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NCT07264010Possibly a fitNot yet recruiting

Sorafenib and venetoclax for MRD-positive AML

Acute Myeloid Leukaemia (AML)Measurable Residual Disease (MRD)

Treatments studied

Part of Blood & lymphatic, Cancer clinical trials.

This trial tests if combining sorafenib and venetoclax can help people with acute myeloid leukemia (AML) who still have minimal residual disease (MRD) after treatment. The goal is to prevent the leukemia from coming back.

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

Phase
Phase 2/Phase 3
Enrollment
87 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You must have acute myeloid leukemia (AML) with minimal residual disease (MRD) left after earlier treatment.
  • Your liver and kidneys must work well enough (bilirubin ≤ 35 μmol/L, AST/ALT less than 2 times normal, creatinine ≤ 150 μmol/L).
  • Your heart must function normally (ejection fraction ≥ 50%, NYHA class I or II).
  • You must be able to perform daily activities with little help (ECOG score 0-2).
  • If you could become pregnant, you must have a negative pregnancy test and agree to use birth control during treatment. Men must also use contraception during and for 3 months after treatment.

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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