Clin2
NCT04708054Possibly a fitRecruiting

Venetoclax with busulfan chemo for high-risk AML or MDS

Acute Myeloid LeukemiaChronic Myelomonocytic LeukemiaMyelodysplastic Syndrome

Treatments studied

Part of Blood & lymphatic, Cancer clinical trials.

This study tests whether adding venetoclax to a specific busulfan-based chemotherapy plan improves outcomes for people with high-risk AML or MDS. It mainly targets patients whose leukemia/marrow disease still has high-risk features or measurable disease after initial treatment.

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

Phase
Phase 2/Phase 3
Enrollment
324 people
Ages
18 years to 70 years
Study type
Interventional

Who can take part

  • You are an adult (about age 18–70 for one part, 18–65 for another part).
  • You have AML, MDS, or CMML with specific “high-risk” lab or genetic features, or disease not fully in remission.
  • A compatible donor is available for stem cell transplant (matched sibling or closely matched donor, or a haploidentical related donor in part of the study).
  • You must agree to join and be able to follow study procedures (informed consent).
  • Your liver and kidney tests are strong enough (for example, kidney clearance at least 50 mL/min).
  • You cannot have certain exclusions like HIV, active uncontrolled infection, or prior allogeneic stem cell transplant.

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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