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NCT06033586: THRIVE
Study to Evaluate the Long-term Safety of Rusfertide (PTG-300) in Subjects With Polycythemia Vera
Phase 3 trial testing Open-label rusfertide in Polycythemia Vera in 46 participants. Participants enrolled and being followed up; not accepting new ones.
1 April 2026
Quick facts
| Lead sponsor | Protagonist Therapeutics, Inc. |
|---|---|
| Phase | Phase 3 |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 46 |
| Start date | 22 January 2024 |
| Primary completion | 1 April 2026 |
| Estimated completion | 1 April 2027 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Open-label rusfertide — full drug profile →
Conditions studied
- Polycythemia Vera — all drugs for Polycythemia Vera →
Sponsor
Protagonist Therapeutics, Inc. — full company profile →
Who can join
18 and older, any sex, with Polycythemia Vera. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this clinical trial is to assess long-term safety and efficacy of rusfertide in subjects with polycythemia vera. Subjects who complete dosing with rusfertide until the end-of-treatment visit of a Phase 2 rusfertide study and meet the inclusion/exclusion criteria for this study, are eligible to participate in this open-label study and continue treatment with rusfertide.
Publications & conference data
4 peer-reviewed publications reference this trial (live from Europe PMC):
-
Advance in peptide-based drug development: delivery platforms, therapeutics and vaccines.
Xiao W, Jiang W, Chen Z, Huang Y, et al · · 2025 · cited 144× · PMID 40038239 · DOI 10.1038/s41392-024-02107-5 -
Modern and multidisciplinary care in polycythemia vera.
Palandri F, Sartor C, Pileri A, Addimanda O, et al · · 2026 · PMID 41999414 · DOI 10.1007/s00277-026-06970-w -
Advances in polycythemia vera treatment with targeted therapies and clinical trials.
Hassanien D, AlYafei RA, Metwally OH, Alremawi I, et al · · 2025 · PMID 41144126 · DOI 10.1007/s12672-025-03703-9 -
EHA2024 Hybrid Congress
· 2024
Verify or expand the search:
- PubMed search for NCT06033586
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Protagonist Therapeutics, Inc. trials
Trials by the same sponsor.
- NCT07153146 — Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of PN-881 in Healthy Subjects. · Phase 1 · recruiting
- NCT04819620 — Pharmacokinetics of PN-232 in Healthy Volunteers · Phase 1 · completed
- NCT04767802 — PTG-300 in Patients With Polycythemia Vera and Elevated Hematocrit · Phase 2 · completed
- NCT04621630 — Pharmacokinetics of PN-235 in Healthy Volunteers · Phase 1 · completed
- NCT04516382 — Pharmacokinetics and Pharmacodynamics of Different PTG-300 Regimens in Healthy Volunteers · Phase 1 · completed
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06033586 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Protagonist Therapeutics, Inc.
- Last refreshed: 6 August 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06033586.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing