| Symbol | AKBA |
|---|---|
| Name | AKEBIA THERAPEUTICS, INC. |
| Sector | HEALTH CARE |
| Region | North America |
| Industry | Biotechnology: Pharmaceutical Preparations |
| Address | 245 FIRST STREET,SUITE 1100, CAMBRIDGE, Massachusetts, 02142, United States |
| Telephone | +1 617 871-2098 |
| Fax | — |
| — | |
| Website | https://www.akebia.com |
| Incorporation | UNDEFINED |
| Incorporated On | — |
| Employees | — |
| Fiscal Year | — |
| Public Since | — |
| Exchanges | NASDAQ |
| Auditor | — |
| Audit Status | NOT PROVIDED |
| Reporting Status | — |
| CIK | 0001517022 |
| Description | Akebia Therapeutics Inc is a biopharmaceutical company. It focuses on the development and commercialization of novel therapeutics to patients with kidney disease through hypoxia-inducible factor (HIF) biology. Its lead product candidate is Vadadustat, an oral therapy, which is used for the treatment of anemia related to chronic kidney disease in non-dialysis and dialysis patients. The company is also developing a HIF-based portfolio of product for the treatment of anemia. Geographically, all the business activity is functioned through the region of United States. Additional info from NASDAQ: |
Butler John P. 🟡 adjusted position in 0 shares (1 derivative) of Akebia Therapeutics, Inc. (AKBA) at $0.63 Transaction Date: Aug 06, 2026 | Filing ID: 000004
Read moreAkebia Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Read moreAkebia Therapeutics Announces Initiation of a Phase 2 Basket Trial to Study Ebribafusp, a Next-Generation Complement Inhibitor in Rare Kidney Diseases
Read moreAkebia Therapeutics to Report Second Quarter 2026 Financial Results and Discuss Recent Business Highlights
Read moreAkebia Therapeutics Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Read more(99% Positive) AKEBIA THERAPEUTICS, INC. (AKBA) Announces Clinical Development Update
Read more📋 Ostrowski Erik (Officer) plans to sell 56K shares of Akebia Therapeutics, Inc. (at $1.11 each, total $62K) Filed: Jun 29, 2026 | ID: 000044
Read moreWolf Myles 🟢 acquired 89.3K shares (1 derivative) of Akebia Therapeutics, Inc. (AKBA) at $1.02 Transaction Date: Jun 17, 2026 | Filing ID: 000001
Read moreSmith Cynthia 🟢 acquired 89.3K shares (1 derivative) of Akebia Therapeutics, Inc. (AKBA) at $1.02 Transaction Date: Jun 17, 2026 | Filing ID: 000003
Read moreROGERS MICHAEL W 🟢 acquired 89.3K shares (1 derivative) of Akebia Therapeutics, Inc. (AKBA) at $1.02 Transaction Date: Jun 17, 2026 | Filing ID: 000001
Read more| Trial ID | Title | Phase | Indication | Status | Start Date | Completion Date | Source |
|---|---|---|---|---|---|---|---|
| NCT06419205 | A Phase 2 Study to Evaluate the Safety, PD, PK, and Clinical Activity of ADX-09… | Phase2 | IgA Nephropathy | Recruiting | 2026-07-30 | 2028-02-01 | ClinicalTrials.gov |
| NCT07565701 | Safety and Efficacy of a Phased Transition From Epogen to Three Times Weekly Or… | Phase3 | Anemia Associated With Chronic Kidney Disease | Not_Yet_Recruiting | 2026-04-01 | 2027-06-01 | ClinicalTrials.gov |
| NCT07429006 | SAD and MAD Study of AKB-9090 in Healthy Adult Participants | Phase1 | Healthy Volunteers | Recruiting | 2026-03-16 | 2026-12-01 | ClinicalTrials.gov |
| NCT07268638 | A Study of Praliciguat in Participants With Focal Segmental Glomerulosclerosis … | Phase2 | Focal Segmental Glomerulosclerosis | Recruiting | 2025-12-03 | 2028-01-01 | ClinicalTrials.gov |
| NCT07086755 | Vadadustat for the Treatment of Nonintubated Acute Respiratory Distress Syndrom… | Phase2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | Recruiting | 2025-10-23 | 2031-05-31 | ClinicalTrials.gov |
| NCT06901505 | To Evaluate the Efficacy of Three Times Weekly (TIW) Vadadustat Compared to Sta… | Phase3 | Anemia of Chronic Kidney Disease | Completed | 2025-07-24 | 2026-08-12 | ClinicalTrials.gov |
| NCT05082584 | Study to Evaluate the Safety and Efficacy of Oral Vadadustat in Pediatric Parti… | Phase3 | Anemia of Chronic Kidney Disease | Withdrawn | 2025-01-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT05082571 | Study to Evaluate the Safety and Efficacy of Oral Vadadustat in Pediatric Parti… | Phase3 | Anemia of Chronic Kidney Disease | Withdrawn | 2025-01-01 | 2026-10-01 | ClinicalTrials.gov |
| NCT06520826 | Vafseo Outcomes In-Center Experience | Phase3 | Anemia of Chronic Kidney Disease | Active_Not_Recruiting | 2024-11-20 | 2026-06-30 | ClinicalTrials.gov |
| NCT05085275 | Ferric Citrate for the Prevention of Renal Failure in Adults With Advanced Chro… | Phase3 | Anemia, Iron Deficiency | Completed | 2022-03-30 | 2024-01-24 | ClinicalTrials.gov |
| NCT04922645 | Auryxia (Ferric Citrate) Therapy for In-Center and Home Dialysis Participants | Phase4 | Hyperphosphatemia | Completed | 2021-06-29 | 2022-09-15 | ClinicalTrials.gov |
| NCT04707768 | Study Evaluating the Efficacy and Safety of Dose Conversion From a Long-acting … | Phase3 | Anemia Associated With Chronic Kidney Disease (CKD) | Completed | 2021-06-18 | 2023-01-30 | ClinicalTrials.gov |
| NCT04478071 | Vadadustat for the Prevention and Treatment of Acute Respiratory Distress Syndr… | Phase2 | Acute Respiratory Distress Syndrome | Completed | 2020-08-22 | 2022-03-25 | ClinicalTrials.gov |
| NCT04299633 | Study in Healthy Adult Subjects to Assess the Effect of Phosphate Binders on th… | Phase1 | Healthy Volunteers | Completed | 2020-06-15 | 2020-09-28 | ClinicalTrials.gov |
| NCT04313153 | Trial Evaluating the Efficacy and Safety of Oral Vadadustat Once Daily (QD) and… | Phase3 | Anemia | Completed | 2020-05-27 | 2022-06-22 | ClinicalTrials.gov |
| NCT03992066 | Study to Evaluate the Pharmacokinetics, Pharmacodynamics, and Safety of Vadadus… | Phase1 | Anemia Associated With Chronic Kidney Disease | Completed | 2019-05-28 | 2020-07-15 | ClinicalTrials.gov |
| NCT03799627 | Study of Vadadustat in Hemodialysis Participants With Anemia Switching From Epo… | Phase2 | Anemia | Completed | 2019-01-31 | 2020-07-15 | ClinicalTrials.gov |
| NCT03789032 | Study to Evaluate the Effect of Rabeprazole on the Pharmacokinetics of Vadadust… | Phase1 | Drug Interaction Potentiation | Completed | 2018-10-03 | 2018-11-19 | ClinicalTrials.gov |
| NCT03657290 | A Study in Evaluating Bioequivalence of Test and Reference Vadadustat 450 MG an… | Phase1 | Healthy | Completed | 2018-08-03 | 2018-10-16 | ClinicalTrials.gov |
| NCT03801759 | Drug-Drug Interaction Study of Vadadustat With Digoxin, Adefovir and Furosemide | Phase1 | Drug Interaction Potentiation | Completed | 2018-07-20 | 2018-09-30 | ClinicalTrials.gov |
| NCT03801746 | Drug-Drug Interaction Study of Vadadustat With Cyclosporine, Probenecid and Rif… | Phase1 | Drug Interaction Potentiation | Completed | 2018-07-20 | 2018-08-15 | ClinicalTrials.gov |
| NCT03801733 | Drug-Drug Interaction Study of Vadadustat With Rosuvastatin, Sulfasalazine, Pra… | Phase1 | Drug Interaction Potentiation | Completed | 2018-06-17 | 2018-11-24 | ClinicalTrials.gov |
| NCT03799848 | A Single Dose Study of Oral Vadadustat in Subjects With Normal and Impaired Hep… | Phase1 | Hepatic Impairment | Completed | 2018-06-12 | 2018-10-18 | ClinicalTrials.gov |
| NCT03639155 | A Study in Evaluating Bioequivalence Between Test and Reference Formulations of… | Phase1 | Healthy | Completed | 2018-04-12 | 2018-05-23 | ClinicalTrials.gov |
| NCT03242967 | Study to Evaluate Three Times Per Week (TIW) Oral Dosing of Vadadustat for Anem… | Phase3 | Anemia | Withdrawn | 2017-08-01 | 2018-02-12 | ClinicalTrials.gov |
| NCT03140722 | Study to Evaluate Vadadustat for Anemia in Subjects With Dialysis-Dependent Chr… | Phase2 | Anemia | Terminated | 2017-05-02 | 2018-03-21 | ClinicalTrials.gov |
| NCT03054350 | Dose-Finding Study of Vadadustat in Japanese Subjects With Anemia Secondary to … | Phase2 | Anemia | Completed | 2016-12-01 | 2018-01-24 | ClinicalTrials.gov |
| NCT03054337 | Dose-Finding Study of Vadadustat in Japanese Subjects With Anemia Secondary to … | Phase2 | Anemia | Completed | 2016-10-01 | 2017-08-28 | ClinicalTrials.gov |
| NCT02892149 | Efficacy and Safety Study to Evaluate Vadadustat for the Maintenance Treatment … | Phase3 | Anemia | Completed | 2016-08-01 | 2020-03-30 | ClinicalTrials.gov |
| NCT02865850 | Efficacy and Safety Study to Evaluate Vadadustat for the Correction or Maintena… | Phase3 | Anemia | Completed | 2016-07-01 | 2020-03-30 | ClinicalTrials.gov |
| NCT02680574 | Efficacy and Safety Study to Evaluate Vadadustat for the Maintenance Treatment … | Phase3 | Anemia | Completed | 2016-02-01 | 2020-07-31 | ClinicalTrials.gov |
| NCT02648347 | Study to Evaluate Vadadustat for the Correction of Anemia in Participants With … | Phase3 | Anemia | Completed | 2015-12-01 | 2020-07-31 | ClinicalTrials.gov |
| NCT02502500 | Effect of AKB-6548 on the Pharmacokinetics of Celecoxib | Phase1 | Healthy Volunteers | Completed | 2015-07-01 | 2015-09-01 | ClinicalTrials.gov |
| NCT02412449 | Relative Bioavailability of Two Formulations of AKB-6548 and the Food Effect of… | Phase1 | Healthy | Completed | 2015-04-01 | 2015-04-01 | ClinicalTrials.gov |
| NCT02327546 | Effects of Ferrous Sulfate on the Pharmacokinetics of AKB-6548 | Phase1 | Healthy Volunteers | Completed | 2014-12-01 | 2015-02-01 | ClinicalTrials.gov |
| NCT02260193 | 16-Week Repeat Oral Dose Study of AKB-6548 for Anemia in Participants With End … | Phase2 | Anemia | Completed | 2014-09-10 | 2015-07-22 | ClinicalTrials.gov |
| NCT02062203 | Effect of AKB-6548 on Cardiac Repolarization Intervals in Healthy Volunteers | Phase1 | Healthy Volunteers | Completed | 2014-01-01 | 2014-04-01 | ClinicalTrials.gov |
| NCT01906489 | 20-Week Repeat Oral Dose Study of AKB-6548 in Participants With Chronic Kidney … | Phase2 | Anemia | Completed | 2013-07-23 | 2014-09-03 | ClinicalTrials.gov |
| NCT01381094 | 42-Day Repeat Oral Dose Study of AKB-6548 in Participants With Chronic Kidney D… | Phase2 | Anemia | Completed | 2011-06-15 | 2012-02-16 | ClinicalTrials.gov |
| NCT01235936 | Safety and Efficacy Study for AKB-6548 in Participants With Chronic Kidney Dise… | Phase2 | Anemia | Completed | 2010-10-21 | 2011-05-01 | ClinicalTrials.gov |
| NCT04707573 | Study to Assess the Safety and Pharmacokinetics of AKB-6548 in Participants Wit… | Phase2 | Chronic Kidney Disease | Completed | 2010-07-08 | 2010-09-24 | ClinicalTrials.gov |
| Product Name | Type | Development Stage | Therapeutic Area | Study Status | Trial ID |
|---|---|---|---|---|---|
| Vadadustat | Other | Phase PHASE3 | Anemia of Chronic Kidney Disease | COMPLETED | NCT06901505 |
| Erythropoiesis-Stimulating Agent (ESA) | Other | Phase PHASE3 | Anemia of Chronic Kidney Disease | COMPLETED | NCT06901505 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | RECRUITING | NCT07086755 |
| Vadadustat 1200mg | Other | Phase PHASE2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | RECRUITING | NCT07086755 |
| Vadadustat 900mg | Other | Phase PHASE2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | RECRUITING | NCT07086755 |
| ADX-097 | Other | Phase PHASE2 | IgA Nephropathy | RECRUITING | NCT06419205 |
| ADX-097 | Other | Phase PHASE2 | IgA Nephropathy | NOT_YET_RECRUITING | NCT06419205 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Epoetin alga (Epogen)/vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease | NOT_YET_RECRUITING | NCT07565701 |
| Epoetin alga (Epogen)/vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease | NOT_YET_RECRUITING | NCT07565701 |
| Epoetin alga (Epogen)/vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease | NOT_YET_RECRUITING | NCT07565701 |
| Epoetin alga (Epogen)/vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease | NOT_YET_RECRUITING | NCT07565701 |
| Epoetin alga (Epogen)/vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease | NOT_YET_RECRUITING | NCT07565701 |
| Epoetin alga (Epogen)/vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease | NOT_YET_RECRUITING | NCT07565701 |
| Epoetin alga (Epogen)/vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease | NOT_YET_RECRUITING | NCT07565701 |
| Epoetin alga (Epogen)/vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease | NOT_YET_RECRUITING | NCT07565701 |
| Placebo | Other | Phase PHASE2 | Anemia | COMPLETED | NCT03054350 |
| Vadadustat | Other | Phase PHASE2 | Anemia | COMPLETED | NCT03054350 |
| Placebo | Other | Phase PHASE2 | Anemia | COMPLETED | NCT03054337 |
| Vadadustat | Other | Phase PHASE2 | Anemia | COMPLETED | NCT03054337 |
| Vadadustat | Other | Phase PHASE2 | Chronic Kidney Disease | COMPLETED | NCT04707573 |
| Placebo | Other | Phase PHASE2 | Anemia | COMPLETED | NCT01381094 |
| AKB-6548 | Other | Phase PHASE2 | Anemia | COMPLETED | NCT01381094 |
| AKB-6548 | Other | Phase PHASE2 | Anemia | COMPLETED | NCT01235936 |
| Darbepoetin alfa | Other | Phase PHASE3 | Anemia | WITHDRAWN | NCT03242967 |
| Vadadustat | Other | Phase PHASE3 | Anemia | WITHDRAWN | NCT03242967 |
| AKB-6548 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02502500 |
| Celecoxib | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02502500 |
| AKB-6548 tablet, test formulation given in the fed state | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02412449 |
| AKB-6548 tablet, test formulation given in the fasted state. | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02412449 |
| AKB-6548 tablet, reference formulation given in the fasted state | Other | Phase PHASE1 | Healthy | COMPLETED | NCT02412449 |
| Ferrous Sulfate | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02327546 |
| AKB-6548 | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02327546 |
| Moxifloxacin | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02062203 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02062203 |
| AKB-6548 (supratherapeutic dose) | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02062203 |
| AKB-6548 (therapeutic dose) | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02062203 |
| Digoxin | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801759 |
| Adefovir | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801759 |
| Furosemide | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801759 |
| Vadadustat | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801759 |
| Cyclosporins | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801746 |
| Probenecid | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801746 |
| Rifampin | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801746 |
| vadadustat | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801746 |
| Sulfasalazine | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Pravastatin | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Atorvastatin | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Rosuvastatin | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Simvastatin | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Vadadustat | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Vadadustat | Other | Phase PHASE1 | Hepatic Impairment | COMPLETED | NCT03799848 |
| Rabeprazole | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03789032 |
| Vadadustat | Other | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03789032 |
| vadadustat | Other | Phase PHASE1 | Healthy | COMPLETED | NCT03657290 |
| vadadustat test tablets | Other | Phase PHASE1 | Healthy | COMPLETED | NCT03639155 |
| vadadustat reference tablets | Other | Phase PHASE1 | Healthy | COMPLETED | NCT03639155 |
| Epoetin alfa | Other | Phase PHASE1 | Anemia Associated With Chronic Kidney Disease | COMPLETED | NCT03992066 |
| Darbepoetin alfa | Other | Phase PHASE1 | Anemia Associated With Chronic Kidney Disease | COMPLETED | NCT03992066 |
| Vadadustat | Other | Phase PHASE1 | Anemia Associated With Chronic Kidney Disease | COMPLETED | NCT03992066 |
| Auryxia® | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT04299633 |
| Calcium acetate | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT04299633 |
| Sevelamer carbonate | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT04299633 |
| Vadadustat | Other | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT04299633 |
| epoetin alfa | Other | Phase PHASE2 | Anemia | TERMINATED | NCT03140722 |
| vadadustat | Other | Phase PHASE2 | Anemia | TERMINATED | NCT03140722 |
| Darbepoetin alfa | Other | Phase PHASE3 | Anemia | COMPLETED | NCT02680574 |
| Vadadustat | Other | Phase PHASE3 | Anemia | COMPLETED | NCT02680574 |
| Darbepoetin alfa | Other | Phase PHASE3 | Anemia | COMPLETED | NCT02648347 |
| Vadadustat | Other | Phase PHASE3 | Anemia | COMPLETED | NCT02648347 |
| Darbepoetin alfa | Other | Phase PHASE3 | Anemia | COMPLETED | NCT02892149 |
| Vadadustat | Other | Phase PHASE3 | Anemia | COMPLETED | NCT02892149 |
| AKB-6548 | Other | Phase PHASE2 | Anemia | COMPLETED | NCT02260193 |
| Darbepoetin alfa | Other | Phase PHASE3 | Anemia | COMPLETED | NCT02865850 |
| Vadadustat | Other | Phase PHASE3 | Anemia | COMPLETED | NCT02865850 |
| Placebo | Other | Phase PHASE2 | Anemia | COMPLETED | NCT01906489 |
| AKB-6548 | Other | Phase PHASE2 | Anemia | COMPLETED | NCT01906489 |
| Vadadustat TIW | Other | Phase PHASE2 | Anemia | COMPLETED | NCT03799627 |
| Epoetin Alfa | Other | Phase PHASE2 | Anemia | COMPLETED | NCT03799627 |
| Vadadustat | Other | Phase PHASE2 | Anemia | COMPLETED | NCT03799627 |
| Standard of care phosphate-lowering therapy | Drug | Phase PHASE4 | Hyperphosphatemia | COMPLETED | NCT04922645 |
| Ferric Citrate 1 gram Oral Tablet | Other | Phase PHASE4 | Hyperphosphatemia | COMPLETED | NCT04922645 |
| Mircera® | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease (CKD) | COMPLETED | NCT04707768 |
| Vadadustat | Other | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease (CKD) | COMPLETED | NCT04707768 |
| placebo | Other | Phase PHASE2 | Acute Respiratory Distress Syndrome | COMPLETED | NCT04478071 |
| vadadustat | Other | Phase PHASE2 | Acute Respiratory Distress Syndrome | COMPLETED | NCT04478071 |
| Darbepoetin alfa | Other | Phase PHASE3 | Anemia | COMPLETED | NCT04313153 |
| Vadadustat | Other | Phase PHASE3 | Anemia | COMPLETED | NCT04313153 |
| Placebo | Other | Phase PHASE3 | Anemia, Iron Deficiency | COMPLETED | NCT05085275 |
| Ferric Citrate 1 GM Oral Tablet [AURYXIA] | Other | Phase PHASE3 | Anemia, Iron Deficiency | COMPLETED | NCT05085275 |
| Erythropoiesis Stimulating Agent | Other | Phase PHASE3 | Anemia of Chronic Kidney Disease | ACTIVE_NOT_RECRUITING | NCT06520826 |
| Vadadustat | Other | Phase PHASE3 | Anemia of Chronic Kidney Disease | ACTIVE_NOT_RECRUITING | NCT06520826 |
| Vadadustat | Other | Phase PHASE3 | Anemia of Chronic Kidney Disease | WITHDRAWN | NCT05082584 |
| vadadustat | Other | Phase PHASE3 | Anemia of Chronic Kidney Disease | WITHDRAWN | NCT05082571 |
| Placebo | Other | Phase PHASE2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | RECRUITING | NCT07086755 |
| Vadadustat 1200mg | Other | Phase PHASE2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | RECRUITING | NCT07086755 |
| Vadadustat 900mg | Other | Phase PHASE2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | RECRUITING | NCT07086755 |
| Vadadustat | Other | Phase PHASE3 | Anemia of Chronic Kidney Disease | ACTIVE_NOT_RECRUITING | NCT06901505 |
| Erythropoiesis-Stimulating Agent (ESA) | Other | Phase PHASE3 | Anemia of Chronic Kidney Disease | ACTIVE_NOT_RECRUITING | NCT06901505 |
| Placebo | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07429006 |
| AKB-9090 | Other | Phase PHASE1 | Healthy Volunteers | RECRUITING | NCT07429006 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Placebo | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Praliciguat | Other | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| AKB-9090 | DRUG | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07429006 |
| Praliciguat | DRUG | Phase PHASE2 | Focal Segmental Glomerulosclerosis | RECRUITING | NCT07268638 |
| Vadadustat 1200mg | DRUG | Phase PHASE2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | RECRUITING | NCT07086755 |
| Vadadustat 900mg | DRUG | Phase PHASE2 | Nonintubated Acute Respiratory Distress Syndrome (ARDS) | RECRUITING | NCT07086755 |
| Erythropoiesis-Stimulating Agent (ESA) | DRUG | Phase PHASE3 | Anemia of Chronic Kidney Disease | ACTIVE_NOT_RECRUITING | NCT06901505 |
| Erythropoiesis Stimulating Agent | DRUG | Phase PHASE3 | Anemia of Chronic Kidney Disease | ACTIVE_NOT_RECRUITING | NCT06520826 |
| Ferric Citrate 1 GM Oral Tablet [AURYXIA] | DRUG | Phase PHASE3 | Anemia, Iron Deficiency | COMPLETED | NCT05085275 |
| Standard of care phosphate-lowering therapy | DRUG | Phase PHASE4 | Hyperphosphatemia | COMPLETED | NCT04922645 |
| Ferric Citrate 1 gram Oral Tablet | DRUG | Phase PHASE4 | Hyperphosphatemia | COMPLETED | NCT04922645 |
| Mircera® | DRUG | Phase PHASE3 | Anemia Associated With Chronic Kidney Disease (CKD) | COMPLETED | NCT04707768 |
| placebo | DRUG | Phase PHASE2 | Acute Respiratory Distress Syndrome | COMPLETED | NCT04478071 |
| Auryxia® | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT04299633 |
| Calcium acetate | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT04299633 |
| Sevelamer carbonate | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT04299633 |
| Epoetin alfa | DRUG | Phase PHASE1 | Anemia Associated With Chronic Kidney Disease | COMPLETED | NCT03992066 |
| Digoxin | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801759 |
| Adefovir | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801759 |
| Furosemide | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801759 |
| Cyclosporins | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801746 |
| Probenecid | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801746 |
| Rifampin | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801746 |
| Sulfasalazine | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Pravastatin | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Atorvastatin | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Rosuvastatin | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Simvastatin | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03801733 |
| Vadadustat TIW | DRUG | Phase PHASE2 | Anemia | COMPLETED | NCT03799627 |
| Epoetin Alfa | DRUG | Phase PHASE2 | Anemia | COMPLETED | NCT03799627 |
| Rabeprazole | DRUG | Phase PHASE1 | Drug Interaction Potentiation | COMPLETED | NCT03789032 |
| vadadustat test tablets | DRUG | Phase PHASE1 | Healthy | COMPLETED | NCT03639155 |
| vadadustat reference tablets | DRUG | Phase PHASE1 | Healthy | COMPLETED | NCT03639155 |
| epoetin alfa | DRUG | Phase PHASE2 | Anemia | TERMINATED | NCT03140722 |
| vadadustat | DRUG | Phase PHASE3 | Anemia of Chronic Kidney Disease | WITHDRAWN | NCT05082571 |
| Darbepoetin alfa | DRUG | Phase PHASE3 | Anemia | COMPLETED | NCT04313153 |
| Vadadustat | DRUG | Phase PHASE3 | Anemia of Chronic Kidney Disease | ACTIVE_NOT_RECRUITING | NCT06901505 |
| Celecoxib | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02502500 |
| AKB-6548 tablet, test formulation given in the fed state | DRUG | Phase PHASE1 | Healthy | COMPLETED | NCT02412449 |
| AKB-6548 tablet, test formulation given in the fasted state. | DRUG | Phase PHASE1 | Healthy | COMPLETED | NCT02412449 |
| AKB-6548 tablet, reference formulation given in the fasted state | DRUG | Phase PHASE1 | Healthy | COMPLETED | NCT02412449 |
| Ferrous Sulfate | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02327546 |
| Moxifloxacin | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02062203 |
| AKB-6548 (supratherapeutic dose) | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02062203 |
| AKB-6548 (therapeutic dose) | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02062203 |
| Placebo | OTHER | Phase PHASE1 | Healthy Volunteers | NOT_YET_RECRUITING | NCT07429006 |
| AKB-6548 | DRUG | Phase PHASE1 | Healthy Volunteers | COMPLETED | NCT02502500 |