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Study to Evaluate the Safety and Efficacy of Oral Vadadustat in Pediatric Participants With Anemia of Chronic Kidney Disease

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NCT05082571

Sponsored by Akebia Therapeutics (industry) · AKBA — their whole pipeline →.

Phase
Phase 3
Status
Withdrawn
Study type
Interventional
Design
Na · None · Treatment
Enrollment
0actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

Sponsor decision

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartJan 2025estimatedWhen the study began enrolling
Primary completionJul 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionOct 2026estimatedThe whole study's end, after follow-up
First posted2021-10-19actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-01actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Anemia of Chronic Kidney Disease

Intervention

  • Drug: vadadustat — also filed as AKB-6548

Primary outcome

what the primary-completion date above is the date OF
Mean Change in Hemoglobin (Hb) Values Between Baseline and the Primary Evaluation Period (Average Hb From Weeks 21 to 28)
measured Baseline; Weeks 21 to 28

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