drugset / Trial / NCT05210790

A Phase 3 Study of Rusfertide in Patients With Polycythemia Vera

NCT05210790 ↗

Phase 3 Active not recruiting 293 enrolled Protagonist Therapeutics, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

The study is designed to evaluate the safety and efficacy of rusfertide in subjects with polycythemia vera (PV) in maintaining hematocrit control and in improving symptoms of PV.

Timeline

Start
2022-04-01
Primary completion
2025-02-21
Completion
2027-06

Outcome

Met primary endpoint

release “VERIFY study evaluating rusfertide in patients with polycythemia vera (PV), which met the primary and all key secondary endpoints.” takeda.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Rusfertide Peptide — —