← Eichor
Study identifier: NCT05342584 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Venetoclax Plus Intensive Chemotherapy in AML and Advanced MDS

Condition: Acute Myeloid Leukemia · Myelodysplastic Syndromes  ·  Sponsor: Montefiore Medical Center

PhasePhase 1
Planned participants99
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is a Phase 1b, open-label study evaluating Venetoclax in combination with intensive induction and consolidation chemotherapy in previously untreated, adult patients with acute myeloid leukemia. In Part 1, the dose escalation phase, the safety and tolerability of the combination with Venetoclax at different doses and duration will inform the appropriate dose(s) and regimen(s) for Part 2. In Part 2, the dose expansion phase, a maximum of 28 additional patients will be randomized 1:1 to the MTD determined in Part 1 and the starting dose (assuming the MTD is not the starting dose), to further evaluate the safety and efficacy of the study drug combination.

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

Talk to the study team

Ioannis Mantzaris, MD  ·  718-920-4826  ·  imantzar@montefiore.org

Always discuss trial participation with your own doctor first.

Locations (1)

Montefiore Einstein Cancer Center and Children's Hospital at Montefiore (CHAM)The Bronx, New York, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT05342584