Clin2
NCT07357727Possibly a fitRecruiting

Study of Pelabresib and Ruxolitinib for Myelofibrosis

Primary Myelofibrosis (PMF)Post-polycythemia Vera Myelofibrosis (PPV-MF)Post-essential Thrombocythemia Myelofibrosis (PET-MF)

Treatments studied

Part of Blood & lymphatic clinical trials.

This trial tests a combination of two drugs (pelabresib and ruxolitinib) for people with myelofibrosis whose spleen is enlarged and who have bothersome symptoms. It aims to see if adding pelabresib to standard care helps control the disease better.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 3
Enrollment
460 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You must have a confirmed diagnosis of myelofibrosis (primary or linked to another blood condition).
  • Your risk category must be at least intermediate-1 (medium risk) or higher on the DIPSS scale.
  • Your spleen must be enlarged to at least 450 cubic centimeters on a scan.
  • You should have significant symptoms (like fatigue, pain, or fever) that score 15 or more on a symptom checklist.
  • Your platelet count must be at least 100,000 per microliter of blood, without needing blood transfusions or growth factors for the last month.
  • You cannot have had prior treatment with JAK inhibitors (like ruxolitinib) or BET inhibitors.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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