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Study identifier: NCT07672262 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

VA Consolidation in Intermediate-Risk AML

Condition: Acute Myeloid Leukemia · Intermediate Risk Acute Myeloid Leukemia · Consolidation Therapy  ·  Sponsor: The First Affiliated Hospital of Soochow University

PhasePhase 2
Planned participants226
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This clinical trial aims to compare the efficacy and safety of venetoclax-based consolidation therapy versus conventional consolidation chemotherapy (intermediate/high-dose cytarabine) in newly diagnosed adult patients with intermediate-risk acute myeloid leukemia (AML). Participants must have achieved complete remission (CR) or CR with incomplete hematologic recovery (CRi) after induction therapy with venetoclax and azacitidine and are planned to undergo allogeneic hematopoietic stem cell transplantation (allo-HSCT).

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

Talk to the study team

Qi Qu  ·  +86-512-676976801  ·  quqimedsz@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

The First Affiliated Hospital of Soochow UniversitySuzhou, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07672262