drugset / Trial / NCT04313153

Trial Evaluating the Efficacy and Safety of Oral Vadadustat Once Daily (QD) and Three Times Weekly (TIW) for the Maintenance Treatment of Anemia in Hemodialysis Subjects Converting From Erythropoiesis-Stimulating Agents (ESAs)

NCT04313153

RandomizedParallel-groupOpen-labelTreatment

Summary

This trial will be conducted to demonstrate the efficacy and safety of vadadustat compared to darbepoetin alfa for the maintenance treatment of anemia in hemodialysis participants after conversion from current erythropoiesis-stimulating agent (ESA) therapy.

Timeline

Start
2020-05-27
Primary completion
2021-11-26
Completion
2022-06-22

Drugs

EvaluationDrugModalityDoseRoute
Comparator Darbepoetin alfa Protein / enzyme biologic Intravenous
Subject Vadadustat Small molecule 300 mg Oral
Subject Vadadustat Small molecule 450 mg Oral
Subject Vadadustat Small molecule 600 mg Oral
Subject Vadadustat Small molecule 750 mg Oral

Indications