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NCT06479135Possibly a fitRecruiting

Study of new drug added to ruxolitinib for myelofibrosis

MyelofibrosisPost-PV MFPost-ET MyelofibrosisPrimary MyelofibrosisMF

Treatments studied

Part of Blood & lymphatic clinical trials.

This trial tests a new drug called Navtemadlin when added to the standard treatment ruxolitinib for people with myelofibrosis who are not getting the best results from ruxolitinib alone. It may help improve response and control the disease.

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

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

Who can take part

  • You have a confirmed diagnosis of primary myelofibrosis, or myelofibrosis that started from essential thrombocythemia or polycythemia vera.
  • You are at high, intermediate-1, or intermediate-2 risk according to a standard scoring system (IPSS).
  • You have not been treated with any JAK inhibitor before.
  • You have not had your spleen removed or spleen radiation in the last 3 months.
  • You have not taken certain other drugs (BCL-XL, BET, MDM2, PI3K, PIM, or XPO1 inhibitors) before.
  • You are not currently eligible for a bone marrow transplant, and your blood or bone marrow blasts are below 10%.
  • Your myelofibrosis cells have a normal (wild-type) TP53 gene, and you are on a stable dose of ruxolitinib yet still have a suboptimal response.

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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