Hepcidin Mimetic in Patients With Polycythemia Vera (REVIVE)
NCT04057040 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 70
Last updated 2025-08-07
Summary
This is a Phase 2 study with an open-label dose escalation phase followed by a blinded withdrawal phase and an open label extension. The study is designed to monitor the PTG-300 safety profile and to obtain preliminary evidence of efficacy of PTG-300 for the treatment of phlebotomy-requiring polycythemia vera.
Conditions
Interventions
- DRUG
-
PTG-300
Active
- DRUG
-
Placebo
Sponsors & Collaborators
-
Protagonist Therapeutics, Inc.
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-10-01
- Primary Completion
- 2023-02-14
- Completion
- 2024-06-17
- FDA Drug
- Yes
Countries
- United States
- India
Study Locations
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