RecruitingPhase 3NCT07429266

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

A Phase 3 Randomized, Double-blind, Placebo-controlled Global Study of Sapablursen in Polycythemia Vera


Sponsor

Ono Pharmaceutical Co., Ltd.

Enrollment

250 participants

Start Date

May 25, 2026

Study Type

INTERVENTIONAL

Conditions

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

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Placebo and a drug called Sapablursen for people with polycythemia vera. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSapablursen

Administered subcutaneously (SC)

DRUGPlacebo

Administered SC


Locations(6)

Regis Clinical Research LLC.

Miami, Florida, United States

Florida Clinical Trials Group

Plantation, Florida, United States

Florida Clinical Trials Group

Tamarac, Florida, United States

The Center for Cancer & Blood Disorders

Bethesda, Maryland, United States

Montefiore Medical Center

The Bronx, New York, United States

Gabrail Cancer Center Research

Canton, Ohio, United States

View Full Details on ClinicalTrials.gov

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NCT07429266


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