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Study identifier: NCT06773208 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

A Study of Azacitidine and Venetoclax in People With Acute Myeloid Leukemia (AML)

Condition: Acute Myeloid Leukemia (AML)  ·  Sponsor: Memorial Sloan Kettering Cancer Center

PhasePhase 2
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to find out if azacitidine and venetoclax are an effective treatment approach to get rid of or lower measurable residual disease (MRD) in people with acute myeloid leukemia (AML) who have received standard chemotherapy and are planning to have an allogeneic hematopoietic stem cell transplant (HSCT). Allogeneic HSCT, sometimes called a bone marrow transplant, involves receiving healthy blood-forming cells (stem cells) from a donor in order to replace the patient's immune system and lower the chances of the disease returning (relapse).

This description comes directly from the study's public registry record.

Talk to the study team

Meira Yisraeli Salman, MD  ·  646-608-3982  ·  yisraem@mskcc.org

Eytan Stein, MD  ·  646-608-3749  ·  steine@mskcc.org

Always discuss trial participation with your own doctor first.

Locations (7)

Memorial Sloan Kettering at Basking Ridge (All Protocol Activities)Basking Ridge, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Monmouth (All Protocol Activities)Middletown, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Bergen (All Protocol Activities)Montvale, New Jersey, United StatesRecruiting
Memorial Sloan Kettering Suffolk-Commack (All Protocol Activities)Commack, New York, United StatesRecruiting
Memorial Sloan Kettering Westchester (Limited Protocol Activities)Harrison, New York, United StatesRecruiting
Memorial Sloan Kettering Cancer Center (All Protocol Activities)New York, New York, United StatesRecruiting
Memorial Sloan Kettering Nassau (All Protocol Activities)Rockville Centre, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06773208