Clin2
NCT07623200Possibly a fitRecruiting

New drug for high-risk essential thrombocythemia with specific genetic mutation

Essential Thrombocythemia

Treatments studied

Part of Blood & lymphatic clinical trials.

This study tests a new drug called INCA033989 for people with a high-risk form of essential thrombocythemia (a blood disorder causing too many platelets) who have a specific genetic change called mutCALR. The trial compares this new drug to the best currently available treatments.

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

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

Who can take part

  • You have been diagnosed with high-risk essential thrombocythemia (ET)
  • Your ET is caused by a specific genetic mutation called CALR mutation (mutCALR)
  • You have previously been treated with at least one blood-thinning or platelet-reducing medication
  • You have not had any major bleeding or blood clots in the past 3 months
  • You have not previously had a stem cell transplant
  • You do not have any other blood cancers or untreated cancers (though past cancers treated with curative intent are okay if cancer-free for 2+ years)

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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