Ozmosi | Daprodustat Drug Profile
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Daprodustat

Pronounced as: dap-roe-DUE-stat

Alternative Names: daprodustat, gsk1278863, JESDUVROQ
Clinical Status: Active
Latest Update: 2026-01-20
Latest Update Note: Clinical Trial Update

Product Description

Daprodustat (Jesduvroq), a HIF-PHI, belongs to a novel class of oral medicines for the treatment of anaemia of CKD in adult patients on dialysis. Inhibition of oxygen-sensing prolyl hydroxylase enzymes stabilises hypoxia-inducible factors, which can lead to transcription of erythropoietin and other genes involved in the correction of anaemia, similar to the physiological effects that occur in the human body at high altitude (Sourced from: https://www.gsk.com/en-gb/media/press-releases/jesduvroq-daprodustat-approved-by-us-fda-for-anaemia-of-chronic-kidney-disease-in-adults-on-dialysis/)

Mechanisms of Action: HIF Inhibitor

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: *

Approval Status: Approved

Approved Countries: Japan | United States

Approved Indications: None

Known Adverse Events: None

Company: GSK
Company Location: Europe
Company Founding Year: 2000
Additional Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Daprodustat

Countries in Clinic: Argentina, Belgium, Canada, France, Germany, Italy, Japan, Netherlands, Poland, Russia, South Korea, Spain, Turkey, United Kingdom, United States, Unknown Location

Active Clinical Trial Count: 3

Recent & Upcoming Milestones

Highest Development Phases

Phase 3: Anemia|Kidney Failure, Chronic

Trial ID

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

Latest Trial Update Date

Data Updated

NCT07300111

QLG1218-301

P3

Not yet recruiting

Anemia

2027-05-01

12%

2025-12-24

Primary Endpoints

NCT05682326

ASCEND-P

P3

Completed

Anemia|Kidney Failure, Chronic

2024-10-18

29%

2025-11-11

jRCT2041220113

jRCT2041220113

P3

Not yet recruiting

Anemia

2028-05-17