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Study identifier: NCT05939180 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

VA vs DA for Newly Diagnosed Hig-risk AML

Condition: Acute Myeloid Leukemia  ·  Sponsor: The First Affiliated Hospital of Soochow University

PhasePhase 2/Phase 3
Planned participants116
Who can joinAll sexes, 18 Years to 64 Years
Healthy volunteersNo

About this study

This is an open-label, multicenter, phase 2b, randomized study aiming to compare the efficacy and safety of venetoclax plus azacytidine Versus daunorubicin plus cytarabine (conventional 7+3 regimen) in adult acute myeloid leukemia (AML) patients with adverse risk featuress. Participants will be 1:1 randomly assigned to the VA and DA groups. Once remission was achieved, consolidated chemotherapy will be performed and allogeneic hematopoietic stem cell transplantation is strongly recommended. After completion of the study intervention, participants will be followed-up every 1 to 2 months for up to 2 years.

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

Talk to the study team

Su-ning Chen  ·  008613814881746  ·  chensuning@sina.com

Always discuss trial participation with your own doctor first.

Locations (2)

The First Affiliated Hospital of Soochow University, Jiangsu Institute of HematologySuzhou, Jiangsu, ChinaRecruiting
Ethical Committee of the First Affliated Hospital of Soochow UniversitySuzhou, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05939180