OncoMatch

OncoMatch/Clinical Trials/NCT06773208

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

Is NCT06773208 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Azacitidine (AZC) and Venetoclax for acute myeloid leukemia (aml).

Phase 2RecruitingMemorial Sloan Kettering Cancer CenterNCT06773208Data as of May 2026

Treatment: Azacitidine (AZC) · VenetoclaxThe 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).

Check if I qualify

Extracted eligibility criteria

Cancer type

Acute Myeloid Leukemia

Performance status

ECOG 0–3(Limited self-care)

Prior therapy

Max 3 prior lines
Min 1 prior line

Must have received: intensive chemotherapy — remission induction

Patient has received 1-3 cycles of intensive chemotherapy for remission induction

Cannot have received: venetoclax containing regimen (venetoclax)

Patient has received previous therapy with a venetoclax containing regimen

Lab requirements

Kidney function

Creatinine clearance greater than 30 mL/min based on Cockroft-Gault GFR estimation

Liver function

AST and ALT ≤ 2.5 x ULN; total bilirubin < 1.5 x ULN (or direct bilirubin normal in subjects with total bilirubin > 1.5 ULN), except in cases of Gilbert's disease

adequate organ function defined as: 1. Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x ULN 2. Serum total bilirubin < 1.5 x ULN (or direct bilirubin normal in subjects with total bilirubin > 1.5 ULN). Except in cases of Gilbert's disease. 3. Creatinine clearance greater than 30 mL/min based on the Cockroft-Gault glomerular filtration rate (GFR) estimation.

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • Memorial Sloan Kettering at Basking Ridge (All Protocol Activities) · Basking Ridge, New Jersey
  • Memorial Sloan Kettering Monmouth (All Protocol Activities) · Middletown, New Jersey
  • Memorial Sloan Kettering Bergen (All Protocol Activities) · Montvale, New Jersey
  • Memorial Sloan Kettering Suffolk-Commack (All Protocol Activities) · Commack, New York
  • Memorial Sloan Kettering Westchester (Limited Protocol Activities) · Harrison, New York

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify