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Clinical Trials in the USA / NCT07429266
Recruiting Phase 3

INTREPID: A Study of Sapablursen Evaluating the Safety and Efficacy in Participants With Polycythemia Vera (PV)

NCT07429266 · tracked via the Priya Life Science USA tracker
Sponsor
Ono Pharmaceutical Co., Ltd.
Phase
Phase 3
Started
2026-05-25
Last updated
2026-09-08

Condition(s) studied

Polycythemia Vera

Investigational drug(s) / intervention(s)

SapablursenPlacebo

Sapablursen: Administered subcutaneously (SC)

Placebo: Administered SC

Study summary

The purpose of this study is to evaluate the efficacy and safety of sapablursen when added on to current standard of care (SOC) for Polycythemia Vera (PV) therapy. The study will be conducted in three sequential parts (Part 1a blinded treatment, Part 1b open-label treatment, \& Part 2 long-term extension). Participants may receive treatment for up to 156 weeks.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: 1. Meet revised 2022 World Health Organization (WHO) and 2022 International Consensus Classification criteria for the diagnosis of PV. 2. Participants must be phlebotomy-dependent. 3. Hct less than (\<) 45% at study start. 4. Participants receiving Cytoreduction therapy (CRT) must be on a stable regimen at study start. 5. Adequate organ function and electrolytes. Exclusion Criteria: 1. Prior treatment of PV with Transmembrane serine protease 6 (TMPRSS6) inhibitors, including sapablursen, or hepcidin mimetics. 2. Clinically significant thrombosis (eg, myocardial infarction, stroke, deep vein thrombosis or splenic vein thrombosis) within 1 month prior to randomization. 3. Participants who require phlebotomy at Hct levels \<45%. 4. Meet the criteria for post-PV myelofibrosis as defined by the International Working Group-Myeloproliferative Neoplasms Research and Treatment. 5. Any serious or unstable medical condition or uncontrolled psychiatric condition that would interfere with their ability to comply with study requirements.

Primary outcome measure(s)

Trial sites (10)

FacilityCityRegionStatus
Regis Clinical Research LLC. Miami Florida Recruiting
Florida Clinical Trials Group Plantation Florida Recruiting
Florida Clinical Trials Group Tamarac Florida Recruiting
Central Georgia Cancer Care Macon Georgia Recruiting
The Center for Cancer & Blood Disorders Bethesda Maryland Recruiting
The Cancer and Hematology Centers Grand Rapids Michigan Recruiting
Montefiore Medical Center The Bronx New York Recruiting
Gabrail Cancer Center Research Canton Ohio Recruiting
Perth Blood Institute West Perth Western Australia Recruiting
Japanese Red Cross Nagasaki Genbaku Hospital Nagasaki Japan Recruiting

More Ono Pharmaceutical Co., Ltd. trials in the USA

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07429266 on ClinicalTrials.gov ↗ ← All trials in the USA