| Symbol | EBS |
|---|---|
| Name | EMERGENT BIOSOLUTIONS INC. |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Biotechnology: Pharmaceutical Preparations |
| Address | 400 PROFESSIONAL DRIVE,SUITE 400, GAITHERSBURG, Maryland, 20879, United States |
| Telephone | +1 240 631-3200 |
| Fax | — |
| — | |
| Website | https://www.emergentbiosolutions.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001367644 |
| Description | Emergent BioSolutions offers public health products to government and healthcare providers. The company has four main units: vaccines, which produces specialty vaccines for public health threats; devices, such as nasal sprays, skin lotions, and injections; therapeutics, which includes antibody-based treatments; and contract development and manufacturing, which brings treatments to market through collaboration with the pharmaceutical and biotechnology industries and the United States government. Most revenue comes from U.S. government purchases of vaccine, device, and therapeutic products. Additional info from NASDAQ: |
Director Dayal Sujata Tyagi 🟡 adjusted position in 22.9K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $8.94 Transaction Date: Apr 30, 2026 | Filing ID: 000004
Read moreDirector DeGolyer Donald W 🟡 adjusted position in 21.2K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $8.96 Transaction Date: Apr 30, 2026 | Filing ID: 000004
Read moreDirector Katkin Keith 🟡 adjusted position in 21.2K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $8.28 Transaction Date: Apr 30, 2026 | Filing ID: 000002
Read moreDirector White Marvin L 🟢 acquired 36.6K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $7.99 Transaction Date: Apr 30, 2026 | Filing ID: 000002
Read moreDirector FOWLER JOHN D JR 🟢 acquired 36.6K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $7.99 Transaction Date: Apr 30, 2026 | Filing ID: 000012
Read moreDirector Richard Ronald 🟢 acquired 36.6K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $7.99 Transaction Date: Apr 30, 2026 | Filing ID: 000004
Read moreDirector Zoon Kathryn C 🟡 adjusted position in 19.4K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $8.97 Transaction Date: Apr 30, 2026 | Filing ID: 000003
Read moreDirector Fowler Neal Franklin 🟢 acquired 36.6K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $7.99 Transaction Date: Apr 30, 2026 | Filing ID: 000003
Read moreDirector Harsanyi Zsolt 🟢 acquired 36.6K shares (1 derivative) of Emergent BioSolutions Inc. (EBS) at $7.99 Transaction Date: Apr 30, 2026 | Filing ID: 000005
Read moreWilliams Paul Anthony 🟢 acquired 100.1K shares of Emergent BioSolutions Inc. (EBS) Transaction Date: Apr 29, 2026 | Filing ID: 000017
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT07268612 | Evaluation of Clinical Benefit and Safety Following CYFENDUS Administration for… | — | Anthrax | Not_Yet_Recruiting | 2035-11-01 | 2037-11-01 | ClinicalTrials.gov |
| NCT03569553 | A Field Study Evaluating Clinical Benefit and Safety of AIGIV (ANTHRASIL®) in I… | — | Inhalational Anthrax | Not_Yet_Recruiting | 2027-05-30 | 2027-07-01 | ClinicalTrials.gov |
| NCT07478471 | Observational Study of Raxibacumab in Sporadic Cases of Systemic Anthrax | — | Infections, Bacterial | Not_Yet_Recruiting | 2027-05-01 | 2030-12-01 | ClinicalTrials.gov |
| NCT02177721 | Clinical Benefit and Safety of Raxibacumab in Patients With Symptomatic Inhalat… | Phase4 | Infections, Bacterial | Not_Yet_Recruiting | 2027-01-01 | 2035-12-01 | ClinicalTrials.gov |
| NCT03569514 | Observational Study Evaluating Clinical Benefit and Safety of AIGIV (ANTHRASIL®… | — | Anthrax | Not_Yet_Recruiting | 2026-11-30 | 2027-08-01 | ClinicalTrials.gov |
| NCT05935917 | Study Evaluating the Bioequivalence of Brincidofovir Form H and Form II Tablets… | Phase1 | Smallpox | Completed | 2023-05-30 | 2023-09-27 | ClinicalTrials.gov |
| NCT05349617 | Safety and Immunogenicity of CHIKV VLP Vaccine PXVX0317 in Adults ≥65 Years | Phase3 | Chikungunya Virus | Completed | 2022-05-12 | 2023-08-08 | ClinicalTrials.gov |
| NCT05377255 | Pharmacokinetics (PK) and Safety of Multiple Doses of Intranasal Naloxone in He… | Phase1 | Opioid Overdose | Completed | 2022-03-28 | 2022-05-10 | ClinicalTrials.gov |
| NCT05194358 | Study of SIAN Nasal Spray in Healthy Adults | Phase1 | Cyanide Poisoning | Completed | 2021-12-21 | 2023-10-13 | ClinicalTrials.gov |
| NCT05142306 | A COVID-19 Study to Evaluate Safety and PK of COVID-HIG Administered Through IM… | Phase1 | SARS-CoV-2 Infection | Completed | 2021-12-07 | 2022-05-31 | ClinicalTrials.gov |
| NCT05155319 | Universal Influenza A Vaccine in Healthy Adults | Phase1 | Human Influenza | Completed | 2021-12-01 | 2023-10-10 | ClinicalTrials.gov |
| NCT05065983 | A Study to Assess the Safety and Immunogenicity of PXVX0317 Chikungunya Virus V… | Phase2 | Chikungunya Virus | Completed | 2021-10-11 | 2022-05-05 | ClinicalTrials.gov |
| NCT05072080 | A Phase 3 Trial of the VLP-Based Chikungunya Vaccine PXVX0317 (CHIKV VLP Vaccin… | Phase3 | Chikungunya Virus | Completed | 2021-09-29 | 2023-04-03 | ClinicalTrials.gov |
| NCT04661839 | A COVID-19 Study to Evaluate Safety and Pharmacokinetics of COVID-HIGIV Adminis… | Phase1 | COVID-19 | Completed | 2020-12-24 | 2021-07-27 | ClinicalTrials.gov |
| NCT03992872 | Phase 2 Open-label Study of Alum-adjuvanted Chikungunya Virus-like Particle Vac… | Phase2 | Chikungunya | Completed | 2019-11-20 | 2021-01-19 | ClinicalTrials.gov |
| NCT04067011 | Velocity 2: An Anthrax Vaccine and Antibiotics Clinical Study | Phase2 | Anthrax | Completed | 2019-08-12 | 2020-03-19 | ClinicalTrials.gov |
| NCT03877926 | VELOCITY: An Anthrax Vaccine Clinical Study | Phase3 | Anthrax | Completed | 2019-03-11 | 2020-08-06 | ClinicalTrials.gov |
| NCT03624946 | Study in Healthy Volunteers Evaluating Safety and Pharmacokinetics of Zika Viru… | Phase1 | Zika Virus Infection | Completed | 2018-06-27 | 2019-03-06 | ClinicalTrials.gov |
| NCT03483961 | Trial of a Chikungunya Vaccine, PXVX0317 CHIKV-VLP, in Healthy Adults | Phase2 | Chikungunya Virus Infection | Completed | 2018-04-18 | 2020-09-21 | ClinicalTrials.gov |
| NCT03425149 | Randomized, Placebo-controlled, Observer-blinded Phase 1 Safety and Immunogenic… | Phase1 | Zika Virus | Completed | 2018-02-24 | 2018-11-16 | ClinicalTrials.gov |
| NCT03315104 | Exploring Safety & Clinical Benefit of Anti-Influenza Immunoglobulin Intravenou… | Phase2 | Influenza A H3N2 | Completed | 2017-11-17 | 2019-06-17 | ClinicalTrials.gov |
| NCT03220737 | VAXCHORA Pediatric Study to Assess Safety and Immunogenicity | Phase4 | Cholera (Disorder) | Completed | 2017-07-21 | 2020-03-06 | ClinicalTrials.gov |
| NCT03160339 | A Study to Assess the Safety, Pharmacodynamics, and Immunogenicity of PXVX0047 | Phase1 | Adenoviral Infection | Terminated | 2017-05-01 | 2017-11-27 | ClinicalTrials.gov |
| NCT02696291 | Safety and Pharmacokinetics of UV-4B Solution Administered Orally as Multiple A… | Phase1 | Viral Infection | Terminated | 2016-05-27 | 2017-03-02 | ClinicalTrials.gov |
| NCT02443623 | VA-008 ACAM2000® Vaccination of Plasma Donors for the Production of VIGIV | Phase4 | Smallpox Vaccine Adverse Reaction | Completed | 2015-09-01 | 2021-08-01 | ClinicalTrials.gov |
| NCT02391909 | Phase 4 Study To Assess The Safety Of Vivotif At Different Release Titers Among… | — | Typhoid Fever | Completed | 2015-08-26 | 2017-02-21 | ClinicalTrials.gov |
| NCT02771730 | Study to Evaluate the Safety and Immunogenicity of an Oral HIV Vaccine in Healt… | Phase1 | Healthy Volunteer | Terminated | 2015-03-01 | 2017-02-01 | ClinicalTrials.gov |
| NCT02339155 | Effect of Raxibacumab on Immunogenicity of Anthrax Vaccine Adsorbed | Phase4 | Infections, Bacterial | Completed | 2015-02-24 | 2017-06-06 | ClinicalTrials.gov |
| NCT02055183 | BT-010 Registry for the Evaluation of Safety and Clinical Outcomes in Patients … | — | Botulism | Completed | 2014-10-01 | 2017-07-01 | ClinicalTrials.gov |
| NCT02051062 | BT-011 Pharmacokinetics of Botulism Antitoxin Heptavalent in Pediatric Patients | Phase4 | Botulism | Enrolling_By_Invitation | 2014-10-01 | 2028-07-31 | ClinicalTrials.gov |
| NCT02061358 | Study to Determine the Safety, Tolerability and Pharmacokinetics of UV-4B Solut… | Phase1 | Viral Infection | Completed | 2014-07-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02145377 | PXVX0200 (CVD103-HgR) vs Shanchol in Mali | Phase2 | Cholera | Completed | 2014-07-01 | 2015-03-01 | ClinicalTrials.gov |
| NCT02094586 | A Phase 3 Lot to Lot Consistency Study of Live Oral Cholera Vaccine, PXVX0200 i… | Phase3 | Cholera | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT02100631 | A Study of Live Oral Cholera Vaccine, PXVX200 in Healthy Older Adults | Phase3 | Cholera | Completed | 2014-05-01 | 2015-06-01 | ClinicalTrials.gov |
| NCT01989533 | Study of Safety and Immunogenicity of HIV Vaccines in Healthy Volunteers | Phase1 | Vaccine Response | Completed | 2013-11-19 | 2019-04-08 | ClinicalTrials.gov |
| NCT01979406 | A Phase 1 Ascending Dose Study to Assess the Safety and Immunogenicity of Adeno… | Phase1 | Anthrax Infection | Completed | 2013-11-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT01895855 | Safety and Efficacy Challenge Study of Live Oral Cholera Vaccine Candidate,PXVX… | Phase3 | Cholera | Completed | 2013-09-01 | 2014-11-01 | ClinicalTrials.gov |
| NCT01770743 | A Phase 2 Safety and Immunogenicity Study for an Anthrax Vaccine Using 3 Schedu… | Phase2 | Anthrax | Completed | 2013-01-01 | 2014-12-01 | ClinicalTrials.gov |
| NCT01753115 | Ciprofloxacin BioThrax Co-Administration Study | Phase2 | Anthrax | Completed | 2012-12-01 | 2013-08-01 | ClinicalTrials.gov |
| NCT01683773 | Safety Study of Tuberculosis Vaccines AERAS-402 and MVA85A | Phase1 | Tuberculosis | Completed | 2012-09-01 | 2014-08-01 | ClinicalTrials.gov |
| NCT01653392 | BioThrax® (Anthrax) Vaccine in Pregnancy Registry | — | Pregnancy Complications | Completed | 2012-07-01 | 2020-02-01 | ClinicalTrials.gov |
| NCT01585181 | Safety and Immunogenicity of the Live Oral Cholera Vaccine Candidate PXVX0200 | Phase1 | Cholera | Completed | 2012-04-01 | 2013-01-01 | ClinicalTrials.gov |
| NCT01491607 | Immunogenicity and Safety Study of a Three-Dose BioThrax® Regimen for Post-Expo… | Phase3 | Anthrax | Completed | 2011-11-01 | 2012-05-01 | ClinicalTrials.gov |
| NCT01395082 | ACAM2000® Myopericarditis Registry | — | Myocarditis | Completed | 2011-04-01 | 2019-02-04 | ClinicalTrials.gov |
| NCT01263691 | Safety, Tolerability and Immunogenicity Study of AV7909 Anthrax Vaccine in Heal… | Phase1 | Bacillus Anthracis (Anthrax) Infection | Completed | 2010-12-01 | 2012-06-01 | ClinicalTrials.gov |
| NCT01158157 | VA-006 Vaccinia Vaccine (ACAM2000) for the Production of VIGIV | Phase3 | Smallpox Vaccine Adverse Reaction | Completed | 2010-09-13 | 2012-02-14 | ClinicalTrials.gov |
| NCT01202695 | Safety and Pharmacokinetics Study of Human Monoclonal Antibody (AVP-21D9) | Phase1 | Anthrax | Completed | 2010-08-01 | 2011-06-01 | ClinicalTrials.gov |
| NCT01006798 | Safety and Immunogenicity of Replication-Competent Adenovirus 4-vectored Vaccin… | Phase1 | Bird Flu | Completed | 2009-10-01 | 2011-09-01 | ClinicalTrials.gov |
| NCT01540929 | Post-licensure Department of Defense (DOD) Screening Accuracy Study in Military… | — | Smallpox | Completed | 2009-09-01 | 2012-09-01 | ClinicalTrials.gov |
| NCT01311674 | Hepatitis B Virus Antibody Booster Program for the Production of Hepatitis B Im… | Phase3 | Healthy Volunteers | Terminated | 2009-09-01 | 2011-03-11 | ClinicalTrials.gov |
| NCT00845650 | Safety and Pharmacokinetics Study of Anthrax Immune Globulin Intravenous (AIGIV) | Phase1 | Anthrax | Completed | 2009-02-01 | 2010-10-01 | ClinicalTrials.gov |
| NCT00928577 | Safety Surveillance Cohort Study of Vaccinia Vaccine (ACAM2000®) | — | Smallpox | Completed | 2008-12-01 | 2015-12-01 | ClinicalTrials.gov |
| NCT00927719 | Safety Surveillance Study of ACAM2000® Vaccinia Vaccine | — | Smallpox | Completed | 2008-12-01 | 2017-12-31 | ClinicalTrials.gov |
| NCT00679172 | Immunogenicity, Safety and Tolerability of the Typhoid Fever Vaccine Candidate … | Phase2 | Typhoid | Completed | 2008-05-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00634933 | Study Evaluating 2 Dosing Regimens Of TRU-015 In Rheumatoid Arthritis | Phase2 | Arthritis, Rheumatoid | Terminated | 2008-03-01 | 2012-10-01 | ClinicalTrials.gov |
| NCT00639678 | A Study to Evaluate the Safety and Tolerability of Raxibacumab in Healthy Subje… | Phase3 | Healthy | Completed | 2008-03-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00636519 | Botulism Antitoxin Effects on Paralysis Induced by Botulinum Neurotoxins in the… | Phase1 | Healthy Volunteers | Completed | 2008-02-01 | 2009-10-01 | ClinicalTrials.gov |
| NCT02016963 | An Open-label, Nonrandomized Study to Evaluate the Safety and Immunogenicity of… | Phase2 | Therapeutic Treatment of Inhalation Anthrax | Completed | 2008-01-31 | 2008-05-31 | ClinicalTrials.gov |
| NCT01374984 | VA-005 Clinical Outcomes of VIGIV Treatment of Smallpox Vaccination Complicatio… | — | Complication of Smallpox Vaccination | Enrolling_By_Invitation | 2007-08-01 | 2027-08-01 | ClinicalTrials.gov |
| NCT00448253 | Safety and Pharmacokinetic Study of Anthrax Immune Globulin Derived From Human … | Phase1 | Symptoms of Inhalational Anthrax | Completed | 2007-07-01 | 2008-09-01 | ClinicalTrials.gov |
| NCT00893516 | CD4 in Combination With CHOP in Treating Non-cutaneous Peripheral TCell Lymphoma | Phase2 | T-cell Lymphoma | Terminated | 2007-05-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00360737 | Safety Study of 7 Botulinum Antitoxin Serotypes Derived From Horses | Phase1 | Healthy | Completed | 2006-07-01 | 2010-04-01 | ClinicalTrials.gov |
| NCT00877656 | HuMax-CD4 in Non-Cutaneous T-Cell Lymphoma | Phase2 | T Cell Lymphoma | Completed | 2005-08-01 | 2008-12-01 | ClinicalTrials.gov |
| NCT00053495 | Effect of Dose, Safety, Tolerability of a New Smallpox Vaccine in Adults Withou… | Phase2 | Smallpox | Completed | 2003-01-01 | 2003-11-01 | ClinicalTrials.gov |
| NCT00053482 | Dose Study of ACAM2000 Smallpox Vaccine in Previously Vaccinated Adults | Phase2 | Smallpox | Completed | 2003-01-01 | 2003-10-01 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AV7909 | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| Placebo | Other | Phase PHASE1 | Zika Virus Infection | COMPLETED | NCT03624946 |
| Zika Virus Immune Globulin (ZIKV-IG) | Other | Phase PHASE1 | Zika Virus Infection | COMPLETED | NCT03624946 |
| Placebo | Other | Phase PHASE1 | Human Influenza | COMPLETED | NCT05155319 |
| UFluA 60 µg each antigen/dose | Other | Phase PHASE1 | Human Influenza | COMPLETED | NCT05155319 |
| UFluA 20 µg each antigen/dose | Other | Phase PHASE1 | Human Influenza | COMPLETED | NCT05155319 |
| Prednisone | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| Methylprednisolone | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| TRU-015 | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| Prednisone | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| Methylprednisolone | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| TRU-015 | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| Prednisone | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| Methylprednisolone | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| TRU-015 | Other | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| MVA85A | Other | Phase PHASE1 | Tuberculosis | COMPLETED | NCT01683773 |
| AERAS-402 | Other | Phase PHASE1 | Tuberculosis | COMPLETED | NCT01683773 |
| Raxibacumab | Other | Phase PHASE2 | Therapeutic Treatment of Inhalation Anthrax | COMPLETED | NCT02016963 |
| Placebo | Other | Phase PHASE1 | Zika Virus | COMPLETED | NCT03425149 |
| VLA1601 | Other | Phase PHASE1 | Zika Virus | COMPLETED | NCT03425149 |
| Shanchol | Other | Phase PHASE2 | Cholera | COMPLETED | NCT02145377 |
| Placebo | Other | Phase PHASE2 | Cholera | COMPLETED | NCT02145377 |
| PXVX0200 10E9 | Other | Phase PHASE2 | Cholera | COMPLETED | NCT02145377 |
| PXVX0200 10E8 | Other | Phase PHASE2 | Cholera | COMPLETED | NCT02145377 |
| gp 120 Protein Boost | Other | Phase PHASE1 | Vaccine Response | COMPLETED | NCT01989533 |
| Ad4-EnvC150 | Other | Phase PHASE1 | Vaccine Response | COMPLETED | NCT01989533 |
| Ad4-mgag | Other | Phase PHASE1 | Vaccine Response | COMPLETED | NCT01989533 |
| Placebo | Other | Phase PHASE1 | Cholera | COMPLETED | NCT01585181 |
| PXVX0200 | Other | Phase PHASE1 | Cholera | COMPLETED | NCT01585181 |
| Placebo | Other | Phase PHASE4 | Cholera (Disorder) | COMPLETED | NCT03220737 |
| VAXCHORA (Cholera Vaccine, Live, Oral) | Other | Phase PHASE4 | Cholera (Disorder) | COMPLETED | NCT03220737 |
| Placebo | Other | Phase PHASE3 | Cholera | COMPLETED | NCT02100631 |
| PXVX0200 | Other | Phase PHASE3 | Cholera | COMPLETED | NCT02100631 |
| Placebo | Other | Phase PHASE3 | Cholera | COMPLETED | NCT02094586 |
| PXVX0200 Lot C | Other | Phase PHASE3 | Cholera | COMPLETED | NCT02094586 |
| PXVX0200 Lot B | Other | Phase PHASE3 | Cholera | COMPLETED | NCT02094586 |
| PXVX0200 Lot A | Other | Phase PHASE3 | Cholera | COMPLETED | NCT02094586 |
| placebo | Other | Phase PHASE3 | Cholera | COMPLETED | NCT01895855 |
| PXVX0200 | Other | Phase PHASE3 | Cholera | COMPLETED | NCT01895855 |
| CHIKV VLP, adjuvanted | Other | Phase PHASE2 | Chikungunya Virus | COMPLETED | NCT05065983 |
| Placebo | Other | Phase PHASE2 | Chikungunya Virus Infection | COMPLETED | NCT03483961 |
| CHIKV VLP/adjuvanted | Other | Phase PHASE2 | Chikungunya Virus Infection | COMPLETED | NCT03483961 |
| CHIKV VLP/unadjuvanted | Other | Phase PHASE2 | Chikungunya Virus Infection | COMPLETED | NCT03483961 |
| Vivotif | Other | Preclinical | Typhoid Fever | COMPLETED | NCT02391909 |
| BAT | Other | Preclinical | Botulism | COMPLETED | NCT02055183 |
| Observational Intervention | Other | Preclinical | Pregnancy Complications | COMPLETED | NCT01653392 |
| Placebo | Other | Phase PHASE1 | Anthrax | COMPLETED | NCT01202695 |
| AVP-21D9 | Other | Phase PHASE1 | Anthrax | COMPLETED | NCT01202695 |
| Placebo for FLU-IGIV | Other | Phase PHASE2 | Influenza A H3N2 | COMPLETED | NCT03315104 |
| FLU-IGIV | Other | Phase PHASE2 | Influenza A H3N2 | COMPLETED | NCT03315104 |
| Teva Ad4/Ad7 Vaccine | Other | Phase PHASE1 | Adenoviral Infection | TERMINATED | NCT03160339 |
| PXVX0047 Vaccine | Other | Phase PHASE1 | Adenoviral Infection | TERMINATED | NCT03160339 |
| AIDSVAX B/E | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT02771730 |
| Placebo Comparator | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT02771730 |
| Ad4-EnvC150 | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT02771730 |
| Ad4-mgag | Other | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT02771730 |
| Placebo | Other | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B Y mg (dose to be determined) oral solution | Other | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B X mg (dose to be determined) oral solution | Other | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B 150 mg oral solution | Other | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B 75 mg oral solution | Other | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B 30 mg oral solution | Other | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| Vaccination with ACAM2000 | Other | Phase PHASE4 | Smallpox Vaccine Adverse Reaction | COMPLETED | NCT02443623 |
| Diphenhydramine | Other | Phase PHASE4 | Infections, Bacterial | COMPLETED | NCT02339155 |
| Raxibacumab | Other | Phase PHASE4 | Infections, Bacterial | COMPLETED | NCT02339155 |
| AVA | Other | Phase PHASE4 | Infections, Bacterial | COMPLETED | NCT02339155 |
| Placebo | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 1000 mg | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 720 mg | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 360 mg | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 180 mg | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 90 mg | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 30 mg | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 10 mg | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 3 mg | Other | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| Ad4-PA-GPI-1 | Other | Phase PHASE1 | Anthrax Infection | COMPLETED | NCT01979406 |
| Ad4-PA-1 | Other | Phase PHASE1 | Anthrax Infection | COMPLETED | NCT01979406 |
| AVA | Other | Phase PHASE1 | Anthrax Infection | COMPLETED | NCT01979406 |
| BioThrax | Other | Phase PHASE2 | Anthrax | COMPLETED | NCT01770743 |
| AV7909 | Other | Phase PHASE2 | Anthrax | COMPLETED | NCT01770743 |
| hepatitis B vaccine | Other | Phase PHASE3 | Healthy Volunteers | TERMINATED | NCT01311674 |
| Control | Other | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| AV7909 Formulation 4 | Other | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| AV7909 Formulation 3 | Other | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| AV7909 Formulation 2 | Other | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| AV7909 Formulation 1 | Other | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| BioThrax | Other | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| ACAM2000 | Other | Phase PHASE3 | Smallpox Vaccine Adverse Reaction | COMPLETED | NCT01158157 |
| Sanofi Pasteur Influenza Virus Vaccine, H5N1 | Other | Phase PHASE1 | Bird Flu | COMPLETED | NCT01006798 |
| Ad4-H5-Vtn | Other | Phase PHASE1 | Bird Flu | COMPLETED | NCT01006798 |
| Placebo | Other | Phase PHASE1 | Bird Flu | COMPLETED | NCT01006798 |
| BioThrax | Other | Phase PHASE3 | Anthrax | COMPLETED | NCT01491607 |
| Placebo | Other | Phase PHASE3 | Chikungunya Virus | COMPLETED | NCT05072080 |
| CHIKV VLP/adjuvant | Other | Phase PHASE3 | Chikungunya Virus | COMPLETED | NCT05072080 |
| Chikungunya | Other | Phase PHASE2 | Chikungunya | COMPLETED | NCT03992872 |
| Placebo | Other | Phase PHASE3 | Chikungunya Virus | COMPLETED | NCT05349617 |
| CHIKV VLP/adjuvant | Other | Phase PHASE3 | Chikungunya Virus | COMPLETED | NCT05349617 |
| Brincidofovir | Other | Phase PHASE1 | Smallpox | COMPLETED | NCT05935917 |
| Stabilized Isoamyl Nitrite (SIAN) | Other | Phase PHASE1 | Cyanide Poisoning | COMPLETED | NCT05194358 |
| COVID-HIG | Other | Phase PHASE1 | SARS-CoV-2 Infection | COMPLETED | NCT05142306 |
| Placebo (saline) | Other | Phase PHASE1 | COVID-19 | COMPLETED | NCT04661839 |
| COVID-HIGIV | Other | Phase PHASE1 | COVID-19 | COMPLETED | NCT04661839 |
| Ciprofloxacin | Other | Phase PHASE2 | Anthrax | COMPLETED | NCT01753115 |
| BioThrax | Other | Phase PHASE2 | Anthrax | COMPLETED | NCT01753115 |
| AV7909 | Other | Phase PHASE2 | Anthrax | COMPLETED | NCT04067011 |
| Doxycycline 100Mg Tablet | Other | Phase PHASE2 | Anthrax | COMPLETED | NCT04067011 |
| Ciprofloxacin 500Mg Tablet | Other | Phase PHASE2 | Anthrax | COMPLETED | NCT04067011 |
| VIGIV | Other | Preclinical | Complication of Smallpox Vaccination | ENROLLING_BY_INVITATION | NCT01374984 |
| Blood sample collection | Other | Phase PHASE4 | Botulism | ENROLLING_BY_INVITATION | NCT02051062 |
| 8 mg naloxone NARCAN Nasal Spray | Other | Phase PHASE1 | Opioid Overdose | COMPLETED | NCT05377255 |
| 16 mg naloxone AP003 | Other | Phase PHASE1 | Opioid Overdose | COMPLETED | NCT05377255 |
| Collection of samples | BIOLOGICAL | Preclinical | Infections, Bacterial | NOT_YET_RECRUITING | NCT07478471 |
| CYFENDUS | BIOLOGICAL | Preclinical | Anthrax | NOT_YET_RECRUITING | NCT07268612 |
| Brincidofovir | DRUG | Phase PHASE1 | Smallpox | COMPLETED | NCT05935917 |
| Stabilized Isoamyl Nitrite (SIAN) | DRUG | Phase PHASE1 | Cyanide Poisoning | COMPLETED | NCT05194358 |
| UFluA 60 µg each antigen/dose | BIOLOGICAL | Phase PHASE1 | Human Influenza | COMPLETED | NCT05155319 |
| UFluA 20 µg each antigen/dose | BIOLOGICAL | Phase PHASE1 | Human Influenza | COMPLETED | NCT05155319 |
| COVID-HIG | BIOLOGICAL | Phase PHASE1 | SARS-CoV-2 Infection | COMPLETED | NCT05142306 |
| CHIKV VLP/adjuvant | BIOLOGICAL | Phase PHASE3 | Chikungunya Virus | COMPLETED | NCT05349617 |
| CHIKV VLP, adjuvanted | BIOLOGICAL | Phase PHASE2 | Chikungunya Virus | COMPLETED | NCT05065983 |
| Placebo (saline) | OTHER | Phase PHASE1 | COVID-19 | COMPLETED | NCT04661839 |
| COVID-HIGIV | BIOLOGICAL | Phase PHASE1 | COVID-19 | COMPLETED | NCT04661839 |
| Doxycycline 100Mg Tablet | DRUG | Phase PHASE2 | Anthrax | COMPLETED | NCT04067011 |
| Ciprofloxacin 500Mg Tablet | DRUG | Phase PHASE2 | Anthrax | COMPLETED | NCT04067011 |
| Chikungunya | BIOLOGICAL | Phase PHASE2 | Chikungunya | COMPLETED | NCT03992872 |
| Zika Virus Immune Globulin (ZIKV-IG) | BIOLOGICAL | Phase PHASE1 | Zika Virus Infection | COMPLETED | NCT03624946 |
| AIGIV | DRUG | Preclinical | Inhalational Anthrax | NOT_YET_RECRUITING | NCT03569553 |
| CHIKV VLP/adjuvanted | BIOLOGICAL | Phase PHASE2 | Chikungunya Virus Infection | COMPLETED | NCT03483961 |
| CHIKV VLP/unadjuvanted | BIOLOGICAL | Phase PHASE2 | Chikungunya Virus Infection | COMPLETED | NCT03483961 |
| VLA1601 | BIOLOGICAL | Phase PHASE1 | Zika Virus | COMPLETED | NCT03425149 |
| Placebo for FLU-IGIV | OTHER | Phase PHASE2 | Influenza A H3N2 | COMPLETED | NCT03315104 |
| FLU-IGIV | BIOLOGICAL | Phase PHASE2 | Influenza A H3N2 | COMPLETED | NCT03315104 |
| VAXCHORA (Cholera Vaccine, Live, Oral) | BIOLOGICAL | Phase PHASE4 | Cholera (Disorder) | COMPLETED | NCT03220737 |
| Teva Ad4/Ad7 Vaccine | BIOLOGICAL | Phase PHASE1 | Adenoviral Infection | TERMINATED | NCT03160339 |
| PXVX0047 Vaccine | BIOLOGICAL | Phase PHASE1 | Adenoviral Infection | TERMINATED | NCT03160339 |
| AIDSVAX B/E | BIOLOGICAL | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT02771730 |
| Placebo Comparator | OTHER | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT02771730 |
| UV-4B Y mg (dose to be determined) oral solution | DRUG | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B X mg (dose to be determined) oral solution | DRUG | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B 150 mg oral solution | DRUG | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B 75 mg oral solution | DRUG | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| UV-4B 30 mg oral solution | DRUG | Phase PHASE1 | Viral Infection | TERMINATED | NCT02696291 |
| Vaccination with ACAM2000 | BIOLOGICAL | Phase PHASE4 | Smallpox Vaccine Adverse Reaction | COMPLETED | NCT02443623 |
| Vivotif | BIOLOGICAL | Preclinical | Typhoid Fever | COMPLETED | NCT02391909 |
| Diphenhydramine | DRUG | Phase PHASE4 | Infections, Bacterial | COMPLETED | NCT02339155 |
| Sample Collection | BIOLOGICAL | Phase PHASE4 | Infections, Bacterial | NOT_YET_RECRUITING | NCT02177721 |
| Shanchol | BIOLOGICAL | Phase PHASE2 | Cholera | COMPLETED | NCT02145377 |
| PXVX0200 10E9 | BIOLOGICAL | Phase PHASE2 | Cholera | COMPLETED | NCT02145377 |
| PXVX0200 10E8 | BIOLOGICAL | Phase PHASE2 | Cholera | COMPLETED | NCT02145377 |
| PXVX0200 Lot C | BIOLOGICAL | Phase PHASE3 | Cholera | COMPLETED | NCT02094586 |
| PXVX0200 Lot B | BIOLOGICAL | Phase PHASE3 | Cholera | COMPLETED | NCT02094586 |
| PXVX0200 Lot A | BIOLOGICAL | Phase PHASE3 | Cholera | COMPLETED | NCT02094586 |
| UV-4B 1000 mg | DRUG | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 720 mg | DRUG | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 360 mg | DRUG | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 180 mg | DRUG | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 90 mg | DRUG | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 30 mg | DRUG | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 10 mg | DRUG | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| UV-4B 3 mg | DRUG | Phase PHASE1 | Viral Infection | COMPLETED | NCT02061358 |
| BAT | DRUG | Preclinical | Botulism | COMPLETED | NCT02055183 |
| Blood sample collection | BIOLOGICAL | Phase PHASE4 | Botulism | ENROLLING_BY_INVITATION | NCT02051062 |
| Raxibacumab | BIOLOGICAL | Phase PHASE4 | Infections, Bacterial | COMPLETED | NCT02339155 |
| gp 120 Protein Boost | BIOLOGICAL | Phase PHASE1 | Vaccine Response | COMPLETED | NCT01989533 |
| Ad4-EnvC150 | BIOLOGICAL | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT02771730 |
| Ad4-mgag | BIOLOGICAL | Phase PHASE1 | Healthy Volunteer | TERMINATED | NCT02771730 |
| Ad4-PA-GPI-1 | BIOLOGICAL | Phase PHASE1 | Anthrax Infection | COMPLETED | NCT01979406 |
| Ad4-PA-1 | BIOLOGICAL | Phase PHASE1 | Anthrax Infection | COMPLETED | NCT01979406 |
| AVA | BIOLOGICAL | Phase PHASE4 | Infections, Bacterial | COMPLETED | NCT02339155 |
| AV7909 | BIOLOGICAL | Phase PHASE2 | Anthrax | COMPLETED | NCT04067011 |
| Ciprofloxacin | DRUG | Phase PHASE2 | Anthrax | COMPLETED | NCT01753115 |
| MVA85A | BIOLOGICAL | Phase PHASE1 | Tuberculosis | COMPLETED | NCT01683773 |
| AERAS-402 | BIOLOGICAL | Phase PHASE1 | Tuberculosis | COMPLETED | NCT01683773 |
| Observational Intervention | BIOLOGICAL | Preclinical | Pregnancy Complications | COMPLETED | NCT01653392 |
| PXVX0200 | BIOLOGICAL | Phase PHASE3 | Cholera | COMPLETED | NCT02100631 |
| VIGIV | BIOLOGICAL | Preclinical | Complication of Smallpox Vaccination | ENROLLING_BY_INVITATION | NCT01374984 |
| hepatitis B vaccine | BIOLOGICAL | Phase PHASE3 | Healthy Volunteers | TERMINATED | NCT01311674 |
| Control | DRUG | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| AV7909 Formulation 4 | BIOLOGICAL | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| AV7909 Formulation 3 | BIOLOGICAL | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| AV7909 Formulation 2 | BIOLOGICAL | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| AV7909 Formulation 1 | BIOLOGICAL | Phase PHASE1 | Bacillus Anthracis (Anthrax) Infection | COMPLETED | NCT01263691 |
| BioThrax | BIOLOGICAL | Phase PHASE3 | Anthrax | COMPLETED | NCT03877926 |
| AVP-21D9 | DRUG | Phase PHASE1 | Anthrax | COMPLETED | NCT01202695 |
| ACAM2000 | BIOLOGICAL | Phase PHASE3 | Smallpox Vaccine Adverse Reaction | COMPLETED | NCT01158157 |
| Sanofi Pasteur Influenza Virus Vaccine, H5N1 | BIOLOGICAL | Phase PHASE1 | Bird Flu | COMPLETED | NCT01006798 |
| Ad4-H5-Vtn | BIOLOGICAL | Phase PHASE1 | Bird Flu | COMPLETED | NCT01006798 |
| Placebo | BIOLOGICAL | Phase PHASE3 | Chikungunya Virus | COMPLETED | NCT05349617 |
| ACAM2000® smallpox vaccine | BIOLOGICAL | Preclinical | Smallpox | COMPLETED | NCT00927719 |
| CHOP | DRUG | Phase PHASE2 | T-cell Lymphoma | TERMINATED | NCT00893516 |
| CHOP + CD4 | BIOLOGICAL | Phase PHASE2 | T-cell Lymphoma | TERMINATED | NCT00893516 |
| HuMax-CD4 | BIOLOGICAL | Phase PHASE2 | T Cell Lymphoma | COMPLETED | NCT00877656 |
| Gamunex 360 mg/kg | BIOLOGICAL | Phase PHASE1 | Anthrax | COMPLETED | NCT00845650 |
| AIGIV 14.0 mg/kg | BIOLOGICAL | Phase PHASE1 | Anthrax | COMPLETED | NCT00845650 |
| Gamunex 180 mg/kg | BIOLOGICAL | Phase PHASE1 | Anthrax | COMPLETED | NCT00845650 |
| AIGIV 7.0 mg/kg | BIOLOGICAL | Phase PHASE1 | Anthrax | COMPLETED | NCT00845650 |
| Gamunex 90 mg/kg | BIOLOGICAL | Phase PHASE1 | Anthrax | COMPLETED | NCT00845650 |
| AIGIV 3.5 mg/kg | BIOLOGICAL | Phase PHASE1 | Anthrax | COMPLETED | NCT00845650 |
| Placebo (Cohorts 1-4 pooled) | OTHER | Phase PHASE2 | Typhoid | COMPLETED | NCT00679172 |
| Dose of of 1.7 x 10^10 CFU (Cohort 4) | BIOLOGICAL | Phase PHASE2 | Typhoid | COMPLETED | NCT00679172 |
| Dose of 1.1 x 10^10 CFU (Cohort 3) | BIOLOGICAL | Phase PHASE2 | Typhoid | COMPLETED | NCT00679172 |
| Dose of 7.5 x 10^9 CFU (Cohort 2) | BIOLOGICAL | Phase PHASE2 | Typhoid | COMPLETED | NCT00679172 |
| Dose of 5.0 x 10^9 CFU (Cohort 1) | BIOLOGICAL | Phase PHASE2 | Typhoid | COMPLETED | NCT00679172 |
| raxibacumab | DRUG | Phase PHASE3 | Healthy | COMPLETED | NCT00639678 |
| placebo | BIOLOGICAL | Phase PHASE3 | Cholera | COMPLETED | NCT01895855 |
| Botulism Antitoxin Heptavalent (Equine) Types A-G | BIOLOGICAL | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00636519 |
| Botulism Antitoxin Bivalent (Equine) Types A and B | BIOLOGICAL | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT00636519 |
| Prednisone | DRUG | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| Methylprednisolone | DRUG | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| TRU-015 | DRUG | Phase PHASE2 | Arthritis, Rheumatoid | TERMINATED | NCT00634933 |
| NP-015 | BIOLOGICAL | Phase PHASE1 | Symptoms of Inhalational Anthrax | COMPLETED | NCT00448253 |
| Botulinum Antitoxin Heptavalent (A B C D E F G) - (EQUINE) | BIOLOGICAL | Phase PHASE1 | Healthy | COMPLETED | NCT00360737 |
| vaccinia virus (calf lymph): Dryvax | BIOLOGICAL | Phase PHASE2 | Smallpox | COMPLETED | NCT00053495 |
| Vaccinia virus: ACAM2000 smallpox vaccine | BIOLOGICAL | Phase PHASE2 | Smallpox | COMPLETED | NCT00053495 |
| Vaccinia virus (calf lymph) smallpox vaccine: Dryvax® | BIOLOGICAL | Phase PHASE2 | Smallpox | COMPLETED | NCT00053482 |
| ACAM2000 Smallpox Vaccine | BIOLOGICAL | Phase PHASE2 | Smallpox | COMPLETED | NCT00053482 |