Clin2
NCT07340138Possibly a fitRecruiting

Pelabresib and Ruxolitinib combo for myelofibrosis in Japan

Primary Myelofibrosis (PMF)Post-polycythemia Vera Myelofibrosis (Post-PV MF)Post-essential Thrombocythemia Myelofibrosis (Post-ET MF)

Treatments studied

Part of Blood & lymphatic clinical trials.

This study tests adding a new drug (pelabresib) to the standard treatment (ruxolitinib) for Japanese people with myelofibrosis. The goal is to see if the combination helps control symptoms like an enlarged spleen.

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

Phase
Phase 1
Enrollment
6 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You have a type of myelofibrosis (primary or after another blood disorder).
  • Your doctor says you are at intermediate-1, intermediate-2, or high risk.
  • You are already taking ruxolitinib (5 to 25 mg twice daily) for at least 8 weeks.
  • Your spleen is enlarged (felt or seen on scan).
  • Your platelet count is at least 100,000 per microliter of blood (without medication or transfusion to raise it).
  • You have fewer than 5% blasts (immature cells) in your blood.

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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