Elritercept for Myelofibrosis and Anemia

This study is testing a drug called elritercept to see if it can help improve anemia (low red blood cell count) in adults with myelofibrosis (a bone marrow disorder) who are already taking ruxolitinib. You would receive either elritercept or a placebo (an inactive substance that looks like the study drug) through injections. Researchers want to know if elritercept helps you become independent from red blood cell transfusions for at least 12 weeks. They will also look at how elritercept affects tiredness, other myelofibrosis symptoms, physical activity, bone marrow, and the spleen, and if it's safe. The study aims to enroll 324 participants, aged 18 and older, who have been diagnosed with myelofibrosis.

Study design
This study is comparing elritercept to a placebo in 324 participants. It is a double-blinded study, meaning neither you nor your doctors will know if you are receiving elritercept or the placebo.
What's involved
You would receive study treatment for at least 9 months (36 weeks). The trial record does not specify the number of visits or procedures.
Compensation
Not stated in the trial record.
Follow-up
The primary goal is measured during a 36-week treatment period. The trial record does not specify follow-up after this period.

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NCT07623161

A Study to Compare Elritercept to Placebo in Adults With Myelofibrosis and Anemia Who Are Taking Ruxolitinib

Recruiting
PHASE3Ages 18+InterventionalTreatment
Takeda
~324 participants
Updated 2026-07-23 on ClinicalTrials.gov
What's tested:PlaceboElritercept

At a glance

Recruiting sites
1 of 207 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Proportion of Participants Who Are Red Blood Cell-Transfusion Independent (RBC-TI) for Any Consecutive Greater Than or Equal to (≥) 12-Week Period During the 36-Week Double-Blinded Treatment Period
Measured over From Cycle 1 Day 1 through Week 36 (each cycle is 28 days)
Myelofibrosis
Anemia
207 sites across 151 states
Florida5
Texas5
Italy5
Bulgaria4
Ireland4
Spain4
North Carolina3
Pennsylvania3
  • Study Director · STUDY_DIRECTOR · Takeda

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  • Proportion of Participants Who Are Red Blood Cell-Transfusion Independent (RBC-TI) for Any Consecutive Greater Than or Equal to (≥) 12-Week Period During the 36-Week Double-Blinded Treatment PeriodFrom Cycle 1 Day 1 through Week 36 (each cycle is 28 days)

    RBC-TI is defined as no RBC transfusions administered for the specified time period during study treatment.