phase PHASE3 | Dry Eye Syndromes | COMPLETED | NCT02871440 |
| Placebo | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT02616614 |
| Clindamycin/benzoyl peroxide gel | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT02616614 |
| Onexton | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT02616614 |
| Pimecrolimus Cream, 1% | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT02791308 |
| Vehicle cream | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT02791308 |
| Pimecrolimus Cream 1% (Valeant) | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT02791308 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Healthy | COMPLETED | NCT03373162 |
| Placebo/Vehicle cream | Other | Phase PHASE3 | Moderate to Severe Papulopustular Rosacea | COMPLETED | NCT02840461 |
| Ivermectin Cream, 1% | Other | Phase PHASE3 | Moderate to Severe Papulopustular Rosacea | COMPLETED | NCT02840461 |
| Finacea | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT02120924 |
| Vehicle | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT02120924 |
| Azelaic acid | Other | Phase PHASE3 | Rosacea | COMPLETED | NCT02120924 |
| CPC-201 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT02185053 |
| CPC-201 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT02185053 |
| CPC-201 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT02185053 |
| Timolol Vehicle (placebo) | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02247804 |
| Sham: Applicator Without Needle | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02247804 |
| Active Comparator: Timolol 0.5% | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02247804 |
| Bimatoprost SR | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02247804 |
| Vehicle foam | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT02267746 |
| Tazarotene (Actavis) | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT02267746 |
| Tazarotene (Fabior™) | Other | Phase PHASE3 | Acne Vulgaris | COMPLETED | NCT02267746 |
| placebo gel | Other | Phase PHASE3 | Acne | COMPLETED | NCT02651220 |
| Adapalene and Benzoyl Peroxide Gel | Other | Phase PHASE3 | Acne | COMPLETED | NCT02651220 |
| Epiduo® Forte Gel | Other | Phase PHASE3 | Acne | COMPLETED | NCT02651220 |
| Placebo | Other | Approved | Osteoarthritis | COMPLETED | NCT02495857 |
| Euflexxa IA injection | Other | Approved | Osteoarthritis | COMPLETED | NCT02495857 |
| Hyaluronate Injectable Viscosupplement | Other | Approved | Osteoarthritis | COMPLETED | NCT02495857 |
| Placebo | Other | Phase PHASE3 | Ankle Sprain | COMPLETED | NCT02324270 |
| Diclofenac epolamine | Other | Phase PHASE3 | Ankle Sprain | COMPLETED | NCT02324270 |
| Anatomically shaped, silicone-filled breast implants with low projection or extra-full projection | Other | Approved | Breast Augmentation | TERMINATED | NCT01785069 |
| Avinza (morphine sulfate sustained-release) capsules | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00782548 |
| KADIAN (morphine sulfate sustained-release) capsules | Other | Phase PHASE4 | Healthy | COMPLETED | NCT00782548 |
| KADIAN Capsule + alcohol (under fed conditions) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00768183 |
| morphine sulfate IR oral solution + water | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00768183 |
| KADIAN Capsule + water (under fasting conditions) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00768183 |
| KADIAN Capsule + alcohol (under fasting conditions) | Other | Phase PHASE1 | Healthy | COMPLETED | NCT00768183 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03668600 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03668600 |
| Radiotherapy | Drug | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Veliparib | Other | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Carboplatin | Other | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Placebo for Veliparib | Other | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Paclitaxel | Other | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Radiotherapy | Drug | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Veliparib | Other | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Carboplatin | Other | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Placebo for Veliparib | Other | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Paclitaxel | Other | Phase PHASE1 | Non-small Cell Lung Cancer Stage III | TERMINATED | NCT02412371 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03675776 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03675776 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03675776 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03675776 |
| Sham Procedure | Procedure | Phase PHASE3 | Macular Degeneration | COMPLETED | NCT02462486 |
| Ranibizumab | Other | Phase PHASE3 | Macular Degeneration | COMPLETED | NCT02462486 |
| Abicipar Pegol | Other | Phase PHASE3 | Macular Degeneration | COMPLETED | NCT02462486 |
| Abicipar pegol | Other | Phase PHASE2 | Macular Degeneration | COMPLETED | NCT03539549 |
| Pancrelipase | Other | Phase PHASE2 | Pancreatic Cancer | TERMINATED | NCT03469258 |
| TrueTear | Other | Approved | Cataract | COMPLETED | NCT03637348 |
| Placebo | Other | Phase PHASE2 | Depressive Disorder, Major | TERMINATED | NCT03352453 |
| Rapastinel | Other | Phase PHASE2 | Depressive Disorder, Major | TERMINATED | NCT03352453 |
| Placebo | Other | Phase PHASE2 | Depressive Disorder, Major | TERMINATED | NCT03352453 |
| Rapastinel | Other | Phase PHASE2 | Depressive Disorder, Major | TERMINATED | NCT03352453 |
| Placebo | Other | Phase PHASE2 | Depressive Disorder, Major | TERMINATED | NCT03352453 |
| Rapastinel | Other | Phase PHASE2 | Depressive Disorder, Major | TERMINATED | NCT03352453 |
| Placebo | Other | Phase PHASE4 | Chronic Migraine | COMPLETED | NCT01700387 |
| Topiramate | Other | Phase PHASE4 | Chronic Migraine | COMPLETED | NCT01700387 |
| onabotulinumtoxinA | Other | Phase PHASE4 | Chronic Migraine | COMPLETED | NCT01700387 |
| Mometasone nasal spray | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT01850823 |
| Mometasone Nasal Spray | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT01850823 |
| placebo | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT01850823 |
| Mometasone nasal spray | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT01850823 |
| Mometasone Nasal Spray | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT01850823 |
| placebo | Other | Phase PHASE3 | Seasonal Allergic Rhinitis | COMPLETED | NCT01850823 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03560518 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03560518 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03560518 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03560518 |
| Refresh Endura | Other | Phase PHASE4 | Primary Sjogren Syndrome | COMPLETED | NCT02004067 |
| Restasis | Other | Phase PHASE4 | Primary Sjogren Syndrome | COMPLETED | NCT02004067 |
| Ceftazidime-avibactam | Other | Preclinical | Bacterial Infections | COMPLETED | NCT04358991 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03614156 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03614156 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03614156 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03614156 |
| Placebo | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03614156 |
| Rapastinel | Other | Phase PHASE3 | Depressive Disorder, Major | TERMINATED | NCT03614156 |
| placebo | Other | Phase PHASE4 | Spinal Cord Injury | COMPLETED | NCT00320281 |
| botulinum toxin A | Other | Phase PHASE4 | Spinal Cord Injury | COMPLETED | NCT00320281 |
| placebo | Other | Phase PHASE4 | Spinal Cord Injury | COMPLETED | NCT00320281 |
| botulinum toxin A | Other | Phase PHASE4 | Spinal Cord Injury | COMPLETED | NCT00320281 |
| ZELTIQ thermoelectric device | Device | Approved | Subcutaneous Fat | UNKNOWN | NCT04553627 |
| Thermalon Dry Eye Compress | Other | Approved | Meibomian Glands | COMPLETED | NCT03226769 |
| TrueTear™ | Other | Approved | Meibomian Glands | COMPLETED | NCT03226769 |
| Telemedicine follow-up visit | Other | Preclinical | Cervical Dystonia | COMPLETED | NCT03969537 |
| Telemedicine follow-up visit | Other | Preclinical | Cervical Dystonia | COMPLETED | NCT03969537 |
| Bevacizumab Injectable Product | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT04619303 |
| Dexamethasone intravitreal implant | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT04619303 |
| Placebo (Saline) | Other | Approved | Post-stroke Shoulder Pain and Spasticity | COMPLETED | NCT00661089 |
| Botulinum Toxin Type A - OnabotulinumtoxinA | Other | Approved | Post-stroke Shoulder Pain and Spasticity | COMPLETED | NCT00661089 |
| Placebo (Saline) | Other | Approved | Post-stroke Shoulder Pain and Spasticity | COMPLETED | NCT00661089 |
| Botulinum Toxin Type A - OnabotulinumtoxinA | Other | Approved | Post-stroke Shoulder Pain and Spasticity | COMPLETED | NCT00661089 |
| Phacoemulsification | Other | Preclinical | Glaucoma | COMPLETED | NCT03868254 |
| XEN Group | Other | Preclinical | Glaucoma | COMPLETED | NCT03868254 |
| Laser Photocoagulation | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT02121262 |
| Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT02121262 |
| Laser Photocoagulation | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT02121262 |
| Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT02121262 |
| adalimumab (ADA) | Other | Phase PHASE4 | Psoriatic Arthritis | COMPLETED | NCT02814175 |
| methotrexate (MTX) | Other | Phase PHASE4 | Psoriatic Arthritis | COMPLETED | NCT02814175 |
| adalimumab (ADA) | Other | Phase PHASE4 | Psoriatic Arthritis | COMPLETED | NCT02814175 |
| methotrexate (MTX) | Other | Phase PHASE4 | Psoriatic Arthritis | COMPLETED | NCT02814175 |
| Bacteriostatic normal saline | Other | Approved | Herpes Labialis | TERMINATED | NCT01225341 |
| onabotulinumtoxinA | Other | Approved | Herpes Labialis | TERMINATED | NCT01225341 |
| Bacteriostatic normal saline | Other | Approved | Herpes Labialis | TERMINATED | NCT01225341 |
| onabotulinumtoxinA | Other | Approved | Herpes Labialis | TERMINATED | NCT01225341 |
| AGN-190584 Vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02780115 |
| AGN-199201 Vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02780115 |
| AGN-190584 ophthalmic solution | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02780115 |
| AGN-199201 ophthalmic solution | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02780115 |
| AGN-190584 Vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02780115 |
| AGN-199201 Vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02780115 |
| AGN-190584 ophthalmic solution | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02780115 |
| AGN-199201 ophthalmic solution | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02780115 |
| AGN-199201 vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-199201 + AGN-190584 Combination | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-190584 vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-190584 ophthalmic solution | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-199201 ophthalmic solution | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-199201 vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-199201 + AGN-190584 Combination | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-190584 vehicle | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-190584 ophthalmic solution | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| AGN-199201 ophthalmic solution | Other | Phase PHASE2 | Presbyopia | COMPLETED | NCT02595528 |
| No-treatment control | Drug | Approved | Nose Enhancement | COMPLETED | NCT03430986 |
| JUVÉDERM® VOLUMA® with Lidocaine | Other | Approved | Nose Enhancement | COMPLETED | NCT03430986 |
| Juvéderm® VOLUMA™ with Lidocaine | Other | Phase PHASE4 | Contour | COMPLETED | NCT03425253 |
| BELKYRA® | Other | Phase PHASE4 | Contour | COMPLETED | NCT03425253 |
| Botox | Other | Phase PHASE4 | Stroke | COMPLETED | NCT00178646 |
| Botox | Other | Phase PHASE4 | Stroke | COMPLETED | NCT00178646 |
| Botulinum Toxin Type A | Other | Phase PHASE4 | Depression | COMPLETED | NCT01004042 |
| Irinotecan | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| ABT-165 | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Fluorouracil - infusion | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Bevacizumab | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Fluorouracil - bolus | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Leucovorin | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Irinotecan | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| ABT-165 | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Fluorouracil - infusion | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Bevacizumab | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Fluorouracil - bolus | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Leucovorin | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| bimatoprost 0.03% ophthalmic solution | Other | Phase EARLY_PHASE1 | Dermatochalasis | COMPLETED | NCT02830776 |
| TrueTear™ Application | Other | Approved | Dry Eye Syndromes | TERMINATED | NCT03274999 |
| Galcanezumab | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04179474 |
| Erenumab | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04179474 |
| Ubrogepant | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04179474 |
| Galcanezumab | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04179474 |
| Erenumab | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04179474 |
| Ubrogepant | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04179474 |
| intravitreal bevacizumab | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT01571232 |
| dexamethasone intravitreal implant | Other | Phase PHASE2 | Diabetic Macular Edema | COMPLETED | NCT01571232 |
| CoolSculpting® System | Other | Approved | Body Fat Disorder | COMPLETED | NCT04142450 |
| Deoxycholic Acid | Other | Phase PHASE4 | Brassiere Strap Fat (BSF) | COMPLETED | NCT04089722 |
| Refresh Tears 0.5% Lubricant Eye Drops | Other | Phase PHASE2 | Congenital Hereditary Endothelial Dystrophy of Cornea | UNKNOWN | NCT04843839 |
| Nepafenac 0.1% Oph Susp | Other | Phase PHASE2 | Congenital Hereditary Endothelial Dystrophy of Cornea | UNKNOWN | NCT04843839 |
| Normal saline | Other | Phase PHASE2 | Masseter Muscle Prominence | COMPLETED | NCT03861936 |
| OnabotulinumtoxinA | Other | Phase PHASE2 | Masseter Muscle Prominence | COMPLETED | NCT03861936 |
| Normal saline | Other | Phase PHASE2 | Masseter Muscle Prominence | COMPLETED | NCT03861936 |
| OnabotulinumtoxinA | Other | Phase PHASE2 | Masseter Muscle Prominence | COMPLETED | NCT03861936 |
| pancrelipase | Other | Phase PHASE4 | Celiac Disease | TERMINATED | NCT02475369 |
| pancrelipase | Other | Phase PHASE4 | Celiac Disease | TERMINATED | NCT02475369 |
| Eluxadoline | Other | Phase PHASE4 | Irritable Bowel Syndrome With Diarrhea | COMPLETED | NCT03441581 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03700320 |
| Standard of Care (SOC) Migraine Preventive Medication | Drug | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03700320 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03700320 |
| Standard of Care (SOC) Migraine Preventive Medication | Drug | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03700320 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03700320 |
| Standard of Care (SOC) Migraine Preventive Medication | Drug | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03700320 |
| Placebo | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03777059 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03777059 |
| Juvéderm® VOLIFT™ with Lidocaine | Other | Phase PHASE4 | Lip Augmentation | COMPLETED | NCT03796728 |
| Timolol Vehicle (placebo) | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02250651 |
| Active Comparator: Timolol 0.5% | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02250651 |
| Sham: Applicator Without Needle | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02250651 |
| Bimatoprost SR | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02250651 |
| Relamorelin | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03285308 |
| Placebo | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03285308 |
| Relamorelin | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03426345 |
| Placebo | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03426345 |
| Relamorelin | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03426345 |
| Placebo | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03426345 |
| Intranasal Tear Neurostimulator (ITN) [TrueTear®] | Other | Approved | Dry Eye Syndromes | TERMINATED | NCT03827564 |
| Juvederm® VOLITE | Other | Approved | Healthy Adults | COMPLETED | NCT04206293 |
| Placebos | Other | Phase PHASE4 | None (i.e. Healthy Volunteers) | UNKNOWN | NCT03249311 |
| Duloxetine | Other | Phase PHASE4 | None (i.e. Healthy Volunteers) | UNKNOWN | NCT03249311 |
| Levomilnacipran | Other | Phase PHASE4 | None (i.e. Healthy Volunteers) | UNKNOWN | NCT03249311 |
| OnabotulinumtoxinA | Other | Phase EARLY_PHASE1 | Glabellar Frown Lines | UNKNOWN | NCT05083286 |
| OnabotulinumtoxinA | Other | Phase EARLY_PHASE1 | Glabellar Frown Lines | UNKNOWN | NCT05083286 |
| Ceftaroline Fosamil | Other | Phase PHASE1 | Hematogenously Acquired Staphylococcus Aureus Osteomyelitis | COMPLETED | NCT02335905 |
| botulinum toxin | Other | Phase PHASE2 | Non-relaxing Puborectalis Syndrome | TERMINATED | NCT01780636 |
| JUVÉDERM VOLBELLA® XC injectable gel | Other | Phase PHASE3 | Infraorbital Hollowing | COMPLETED | NCT03418545 |
| JUVÉDERM VOLBELLA® XC injectable gel | Other | Phase PHASE3 | Infraorbital Hollowing | COMPLETED | NCT03418545 |
| Placebo | Other | Phase PHASE1 | Facial Fine Lines | COMPLETED | NCT04631588 |
| Botox | Other | Phase PHASE1 | Facial Fine Lines | COMPLETED | NCT04631588 |
| XEN45 gel stent implantation | Other | Approved | Glaucoma | UNKNOWN | NCT05130554 |
| Ultrasound | Other | Approved | Spasticity | COMPLETED | NCT02334683 |
| Electrical stimulation | Other | Approved | Spasticity | COMPLETED | NCT02334683 |
| Ultrasound | Other | Approved | Spasticity | COMPLETED | NCT02334683 |
| Electrical stimulation | Other | Approved | Spasticity | COMPLETED | NCT02334683 |
| Relamorelin 10 μg | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03786380 |
| Relamorelin | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03420781 |
| Placebo | Other | Phase PHASE3 | Gastroparesis | TERMINATED | NCT03420781 |
| Pilocarpine HCl Ophthalmic Solution | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT03804268 |
| Vehicle | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT03804268 |
| Pilocarpine HCl Ophthalmic Solution | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT03804268 |
| Vehicle | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT03804268 |
| Vehicle | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT03857542 |
| Pilocarpine HCl Ophthalmic Solution | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT03857542 |
| Vehicle | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT03857542 |
| Pilocarpine HCl Ophthalmic Solution | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT03857542 |
| Botox | Other | Phase PHASE4 | Stroke | TERMINATED | NCT03367429 |
| Sham Selective Laser Trabeculoplasty | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT02636946 |
| Selective Laser Trabeculoplasty | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT02636946 |
| Sham Bimatoprost SR | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT02636946 |
| Bimatoprost SR | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT02636946 |
| Control | Other | Approved | Pigmentation | COMPLETED | NCT03065582 |
| Topical Product C | Other | Approved | Pigmentation | COMPLETED | NCT03065582 |
| Topical Product B | Other | Approved | Pigmentation | COMPLETED | NCT03065582 |
| Topical Product A | Other | Approved | Pigmentation | COMPLETED | NCT03065582 |
| Placebo | Other | Phase PHASE2 | Covid19 | TERMINATED | NCT04500418 |
| Cenicriviroc (CVC) | Other | Phase PHASE2 | Covid19 | TERMINATED | NCT04500418 |
| Placebo | Other | Phase PHASE1 | Myofascial Pain Syndromes | COMPLETED | NCT02173405 |
| OnabotulinumtoxinA | Other | Phase PHASE1 | Myofascial Pain Syndromes | COMPLETED | NCT02173405 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT03939312 |
| Placebo | Other | Phase PHASE2 | Dystonia Disorder | UNKNOWN | NCT04277247 |
| Botulinum toxin type A | Other | Phase PHASE2 | Dystonia Disorder | UNKNOWN | NCT04277247 |
| Androderm® | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT04320745 |
| Trabeculectomy | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT03654885 |
| XEN-45 Gel Stent | Other | Phase PHASE4 | Glaucoma | COMPLETED | NCT03654885 |
| EARFOLD® | Other | Phase PHASE4 | Prominent Ears | COMPLETED | NCT03194269 |
| Juvéderm® VOLIFT™ with Lidocaine | Other | Phase PHASE4 | Marionette Lines Forehead Contouring | COMPLETED | NCT05077488 |
| Dalbavancin | Other | Phase PHASE4 | Skin Infection | TERMINATED | NCT03372941 |
| Juvéderm® VOLIFT with Lidocaine | Other | Phase PHASE4 | Skin Depressions | COMPLETED | NCT04390581 |
| Placebo | Other | Phase PHASE2 | HIV Infections | WITHDRAWN | NCT04334915 |
| Cenicriviroc Mesylate (CVC) | Other | Phase PHASE2 | HIV Infections | WITHDRAWN | NCT04334915 |
| BOTOX® | Other | Phase PHASE3 | Urinary Incontinence | TERMINATED | NCT02097121 |
| No-treatment control | Drug | Phase PHASE3 | Jawline Definition | COMPLETED | NCT03712137 |
| VOLUX XC | Other | Phase PHASE3 | Jawline Definition | COMPLETED | NCT03712137 |
| Placebo | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT03855137 |
| Atogepant 60 mg | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT03855137 |
| Atogepant 30 mg | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT03855137 |
| JUVÉDERM VOLUX® | Other | Preclinical | Chin Retrusion | COMPLETED | NCT04687046 |
| JUVÉDERM VOLUX® | Other | Preclinical | Chin Retrusion | COMPLETED | NCT04687046 |
| Vehicle | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT04983589 |
| Pilocarpine HCl | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT04983589 |
| Vehicle | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT04983589 |
| Pilocarpine HCl | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT04983589 |
| OZURDEX | Other | Phase PHASE4 | Macular Edema | COMPLETED | NCT03908307 |
| Normal saline pyloric injection | Other | Phase PHASE4 | Bariatric Surgery | COMPLETED | NCT03701919 |
| Botulinum toxin pyloroplasty | Other | Phase PHASE4 | Bariatric Surgery | COMPLETED | NCT03701919 |
| Placebo | Other | Phase PHASE2 | Platysma Prominence | COMPLETED | NCT03915067 |
| BOTOX® purified neurotoxin complex | Other | Phase PHASE2 | Platysma Prominence | COMPLETED | NCT03915067 |
| XEN45 | Other | Phase PHASE3 | Glaucoma | COMPLETED | NCT03362931 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT04829747 |
| Placebo arm | Other | Phase PHASE4 | Bruxism | COMPLETED | NCT00908050 |
| Botulinum toxin type A | Other | Phase PHASE4 | Bruxism | COMPLETED | NCT00908050 |
| CoolSculpting® System | Other | Approved | Non-invasive Fat Reduction | COMPLETED | NCT03909100 |
| CoolSculpting® System | Other | Approved | Non-invasive Fat Reduction | COMPLETED | NCT03909100 |
| TrueTear Intranasal Tear Neurostimulator | Other | Approved | Dry Eye Syndromes | COMPLETED | NCT03719885 |
| TrueTear Intranasal Tear Neurostimulator | Other | Approved | Dry Eye Syndromes | COMPLETED | NCT03719885 |
| Placebo | Other | Phase PHASE2 | Glabellar Lines | COMPLETED | NCT04096326 |
| AGN-151586 | Other | Phase PHASE2 | Glabellar Lines | COMPLETED | NCT04096326 |
| Metronidazole Gel | Other | Phase PHASE4 | Vaginosis, Bacterial | COMPLETED | NCT02392026 |
| Metronidazole Gel | Other | Phase PHASE4 | Vaginosis, Bacterial | COMPLETED | NCT02392026 |
| JUVÉDERM VOLUX® | Other | Phase PHASE3 | Chin Retrusion | COMPLETED | NCT04559984 |
| JUVÉDERM VOLUX® | Other | Phase PHASE3 | Chin Retrusion | COMPLETED | NCT04559984 |
| Placebo | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT04740827 |
| Atogepant 60 mg | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT04740827 |
| SkinMedica | Other | Phase PHASE4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | COMPLETED | NCT03712449 |
| BELKYRA® | Other | Phase PHASE4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | COMPLETED | NCT03712449 |
| BOTOX Cosmetic® | Other | Phase PHASE4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | COMPLETED | NCT03712449 |
| JUVÉDERM® | Other | Phase PHASE4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | COMPLETED | NCT03712449 |
| SkinMedica | Other | Phase PHASE4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | COMPLETED | NCT03712449 |
| BELKYRA® | Other | Phase PHASE4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | COMPLETED | NCT03712449 |
| BOTOX Cosmetic® | Other | Phase PHASE4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | COMPLETED | NCT03712449 |
| JUVÉDERM® | Other | Phase PHASE4 | Facial Rhytides, Skin Folds, Loss of Volume and Skin Quality | COMPLETED | NCT03712449 |
| Reminyl 4 mg Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01190748 |
| Galantamine 4 mg Tablet, single dose | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01190748 |
| XEN Glaucoma Stent | Other | Preclinical | Refractory Glaucoma | COMPLETED | NCT04303897 |
| XEN Glaucoma Stent | Other | Preclinical | Refractory Glaucoma | COMPLETED | NCT04303897 |
| No-treatment control | Drug | Phase PHASE3 | Temple Hollowing | COMPLETED | NCT04414397 |
| JUVÉDERM® VOLUMA® XC | Other | Phase PHASE3 | Temple Hollowing | COMPLETED | NCT04414397 |
| Levothyroxine | Other | Phase PHASE2 | Hypothyroidism | COMPLETED | NCT04124705 |
| Armour® Thyroid | Other | Phase PHASE2 | Hypothyroidism | COMPLETED | NCT04124705 |
| Aflibercept | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT04411693 |
| Dexamethasone implant | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT04411693 |
| Aflibercept | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT04411693 |
| Dexamethasone implant | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT04411693 |
| Corneal topography: Pentacam | Other | Approved | Glaucoma, Open-Angle | COMPLETED | NCT04602923 |
| Corneal topography: OPD-Scan | Other | Approved | Glaucoma, Open-Angle | COMPLETED | NCT04602923 |
| Normal Saline | Other | Phase PHASE2 | Scar | COMPLETED | NCT01177358 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Scar | COMPLETED | NCT01177358 |
| Normal Saline | Other | Phase PHASE2 | Scar | COMPLETED | NCT01177358 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Scar | COMPLETED | NCT01177358 |
| Normal Saline | Other | Phase PHASE2 | Scar | COMPLETED | NCT01177358 |
| Botulinum Toxin Type A | Other | Phase PHASE2 | Scar | COMPLETED | NCT01177358 |
| HArmonyCa Injectable Gel | Other | Phase PHASE4 | Soft Tissue Augmentation | COMPLETED | NCT05119777 |
| VOLBELLA with Lidocaine | Other | Phase PHASE3 | Infraorbital Hollowing | COMPLETED | NCT05088980 |
| JUVÉDERM® VOLUMA® with Lidocaine | Other | Phase PHASE3 | Temple Hollowing | COMPLETED | NCT04891419 |
| Juvéderm Volbella XC | Other | Phase PHASE2 | Dermatological Non-Disease | COMPLETED | NCT04755595 |
| Juvéderm Voluma XC | Other | Phase PHASE2 | Dermatological Non-Disease | COMPLETED | NCT04755595 |
| Botox Cosmetic Injectable Product | Other | Phase PHASE2 | Dermatological Non-Disease | COMPLETED | NCT04755595 |
| Juvéderm Volbella XC | Other | Phase PHASE2 | Dermatological Non-Disease | COMPLETED | NCT04755595 |
| Juvéderm Voluma XC | Other | Phase PHASE2 | Dermatological Non-Disease | COMPLETED | NCT04755595 |
| Botox Cosmetic Injectable Product | Other | Phase PHASE2 | Dermatological Non-Disease | COMPLETED | NCT04755595 |
| HArmonyCa Lidocaine Injectable Gel | Other | Phase PHASE3 | Mid Face Volume Deficit | COMPLETED | NCT05452070 |
| New Emulsion, Optive, Soothe | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT01013077 |
| Soothe, New Emulsion, Optive | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT01013077 |
| Optive, Soothe, New Emulsion | Other | Approved | Dry Eye Syndrome | COMPLETED | NCT01013077 |
| Formulation C: OnabotulinumtoxinA | Other | Phase PHASE2 | Glabellar Lines | COMPLETED | NCT05013424 |
| Formulation B: OnabotulinumtoxinA | Other | Phase PHASE2 | Glabellar Lines | COMPLETED | NCT05013424 |
| Formulation A: OnabotulinumtoxinA | Other | Phase PHASE2 | Glabellar Lines | COMPLETED | NCT05013424 |
| Placebo | Other | Phase PHASE2 | Forehead Lines | COMPLETED | NCT05152576 |
| OnabotulinumtoxinA X | Other | Phase PHASE2 | Forehead Lines | COMPLETED | NCT05152576 |
| Placebo | Other | Phase PHASE2 | Forehead Lines | COMPLETED | NCT05152576 |
| OnabotulinumtoxinA X | Other | Phase PHASE2 | Forehead Lines | COMPLETED | NCT05152576 |
| Placebo | Other | Phase PHASE2 | Glabellar Lines | COMPLETED | NCT05100199 |
| OnabotulinumtoxinA X | Other | Phase PHASE2 | Glabellar Lines | COMPLETED | NCT05100199 |
| Ozurdex | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT03832179 |
| Aflibercept | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT03832179 |
| Ranibizumab | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT03832179 |
| Bevacizumab | Other | Phase PHASE4 | Diabetic Macular Edema | COMPLETED | NCT03832179 |
| Aqueous PGE2 and inflammatory cytokines measurements | Other | Phase PHASE1 | Diabetic Retinopathy | ACTIVE_NOT_RECRUITING | NCT04505566 |
| Placebo - Preservative-free artificial tears | Other | Phase PHASE1 | Diabetic Retinopathy | ACTIVE_NOT_RECRUITING | NCT04505566 |
| Ketorolac 0.45% ophthalmic solution | Other | Phase PHASE1 | Diabetic Retinopathy | ACTIVE_NOT_RECRUITING | NCT04505566 |
| onabotulinumtoxin A | Other | Phase EARLY_PHASE1 | Stress Urinary Incontinence | SUSPENDED | NCT04984317 |
| Cyclophosphamide | Other | Phase PHASE1 | Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05577000 |
| Fludarabine | Other | Phase PHASE1 | Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05577000 |
| Manufactured Anti-BCMA CAR-T cells | Other | Phase PHASE1 | Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05577000 |
| Placebo | Other | Phase PHASE3 | Essential Head Tremor | COMPLETED | NCT02555982 |
| BOTOX ® 200 Unités | Other | Phase PHASE3 | Essential Head Tremor | COMPLETED | NCT02555982 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | TEMPORARILY_NOT_AVAILABLE | NCT04830202 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | AVAILABLE | NCT04278235 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04379050 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Nab-Paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, budigalimab, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT03844048 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| New formulation adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01752855 |
| New formulation adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01752855 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01549834 |
| ABT-126 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01549834 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01549834 |
| ABT-126 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01549834 |
| ABT-126 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01527916 |
| donepezil | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01527916 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01527916 |
| ABT-126 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01527916 |
| donepezil | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01527916 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01527916 |
| Ritonavir | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01221298 |
| Ribavirin | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01221298 |
| ABT-072 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01221298 |
| ABT-450 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01221298 |
| Ritonavir | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01221298 |
| Ribavirin | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01221298 |
| ABT-072 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01221298 |
| ABT-450 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01221298 |
| Placebo | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| Ribavirin | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| Peginterferon alpha-2a | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| Ritonavir | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| ABT-333 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| ABT-072 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| ABT-450 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| Placebo | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| Ribavirin | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| Peginterferon alpha-2a | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| Ritonavir | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| ABT-333 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| ABT-072 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| ABT-450 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT01074008 |
| ABT-333 | Other | Phase PHASE2 | HCV Infection | COMPLETED | NCT00726882 |
| Blood sample collection only | Other | Phase PHASE2 | HCV Infection | COMPLETED | NCT00726882 |
| ABT-333 | Other | Phase PHASE2 | HCV Infection | COMPLETED | NCT00726882 |
| Blood sample collection only | Other | Phase PHASE2 | HCV Infection | COMPLETED | NCT00726882 |
| ABT-333 | Other | Phase PHASE2 | HCV Infection | COMPLETED | NCT00726882 |
| Blood sample collection only | Other | Phase PHASE2 | HCV Infection | COMPLETED | NCT00726882 |
| J-tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| PEG tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| Placebo (PBO) oral capsules | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| Levodopa carbidopa (LC) oral encapsulated immediate release (IR) tablets | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| Placebo gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| Levodopa carbidopa intestinal gel (LCIG) | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| J-tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| PEG tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| Placebo (PBO) oral capsules | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| Levodopa carbidopa (LC) oral encapsulated immediate release (IR) tablets | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| Placebo gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| Levodopa carbidopa intestinal gel (LCIG) | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00357994 |
| J-tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| PEG tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| Levodopa-carbidopa intestinal gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| J-tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| PEG tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| Levodopa-carbidopa intestinal gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| J-tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| PEG tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| Levodopa-carbidopa intestinal gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00335153 |
| placebo | Other | Phase PHASE3 | Plaque Psoriasis | COMPLETED | NCT01646073 |
| Adalimumab | Other | Phase PHASE3 | Plaque Psoriasis | COMPLETED | NCT01646073 |
| placebo | Other | Phase PHASE3 | Plaque Psoriasis | COMPLETED | NCT01646073 |
| Adalimumab | Other | Phase PHASE3 | Plaque Psoriasis | COMPLETED | NCT01646073 |
| Ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| Ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| ABT-450 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| Ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| Ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| ABT-450 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01464827 |
| Immediate post-screening treatment education | Drug | Approved | HIV | UNKNOWN | NCT01892228 |
| ABT-333 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT02534870 |
| ABT-450/r/ABT-267 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT02534870 |
| ABT-333 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT02534870 |
| ABT-450/r/ABT-267 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT02534870 |
| ABT-333 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT02534870 |
| ABT-450/r/ABT-267 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT02534870 |
| ABT-530 | Other | Phase PHASE1 | Hepatic Impairment | COMPLETED | NCT02296905 |
| ABT-493 | Other | Phase PHASE1 | Hepatic Impairment | COMPLETED | NCT02296905 |
| ABT-530 | Other | Phase PHASE1 | Hepatic Impairment | COMPLETED | NCT02296905 |
| ABT-493 | Other | Phase PHASE1 | Hepatic Impairment | COMPLETED | NCT02296905 |
| placebo | Other | Phase PHASE2 | Non-Small -Cell Lung Cancer | COMPLETED | NCT01560104 |
| paclitaxel | Other | Phase PHASE2 | Non-Small -Cell Lung Cancer | COMPLETED | NCT01560104 |
| Carboplatin | Other | Phase PHASE2 | Non-Small -Cell Lung Cancer | COMPLETED | NCT01560104 |
| Veliparib | Other | Phase PHASE2 | Non-Small -Cell Lung Cancer | COMPLETED | NCT01560104 |
| placebo | Other | Phase PHASE2 | Non-Small -Cell Lung Cancer | COMPLETED | NCT01560104 |
| paclitaxel | Other | Phase PHASE2 | Non-Small -Cell Lung Cancer | COMPLETED | NCT01560104 |
| Carboplatin | Other | Phase PHASE2 | Non-Small -Cell Lung Cancer | COMPLETED | NCT01560104 |
| Veliparib | Other | Phase PHASE2 | Non-Small -Cell Lung Cancer | COMPLETED | NCT01560104 |
| biological treatment | Drug | Preclinical | Psoriasis | COMPLETED | NCT01356758 |
| biological treatment | Drug | Preclinical | Psoriasis | COMPLETED | NCT01356758 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | COMPLETED | NCT00775437 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | COMPLETED | NCT00775437 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT01670240 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT01670240 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT01670240 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT01670240 |
| ABT-530 | Other | Phase PHASE1 | Renal Impairment | COMPLETED | NCT02442258 |
| ABT-493 | Other | Phase PHASE1 | Renal Impairment | COMPLETED | NCT02442258 |
| ABT-530 | Other | Phase PHASE1 | Renal Impairment | COMPLETED | NCT02442258 |
| ABT-493 | Other | Phase PHASE1 | Renal Impairment | COMPLETED | NCT02442258 |
| Placebo | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT02531178 |
| ABBV-257 | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT02531178 |
| Placebo | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT02531178 |
| ABBV-257 | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT02531178 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT01958827 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT01958827 |
| ABT-122 | Other | Phase PHASE2 | Psoriatic Arthritis | TERMINATED | NCT02429895 |
| Ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Ombitasvir/Paritaprevir/Ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Ombitasvir/Paritaprevir/Ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Ombitasvir/Paritaprevir/Ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| Ombitasvir/Paritaprevir/Ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02216422 |
| ritonavir | Other | Phase PHASE2 | Hepatitis C Virus | COMPLETED | NCT01458535 |
| ribavirin | Other | Phase PHASE2 | Hepatitis C Virus | COMPLETED | NCT01458535 |
| ABT-267 | Other | Phase PHASE2 | Hepatitis C Virus | COMPLETED | NCT01458535 |
| ABT-450 | Other | Phase PHASE2 | Hepatitis C Virus | COMPLETED | NCT01458535 |
| ritonavir | Other | Phase PHASE2 | Hepatitis C Virus | COMPLETED | NCT01458535 |
| ribavirin | Other | Phase PHASE2 | Hepatitis C Virus | COMPLETED | NCT01458535 |
| ABT-267 | Other | Phase PHASE2 | Hepatitis C Virus | COMPLETED | NCT01458535 |
| ABT-450 | Other | Phase PHASE2 | Hepatitis C Virus | COMPLETED | NCT01458535 |
| jejunal extension tube (J-tube) | Other | Phase PHASE4 | Advanced Idiopathic Parkinson's Disease | COMPLETED | NCT00141518 |
| percutaneous endoscopic gastrostomy tube (PEG tube) | Other | Phase PHASE4 | Advanced Idiopathic Parkinson's Disease | COMPLETED | NCT00141518 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE4 | Advanced Idiopathic Parkinson's Disease | COMPLETED | NCT00141518 |
| Levodopa-carbidopa intestinal gel (LCIG) | Other | Phase PHASE4 | Advanced Idiopathic Parkinson's Disease | COMPLETED | NCT00141518 |
| jejunal extension tube (J-tube) | Other | Phase PHASE4 | Advanced Idiopathic Parkinson's Disease | COMPLETED | NCT00141518 |
| percutaneous endoscopic gastrostomy tube (PEG tube) | Other | Phase PHASE4 | Advanced Idiopathic Parkinson's Disease | COMPLETED | NCT00141518 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE4 | Advanced Idiopathic Parkinson's Disease | COMPLETED | NCT00141518 |
| Levodopa-carbidopa intestinal gel (LCIG) | Other | Phase PHASE4 | Advanced Idiopathic Parkinson's Disease | COMPLETED | NCT00141518 |
| Venetoclax | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | WITHDRAWN | NCT02640833 |
| Duvelisib | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | WITHDRAWN | NCT02640833 |
| Venetoclax | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | WITHDRAWN | NCT02640833 |
| Duvelisib | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | WITHDRAWN | NCT02640833 |
| DSM265 25% SDD powder for suspension | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT02750384 |
| DSM265 50% SDD granules | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT02750384 |
| DSM265 25% SDD powder for suspension | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT02750384 |
| DSM265 50% SDD granules | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT02750384 |
| DSM265 25% SDD powder for suspension | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT02750384 |
| DSM265 50% SDD granules | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT02750384 |
| FOLFIRI | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02033551 |
| Paclitaxel | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02033551 |
| Carboplatin | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02033551 |
| Veliparib | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02033551 |
| FOLFIRI | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02033551 |
| Paclitaxel | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02033551 |
| Carboplatin | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02033551 |
| Veliparib | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02033551 |
| Technetium labelled glucosamine | Other | Preclinical | Rheumatoid Arthritis | NO_LONGER_AVAILABLE | NCT01789151 |
| Technetium labelled glucosamine | Other | Preclinical | Rheumatoid Arthritis | NO_LONGER_AVAILABLE | NCT01789151 |
| Methotrexate | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01162421 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01162421 |
| Methotrexate | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01162421 |
| adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01162421 |
| ABT-122 | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02141997 |
| adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02141997 |
| ABT-122 | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02141997 |
| adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02141997 |
| BI 655066 (low medium i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| Placebo, s.c. | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (high i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (low s.c. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (very low i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (high medium i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (low i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (high s.c. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| Placebo, i.v. | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (very high i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (low medium i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| Placebo, s.c. | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (high i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (low s.c. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (very low i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (high medium i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (low i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (high s.c. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| Placebo, i.v. | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| BI 655066 (very high i.v. dose) | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT01577550 |
| ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | COMPLETED | NCT02399345 |
| sofosbuvir (SOF) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | COMPLETED | NCT02399345 |
| ombitasvir/paritaprevir/ritonavir, dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | COMPLETED | NCT02399345 |
| ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | COMPLETED | NCT02399345 |
| sofosbuvir (SOF) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | COMPLETED | NCT02399345 |
| ombitasvir/paritaprevir/ritonavir, dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV Infection Genotype 1) | COMPLETED | NCT02399345 |
| Adalimumab 40 MG/0.8 ML Subcutaneous Solution [HUMIRA] | Other | Approved | Psoriasis | COMPLETED | NCT01320293 |
| Adalimumab 40 MG/0.8 ML Subcutaneous Solution [HUMIRA] | Other | Approved | Psoriasis | COMPLETED | NCT01320293 |
| Intravenous Paricalcitol | Other | Phase PHASE4 | Endstage Renal Disease | UNKNOWN | NCT03023748 |
| ABT-806 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01406119 |
| ABT-806 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01406119 |
| ABT-555 | Other | Phase PHASE1 | Multiple Sclerosis | TERMINATED | NCT02606630 |
| PET/CT imaging | Other | Phase PHASE4 | Ankylosing Spondyloarthritis | UNKNOWN | NCT02634541 |
| Adalimumab | Other | Phase PHASE4 | Ankylosing Spondyloarthritis | UNKNOWN | NCT02634541 |
| PET/CT imaging | Other | Phase PHASE4 | Ankylosing Spondyloarthritis | UNKNOWN | NCT02634541 |
| Adalimumab | Other | Phase PHASE4 | Ankylosing Spondyloarthritis | UNKNOWN | NCT02634541 |
| Matched Placebo - Sugar Pill | Other | Phase PHASE2 | Alcohol Dependence | COMPLETED | NCT01613014 |
| ABT-436 | Other | Phase PHASE2 | Alcohol Dependence | COMPLETED | NCT01613014 |
| Matched Placebo - Sugar Pill | Other | Phase PHASE2 | Alcohol Dependence | COMPLETED | NCT01613014 |
| ABT-436 | Other | Phase PHASE2 | Alcohol Dependence | COMPLETED | NCT01613014 |
| Hydroxychloroquine | Other | Phase PHASE2 | Prostate Cancer | TERMINATED | NCT01828476 |
| ABT-263 | Other | Phase PHASE2 | Prostate Cancer | TERMINATED | NCT01828476 |
| Abiraterone | Other | Phase PHASE2 | Prostate Cancer | TERMINATED | NCT01828476 |
| Placebo | Other | Phase PHASE3 | Nail Psoriasis | COMPLETED | NCT02016482 |
| Adalimumab | Other | Phase PHASE3 | Nail Psoriasis | COMPLETED | NCT02016482 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | WITHDRAWN | NCT02951117 |
| ABBV-838 | Other | Phase PHASE1 | Multiple Myeloma | WITHDRAWN | NCT02951117 |
| Venetoclax | Other | Phase PHASE1 | Multiple Myeloma | WITHDRAWN | NCT02951117 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | WITHDRAWN | NCT02951117 |
| ABBV-838 | Other | Phase PHASE1 | Multiple Myeloma | WITHDRAWN | NCT02951117 |
| Venetoclax | Other | Phase PHASE1 | Multiple Myeloma | WITHDRAWN | NCT02951117 |
| Chama cha MamaToto | Other | Approved | Pregnancy Related | UNKNOWN | NCT03187873 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02596217 |
| ABBV-066 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02596217 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02596217 |
| ABBV-066 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02596217 |
| ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02219477 |
| dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02219477 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02219477 |
| ABT-122 | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02433340 |
| ABT-122 | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02433340 |
| ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02442271 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02442271 |
| ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02442271 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02442271 |
| ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02442271 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02442271 |
| ABT-122 | Other | Phase PHASE2 | Psoriatic Arthritis | COMPLETED | NCT02349451 |
| adalimumab | Other | Phase PHASE2 | Psoriatic Arthritis | COMPLETED | NCT02349451 |
| ABT-122 | Other | Phase PHASE2 | Psoriatic Arthritis | COMPLETED | NCT02349451 |
| adalimumab | Other | Phase PHASE2 | Psoriatic Arthritis | COMPLETED | NCT02349451 |
| Placebo for ABT-981 | Other | Phase PHASE2 | Erosive Hand Osteoarthritis | COMPLETED | NCT02384538 |
| ABT-981 | Other | Phase PHASE2 | Erosive Hand Osteoarthritis | COMPLETED | NCT02384538 |
| Placebo for ABT-981 | Other | Phase PHASE2 | Erosive Hand Osteoarthritis | COMPLETED | NCT02384538 |
| ABT-981 | Other | Phase PHASE2 | Erosive Hand Osteoarthritis | COMPLETED | NCT02384538 |
| Atrasentan placebo group | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01424319 |
| Atrasentan high dose group | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01424319 |
| Atrasentan low dose group | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01424319 |
| Atrasentan placebo group | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01424319 |
| Atrasentan high dose group | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01424319 |
| Atrasentan low dose group | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT01424319 |
| ribavirin | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02265237 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02265237 |
| Risankizumab | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Midazolam | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Metoprolol | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Omeprazole | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Warfarin | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Caffeine | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Risankizumab | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Midazolam | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Metoprolol | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Omeprazole | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Warfarin | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Caffeine | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Risankizumab | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Midazolam | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Metoprolol | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Omeprazole | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Warfarin | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| Caffeine | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT02772601 |
| ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02476617 |
| dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02476617 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02476617 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02651194 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02651194 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02442284 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02442284 |
| Placebo for ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02517515 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02517515 |
| Placebo for ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02517515 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02517515 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02493855 |
| Dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02493855 |
| Ombitasvir/ABT-450/Ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02493855 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02493855 |
| Dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02493855 |
| Ombitasvir/ABT-450/Ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02493855 |
| Placebo | Other | Phase PHASE1 | Psoriasis | TERMINATED | NCT03145948 |
| ABBV-553 | Other | Phase PHASE1 | Psoriasis | TERMINATED | NCT03145948 |
| Placebo | Other | Phase PHASE1 | Psoriasis | TERMINATED | NCT03145948 |
| ABBV-553 | Other | Phase PHASE1 | Psoriasis | TERMINATED | NCT03145948 |
| Placebo | Other | Phase PHASE1 | Psoriasis | TERMINATED | NCT03145948 |
| ABBV-553 | Other | Phase PHASE1 | Psoriasis | TERMINATED | NCT03145948 |
| ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01782495 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02207088 |
| dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02207088 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02207088 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02207088 |
| dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02207088 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02207088 |
| Placebo | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02009631 |
| Veliparib (ABT-888) | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02009631 |
| Placebo | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02009631 |
| Veliparib (ABT-888) | Other | Phase PHASE1 | Breast Cancer | COMPLETED | NCT02009631 |
| Ketoconazole | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | COMPLETED | NCT01969669 |
| ABT-199 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | COMPLETED | NCT01969669 |
| Placebo | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT01853033 |
| ABT-122 | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT01853033 |
| ABT-414 | Other | Phase PHASE1 | Squamous Cell Tumors | COMPLETED | NCT01741727 |
| ABT-414 | Other | Phase PHASE1 | Squamous Cell Tumors | COMPLETED | NCT01741727 |
| Tofacitinib | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT01741493 |
| Placebo | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT01741493 |
| ABT-494 | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT01741493 |
| Tofacitinib | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT01741493 |
| Placebo | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT01741493 |
| ABT-494 | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT01741493 |
| Placebo | Other | Phase PHASE1 | Osteoarthritis | COMPLETED | NCT01668511 |
| ABT-981 | Other | Phase PHASE1 | Osteoarthritis | COMPLETED | NCT01668511 |
| Placebo | Other | Phase PHASE1 | Osteoarthritis | COMPLETED | NCT01668511 |
| ABT-981 | Other | Phase PHASE1 | Osteoarthritis | COMPLETED | NCT01668511 |
| paclitaxel | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| carboplatin | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| veliparib (ABT-888) | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| paclitaxel | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| carboplatin | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| veliparib (ABT-888) | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| paclitaxel | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| carboplatin | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| veliparib (ABT-888) | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01617928 |
| radiation | Other | Phase PHASE1 | Locally Advanced Rectal Cancer | COMPLETED | NCT01589419 |
| capecitabine | Other | Phase PHASE1 | Locally Advanced Rectal Cancer | COMPLETED | NCT01589419 |
| veliparib | Other | Phase PHASE1 | Locally Advanced Rectal Cancer | COMPLETED | NCT01589419 |
| radiation | Other | Phase PHASE1 | Locally Advanced Rectal Cancer | COMPLETED | NCT01589419 |
| capecitabine | Other | Phase PHASE1 | Locally Advanced Rectal Cancer | COMPLETED | NCT01589419 |
| veliparib | Other | Phase PHASE1 | Locally Advanced Rectal Cancer | COMPLETED | NCT01589419 |
| ABT-348 and azacitidine | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia | COMPLETED | NCT01110473 |
| ABT-348 | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia | COMPLETED | NCT01110473 |
| ABT-348 and azacitidine | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia | COMPLETED | NCT01110473 |
| ABT-348 | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia | COMPLETED | NCT01110473 |
| irinotecan (weekly schedule) | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01009073 |
| irinotecan (3-week schedule) | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01009073 |
| erlotinib | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01009073 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01009073 |
| irinotecan (weekly schedule) | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01009073 |
| irinotecan (3-week schedule) | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01009073 |
| erlotinib | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01009073 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01009073 |
| Placebo for ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00850044 |
| placebo for ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00850044 |
| ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00850044 |
| ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00850044 |
| Placebo for ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00850044 |
| placebo for ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00850044 |
| ritonavir | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00850044 |
| ABT-450 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00850044 |
| adalimumab | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT00650156 |
| adalimumab | Other | Phase PHASE1 | Rheumatoid Arthritis | COMPLETED | NCT00650156 |
| linifanib | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01413893 |
| Matching Placebo | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT01380704 |
| ABT-436 | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT01380704 |
| Matching Placebo | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT01380704 |
| ABT-436 | Other | Phase PHASE1 | Major Depressive Disorder | COMPLETED | NCT01380704 |
| Paclitaxel | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT01225302 |
| Carboplatin | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT01225302 |
| Linifanib | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT01225302 |
| Paclitaxel | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT01225302 |
| Carboplatin | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT01225302 |
| Linifanib | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT01225302 |
| veliparib | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01199224 |
| veliparib | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT01199224 |
| Rifampin | Other | Phase PHASE1 | Lymphoma, Including Chronic Lymphocytic Leukemia | COMPLETED | NCT01121133 |
| navitoclax | Other | Phase PHASE1 | Lymphoma, Including Chronic Lymphocytic Leukemia | COMPLETED | NCT01121133 |
| Rifampin | Other | Phase PHASE1 | Lymphoma, Including Chronic Lymphocytic Leukemia | COMPLETED | NCT01121133 |
| navitoclax | Other | Phase PHASE1 | Lymphoma, Including Chronic Lymphocytic Leukemia | COMPLETED | NCT01121133 |
| Placebo | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00986037 |
| ABT-308 | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00986037 |
| Placebo | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00986037 |
| ABT-308 | Other | Phase PHASE1 | Asthma | COMPLETED | NCT00986037 |
| ABT-263 | Other | Phase PHASE1 | Lymphoid Malignancy | COMPLETED | NCT00982566 |
| paclitaxel | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00891605 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00891605 |
| paclitaxel | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00891605 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00891605 |
| Placebo | Other | Phase PHASE1 | Schizophrenia | COMPLETED | NCT00888693 |
| ABT-288 | Other | Phase PHASE1 | Schizophrenia | COMPLETED | NCT00888693 |
| gemcitabine | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00887757 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00887757 |
| gemcitabine | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00887757 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00887757 |
| ABT-869 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT00733187 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00718380 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00718380 |
| ABT-869 | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT00718380 |
| Placebo | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00696904 |
| ABT-333 | Other | Phase PHASE1 | HCV Infection | COMPLETED | NCT00696904 |
| M200 (Volociximab), Carboplatin, Paclitaxel | Other | Phase PHASE1 | Non-small Cell Lung Cancer | COMPLETED | NCT00654758 |
| M200 (Volociximab), Carboplatin, Paclitaxel | Other | Phase PHASE1 | Non-small Cell Lung Cancer | COMPLETED | NCT00654758 |
| Temozolomide | Other | Phase PHASE1 | Non-hematologic Malignancies | COMPLETED | NCT00526617 |
| ABT-888 | Other | Phase PHASE1 | Non-hematologic Malignancies | COMPLETED | NCT00526617 |
| Temozolomide | Other | Phase PHASE1 | Non-hematologic Malignancies | COMPLETED | NCT00526617 |
| ABT-888 | Other | Phase PHASE1 | Non-hematologic Malignancies | COMPLETED | NCT00526617 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02487199 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02487199 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02487199 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02487199 |
| Placebo | Other | Phase PHASE3 | Obsessive Compulsive Disorder | COMPLETED | NCT01933919 |
| Fluvoxamine maleate | Other | Phase PHASE3 | Obsessive Compulsive Disorder | COMPLETED | NCT01933919 |
| Glecaprevir-pibrentasvir | Other | Phase PHASE4 | Hepatitis C | UNKNOWN | NCT03364725 |
| Testosterone Gel 1.62% | Other | Phase PHASE1 | Hypogonadism | COMPLETED | NCT01133548 |
| Testosterone Gel 1.62% | Other | Phase PHASE1 | Hypogonadism | COMPLETED | NCT01133548 |
| Testosterone Gel 1.62% | Other | Phase PHASE1 | Healthy | COMPLETED | NCT01130298 |
| ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | TERMINATED | NCT02504099 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | TERMINATED | NCT02504099 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | TERMINATED | NCT02504099 |
| Ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02356562 |
| Sofosbuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02356562 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02356562 |
| Ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02356562 |
| Sofosbuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02356562 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02356562 |
| ABT-767 | Other | Phase PHASE1 | Fallopian Tube | COMPLETED | NCT01339650 |
| ABT-767 | Other | Phase PHASE1 | Fallopian Tube | COMPLETED | NCT01339650 |
| adalimumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | COMPLETED | NCT01635764 |
| adalimumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | COMPLETED | NCT01635764 |
| Adalimumab | Other | Approved | Crohn Disease | COMPLETED | NCT02539849 |
| FOS | Other | Approved | Crohn Disease | COMPLETED | NCT02539849 |
| Adalimumab | Other | Approved | Crohn Disease | COMPLETED | NCT02539849 |
| FOS | Other | Approved | Crohn Disease | COMPLETED | NCT02539849 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02068222 |
| ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02068222 |
| ABT-450/ritonavir (r) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02068222 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02068222 |
| ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02068222 |
| ABT-450/ritonavir (r) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02068222 |
| adalimumab | Other | Phase PHASE4 | Moderate to Severe Crohn's Disease | COMPLETED | NCT02148718 |
| adalimumab | Other | Phase PHASE4 | Moderate to Severe Crohn's Disease | COMPLETED | NCT02148718 |
| ABBV-221 | Other | Phase PHASE1 | Head and Neck Squamous Cell Carcinoma | TERMINATED | NCT02365662 |
| ABBV-221 | Other | Phase PHASE1 | Head and Neck Squamous Cell Carcinoma | TERMINATED | NCT02365662 |
| ABBV-221 | Other | Phase PHASE1 | Head and Neck Squamous Cell Carcinoma | TERMINATED | NCT02365662 |
| SC-007 | Other | Phase PHASE1 | Colorectal Cancer (CRC) | TERMINATED | NCT03253185 |
| SC-007 | Other | Phase PHASE1 | Colorectal Cancer (CRC) | TERMINATED | NCT03253185 |
| SC-007 | Other | Phase PHASE1 | Colorectal Cancer (CRC) | TERMINATED | NCT03253185 |
| ABT-126 | Other | Phase PHASE2 | Schizophrenia | TERMINATED | NCT01834638 |
| ABT-126 | Other | Phase PHASE2 | Schizophrenia | TERMINATED | NCT01834638 |
| veliparib (ABT-888) | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT02210663 |
| Adalimumab | Other | Phase PHASE4 | RheumatoId Arthritis | UNKNOWN | NCT02035800 |
| Adalimumab | Other | Phase PHASE4 | RheumatoId Arthritis | UNKNOWN | NCT02035800 |
| Placebo | Other | Phase PHASE1 | Multiple Sclerosis | COMPLETED | NCT02601885 |
| ABT-555 | Other | Phase PHASE1 | Multiple Sclerosis | COMPLETED | NCT02601885 |
| Adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01866592 |
| Adalimumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT01866592 |
| Placebo for adalimumab | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT02015793 |
| Adalimumab | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT02015793 |
| Placebo for adalimumab | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT02015793 |
| Adalimumab | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT02015793 |
| J-tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01960842 |
| PEG tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01960842 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01960842 |
| Levodopa-carbidopa intestinal gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01960842 |
| J-tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01960842 |
| PEG tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01960842 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01960842 |
| Levodopa-carbidopa intestinal gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01960842 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01911845 |
| ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01911845 |
| ABT-450/r/ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01911845 |
| Placebo | Other | Phase PHASE3 | Axial Spondyloarthritis | COMPLETED | NCT01808118 |
| adalimumab | Other | Phase PHASE3 | Axial Spondyloarthritis | COMPLETED | NCT01808118 |
| Placebo | Other | Phase PHASE3 | Axial Spondyloarthritis | COMPLETED | NCT01808118 |
| adalimumab | Other | Phase PHASE3 | Axial Spondyloarthritis | COMPLETED | NCT01808118 |
| ABT-450/ritonavir, ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01672983 |
| ABT-450/ritonavir, ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT01672983 |
| Placebo | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02023099 |
| ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02023099 |
| ABT-199 | Other | Phase PHASE2 | Acute Myelogenous Leukemia | COMPLETED | NCT01994837 |
| ABT-199 | Other | Phase PHASE2 | Acute Myelogenous Leukemia | COMPLETED | NCT01994837 |
| temozolomide | Other | Phase PHASE2 | Ovarian Cancer | COMPLETED | NCT01113957 |
| pegylated liposomal doxorubicin | Other | Phase PHASE2 | Ovarian Cancer | COMPLETED | NCT01113957 |
| ABT-888 | Other | Phase PHASE2 | Ovarian Cancer | COMPLETED | NCT01113957 |
| temozolomide | Other | Phase PHASE2 | Ovarian Cancer | COMPLETED | NCT01113957 |
| pegylated liposomal doxorubicin | Other | Phase PHASE2 | Ovarian Cancer | COMPLETED | NCT01113957 |
| ABT-888 | Other | Phase PHASE2 | Ovarian Cancer | COMPLETED | NCT01113957 |
| Placebo | Other | Phase PHASE2 | Cognitive Deficits in Schizophrenia | COMPLETED | NCT01095562 |
| ABT-126 | Other | Phase PHASE2 | Cognitive Deficits in Schizophrenia | COMPLETED | NCT01095562 |
| Placebo | Other | Phase PHASE2 | Cognitive Deficits in Schizophrenia | COMPLETED | NCT01095562 |
| ABT-126 | Other | Phase PHASE2 | Cognitive Deficits in Schizophrenia | COMPLETED | NCT01095562 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| donepezil | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| ABT-288 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| donepezil | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| ABT-288 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| placebo | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| donepezil | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| ABT-288 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT01018875 |
| 1.75 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| 0.75 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| 0.25 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| Placebo for Atrasentan 0.2 mg/mL solution | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| 1.75 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| 0.75 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| 0.25 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| Placebo for Atrasentan 0.2 mg/mL solution | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| 1.75 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| 0.75 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| 0.25 mg Atrasentan QD | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| Placebo for Atrasentan 0.2 mg/mL solution | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT00920764 |
| etoposide/cisplatin | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00878449 |
| ABT-263 | Other | Phase PHASE1 | Solid Tumors | COMPLETED | NCT00878449 |
| Placebo | Other | Phase PHASE2 | Melanoma | COMPLETED | NCT00804908 |
| ABT-888 | Other | Phase PHASE2 | Melanoma | COMPLETED | NCT00804908 |
| temozolomide | Other | Phase PHASE2 | Melanoma | COMPLETED | NCT00804908 |
| Placebo | Other | Phase PHASE2 | Melanoma | COMPLETED | NCT00804908 |
| ABT-888 | Other | Phase PHASE2 | Melanoma | COMPLETED | NCT00804908 |
| temozolomide | Other | Phase PHASE2 | Melanoma | COMPLETED | NCT00804908 |
| ABT-263 | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT00445198 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01609933 |
| pegylated interferon alpha-2a (pegIFN) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01609933 |
| ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01609933 |
| ABT-450/r | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01609933 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01609933 |
| pegylated interferon alpha-2a (pegIFN) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01609933 |
| ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01609933 |
| ABT-450/r | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01609933 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT01550965 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT01550965 |
| paricalcitol | Other | Phase PHASE3 | End-Stage Renal Disease | COMPLETED | NCT01382212 |
| paricalcitol | Other | Phase PHASE3 | End-Stage Renal Disease | COMPLETED | NCT01382212 |
| paricalcitol | Other | Phase PHASE3 | End-Stage Renal Disease | COMPLETED | NCT01382212 |
| Placebo for ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01314261 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01314261 |
| Pegylated interferon (pegIFN) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01314261 |
| ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01314261 |
| Placebo for ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01314261 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01314261 |
| Pegylated interferon (pegIFN) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01314261 |
| ABT-267 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01314261 |
| Adalimumab delivered in Physiolis autoinjector | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in current autoinjector | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in Physiolis syringe | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in current syringe | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in Physiolis autoinjector | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in current autoinjector | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in Physiolis syringe | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in current syringe | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in Physiolis autoinjector | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in current autoinjector | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in Physiolis syringe | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Adalimumab delivered in current syringe | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01163617 |
| Placebo | Other | Phase PHASE3 | Chronic Kidney Disease Stage 3 and 4 | COMPLETED | NCT01020487 |
| Paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease Stage 3 and 4 | COMPLETED | NCT01020487 |
| Placebo | Other | Phase PHASE3 | Chronic Kidney Disease Stage 3 and 4 | COMPLETED | NCT01020487 |
| Paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease Stage 3 and 4 | COMPLETED | NCT01020487 |
| Ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT00851890 |
| Pegylated interferon | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT00851890 |
| Placebo for ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT00851890 |
| ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT00851890 |
| Ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT00851890 |
| Pegylated interferon | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT00851890 |
| Placebo for ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT00851890 |
| ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT00851890 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00686374 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT00686374 |
| Atorvastatin | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00616772 |
| Placebo | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00616772 |
| ABT-335 | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00616772 |
| Atorvastatin | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00616772 |
| Placebo | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00616772 |
| ABT-335 | Other | Phase PHASE3 | Coronary Artery Disease | COMPLETED | NCT00616772 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01931670 |
| placebo | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01931670 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01931670 |
| placebo | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01931670 |
| placebo | Other | Phase PHASE2 | Endometriosis, Pain | COMPLETED | NCT00619866 |
| Elagolix | Other | Phase PHASE2 | Endometriosis, Pain | COMPLETED | NCT00619866 |
| placebo | Other | Phase PHASE2 | Endometriosis, Pain | COMPLETED | NCT00619866 |
| Elagolix | Other | Phase PHASE2 | Endometriosis, Pain | COMPLETED | NCT00619866 |
| Placebo to Leuprorelin Acetate | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00797225 |
| Placebo to Elagolix | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00797225 |
| Elagolix | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00797225 |
| Leuprorelin Acetate Depot | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00797225 |
| Placebo to Leuprorelin Acetate | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00797225 |
| Placebo to Elagolix | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00797225 |
| Elagolix | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00797225 |
| Leuprorelin Acetate Depot | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00797225 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| ABBV-838 | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| ABBV-838 | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| ABBV-838 | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT02462525 |
| placebo | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01620528 |
| elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01620528 |
| placebo | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01620528 |
| elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01620528 |
| Elagolix | Other | Phase PHASE2 | Endometriosis, Pain | COMPLETED | NCT00973973 |
| Placebo | Other | Phase PHASE2 | Endometriosis, Pain | COMPLETED | NCT00973973 |
| Elagolix | Other | Phase PHASE2 | Endometriosis, Pain | COMPLETED | NCT00973973 |
| Placebo | Other | Phase PHASE2 | Endometriosis, Pain | COMPLETED | NCT00973973 |
| Placebo to DMPA-SC | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00437658 |
| Placebo to Elagolix | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00437658 |
| Subcutaneous depot medroxyprogesterone acetate (DMPA-SC) | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00437658 |
| Elagolix | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00437658 |
| Placebo to DMPA-SC | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00437658 |
| Placebo to Elagolix | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00437658 |
| Subcutaneous depot medroxyprogesterone acetate (DMPA-SC) | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00437658 |
| Elagolix | Other | Phase PHASE2 | Endometriosis | COMPLETED | NCT00437658 |
| paritaprevir/ritonavir/ombitasvir + dasabuvir +/- ribavirin | Other | Phase PHASE4 | Chronic Hepatitis C | COMPLETED | NCT03710252 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02185014 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02185014 |
| Calcifediol | Other | Phase PHASE4 | Secondary Hyperparathyroidism Due to Renal Causes | COMPLETED | NCT01939977 |
| Paricalcitol | Other | Phase PHASE4 | Secondary Hyperparathyroidism Due to Renal Causes | COMPLETED | NCT01939977 |
| Calcifediol | Other | Phase PHASE4 | Secondary Hyperparathyroidism Due to Renal Causes | COMPLETED | NCT01939977 |
| Paricalcitol | Other | Phase PHASE4 | Secondary Hyperparathyroidism Due to Renal Causes | COMPLETED | NCT01939977 |
| Calcifediol | Other | Phase PHASE4 | Secondary Hyperparathyroidism Due to Renal Causes | COMPLETED | NCT01939977 |
| Paricalcitol | Other | Phase PHASE4 | Secondary Hyperparathyroidism Due to Renal Causes | COMPLETED | NCT01939977 |
| Fluorouracil infusion | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Bevacizumab | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| FOLFIRI | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Modified FOLFIRI | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Placebo | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Veliparib | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Fluorouracil infusion | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Bevacizumab | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| FOLFIRI | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Modified FOLFIRI | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Placebo | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Veliparib | Other | Phase PHASE2 | Untreated Metastatic Colorectal Cancer | COMPLETED | NCT02305758 |
| Placebo | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| risankizumab SC | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| risankizumab IV | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| Placebo | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| risankizumab SC | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| risankizumab IV | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| Placebo | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| risankizumab SC | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| risankizumab IV | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02031276 |
| ABBV-176 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | TERMINATED | NCT03145909 |
| ABBV-176 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | TERMINATED | NCT03145909 |
| SC-005 | Other | Phase PHASE1 | Breast Cancer | TERMINATED | NCT03316794 |
| SC-005 | Other | Phase PHASE1 | Breast Cancer | TERMINATED | NCT03316794 |
| SC-005 | Other | Phase PHASE1 | Breast Cancer | TERMINATED | NCT03316794 |
| Rovalpituzumab tesirine | Other | Phase PHASE3 | Small Cell Lung Cancer | WITHDRAWN | NCT03334487 |
| Dexamethasone | Other | Phase PHASE3 | Small Cell Lung Cancer | WITHDRAWN | NCT03334487 |
| Rovalpituzumab tesirine | Other | Phase PHASE3 | Small Cell Lung Cancer | WITHDRAWN | NCT03334487 |
| Dexamethasone | Other | Phase PHASE3 | Small Cell Lung Cancer | WITHDRAWN | NCT03334487 |
| Rovalpituzumab tesirine | Other | Phase PHASE3 | Small Cell Lung Cancer | WITHDRAWN | NCT03334487 |
| Dexamethasone | Other | Phase PHASE3 | Small Cell Lung Cancer | WITHDRAWN | NCT03334487 |
| placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02499783 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02499783 |
| placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02499783 |
| adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02499783 |
| Adalimumab | Other | Phase PHASE3 | Generalized Pustular Psoriasis (GPP) | COMPLETED | NCT02533375 |
| Adalimumab | Other | Preclinical | Ankylosing Spondylitis | COMPLETED | NCT02333383 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01768858 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01768858 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01768858 |
| Glecaprevir/pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03069365 |
| ABBV-399 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT03311477 |
| ABBV-399 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT03311477 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02581189 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02581189 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02581189 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02581189 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02581189 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02581189 |
| ABBV-085 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT02565758 |
| ABBV-085 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT02565758 |
| ABBV-085 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT02565758 |
| risankizumab | Other | Phase PHASE2 | Asthma | COMPLETED | NCT02443298 |
| placebo | Other | Phase PHASE2 | Asthma | COMPLETED | NCT02443298 |
| risankizumab | Other | Phase PHASE2 | Asthma | COMPLETED | NCT02443298 |
| placebo | Other | Phase PHASE2 | Asthma | COMPLETED | NCT02443298 |
| risankizumab | Other | Phase PHASE2 | Asthma | COMPLETED | NCT02443298 |
| placebo | Other | Phase PHASE2 | Asthma | COMPLETED | NCT02443298 |
| Placebo | Other | Phase PHASE3 | Diabetic Nephropathy | TERMINATED | NCT01858532 |
| Atrasentan | Other | Phase PHASE3 | Diabetic Nephropathy | TERMINATED | NCT01858532 |
| Creon36™ | Other | Phase PHASE2 | Chronic Pancreatitis | COMPLETED | NCT02849704 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02582671 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C, Genotype 1 or 4 | COMPLETED | NCT02581163 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C, Genotype 1 or 4 | COMPLETED | NCT02581163 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C, Genotype 1 or 4 | COMPLETED | NCT02581163 |
| caremessage | Other | Approved | Medication Adherence | COMPLETED | NCT03052231 |
| caremessage | Other | Approved | Medication Adherence | COMPLETED | NCT03052231 |
| Atrasentan | Other | Phase PHASE2 | Nephropathy | COMPLETED | NCT02118714 |
| Atrasentan | Other | Phase PHASE2 | Nephropathy | COMPLETED | NCT02118714 |
| ABBV-181 | Other | Phase PHASE1 | Cancer | TERMINATED | NCT03138408 |
| SC-004 | Other | Phase PHASE1 | Cancer | TERMINATED | NCT03138408 |
| ABBV-181 | Other | Phase PHASE1 | Cancer | TERMINATED | NCT03138408 |
| SC-004 | Other | Phase PHASE1 | Cancer | TERMINATED | NCT03138408 |
| placebo for risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03000075 |
| risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03000075 |
| placebo for risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03000075 |
| risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03000075 |
| placebo for risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03000075 |
| risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03000075 |
| risankizumab | Other | Phase PHASE2 | Psoriatic Arthritis | COMPLETED | NCT02986373 |
| risankizumab | Other | Phase PHASE2 | Psoriatic Arthritis | COMPLETED | NCT02986373 |
| placebo for risankizumab | Other | Phase PHASE2 | Arthritis, Psoriatic | COMPLETED | NCT02719171 |
| risankizumab | Other | Phase PHASE2 | Arthritis, Psoriatic | COMPLETED | NCT02719171 |
| risankizumab | Other | Phase PHASE2 | Ankylosing Spondylitis (AS) | COMPLETED | NCT02047110 |
| placebo for risankizumab | Other | Phase PHASE2 | Ankylosing Spondylitis (AS) | COMPLETED | NCT02047110 |
| risankizumab | Other | Phase PHASE2 | Ankylosing Spondylitis (AS) | COMPLETED | NCT02047110 |
| placebo for risankizumab | Other | Phase PHASE2 | Ankylosing Spondylitis (AS) | COMPLETED | NCT02047110 |
| risankizumab | Other | Phase PHASE2 | Ankylosing Spondylitis (AS) | COMPLETED | NCT02047110 |
| placebo for risankizumab | Other | Phase PHASE2 | Ankylosing Spondylitis (AS) | COMPLETED | NCT02047110 |
| Rituximab | Other | Phase PHASE2 | Follicular Lymphoma | COMPLETED | NCT02187861 |
| Bendamustine | Other | Phase PHASE2 | Follicular Lymphoma | COMPLETED | NCT02187861 |
| Venetoclax | Other | Phase PHASE2 | Follicular Lymphoma | COMPLETED | NCT02187861 |
| Rituximab | Other | Phase PHASE2 | Follicular Lymphoma | COMPLETED | NCT02187861 |
| Bendamustine | Other | Phase PHASE2 | Follicular Lymphoma | COMPLETED | NCT02187861 |
| Venetoclax | Other | Phase PHASE2 | Follicular Lymphoma | COMPLETED | NCT02187861 |
| lamivudine | Other | Preclinical | HIV-1 Infection | COMPLETED | NCT02581202 |
| lopinavir/ritonavir | Other | Preclinical | HIV-1 Infection | COMPLETED | NCT02581202 |
| lamivudine | Other | Preclinical | HIV-1 Infection | COMPLETED | NCT02581202 |
| lopinavir/ritonavir | Other | Preclinical | HIV-1 Infection | COMPLETED | NCT02581202 |
| Placebo | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT02198651 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT02198651 |
| Placebo | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT02198651 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT02198651 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01736189 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01736189 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT01736189 |
| Non-steroidal Anti-inflammatory Drugs (NSAIDs) | Drug | Phase PHASE4 | Axial Spondyloarthritis | TERMINATED | NCT02897115 |
| Adalimumab | Other | Phase PHASE4 | Axial Spondyloarthritis | TERMINATED | NCT02897115 |
| Non-steroidal Anti-inflammatory Drugs (NSAIDs) | Drug | Phase PHASE4 | Axial Spondyloarthritis | TERMINATED | NCT02897115 |
| Adalimumab | Other | Phase PHASE4 | Axial Spondyloarthritis | TERMINATED | NCT02897115 |
| Non-steroidal Anti-inflammatory Drugs (NSAIDs) | Drug | Phase PHASE4 | Axial Spondyloarthritis | TERMINATED | NCT02897115 |
| Adalimumab | Other | Phase PHASE4 | Axial Spondyloarthritis | TERMINATED | NCT02897115 |
| Placebo | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03217734 |
| Methotrexate | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03217734 |
| Adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03217734 |
| Placebo | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03217734 |
| Methotrexate | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03217734 |
| Adalimumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT03217734 |
| ABT-414 | Other | Preclinical | Glioblastoma or Solid Tumors, Epidermal Growth Factor Receptor (EGFR) Diagnosis | NO_LONGER_AVAILABLE | NCT03123952 |
| ABT-414 | Other | Preclinical | Glioblastoma or Solid Tumors, Epidermal Growth Factor Receptor (EGFR) Diagnosis | NO_LONGER_AVAILABLE | NCT03123952 |
| ABT-414 | Other | Preclinical | Glioblastoma or Solid Tumors, Epidermal Growth Factor Receptor (EGFR) Diagnosis | NO_LONGER_AVAILABLE | NCT03123952 |
| PTV/r/OBV/DSV | Other | Phase PHASE4 | Hepatitis Viruses | COMPLETED | NCT02874066 |
| PTV/r/OBV/DSV | Other | Phase PHASE4 | Hepatitis Viruses | COMPLETED | NCT02874066 |
| EXVIERA | Other | Phase PHASE4 | HCV Coinfection | COMPLETED | NCT03050905 |
| VEKIRAX | Other | Phase PHASE4 | HCV Coinfection | COMPLETED | NCT03050905 |
| EXVIERA | Other | Phase PHASE4 | HCV Coinfection | COMPLETED | NCT03050905 |
| VEKIRAX | Other | Phase PHASE4 | HCV Coinfection | COMPLETED | NCT03050905 |
| Adalimumab | Other | Preclinical | Hidradenitis Suppurativa | COMPLETED | NCT02739828 |
| Adalimumab | Other | Preclinical | Hidradenitis Suppurativa | COMPLETED | NCT02739828 |
| Adalimumab | Other | Preclinical | Hidradenitis Suppurativa | COMPLETED | NCT02739828 |
| ABT450r-ABT267-ABT333 +/- Ribavirin | Other | Phase PHASE4 | Hepatitis C | COMPLETED | NCT02734173 |
| Fecal calprotectin | Other | Approved | Spondyloarthropathy | COMPLETED | NCT03064815 |
| PROMETHEUS® IBD sgi Diagnostic™ | Other | Approved | Spondyloarthropathy | COMPLETED | NCT03064815 |
| colonoscopy | Other | Approved | Spondyloarthropathy | COMPLETED | NCT03064815 |
| Videocapsule endoscopy | Other | Approved | Spondyloarthropathy | COMPLETED | NCT03064815 |
| Fecal calprotectin | Other | Approved | Spondyloarthropathy | COMPLETED | NCT03064815 |
| PROMETHEUS® IBD sgi Diagnostic™ | Other | Approved | Spondyloarthropathy | COMPLETED | NCT03064815 |
| colonoscopy | Other | Approved | Spondyloarthropathy | COMPLETED | NCT03064815 |
| Videocapsule endoscopy | Other | Approved | Spondyloarthropathy | COMPLETED | NCT03064815 |
| ABBV-8E12 | Other | Preclinical | Primary Tauopathy Corticobasal Degeneration Syndrome (CBD) | NO_LONGER_AVAILABLE | NCT03744546 |
| ABBV-8E12 | Other | Preclinical | Primary Tauopathy Corticobasal Degeneration Syndrome (CBD) | NO_LONGER_AVAILABLE | NCT03744546 |
| dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | WITHDRAWN | NCT03785184 |
| lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | WITHDRAWN | NCT03785184 |
| venetoclax | Other | Phase PHASE2 | Multiple Myeloma | WITHDRAWN | NCT03785184 |
| dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | WITHDRAWN | NCT03785184 |
| lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | WITHDRAWN | NCT03785184 |
| venetoclax | Other | Phase PHASE2 | Multiple Myeloma | WITHDRAWN | NCT03785184 |
| Placebo | Other | Phase PHASE2 | Knee Osteoarthritis | COMPLETED | NCT02087904 |
| ABT-981 | Other | Phase PHASE2 | Knee Osteoarthritis | COMPLETED | NCT02087904 |
| Placebo | Other | Phase PHASE2 | Knee Osteoarthritis | COMPLETED | NCT02087904 |
| ABT-981 | Other | Phase PHASE2 | Knee Osteoarthritis | COMPLETED | NCT02087904 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03212521 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03212521 |
| rovalpituzumab tesirine | Other | Preclinical | Small Cell Lung Cancer | NO_LONGER_AVAILABLE | NCT03503890 |
| rovalpituzumab tesirine | Other | Preclinical | Small Cell Lung Cancer | NO_LONGER_AVAILABLE | NCT03503890 |
| rovalpituzumab tesirine | Other | Preclinical | Small Cell Lung Cancer | NO_LONGER_AVAILABLE | NCT03503890 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT02668640 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT02668640 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT02668640 |
| Standard of Care (SOC) Physiotherapy | Drug | Preclinical | Axial Spondyloarthritis | TERMINATED | NCT03258814 |
| Active Supervised Training (AST) | Other | Preclinical | Axial Spondyloarthritis | TERMINATED | NCT03258814 |
| Standard of Care (SOC) Physiotherapy | Drug | Preclinical | Axial Spondyloarthritis | TERMINATED | NCT03258814 |
| Active Supervised Training (AST) | Other | Preclinical | Axial Spondyloarthritis | TERMINATED | NCT03258814 |
| Placebo | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02672852 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02672852 |
| Placebo | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02672852 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02672852 |
| Placebo | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02672852 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02672852 |
| Patient support program | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Patient support program | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Patient support program | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Ribavirin | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Dasabuvir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| Ombitasvir/paritaprevir/ritonavir | Other | Preclinical | Chronic Hepatitis C | COMPLETED | NCT02803138 |
| carboplatin | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| veliparib | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| paclitaxel | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| nivolumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| pemetrexed | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| carboplatin | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| veliparib | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| paclitaxel | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| nivolumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| pemetrexed | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | COMPLETED | NCT02944396 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT02056184 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT02056184 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT02056184 |
| AbbVie Care 2.0 | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT02750800 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT02750800 |
| AbbVie Care 2.0 | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT02750800 |
| Adalimumab | Other | Preclinical | Rheumatoid Arthritis | COMPLETED | NCT02750800 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03235349 |
| estradiol/norethindrone acetate (E2/NETA) | Other | Phase PHASE3 | Endometriosis | TERMINATED | NCT03343067 |
| elagolix | Other | Phase PHASE3 | Endometriosis | TERMINATED | NCT03343067 |
| estradiol/norethindrone acetate (E2/NETA) | Other | Phase PHASE3 | Endometriosis | TERMINATED | NCT03343067 |
| elagolix | Other | Phase PHASE3 | Endometriosis | TERMINATED | NCT03343067 |
| estradiol/norethindrone acetate (E2/NETA) | Other | Phase PHASE3 | Endometriosis | TERMINATED | NCT03343067 |
| elagolix | Other | Phase PHASE3 | Endometriosis | TERMINATED | NCT03343067 |
| ABBV-8E12 | Other | Phase PHASE1 | Progressive Supranuclear Palsy (PSP) | COMPLETED | NCT03413319 |
| ABBV-8E12 | Other | Phase PHASE1 | Progressive Supranuclear Palsy (PSP) | COMPLETED | NCT03413319 |
| Adalimumab | Other | Preclinical | Psoriasis | COMPLETED | NCT01387815 |
| Adalimumab | Other | Preclinical | Psoriasis | COMPLETED | NCT01387815 |
| ribavirin | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02609659 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02609659 |
| ribavirin | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02609659 |
| ombitasvir/paritaprevir/ritonavir and dasabuvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02609659 |
| ABT-199 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | COMPLETED | NCT01969695 |
| ABT-199 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | COMPLETED | NCT01969695 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03222583 |
| Placebo | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03222583 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03222583 |
| Placebo | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03222583 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03222583 |
| Placebo | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03222583 |
| pibrentasvir | Other | Preclinical | Hepatitis C Virus Infection | APPROVED_FOR_MARKETING | NCT03123965 |
| glecaprevir | Other | Preclinical | Hepatitis C Virus Infection | APPROVED_FOR_MARKETING | NCT03123965 |
| pibrentasvir | Other | Preclinical | Hepatitis C Virus Infection | APPROVED_FOR_MARKETING | NCT03123965 |
| glecaprevir | Other | Preclinical | Hepatitis C Virus Infection | APPROVED_FOR_MARKETING | NCT03123965 |
| ABBV-181 | Other | Phase PHASE1 | Colorectal Cancer | TERMINATED | NCT03035279 |
| SC-006 | Other | Phase PHASE1 | Colorectal Cancer | TERMINATED | NCT03035279 |
| ABBV-181 | Other | Phase PHASE1 | Colorectal Cancer | TERMINATED | NCT03035279 |
| SC-006 | Other | Phase PHASE1 | Colorectal Cancer | TERMINATED | NCT03035279 |
| Ribavirin 200Mg Tablet | Other | Phase PHASE3 | Hepatitis C | COMPLETED | NCT03092375 |
| Glecaprevir/Pibrentasvir (G/P) 300mg/120mg | Other | Phase PHASE3 | Hepatitis C | COMPLETED | NCT03092375 |
| Ribavirin 200Mg Tablet | Other | Phase PHASE3 | Hepatitis C | COMPLETED | NCT03092375 |
| Glecaprevir/Pibrentasvir (G/P) 300mg/120mg | Other | Phase PHASE3 | Hepatitis C | COMPLETED | NCT03092375 |
| Punch Biopsy | Other | Approved | Psoriasis | COMPLETED | NCT03048721 |
| Skin Tape Stripping | Other | Approved | Psoriasis | COMPLETED | NCT03048721 |
| Punch Biopsy | Other | Approved | Psoriasis | COMPLETED | NCT03048721 |
| Skin Tape Stripping | Other | Approved | Psoriasis | COMPLETED | NCT03048721 |
| Punch Biopsy | Other | Approved | Psoriasis | COMPLETED | NCT03048721 |
| Skin Tape Stripping | Other | Approved | Psoriasis | COMPLETED | NCT03048721 |
| DSM265 25% SDD, 400 mg fasted | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT03637517 |
| DSM265-TPGS 34% SDD, 400 mg fed | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT03637517 |
| DSM265-TPGS 34% SDD, 400 mg fasted | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT03637517 |
| DSM265 25% SDD, 400 mg fasted | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT03637517 |
| DSM265-TPGS 34% SDD, 400 mg fed | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT03637517 |
| DSM265-TPGS 34% SDD, 400 mg fasted | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT03637517 |
| Etoposide | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Cisplatin | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Rovalpituzumab Tesirine | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Etoposide | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Cisplatin | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Rovalpituzumab Tesirine | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Etoposide | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Cisplatin | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Rovalpituzumab Tesirine | Other | Phase PHASE1 | Small Cell Lung Cancer | TERMINATED | NCT02819999 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03219216 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03219216 |
| Pancreatic Enzyme | Other | Phase PHASE2 | Short Bowel Syndrome | COMPLETED | NCT03097029 |
| Pancreatic Enzyme | Other | Phase PHASE2 | Short Bowel Syndrome | COMPLETED | NCT03097029 |
| Risankizumab 180 mg SC | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02513459 |
| Risankizumab 600 mg IV | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02513459 |
| Risankizumab 180 mg SC | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02513459 |
| Risankizumab 600 mg IV | Other | Phase PHASE2 | Crohn Disease | COMPLETED | NCT02513459 |
| adalimumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | COMPLETED | NCT02904902 |
| adalimumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | COMPLETED | NCT02904902 |
| Adalimumab | Other | Phase PHASE4 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT02808975 |
| Placebo | Other | Phase PHASE4 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT02808975 |
| Adalimumab | Other | Phase PHASE4 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT02808975 |
| Placebo | Other | Phase PHASE4 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT02808975 |
| Placebo | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT02289690 |
| Etoposide | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT02289690 |
| Carboplatin | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT02289690 |
| Veliparib | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT02289690 |
| Placebo | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT02289690 |
| Etoposide | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT02289690 |
| Carboplatin | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT02289690 |
| Veliparib | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT02289690 |
| Lomustine | Other | Phase PHASE2 | Glioblastoma | COMPLETED | NCT02343406 |
| Temozolomide | Other | Phase PHASE2 | Glioblastoma | COMPLETED | NCT02343406 |
| Depatuxizumab mafodotin | Other | Phase PHASE2 | Glioblastoma | COMPLETED | NCT02343406 |
| Prednisone | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Vincristine | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Doxorubicin | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Rituximab | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Obinutuzumab | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Cyclophosphamide | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Venetoclax | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Prednisone | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Vincristine | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Doxorubicin | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Rituximab | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Obinutuzumab | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Cyclophosphamide | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Venetoclax | Other | Phase PHASE1 | Lymphoma, Non-Hodgkin | COMPLETED | NCT02055820 |
| Placebo for Elagolix | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02654054 |
| Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02654054 |
| Placebo for Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02654054 |
| Elagolix | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02654054 |
| Placebo for Elagolix | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02654054 |
| Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02654054 |
| Placebo for Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02654054 |
| Elagolix | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02654054 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03089944 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT03089944 |
| Intensity modulated radiation therapy | Drug | Phase PHASE1 | Pancreatic Cancer | COMPLETED | NCT01908478 |
| Gemcitabine | Other | Phase PHASE1 | Pancreatic Cancer | COMPLETED | NCT01908478 |
| Veliparib | Other | Phase PHASE1 | Pancreatic Cancer | COMPLETED | NCT01908478 |
| Intensity modulated radiation therapy | Drug | Phase PHASE1 | Pancreatic Cancer | COMPLETED | NCT01908478 |
| Gemcitabine | Other | Phase PHASE1 | Pancreatic Cancer | COMPLETED | NCT01908478 |
| Veliparib | Other | Phase PHASE1 | Pancreatic Cancer | COMPLETED | NCT01908478 |
| Placebo | Other | Phase PHASE2 | Atopic Dermatitis | COMPLETED | NCT02925117 |
| Upadacitinib | Other | Phase PHASE2 | Atopic Dermatitis | COMPLETED | NCT02925117 |
| Placebo | Other | Phase PHASE2 | Atopic Dermatitis | COMPLETED | NCT02925117 |
| Upadacitinib | Other | Phase PHASE2 | Atopic Dermatitis | COMPLETED | NCT02925117 |
| Nivolumab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT02955251 |
| ABBV-428 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT02955251 |
| Nivolumab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT02955251 |
| ABBV-428 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT02955251 |
| Nivolumab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT02955251 |
| ABBV-428 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT02955251 |
| E2/NETA placebo | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01817530 |
| 1 mg estradiol / 0.5 mg norethindrone acetate | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01817530 |
| 0.5 mg estradiol / 0.1 mg norethindrone acetate | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01817530 |
| Elagolix | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01817530 |
| Elagolix placebo | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01817530 |
| Jejunal extension tube | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT02799381 |
| Percutaneous endoscopic gastrostomy tube | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT02799381 |
| CADD-Legacy ambulatory infusion pump | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT02799381 |
| Levodopa-Carbidopa Intestinal Gel (LCIG) | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT02799381 |
| Optimized antiparkinsonian treatment | Drug | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT02799381 |
| ABT-414 | Other | Phase PHASE1 | Malignant Glioma | COMPLETED | NCT02590263 |
| Temozolomide | Other | Phase PHASE1 | Malignant Glioma | COMPLETED | NCT02590263 |
| Whole Brain Radiation | Other | Phase PHASE1 | Malignant Glioma | COMPLETED | NCT02590263 |
| ABT-414 | Other | Phase PHASE1 | Malignant Glioma | COMPLETED | NCT02590263 |
| Temozolomide | Other | Phase PHASE1 | Malignant Glioma | COMPLETED | NCT02590263 |
| Whole Brain Radiation | Other | Phase PHASE1 | Malignant Glioma | COMPLETED | NCT02590263 |
| ABT-530 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT02441283 |
| ABT-493 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT02441283 |
| ABT-530 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT02441283 |
| ABT-493 | Other | Phase PHASE2 | Hepatitis C | COMPLETED | NCT02441283 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT02065557 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT02065557 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT02065557 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT02065557 |
| Dexamethasone | Other | Phase PHASE1 | Malignant Melanoma | TERMINATED | NCT02709889 |
| Rovalpituzumab tesirine | Other | Phase PHASE1 | Malignant Melanoma | TERMINATED | NCT02709889 |
| Endoscopic balloon dilatation | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Thiopurine | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Adalimumab Injection | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Endoscopic balloon dilatation | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Thiopurine | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Adalimumab Injection | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Endoscopic balloon dilatation | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Thiopurine | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Adalimumab Injection | Other | Phase PHASE4 | Crohn Disease | UNKNOWN | NCT03220841 |
| Capecitabine | Other | Phase PHASE1 | Breast Cancer | TERMINATED | NCT04274933 |
| Venetoclax | Other | Phase PHASE1 | Breast Cancer | TERMINATED | NCT04274933 |
| Capecitabine | Other | Phase PHASE1 | Breast Cancer | TERMINATED | NCT04274933 |
| Venetoclax | Other | Phase PHASE1 | Breast Cancer | TERMINATED | NCT04274933 |
| Liver vein catheterization | Other | Preclinical | Hepatitis C | COMPLETED | NCT02526641 |
| Galactose Elimination Capacity (GEC) | Other | Preclinical | Hepatitis C | COMPLETED | NCT02526641 |
| Functional Hepatic Nitrogen Clearance (FHNC) | Other | Preclinical | Hepatitis C | COMPLETED | NCT02526641 |
| Placebo to veliparib | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Paclitaxel | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Veliparib | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Carboplatin | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Placebo to veliparib | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Paclitaxel | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Veliparib | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Carboplatin | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Placebo to veliparib | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Paclitaxel | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Veliparib | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Carboplatin | Other | Phase PHASE3 | Squamous Non-Small Cell Lung Cancer | COMPLETED | NCT02106546 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis (UC) | COMPLETED | NCT02065622 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis (UC) | COMPLETED | NCT02065622 |
| ABBV-927 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| ABBV-368 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| ABBV-181 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| ABBV-927 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| ABBV-368 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| ABBV-181 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| ABBV-927 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| ABBV-368 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| ABBV-181 | Other | Phase PHASE1 | Head and Neck Cancer | TERMINATED | NCT03818542 |
| rovalpituzumab tesirine | Other | Phase PHASE2 | Cancer | COMPLETED | NCT03543358 |
| rovalpituzumab tesirine | Other | Phase PHASE2 | Cancer | COMPLETED | NCT03543358 |
| rovalpituzumab tesirine | Other | Phase PHASE2 | Cancer | COMPLETED | NCT03543358 |
| Veliparib | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Carboplatin | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Paclitaxel | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Doxorubicin | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Placebo | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Cyclophosphamide | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Veliparib | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Carboplatin | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Paclitaxel | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Doxorubicin | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Placebo | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| Cyclophosphamide | Other | Phase PHASE3 | Triple Negative Breast Cancer | COMPLETED | NCT02032277 |
| ombitasvir, paritaprevir/r, dasabuvir | Other | Phase PHASE4 | Hepatitis C, Chronic | COMPLETED | NCT02461745 |
| ombitasvir, paritaprevir/r, dasabuvir + ribavirin | Other | Phase PHASE4 | Hepatitis C, Chronic | COMPLETED | NCT02461745 |
| ombitasvir, paritaprevir/r, dasabuvir | Other | Phase PHASE4 | Hepatitis C, Chronic | COMPLETED | NCT02461745 |
| ombitasvir, paritaprevir/r, dasabuvir + ribavirin | Other | Phase PHASE4 | Hepatitis C, Chronic | COMPLETED | NCT02461745 |
| placebo for rizankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03518047 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03518047 |
| placebo for rizankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03518047 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03518047 |
| Placebo solution for IV infusion on Day 15 | Other | Phase PHASE2 | Progressive Supranuclear Palsy (PSP) | TERMINATED | NCT03391765 |
| ABBV-8E12 | Other | Phase PHASE2 | Progressive Supranuclear Palsy (PSP) | TERMINATED | NCT03391765 |
| Placebo solution for IV infusion on Day 15 | Other | Phase PHASE2 | Progressive Supranuclear Palsy (PSP) | TERMINATED | NCT03391765 |
| ABBV-8E12 | Other | Phase PHASE2 | Progressive Supranuclear Palsy (PSP) | TERMINATED | NCT03391765 |
| Placebo solution for IV infusion on Day 15 | Other | Phase PHASE2 | Progressive Supranuclear Palsy (PSP) | TERMINATED | NCT03391765 |
| ABBV-8E12 | Other | Phase PHASE2 | Progressive Supranuclear Palsy (PSP) | TERMINATED | NCT03391765 |
| ABBV-8E12 | Other | Phase PHASE2 | Progressive Supranuclear Palsy | TERMINATED | NCT02985879 |
| Placebo | Other | Phase PHASE2 | Progressive Supranuclear Palsy | TERMINATED | NCT02985879 |
| ABBV-8E12 | Other | Phase PHASE2 | Progressive Supranuclear Palsy | TERMINATED | NCT02985879 |
| Placebo | Other | Phase PHASE2 | Progressive Supranuclear Palsy | TERMINATED | NCT02985879 |
| ABBV-8E12 | Other | Phase PHASE2 | Progressive Supranuclear Palsy | TERMINATED | NCT02985879 |
| Placebo | Other | Phase PHASE2 | Progressive Supranuclear Palsy | TERMINATED | NCT02985879 |
| Irinotecan | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| ABT-165 | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Fluorouracil - infusion | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Bevacizumab | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Fluorouracil - bolus | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Leucovorin | Other | Phase PHASE2 | Cancer | TERMINATED | NCT03368859 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Cancer | TERMINATED | NCT04274907 |
| Venetoclax | Other | Phase PHASE1 | Non Small Cell Lung Cancer | TERMINATED | NCT04274907 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Cancer | TERMINATED | NCT04274907 |
| Venetoclax | Other | Phase PHASE1 | Non Small Cell Lung Cancer | TERMINATED | NCT04274907 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02065570 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02065570 |
| Placebo | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02065570 |
| Adalimumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT02065570 |
| Dexamethasone | Other | Phase PHASE3 | Small Cell Lung Cancer | COMPLETED | NCT03061812 |
| Topotecan | Other | Phase PHASE3 | Small Cell Lung Cancer | COMPLETED | NCT03061812 |
| Rovalpituzumab tesirine | Other | Phase PHASE3 | Small Cell Lung Cancer | COMPLETED | NCT03061812 |
| Pemetrexed | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Veliparib | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Cisplatin | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Carboplatin | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Paclitaxel | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Pemetrexed | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Veliparib | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Cisplatin | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Carboplatin | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Paclitaxel | Other | Phase PHASE3 | Non-squamous Non-small Cell Lung Cancer | COMPLETED | NCT02264990 |
| Venetoclax (RP2D) | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Irinotecan 60 mg/m2 | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 600 | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 400 | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 200 MG | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 100 MG | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 50 MG | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax (RP2D) | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Irinotecan 60 mg/m2 | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 600 | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 400 | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 200 MG | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 100 MG | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| Venetoclax 50 MG | Other | Phase PHASE1 | Relapsed Small Cell Lung Cancer | WITHDRAWN | NCT04543916 |
| adalimumab | Other | Phase PHASE3 | Pyoderma Gangrenosum | COMPLETED | NCT03311464 |
| Placebo solution for risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875482 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875482 |
| Placebo solution for risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875482 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875482 |
| No pancreatic enzyme replacement therapy | Drug | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| PERTZYE | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| other non-sponsor pancreatic enzyme replacement therapy | Drug | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| ZENPEP | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| CREON | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| PANCREAZE | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| ULTRESA | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| No pancreatic enzyme replacement therapy | Drug | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| PERTZYE | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| other non-sponsor pancreatic enzyme replacement therapy | Drug | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| ZENPEP | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| CREON | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| PANCREAZE | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| ULTRESA | Other | Preclinical | Fibrosing Colonopathy | TERMINATED | NCT01652157 |
| ABBV-744 | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT03360006 |
| ABBV-744 | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT03360006 |
| ABBV-744 | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT03360006 |
| rituximab / IDEC-C2B8 | Other | Phase PHASE1 | Non-Hodgkin Lymphoma (NHL) | COMPLETED | NCT02265731 |
| venetoclax | Other | Phase PHASE1 | Non-Hodgkin Lymphoma (NHL) | COMPLETED | NCT02265731 |
| azacitadine | Other | Phase PHASE1 | Non-Hodgkin Lymphoma (NHL) | COMPLETED | NCT02265731 |
| rituximab / IDEC-C2B8 | Other | Phase PHASE1 | Non-Hodgkin Lymphoma (NHL) | COMPLETED | NCT02265731 |
| venetoclax | Other | Phase PHASE1 | Non-Hodgkin Lymphoma (NHL) | COMPLETED | NCT02265731 |
| azacitadine | Other | Phase PHASE1 | Non-Hodgkin Lymphoma (NHL) | COMPLETED | NCT02265731 |
| dexamethasone | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT01794507 |
| bortezomib | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT01794507 |
| ABT-199 | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT01794507 |
| Paclitaxel | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Carboplatin | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Veliparib, tablet | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Veliparib, capsule | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Paclitaxel | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Carboplatin | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Veliparib, tablet | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Veliparib, capsule | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05268068 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05268068 |
| Placebo | Other | Phase PHASE4 | Uterine Fibroids | COMPLETED | NCT03886220 |
| Elagolix | Other | Phase PHASE4 | Uterine Fibroids | COMPLETED | NCT03886220 |
| Pneumococcal 13-valent conjugate vaccine (PCV-13) | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02049138 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02049138 |
| Pneumococcal 13-valent conjugate vaccine (PCV-13) | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02049138 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02049138 |
| Epcoritamab | Other | Preclinical | Lymphoma | NO_LONGER_AVAILABLE | NCT05692050 |
| Epcoritamab | Other | Preclinical | Lymphoma | NO_LONGER_AVAILABLE | NCT05692050 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Carfilzomib | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Lemzoparlimab | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Carfilzomib | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Lemzoparlimab | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Placebo | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04223804 |
| ABBV-181 | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04223804 |
| ABBV-CLS-7262 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT05763459 |
| ABBV-CLS-7262 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT05763459 |
| Placebo for venetoclax | Other | Phase PHASE3 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT02755597 |
| Dexamethasone | Other | Phase PHASE3 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT02755597 |
| Bortezomib | Other | Phase PHASE3 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT02755597 |
| Venetoclax | Other | Phase PHASE3 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT02755597 |
| Placebo for venetoclax | Other | Phase PHASE3 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT02755597 |
| Dexamethasone | Other | Phase PHASE3 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT02755597 |
| Bortezomib | Other | Phase PHASE3 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT02755597 |
| Venetoclax | Other | Phase PHASE3 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT02755597 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Azacitidine | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Venetoclax | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Matching Placebo for PVEK | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Pivekimab Sunirine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | TEMPORARILY_NOT_AVAILABLE | NCT04830202 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | AVAILABLE | NCT04278235 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04379050 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Liposomal daunorubicin and cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Daunorubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Idarubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Nab-Paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, budigalimab, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| TTX-030, nab-paclitaxel and gemcitabine | Other | Phase PHASE2 | Pancreatic Cancer | COMPLETED | NCT06119217 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT03844048 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Iberdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Liposomal daunorubicin and cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Daunorubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Idarubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Iberdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Matching Placebo for PVEK | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Pivekimab Sunirine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Azacitidine | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Venetoclax | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT03781167 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT03781167 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT03781167 |
| Midazolam | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05895266 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05895266 |
| Midazolam | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05895266 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05895266 |
| Placebo | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT03518034 |
| AndroGel® | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT03518034 |
| BOTOX Dose C | Other | Phase PHASE2 | Ventral Hernia | WITHDRAWN | NCT05606757 |
| BOTOX Dose B | Other | Phase PHASE2 | Ventral Hernia | WITHDRAWN | NCT05606757 |
| Placebo for BOTOX | Other | Phase PHASE2 | Ventral Hernia | WITHDRAWN | NCT05606757 |
| BOTOX Dose A | Other | Phase PHASE2 | Ventral Hernia | WITHDRAWN | NCT05606757 |
| BOTOX Dose C | Other | Phase PHASE2 | Ventral Hernia | WITHDRAWN | NCT05606757 |
| BOTOX Dose B | Other | Phase PHASE2 | Ventral Hernia | WITHDRAWN | NCT05606757 |
| Placebo for BOTOX | Other | Phase PHASE2 | Ventral Hernia | WITHDRAWN | NCT05606757 |
| BOTOX Dose A | Other | Phase PHASE2 | Ventral Hernia | WITHDRAWN | NCT05606757 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Liposomal daunorubicin and cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Daunorubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Idarubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Iberdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Matching Placebo for PVEK | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Pivekimab Sunirine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Azacitidine | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Venetoclax | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis (AD) | WITHDRAWN | NCT04666675 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis (AD) | WITHDRAWN | NCT04666675 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis (AD) | WITHDRAWN | NCT04666675 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis (AD) | WITHDRAWN | NCT04666675 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis (AD) | WITHDRAWN | NCT04666675 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis (AD) | WITHDRAWN | NCT04666675 |
| Standard cytotherapy | Drug | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Nivolumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Ramucirumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Bemarituzumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| ABT-806 | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Trastuzumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Standard cytotherapy | Drug | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Nivolumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Ramucirumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Bemarituzumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| ABT-806 | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Trastuzumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Standard cytotherapy | Drug | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Nivolumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Ramucirumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Bemarituzumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| ABT-806 | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Trastuzumab | Other | Phase PHASE2 | Adenocarcinoma | COMPLETED | NCT02213289 |
| Placebo | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01893996 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01893996 |
| Placebo | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01893996 |
| Adalimumab | Other | Phase PHASE4 | Rheumatoid Arthritis | COMPLETED | NCT01893996 |
| Radiation | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Temozolomide | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Depatuxizumab mafodotin | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Ophthalmic steroid ointment | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Cold compress | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Vasoconstrictor eye drops | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Steroid eye drops | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Radiation | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Temozolomide | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Depatuxizumab mafodotin | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Ophthalmic steroid ointment | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Cold compress | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Vasoconstrictor eye drops | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Steroid eye drops | Other | Phase PHASE3 | Glioblastoma Multiforme | TERMINATED | NCT03419403 |
| Placebo for upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Placebo for elsubrutinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Elsubrutinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Placebo for upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Placebo for elsubrutinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Elsubrutinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Placebo for upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Placebo for elsubrutinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| Elsubrutinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03682705 |
| ABBV-321 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT03234712 |
| Placebo for ABBV-157 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03922607 |
| ABBV-157 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03922607 |
| Placebo for ABBV-157 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03922607 |
| ABBV-157 | Other | Phase PHASE1 | Psoriasis | COMPLETED | NCT03922607 |
| Autoinjector | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875508 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875508 |
| Autoinjector | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875508 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875508 |
| Autoinjector | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875508 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03875508 |
| ABT-SLV187 | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02082249 |
| ABT-SLV187 | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02082249 |
| ABT-SLV187 | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02082249 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Pomalidomide | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Venetoclax | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Pomalidomide | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Venetoclax | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Pomalidomide | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Venetoclax | Other | Phase PHASE2 | Multiple Myeloma | TERMINATED | NCT03567616 |
| Placebo | Other | Phase PHASE1 | Alzheimer's Disease | TERMINATED | NCT02573740 |
| ABT-957 | Other | Phase PHASE1 | Alzheimer's Disease | TERMINATED | NCT02573740 |
| Placebo | Other | Phase PHASE1 | Alzheimer's Disease | TERMINATED | NCT02573740 |
| ABT-957 | Other | Phase PHASE1 | Alzheimer's Disease | TERMINATED | NCT02573740 |
| Placebo for ABT-957 | Other | Phase PHASE1 | Alzheimer's Disease | TERMINATED | NCT02220738 |
| ABT-957 | Other | Phase PHASE1 | Alzheimer's Disease | TERMINATED | NCT02220738 |
| Placebo for ABT-957 | Other | Phase PHASE1 | Alzheimer's Disease | TERMINATED | NCT02220738 |
| ABT-957 | Other | Phase PHASE1 | Alzheimer's Disease | TERMINATED | NCT02220738 |
| Placebo | Other | Phase PHASE2 | Acute Kidney Injury | COMPLETED | NCT01777165 |
| ABT-719 | Other | Phase PHASE2 | Acute Kidney Injury | COMPLETED | NCT01777165 |
| Placebo | Other | Phase PHASE2 | Acute Kidney Injury | COMPLETED | NCT01777165 |
| ABT-719 | Other | Phase PHASE2 | Acute Kidney Injury | COMPLETED | NCT01777165 |
| Placebo | Other | Phase PHASE2 | Acute Kidney Injury | COMPLETED | NCT01777165 |
| ABT-719 | Other | Phase PHASE2 | Acute Kidney Injury | COMPLETED | NCT01777165 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT01678755 |
| ABT-126 | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT01678755 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT01678755 |
| ABT-126 | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT01678755 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT01655680 |
| ABT-126 | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT01655680 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT01655680 |
| ABT-126 | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT01655680 |
| placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT01468207 |
| adalimumab | Other | Phase PHASE3 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT01468207 |
| placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT01468207 |
| adalimumab | Other | Phase PHASE3 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT01468207 |
| Placebo | Other | Phase PHASE3 | Peripheral Spondyloarthritis | COMPLETED | NCT01064856 |
| Adalimumab | Other | Phase PHASE3 | Peripheral Spondyloarthritis | COMPLETED | NCT01064856 |
| Placebo | Other | Phase PHASE3 | Peripheral Spondyloarthritis | COMPLETED | NCT01064856 |
| Adalimumab | Other | Phase PHASE3 | Peripheral Spondyloarthritis | COMPLETED | NCT01064856 |
| Placebo | Other | Phase PHASE3 | Peripheral Spondyloarthritis | COMPLETED | NCT01064856 |
| Adalimumab | Other | Phase PHASE3 | Peripheral Spondyloarthritis | COMPLETED | NCT01064856 |
| adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00573794 |
| adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00573794 |
| adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT00573794 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT02292719 |
| Sofosbuvir | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT02292719 |
| OBV/PTV/r | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT02292719 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT02292719 |
| Sofosbuvir | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT02292719 |
| OBV/PTV/r | Other | Phase PHASE2 | Chronic Hepatitis C Virus Infection | COMPLETED | NCT02292719 |
| Dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02219503 |
| Ombitasvir/Paritaprevir/Ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02219503 |
| Dasabuvir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02219503 |
| Ombitasvir/Paritaprevir/Ritonavir | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT02219503 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01995071 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01995071 |
| ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01995071 |
| ABT-493 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01995071 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01995071 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01995071 |
| ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01995071 |
| ABT-493 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT01995071 |
| ribavirin | Other | Phase PHASE2 | Hepatitis C Virus Infection | COMPLETED | NCT01939197 |
| ABT-333 | Other | Phase PHASE2 | Hepatitis C Virus Infection | COMPLETED | NCT01939197 |
| ABT-450/r/ABT-267 | Other | Phase PHASE2 | Hepatitis C Virus Infection | COMPLETED | NCT01939197 |
| ribavirin | Other | Phase PHASE2 | Hepatitis C Virus Infection | COMPLETED | NCT01939197 |
| ABT-333 | Other | Phase PHASE2 | Hepatitis C Virus Infection | COMPLETED | NCT01939197 |
| ABT-450/r/ABT-267 | Other | Phase PHASE2 | Hepatitis C Virus Infection | COMPLETED | NCT01939197 |
| Placebo for Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01833533 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01833533 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01833533 |
| Placebo for Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01833533 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01833533 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01833533 |
| Placebo for ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01767116 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01767116 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01767116 |
| Placebo for ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01767116 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01767116 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01767116 |
| Placebo for ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| Placebo for ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| Placebo for ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| Placebo for ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| Placebo for ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| Placebo for ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01716585 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01674725 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01674725 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01674725 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01674725 |
| placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT01468233 |
| adalimumab | Other | Phase PHASE3 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT01468233 |
| placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT01468233 |
| adalimumab | Other | Phase PHASE3 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT01468233 |
| placebo for adalimumab | Other | Phase PHASE3 | Enthesitis Related Arthritis (ERA) | COMPLETED | NCT01166282 |
| adalimumab | Other | Phase PHASE3 | Enthesitis Related Arthritis (ERA) | COMPLETED | NCT01166282 |
| placebo for adalimumab | Other | Phase PHASE3 | Enthesitis Related Arthritis (ERA) | COMPLETED | NCT01166282 |
| adalimumab | Other | Phase PHASE3 | Enthesitis Related Arthritis (ERA) | COMPLETED | NCT01166282 |
| adalimumab | Other | Phase PHASE3 | Uveitis | COMPLETED | NCT01148225 |
| adalimumab | Other | Phase PHASE3 | Uveitis | COMPLETED | NCT01148225 |
| secukinumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03478787 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03478787 |
| Elagolix | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02925494 |
| Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02925494 |
| Elagolix | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02925494 |
| Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02925494 |
| ABT-493 coformulated with ABT-530 | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02738138 |
| ABT-493 coformulated with ABT-530 | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02738138 |
| glecaprevir/pibrentasvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02692703 |
| glecaprevir/pibrentasvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02692703 |
| Placebo for Elagolix | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02691494 |
| Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02691494 |
| Placebo for Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02691494 |
| Elagolix | Other | Phase PHASE3 | Uterine Fibroids | COMPLETED | NCT02691494 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02642432 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02642432 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02636595 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02636595 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02636595 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02604017 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02604017 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02604017 |
| ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243280 |
| ABT-493 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243280 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT02143713 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT02143713 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01760954 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT01760954 |
| Progesterone | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Estradiol | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Estradiol/Norethindrone acetate (E2/NETA) | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Placebo | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Elagolix | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Progesterone | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Estradiol | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Estradiol/Norethindrone acetate (E2/NETA) | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Placebo | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| Elagolix | Other | Phase PHASE2 | Heavy Uterine Bleeding | COMPLETED | NCT01441635 |
| ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02723084 |
| sofosbuvir (SOF) | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02723084 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02723084 |
| ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02723084 |
| sofosbuvir (SOF) | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02723084 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02723084 |
| OBV/PTV/r | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02707952 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02707952 |
| OBV/PTV/r | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02707952 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02707952 |
| OBV/PTV/r | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02707952 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus | COMPLETED | NCT02707952 |
| Placebo for ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02640482 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection | COMPLETED | NCT02640482 |
| Levodopa-carbidopa Immediate Release (LC-IR) Tablets | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01736176 |
| Percutaneous Endoscopic Gastrostomy with Jejunal Extension (PEG-J) | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01736176 |
| Levodopa-Carbidopa Intestinal Gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01736176 |
| Levodopa-carbidopa Immediate Release (LC-IR) Tablets | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01736176 |
| Percutaneous Endoscopic Gastrostomy with Jejunal Extension (PEG-J) | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01736176 |
| Levodopa-Carbidopa Intestinal Gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT01736176 |
| Placebo for adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03823391 |
| Adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03823391 |
| Placebo for ABBV-3373 | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03823391 |
| ABBV-3373 | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03823391 |
| Placebo for adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03823391 |
| Adalimumab | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03823391 |
| Placebo for ABBV-3373 | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03823391 |
| ABBV-3373 | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03823391 |
| blood drawing | Other | Approved | Chronic Hepatitis C | COMPLETED | NCT03155113 |
| blood drawing | Other | Approved | Chronic Hepatitis C | COMPLETED | NCT03155113 |
| Vinorelbine | Other | Preclinical | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | NO_LONGER_AVAILABLE | NCT02985658 |
| Cisplatin | Other | Preclinical | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | NO_LONGER_AVAILABLE | NCT02985658 |
| Veliparib | Other | Preclinical | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | NO_LONGER_AVAILABLE | NCT02985658 |
| Vinorelbine | Other | Preclinical | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | NO_LONGER_AVAILABLE | NCT02985658 |
| Cisplatin | Other | Preclinical | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | NO_LONGER_AVAILABLE | NCT02985658 |
| Veliparib | Other | Preclinical | Metastatic Breast Cancer With BRCA 1 or BRCA 2 Genetic Mutation | NO_LONGER_AVAILABLE | NCT02985658 |
| ABBV-467 | Other | Phase PHASE1 | Multiple Myeloma (MM) | TERMINATED | NCT04178902 |
| ABBV-467 | Other | Phase PHASE1 | Multiple Myeloma (MM) | TERMINATED | NCT04178902 |
| ABBV-467 | Other | Phase PHASE1 | Multiple Myeloma (MM) | TERMINATED | NCT04178902 |
| ABBV-467 | Other | Phase PHASE1 | Multiple Myeloma (MM) | TERMINATED | NCT04178902 |
| Dexamethasone | Other | Phase PHASE3 | Small Cell Lung Cancer | TERMINATED | NCT03033511 |
| Rovalpituzumab tesirine | Other | Phase PHASE3 | Small Cell Lung Cancer | TERMINATED | NCT03033511 |
| Placebo for rovalpituzumab tesirine | Other | Phase PHASE3 | Small Cell Lung Cancer | TERMINATED | NCT03033511 |
| Placebo for dexamethasone | Other | Phase PHASE3 | Small Cell Lung Cancer | TERMINATED | NCT03033511 |
| Dexamethasone | Other | Phase PHASE3 | Small Cell Lung Cancer | TERMINATED | NCT03033511 |
| Rovalpituzumab tesirine | Other | Phase PHASE3 | Small Cell Lung Cancer | TERMINATED | NCT03033511 |
| Placebo for rovalpituzumab tesirine | Other | Phase PHASE3 | Small Cell Lung Cancer | TERMINATED | NCT03033511 |
| Placebo for dexamethasone | Other | Phase PHASE3 | Small Cell Lung Cancer | TERMINATED | NCT03033511 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02966795 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT02966795 |
| Long- and intermediate- acting insulins | Other | Preclinical | Diabetes | COMPLETED | NCT02922179 |
| placebo for adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02694523 |
| placebo for risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02694523 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02694523 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02694523 |
| placebo for adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02694523 |
| placebo for risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02694523 |
| adalimumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02694523 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02694523 |
| placebo for ustekinumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02684370 |
| ustekinumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02684370 |
| placebo for risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02684370 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02684370 |
| Rovalpituzumab tesirine | Other | Phase PHASE2 | Small Cell Lung Cancer | COMPLETED | NCT02674568 |
| Rovalpituzumab tesirine | Other | Phase PHASE2 | Small Cell Lung Cancer | COMPLETED | NCT02674568 |
| Daclatasvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02640157 |
| Sofosbuvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02640157 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02640157 |
| Daclatasvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02640157 |
| Sofosbuvir | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02640157 |
| ABT-493/ABT-530 | Other | Phase PHASE3 | Chronic Hepatitis C | COMPLETED | NCT02640157 |
| dasabuvir | Other | Phase PHASE3 | Hepatitis C Infection | COMPLETED | NCT02582632 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Hepatitis C Infection | COMPLETED | NCT02582632 |
| dasabuvir | Other | Phase PHASE3 | Hepatitis C Infection | COMPLETED | NCT02582632 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Hepatitis C Infection | COMPLETED | NCT02582632 |
| dasabuvir | Other | Phase PHASE3 | Hepatitis C Infection | COMPLETED | NCT02582632 |
| ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE3 | Hepatitis C Infection | COMPLETED | NCT02582632 |
| RBV | Other | Phase PHASE3 | HCV | COMPLETED | NCT02247401 |
| 2 DAA | Other | Phase PHASE3 | HCV | COMPLETED | NCT02247401 |
| ABT-493/ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243293 |
| ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243293 |
| ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243293 |
| ABT-493 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243293 |
| ABT-493/ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243293 |
| ribavirin (RBV) | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243293 |
| ABT-530 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243293 |
| ABT-493 | Other | Phase PHASE2 | Chronic Hepatitis C | COMPLETED | NCT02243293 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02066389 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02066389 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02066389 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02066389 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02066389 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02066389 |
| Ribavirin | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02023112 |
| ABT-450/r/ABT-267 | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02023112 |
| Ribavirin | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02023112 |
| ABT-450/r/ABT-267 | Other | Phase PHASE3 | Hepatitis C Virus | COMPLETED | NCT02023112 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Hepatitis C, Chronic | COMPLETED | NCT01685203 |
| ABT-267 | Other | Phase PHASE2 | Hepatitis C, Chronic | COMPLETED | NCT01685203 |
| ABT-450/r | Other | Phase PHASE2 | Hepatitis C, Chronic | COMPLETED | NCT01685203 |
| Ribavirin (RBV) | Other | Phase PHASE2 | Hepatitis C, Chronic | COMPLETED | NCT01685203 |
| ABT-267 | Other | Phase PHASE2 | Hepatitis C, Chronic | COMPLETED | NCT01685203 |
| ABT-450/r | Other | Phase PHASE2 | Hepatitis C, Chronic | COMPLETED | NCT01685203 |
| Darbepoetin alfa | Other | Phase PHASE4 | Moderate to Severe Secondary Hyperparathyroidism | COMPLETED | NCT01506947 |
| Paricalcitol | Other | Phase PHASE4 | Moderate to Severe Secondary Hyperparathyroidism | COMPLETED | NCT01506947 |
| Darbepoetin alfa | Other | Phase PHASE4 | Moderate to Severe Secondary Hyperparathyroidism | COMPLETED | NCT01506947 |
| Paricalcitol | Other | Phase PHASE4 | Moderate to Severe Secondary Hyperparathyroidism | COMPLETED | NCT01506947 |
| Placebo for ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| Placebo for ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| Placebo for ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| Placebo for ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| Placebo for ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| Placebo for ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| Ribavirin | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| ABT-450/r/ABT-267, ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Infection | COMPLETED | NCT01715415 |
| ABT-126 | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT01690195 |
| ABT-126 | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT01690195 |
| Bendamustine | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | COMPLETED | NCT01594229 |
| Rituximab | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | COMPLETED | NCT01594229 |
| ABT-199 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | COMPLETED | NCT01594229 |
| Veliparib | Other | Phase PHASE1 | Gastric Cancer | COMPLETED | NCT01123876 |
| Veliparib | Other | Phase PHASE1 | Gastric Cancer | COMPLETED | NCT01123876 |
| gemcitabine | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01063816 |
| carboplatin | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01063816 |
| veliparib (ABT-888) | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01063816 |
| gemcitabine | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01063816 |
| carboplatin | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01063816 |
| veliparib (ABT-888) | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01063816 |
| Rovalpituzumab tesirine | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT03086239 |
| Rovalpituzumab tesirine | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT03086239 |
| placebo for ustekinumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02684357 |
| placebo for risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02684357 |
| ustekinumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02684357 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT02684357 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01960855 |
| ABT-494 | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01960855 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01960855 |
| ABT-494 | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01960855 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01960855 |
| ABT-494 | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT01960855 |
| Placebo for ABBV-2B04 | Other | Phase PHASE1 | CoronaVirus Disease-2019 (COVID-19) | COMPLETED | NCT04644120 |
| ABBV-2B04 | Other | Phase PHASE1 | CoronaVirus Disease-2019 (COVID-19) | COMPLETED | NCT04644120 |
| Placebo for ABBV-47D11 | Other | Phase PHASE1 | CoronaVirus Disease-2019 (COVID-19) | COMPLETED | NCT04644120 |
| ABBV-47D11 | Other | Phase PHASE1 | CoronaVirus Disease-2019 (COVID-19) | COMPLETED | NCT04644120 |
| Placebo for upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | TERMINATED | NCT03823378 |
| Placebo for elsubrutinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | TERMINATED | NCT03823378 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | TERMINATED | NCT03823378 |
| Elsubrutinib | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | TERMINATED | NCT03823378 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT02955212 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT02955212 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT02955212 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT02955212 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT02955212 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT02955212 |
| Ribavirin solution | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Dasabuvir mini tablet | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ritonavir mini tablet | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Paritaprevir mini tablet | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ombitasvir mini tablet | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ribavirin solution | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Dasabuvir mini tablet | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ritonavir mini tablet | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Paritaprevir mini tablet | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ombitasvir mini tablet | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ribavirin | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Dasabuvir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Ombitasvir/paritaprevir/ritonavir | Other | Phase PHASE2 | Chronic Hepatitis C Infection | COMPLETED | NCT02486406 |
| Venetoclax | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Chemotherapy | Drug | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Navitoclax | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Venetoclax | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Chemotherapy | Drug | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Navitoclax | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Venetoclax | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Chemotherapy | Drug | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Navitoclax | Other | Phase PHASE1 | Acute Lymphoblastic Leukemia (ALL) | COMPLETED | NCT03181126 |
| Paclitaxel | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Temozolomide | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Carboplatin | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Veliparib | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Placebo | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Paclitaxel | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Temozolomide | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Carboplatin | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Veliparib | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Placebo | Other | Phase PHASE2 | Metastatic Breast Cancer | COMPLETED | NCT01506609 |
| Placebo | Other | Phase PHASE2 | Osteoarthritis, Knee | COMPLETED | NCT02471118 |
| Adalimumab 40 mg | Other | Phase PHASE2 | Osteoarthritis, Knee | COMPLETED | NCT02471118 |
| Mavyret | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT02946034 |
| Viekira Pak ± ribavirin | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT02946034 |
| Mavyret | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT02946034 |
| Viekira Pak ± ribavirin | Other | Phase PHASE4 | Chronic Kidney Disease | COMPLETED | NCT02946034 |
| CREON | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency (EPI) | WITHDRAWN | NCT04315311 |
| CREON | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency (EPI) | WITHDRAWN | NCT04315311 |
| CREON | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency (EPI) | WITHDRAWN | NCT04315311 |
| Risankizumab | Other | Phase PHASE2 | Dermatitis | COMPLETED | NCT03706040 |
| Placebo | Other | Phase PHASE2 | Dermatitis | COMPLETED | NCT03706040 |
| Risankizumab | Other | Phase PHASE2 | Dermatitis | COMPLETED | NCT03706040 |
| Placebo | Other | Phase PHASE2 | Dermatitis | COMPLETED | NCT03706040 |
| Risankizumab | Other | Phase PHASE2 | Dermatitis | COMPLETED | NCT03706040 |
| Placebo | Other | Phase PHASE2 | Dermatitis | COMPLETED | NCT03706040 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03022045 |
| AMG 176 | Other | Phase PHASE1 | Acute Myeloid Leukemia | TERMINATED | NCT03797261 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | TERMINATED | NCT03797261 |
| AMG 176 | Other | Phase PHASE1 | Acute Myeloid Leukemia | TERMINATED | NCT03797261 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | TERMINATED | NCT03797261 |
| AMG 176 | Other | Phase PHASE1 | Acute Myeloid Leukemia | TERMINATED | NCT03797261 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | TERMINATED | NCT03797261 |
| upadacitinib 15mg/day | Other | Phase PHASE3 | Rheumatoid Arthritis | UNKNOWN | NCT05121298 |
| upadacitinib 15mg/day | Other | Phase PHASE3 | Rheumatoid Arthritis | UNKNOWN | NCT05121298 |
| Paclitaxel | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Carboplatin | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Veliparib, tablet | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Veliparib, capsule | Other | Phase PHASE1 | Cancer - Ovarian | WITHDRAWN | NCT03400306 |
| Placebo ABBV-0805 | Other | Phase PHASE1 | Parkinson's Disease | WITHDRAWN | NCT04127695 |
| ABBV-0805 | Other | Phase PHASE1 | Parkinson's Disease | WITHDRAWN | NCT04127695 |
| Placebo ABBV-0805 | Other | Phase PHASE1 | Parkinson's Disease | WITHDRAWN | NCT04127695 |
| ABBV-0805 | Other | Phase PHASE1 | Parkinson's Disease | WITHDRAWN | NCT04127695 |
| ABT-199 (Safety Expansion Cohort) | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia | COMPLETED | NCT01889186 |
| ABT-199 (Main Cohort) | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia | COMPLETED | NCT01889186 |
| Placebo | Other | Phase PHASE2 | Sjogren's Syndrome (SS) | WITHDRAWN | NCT05217472 |
| Ravagalimab | Other | Phase PHASE2 | Sjogren's Syndrome (SS) | WITHDRAWN | NCT05217472 |
| Ravaglimab | Other | Phase PHASE2 | Sjogren's Syndrome (SS) | WITHDRAWN | NCT05217472 |
| Alvocidib | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03441555 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03441555 |
| Alvocidib | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03441555 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03441555 |
| Sleep Headband | Other | Phase PHASE1 | Atopic Dermatitis | TERMINATED | NCT04262791 |
| Wrist Actigraphy Device | Device | Phase PHASE1 | Atopic Dermatitis | TERMINATED | NCT04262791 |
| Sleep Headband | Other | Phase PHASE1 | Atopic Dermatitis | TERMINATED | NCT04262791 |
| Wrist Actigraphy Device | Device | Phase PHASE1 | Atopic Dermatitis | TERMINATED | NCT04262791 |
| ABT-199 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT01328626 |
| ABT-199 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT01328626 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis (UC) | COMPLETED | NCT03653026 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis (UC) | COMPLETED | NCT03653026 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis (UC) | COMPLETED | NCT03653026 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis (UC) | COMPLETED | NCT03653026 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05274100 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05274087 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05274087 |
| risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05283694 |
| risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05283694 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05283681 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05283681 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05283681 |
| Dalbavancin | Other | Phase PHASE1 | Bacterial Infections | TERMINATED | NCT02688790 |
| Dalbavancin | Other | Phase PHASE1 | Bacterial Infections | TERMINATED | NCT02688790 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05305222 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05305222 |
| Placebo | Other | Phase PHASE3 | Schizophrenia | TERMINATED | NCT03593213 |
| Cariprazine | Other | Phase PHASE3 | Schizophrenia | TERMINATED | NCT03593213 |
| Placebo | Other | Phase PHASE3 | Schizophrenia | TERMINATED | NCT03593213 |
| Cariprazine | Other | Phase PHASE3 | Schizophrenia | TERMINATED | NCT03593213 |
| Placebo | Other | Phase PHASE2 | Generalized Anxiety Disorder | WITHDRAWN | NCT04965272 |
| Cariprazine 3.0 mg/day | Other | Phase PHASE2 | Generalized Anxiety Disorder | WITHDRAWN | NCT04965272 |
| Cariprazine 1.5 mg/day | Other | Phase PHASE2 | Generalized Anxiety Disorder | WITHDRAWN | NCT04965272 |
| Cariprazine 0.75 mg/day | Other | Phase PHASE2 | Generalized Anxiety Disorder | WITHDRAWN | NCT04965272 |
| Placebo | Other | Phase PHASE2 | Generalized Anxiety Disorder | WITHDRAWN | NCT04965272 |
| Cariprazine 3.0 mg/day | Other | Phase PHASE2 | Generalized Anxiety Disorder | WITHDRAWN | NCT04965272 |
| Cariprazine 1.5 mg/day | Other | Phase PHASE2 | Generalized Anxiety Disorder | WITHDRAWN | NCT04965272 |
| Cariprazine 0.75 mg/day | Other | Phase PHASE2 | Generalized Anxiety Disorder | WITHDRAWN | NCT04965272 |
| Cariprazine | Other | Phase PHASE1 | Autism Spectrum Disorder | COMPLETED | NCT04382885 |
| Cariprazine | Other | Phase PHASE1 | Autism Spectrum Disorder | COMPLETED | NCT04382885 |
| Cariprazine | Other | Phase PHASE1 | Autism Spectrum Disorder | COMPLETED | NCT04382885 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03000257 |
| Rovalpituzumab Tesirine | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03000257 |
| Venetoclax | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03000257 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03000257 |
| Rovalpituzumab Tesirine | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03000257 |
| Venetoclax | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03000257 |
| Standard of Care | Other | Phase PHASE2 | Endocarditis | TERMINATED | NCT03148756 |
| Dalbavancin | Other | Phase PHASE2 | Endocarditis | TERMINATED | NCT03148756 |
| Standard of Care | Other | Phase PHASE2 | Endocarditis | TERMINATED | NCT03148756 |
| Dalbavancin | Other | Phase PHASE2 | Endocarditis | TERMINATED | NCT03148756 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT03071757 |
| ABBV-368 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT03071757 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT03071757 |
| ABBV-368 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT03071757 |
| Ribavirin | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02939989 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02939989 |
| Sofosbuvir | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02939989 |
| Ribavirin | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02939989 |
| Glecaprevir/Pibrentasvir | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02939989 |
| Sofosbuvir | Other | Phase PHASE3 | Hepatitis C Virus Infection | COMPLETED | NCT02939989 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT04509622 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT04509622 |
| ABT199 | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | COMPLETED | NCT02677324 |
| ABT199 | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | COMPLETED | NCT02677324 |
| Risankizumab | Other | Preclinical | Crohn's Disease | NO_LONGER_AVAILABLE | NCT03914261 |
| Risankizumab | Other | Preclinical | Crohn's Disease | NO_LONGER_AVAILABLE | NCT03914261 |
| Veliparib | Other | Preclinical | Solid Tumors With Documented BRCA, BARD, or PALB or Other Acceptable DNA Mutations or Anomalies That Are Scientifically Sound | NO_LONGER_AVAILABLE | NCT03123211 |
| ABT-199 and Ibrutinib Combination | Other | Phase PHASE1 | Lymphoma, Mantle-Cell | COMPLETED | NCT02419560 |
| Placebo | Other | Phase PHASE2 | CoronaVirus Induced Disease-2019 (COVID-19) | COMPLETED | NCT04375397 |
| Ibrutinib | Other | Phase PHASE2 | CoronaVirus Induced Disease-2019 (COVID-19) | COMPLETED | NCT04375397 |
| Placebo | Other | Phase PHASE2 | CoronaVirus Induced Disease-2019 (COVID-19) | COMPLETED | NCT04375397 |
| Ibrutinib | Other | Phase PHASE2 | CoronaVirus Induced Disease-2019 (COVID-19) | COMPLETED | NCT04375397 |
| Placebo | Other | Phase PHASE2 | CoronaVirus Induced Disease-2019 (COVID-19) | COMPLETED | NCT04375397 |
| Ibrutinib | Other | Phase PHASE2 | CoronaVirus Induced Disease-2019 (COVID-19) | COMPLETED | NCT04375397 |
| Placebo | Other | Phase PHASE2 | Polycystic Ovary Syndrome | COMPLETED | NCT03951077 |
| Elagolix | Other | Phase PHASE2 | Polycystic Ovary Syndrome | COMPLETED | NCT03951077 |
| Placebo | Other | Phase PHASE2 | Polycystic Ovary Syndrome | COMPLETED | NCT03951077 |
| Elagolix | Other | Phase PHASE2 | Polycystic Ovary Syndrome | COMPLETED | NCT03951077 |
| risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03104413 |
| risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03104413 |
| placebo for risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03104413 |
| risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03104413 |
| risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03104413 |
| placebo for risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03104413 |
| Ubrogepant | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04818515 |
| Atogepant | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04818515 |
| Ubrogepant | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04818515 |
| Atogepant | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04818515 |
| Ubrogepant | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04818515 |
| Atogepant | Other | Phase PHASE1 | Migraine | COMPLETED | NCT04818515 |
| Upadacitinib | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT02819635 |
| Placebo | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT02819635 |
| risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03105128 |
| risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03105128 |
| placebo for risankizumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03105128 |
| risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03105128 |
| risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03105128 |
| placebo for risankizumab | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03105128 |
| Ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02167945 |
| ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02167945 |
| ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02167945 |
| Ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02167945 |
| ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02167945 |
| ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02167945 |
| Colonoscopy | Other | Approved | CD | COMPLETED | NCT03498625 |
| Colonoscopy | Other | Approved | CD | COMPLETED | NCT03498625 |
| Colonoscopy | Other | Approved | CD | UNKNOWN | NCT03487900 |
| Colonoscopy | Other | Approved | CD | UNKNOWN | NCT03487900 |
| Placebo for risankizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT03926169 |
| Risankizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT03926169 |
| Placebo for risankizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT03926169 |
| Risankizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT03926169 |
| Placebo for risankizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT03926169 |
| Risankizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | COMPLETED | NCT03926169 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03345836 |
| Matching Placebo for Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03345836 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03345836 |
| Matching Placebo for Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03345836 |
| Glecaprevir/pibrentasvir | Other | Phase PHASE3 | Hepatitis C, Acute | COMPLETED | NCT02634008 |
| Ribavirin | Other | Phase PHASE3 | Hepatitis C, Acute | COMPLETED | NCT02634008 |
| Dasabuvir | Other | Phase PHASE3 | Hepatitis C, Acute | COMPLETED | NCT02634008 |
| Paritaprevir/ritonavir/ombitasvir | Other | Phase PHASE3 | Hepatitis C, Acute | COMPLETED | NCT02634008 |
| placebo for ABBV-8E12 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT02880956 |
| ABBV-8E12 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT02880956 |
| placebo for ABBV-8E12 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT02880956 |
| ABBV-8E12 | Other | Phase PHASE2 | Alzheimer's Disease | COMPLETED | NCT02880956 |
| Cytarabine | Other | Phase PHASE1 | Acute Myelogenous Leukemia | COMPLETED | NCT02287233 |
| Venetoclax | Other | Phase PHASE1 | Acute Myelogenous Leukemia | COMPLETED | NCT02287233 |
| Cytarabine | Other | Phase PHASE1 | Acute Myelogenous Leukemia | COMPLETED | NCT02287233 |
| Venetoclax | Other | Phase PHASE1 | Acute Myelogenous Leukemia | COMPLETED | NCT02287233 |
| Cytarabine | Other | Phase PHASE1 | Acute Myelogenous Leukemia | COMPLETED | NCT02287233 |
| Venetoclax | Other | Phase PHASE1 | Acute Myelogenous Leukemia | COMPLETED | NCT02287233 |
| ABBV-184 | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04272203 |
| ABBV-184 | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04272203 |
| Venetoclax | Other | Phase PHASE1 | Renal Impairment | COMPLETED | NCT04810598 |
| Venetoclax | Other | Phase PHASE1 | Renal Impairment | COMPLETED | NCT04810598 |
| Venetoclax | Other | Phase PHASE1 | Renal Impairment | COMPLETED | NCT04810598 |
| Antidepressant Therapy (ADT) | Drug | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03739203 |
| Placebo | Other | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03739203 |
| Cariprazine | Other | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03739203 |
| Antidepressant Therapy (ADT) | Drug | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03739203 |
| Placebo | Other | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03739203 |
| Cariprazine | Other | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03739203 |
| Tilavonemab | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT03712787 |
| Tilavonemab | Other | Phase PHASE2 | Alzheimer's Disease | TERMINATED | NCT03712787 |
| Placebo | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04799353 |
| Budigalimab | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04799353 |
| Placebo | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04799353 |
| Budigalimab | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04799353 |
| Placebo | Other | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03738215 |
| Cariprazine | Other | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03738215 |
| Placebo | Other | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03738215 |
| Cariprazine | Other | Phase PHASE3 | Major Depressive Disorder | COMPLETED | NCT03738215 |
| Placebo for ABBV-990 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT05475821 |
| ABBV-990 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT05475821 |
| Home titration | Other | Preclinical | Parkinson Disease | COMPLETED | NCT04196647 |
| Home titration | Other | Preclinical | Parkinson Disease | COMPLETED | NCT04196647 |
| methotrexate | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03219437 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03219437 |
| methotrexate | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03219437 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03219437 |
| Placebo | Other | Phase PHASE4 | Anxiety Disorders,Generalized Anxiety Disorder | COMPLETED | NCT03924323 |
| Escitalopram | Other | Phase PHASE4 | Anxiety Disorders,Generalized Anxiety Disorder | COMPLETED | NCT03924323 |
| Placebo for ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04380142 |
| Levodopa/Carbidopa (LD/CD) | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04380142 |
| Placebo for Levodopa/Carbidopa (LD/CD) | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04380142 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04380142 |
| Placebo for ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04380142 |
| Levodopa/Carbidopa (LD/CD) | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04380142 |
| Placebo for Levodopa/Carbidopa (LD/CD) | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04380142 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | COMPLETED | NCT04380142 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03345849 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03345849 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03345849 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | COMPLETED | NCT03345849 |
| Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J) | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00660673 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00660673 |
| Levodopa-Carbidopa Intestinal Gel (LCIG) | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00660673 |
| Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J) | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00660673 |
| CADD-Legacy® 1400 ambulatory infusion pump | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00660673 |
| Levodopa-Carbidopa Intestinal Gel (LCIG) | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT00660673 |
| Placebo | Other | Phase PHASE3 | Palmoplantar Pustulosis (PPP) | COMPLETED | NCT04451720 |
| Risankizumab | Other | Phase PHASE3 | Palmoplantar Pustulosis (PPP) | COMPLETED | NCT04451720 |
| Cedirogant | Other | Phase PHASE1 | Hepatic Impairment | TERMINATED | NCT05376839 |
| Comparator 2 | Other | Preclinical | Psoriasis | WITHDRAWN | NCT04799990 |
| Comparator 1 | Other | Preclinical | Psoriasis | WITHDRAWN | NCT04799990 |
| Risankizumab | Other | Preclinical | Psoriasis | WITHDRAWN | NCT04799990 |
| Comparator 2 | Other | Preclinical | Psoriasis | WITHDRAWN | NCT04799990 |
| Comparator 1 | Other | Preclinical | Psoriasis | WITHDRAWN | NCT04799990 |
| Risankizumab | Other | Preclinical | Psoriasis | WITHDRAWN | NCT04799990 |
| FOLFIRI | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03082209 |
| Bevacizumab | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03082209 |
| Venetoclax | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03082209 |
| ABBV-621 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03082209 |
| FOLFIRI | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03082209 |
| Bevacizumab | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03082209 |
| Venetoclax | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03082209 |
| ABBV-621 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03082209 |
| AndroGel 1.62% | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT04274894 |
| AndroGel 1.62% | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT04274894 |
| Ibrutinib | Other | Phase PHASE2 | Leukemia | COMPLETED | NCT03873493 |
| Venetoclax | Other | Phase PHASE2 | Leukemia | COMPLETED | NCT03873493 |
| Ibrutinib | Other | Phase PHASE2 | Leukemia | COMPLETED | NCT03873493 |
| Venetoclax | Other | Phase PHASE2 | Leukemia | COMPLETED | NCT03873493 |
| Venetoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02141282 |
| Dinaciclib | Other | Phase PHASE1 | Cancer - Acute Myeloid Leukemia | TERMINATED | NCT03484520 |
| Venetoclax | Other | Phase PHASE1 | Cancer - Acute Myeloid Leukemia | TERMINATED | NCT03484520 |
| Navocaftor | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05538585 |
| Galicaftor | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05538585 |
| Navocaftor | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05538585 |
| Galicaftor | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05538585 |
| Epcoritamab | Other | Preclinical | Lymphoma | NO_LONGER_AVAILABLE | NCT05692050 |
| ABBV-992 | Other | Phase PHASE1 | B-cell Lymphoma | TERMINATED | NCT04804254 |
| ABBV-623 | Other | Phase PHASE1 | B-cell Lymphoma | TERMINATED | NCT04804254 |
| ABBV-992 | Other | Phase PHASE1 | B-cell Lymphoma | TERMINATED | NCT04804254 |
| ABBV-623 | Other | Phase PHASE1 | B-cell Lymphoma | TERMINATED | NCT04804254 |
| Placebo | Other | Phase PHASE2 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT04430855 |
| Upadacitinib | Other | Phase PHASE2 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT04430855 |
| Placebo | Other | Phase PHASE2 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT04430855 |
| Upadacitinib | Other | Phase PHASE2 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT04430855 |
| Placebo | Other | Phase PHASE2 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT04430855 |
| Upadacitinib | Other | Phase PHASE2 | Hidradenitis Suppurativa (HS) | COMPLETED | NCT04430855 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706847 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706847 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706847 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706847 |
| Midazolam | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05530278 |
| Navocaftor | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05530278 |
| ABBV-576 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05530278 |
| Galicaftor | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05530278 |
| Midazolam | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05530278 |
| Navocaftor | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05530278 |
| ABBV-576 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05530278 |
| Galicaftor | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05530278 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT02980731 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT02980731 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04196283 |
| Nab-paclitaxel | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04196283 |
| Tilsotolimod | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04196283 |
| ABBV-368 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04196283 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04196283 |
| Nab-paclitaxel | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04196283 |
| Tilsotolimod | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04196283 |
| ABBV-368 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04196283 |
| Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT04976777 |
| Approved DEX PS DDS Applicator | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT04976777 |
| Updated DEX PS DDS Applicator | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT04976777 |
| Dexamethasone | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT04976777 |
| Approved DEX PS DDS Applicator | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT04976777 |
| Updated DEX PS DDS Applicator | Other | Phase PHASE3 | Macular Edema | COMPLETED | NCT04976777 |
| Topical Corticosteroids (TCS) | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03661138 |
| Placebo for upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03661138 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03661138 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Carfilzomib | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Lemzoparlimab | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04895410 |
| Placebo | Other | Phase PHASE2 | Ankylosing Spondylitis (AS) | COMPLETED | NCT03178487 |
| Upadacitinib | Other | Phase PHASE2 | Ankylosing Spondylitis (AS) | COMPLETED | NCT03178487 |
| Placebo | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04223804 |
| ABBV-181 | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04223804 |
| ABBV-154 Dose Formulation B | Other | Phase PHASE1 | ABBV-154 | COMPLETED | NCT05556226 |
| ABBV-154 Dose Formulation A | Other | Phase PHASE1 | ABBV-154 | COMPLETED | NCT05556226 |
| Ravagalimab 300 mg | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03695185 |
| Ravagalimab 600 mg | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03695185 |
| Ravagalimab 300 mg | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03695185 |
| Ravagalimab 600 mg | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03695185 |
| Ravagalimab 300 mg | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03695185 |
| Ravagalimab 600 mg | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03695185 |
| Decitabine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03941964 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03941964 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03941964 |
| Decitabine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03941964 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03941964 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03941964 |
| ABBV-951 | Other | Phase PHASE1 | Parkinson's Disease | COMPLETED | NCT05094050 |
| ABBV-951 | Other | Phase PHASE1 | Parkinson's Disease | COMPLETED | NCT05094050 |
| ABBV-552 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05686980 |
| ABBV-552 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05686980 |
| Ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02219490 |
| ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02219490 |
| ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02219490 |
| Ribavirin (RBV) | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02219490 |
| ABT-333 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02219490 |
| ABT-450/r/ABT-267 | Other | Phase PHASE3 | Chronic Hepatitis C Virus (HCV) Infection Genotype 1 | COMPLETED | NCT02219490 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02756611 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02756611 |
| Dexamethasone | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT01794520 |
| Venetoclax | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT01794520 |
| Dexamethasone | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT01794520 |
| Venetoclax | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | COMPLETED | NCT01794520 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02675426 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02675426 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02675426 |
| Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02675426 |
| Risankizumab Dose B | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05567029 |
| Risankizumab Dose A | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05567029 |
| Risankizumab Dose B | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05567029 |
| Risankizumab Dose A | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05567029 |
| Glecaprevir + Pibrentasvir Pediatric Formulation | Other | Phase PHASE2 | Hepatitis C Virus (HCV) | COMPLETED | NCT03067129 |
| Glecaprevir/Pibrentasvir Adult Formulation | Other | Phase PHASE2 | Hepatitis C Virus (HCV) | COMPLETED | NCT03067129 |
| azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | COMPLETED | NCT02966782 |
| venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | COMPLETED | NCT02966782 |
| azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | COMPLETED | NCT02966782 |
| venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | COMPLETED | NCT02966782 |
| azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | COMPLETED | NCT02966782 |
| venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | COMPLETED | NCT02966782 |
| Placebo for ABT-414 | Other | Phase PHASE3 | Glioblastoma | COMPLETED | NCT02573324 |
| Radiation | Other | Phase PHASE3 | Glioblastoma | COMPLETED | NCT02573324 |
| Depatuxizumab mafodotin | Other | Phase PHASE3 | Glioblastoma | COMPLETED | NCT02573324 |
| Temozolomide | Other | Phase PHASE3 | Glioblastoma | COMPLETED | NCT02573324 |
| Placebo for ABT-414 | Other | Phase PHASE3 | Glioblastoma | COMPLETED | NCT02573324 |
| Radiation | Other | Phase PHASE3 | Glioblastoma | COMPLETED | NCT02573324 |
| Depatuxizumab mafodotin | Other | Phase PHASE3 | Glioblastoma | COMPLETED | NCT02573324 |
| Temozolomide | Other | Phase PHASE3 | Glioblastoma | COMPLETED | NCT02573324 |
| Azacitidine | Other | Phase PHASE1 | Acute Myelogenous Leukemia | TERMINATED | NCT02203773 |
| Decitabine | Other | Phase PHASE1 | Acute Myelogenous Leukemia | TERMINATED | NCT02203773 |
| ABT-199 | Other | Phase PHASE1 | Acute Myelogenous Leukemia | TERMINATED | NCT02203773 |
| Posaconazole | Other | Phase PHASE1 | Acute Myelogenous Leukemia | TERMINATED | NCT02203773 |
| venetoclax | Other | Phase PHASE1 | Malignancies | COMPLETED | NCT03236857 |
| chemotherapy | Drug | Phase PHASE1 | Malignancies | COMPLETED | NCT03236857 |
| venetoclax | Other | Phase PHASE1 | Malignancies | COMPLETED | NCT03236857 |
| chemotherapy | Drug | Phase PHASE1 | Malignancies | COMPLETED | NCT03236857 |
| Epcoritamab | Other | Preclinical | Large B-cell Lymphoma | APPROVED_FOR_MARKETING | NCT05733650 |
| Placebo | Other | Phase PHASE3 | Migraine | COMPLETED | NCT04492020 |
| Ubrogepant 100 mg | Other | Phase PHASE3 | Migraine | COMPLETED | NCT04492020 |
| Placebo | Other | Phase PHASE3 | Migraine | COMPLETED | NCT04492020 |
| Ubrogepant 100 mg | Other | Phase PHASE3 | Migraine | COMPLETED | NCT04492020 |
| Therapy Education | Drug | Phase PHASE4 | Ulcerative Colitis | RECRUITING | NCT04183608 |
| e-Monitoring | Other | Phase PHASE4 | Ulcerative Colitis | RECRUITING | NCT04183608 |
| Calprotectin | Other | Phase PHASE4 | Ulcerative Colitis | RECRUITING | NCT04183608 |
| Adalimumab | Other | Phase PHASE4 | Ulcerative Colitis | RECRUITING | NCT04183608 |
| Therapy Education | Drug | Phase PHASE4 | Ulcerative Colitis | RECRUITING | NCT04183608 |
| e-Monitoring | Other | Phase PHASE4 | Ulcerative Colitis | RECRUITING | NCT04183608 |
| Calprotectin | Other | Phase PHASE4 | Ulcerative Colitis | RECRUITING | NCT04183608 |
| Adalimumab | Other | Phase PHASE4 | Ulcerative Colitis | RECRUITING | NCT04183608 |
| Placebo | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency (EPI) | TERMINATED | NCT03859869 |
| Pancrelipase | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency (EPI) | TERMINATED | NCT03859869 |
| Rituximab | Other | Phase PHASE1 | Small Lymphocytic Lymphoma | COMPLETED | NCT01682616 |
| ABT-199 | Other | Phase PHASE1 | Small Lymphocytic Lymphoma | COMPLETED | NCT01682616 |
| Rituximab | Other | Phase PHASE1 | Small Lymphocytic Lymphoma | COMPLETED | NCT01682616 |
| ABT-199 | Other | Phase PHASE1 | Small Lymphocytic Lymphoma | COMPLETED | NCT01682616 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02720523 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02720523 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02720523 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02720523 |
| Upadacitinib | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02720523 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | COMPLETED | NCT02720523 |
| Placebo | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| BOTOX | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| AGN-151586 | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| Placebo | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| BOTOX | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| AGN-151586 | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT05496335 |
| LUMIGAN | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT04285580 |
| Bimatoprost SR | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT04285580 |
| LUMIGAN | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT04285580 |
| Bimatoprost SR | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT04285580 |
| ABT-263 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | COMPLETED | NCT00481091 |
| Placebo ABBV-2222 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| ABBV-2222 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| Placebo ABBV-3067 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| ABBV-3067 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| Placebo ABBV-2222 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| ABBV-2222 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| Placebo ABBV-3067 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| ABBV-3067 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| Placebo ABBV-2222 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| ABBV-2222 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| Placebo ABBV-3067 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| ABBV-3067 | Other | Phase PHASE2 | Cystic Fibrosis | COMPLETED | NCT03969888 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706873 |
| Placebo to Methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706873 |
| Methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706873 |
| Placebo to Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706873 |
| Questionnaires and dry eye tests | Other | Preclinical | Dry Eye | UNKNOWN | NCT05938985 |
| Questionnaires and dry eye tests | Other | Preclinical | Dry Eye | UNKNOWN | NCT05938985 |
| ABBV-903 Tablet Form 2 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05836506 |
| ABBV-903 Tablet Form 1 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05836506 |
| ABBV-903 Tablet Form 2 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05836506 |
| ABBV-903 Tablet Form 1 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05836506 |
| Ilorasertib | Other | Phase PHASE2 | Advanced Cancers | TERMINATED | NCT02478320 |
| Ilorasertib | Other | Phase PHASE2 | Advanced Cancers | TERMINATED | NCT02478320 |
| Placebo for upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Placebo for elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Placebo for upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Placebo for elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Placebo for upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Placebo for elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT03978520 |
| GEN1044 is an immunoglobulin G1 (IgG1) bispecific antibody targeting CD3 and 5T4. | Other | Phase PHASE1 | Locally Advanced or Metastatic Solid Tumor(s) | TERMINATED | NCT04424641 |
| GEN1044 is an immunoglobulin G1 (IgG1) bispecific antibody targeting CD3 and 5T4. | Other | Phase PHASE1 | Locally Advanced or Metastatic Solid Tumor(s) | TERMINATED | NCT04424641 |
| Placebo to match OBV/PTV/r and DSV | Other | Phase PHASE4 | Hepatitis C, Chronic | TERMINATED | NCT03003338 |
| OBV/PTV/r and DSV | Other | Phase PHASE4 | Hepatitis C, Chronic | TERMINATED | NCT03003338 |
| Placebo to match OBV/PTV/r and DSV | Other | Phase PHASE4 | Hepatitis C, Chronic | TERMINATED | NCT03003338 |
| OBV/PTV/r and DSV | Other | Phase PHASE4 | Hepatitis C, Chronic | TERMINATED | NCT03003338 |
| Placebo to match OBV/PTV/r and DSV | Other | Phase PHASE4 | Hepatitis C, Chronic | TERMINATED | NCT03003338 |
| OBV/PTV/r and DSV | Other | Phase PHASE4 | Hepatitis C, Chronic | TERMINATED | NCT03003338 |
| Surveys | Other | Approved | Inflammatory Bowel Diseases | COMPLETED | NCT03757533 |
| Health Coaching | Other | Approved | Inflammatory Bowel Diseases | COMPLETED | NCT03757533 |
| Surveys | Other | Approved | Inflammatory Bowel Diseases | COMPLETED | NCT03757533 |
| Health Coaching | Other | Approved | Inflammatory Bowel Diseases | COMPLETED | NCT03757533 |
| Surveys | Other | Approved | Inflammatory Bowel Diseases | COMPLETED | NCT03757533 |
| Health Coaching | Other | Approved | Inflammatory Bowel Diseases | COMPLETED | NCT03757533 |
| Hypofractionated WPRT | Other | Phase PHASE2 | Prostate Cancer | ACTIVE_NOT_RECRUITING | NCT04197141 |
| Conventionally-fractionated WPRT | Other | Phase PHASE2 | Prostate Cancer | ACTIVE_NOT_RECRUITING | NCT04197141 |
| Hypofractionated WPRT | Other | Phase PHASE2 | Prostate Cancer | ACTIVE_NOT_RECRUITING | NCT04197141 |
| Conventionally-fractionated WPRT | Other | Phase PHASE2 | Prostate Cancer | ACTIVE_NOT_RECRUITING | NCT04197141 |
| Ruxolitinib | Other | Phase PHASE1 | Myelofibrosis (MF) | TERMINATED | NCT04480086 |
| Navitoclax | Other | Phase PHASE1 | Myelofibrosis (MF) | TERMINATED | NCT04480086 |
| Mivebresib | Other | Phase PHASE1 | Myelofibrosis (MF) | TERMINATED | NCT04480086 |
| Ruxolitinib | Other | Phase PHASE1 | Myelofibrosis (MF) | TERMINATED | NCT04480086 |
| Navitoclax | Other | Phase PHASE1 | Myelofibrosis (MF) | TERMINATED | NCT04480086 |
| Mivebresib | Other | Phase PHASE1 | Myelofibrosis (MF) | TERMINATED | NCT04480086 |
| Venetoclax | Other | Preclinical | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT03873857 |
| Venetoclax | Other | Preclinical | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT03873857 |
| Pancrelipase | Other | Phase PHASE4 | Cystic Fibrosis | COMPLETED | NCT03924947 |
| Placebo | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT03573297 |
| Cariprazine | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT03573297 |
| Placebo | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT03573297 |
| Cariprazine | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT03573297 |
| Placebo | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT03573297 |
| Cariprazine | Other | Phase PHASE3 | Bipolar I Disorder | COMPLETED | NCT03573297 |
| Venetoclax | Other | Phase PHASE1 | Castration Levels of Testosterone | COMPLETED | NCT03751436 |
| Enzalutamide | Other | Phase PHASE1 | Castration Levels of Testosterone | COMPLETED | NCT03751436 |
| Venetoclax | Other | Phase PHASE1 | Castration Levels of Testosterone | COMPLETED | NCT03751436 |
| Enzalutamide | Other | Phase PHASE1 | Castration Levels of Testosterone | COMPLETED | NCT03751436 |
| Rituximab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02005471 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02005471 |
| Bendamustine | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02005471 |
| Rituximab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02005471 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02005471 |
| Bendamustine | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02005471 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05995366 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05995366 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05691699 |
| Placebo for ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05691699 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05691699 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05691699 |
| Placebo for ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05691699 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05691699 |
| Midazolam | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05895266 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT05895266 |
| Placebo for ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT06009237 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT06009237 |
| Placebo for ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT06009237 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT06009237 |
| Placebo for ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT06009237 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT06009237 |
| Placebo for ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT06009237 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | TERMINATED | NCT06009237 |
| Risankizumab | Other | Phase PHASE3 | Plaque Psoriasis | COMPLETED | NCT04102007 |
| Percutaneous endoscopic gastrostomy with a jejunal (PEG-J) tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02549092 |
| Nasojejunal (NJ) tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02549092 |
| Levodopa-Carbidopa Intestinal Gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02549092 |
| Optimized Medical Treatment | Drug | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02549092 |
| Percutaneous endoscopic gastrostomy with a jejunal (PEG-J) tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02549092 |
| Nasojejunal (NJ) tube | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02549092 |
| Levodopa-Carbidopa Intestinal Gel | Other | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02549092 |
| Optimized Medical Treatment | Drug | Phase PHASE3 | Advanced Parkinson's Disease | COMPLETED | NCT02549092 |
| Placebo | Other | Phase PHASE2 | Psoriasis | TERMINATED | NCT05044234 |
| Cedirogant | Other | Phase PHASE2 | Psoriasis | TERMINATED | NCT05044234 |
| Placebo | Other | Phase PHASE2 | Psoriasis | TERMINATED | NCT05044234 |
| Cedirogant | Other | Phase PHASE2 | Psoriasis | TERMINATED | NCT05044234 |
| Placebo | Other | Phase PHASE2 | Psoriasis | TERMINATED | NCT05044234 |
| Cedirogant | Other | Phase PHASE2 | Psoriasis | TERMINATED | NCT05044234 |
| Venetoclax | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05909553 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01946074 |
| ABT-165 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01946074 |
| FOLFIRI | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01946074 |
| paclitaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01946074 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01946074 |
| ABT-165 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01946074 |
| FOLFIRI | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01946074 |
| paclitaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT01946074 |
| placebo | Other | Phase PHASE2 | Multiple Sclerosis (MS) | COMPLETED | NCT03737812 |
| elezanumab | Other | Phase PHASE2 | Multiple Sclerosis (MS) | COMPLETED | NCT03737812 |
| placebo | Other | Phase PHASE2 | Multiple Sclerosis (MS) | COMPLETED | NCT03737812 |
| elezanumab | Other | Phase PHASE2 | Multiple Sclerosis (MS) | COMPLETED | NCT03737812 |
| placebo | Other | Phase PHASE2 | Multiple Sclerosis (MS) | COMPLETED | NCT03737851 |
| elezanumab | Other | Phase PHASE2 | Multiple Sclerosis (MS) | COMPLETED | NCT03737851 |
| placebo | Other | Phase PHASE2 | Multiple Sclerosis (MS) | COMPLETED | NCT03737851 |
| elezanumab | Other | Phase PHASE2 | Multiple Sclerosis (MS) | COMPLETED | NCT03737851 |
| ABT-494 | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT02365649 |
| Placebo | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT02365649 |
| ABT-494 | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT02365649 |
| Placebo | Other | Phase PHASE2 | Crohn's Disease | COMPLETED | NCT02365649 |
| Placebo Methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706951 |
| Placebo Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706951 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706951 |
| Methotrexate | Other | Phase PHASE3 | Rheumatoid Arthritis | COMPLETED | NCT02706951 |
| Vehicle | Other | Phase PHASE1 | Presbyopia | TERMINATED | NCT04403763 |
| AGN-241622 | Other | Phase PHASE1 | Presbyopia | TERMINATED | NCT04403763 |
| Vehicle | Other | Phase PHASE1 | Presbyopia | TERMINATED | NCT04403763 |
| AGN-241622 | Other | Phase PHASE1 | Presbyopia | TERMINATED | NCT04403763 |
| Vehicle | Other | Phase PHASE1 | Presbyopia | TERMINATED | NCT04403763 |
| AGN-241622 | Other | Phase PHASE1 | Presbyopia | TERMINATED | NCT04403763 |
| Budigalimab | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT03639194 |
| ABBV-011 | Other | Phase PHASE1 | Small Cell Lung Cancer | COMPLETED | NCT03639194 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Azacitidine | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Lemzoparlimab | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Azacitidine | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Lemzoparlimab | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Azacitidine | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Lemzoparlimab | Other | Phase PHASE1 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04912063 |
| Placebo | Other | Phase PHASE2 | COVID-19 | COMPLETED | NCT04372628 |
| Lopinavir/Ritonavir 400 mg/100 mg | Other | Phase PHASE2 | COVID-19 | COMPLETED | NCT04372628 |
| Placebo | Other | Phase PHASE2 | COVID-19 | COMPLETED | NCT04372628 |
| Lopinavir/Ritonavir 400 mg/100 mg | Other | Phase PHASE2 | COVID-19 | COMPLETED | NCT04372628 |
| Placebo | Other | Phase PHASE2 | COVID-19 | COMPLETED | NCT04372628 |
| Lopinavir/Ritonavir 400 mg/100 mg | Other | Phase PHASE2 | COVID-19 | COMPLETED | NCT04372628 |
| Venetoclax Oral Tablet | Other | Phase PHASE1 | Relapsed Adult AML | ACTIVE_NOT_RECRUITING | NCT04330820 |
| Venetoclax Oral Tablet | Other | Phase PHASE1 | Relapsed Adult AML | UNKNOWN | NCT04330820 |
| Placebo for ABBV-382 | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04554966 |
| ABBV-382 | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04554966 |
| Placebo for ABBV-382 | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04554966 |
| ABBV-382 | Other | Phase PHASE1 | Human Immunodeficiency Virus (HIV) | COMPLETED | NCT04554966 |
| Aflibercept | Other | Phase PHASE4 | Diabetic Macular Edema | UNKNOWN | NCT05990829 |
| Ozurdex | Other | Phase PHASE4 | Diabetic Macular Edema | UNKNOWN | NCT05990829 |
| Aflibercept | Other | Phase PHASE4 | Diabetic Macular Edema | UNKNOWN | NCT05990829 |
| Ozurdex | Other | Phase PHASE4 | Diabetic Macular Edema | UNKNOWN | NCT05990829 |
| ABBV-CLS-7262 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT06145607 |
| ABBV-CLS-7262 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT06145607 |
| Ubrogepant | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05892757 |
| Atogepant | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05892757 |
| Ubrogepant | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05892757 |
| Atogepant | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT05892757 |
| Placebo | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT03518034 |
| AndroGel® | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT03518034 |
| Placebo | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT03518034 |
| AndroGel® | Other | Phase PHASE4 | Hypogonadism | COMPLETED | NCT03518034 |
| Lutikizumab Dose B | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06067568 |
| Lutikizumab Dose A | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06067568 |
| Lutikizumab Dose B | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06067568 |
| Lutikizumab Dose A | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06067568 |
| Lutikizumab Dose B | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06067568 |
| Lutikizumab Dose A | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06067568 |
| Placebo to upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03738397 |
| Placebo to dupilumab | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03738397 |
| Dupilumab | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03738397 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03738397 |
| Placebo to upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03738397 |
| Placebo to dupilumab | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03738397 |
| Dupilumab | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03738397 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03738397 |
| dexamethasone implant | Other | Preclinical | Diabetic Macular Edema | UNKNOWN | NCT06332690 |
| dexamethasone implant | Other | Preclinical | Diabetic Macular Edema | RECRUITING | NCT06332690 |
| CREON | Other | Preclinical | Chronic Pancreatitis | COMPLETED | NCT04949828 |
| Placebo | Other | Phase PHASE1 | Moderate to Severe Glabellar Lines | COMPLETED | NCT06151561 |
| AGN-151586 | Other | Phase PHASE1 | Moderate to Severe Glabellar Lines | COMPLETED | NCT06151561 |
| Unspecific group training | Other | Approved | Parkinson's Disease | COMPLETED | NCT02048605 |
| Psycho-social CBT based training | Other | Approved | Parkinson's Disease | COMPLETED | NCT02048605 |
| AGN-190584 | Other | Phase PHASE4 | Presbyopia | WITHDRAWN | NCT05624320 |
| AGN-190584 | Other | Phase PHASE4 | Presbyopia | WITHDRAWN | NCT05624320 |
| ABBV-552 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06278766 |
| ABBV-552 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06278766 |
| Apremilast | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04908475 |
| Risankizumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04908475 |
| Apremilast | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04908475 |
| Risankizumab | Other | Phase PHASE4 | Psoriasis | COMPLETED | NCT04908475 |
| Veliparib | Other | Phase PHASE2 | Cancer | WITHDRAWN | NCT03044795 |
| Veliparib | Other | Phase PHASE2 | Cancer | WITHDRAWN | NCT03044795 |
| Venetoclax | Other | Preclinical | Myelofibrosis | NO_LONGER_AVAILABLE | NCT03592576 |
| Navitoclax | Other | Preclinical | Myelofibrosis | NO_LONGER_AVAILABLE | NCT03592576 |
| Venetoclax | Other | Preclinical | Myelofibrosis | NO_LONGER_AVAILABLE | NCT03592576 |
| Navitoclax | Other | Preclinical | Myelofibrosis | NO_LONGER_AVAILABLE | NCT03592576 |
| Sham Selective Laser Trabeculoplasty | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02507687 |
| Selective Laser Trabeculoplasty | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02507687 |
| Sham Bimatoprost SR | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02507687 |
| Bimatoprost SR | Other | Phase PHASE3 | Glaucoma, Open-Angle | COMPLETED | NCT02507687 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06054425 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06054425 |
| Placebo | Other | Phase PHASE2 | Post-Operative Atrial Fibrillation | COMPLETED | NCT03779841 |
| AGN-151607 | Other | Phase PHASE2 | Post-Operative Atrial Fibrillation | COMPLETED | NCT03779841 |
| Placebo | Other | Phase PHASE2 | Post-Operative Atrial Fibrillation | COMPLETED | NCT03779841 |
| AGN-151607 | Other | Phase PHASE2 | Post-Operative Atrial Fibrillation | COMPLETED | NCT03779841 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248867 |
| Placebo | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248867 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248867 |
| Placebo | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248867 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248893 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04905810 |
| Decitabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04905810 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04905810 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04905810 |
| Decitabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04905810 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04905810 |
| Leuprolide Acetate (LA) | Other | Phase PHASE3 | Central Precocious Puberty (CPP) | COMPLETED | NCT03695237 |
| Leuprolide Acetate (LA) | Other | Phase PHASE3 | Central Precocious Puberty (CPP) | COMPLETED | NCT03695237 |
| Leuprolide Acetate (LA) | Other | Phase PHASE3 | Central Precocious Puberty (CPP) | COMPLETED | NCT03695237 |
| 18F-FluorApoTrace | Other | Phase EARLY_PHASE1 | Diffuse Large B Cell Lymphoma | TERMINATED | NCT05048732 |
| 18F-FluorApoTrace | Other | Phase EARLY_PHASE1 | Diffuse Large B Cell Lymphoma | TERMINATED | NCT05048732 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT04713592 |
| Placebo for Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT04713592 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT04713592 |
| Placebo for Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT04713592 |
| RGX-314 | Other | Phase PHASE2 | Neovascular Age-related Macular Degeneration | ENROLLING_BY_INVITATION | NCT03999801 |
| Venetoclax | Other | Phase PHASE1 | Healthy Volunteers | WITHDRAWN | NCT06070948 |
| Venetoclax | Other | Phase PHASE1 | Healthy Volunteers | WITHDRAWN | NCT06070948 |
| Pemetrexed | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Carboplatin | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Cisplatin | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Osimertinib | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Pemetrexed | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Carboplatin | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Cisplatin | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Osimertinib | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non-Small Cell Lung Cancer | WITHDRAWN | NCT06093503 |
| Moxifloxacin 400mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT06310876 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT06310876 |
| ABBV-CLS-7262 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT06310876 |
| Moxifloxacin 400mg | Other | Phase PHASE1 | Healthy | COMPLETED | NCT06310876 |
| Placebo | Other | Phase PHASE1 | Healthy | COMPLETED | NCT06310876 |
| ABBV-CLS-7262 | Other | Phase PHASE1 | Healthy | COMPLETED | NCT06310876 |
| Placebo for ABBV-950 | Other | Phase PHASE1 | Upper Limb Spasticity | TERMINATED | NCT05956509 |
| BOTOX | Other | Phase PHASE1 | Upper Limb Spasticity | TERMINATED | NCT05956509 |
| ABBV-950 | Other | Phase PHASE1 | Upper Limb Spasticity | TERMINATED | NCT05956509 |
| Placebo for ABBV-950 | Other | Phase PHASE1 | Upper Limb Spasticity | TERMINATED | NCT05956509 |
| BOTOX | Other | Phase PHASE1 | Upper Limb Spasticity | TERMINATED | NCT05956509 |
| ABBV-950 | Other | Phase PHASE1 | Upper Limb Spasticity | TERMINATED | NCT05956509 |
| Cytochrome P450 (CYP) Substrates | Other | Phase PHASE1 | Ulcerative Colitis (UC) | COMPLETED | NCT04254783 |
| Risankizumab | Other | Phase PHASE1 | Ulcerative Colitis (UC) | COMPLETED | NCT04254783 |
| Cytochrome P450 (CYP) Substrates | Other | Phase PHASE1 | Ulcerative Colitis (UC) | COMPLETED | NCT04254783 |
| Risankizumab | Other | Phase PHASE1 | Ulcerative Colitis (UC) | COMPLETED | NCT04254783 |
| ABBV-119 | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| Navocaftor | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| Placebo | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| Galicaftor | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| ABBV-576 | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| ABBV-119 | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| Navocaftor | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| Placebo | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| Galicaftor | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| ABBV-576 | Other | Phase PHASE2 | Cystic Fibrosis (CF) | TERMINATED | NCT04853368 |
| No intervention, this is an observational study | Other | Preclinical | Acute Pancreatitis | COMPLETED | NCT03063398 |
| No intervention, this is an observational study | Other | Preclinical | Acute Pancreatitis | COMPLETED | NCT03063398 |
| Placebo for upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03086343 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03086343 |
| Placebo for abatacept (0.9% Sodium Chloride Injection or Solution for Infusion) | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03086343 |
| Abatacept | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03086343 |
| Placebo for upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03086343 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03086343 |
| Placebo for abatacept (0.9% Sodium Chloride Injection or Solution for Infusion) | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03086343 |
| Abatacept | Other | Phase PHASE3 | Rheumatoid Arthritis (RA) | COMPLETED | NCT03086343 |
| [14C] ABBV-CLS-7262 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06425003 |
| [14C] ABBV-CLS-7262 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06425003 |
| CREON | Other | Phase PHASE4 | Cystic Fibrosis | COMPLETED | NCT05069597 |
| CREON | Other | Phase PHASE4 | Cystic Fibrosis | COMPLETED | NCT05069597 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT03406156 |
| Bendamustine | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT03406156 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT03406156 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT03406156 |
| Bendamustine | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT03406156 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT03406156 |
| Ubrogepant 100 MG [Ubrelvy] | Other | Phase PHASE4 | Headache, Migraine | ACTIVE_NOT_RECRUITING | NCT05503082 |
| Ubrogepant 50 MG [Ubrelvy] | Other | Phase PHASE4 | Headache, Migraine | ACTIVE_NOT_RECRUITING | NCT05503082 |
| Ubrogepant 100 MG [Ubrelvy] | Other | Phase PHASE4 | Headache, Migraine | ACTIVE_NOT_RECRUITING | NCT05503082 |
| Ubrogepant 50 MG [Ubrelvy] | Other | Phase PHASE4 | Headache, Migraine | ACTIVE_NOT_RECRUITING | NCT05503082 |
| Placebo | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT04994535 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT04994535 |
| Placebo | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT04994535 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT04994535 |
| Placebo | Other | Phase PHASE4 | Social Anxiety Disorder | COMPLETED | NCT05384483 |
| Cariprazine | Other | Phase PHASE4 | Social Anxiety Disorder | COMPLETED | NCT05384483 |
| Placebo | Other | Phase PHASE4 | Social Anxiety Disorder | COMPLETED | NCT05384483 |
| Cariprazine | Other | Phase PHASE4 | Social Anxiety Disorder | COMPLETED | NCT05384483 |
| Placebo Microcrystalline Cellulose | Other | Approved | Adjuvant Zinc May Increase the Efficacy of Botulinum Toxin | WITHDRAWN | NCT05894109 |
| zinc citrate 50 mg | Other | Approved | Adjuvant Zinc May Increase the Efficacy of Botulinum Toxin | WITHDRAWN | NCT05894109 |
| Clindamycin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Cefadroxil | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Flucloxacillin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Oxacillin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Vancomycin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Dalbavancin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Clindamycin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Cefadroxil | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Flucloxacillin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Oxacillin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Vancomycin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| Dalbavancin | Other | Phase PHASE3 | Methicillin-Resistant Staphylococcus Aureus | COMPLETED | NCT02814916 |
| OnabotulinumtoxinA 145 UNT [Botox] | Other | Phase PHASE4 | Drug-resistant Focal Seizure | TERMINATED | NCT05605756 |
| Epcoritamab | Other | Phase PHASE2 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT05451810 |
| Epcoritamab | Other | Phase PHASE2 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT05451810 |
| Osimertinib | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT04720976 |
| Sotorasib | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT04720976 |
| Pembrolizumab | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT04720976 |
| Binimetinib | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT04720976 |
| JAB-3312 | Other | Phase PHASE1 | Solid Tumor | COMPLETED | NCT04720976 |
| VOLITE XC | Other | Phase PHASE3 | Neck Lines | COMPLETED | NCT05316233 |
| VOLITE XC | Other | Phase PHASE3 | Neck Lines | COMPLETED | NCT05316233 |
| Placebo | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT04073303 |
| Botulinum Toxin Type A | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT04073303 |
| Breath Test | Other | Preclinical | IBD | ACTIVE_NOT_RECRUITING | NCT04827368 |
| Breath Test | Other | Preclinical | IBD | ACTIVE_NOT_RECRUITING | NCT04827368 |
| Lenalidomide | Other | Phase PHASE3 | Follicular Lymphoma (FL) | ACTIVE_NOT_RECRUITING | NCT05409066 |
| Rituximab | Other | Phase PHASE3 | Follicular Lymphoma (FL) | ACTIVE_NOT_RECRUITING | NCT05409066 |
| Epcoritamab | Other | Phase PHASE3 | Follicular Lymphoma (FL) | ACTIVE_NOT_RECRUITING | NCT05409066 |
| Lenalidomide | Other | Phase PHASE3 | Follicular Lymphoma (FL) | ACTIVE_NOT_RECRUITING | NCT05409066 |
| Rituximab | Other | Phase PHASE3 | Follicular Lymphoma (FL) | ACTIVE_NOT_RECRUITING | NCT05409066 |
| Epcoritamab | Other | Phase PHASE3 | Follicular Lymphoma (FL) | ACTIVE_NOT_RECRUITING | NCT05409066 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04086264 |
| IMGN632 | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04086264 |
| Azacitidine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04086264 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04086264 |
| IMGN632 | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04086264 |
| Azacitidine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04086264 |
| Bevacizumab | Other | Phase PHASE3 | Metastatic Colorectal Cancer | RECRUITING | NCT06614192 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Metastatic Colorectal Cancer | RECRUITING | NCT06614192 |
| Telisotuzumab Adizutecan | Other | Phase PHASE3 | Metastatic Colorectal Cancer | RECRUITING | NCT06614192 |
| Bevacizumab | Other | Phase PHASE3 | Metastatic Colorectal Cancer | RECRUITING | NCT06614192 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Metastatic Colorectal Cancer | RECRUITING | NCT06614192 |
| Telisotuzumab Adizutecan | Other | Phase PHASE3 | Metastatic Colorectal Cancer | RECRUITING | NCT06614192 |
| VEGFR TKI | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04417465 |
| PD-1 inhibitor | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04417465 |
| ABBV-CLS-579 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | COMPLETED | NCT04417465 |
| Adalimumab | Other | Phase PHASE2 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT06257875 |
| Lutikizumab | Other | Phase PHASE2 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT06257875 |
| Venetoclax | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06742086 |
| Venetoclax | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06742086 |
| Venetoclax | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06742086 |
| risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT05283135 |
| risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT05283135 |
| risankizumab | Other | Phase PHASE2 | Psoriasis | COMPLETED | NCT05283135 |
| Carboplatin | Other | Phase PHASE2 | High Grade Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05456685 |
| Mirvetuximab soravtansine | Other | Phase PHASE2 | High Grade Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05456685 |
| Placebo | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT06834789 |
| OnabotulinumtoxinA | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT06834789 |
| AGN-151586 | Other | Phase PHASE1 | Glabellar Lines | COMPLETED | NCT06834789 |
| Topical corticosteroids (TCS) | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT03568318 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT03568318 |
| Placebo | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT03568318 |
| Topical corticosteroids (TCS) | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT03568318 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT03568318 |
| Placebo | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT03568318 |
| GUB014295-PLACEBO | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06144684 |
| GUB014295 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06144684 |
| Bevacizumab | Other | Phase PHASE1 | Ovarian Cancer | RECRUITING | NCT07278336 |
| ABBV-901 | Other | Phase PHASE1 | Ovarian Cancer | RECRUITING | NCT07278336 |
| Upadacitinib | Other | Preclinical | Crohn Disease | AVAILABLE | NCT04159597 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | AVAILABLE | NCT04278235 |
| SYFOVRE | Other | Phase PHASE1 | Geographic Atrophy | RECRUITING | NCT07160179 |
| ABBV-6628 | Other | Phase PHASE1 | Geographic Atrophy | RECRUITING | NCT07160179 |
| SYFOVRE | Other | Phase PHASE1 | Geographic Atrophy | RECRUITING | NCT07160179 |
| ABBV-6628 | Other | Phase PHASE1 | Geographic Atrophy | RECRUITING | NCT07160179 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Risankizumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Adalimumab | Other | Phase PHASE3 | Juvenile Psoriatic Arthritis | RECRUITING | NCT06100744 |
| Placebo | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248880 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248880 |
| Placebo | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248880 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT05248880 |
| Prednisolone | Other | Phase PHASE3 | Takayasu Arteritis (TAK) | ACTIVE_NOT_RECRUITING | NCT04161898 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Takayasu Arteritis (TAK) | ACTIVE_NOT_RECRUITING | NCT04161898 |
| Upadacitinib | Other | Phase PHASE3 | Takayasu Arteritis (TAK) | ACTIVE_NOT_RECRUITING | NCT04161898 |
| Pivekimab Sunirine | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Multigated Acquisition Scan | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Idarubicin | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Granulocyte Colony-Stimulating Factor | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Fludarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Echocardiography | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Cytarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Bone Marrow Aspiration | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Biospecimen Collection | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT06034470 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-453 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-453 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | ACTIVE_NOT_RECRUITING | NCT07361367 |
| No Intervention | Other | Phase PHASE3 | Breast Reconstruction | RECRUITING | NCT06575192 |
| ARTIA Reconstructive Tissue Matrix | Other | Phase PHASE3 | Breast Reconstruction | RECRUITING | NCT06575192 |
| Placebo for Risankizumab | Other | Phase PHASE4 | Genital Psoriasis | COMPLETED | NCT05969223 |
| Risankizumab | Other | Phase PHASE4 | Genital Psoriasis | COMPLETED | NCT05969223 |
| Placebo for Risankizumab | Other | Phase PHASE4 | Genital Psoriasis | COMPLETED | NCT05969223 |
| Risankizumab | Other | Phase PHASE4 | Genital Psoriasis | COMPLETED | NCT05969223 |
| Bendamustine | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Obinutuzumab | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Cyclophosphamide | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Vincristine | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Doxorubicin | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Lenalidomide | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Rituximab | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Prednisone | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Epcoritamab | Other | Phase PHASE3 | Follicular Lymphoma (FL) | RECRUITING | NCT06191744 |
| Placebo | Other | Phase PHASE3 | Systemic Lupus Erythematosus | RECRUITING | NCT05843643 |
| Upadacitinib | Other | Phase PHASE3 | Systemic Lupus Erythematosus | RECRUITING | NCT05843643 |
| Placebo | Other | Phase PHASE3 | Systemic Lupus Erythematosus | RECRUITING | NCT05843643 |
| Upadacitinib | Other | Phase PHASE3 | Systemic Lupus Erythematosus | RECRUITING | NCT05843643 |
| Vedolizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT06880744 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT06880744 |
| Vedolizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT06880744 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT06880744 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| ABBV-101 | Other | Phase PHASE1 | Hematologic Cancer | ACTIVE_NOT_RECRUITING | NCT05753501 |
| Upadacitinib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07425899 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07425899 |
| ABBV-438 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT07409246 |
| ABBV-932 | Other | Phase PHASE2 | Bipolar I or II Disorder | RECRUITING | NCT07220460 |
| ABBV-932 | Other | Phase PHASE2 | Bipolar I or II Disorder | RECRUITING | NCT07220460 |
| Gemcitabine | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Oxaliplatin | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Lenalidomide | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Rituximab | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Epcoritamab | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Gemcitabine | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Oxaliplatin | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Lenalidomide | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Rituximab | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Epcoritamab | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT06508658 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | RECRUITING | NCT07323641 |
| Survey Administration | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | RECRUITING | NCT07323641 |
| Osimertinib | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | RECRUITING | NCT07323641 |
| Magnetic Resonance Imaging | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | RECRUITING | NCT07323641 |
| Computed Tomography | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | RECRUITING | NCT07323641 |
| Biospecimen Collection | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | RECRUITING | NCT07323641 |
| Biopsy Procedure | Procedure | Phase PHASE2 | Lung Non-Small Cell Carcinoma | RECRUITING | NCT07323641 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Liposomal daunorubicin and cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Daunorubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Idarubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Iberdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Matching Placebo for PVEK | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Pivekimab Sunirine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Azacitidine | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Venetoclax | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| ethinyl estradiol/levonorgestrel | Other | Phase PHASE1 | Hematologic Malignancies | RECRUITING | NCT03557619 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Malignancies | RECRUITING | NCT03557619 |
| ethinyl estradiol/levonorgestrel | Other | Phase PHASE1 | Hematologic Malignancies | RECRUITING | NCT03557619 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Malignancies | RECRUITING | NCT03557619 |
| ethinyl estradiol/levonorgestrel | Other | Phase PHASE1 | Hematologic Malignancies | RECRUITING | NCT03557619 |
| Venetoclax | Other | Phase PHASE1 | Hematologic Malignancies | RECRUITING | NCT03557619 |
| Placebo | Other | Phase PHASE4 | Overactive Detrusor | COMPLETED | NCT01192568 |
| Oxybutynin | Other | Phase PHASE4 | Overactive Detrusor | COMPLETED | NCT01192568 |
| Carboplatin | Other | Preclinical | Metastatic Non Small Cell Lung Cancer | COMPLETED | NCT06585189 |
| Cisplatin | Other | Preclinical | Metastatic Non Small Cell Lung Cancer | COMPLETED | NCT06585189 |
| Pemetrexed | Other | Preclinical | Metastatic Non Small Cell Lung Cancer | COMPLETED | NCT06585189 |
| Pembrolizumab | Other | Preclinical | Metastatic Non Small Cell Lung Cancer | COMPLETED | NCT06585189 |
| Carboplatin | Other | Preclinical | Metastatic Non Small Cell Lung Cancer | COMPLETED | NCT06585189 |
| Cisplatin | Other | Preclinical | Metastatic Non Small Cell Lung Cancer | COMPLETED | NCT06585189 |
| Pemetrexed | Other | Preclinical | Metastatic Non Small Cell Lung Cancer | COMPLETED | NCT06585189 |
| Pembrolizumab | Other | Preclinical | Metastatic Non Small Cell Lung Cancer | COMPLETED | NCT06585189 |
| RGX-314 | Other | Phase PHASE2 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT04832724 |
| RGX-314 | Other | Phase PHASE2 | Neovascular Age-related Macular Degeneration | COMPLETED | NCT04832724 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | WITHDRAWN | NCT06390722 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | WITHDRAWN | NCT06390722 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | WITHDRAWN | NCT06390722 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | WITHDRAWN | NCT06390722 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | WITHDRAWN | NCT06390722 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | WITHDRAWN | NCT06390722 |
| Placebo for Albendazole | Other | Phase PHASE2 | Onchocerciasis | TERMINATED | NCT04913610 |
| Albendazole | Other | Phase PHASE2 | Onchocerciasis | TERMINATED | NCT04913610 |
| Placebo for ABBV-4083 | Other | Phase PHASE2 | Onchocerciasis | TERMINATED | NCT04913610 |
| ABBV-4083 | Other | Phase PHASE2 | Onchocerciasis | TERMINATED | NCT04913610 |
| Placebo for Albendazole | Other | Phase PHASE2 | Onchocerciasis | TERMINATED | NCT04913610 |
| Albendazole | Other | Phase PHASE2 | Onchocerciasis | TERMINATED | NCT04913610 |
| Placebo for ABBV-4083 | Other | Phase PHASE2 | Onchocerciasis | TERMINATED | NCT04913610 |
| ABBV-4083 | Other | Phase PHASE2 | Onchocerciasis | TERMINATED | NCT04913610 |
| ABBV-903 | Other | Phase PHASE1 | Healthy Volunteers | WITHDRAWN | NCT06078202 |
| Letrozole | Other | Preclinical | Metastatic Breast Cancer | COMPLETED | NCT06607601 |
| Palbociclib | Other | Preclinical | Metastatic Breast Cancer | COMPLETED | NCT06607601 |
| Letrozole | Other | Preclinical | Metastatic Breast Cancer | COMPLETED | NCT06607601 |
| Palbociclib | Other | Preclinical | Metastatic Breast Cancer | COMPLETED | NCT06607601 |
| Carboplatin | Other | Preclinical | Metastatic Nonsmall Cell Lung Cancer | COMPLETED | NCT06607393 |
| Cisplatin | Other | Preclinical | Metastatic Nonsmall Cell Lung Cancer | COMPLETED | NCT06607393 |
| Pemetrexed | Other | Preclinical | Metastatic Nonsmall Cell Lung Cancer | COMPLETED | NCT06607393 |
| Pembrolizumab | Other | Preclinical | Metastatic Nonsmall Cell Lung Cancer | COMPLETED | NCT06607393 |
| Carboplatin | Other | Preclinical | Metastatic Nonsmall Cell Lung Cancer | COMPLETED | NCT06607393 |
| Cisplatin | Other | Preclinical | Metastatic Nonsmall Cell Lung Cancer | COMPLETED | NCT06607393 |
| Pemetrexed | Other | Preclinical | Metastatic Nonsmall Cell Lung Cancer | COMPLETED | NCT06607393 |
| Pembrolizumab | Other | Preclinical | Metastatic Nonsmall Cell Lung Cancer | COMPLETED | NCT06607393 |
| Juvéderm® VOLUMA® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Juvéderm® VOLIFT® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Juvéderm® VOLBELLA® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| BOTOX®/VISTABEL® | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Juvéderm® VOLUMA® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Juvéderm® VOLIFT® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Juvéderm® VOLBELLA® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| BOTOX®/VISTABEL® | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Juvéderm® VOLUMA® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Juvéderm® VOLIFT® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Juvéderm® VOLBELLA® with Lidocaine | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| BOTOX®/VISTABEL® | Other | Phase PHASE4 | Facial Corrections | COMPLETED | NCT05647551 |
| Placebo | Other | Phase PHASE2 | Crohn's Disease | TERMINATED | NCT05068284 |
| ABBV-154 | Other | Phase PHASE2 | Crohn's Disease | TERMINATED | NCT05068284 |
| Placebo | Other | Phase PHASE2 | Crohn's Disease | TERMINATED | NCT05068284 |
| ABBV-154 | Other | Phase PHASE2 | Crohn's Disease | TERMINATED | NCT05068284 |
| ABBV-668 ER | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06477926 |
| ABBV-668 IR | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06477926 |
| ABBV-668 ER | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06477926 |
| ABBV-668 IR | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06477926 |
| ABBV-668 ER | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06477926 |
| ABBV-668 IR | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06477926 |
| Ubrogepant | Other | Phase PHASE4 | Episodic Migraine | COMPLETED | NCT05264129 |
| Atogepant | Other | Phase PHASE4 | Episodic Migraine | COMPLETED | NCT05264129 |
| Ubrogepant | Other | Phase PHASE4 | Episodic Migraine | COMPLETED | NCT05264129 |
| Atogepant | Other | Phase PHASE4 | Episodic Migraine | COMPLETED | NCT05264129 |
| Placebo | Other | Phase PHASE2 | Non-Segmental Vitiligo | COMPLETED | NCT04927975 |
| Upadacitinib | Other | Phase PHASE2 | Non-Segmental Vitiligo | COMPLETED | NCT04927975 |
| Placebo | Other | Phase PHASE2 | Non-Segmental Vitiligo | COMPLETED | NCT04927975 |
| Upadacitinib | Other | Phase PHASE2 | Non-Segmental Vitiligo | COMPLETED | NCT04927975 |
| Placebo | Other | Phase PHASE2 | Non-Segmental Vitiligo | COMPLETED | NCT04927975 |
| Upadacitinib | Other | Phase PHASE2 | Non-Segmental Vitiligo | COMPLETED | NCT04927975 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | TERMINATED | NCT04888585 |
| ABBV-154 | Other | Phase PHASE2 | Rheumatoid Arthritis (RA) | TERMINATED | NCT04888585 |
| Vehicle | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT04837482 |
| AGN-190584 | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT04837482 |
| Vehicle | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT04837482 |
| AGN-190584 | Other | Phase PHASE3 | Presbyopia | COMPLETED | NCT04837482 |
| ABBV-444 | Other | Phase PHASE3 | Dry Eye Syndrome | COMPLETED | NCT05878067 |
| ABBV-444 | Other | Phase PHASE3 | Dry Eye Syndrome | COMPLETED | NCT05878067 |
| Glucocorticoid | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| Placebo | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| ABBV-154 | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| Glucocorticoid | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| Placebo | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| ABBV-154 | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| Glucocorticoid | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| Placebo | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| ABBV-154 | Other | Phase PHASE2 | Polymyalgia Rheumatica | TERMINATED | NCT04972968 |
| Ravagalimab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06402513 |
| Ravagalimab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06402513 |
| Ravagalimab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06402513 |
| Placebo to Veliparib | Other | Phase PHASE3 | Ovarian Cancer | TERMINATED | NCT02470585 |
| Carboplatin | Other | Phase PHASE3 | Ovarian Cancer | TERMINATED | NCT02470585 |
| Paclitaxel | Other | Phase PHASE3 | Ovarian Cancer | TERMINATED | NCT02470585 |
| Veliparib | Other | Phase PHASE3 | Ovarian Cancer | TERMINATED | NCT02470585 |
| ABBV-951 | Other | Phase PHASE1 | Parkinson's Disease (PD) | COMPLETED | NCT03374917 |
| ABBV-951 | Other | Phase PHASE1 | Parkinson's Disease (PD) | COMPLETED | NCT03374917 |
| ABBV-951 | Other | Phase PHASE1 | Parkinson's Disease (PD) | COMPLETED | NCT03033498 |
| ABBV-951 | Other | Phase PHASE1 | Parkinson's Disease (PD) | COMPLETED | NCT03033498 |
| ABBV-951 | Other | Phase PHASE1 | Parkinson's Disease (PD) | COMPLETED | NCT03033498 |
| Placebo | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT04949399 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT04949399 |
| Placebo | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT04949399 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT04949399 |
| standard of care chemotherapy plus gemtuzumab ozogamicin | Drug | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT05904106 |
| Venetoclax plus Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT05904106 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT05134649 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Platysma Prominence | COMPLETED | NCT05134649 |
| Ibrutinib 420 mg | Other | Phase PHASE1 | Breast Neoplasms | ACTIVE_NOT_RECRUITING | NCT03379428 |
| Ibrutinib 840 mg | Other | Phase PHASE1 | Breast Neoplasms | ACTIVE_NOT_RECRUITING | NCT03379428 |
| Ibrutinib 560 mg | Other | Phase PHASE1 | Breast Neoplasms | ACTIVE_NOT_RECRUITING | NCT03379428 |
| Trastuzumab | Other | Phase PHASE1 | Breast Neoplasms | ACTIVE_NOT_RECRUITING | NCT03379428 |
| Ibrutinib 420 mg | Other | Phase PHASE1 | Breast Neoplasms | ACTIVE_NOT_RECRUITING | NCT03379428 |
| Ibrutinib 840 mg | Other | Phase PHASE1 | Breast Neoplasms | ACTIVE_NOT_RECRUITING | NCT03379428 |
| Ibrutinib 560 mg | Other | Phase PHASE1 | Breast Neoplasms | ACTIVE_NOT_RECRUITING | NCT03379428 |
| Trastuzumab | Other | Phase PHASE1 | Breast Neoplasms | ACTIVE_NOT_RECRUITING | NCT03379428 |
| Androgen suppression plus radiation therapy | Drug | Phase PHASE2 | Adenocarcinoma of the Prostate | COMPLETED | NCT01255891 |
| Androgen suppression plus radiation therapy | Drug | Phase PHASE2 | Adenocarcinoma of the Prostate | COMPLETED | NCT01255891 |
| MRE | Other | Approved | Crohn Disease | RECRUITING | NCT05420233 |
| MRE | Other | Approved | Crohn Disease | RECRUITING | NCT05420233 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03047395 |
| risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT03047395 |
| IMGN632 | Other | Phase PHASE1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | ACTIVE_NOT_RECRUITING | NCT03386513 |
| IMGN632 | Other | Phase PHASE1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | ACTIVE_NOT_RECRUITING | NCT03386513 |
| Placebo for E2/NETA | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT03213457 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT03213457 |
| Placebo for Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT03213457 |
| Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT03213457 |
| Placebo for E2/NETA | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT03213457 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT03213457 |
| Placebo for Elagolix | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT03213457 |
| Estradiol/Norethindrone Acetate | Other | Phase PHASE3 | Endometriosis | COMPLETED | NCT03213457 |
| Ibrutinib | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Bendamustine | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Rituximab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Cyclophosphamide | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Fludarabine | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Ibrutinib | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Bendamustine | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Rituximab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Cyclophosphamide | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Fludarabine | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | COMPLETED | NCT02950051 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Ibrutinib | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Ibrutinib | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Ibrutinib | Other | Phase PHASE3 | Chronic Lymphoid Leukemia | ACTIVE_NOT_RECRUITING | NCT04608318 |
| Lenalidomide | Other | Phase PHASE1 | B-Cell Non-Hodgkin Lymphoma | ACTIVE_NOT_RECRUITING | NCT05201248 |
| Prednisone | Other | Phase PHASE1 | B-Cell Non-Hodgkin Lymphoma | ACTIVE_NOT_RECRUITING | NCT05201248 |
| Vincristine | Other | Phase PHASE1 | B-Cell Non-Hodgkin Lymphoma | ACTIVE_NOT_RECRUITING | NCT05201248 |
| Doxorubicin | Other | Phase PHASE1 | B-Cell Non-Hodgkin Lymphoma | ACTIVE_NOT_RECRUITING | NCT05201248 |
| Rituximab | Other | Phase PHASE1 | B-Cell Non-Hodgkin Lymphoma | ACTIVE_NOT_RECRUITING | NCT05201248 |
| Cyclophosphamide | Other | Phase PHASE1 | B-Cell Non-Hodgkin Lymphoma | ACTIVE_NOT_RECRUITING | NCT05201248 |
| Epcoritamab | Other | Phase PHASE1 | B-Cell Non-Hodgkin Lymphoma | ACTIVE_NOT_RECRUITING | NCT05201248 |
| modified FOLFIRINOX | Other | Phase PHASE1 | Pancreatic Cancer | TERMINATED | NCT04807972 |
| Budiglimab | Other | Phase PHASE1 | Pancreatic Cancer | TERMINATED | NCT04807972 |
| ABBV-927 | Other | Phase PHASE1 | Pancreatic Cancer | TERMINATED | NCT04807972 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT04195698 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT04195698 |
| Placebo for Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Placebo for Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Placebo for Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Placebo for Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Placebo for Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Upadacitinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Placebo for Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Elsubrutinib | Other | Phase PHASE2 | Systemic Lupus Erythematosus (SLE) | COMPLETED | NCT04451772 |
| Upadacitinib | Other | Phase PHASE4 | Prurigo Nodularis | RECRUITING | NCT06773403 |
| risankizumab SC | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| placebo for risankizumab | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| risankizumab IV | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| risankizumab SC | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| placebo for risankizumab | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| risankizumab IV | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| risankizumab SC | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| placebo for risankizumab | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| risankizumab IV | Other | Phase PHASE2 | Ulcerative Colitis (UC) | COMPLETED | NCT03398148 |
| Placebo for ABBV-141 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06148181 |
| ABBV-141 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06148181 |
| OnabotulinumtoxinA 145 UNT [Botox] | Other | Phase PHASE4 | Drug-resistant Focal Seizure | TERMINATED | NCT05605756 |
| Lutikizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | RECRUITING | NCT06524635 |
| Itraconazole (ITZ) | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06722430 |
| Icalcaprant | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06722430 |
| Itraconazole (ITZ) | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06722430 |
| Icalcaprant | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06722430 |
| Icalcaprant | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06722417 |
| Icalcaprant | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06722417 |
| Methotrexate | Other | Preclinical | Juvenile Idiopathic Arthritis | COMPLETED | NCT00783510 |
| adalimumab | Other | Preclinical | Juvenile Idiopathic Arthritis | COMPLETED | NCT00783510 |
| Methotrexate | Other | Preclinical | Juvenile Idiopathic Arthritis | COMPLETED | NCT00783510 |
| adalimumab | Other | Preclinical | Juvenile Idiopathic Arthritis | COMPLETED | NCT00783510 |
| Methotrexate | Other | Preclinical | Juvenile Idiopathic Arthritis | COMPLETED | NCT00783510 |
| adalimumab | Other | Preclinical | Juvenile Idiopathic Arthritis | COMPLETED | NCT00783510 |
| Bimatoprost Sustained Release Implant | Other | Preclinical | Open-angle Glaucoma | NO_LONGER_AVAILABLE | NCT05338606 |
| Bimatoprost Sustained Release Implant | Other | Preclinical | Open-angle Glaucoma | NO_LONGER_AVAILABLE | NCT05338606 |
| Upadacitinib (ABT-494) | Other | Phase PHASE1 | Atopic Dermatitis | COMPLETED | NCT03646604 |
| Upadacitinib (ABT-494) | Other | Phase PHASE1 | Atopic Dermatitis | COMPLETED | NCT03646604 |
| Upadacitinib (ABT-494) | Other | Phase PHASE1 | Atopic Dermatitis | COMPLETED | NCT03646604 |
| HAC 20L | Other | Phase PHASE2 | Nasolabial Folds | COMPLETED | NCT06018987 |
| No-Treatment Control | Drug | Phase PHASE2 | Nasolabial Folds | COMPLETED | NCT06018987 |
| HAC 20L | Other | Phase PHASE2 | Nasolabial Folds | COMPLETED | NCT06018987 |
| No-Treatment Control | Drug | Phase PHASE2 | Nasolabial Folds | COMPLETED | NCT06018987 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT05601882 |
| Dupilumab | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT05601882 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT05601882 |
| Dupilumab | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT05601882 |
| Celecoxib | Other | Phase PHASE1 | Myeloproliferative Neoplasm | ACTIVE_NOT_RECRUITING | NCT04041050 |
| Ruxolitinib | Other | Phase PHASE1 | Myeloproliferative Neoplasm | ACTIVE_NOT_RECRUITING | NCT04041050 |
| Navitoclax | Other | Phase PHASE1 | Myeloproliferative Neoplasm | ACTIVE_NOT_RECRUITING | NCT04041050 |
| Celecoxib | Other | Phase PHASE1 | Myeloproliferative Neoplasm | ACTIVE_NOT_RECRUITING | NCT04041050 |
| Ruxolitinib | Other | Phase PHASE1 | Myeloproliferative Neoplasm | ACTIVE_NOT_RECRUITING | NCT04041050 |
| Navitoclax | Other | Phase PHASE1 | Myeloproliferative Neoplasm | ACTIVE_NOT_RECRUITING | NCT04041050 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06487572 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06487572 |
| Drug: Placebo for ABBV-1088 | Drug | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06414798 |
| Drug: ABBV-1088 | Drug | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06414798 |
| Drug: Placebo for ABBV-1088 | Drug | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06414798 |
| Drug: ABBV-1088 | Drug | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06414798 |
| Paclitaxel | Other | Phase PHASE3 | Metastatic Breast Cancer | COMPLETED | NCT02163694 |
| Carboplatin | Other | Phase PHASE3 | Metastatic Breast Cancer | COMPLETED | NCT02163694 |
| Veliparib | Other | Phase PHASE3 | Metastatic Breast Cancer | COMPLETED | NCT02163694 |
| Veliparib Placebo | Other | Phase PHASE3 | Metastatic Breast Cancer | COMPLETED | NCT02163694 |
| Paclitaxel | Other | Phase PHASE3 | Metastatic Breast Cancer | COMPLETED | NCT02163694 |
| Carboplatin | Other | Phase PHASE3 | Metastatic Breast Cancer | COMPLETED | NCT02163694 |
| Veliparib | Other | Phase PHASE3 | Metastatic Breast Cancer | COMPLETED | NCT02163694 |
| Veliparib Placebo | Other | Phase PHASE3 | Metastatic Breast Cancer | COMPLETED | NCT02163694 |
| Lab work | Other | Phase EARLY_PHASE1 | Infertility | COMPLETED | NCT04445025 |
| Leuprolide Acetate 3.75 MG/ML | Other | Phase EARLY_PHASE1 | Infertility | COMPLETED | NCT04445025 |
| Elagolix 200 MG | Other | Phase EARLY_PHASE1 | Infertility | COMPLETED | NCT04445025 |
| Lab work | Other | Phase EARLY_PHASE1 | Infertility | COMPLETED | NCT04445025 |
| Leuprolide Acetate 3.75 MG/ML | Other | Phase EARLY_PHASE1 | Infertility | COMPLETED | NCT04445025 |
| Elagolix 200 MG | Other | Phase EARLY_PHASE1 | Infertility | COMPLETED | NCT04445025 |
| ABT-263 | Other | Phase PHASE1 | CD20-Positive Lymphoid Malignancies | COMPLETED | NCT00788684 |
| rituximab | Other | Phase PHASE1 | CD20-Positive Lymphoid Malignancies | COMPLETED | NCT00788684 |
| ABT-263 | Other | Phase PHASE1 | CD20-Positive Lymphoid Malignancies | COMPLETED | NCT00788684 |
| rituximab | Other | Phase PHASE1 | CD20-Positive Lymphoid Malignancies | COMPLETED | NCT00788684 |
| Glecaprevir and Pibrentasvir | Other | Phase PHASE4 | Hepatitis C | TERMINATED | NCT05582681 |
| HCV education from a health care provider | Other | Phase PHASE4 | Hepatitis C | TERMINATED | NCT05582681 |
| Cepheid POC HCV Viremia (RNA) test | Other | Phase PHASE4 | Hepatitis C | TERMINATED | NCT05582681 |
| Glecaprevir and Pibrentasvir | Other | Phase PHASE4 | Hepatitis C | TERMINATED | NCT05582681 |
| HCV education from a health care provider | Other | Phase PHASE4 | Hepatitis C | TERMINATED | NCT05582681 |
| Cepheid POC HCV Viremia (RNA) test | Other | Phase PHASE4 | Hepatitis C | TERMINATED | NCT05582681 |
| Budigalimab | Other | Phase PHASE1 | Hepatocellular Carcinoma (HCC) | RECRUITING | NCT06487559 |
| Livmoniplimab | Other | Phase PHASE1 | Hepatocellular Carcinoma (HCC) | RECRUITING | NCT06487559 |
| Budigalimab | Other | Phase PHASE1 | Hepatocellular Carcinoma (HCC) | RECRUITING | NCT06487559 |
| Livmoniplimab | Other | Phase PHASE1 | Hepatocellular Carcinoma (HCC) | RECRUITING | NCT06487559 |
| ELAPR002f Injectable Gel | Other | Phase PHASE2 | Skin Quality Deficit | COMPLETED | NCT06151535 |
| ELAPR002f Injectable Gel | Other | Phase PHASE2 | Skin Quality Deficit | COMPLETED | NCT06151535 |
| ELAPR002f Injectable Gel | Other | Phase PHASE2 | Skin Quality Deficit | COMPLETED | NCT06151535 |
| ABBV-787 | Other | Phase PHASE1 | Acute Myeloid Leukemia | TERMINATED | NCT06068868 |
| ABBV-787 | Other | Phase PHASE1 | Acute Myeloid Leukemia | TERMINATED | NCT06068868 |
| Cyclin D1 gene (CCDN1) /immunoglobulin heavy chain (IGH) fluorescence in situ hybridization (FISH) assay | Other | Phase PHASE1 | AL Amyloidosis | WITHDRAWN | NCT05486481 |
| Daratumumab | Other | Phase PHASE1 | AL Amyloidosis | WITHDRAWN | NCT05486481 |
| Dexamethasone | Other | Phase PHASE1 | AL Amyloidosis | WITHDRAWN | NCT05486481 |
| Venetoclax | Other | Phase PHASE1 | AL Amyloidosis | WITHDRAWN | NCT05486481 |
| Venetoclax | Other | Phase PHASE2 | Chronic Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT05701215 |
| Venetoclax | Other | Phase PHASE2 | Chronic Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT05701215 |
| Placebo for ABBV-932 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06024239 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06024239 |
| Placebo for ABBV-932 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06024239 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06024239 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05861427 |
| Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05861427 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05861427 |
| Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05861427 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05861427 |
| Atogepant | Other | Phase PHASE3 | Migraine | COMPLETED | NCT05861427 |
| Elagolix | Other | Phase PHASE4 | Mild Autonomous Cortisol Excess | TERMINATED | NCT05038878 |
| Placebo | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT06308198 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT06308198 |
| Placebo | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT06308198 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT06308198 |
| Placebo | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT06308198 |
| AGN-151586 | Other | Phase PHASE3 | Glabellar Lines | COMPLETED | NCT06308198 |
| No Interventions | Other | Preclinical | Interstitial Lung Disease | RECRUITING | NCT06644144 |
| Placebo | Other | Phase PHASE2 | Panic Disorder | COMPLETED | NCT05941442 |
| Darigabat | Other | Phase PHASE2 | Panic Disorder | COMPLETED | NCT05941442 |
| Placebo | Other | Phase PHASE2 | Panic Disorder | COMPLETED | NCT05941442 |
| Darigabat | Other | Phase PHASE2 | Panic Disorder | COMPLETED | NCT05941442 |
| Emraclidine | Other | Phase PHASE1 | Renal Impairment | COMPLETED | NCT05940402 |
| Emraclidine | Other | Phase PHASE1 | Hepatic Impairment | COMPLETED | NCT05935033 |
| Emraclidine | Other | Phase PHASE1 | Hepatic Impairment | COMPLETED | NCT05935033 |
| Placebo | Other | Phase PHASE3 | Autism Spectrum Disorder | COMPLETED | NCT05439616 |
| Cariprazine | Other | Phase PHASE3 | Autism Spectrum Disorder | COMPLETED | NCT05439616 |
| Placebo | Other | Phase PHASE3 | Autism Spectrum Disorder | COMPLETED | NCT05439616 |
| Cariprazine | Other | Phase PHASE3 | Autism Spectrum Disorder | COMPLETED | NCT05439616 |
| Placebo | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04542499 |
| Tavapadon | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04542499 |
| Placebo | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04542499 |
| Tavapadon | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04542499 |
| Placebo | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04542499 |
| Tavapadon | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04542499 |
| Glecaprevir/Pibrentasvir (GLE/PIB) | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT04903626 |
| Glecaprevir/Pibrentasvir (GLE/PIB) | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT04903626 |
| Glecaprevir/Pibrentasvir (GLE/PIB) | Other | Phase PHASE3 | Hepatitis C Virus (HCV) | COMPLETED | NCT04903626 |
| Epcoritamab | Other | Phase PHASE1 | Non-hodgkin Lymphoma | ACTIVE_NOT_RECRUITING | NCT05206357 |
| Telehealth in Parole/Probation Office | Other | Approved | Hepatitis C | COMPLETED | NCT05413785 |
| Telehealth in Parole/Probation Office | Other | Approved | Hepatitis C | COMPLETED | NCT05413785 |
| Telehealth in Parole/Probation Office | Other | Approved | Hepatitis C | COMPLETED | NCT05413785 |
| Placebo | Other | Phase PHASE1 | Healthy Participants | COMPLETED | NCT05644977 |
| Emraclidine | Other | Phase PHASE1 | Healthy Participants | COMPLETED | NCT05644977 |
| Placebo | Other | Phase PHASE1 | Healthy Participants | COMPLETED | NCT05644977 |
| Emraclidine | Other | Phase PHASE1 | Healthy Participants | COMPLETED | NCT05644977 |
| Placebo for BOTOX | Other | Phase PHASE2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | COMPLETED | NCT05141006 |
| BOTOX | Other | Phase PHASE2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | COMPLETED | NCT05141006 |
| Placebo for BOTOX | Other | Phase PHASE2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | COMPLETED | NCT05141006 |
| BOTOX | Other | Phase PHASE2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | COMPLETED | NCT05141006 |
| Placebo for BOTOX | Other | Phase PHASE2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | COMPLETED | NCT05141006 |
| BOTOX | Other | Phase PHASE2 | Interstitial Cystitis/Bladder Pain Syndrome (IC/BPS) | COMPLETED | NCT05141006 |
| Placebo | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT04073303 |
| Botulinum Toxin Type A | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT04073303 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03573024 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03573024 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03573024 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03573024 |
| Epcoritamab | Other | Phase PHASE1 | Non-Hodgkin Lymphoma | RECRUITING | NCT06447376 |
| Siltuximab | Other | Phase PHASE1 | Non-Hodgkin Lymphoma | RECRUITING | NCT06447376 |
| Epcoritamab | Other | Phase PHASE1 | Non-Hodgkin Lymphoma | RECRUITING | NCT06447376 |
| Siltuximab | Other | Phase PHASE1 | Non-Hodgkin Lymphoma | RECRUITING | NCT06447376 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06571266 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06571266 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT05216263 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT05216263 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04570631 |
| Bortezomib | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04570631 |
| Eftozanermin alfa | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04570631 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04570631 |
| Bortezomib | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04570631 |
| Eftozanermin alfa | Other | Phase PHASE1 | Multiple Myeloma | TERMINATED | NCT04570631 |
| Ustekinumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT04435600 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT04435600 |
| Ustekinumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT04435600 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | COMPLETED | NCT04435600 |
| Lifitegrast 5% Ophthalmic Solution | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| AGN-231868 Vehicle | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| AGN-242428 Vehicle | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| AGN-231868 | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| AGN-242428 | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| Lifitegrast 5% Ophthalmic Solution | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| AGN-231868 Vehicle | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| AGN-242428 Vehicle | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| AGN-231868 | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| AGN-242428 | Other | Phase PHASE1 | Dry Eye Disease | COMPLETED | NCT04030962 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Colorectal Cancer | RECRUITING | NCT06464692 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Colorectal Cancer | RECRUITING | NCT06464692 |
| Placebo for Topiramate | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Topiramate | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Placebo for Topiramate | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Topiramate | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Placebo for Topiramate | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Topiramate | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Atogepant | Other | Phase PHASE3 | Migraine | ACTIVE_NOT_RECRUITING | NCT05748483 |
| Budigalimab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT03821935 |
| Livmoniplimab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT03821935 |
| Budigalimab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT03821935 |
| Livmoniplimab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT03821935 |
| Budigalimab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT03821935 |
| Livmoniplimab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT03821935 |
| Adalimumab | Other | Approved | Crohn Disease | ACTIVE_NOT_RECRUITING | NCT03261102 |
| Adalimumab | Other | Approved | Crohn Disease | ACTIVE_NOT_RECRUITING | NCT03261102 |
| Placebo for ABBV-382 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06632938 |
| ABBV-382 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06632938 |
| Placebo for ABBV-382 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06632938 |
| ABBV-382 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06632938 |
| Placebo for ABBV-382 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06632938 |
| ABBV-382 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06632938 |
| CVL-865 | Other | Phase PHASE2 | Seizures | COMPLETED | NCT04244175 |
| Placebo | Other | Phase PHASE2 | Seizures | COMPLETED | NCT04244175 |
| CVL-865 | Other | Phase PHASE2 | Seizures | COMPLETED | NCT04244175 |
| Placebo | Other | Phase PHASE2 | Seizures | COMPLETED | NCT04244175 |
| Programmed Cell Death-1 (PD-1) Inhibitor | Other | Phase PHASE1 | Advanced Solid Tumor Cancer | RECRUITING | NCT04777994 |
| Vascular Endothelial Growth Factor Receptor (VEGFR) Tyrosine Kinase Inhibitor (TKI) | Other | Phase PHASE1 | Advanced Solid Tumor Cancer | RECRUITING | NCT04777994 |
| ABBV-CLS-484 | Other | Phase PHASE1 | Advanced Solid Tumor Cancer | RECRUITING | NCT04777994 |
| Epcoritamab, lenalidomide and rituximab | Other | Phase PHASE2 | Relapsed/Refractory Large B-cell Lymphoma | RECRUITING | NCT06414148 |
| Epcoritamab | Other | Phase PHASE2 | Relapsed/Refractory Large B-cell Lymphoma | RECRUITING | NCT06414148 |
| Epcoritamab, lenalidomide and rituximab | Other | Phase PHASE2 | Relapsed/Refractory Large B-cell Lymphoma | RECRUITING | NCT06414148 |
| Epcoritamab | Other | Phase PHASE2 | Relapsed/Refractory Large B-cell Lymphoma | RECRUITING | NCT06414148 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06300580 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06300580 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06300580 |
| Standard Chemotherapy | Drug | Phase PHASE1 | Leukemia | RECRUITING | NCT03319901 |
| Venetoclax | Other | Phase PHASE1 | Leukemia | RECRUITING | NCT03319901 |
| Standard Chemotherapy | Drug | Phase PHASE1 | Leukemia | RECRUITING | NCT03319901 |
| Venetoclax | Other | Phase PHASE1 | Leukemia | RECRUITING | NCT03319901 |
| Saline Active Control | Other | Phase PHASE3 | Atrophic Acne Scars | ACTIVE_NOT_RECRUITING | NCT05995340 |
| ELAPR002f Injectable Gel | Other | Phase PHASE3 | Atrophic Acne Scars | ACTIVE_NOT_RECRUITING | NCT05995340 |
| Saline Active Control | Other | Phase PHASE3 | Atrophic Acne Scars | ACTIVE_NOT_RECRUITING | NCT05995340 |
| ELAPR002f Injectable Gel | Other | Phase PHASE3 | Atrophic Acne Scars | ACTIVE_NOT_RECRUITING | NCT05995340 |
| Saline Active Control | Other | Phase PHASE3 | Atrophic Acne Scars | ACTIVE_NOT_RECRUITING | NCT05995340 |
| ELAPR002f Injectable Gel | Other | Phase PHASE3 | Atrophic Acne Scars | ACTIVE_NOT_RECRUITING | NCT05995340 |
| Adalimumab | Other | Phase PHASE4 | Non-infectious Intermediate Posterior- or Pan-uveitis | COMPLETED | NCT05414201 |
| Adalimumab | Other | Phase PHASE4 | Non-infectious Intermediate Posterior- or Pan-uveitis | COMPLETED | NCT05414201 |
| ABT-199 | Other | Phase PHASE2 | Chronic Lymphocytic Leucemia | COMPLETED | NCT02401503 |
| GA101 | Other | Phase PHASE2 | Chronic Lymphocytic Leucemia | COMPLETED | NCT02401503 |
| Bendamustine | Other | Phase PHASE2 | Chronic Lymphocytic Leucemia | COMPLETED | NCT02401503 |
| Venetoclax Oral Tablet [Venclexta] | Other | Phase PHASE2 | Mantle Cell Lymphoma | TERMINATED | NCT05025423 |
| Venetoclax Oral Tablet [Venclexta] | Other | Phase PHASE2 | Mantle Cell Lymphoma | TERMINATED | NCT05025423 |
| Venetoclax Oral Tablet [Venclexta] | Other | Phase PHASE2 | Mantle Cell Lymphoma | TERMINATED | NCT05025423 |
| Sanacoach Parkinson (SCP) | Other | Approved | Parkinson Disease | ACTIVE_NOT_RECRUITING | NCT05164783 |
| No Intervention | Other | Preclinical | Diabetic Retinopathy, DR | ENROLLING_BY_INVITATION | NCT05296447 |
| No Intervention | Other | Preclinical | Diabetic Retinopathy, DR | ENROLLING_BY_INVITATION | NCT05296447 |
| No intervention. | Other | Preclinical | Neovascular Age-Related Macular Degeneration (nAMD) | ENROLLING_BY_INVITATION | NCT05210803 |
| No intervention. | Other | Preclinical | Neovascular Age-Related Macular Degeneration (nAMD) | ENROLLING_BY_INVITATION | NCT05210803 |
| No intervention. | Other | Preclinical | Neovascular Age-Related Macular Degeneration (nAMD) | ENROLLING_BY_INVITATION | NCT05210803 |
| Venetoclax | Other | Phase PHASE3 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03539744 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03539744 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03539744 |
| Venetoclax | Other | Phase PHASE3 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03539744 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03539744 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03539744 |
| Upadacitinib Oral Product | Other | Phase PHASE3 | Colitis, Ulcerative | RECRUITING | NCT06660693 |
| Upadacitinib Oral Product | Other | Phase PHASE3 | Colitis, Ulcerative | RECRUITING | NCT06660693 |
| Tavapadon | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06895356 |
| Tavapadon | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06895356 |
| NX-13 Placebo | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| NX-13 750mg | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| NX-13 250mg | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| NX-13 Placebo | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| NX-13 750mg | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| NX-13 250mg | Other | Phase PHASE2 | Ulcerative Colitis | TERMINATED | NCT05785715 |
| Venetoclax | Other | Phase PHASE2 | Marginal Zone Lymphoma | ACTIVE_NOT_RECRUITING | NCT04416451 |
| Rituximab | Other | Phase PHASE2 | Marginal Zone Lymphoma | ACTIVE_NOT_RECRUITING | NCT04416451 |
| Osimertinib | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT04721015 |
| Docetaxel | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT04721015 |
| ABBV-637 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT04721015 |
| Osimertinib | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT04721015 |
| Docetaxel | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT04721015 |
| ABBV-637 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT04721015 |
| Venetoclax | Other | Phase PHASE2 | Mantle Cell Lymphoma (MCL) | COMPLETED | NCT04477486 |
| Ibrutinib | Other | Phase PHASE2 | Mantle Cell Lymphoma (MCL) | COMPLETED | NCT04477486 |
| Venetoclax | Other | Phase PHASE2 | Mantle Cell Lymphoma (MCL) | COMPLETED | NCT04477486 |
| Ibrutinib | Other | Phase PHASE2 | Mantle Cell Lymphoma (MCL) | COMPLETED | NCT04477486 |
| Next Generation Emulsion Preservative Free Eye Drops (NGE-UD) | Other | Preclinical | Dry Eye | COMPLETED | NCT06443775 |
| Next Generation Emulsion Preservative Free Eye Drops (NGE-UD) | Other | Preclinical | Dry Eye | COMPLETED | NCT06443775 |
| Placebo for CVC 300 mg | Other | Phase PHASE2 | HIV-1-infection | COMPLETED | NCT05630885 |
| Placebo for CVC 150 mg | Other | Phase PHASE2 | HIV-1-infection | COMPLETED | NCT05630885 |
| CVC 300 mg | Other | Phase PHASE2 | HIV-1-infection | COMPLETED | NCT05630885 |
| CVC 150 mg | Other | Phase PHASE2 | HIV-1-infection | COMPLETED | NCT05630885 |
| Placebo for CVC 300 mg | Other | Phase PHASE2 | HIV-1-infection | COMPLETED | NCT05630885 |
| Placebo for CVC 150 mg | Other | Phase PHASE2 | HIV-1-infection | COMPLETED | NCT05630885 |
| CVC 300 mg | Other | Phase PHASE2 | HIV-1-infection | COMPLETED | NCT05630885 |
| CVC 150 mg | Other | Phase PHASE2 | HIV-1-infection | COMPLETED | NCT05630885 |
| Ruxolitinib | Other | Phase PHASE1 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04454658 |
| Navitoclax | Other | Phase PHASE1 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04454658 |
| ABBV-744 | Other | Phase PHASE1 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04454658 |
| Ruxolitinib | Other | Phase PHASE1 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04454658 |
| Navitoclax | Other | Phase PHASE1 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04454658 |
| ABBV-744 | Other | Phase PHASE1 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04454658 |
| Placebo | Other | Phase PHASE1 | Alzheimer Disease | COMPLETED | NCT06406348 |
| ALIA-1758 | Other | Phase PHASE1 | Alzheimer Disease | COMPLETED | NCT06406348 |
| Placebo | Other | Phase PHASE1 | Alzheimer Disease | COMPLETED | NCT06406348 |
| ALIA-1758 | Other | Phase PHASE1 | Alzheimer Disease | COMPLETED | NCT06406348 |
| Placebo | Other | Phase PHASE1 | Alzheimer Disease | COMPLETED | NCT06406348 |
| ALIA-1758 | Other | Phase PHASE1 | Alzheimer Disease | COMPLETED | NCT06406348 |
| 100mg Eluxadoline | Other | Phase PHASE3 | Irritable Bowel Syndrome | ENROLLING_BY_INVITATION | NCT04880876 |
| 25mg Eluxadoline | Other | Phase PHASE3 | Irritable Bowel Syndrome | ENROLLING_BY_INVITATION | NCT04880876 |
| 100mg Eluxadoline | Other | Phase PHASE3 | Irritable Bowel Syndrome | ENROLLING_BY_INVITATION | NCT04880876 |
| 25mg Eluxadoline | Other | Phase PHASE3 | Irritable Bowel Syndrome | ENROLLING_BY_INVITATION | NCT04880876 |
| Comparator | Other | Preclinical | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | RECRUITING | NCT04846959 |
| Risankizumab | Other | Preclinical | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | RECRUITING | NCT04846959 |
| Comparator | Other | Preclinical | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | RECRUITING | NCT04846959 |
| Risankizumab | Other | Preclinical | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | RECRUITING | NCT04846959 |
| Comparator | Other | Preclinical | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | RECRUITING | NCT04846959 |
| Risankizumab | Other | Preclinical | Plaque Psoriasis, Psoriatic Arthritis, Crohn's Disease, or Other Conditions for Which Risankizumab is an FDA-approved Treatment | RECRUITING | NCT04846959 |
| Venetoclax | Other | Phase PHASE1 | Refractory Follicular Lymphoma | COMPLETED | NCT02956382 |
| Ibrutinib | Other | Phase PHASE1 | Refractory Follicular Lymphoma | COMPLETED | NCT02956382 |
| Venetoclax | Other | Phase PHASE1 | Refractory Follicular Lymphoma | COMPLETED | NCT02956382 |
| Ibrutinib | Other | Phase PHASE1 | Refractory Follicular Lymphoma | COMPLETED | NCT02956382 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT06673238 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT06673238 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT06673238 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT06673238 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | ENROLLING_BY_INVITATION | NCT05127954 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | ENROLLING_BY_INVITATION | NCT05127954 |
| Atogepant 60 mg | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT04437433 |
| Atogepant 60 mg | Other | Phase PHASE3 | Chronic Migraine | COMPLETED | NCT04437433 |
| Elagolix Placebo | Other | Phase PHASE3 | Heavy Menstrual Bleeding | COMPLETED | NCT03271489 |
| E2/NETA Placebo | Other | Phase PHASE3 | Heavy Menstrual Bleeding | COMPLETED | NCT03271489 |
| Estradiol /norethindrone acetate (E2/NETA) | Other | Phase PHASE3 | Heavy Menstrual Bleeding | COMPLETED | NCT03271489 |
| Elagolix | Other | Phase PHASE3 | Heavy Menstrual Bleeding | COMPLETED | NCT03271489 |
| Elagolix Placebo | Other | Phase PHASE3 | Heavy Menstrual Bleeding | COMPLETED | NCT03271489 |
| E2/NETA Placebo | Other | Phase PHASE3 | Heavy Menstrual Bleeding | COMPLETED | NCT03271489 |
| Estradiol /norethindrone acetate (E2/NETA) | Other | Phase PHASE3 | Heavy Menstrual Bleeding | COMPLETED | NCT03271489 |
| Elagolix | Other | Phase PHASE3 | Heavy Menstrual Bleeding | COMPLETED | NCT03271489 |
| CVL-231 30 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05443724 |
| Placebo | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04201093 |
| Tavapadon | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04201093 |
| Upadacitinib | Other | Phase PHASE4 | Atopic Dermatitis | COMPLETED | NCT05507580 |
| Upadacitinib | Other | Phase PHASE4 | Atopic Dermatitis | COMPLETED | NCT05507580 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | ACTIVE_NOT_RECRUITING | NCT04273139 |
| IBRUTINIB | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | ACTIVE_NOT_RECRUITING | NCT04273139 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | ACTIVE_NOT_RECRUITING | NCT04273139 |
| IBRUTINIB | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | ACTIVE_NOT_RECRUITING | NCT04273139 |
| ABT-494 | Other | Phase PHASE2 | Crohn's Disease (CD) | COMPLETED | NCT02782663 |
| ABT-494 | Other | Phase PHASE2 | Crohn's Disease (CD) | COMPLETED | NCT02782663 |
| Placebo | Other | Phase PHASE1 | ALS | TERMINATED | NCT04948645 |
| Fosigotifator | Other | Phase PHASE1 | ALS | TERMINATED | NCT04948645 |
| Placebo | Other | Phase PHASE1 | ALS | TERMINATED | NCT04948645 |
| Fosigotifator | Other | Phase PHASE1 | ALS | TERMINATED | NCT04948645 |
| onabotulinum toxin A | Other | Phase PHASE2 | Neuropathic Pain | COMPLETED | NCT03848143 |
| Placebo | Other | Phase PHASE3 | Myelodysplastic Syndrome (MDS) | ACTIVE_NOT_RECRUITING | NCT04401748 |
| Azacitidine | Other | Phase PHASE3 | Myelodysplastic Syndrome (MDS) | ACTIVE_NOT_RECRUITING | NCT04401748 |
| Venetoclax | Other | Phase PHASE3 | Myelodysplastic Syndrome (MDS) | ACTIVE_NOT_RECRUITING | NCT04401748 |
| Placebo | Other | Phase PHASE3 | Myelodysplastic Syndrome (MDS) | ACTIVE_NOT_RECRUITING | NCT04401748 |
| Azacitidine | Other | Phase PHASE3 | Myelodysplastic Syndrome (MDS) | ACTIVE_NOT_RECRUITING | NCT04401748 |
| Venetoclax | Other | Phase PHASE3 | Myelodysplastic Syndrome (MDS) | ACTIVE_NOT_RECRUITING | NCT04401748 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | ACTIVE_NOT_RECRUITING | NCT04379050 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | ACTIVE_NOT_RECRUITING | NCT04379050 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | ACTIVE_NOT_RECRUITING | NCT04379050 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | ACTIVE_NOT_RECRUITING | NCT04379050 |
| Upadacitinib | Other | Phase PHASE1 | Juvenile Idiopathic Arthritis (JIA) | ACTIVE_NOT_RECRUITING | NCT03725007 |
| Risankizumab | Other | Phase PHASE3 | Psoriatic Arthritis | ACTIVE_NOT_RECRUITING | NCT03675308 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis | ACTIVE_NOT_RECRUITING | NCT03675308 |
| Risankizumab | Other | Phase PHASE3 | Psoriatic Arthritis | ACTIVE_NOT_RECRUITING | NCT03675308 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis | ACTIVE_NOT_RECRUITING | NCT03675308 |
| Risankizumab | Other | Phase PHASE3 | Psoriatic Arthritis | ACTIVE_NOT_RECRUITING | NCT03675308 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis | ACTIVE_NOT_RECRUITING | NCT03675308 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03345823 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03345823 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Azacitidine | Other | Phase PHASE1 | Myelodysplastic Syndromes (MDS) | ACTIVE_NOT_RECRUITING | NCT02942290 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT02629159 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT02629159 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT02629159 |
| Placebo for Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT02629159 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT02629159 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT02629159 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT02629159 |
| Placebo for Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT02629159 |
| Donor Lymphocyte Infusion | Other | Phase PHASE1 | Acute Myeloid Leukemia | SUSPENDED | NCT06158100 |
| Azacitidine | Other | Phase PHASE1 | Acute Myeloid Leukemia | SUSPENDED | NCT06158100 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | SUSPENDED | NCT06158100 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT06953934 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT06953934 |
| Etentamig | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05286229 |
| Etentamig | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05286229 |
| Gemcitabine | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Paclitaxel | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Docetaxel | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Budigalimab | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Livmoniplimab | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Gemcitabine | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Paclitaxel | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Docetaxel | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Budigalimab | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Livmoniplimab | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Gemcitabine | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Paclitaxel | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Docetaxel | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Budigalimab | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Livmoniplimab | Other | Phase PHASE2 | Urothelial Carcinoma | ACTIVE_NOT_RECRUITING | NCT06632951 |
| Atogepant | Other | Phase PHASE3 | Migraine Prophylaxis | ENROLLING_BY_INVITATION | NCT05707949 |
| Atogepant | Other | Phase PHASE3 | Migraine Prophylaxis | ENROLLING_BY_INVITATION | NCT05707949 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis (UC) | WITHDRAWN | NCT05316220 |
| Mesalamine | Other | Phase PHASE3 | Ulcerative Colitis (UC) | WITHDRAWN | NCT05316220 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis (UC) | WITHDRAWN | NCT05316220 |
| Mesalamine | Other | Phase PHASE3 | Ulcerative Colitis (UC) | WITHDRAWN | NCT05316220 |
| Azacitidine | Other | Phase PHASE4 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT05144243 |
| Venetoclax | Other | Phase PHASE4 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT05144243 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | ACTIVE_NOT_RECRUITING | NCT04862286 |
| Risankizumab | Other | Phase PHASE3 | Psoriasis | ACTIVE_NOT_RECRUITING | NCT04862286 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | ACTIVE_NOT_RECRUITING | NCT04750226 |
| ABBV-951 | Other | Phase PHASE3 | Parkinson's Disease (PD) | ACTIVE_NOT_RECRUITING | NCT04750226 |
| Nab-paclitaxel | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| Carboplatin | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| ABBV-181 | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| ABBV-368 | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| ABBV-927 | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| Nab-paclitaxel | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| Carboplatin | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| ABBV-181 | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| ABBV-368 | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| ABBV-927 | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT03893955 |
| Restylane® Perlane® Lidocaine | Other | Phase PHASE3 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07032597 |
| HArmonyCa Lidocaine Injectable Gel | Other | Phase PHASE3 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07032597 |
| Restylane® Perlane® Lidocaine | Other | Phase PHASE3 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07032597 |
| HArmonyCa Lidocaine Injectable Gel | Other | Phase PHASE3 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07032597 |
| Restylane® Perlane® Lidocaine | Other | Phase PHASE3 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07032597 |
| HArmonyCa Lidocaine Injectable Gel | Other | Phase PHASE3 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07032597 |
| Placebo | Other | Phase PHASE3 | Forehead Lines | ACTIVE_NOT_RECRUITING | NCT06794866 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Forehead Lines | ACTIVE_NOT_RECRUITING | NCT06794866 |
| Placebo | Other | Phase PHASE3 | Forehead Lines | ACTIVE_NOT_RECRUITING | NCT06794866 |
| OnabotulinumtoxinA | Other | Phase PHASE3 | Forehead Lines | ACTIVE_NOT_RECRUITING | NCT06794866 |
| Sorafenib | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Lenvatinib | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Livmoniplimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Budigalimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Sorafenib | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Lenvatinib | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Livmoniplimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Budigalimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Sorafenib | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Lenvatinib | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Livmoniplimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Budigalimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT05822752 |
| Lenalidomide | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05308654 |
| Daratumumab | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05308654 |
| Dexamethasone | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05308654 |
| ABBV-453 | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05308654 |
| Lenalidomide | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05308654 |
| Daratumumab | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05308654 |
| Dexamethasone | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05308654 |
| ABBV-453 | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05308654 |
| Bortezomib | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Venetoclax | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Bortezomib | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Venetoclax | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Bortezomib | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Venetoclax | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03314181 |
| Risankizumab On-Body Injector (OBI) | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Placebo for Risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Placebo for Risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Risankizumab On-Body Injector (OBI) | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Placebo for Risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Risankizumab IV | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Placebo for Risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT03105102 |
| Erlotinib | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Telisotuzumab vedotin | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Nivolumab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Osimertinib | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Erlotinib | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Telisotuzumab vedotin | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Nivolumab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Osimertinib | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Erlotinib | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Telisotuzumab vedotin | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Nivolumab | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Osimertinib | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02099058 |
| Tremelimumab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Bevacizumab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Atezolizumab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Durvalumab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Budigalimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Livmoniplimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Tremelimumab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Bevacizumab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Atezolizumab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Durvalumab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Budigalimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Livmoniplimab | Other | Phase PHASE2 | Hepatocellular Carcinoma | RECRUITING | NCT06109272 |
| Positron Emission Tomography | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | RECRUITING | NCT06672705 |
| Epcoritamab | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | RECRUITING | NCT06672705 |
| Computed Tomography | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | RECRUITING | NCT06672705 |
| Biospecimen Collection | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | RECRUITING | NCT06672705 |
| Biopsy | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma Post-Transplant Lymphoproliferative Disorder | RECRUITING | NCT06672705 |
| Optive MEGA-3 (OM3) | Other | Preclinical | Dry Eye | COMPLETED | NCT06439394 |
| Optive MEGA-3 (OM3) | Other | Preclinical | Dry Eye | COMPLETED | NCT06439394 |
| Optive MEGA-3 (OM3) | Other | Preclinical | Dry Eye | COMPLETED | NCT06439394 |
| Fluorescence Imaging | Other | Phase PHASE2 | IBD | RECRUITING | NCT03938701 |
| Adalimumab-800CW | Other | Phase PHASE2 | IBD | RECRUITING | NCT03938701 |
| Fluorescence Imaging | Other | Phase PHASE2 | IBD | RECRUITING | NCT03938701 |
| Adalimumab-800CW | Other | Phase PHASE2 | IBD | RECRUITING | NCT03938701 |
| Fluorescence Imaging | Other | Phase PHASE2 | IBD | RECRUITING | NCT03938701 |
| Adalimumab-800CW | Other | Phase PHASE2 | IBD | RECRUITING | NCT03938701 |
| Bimatoprost (SR) | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT03850782 |
| Bimatoprost (SR) | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT03850782 |
| Bimatoprost (SR) | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT03850782 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | ACTIVE_NOT_RECRUITING | NCT02993523 |
| Placebo for BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06137287 |
| BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06137287 |
| Venetoclax | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Questionnaire Administration | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Multigated Acquisition Scan | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Lumbar Puncture | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Echocardiography | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Cytarabine | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Cladribine | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Bone Marrow Biopsy | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Bone Marrow Aspiration | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Biospecimen Collection | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Azacitidine | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Pegylated liposomal doxorubicin | Other | Phase PHASE3 | Epithelial Ovarian Cancer | COMPLETED | NCT04209855 |
| Topotecan | Other | Phase PHASE3 | Epithelial Ovarian Cancer | COMPLETED | NCT04209855 |
| Paclitaxel | Other | Phase PHASE3 | Epithelial Ovarian Cancer | COMPLETED | NCT04209855 |
| Mirvetuximab Soravtansine | Other | Phase PHASE3 | Epithelial Ovarian Cancer | COMPLETED | NCT04209855 |
| Placebo | Other | Phase PHASE3 | Forehead Lines | COMPLETED | NCT06174688 |
| BOTOX | Other | Phase PHASE3 | Forehead Lines | COMPLETED | NCT06174688 |
| Placebo | Other | Phase PHASE3 | Forehead Lines | COMPLETED | NCT06174688 |
| BOTOX | Other | Phase PHASE3 | Forehead Lines | COMPLETED | NCT06174688 |
| Standard of Care | Other | Phase PHASE3 | Open-Angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT03891446 |
| Bimatoprost SR | Other | Phase PHASE3 | Open-Angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT03891446 |
| Standard of Care | Other | Phase PHASE3 | Open-Angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT03891446 |
| Bimatoprost SR | Other | Phase PHASE3 | Open-Angle Glaucoma | ACTIVE_NOT_RECRUITING | NCT03891446 |
| Risankizumab | Other | Phase PHASE3 | Psoriatic Arthritis (PsA) | ACTIVE_NOT_RECRUITING | NCT03671148 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis (PsA) | ACTIVE_NOT_RECRUITING | NCT03671148 |
| Risankizumab | Other | Phase PHASE3 | Psoriatic Arthritis (PsA) | ACTIVE_NOT_RECRUITING | NCT03671148 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis (PsA) | ACTIVE_NOT_RECRUITING | NCT03671148 |
| Risankizumab | Other | Phase PHASE3 | Psoriatic Arthritis (PsA) | ACTIVE_NOT_RECRUITING | NCT03671148 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis (PsA) | ACTIVE_NOT_RECRUITING | NCT03671148 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07136103 |
| ABBV-277 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07136103 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07136103 |
| ABBV-277 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07136103 |
| Placebo for risankizumab | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT06063967 |
| Risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT06063967 |
| Placebo for risankizumab | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT06063967 |
| Risankizumab SC | Other | Phase PHASE3 | Crohn's Disease | ACTIVE_NOT_RECRUITING | NCT06063967 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT07071532 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT07071532 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT07071532 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT07071532 |
| Upadacitinib | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104374 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104374 |
| Upadacitinib | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104374 |
| Placebo | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104374 |
| Emraclidine 30 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Emraclidine 10 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Emraclidine 30 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Emraclidine 10 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Emraclidine 30 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Emraclidine 10 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227690 |
| Placebo | Other | Phase PHASE2 | Irritable Bowel Syndrome | RECRUITING | NCT03339128 |
| Eluxadoline | Other | Phase PHASE2 | Irritable Bowel Syndrome | RECRUITING | NCT03339128 |
| Placebo | Other | Phase PHASE2 | Irritable Bowel Syndrome | RECRUITING | NCT03339128 |
| Eluxadoline | Other | Phase PHASE2 | Irritable Bowel Syndrome | RECRUITING | NCT03339128 |
| Placebo | Other | Phase PHASE2 | Irritable Bowel Syndrome | RECRUITING | NCT03339128 |
| Eluxadoline | Other | Phase PHASE2 | Irritable Bowel Syndrome | RECRUITING | NCT03339128 |
| Radiation | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Erwinia asparaginase | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Pegaspargase | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Intrathecal Triples | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Leucovorin | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Etoposide | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Cyclophosphamide | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Mercaptopurine | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Methotrexate | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Blinatumomab | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Cytarabine | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Dasatinib | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Calaspargase Pegol | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Vincristine | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Dexamethasone | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Navitoclax | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Venetoclax | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Radiation | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Erwinia asparaginase | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Pegaspargase | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Intrathecal Triples | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Leucovorin | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Etoposide | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Cyclophosphamide | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Mercaptopurine | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Methotrexate | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Blinatumomab | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Cytarabine | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Dasatinib | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Calaspargase Pegol | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Vincristine | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Dexamethasone | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Navitoclax | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Venetoclax | Other | Phase PHASE1 | Refractory Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05192889 |
| Placebo to Adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Placebo to Upadacitinib | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Upadacitinib | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Placebo to Adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Placebo to Upadacitinib | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Upadacitinib | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Placebo to Adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Placebo to Upadacitinib | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Upadacitinib | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| Adalimumab | Other | Phase PHASE3 | Psoriatic Arthritis | COMPLETED | NCT03104400 |
| MedicWise | Other | Approved | Crohn Disease | RECRUITING | NCT06742385 |
| MedicWise | Other | Approved | Crohn Disease | RECRUITING | NCT06742385 |
| Loncastuximab Tesirine and Epcoritamab | Other | Phase PHASE2 | Aggressive Diffuse Large B-cell Lymphoma | NOT_YET_RECRUITING | NCT07197307 |
| Loncastuximab Tesirine and Epcoritamab | Other | Phase PHASE2 | Aggressive Diffuse Large B-cell Lymphoma | NOT_YET_RECRUITING | NCT07197307 |
| Fosigotifator | Other | Phase PHASE1 | Vanishing White Matter Disease | RECRUITING | NCT05757141 |
| Placebo | Other | Phase PHASE1 | Major Depressive Disorder (MDD) | TERMINATED | NCT06618118 |
| Fosigotifator | Other | Phase PHASE1 | Major Depressive Disorder (MDD) | TERMINATED | NCT06618118 |
| Placebo | Other | Phase PHASE1 | Major Depressive Disorder (MDD) | TERMINATED | NCT06618118 |
| Fosigotifator | Other | Phase PHASE1 | Major Depressive Disorder (MDD) | TERMINATED | NCT06618118 |
| Placebo | Other | Phase PHASE1 | Major Depressive Disorder (MDD) | TERMINATED | NCT06618118 |
| Fosigotifator | Other | Phase PHASE1 | Major Depressive Disorder (MDD) | TERMINATED | NCT06618118 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| Placebo | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT03069352 |
| ABBV-101 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06887010 |
| ABBV-101 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06887010 |
| ABBV-101 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06887010 |
| Best Supportive Care (BSC) | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Best Supportive Care (BSC) | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | TERMINATED | NCT04161885 |
| Placebo for ABBV-552 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05771428 |
| ABBV-552 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05771428 |
| Placebo for ABBV-552 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05771428 |
| ABBV-552 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05771428 |
| Placebo for ABBV-552 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05771428 |
| ABBV-552 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05771428 |
| Obinutuzumab | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT05105841 |
| Ibrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT05105841 |
| Venetoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | COMPLETED | NCT05105841 |
| Biospecimen Collection | Other | Phase PHASE1 | Acute Biphenotypic Leukemia | RECRUITING | NCT04797767 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Acute Biphenotypic Leukemia | RECRUITING | NCT04797767 |
| Bone Marrow Aspiration | Other | Phase PHASE1 | Acute Biphenotypic Leukemia | RECRUITING | NCT04797767 |
| Venetoclax | Other | Phase PHASE1 | Acute Biphenotypic Leukemia | RECRUITING | NCT04797767 |
| Recombinant Granulocyte Colony-Stimulating Factor | Other | Phase PHASE1 | Acute Biphenotypic Leukemia | RECRUITING | NCT04797767 |
| Mitoxantrone | Other | Phase PHASE1 | Acute Biphenotypic Leukemia | RECRUITING | NCT04797767 |
| Cytarabine | Other | Phase PHASE1 | Acute Biphenotypic Leukemia | RECRUITING | NCT04797767 |
| Cladribine | Other | Phase PHASE1 | Acute Biphenotypic Leukemia | RECRUITING | NCT04797767 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT02632175 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT02632175 |
| Adalimumab | Other | Phase PHASE3 | Ulcerative Colitis | COMPLETED | NCT02632175 |
| Carboplatin | Other | Phase PHASE1 | Advanced Solid Tumors | ACTIVE_NOT_RECRUITING | NCT05599984 |
| Budigalimab | Other | Phase PHASE1 | Advanced Solid Tumors | ACTIVE_NOT_RECRUITING | NCT05599984 |
| Cisplatin | Other | Phase PHASE1 | Advanced Solid Tumors | ACTIVE_NOT_RECRUITING | NCT05599984 |
| ABBV-706 | Other | Phase PHASE1 | Advanced Solid Tumors | ACTIVE_NOT_RECRUITING | NCT05599984 |
| Carboplatin | Other | Phase PHASE1 | Advanced Solid Tumors | ACTIVE_NOT_RECRUITING | NCT05599984 |
| Budigalimab | Other | Phase PHASE1 | Advanced Solid Tumors | ACTIVE_NOT_RECRUITING | NCT05599984 |
| Cisplatin | Other | Phase PHASE1 | Advanced Solid Tumors | ACTIVE_NOT_RECRUITING | NCT05599984 |
| ABBV-706 | Other | Phase PHASE1 | Advanced Solid Tumors | ACTIVE_NOT_RECRUITING | NCT05599984 |
| Placebo | Other | Phase PHASE3 | Schizophrenia | TERMINATED | NCT05368558 |
| Cariprazine | Other | Phase PHASE3 | Schizophrenia | TERMINATED | NCT05368558 |
| Placebo | Other | Phase PHASE3 | Schizophrenia | TERMINATED | NCT05368558 |
| Cariprazine | Other | Phase PHASE3 | Schizophrenia | TERMINATED | NCT05368558 |
| Pancrelipase Capsules | Other | Phase PHASE4 | Exocrine Pancreatic Insufficiency | RECRUITING | NCT06477159 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non Small Cell Lung Cancer | TERMINATED | NCT05513703 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non Small Cell Lung Cancer | TERMINATED | NCT05513703 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03569293 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03569293 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03569293 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03569293 |
| Budigalimab | Other | Phase PHASE1 | Solid Tumors | TERMINATED | NCT06158958 |
| ABBV-303 | Other | Phase PHASE1 | Solid Tumors | TERMINATED | NCT06158958 |
| Cariprazine Flexible Dose | Other | Phase PHASE3 | Schizophrenia | COMPLETED | NCT04578756 |
| Cariprazine Flexible Dose | Other | Phase PHASE3 | Schizophrenia | COMPLETED | NCT04578756 |
| Epcoritamab | Other | Phase PHASE2 | Marginal Zone Lymphoma | RECRUITING | NCT06796998 |
| Carboplatin | Other | Phase PHASE2 | High Grade Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05456685 |
| Mirvetuximab soravtansine | Other | Phase PHASE2 | High Grade Ovarian Cancer | ACTIVE_NOT_RECRUITING | NCT05456685 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227703 |
| Emraclidine 30 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227703 |
| Emraclidine 15 mg | Other | Phase PHASE2 | Schizophrenia | COMPLETED | NCT05227703 |
| Placebo for ABBV-382 | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| ABBV-382 | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Placebo for Budigalimab | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Budigalimab | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Placebo for ABBV-382 | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| ABBV-382 | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Placebo for Budigalimab | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Budigalimab | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Placebo for ABBV-382 | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| ABBV-382 | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Placebo for Budigalimab | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Budigalimab | Other | Phase PHASE2 | Human Immuno-deficiency Virus (HIV) Disease | TERMINATED | NCT06032546 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| Trifluridine/Tipiracil | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| ABBV-400 | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| Trifluridine/Tipiracil | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| ABBV-400 | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| Trifluridine/Tipiracil | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| ABBV-400 | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT05029882 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07222709 |
| ABBV-1042 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07222709 |
| Itraconazole (ITZ) | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| Placebo for ABBV-1088 | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| ABBV-1088 | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| Itraconazole (ITZ) | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| Placebo for ABBV-1088 | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| ABBV-1088 | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| Itraconazole (ITZ) | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| Placebo for ABBV-1088 | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| ABBV-1088 | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT06579300 |
| Olaparib | Other | Phase PHASE2 | Ovary Cancer | RECRUITING | NCT05887609 |
| Mirvetuximab Soravtansine-gynx | Other | Phase PHASE2 | Ovary Cancer | RECRUITING | NCT05887609 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | ACTIVE_NOT_RECRUITING | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | ACTIVE_NOT_RECRUITING | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | ACTIVE_NOT_RECRUITING | NCT04630652 |
| Punch biopsies of the skin at week 28 visit | Other | Phase PHASE4 | Psoriasis | ACTIVE_NOT_RECRUITING | NCT04630652 |
| Punch biopsies of the skin at baseline visit | Other | Phase PHASE4 | Psoriasis | ACTIVE_NOT_RECRUITING | NCT04630652 |
| Risankizumab-Rzaa | Other | Phase PHASE4 | Psoriasis | ACTIVE_NOT_RECRUITING | NCT04630652 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | RECRUITING | NCT06428019 |
| Acalabrutinib | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | RECRUITING | NCT06428019 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | RECRUITING | NCT06428019 |
| Telisotuzumab vedotin | Other | Phase PHASE2 | Non-small Cell Lung Cancer | ACTIVE_NOT_RECRUITING | NCT03539536 |
| Obinutuzumab | Other | Phase PHASE3 | Lymphocytic Leukemia, Chronic | COMPLETED | NCT02242942 |
| Venetoclax | Other | Phase PHASE3 | Lymphocytic Leukemia, Chronic | COMPLETED | NCT02242942 |
| Chlorambucil | Other | Phase PHASE3 | Lymphocytic Leukemia, Chronic | COMPLETED | NCT02242942 |
| Obinutuzumab | Other | Phase PHASE3 | Lymphocytic Leukemia, Chronic | COMPLETED | NCT02242942 |
| Venetoclax | Other | Phase PHASE3 | Lymphocytic Leukemia, Chronic | COMPLETED | NCT02242942 |
| Chlorambucil | Other | Phase PHASE3 | Lymphocytic Leukemia, Chronic | COMPLETED | NCT02242942 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| NB-UVB (narrow-band ultraviolet B) Phototherapy | Drug | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Placebo | Other | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Upadacitinib | Other | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| NB-UVB (narrow-band ultraviolet B) Phototherapy | Drug | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Placebo | Other | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Upadacitinib | Other | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| NB-UVB (narrow-band ultraviolet B) Phototherapy | Drug | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Placebo | Other | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Upadacitinib | Other | Phase PHASE3 | Vitiligo | ACTIVE_NOT_RECRUITING | NCT06118411 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Placebo for Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06417775 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Liposomal daunorubicin and cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Daunorubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Idarubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Liposomal daunorubicin and cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Daunorubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Idarubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT04801797 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06937619 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06937619 |
| Placebo | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06399718 |
| BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06399718 |
| Placebo | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06399718 |
| BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06399718 |
| Trabeculectomy | Other | Phase PHASE4 | Open-angle Glaucoma | RECRUITING | NCT05821855 |
| XEN45 Glaucoma Treatment System | Drug | Phase PHASE4 | Open-angle Glaucoma | RECRUITING | NCT05821855 |
| Trabeculectomy | Other | Phase PHASE4 | Open-angle Glaucoma | RECRUITING | NCT05821855 |
| XEN45 Glaucoma Treatment System | Drug | Phase PHASE4 | Open-angle Glaucoma | RECRUITING | NCT05821855 |
| Combined Oral Contraceptive | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Placebo | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Combined Oral Contraceptive | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Placebo | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Elagolix | Other | Phase PHASE3 | Endometriosis | ACTIVE_NOT_RECRUITING | NCT04333576 |
| Placebo | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04223193 |
| Tavapadon | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04223193 |
| Placebo | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04223193 |
| Tavapadon | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04223193 |
| Saline Control | Other | Phase PHASE3 | Acne Scars | RECRUITING | NCT07207369 |
| ELAPR002f Injectable Gel | Other | Phase PHASE3 | Acne Scars | RECRUITING | NCT07207369 |
| Saline Control | Other | Phase PHASE3 | Acne Scars | RECRUITING | NCT07207369 |
| ELAPR002f Injectable Gel | Other | Phase PHASE3 | Acne Scars | RECRUITING | NCT07207369 |
| BOTOX | Other | Phase PHASE4 | Upper Facial Lines | COMPLETED | NCT06218251 |
| Venetoclax combined with Orelabrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | RECRUITING | NCT06958705 |
| Venetoclax combined with Acalabrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | RECRUITING | NCT06958705 |
| Venetoclax combined with Zanubrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | RECRUITING | NCT06958705 |
| Venetoclax combined with Ibrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | RECRUITING | NCT06958705 |
| Venetoclax combined with Orelabrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | RECRUITING | NCT06958705 |
| Venetoclax combined with Acalabrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | RECRUITING | NCT06958705 |
| Venetoclax combined with Zanubrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | RECRUITING | NCT06958705 |
| Venetoclax combined with Ibrutinib | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) / Small Lymphocytic Lymphoma (SLL) | RECRUITING | NCT06958705 |
| FCR | Other | Phase PHASE2 | Intermediate Risk Chronic Lymphocytic Leukemia | COMPLETED | NCT04010968 |
| venetoclax and ibrutinib (I+VEN) | Other | Phase PHASE2 | Intermediate Risk Chronic Lymphocytic Leukemia | COMPLETED | NCT04010968 |
| FCR | Other | Phase PHASE2 | Intermediate Risk Chronic Lymphocytic Leukemia | COMPLETED | NCT04010968 |
| venetoclax and ibrutinib (I+VEN) | Other | Phase PHASE2 | Intermediate Risk Chronic Lymphocytic Leukemia | COMPLETED | NCT04010968 |
| DRC | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT05099471 |
| Venetoclax; Rituximab | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT05099471 |
| Control | Other | Phase PHASE3 | Perioral Lines | COMPLETED | NCT05454033 |
| JUVÉDERM® VOLITE™ | Other | Phase PHASE3 | Perioral Lines | COMPLETED | NCT05454033 |
| First line therapy | Drug | Preclinical | CLL/SLL | ACTIVE_NOT_RECRUITING | NCT05590702 |
| First line therapy | Drug | Preclinical | CLL/SLL | ACTIVE_NOT_RECRUITING | NCT05590702 |
| Usual care | Other | Approved | Hepatitis C Virus Infection, Response to Therapy of | COMPLETED | NCT04677153 |
| Test and treat plus peer mentors | Other | Approved | Hepatitis C Virus Infection, Response to Therapy of | COMPLETED | NCT04677153 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03607422 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | COMPLETED | NCT03607422 |
| Carboplatin | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Bevacizumab | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Ovarian Cancer | RECRUITING | NCT07059845 |
| Paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) | TERMINATED | NCT04064827 |
| Paricalcitol | Other | Phase PHASE3 | Chronic Kidney Disease (CKD) | TERMINATED | NCT04064827 |
| Control | Other | Phase PHASE3 | Neck Lines | COMPLETED | NCT05741034 |
| JUVÉDERM® VOLITE™ | Other | Phase PHASE3 | Neck Lines | COMPLETED | NCT05741034 |
| Control | Other | Phase PHASE3 | Neck Lines | COMPLETED | NCT05741034 |
| JUVÉDERM® VOLITE™ | Other | Phase PHASE3 | Neck Lines | COMPLETED | NCT05741034 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Quality-of-Life Assessment | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Laboratory Biomarker Analysis | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Biospecimen Collection | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Decitabine | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Venetoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Navitoclax | Other | Phase PHASE1 | Myelodysplastic Syndrome | ACTIVE_NOT_RECRUITING | NCT05564650 |
| Venetoclax | Other | Phase PHASE2 | Lymphoma, Mantle-Cell | COMPLETED | NCT03567876 |
| Venetoclax | Other | Phase PHASE2 | Lymphoma, Mantle-Cell | COMPLETED | NCT03567876 |
| Gilteritinib | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Etoposide | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Mitoxantrone Hydrochloride | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Idarubicin Hydrochloride | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Fludarabine Phosphate | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Daunorubicin Hydrochloride | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Placebo | Other | Phase PHASE3 | Episodic Migraine | TERMINATED | NCT05028569 |
| BOTOX | Other | Phase PHASE3 | Episodic Migraine | TERMINATED | NCT05028569 |
| Placebo | Other | Phase PHASE3 | Episodic Migraine | TERMINATED | NCT05028569 |
| BOTOX | Other | Phase PHASE3 | Episodic Migraine | TERMINATED | NCT05028569 |
| Placebo | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06068855 |
| BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06068855 |
| Placebo | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06068855 |
| BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06068855 |
| Placebo | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05291234 |
| ABBV-916 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05291234 |
| Placebo | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05291234 |
| ABBV-916 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05291234 |
| Placebo | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05291234 |
| ABBV-916 | Other | Phase PHASE2 | Alzheimer's Disease (AD) | COMPLETED | NCT05291234 |
| Docetaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| Paclitaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| ABBV-155 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| Docetaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| Paclitaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| ABBV-155 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| Docetaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| Paclitaxel | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| ABBV-155 | Other | Phase PHASE1 | Advanced Solid Tumors | COMPLETED | NCT03595059 |
| Placebo | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06387394 |
| BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06387394 |
| Placebo | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06387394 |
| BOTOX | Other | Phase PHASE3 | Masseter Muscle Prominence | COMPLETED | NCT06387394 |
| CVL-865 | Other | Phase PHASE2 | Seizures | TERMINATED | NCT04686786 |
| CVL-865 | Other | Phase PHASE2 | Seizures | TERMINATED | NCT04686786 |
| Irinotecan | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Fluorouracil | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Folinic Acid | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Bevacizumab | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| ABBV-400 | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Irinotecan | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Fluorouracil | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Folinic Acid | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Bevacizumab | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| ABBV-400 | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Irinotecan | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Fluorouracil | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Folinic Acid | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Bevacizumab | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| ABBV-400 | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Irinotecan | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Fluorouracil | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Folinic Acid | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| Bevacizumab | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| ABBV-400 | Other | Phase PHASE2 | Unresectable Metastatic Colorectal Cancer | ACTIVE_NOT_RECRUITING | NCT06107413 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| ABBV-383 (Etentamig) | Other | Phase PHASE1 | Immunoglobulin Light Chain (AL) Amyloidosis | RECRUITING | NCT06158854 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Placebo | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| ABBV-295 | Other | Phase PHASE1 | Obesity | RECRUITING | NCT07291232 |
| Risankizumab | Other | Phase PHASE2 | Psoriatic Arthritis | RECRUITING | NCT06865105 |
| Lutikizumab | Other | Phase PHASE2 | Psoriatic Arthritis | RECRUITING | NCT06865105 |
| Risankizumab | Other | Phase PHASE2 | Psoriatic Arthritis | RECRUITING | NCT06865105 |
| Lutikizumab | Other | Phase PHASE2 | Psoriatic Arthritis | RECRUITING | NCT06865105 |
| Atogepant 60 mg | Other | Phase PHASE3 | Episodic Migraine | COMPLETED | NCT04686136 |
| Daratumumab | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Pomalidomide | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Lenalidomide | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Dexamethasone | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Etentamig | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Daratumumab | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Pomalidomide | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Lenalidomide | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Dexamethasone | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Etentamig | Other | Phase PHASE1 | Relapsed/Refractory Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT05259839 |
| Placebo | Other | Phase PHASE2 | Acute Ischemic Stroke | COMPLETED | NCT04309474 |
| Elezanumab | Other | Phase PHASE2 | Acute Ischemic Stroke | COMPLETED | NCT04309474 |
| Placebo | Other | Phase PHASE2 | Acute Ischemic Stroke | COMPLETED | NCT04309474 |
| Elezanumab | Other | Phase PHASE2 | Acute Ischemic Stroke | COMPLETED | NCT04309474 |
| Rituximab | Other | Phase PHASE2 | Follicular Lymphoma | RECRUITING | NCT05783609 |
| Epcoritamab | Other | Phase PHASE2 | Follicular Lymphoma | RECRUITING | NCT05783609 |
| ABBV-668 | Other | Phase PHASE2 | Ulcerative Colitis | COMPLETED | NCT05570006 |
| ABBV-668 | Other | Phase PHASE2 | Ulcerative Colitis | COMPLETED | NCT05570006 |
| Tavapadon | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04760769 |
| Tavapadon | Other | Phase PHASE3 | Parkinson Disease | COMPLETED | NCT04760769 |
| Upadacitinib Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT07023302 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT07023302 |
| Venetoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT02966756 |
| Venetoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT02966756 |
| Venetoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT02966756 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06946524 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06946524 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06946524 |
| HAC 22L | Other | Phase PHASE3 | Facial Volume Deficit | COMPLETED | NCT05818709 |
| HAC 22L | Other | Phase PHASE3 | Facial Volume Deficit | COMPLETED | NCT05818709 |
| Upadacitinib | Other | Phase PHASE3 | Ulcerative Colitis | ACTIVE_NOT_RECRUITING | NCT05782907 |
| Pivekimab Sunirine | Other | Phase PHASE1 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07306832 |
| Pivekimab Sunirine | Other | Phase PHASE1 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07306832 |
| Placebo for ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07024797 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07024797 |
| Placebo for ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07024797 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07024797 |
| Placebo for ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07024797 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07024797 |
| ABBV-1354 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT07219017 |
| Levothyroxine | Other | Phase PHASE2 | Hypothyroidism | RECRUITING | NCT06345339 |
| Armour Thyroid | Other | Phase PHASE2 | Hypothyroidism | RECRUITING | NCT06345339 |
| Levothyroxine | Other | Phase PHASE2 | Hypothyroidism | RECRUITING | NCT06345339 |
| Armour Thyroid | Other | Phase PHASE2 | Hypothyroidism | RECRUITING | NCT06345339 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | NOT_YET_RECRUITING | NCT07323641 |
| Survey Administration | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | NOT_YET_RECRUITING | NCT07323641 |
| Osimertinib | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | NOT_YET_RECRUITING | NCT07323641 |
| Magnetic Resonance Imaging | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | NOT_YET_RECRUITING | NCT07323641 |
| Computed Tomography | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | NOT_YET_RECRUITING | NCT07323641 |
| Biospecimen Collection | Other | Phase PHASE2 | Lung Non-Small Cell Carcinoma | NOT_YET_RECRUITING | NCT07323641 |
| Biopsy Procedure | Procedure | Phase PHASE2 | Lung Non-Small Cell Carcinoma | NOT_YET_RECRUITING | NCT07323641 |
| Venetoclax | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04572763 |
| Copanlisib | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04572763 |
| Venetoclax | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04572763 |
| Copanlisib | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04572763 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Non-Surgical Fat Reduction | ACTIVE_NOT_RECRUITING | NCT07122583 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Non-Surgical Fat Reduction | ACTIVE_NOT_RECRUITING | NCT07122583 |
| ABBV-453 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT06291220 |
| Obinutuzumab | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT06291220 |
| ABBV-453 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT06291220 |
| Obinutuzumab | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT06291220 |
| ABBV-453 | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT06291220 |
| Obinutuzumab | Other | Phase PHASE1 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT06291220 |
| Cytarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT05342584 |
| Daunorubicin | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT05342584 |
| Venetoclax Oral Tablet | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT05342584 |
| Cytarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT05342584 |
| Daunorubicin | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT05342584 |
| Venetoclax Oral Tablet | Other | Phase PHASE1 | Acute Myeloid Leukemia | RECRUITING | NCT05342584 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian | RECRUITING | NCT06682988 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Advanced High-Grade Epithelial Ovarian | RECRUITING | NCT06682988 |
| Mirvetuximab soravtansine | Other | Phase PHASE2 | Ovarian Cancer | COMPLETED | NCT05041257 |
| Best Available Therapy (BAT) | Drug | Phase PHASE3 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04468984 |
| Ruxolitinib | Other | Phase PHASE3 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04468984 |
| Navitoclax | Other | Phase PHASE3 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04468984 |
| Best Available Therapy (BAT) | Drug | Phase PHASE3 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04468984 |
| Ruxolitinib | Other | Phase PHASE3 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04468984 |
| Navitoclax | Other | Phase PHASE3 | Myelofibrosis (MF) | ACTIVE_NOT_RECRUITING | NCT04468984 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02988960 |
| ABBV-927 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02988960 |
| ABBV-181 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02988960 |
| ABBV-927 | Other | Phase PHASE1 | Advanced Solid Tumors Cancer | ACTIVE_NOT_RECRUITING | NCT02988960 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07306754 |
| ABBV-243 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07306754 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07306754 |
| ABBV-243 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07306754 |
| Azacitidine | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Venetoclax | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Placebo for ABBV-932 | Other | Phase PHASE2 | Bipolar I Disorder | COMPLETED | NCT06605599 |
| ABBV-932 | Other | Phase PHASE2 | Bipolar I Disorder | COMPLETED | NCT06605599 |
| Placebo for ABBV-932 | Other | Phase PHASE2 | Bipolar I Disorder | COMPLETED | NCT06605599 |
| ABBV-932 | Other | Phase PHASE2 | Bipolar I Disorder | COMPLETED | NCT06605599 |
| Adalimumab Matching Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT05814627 |
| Upadacitinib Matching Placebo | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT05814627 |
| Adalimumab | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT05814627 |
| Upadacitinib | Other | Phase PHASE3 | Rheumatoid Arthritis | ACTIVE_NOT_RECRUITING | NCT05814627 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis (UC) | ACTIVE_NOT_RECRUITING | NCT03006068 |
| Upadacitinib (ABT-494) | Other | Phase PHASE3 | Ulcerative Colitis (UC) | ACTIVE_NOT_RECRUITING | NCT03006068 |
| Placebo | Other | Phase PHASE3 | Ulcerative Colitis (UC) | ACTIVE_NOT_RECRUITING | NCT03006068 |
| Upadacitinib (ABT-494) | Other | Phase PHASE3 | Ulcerative Colitis (UC) | ACTIVE_NOT_RECRUITING | NCT03006068 |
| AGN-151597 | Other | Phase PHASE1 | Advanced Retinitis Pigmentosa | COMPLETED | NCT02556736 |
| AGN-151597 | Other | Phase PHASE1 | Advanced Retinitis Pigmentosa | COMPLETED | NCT02556736 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Cytarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fludarabine | Other | Phase PHASE3 | Acute Myeloid Leukemia | RECRUITING | NCT05183035 |
| Fosigotifator | Other | Preclinical | Vanishing White Matter | NO_LONGER_AVAILABLE | NCT06594016 |
| Fosigotifator | Other | Preclinical | Vanishing White Matter | NO_LONGER_AVAILABLE | NCT06594016 |
| Fosigotifator | Other | Preclinical | Vanishing White Matter | NO_LONGER_AVAILABLE | NCT06594016 |
| Rituximab | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Prednisone | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Positron Emission Tomography | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Multigated Acquisition Scan | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Fludeoxyglucose F-18 | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Etoposide | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Epcoritamab | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Echocardiography Test | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Doxorubicin | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Cyclophosphamide | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Computed Tomography | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Bone Marrow Biopsy | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Bone Marrow Aspiration | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Biospecimen Collection | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| ABBV-CLS-616 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| ABBV-CLS-616 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| Itraconazole | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| ABBV-CLS-616 | Other | Phase PHASE1 | Healthy Volunteer | COMPLETED | NCT06698926 |
| GUB014295-PLACEBO | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06144684 |
| GUB014295 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT06144684 |
| ABBV-319 | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | RECRUITING | NCT05512390 |
| Cytarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Daunorubicin | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Cytarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Daunorubicin | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03709758 |
| Atogepant | Other | Preclinical | Chronic Migraine | RECRUITING | NCT06603558 |
| Itraconazole (ITZ) | Other | Phase PHASE1 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT06084481 |
| ABBV-400 | Other | Phase PHASE1 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT06084481 |
| Itraconazole (ITZ) | Other | Phase PHASE1 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT06084481 |
| ABBV-400 | Other | Phase PHASE1 | Hepatocellular Carcinoma | ACTIVE_NOT_RECRUITING | NCT06084481 |
| Placebo for BOTOX | Other | Phase PHASE2 | Upper Limb Essential Tremor (UL ET) | COMPLETED | NCT05216250 |
| BOTOX | Other | Phase PHASE2 | Upper Limb Essential Tremor (UL ET) | COMPLETED | NCT05216250 |
| Placebo for BOTOX | Other | Phase PHASE2 | Upper Limb Essential Tremor (UL ET) | COMPLETED | NCT05216250 |
| BOTOX | Other | Phase PHASE2 | Upper Limb Essential Tremor (UL ET) | COMPLETED | NCT05216250 |
| Placebo for BOTOX | Other | Phase PHASE2 | Upper Limb Essential Tremor (UL ET) | COMPLETED | NCT05216250 |
| BOTOX | Other | Phase PHASE2 | Upper Limb Essential Tremor (UL ET) | COMPLETED | NCT05216250 |
| placebo for risankizumab | Other | Phase PHASE3 | Ulcerative Colitis (UC) | ACTIVE_NOT_RECRUITING | NCT03398135 |
| risankizumab | Other | Phase PHASE3 | Ulcerative Colitis (UC) | ACTIVE_NOT_RECRUITING | NCT03398135 |
| placebo for risankizumab | Other | Phase PHASE3 | Ulcerative Colitis (UC) | ACTIVE_NOT_RECRUITING | NCT03398135 |
| risankizumab | Other | Phase PHASE3 | Ulcerative Colitis (UC) | ACTIVE_NOT_RECRUITING | NCT03398135 |
| Navitoclax | Other | Phase PHASE2 | Myelofibrosis (MF) | COMPLETED | NCT03222609 |
| Ruxolitinib | Other | Phase PHASE2 | Myelofibrosis (MF) | COMPLETED | NCT03222609 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Placebo | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| MEDI0618 | Other | Phase PHASE2 | Migraine | RECRUITING | NCT06602479 |
| Antidepressant Therapy (ADT) | Drug | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| Placebo for ABBV-932 | Other | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| ABBV-932 | Other | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| Antidepressant Therapy (ADT) | Drug | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| Placebo for ABBV-932 | Other | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| ABBV-932 | Other | Phase PHASE2 | Generalized Anxiety Disorder (GAD) | RECRUITING | NCT06846320 |
| Amrubicin | Other | Phase PHASE3 | Small Cell Lung Cancer | NOT_YET_RECRUITING | NCT07365241 |
| Lurbinectedin | Other | Phase PHASE3 | Small Cell Lung Cancer | NOT_YET_RECRUITING | NCT07365241 |
| Topotecan | Other | Phase PHASE3 | Small Cell Lung Cancer | NOT_YET_RECRUITING | NCT07365241 |
| ABBV-706 | Other | Phase PHASE3 | Small Cell Lung Cancer | NOT_YET_RECRUITING | NCT07365241 |
| Amrubicin | Other | Phase PHASE3 | Small Cell Lung Cancer | NOT_YET_RECRUITING | NCT07365241 |
| Lurbinectedin | Other | Phase PHASE3 | Small Cell Lung Cancer | NOT_YET_RECRUITING | NCT07365241 |
| Topotecan | Other | Phase PHASE3 | Small Cell Lung Cancer | NOT_YET_RECRUITING | NCT07365241 |
| ABBV-706 | Other | Phase PHASE3 | Small Cell Lung Cancer | NOT_YET_RECRUITING | NCT07365241 |
| ABBV-291 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | RECRUITING | NCT06667687 |
| ABBV-291 | Other | Phase PHASE1 | Non-Hodgkin's Lymphoma | RECRUITING | NCT06667687 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT07007091 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT07007091 |
| Decitabine | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| Venetoclax | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| Navitoclax | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| Decitabine | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| Venetoclax | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| Navitoclax | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| Decitabine | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| Venetoclax | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| Navitoclax | Other | Phase PHASE1 | Myeloid Malignancy | ACTIVE_NOT_RECRUITING | NCT05455294 |
| ABBV-706 | Other | Preclinical | Small Cell Lung Cancer | AVAILABLE | NCT07310277 |
| Glecaprevir/pibrentasvir | Other | Phase PHASE1 | Hepatitis C | NOT_YET_RECRUITING | NCT07040319 |
| Inotuzumab Ozogamicin | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Dexamethasone | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Venetoclax | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Inotuzumab Ozogamicin | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Dexamethasone | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Venetoclax | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Inotuzumab Ozogamicin | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Dexamethasone | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Venetoclax | Other | Phase PHASE1 | B-cell Acute Lymphoblastic Leukemia | ACTIVE_NOT_RECRUITING | NCT05016947 |
| Upadacitinib | Other | Preclinical | Crohn Disease | AVAILABLE | NCT04159597 |
| Upadacitinib | Other | Preclinical | Crohn Disease | AVAILABLE | NCT04159597 |
| Venetoclax | Other | Preclinical | Chronic Lymphocytic Leukemia (CLL) | AVAILABLE | NCT03123029 |
| Venetoclax | Other | Preclinical | Chronic Lymphocytic Leukemia (CLL) | AVAILABLE | NCT03123029 |
| Venetoclax | Other | Preclinical | Chronic Lymphocytic Leukemia (CLL) | AVAILABLE | NCT03123029 |
| Oral Prednisone - Hospital Dose Steroids | Other | Phase PHASE4 | Ulcerative Colitis Acute | RECRUITING | NCT07258771 |
| Oral prednisolone Taper | Other | Phase PHASE4 | Ulcerative Colitis Acute | RECRUITING | NCT07258771 |
| Oral Upadacitinib Placebo | Other | Phase PHASE4 | Ulcerative Colitis Acute | RECRUITING | NCT07258771 |
| Intravenous Methylprednisolone | Other | Phase PHASE4 | Ulcerative Colitis Acute | RECRUITING | NCT07258771 |
| Oral Upadacitinib | Other | Phase PHASE4 | Ulcerative Colitis Acute | RECRUITING | NCT07258771 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Upadacitinib | Other | Preclinical | Axial Spondylarthritis (r-axSpA) | RECRUITING | NCT05094128 |
| Venetoclax | Other | Phase PHASE1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | COMPLETED | NCT03485547 |
| Venetoclax | Other | Phase PHASE1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | COMPLETED | NCT03485547 |
| Venetoclax | Other | Phase PHASE1 | Blastic Plasmacytoid Dendritic Cell Neoplasm | COMPLETED | NCT03485547 |
| Elezanumab | Other | Preclinical | Acute Spinal Cord Injury (SCI) | AVAILABLE | NCT04278235 |
| Alternately treated with VA/low CHA regimen | Other | Phase PHASE2 | Intensive Chemotherapy Unfit | RECRUITING | NCT07172204 |
| Alternately treated with VA/low CHA regimen | Other | Phase PHASE2 | Intensive Chemotherapy Unfit | RECRUITING | NCT07172204 |
| Placebo | Other | Phase PHASE2 | Autosomal Dominant Polycystic Kidney Disease | RECRUITING | NCT06902558 |
| ABBV-CLS-628 | Other | Phase PHASE2 | Autosomal Dominant Polycystic Kidney Disease | RECRUITING | NCT06902558 |
| Placebo | Other | Phase PHASE2 | Autosomal Dominant Polycystic Kidney Disease | RECRUITING | NCT06902558 |
| ABBV-CLS-628 | Other | Phase PHASE2 | Autosomal Dominant Polycystic Kidney Disease | RECRUITING | NCT06902558 |
| Placebo | Other | Phase PHASE2 | Autosomal Dominant Polycystic Kidney Disease | RECRUITING | NCT06902558 |
| ABBV-CLS-628 | Other | Phase PHASE2 | Autosomal Dominant Polycystic Kidney Disease | RECRUITING | NCT06902558 |
| Telisotuzumab Adizutecan | Other | Preclinical | Solid Tumors | AVAILABLE | NCT05982873 |
| Telisotuzumab Adizutecan | Other | Preclinical | Solid Tumors | AVAILABLE | NCT05982873 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | AVAILABLE | NCT04830202 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | AVAILABLE | NCT04830202 |
| Telisotuzumab vedotin | Other | Preclinical | Non-Small Cell Lung Cancer (NSCLC) | AVAILABLE | NCT04830202 |
| TNB-383B | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03933735 |
| TNB-383B | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03933735 |
| TNB-383B | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT03933735 |
| Obinutuzumab | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT04895436 |
| Venetoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT04895436 |
| Obinutuzumab | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT04895436 |
| Venetoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT04895436 |
| Obinutuzumab | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT04895436 |
| Venetoclax | Other | Phase PHASE2 | Chronic Lymphocytic Leukemia (CLL) | RECRUITING | NCT04895436 |
| Tavapadon | Other | Preclinical | Parkinson Disease | AVAILABLE | NCT07158827 |
| Tavapadon | Other | Preclinical | Parkinson Disease | AVAILABLE | NCT07158827 |
| Placebo | Other | Phase PHASE2 | Schizophrenia | RECRUITING | NCT07145918 |
| Emraclidine | Other | Phase PHASE2 | Schizophrenia | RECRUITING | NCT07145918 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Tocilizumab | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Upadacitinib | Other | Phase PHASE3 | Juvenile Idiopathic Arthritis | RECRUITING | NCT05609630 |
| Biospecimen Collection | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Lumbar Puncture | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Bone Marrow Aspiration and Biopsy | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Blinatumomab | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Venetoclax | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Rituximab | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Prednisone | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Methotrexate | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Dasatinib | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Biospecimen Collection | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Lumbar Puncture | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Bone Marrow Aspiration and Biopsy | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Blinatumomab | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Venetoclax | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Rituximab | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Prednisone | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Methotrexate | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Dasatinib | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Biospecimen Collection | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Lumbar Puncture | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Bone Marrow Aspiration and Biopsy | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Blinatumomab | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Venetoclax | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Rituximab | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Prednisone | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Methotrexate | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Dasatinib | Other | Phase PHASE1 | B Acute Lymphoblastic Leukemia | RECRUITING | NCT04872790 |
| Risankizumab | Other | Phase PHASE3 | Ulcerative Colitis | RECRUITING | NCT07071519 |
| Placebo | Other | Phase PHASE2 | Spinal Cord Injury (SCI) | COMPLETED | NCT04295538 |
| Elezanumab | Other | Phase PHASE2 | Spinal Cord Injury (SCI) | COMPLETED | NCT04295538 |
| Placebo | Other | Phase PHASE2 | Spinal Cord Injury (SCI) | COMPLETED | NCT04295538 |
| Elezanumab | Other | Phase PHASE2 | Spinal Cord Injury (SCI) | COMPLETED | NCT04295538 |
| ABBV-787 | Other | Preclinical | Acute Myeloid Leukemia | NO_LONGER_AVAILABLE | NCT06439966 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| Etentamig (ABBV-383) | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT05650632 |
| ABBV-525 | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | RECRUITING | NCT05618028 |
| ABBV-525 | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | RECRUITING | NCT05618028 |
| ABBV-525 | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | RECRUITING | NCT05618028 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Placebo | Other | Phase PHASE2 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT05139602 |
| Lutikizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT05139602 |
| Placebo | Other | Phase PHASE2 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT05139602 |
| Lutikizumab | Other | Phase PHASE2 | Hidradenitis Suppurativa | ACTIVE_NOT_RECRUITING | NCT05139602 |
| Levonorgestrel/Ethinyl Estradiol | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07414784 |
| ABBV-295 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07414784 |
| Levonorgestrel/Ethinyl Estradiol | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07414784 |
| ABBV-295 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07414784 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Budigalimab | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| ABBV-711 | Other | Phase PHASE1 | Advanced Squamous Tumors | RECRUITING | NCT07241039 |
| Carfilzomib | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Lenalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Carfilzomib | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Lenalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06892522 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06774313 |
| ABBV-142 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06774313 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06774313 |
| ABBV-142 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06774313 |
| Control | Other | Phase PHASE2 | Skin Quality Deficit | COMPLETED | NCT06547125 |
| JUVÉDERM® VOLITE™ | Other | Phase PHASE2 | Skin Quality Deficit | COMPLETED | NCT06547125 |
| Control | Other | Phase PHASE2 | Skin Quality Deficit | COMPLETED | NCT06547125 |
| JUVÉDERM® VOLITE™ | Other | Phase PHASE2 | Skin Quality Deficit | COMPLETED | NCT06547125 |
| Prednisolone | Other | Phase PHASE3 | Takayasu Arteritis (TAK) | ACTIVE_NOT_RECRUITING | NCT04161898 |
| Placebo for Upadacitinib | Other | Phase PHASE3 | Takayasu Arteritis (TAK) | ACTIVE_NOT_RECRUITING | NCT04161898 |
| Upadacitinib | Other | Phase PHASE3 | Takayasu Arteritis (TAK) | ACTIVE_NOT_RECRUITING | NCT04161898 |
| Positron Emission Tomography | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Ibrutinib | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Epcoritamab | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Computed Tomography | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Bone Marrow Aspiration | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Biospecimen Collection | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Positron Emission Tomography | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Ibrutinib | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Epcoritamab | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Computed Tomography | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Bone Marrow Aspiration | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Biospecimen Collection | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Positron Emission Tomography | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Ibrutinib | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Epcoritamab | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Computed Tomography | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Bone Marrow Aspiration | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| Biospecimen Collection | Other | Phase PHASE1 | Recurrent Diffuse Large B-Cell Lymphoma | RECRUITING | NCT06536049 |
| IMGN151 | Other | Phase PHASE1 | Endometrial Cancer | ACTIVE_NOT_RECRUITING | NCT05527184 |
| JUVÉDERM ULTRA PLUS XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM ULTRA XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| SKINVIVE by JUVÉDERM | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM VOLLURE XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM VOLBELLA XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM VOLUMA XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM VOLUX XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM ULTRA PLUS XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM ULTRA XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| SKINVIVE by JUVÉDERM | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM VOLLURE XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM VOLBELLA XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM VOLUMA XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| JUVÉDERM VOLUX XC | Other | Phase PHASE4 | Mid Face Volume Deficit | ACTIVE_NOT_RECRUITING | NCT07186595 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT07141199 |
| ABBV-8736 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT07141199 |
| Pomalidomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Dexamethasone | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Daratumumab | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| ABBV-453 | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06953960 |
| Placebo | Other | Phase PHASE2 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT06718101 |
| Lutikizumab | Other | Phase PHASE2 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT06718101 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT06701331 |
| Placebo | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT06701331 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT06701331 |
| Placebo | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT06701331 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT06701331 |
| Placebo | Other | Phase PHASE3 | Atopic Dermatitis | ACTIVE_NOT_RECRUITING | NCT06701331 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Telisotuzumab Vedotin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06568939 |
| Carboplatin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Cisplatin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Pemetrexed | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Pembrolizumab | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Budigalimab | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Livmoniplimab | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Carboplatin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Cisplatin | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Pemetrexed | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Pembrolizumab | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Budigalimab | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Livmoniplimab | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT06236438 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | RECRUITING | NCT05445778 |
| Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | RECRUITING | NCT05445778 |
| Mirvetuximab soravtansine plus Bevacizumab | Other | Phase PHASE3 | Ovarian Cancer | RECRUITING | NCT05445778 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06849791 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06849791 |
| ABBV-932 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06849791 |
| No Intervention | Other | Phase PHASE3 | Breast Reconstruction | RECRUITING | NCT06575192 |
| ARTIA Reconstructive Tissue Matrix | Other | Phase PHASE3 | Breast Reconstruction | RECRUITING | NCT06575192 |
| Deucravacitinib | Other | Phase PHASE4 | Moderate Plaque Psoriasis | ACTIVE_NOT_RECRUITING | NCT06333860 |
| Risankizumab | Other | Phase PHASE4 | Moderate Plaque Psoriasis | ACTIVE_NOT_RECRUITING | NCT06333860 |
| Placebo | Other | Phase PHASE3 | Spondyloarthritis | COMPLETED | NCT04169373 |
| Upadacitinib | Other | Phase PHASE3 | Spondyloarthritis | COMPLETED | NCT04169373 |
| Placebo | Other | Phase PHASE3 | Spondyloarthritis | COMPLETED | NCT04169373 |
| Upadacitinib | Other | Phase PHASE3 | Spondyloarthritis | COMPLETED | NCT04169373 |
| Placebo | Other | Phase PHASE3 | Spondyloarthritis | COMPLETED | NCT04169373 |
| Upadacitinib | Other | Phase PHASE3 | Spondyloarthritis | COMPLETED | NCT04169373 |
| Placebo | Other | Phase PHASE3 | Spondyloarthritis | COMPLETED | NCT04169373 |
| Upadacitinib | Other | Phase PHASE3 | Spondyloarthritis | COMPLETED | NCT04169373 |
| Placebo | Other | Phase PHASE3 | Giant Cell Arteritis (GCA) | COMPLETED | NCT03725202 |
| Corticosteroid (CS) | Other | Phase PHASE3 | Giant Cell Arteritis (GCA) | COMPLETED | NCT03725202 |
| Upadacitinib | Other | Phase PHASE3 | Giant Cell Arteritis (GCA) | COMPLETED | NCT03725202 |
| Placebo | Other | Phase PHASE3 | Giant Cell Arteritis (GCA) | COMPLETED | NCT03725202 |
| Corticosteroid (CS) | Other | Phase PHASE3 | Giant Cell Arteritis (GCA) | COMPLETED | NCT03725202 |
| Upadacitinib | Other | Phase PHASE3 | Giant Cell Arteritis (GCA) | COMPLETED | NCT03725202 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT06511882 |
| Decitabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT06511882 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | RECRUITING | NCT06511882 |
| Thioguanine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Methotrexate | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Nelarabine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Mercaptopurine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Cytarabine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Cyclophosphamide | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Intrathecal triple therapy (methotrexate + hydrocortisone + cytarabine) | Drug | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Bortezomib | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Venetoclax | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Dasatinib | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Calaspargase pegol | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Daunorubicin | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Vincristine | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Dexamethasone | Other | Phase PHASE2 | T-cell Acute Lymphoblastic Leukemia | RECRUITING | NCT06390319 |
| Risankizumab | Other | Phase PHASE4 | Inflammatory Bowel Disease | COMPLETED | NCT06346288 |
| Breast Milk Sampling | Other | Phase PHASE4 | Inflammatory Bowel Disease | COMPLETED | NCT06346288 |
| XEN45 (Glaucoma Gel Stent) | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT05411198 |
| XEN45 (Glaucoma Gel Stent) | Other | Phase PHASE3 | Open-Angle Glaucoma | COMPLETED | NCT05411198 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06895343 |
| ABBV-701 | Other | Phase PHASE1 | Healthy Volunteer | ACTIVE_NOT_RECRUITING | NCT06895343 |
| CC-99282 | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Polatuzumab Vedotin | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Prednisone | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Doxorubicin Hydrochloride [HCl] | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Cyclophosphamide | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Rituximab | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Ibrutinib | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Lenalidomide | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Epcoritamab | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| ABBV-8736 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07413133 |
| ABBV-8736 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07413133 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Upadacitinib | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Upadacitinib | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Upadacitinib | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Upadacitinib | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT05889182 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Placebo-Matching Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Ubrogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT05125302 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03844815 |
| Decitabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03844815 |
| Venetoclax | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03844815 |
| Decitabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT03844815 |
| ABBV-547 Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07232004 |
| ABBV-547 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07232004 |
| ABBV-547 Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07232004 |
| ABBV-547 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07232004 |
| ABBV-547 Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07232004 |
| ABBV-547 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07232004 |
| Durysta, Bimatoprost Intracameral Implant 10 µg | Other | Phase PHASE4 | Glaucoma | RECRUITING | NCT07217678 |
| Durysta, Bimatoprost Intracameral Implant 10 µg | Other | Phase PHASE4 | Glaucoma | RECRUITING | NCT07217678 |
| Durysta, Bimatoprost Intracameral Implant 10 µg | Other | Phase PHASE4 | Glaucoma | RECRUITING | NCT07217678 |
| Venetoclax | Other | Phase PHASE2 | Chronic Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT05768711 |
| Venetoclax | Other | Phase PHASE2 | Chronic Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT05768711 |
| Venetoclax | Other | Phase PHASE2 | Chronic Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT05768711 |
| Placebo for Atogepant | Other | Phase PHASE3 | Menstrual Migraine (MM) | RECRUITING | NCT06806293 |
| Atogepant | Other | Phase PHASE3 | Menstrual Migraine (MM) | RECRUITING | NCT06806293 |
| Placebo for Atogepant | Other | Phase PHASE3 | Menstrual Migraine (MM) | RECRUITING | NCT06806293 |
| Atogepant | Other | Phase PHASE3 | Menstrual Migraine (MM) | RECRUITING | NCT06806293 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Solid Tumors Harboring MET Amplification | RECRUITING | NCT07196644 |
| Standard of Care | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT07155187 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT07155187 |
| Standard of Care | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT07155187 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Small Cell Lung Cancer | RECRUITING | NCT07155187 |
| Placebo | Other | Phase PHASE2 | Apathy in Dementia | TERMINATED | NCT04958031 |
| CVL-871 3.0 mg | Other | Phase PHASE2 | Apathy in Dementia | TERMINATED | NCT04958031 |
| CVL-871 1.0 mg | Other | Phase PHASE2 | Apathy in Dementia | TERMINATED | NCT04958031 |
| Placebo | Other | Phase PHASE2 | Apathy in Dementia | TERMINATED | NCT04958031 |
| CVL-871 3.0 mg | Other | Phase PHASE2 | Apathy in Dementia | TERMINATED | NCT04958031 |
| CVL-871 1.0 mg | Other | Phase PHASE2 | Apathy in Dementia | TERMINATED | NCT04958031 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07466550 |
| Risankizumab | Other | Phase PHASE1 | Healthy Volunteer | NOT_YET_RECRUITING | NCT07466550 |
| venetoclax + azacitidine +/- donor lymphocyte infusion | Other | Phase PHASE1 | MDS | ACTIVE_NOT_RECRUITING | NCT05226455 |
| REFRESH OPTIVE UD | Other | Phase PHASE3 | Dry Eye Disease | RECRUITING | NCT07284381 |
| ABBV-444 | Other | Phase PHASE3 | Dry Eye Disease | RECRUITING | NCT07284381 |
| REFRESH OPTIVE UD | Other | Phase PHASE3 | Dry Eye Disease | RECRUITING | NCT07284381 |
| ABBV-444 | Other | Phase PHASE3 | Dry Eye Disease | RECRUITING | NCT07284381 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Standard of Care | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Colorectal Cancer | RECRUITING | NCT07023289 |
| Rituximab | Other | Phase PHASE2 | Lymphoma | RECRUITING | NCT06510309 |
| Venetoclax | Other | Phase PHASE2 | Lymphoma | RECRUITING | NCT06510309 |
| Rituximab | Other | Phase PHASE2 | Lymphoma | RECRUITING | NCT06510309 |
| Venetoclax | Other | Phase PHASE2 | Lymphoma | RECRUITING | NCT06510309 |
| Rituximab | Other | Phase PHASE2 | Lymphoma | RECRUITING | NCT06510309 |
| Venetoclax | Other | Phase PHASE2 | Lymphoma | RECRUITING | NCT06510309 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Dexamethasone | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Bortezomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Selinexor | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Elotuzumab | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Pomalidomide | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Carfilzomib | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Etentamig | Other | Phase PHASE3 | Multiple Myeloma | RECRUITING | NCT06158841 |
| Epcoritamab | Other | Phase PHASE2 | Primary CNS Lymphoma (PCNSL) | RECRUITING | NCT06931652 |
| Epcoritamab | Other | Phase PHASE2 | Primary CNS Lymphoma (PCNSL) | RECRUITING | NCT06931652 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT05995353 |
| XEN63 Glaucoma Treatment System | Drug | Phase PHASE3 | Primary Open Angle Glaucoma | RECRUITING | NCT06822738 |
| Placebo | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT06468228 |
| Lutikizumab | Other | Phase PHASE3 | Hidradenitis Suppurativa | RECRUITING | NCT06468228 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Placebo-Matching Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Atogepant | Other | Phase PHASE3 | Episodic Migraine | RECRUITING | NCT05711394 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT03844048 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | ACTIVE_NOT_RECRUITING | NCT03844048 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Icalcaprant | Other | Phase PHASE2 | Major Depressive Disorder | RECRUITING | NCT07276997 |
| Lumigan Vehicle | Other | Phase PHASE1 | Open-angle Glaucoma | RECRUITING | NCT04499248 |
| Sham Administration | Other | Phase PHASE1 | Open-angle Glaucoma | RECRUITING | NCT04499248 |
| Lumigan | Other | Phase PHASE1 | Open-angle Glaucoma | RECRUITING | NCT04499248 |
| AGN-193408 SR | Other | Phase PHASE1 | Open-angle Glaucoma | RECRUITING | NCT04499248 |
| Navitoclax | Other | Phase PHASE3 | Myelofibrosis (MF) | COMPLETED | NCT04472598 |
| Ruxolitinib | Other | Phase PHASE3 | Myelofibrosis (MF) | COMPLETED | NCT04472598 |
| Placebo for Navitoclax | Other | Phase PHASE3 | Myelofibrosis (MF) | COMPLETED | NCT04472598 |
| Navitoclax | Other | Phase PHASE3 | Myelofibrosis (MF) | COMPLETED | NCT04472598 |
| Ruxolitinib | Other | Phase PHASE3 | Myelofibrosis (MF) | COMPLETED | NCT04472598 |
| Placebo for Navitoclax | Other | Phase PHASE3 | Myelofibrosis (MF) | COMPLETED | NCT04472598 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Irinotecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Folinic acid/ Leucovorina | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Telisotuzumab adizutecan | Other | Phase PHASE2 | Metastatic Pancreatic Ductal Adenocarcinoma | NOT_YET_RECRUITING | NCT07490301 |
| Cofetuzumab Pelidotin | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT04189614 |
| Cofetuzumab Pelidotin | Other | Phase PHASE1 | Cancer | ACTIVE_NOT_RECRUITING | NCT04189614 |
| ABBV-324 | Other | Phase PHASE1 | Hepatocellular Cancer | RECRUITING | NCT06858813 |
| Lenvatinib | Other | Phase PHASE1 | Hepatocellular Cancer | RECRUITING | NCT06858813 |
| ABBV-324 | Other | Phase PHASE1 | Hepatocellular Cancer | RECRUITING | NCT06858813 |
| Lenvatinib | Other | Phase PHASE1 | Hepatocellular Cancer | RECRUITING | NCT06858813 |
| Brimonidine tartrate ophthalmic solution eye drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Prednisolone acetate ophthalmic suspension 1% eye drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Lubricating Eye Drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Brimonidine tartrate ophthalmic solution eye drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Prednisolone acetate ophthalmic suspension 1% eye drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Lubricating Eye Drops | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Recurrent Ovarian Cancer | RECRUITING | NCT06365853 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| KYBELLA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| SkinMedica Products | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| JUVÉDERM | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| KYBELLA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| SkinMedica Products | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| CoolSculpting Elite System | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| JUVÉDERM | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| OnabotulinumtoxinA | Other | Phase PHASE4 | Facial Contouring | COMPLETED | NCT06783621 |
| Intravenous (IV) Etentamig | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT06223516 |
| Subcutaneous (SC) Etentamig | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT06223516 |
| Intravenous (IV) Etentamig | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT06223516 |
| Subcutaneous (SC) Etentamig | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT06223516 |
| Intravenous (IV) Etentamig | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT06223516 |
| Subcutaneous (SC) Etentamig | Other | Phase PHASE1 | Multiple Myeloma | ACTIVE_NOT_RECRUITING | NCT06223516 |
| Iberdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Iberdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Oxaliplatin | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Leucovorin | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Fluorouracil | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Budigalimab | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Oxaliplatin | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Leucovorin | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Fluorouracil | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Budigalimab | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Locally Advanced Unresectable or Metastatic Gastric Adenocarcinoma | RECRUITING | NCT06628310 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07502417 |
| Ethinyl Estradiol + Levonorgestrel | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07502417 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07502417 |
| Ethinyl Estradiol + Levonorgestrel | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07502417 |
| Upadacitinib | Other | Phase PHASE4 | UC - Ulcerative Colitis | NOT_YET_RECRUITING | NCT07502339 |
| Venetoclax | Other | Phase PHASE2 | Relapsed or Refractory Acute Myeloid Leukemia (AML) | RECRUITING | NCT06660368 |
| Cladribine, Cytarabine, Mitoxantrone, G-CSF (CLAG-M) regimen | Other | Phase PHASE2 | Relapsed or Refractory Acute Myeloid Leukemia (AML) | RECRUITING | NCT06660368 |
| ABBV-8736 | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Trosunilimab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Lutikizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Risankizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| ABBV-8736 | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Trosunilimab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Lutikizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Risankizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| ABBV-8736 | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Trosunilimab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Lutikizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Risankizumab | Other | Phase PHASE2 | Crohn's Disease | RECRUITING | NCT06548542 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Topiramate 100 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Propranolol 160 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Atogepant 60 mg | Other | Phase PHASE4 | Migraine | RECRUITING | NCT06972056 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Placebo | Other | Phase PHASE4 | Psoriatic Arthritis | RECRUITING | NCT06454188 |
| Upadacitinib 15 MG [Rinvoq] | Other | Phase PHASE4 | Psoriatic Arthritis | RECRUITING | NCT06454188 |
| Placebo | Other | Phase PHASE4 | Psoriatic Arthritis | RECRUITING | NCT06454188 |
| Upadacitinib 15 MG [Rinvoq] | Other | Phase PHASE4 | Psoriatic Arthritis | RECRUITING | NCT06454188 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Bevacizumab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Budigalimab | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Azirkitug | Other | Phase PHASE1 | Non-Small Cell Lung Cancer | RECRUITING | NCT05005403 |
| Placebo for ABBV-142 | Other | Phase PHASE2 | Idiopathic Pulmonary Fibrosis | RECRUITING | NCT07230288 |
| ABBV-142 | Other | Phase PHASE2 | Idiopathic Pulmonary Fibrosis | RECRUITING | NCT07230288 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Placebo for AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| AGN-151607-DP | Other | Phase PHASE2 | Ventral Hernia | RECRUITING | NCT07226791 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Olaparib | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Bevacizumab | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Carboplatin | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| IMGN151 | Other | Phase PHASE2 | Gynecologic Cancers | RECRUITING | NCT07024784 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Placebo for Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Icalcaprant | Other | Phase PHASE2 | Bipolar I Disorder | RECRUITING | NCT06696755 |
| Upadacitinib | Other | Phase PHASE3 | Crohn's Disease | RECRUITING | NCT06332534 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Placebo for ABBV-295 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07514260 |
| ABBV-295 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07514260 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Dupilumab | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06461897 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06461897 |
| Dupilumab | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06461897 |
| Upadacitinib | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06461897 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Ustekinumab | Other | Phase PHASE3 | Crohn's Disease (CD) | ACTIVE_NOT_RECRUITING | NCT04524611 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease (CD) | ACTIVE_NOT_RECRUITING | NCT04524611 |
| Investigator's Choice Chemotherapy | Drug | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT07226752 |
| Epcoritamab | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT07226752 |
| Investigator's Choice Chemotherapy | Drug | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT07226752 |
| Epcoritamab | Other | Phase PHASE3 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT07226752 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| ABBV-969 | Other | Phase PHASE1 | Metastatic Castration-Resistant Prostate Cancer | RECRUITING | NCT06318273 |
| ABBV-969 | Other | Phase PHASE1 | Metastatic Castration-Resistant Prostate Cancer | RECRUITING | NCT06318273 |
| ABBV-969 | Other | Phase PHASE1 | Metastatic Castration-Resistant Prostate Cancer | RECRUITING | NCT06318273 |
| Lenalidomide | Other | Phase PHASE2 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT05660967 |
| Epcoritamab | Other | Phase PHASE2 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT05660967 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Rituximab and Lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, ifosfamide, carboplatin, and etoposide phosphate | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cyclophosphamide, reduced dose of doxorubicin, vincristine, and prednisone | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Epcoritamab | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| gemcitabine and oxaliplatin | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cytarabine, dexamethasone, and oxaliplatin/carboplatin | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab and bendamustine | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab and lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Rituximab and Lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, ifosfamide, carboplatin, and etoposide phosphate | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cyclophosphamide, reduced dose of doxorubicin, vincristine, and prednisone | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Epcoritamab | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| gemcitabine and oxaliplatin | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cytarabine, dexamethasone, and oxaliplatin/carboplatin | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab and bendamustine | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab and lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Rituximab and Lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, ifosfamide, carboplatin, and etoposide phosphate | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cyclophosphamide, reduced dose of doxorubicin, vincristine, and prednisone | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Epcoritamab | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| gemcitabine and oxaliplatin | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cytarabine, dexamethasone, and oxaliplatin/carboplatin | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab and bendamustine | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab and lenalidomide | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone | Other | Phase PHASE1 | Diffuse Large B-Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04663347 |
| Investigator's Choice Chemotherapy | Drug | Phase PHASE3 | Diffuse Large B-cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04628494 |
| Epcoritamab | Other | Phase PHASE3 | Diffuse Large B-cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04628494 |
| Investigator's Choice Chemotherapy | Drug | Phase PHASE3 | Diffuse Large B-cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04628494 |
| Epcoritamab | Other | Phase PHASE3 | Diffuse Large B-cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04628494 |
| Rituximab and lenalidomide | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Epcoritamab (maintenance) | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Gemcitabine and oxaliplatin | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Epcoritamab | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Epcoritamab (monotherapy) | Drug | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Rituximab and lenalidomide | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Epcoritamab (maintenance) | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Gemcitabine and oxaliplatin | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Epcoritamab | Other | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Epcoritamab (monotherapy) | Drug | Phase PHASE1 | Diffuse Large B Cell Lymphoma | ACTIVE_NOT_RECRUITING | NCT04542824 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT04102020 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT04102020 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT04102020 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT04102020 |
| Azacitidine | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT04102020 |
| Venetoclax | Other | Phase PHASE3 | Acute Myeloid Leukemia (AML) | COMPLETED | NCT04102020 |
| Epcoritamab | Other | Phase PHASE1 | DLBCL | ACTIVE_NOT_RECRUITING | NCT03625037 |
| Epcoritamab | Other | Phase PHASE1 | DLBCL | ACTIVE_NOT_RECRUITING | NCT03625037 |
| Placebo for ABBV-142 | Other | Phase PHASE2 | Idiopathic Pulmonary Fibrosis | RECRUITING | NCT07230288 |
| ABBV-142 | Other | Phase PHASE2 | Idiopathic Pulmonary Fibrosis | RECRUITING | NCT07230288 |
| Obinutuzumab | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | RECRUITING | NCT06428019 |
| Acalabrutinib | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | RECRUITING | NCT06428019 |
| Venetoclax | Other | Phase PHASE3 | Chronic Lymphocytic Leukemia | RECRUITING | NCT06428019 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | NOT_YET_RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | NOT_YET_RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | NOT_YET_RECRUITING | NCT07525206 |
| Trifluridine/Tipiracil | Other | Phase PHASE3 | Colorectal Cancer | NOT_YET_RECRUITING | NCT07525206 |
| Bevacizumab | Other | Phase PHASE3 | Colorectal Cancer | NOT_YET_RECRUITING | NCT07525206 |
| Telisotuzumab adizutecan | Other | Phase PHASE3 | Colorectal Cancer | NOT_YET_RECRUITING | NCT07525206 |
| Venetoclax | Other | Phase PHASE2 | Waldenstrom Macroglobulinemia | RECRUITING | NCT07387471 |
| Venetoclax | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Questionnaire Administration | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Multigated Acquisition Scan | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Lumbar Puncture | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Echocardiography | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Cytarabine | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Cladribine | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Bone Marrow Biopsy | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Bone Marrow Aspiration | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Biospecimen Collection | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Azacitidine | Other | Phase PHASE2 | Acute Monocytic Leukemia | RECRUITING | NCT06504459 |
| Olaparib | Other | Phase PHASE2 | Ovary Cancer | RECRUITING | NCT05887609 |
| Mirvetuximab Soravtansine-gynx | Other | Phase PHASE2 | Ovary Cancer | RECRUITING | NCT05887609 |
| CC-99282 | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Polatuzumab Vedotin | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Prednisone | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Doxorubicin Hydrochloride [HCl] | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Cyclophosphamide | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Rituximab | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Ibrutinib | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Lenalidomide | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Epcoritamab | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| CC-99282 | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Polatuzumab Vedotin | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Prednisone | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Doxorubicin Hydrochloride [HCl] | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Cyclophosphamide | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Rituximab | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Ibrutinib | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Lenalidomide | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Epcoritamab | Other | Phase PHASE2 | Non-Hodgkin Lymphoma | RECRUITING | NCT05283720 |
| Usual care | Other | Approved | Hepatitis C Virus Infection, Response to Therapy of | COMPLETED | NCT04677153 |
| Test and treat plus peer mentors | Other | Approved | Hepatitis C Virus Infection, Response to Therapy of | COMPLETED | NCT04677153 |
| Ustekinumab | Other | Phase PHASE3 | Crohn's Disease (CD) | ACTIVE_NOT_RECRUITING | NCT04524611 |
| Risankizumab | Other | Phase PHASE3 | Crohn's Disease (CD) | ACTIVE_NOT_RECRUITING | NCT04524611 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Pivekimab Sunirine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Multigated Acquisition Scan | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Idarubicin | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Granulocyte Colony-Stimulating Factor | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Fludarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Echocardiography | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Cytarabine | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Bone Marrow Biopsy | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Bone Marrow Aspiration | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Biospecimen Collection | Other | Phase PHASE1 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT06034470 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Placebo for ABBV-295 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07514260 |
| ABBV-295 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07514260 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Panitumumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Bevacizumab | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Leucovorin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Oxaliplatin | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Fluorouracil | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Metastatic Colorectal Cancer | RECRUITING | NCT06820463 |
| Deucravacitinib | Other | Phase PHASE4 | Moderate Plaque Psoriasis | COMPLETED | NCT06333860 |
| Risankizumab | Other | Phase PHASE4 | Moderate Plaque Psoriasis | COMPLETED | NCT06333860 |
| Deucravacitinib | Other | Phase PHASE4 | Moderate Plaque Psoriasis | COMPLETED | NCT06333860 |
| Risankizumab | Other | Phase PHASE4 | Moderate Plaque Psoriasis | COMPLETED | NCT06333860 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Upadacitinib | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07425899 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07425899 |
| Risankizumab | Other | Phase PHASE4 | Inflammatory Bowel Disease | COMPLETED | NCT06346288 |
| Breast Milk Sampling | Other | Phase PHASE4 | Inflammatory Bowel Disease | COMPLETED | NCT06346288 |
| Risankizumab | Other | Phase PHASE4 | Inflammatory Bowel Disease | COMPLETED | NCT06346288 |
| Breast Milk Sampling | Other | Phase PHASE4 | Inflammatory Bowel Disease | COMPLETED | NCT06346288 |
| Rituximab | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Prednisone | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Positron Emission Tomography | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Multigated Acquisition Scan | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Fludeoxyglucose F-18 | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Etoposide | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Epcoritamab | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Echocardiography Test | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Doxorubicin | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Cyclophosphamide | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Computed Tomography | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Bone Marrow Biopsy | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Bone Marrow Aspiration | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Biospecimen Collection | Other | Phase PHASE2 | B-Cell Non-Hodgkin Lymphoma | RECRUITING | NCT07097363 |
| Gilteritinib | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Etoposide | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Mitoxantrone Hydrochloride | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Idarubicin Hydrochloride | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Fludarabine Phosphate | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Daunorubicin Hydrochloride | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Gemtuzumab Ozogamicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | SUSPENDED | NCT05955261 |
| ABBV-722 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT07361367 |
| Glecaprevir/pibrentasvir | Other | Phase PHASE1 | Hepatitis C | RECRUITING | NCT07040319 |
| Placebo for Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Atogepant | Other | Phase PHASE3 | Migraine | RECRUITING | NCT06241313 |
| Placebo | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Upadacitinib | Other | Phase PHASE3 | Alopecia Areata | RECRUITING | NCT06012240 |
| Cisplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pemetrexed | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Carboplatin | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Pembrolizumab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Budigalimab | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Telisotuzumab Adizutecan | Other | Phase PHASE1 | Non Small Cell Lung Carcinoma | RECRUITING | NCT06772623 |
| Ranibizumab Control | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Surabgene Lomparvovec (ABBV-RGX-314) | Other | Phase PHASE3 | Neovascular Age-related Macular Degeneration | RECRUITING | NCT07007065 |
| Placebo for Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Atogepant | Other | Phase PHASE3 | Chronic Migraine | RECRUITING | NCT06810505 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Liposomal daunorubicin and cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Daunorubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Idarubicin | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Cytarabine | Other | Phase PHASE2 | Acute Myeloid Leukemia | ACTIVE_NOT_RECRUITING | NCT04801797 |
| Pemetrexed | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Carboplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Cisplatin | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Osimertinib (Osi) | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Telisotuzumab Adizutecan | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Standard of Care | Other | Phase PHASE2 | Non-Squamous Non-Small Cell Lung Cancer | RECRUITING | NCT07005102 |
| Iberdomide | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Etentamig | Other | Phase PHASE1 | Multiple Myeloma | RECRUITING | NCT06896916 |
| Bevacizumab | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Mirvetuximab Soravtansine | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Carboplatin | Other | Phase PHASE2 | Epithelial Ovarian Cancer | RECRUITING | NCT06890338 |
| Dexamethasone | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Daratumumab | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Lenalidomide | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Etentamig | Other | Phase PHASE2 | Multiple Myeloma | RECRUITING | NCT07095452 |
| Ravagalimab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Placebo | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lutikizumab | Other | Phase PHASE2 | Rheumatoid Arthritis | RECRUITING | NCT06972446 |
| Lurbinectedin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Carboplatin | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Etoposide | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Atezolizumab | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| ABBV-706 | Other | Phase PHASE2 | Small Cell Lung Cancer | RECRUITING | NCT07155174 |
| Matching Placebo for PVEK | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Azacitidine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Venetoclax | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Pivekimab Sunirine | Other | Phase PHASE2 | Acute Myeloid Leukemia | NOT_YET_RECRUITING | NCT07581002 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| Emraclidine | Other | Phase PHASE1 | Healthy Volunteer | RECRUITING | NCT07219030 |
| ABBV-319 | Other | Phase PHASE1 | Dry Eye Syndrome | RECRUITING | NCT06977724 |
| VOLUMA XC | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| NOA VOLUME | Other | Phase PHASE3 | Mid Face Volume Deficit | RECRUITING | NCT06734351 |
| Upadacitinib 30mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Dupilumab 300mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Upadacitinib 15mg Dose | Other | Phase PHASE3 | Atopic Dermatitis | RECRUITING | NCT06389136 |
| Placebo | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Cariprazine | Other | Phase PHASE3 | Depression | RECRUITING | NCT04777357 |
| Docetaxel | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Telisotuzumab Vedotin | Other | Phase PHASE3 | Non Small Cell Lung Cancer | RECRUITING | NCT04928846 |
| Azacitidine | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |
| Venetoclax | Other | Phase PHASE4 | Acute Myeloid Leukemia | RECRUITING | NCT07044687 |