INTREPID Study: Sapablursen for Polycythemia Vera

This study, called INTREPID, is looking at a drug called sapablursen for people with Polycythemia Vera (PV). PV is a blood disorder where your body makes too many red blood cells. The study wants to see how safe and effective sapablursen is when added to your usual PV treatment. You might be able to join if you are 18 or older, have been diagnosed with PV, and need regular blood draws (phlebotomy). Your red blood cell count (Hct) needs to be below 45% at the start of the study. The main goal is to see if sapablursen can help you avoid needing phlebotomy between weeks 20 and 32. The study is currently recruiting about 250 participants.

Study design
This is an interventional study with three parts, including a blinded treatment phase where you might receive sapablursen or a placebo (an inactive substance). You could receive treatment for up to 156 weeks.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint measures your need for phlebotomy between week 20 and week 32.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07429266

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

Recruiting
PHASE3Ages 18+InterventionalTreatment
Ono Pharmaceutical Co., Ltd.
~250 participants
Updated 2026-08-20 on ClinicalTrials.gov
What's tested:SapablursenPlacebo

At a glance

Recruiting sites
8 of 8 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Percentage of Participants with Absence of Phlebotomy Eligibility
Measured over Week 20 through Week 32
Polycythemia Vera
8 sites across 6 states
Florida3
Maryland1
Michigan1
New York1
Ohio1
Western Australia1
  • Clinical Team · STUDY_DIRECTOR · Deciphera Pharmaceuticals, LLC

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  • Percentage of Participants with Absence of Phlebotomy EligibilityWeek 20 through Week 32

    Response is defined as absence of phlebotomy eligibility.