Study of Momelotinib and Luspatercept for Myelofibrosis
This study is testing a combination of two drugs, momelotinib and luspatercept, for people with myelofibrosis. Myelofibrosis is a bone marrow disorder that causes scarring in the bone marrow, leading to severe anemia and other symptoms. This study is for you if you have primary myelofibrosis or myelofibrosis that developed after polycythemia vera or essential thrombocythemia, and you need regular blood transfusions. You can join whether or not you've taken a JAK inhibitor (another type of medication for myelofibrosis) before. The main goal is to see how many participants no longer need blood transfusions by Week 24. This study plans to enroll 68 participants, but its current status is unclear.
- Study design
- This is a Phase 2 interventional study, meaning it tests new treatments in a small group of people to see if they are safe and effective. It plans to enroll 68 participants.
- What's involved
- Momelotinib will be taken by mouth, and luspatercept will be given as an injection under the skin. The study will measure if you need fewer blood transfusions up to Week 24.
- Compensation
- Not stated in the trial record.
- Follow-up
- The main goal of the study is measured up to Week 24.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Study of Momelotinib in Combination With Luspatercept in Participants With Transfusion Dependent Myelofibrosis
At a glance
Conditions
NCT06517875
Where you'd take part
This study runs at 33 sites. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
GSK Investigational Site
Ann Arbor, Michiganstudy coordinator listed
Recruiting
GSK Investigational Site
New York, New Yorkstudy coordinator listed
Recruiting
GSK Investigational Site
Nashville, Tennesseestudy coordinator listed
Recruiting
GSK Investigational Site
Houston, Texasstudy coordinator listed
Recruiting
GSK Investigational Site
Seattle, Washingtonstudy coordinator listed
Recruiting
GSK Investigational Site
Vancouver, British Columbia, Canadastudy coordinator listed
Recruiting
GSK Investigational Site
Toronto, Ontario, Canadastudy coordinator listed
Recruiting
GSK Investigational Site
Montreal, Quebec, Canadastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Percentage of Participants with TI Response by Week 24Up to Week 24
TI response is defined as not requiring red blood cell (RBC) transfusion (except in the case of clinically overt bleeding) for any ≥12-week interval.