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Study identifier: NCT07117422 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Venetoclax-Decitabine in Untreated Elderly/Unfit AML

Condition: AML, Adult  ·  Sponsor: The Second Hospital of Hebei Medical University

PhaseNA
Planned participants39
Who can joinAll sexes, 65 Years to no upper limit
Healthy volunteersNo

About this study

Acute myeloid leukemia (AML) is a highly fatal malignancy in China, with particularly poor outcomes in elderly patients. Low-intensity regimens yield low remission rates, and median overall survival (OS) typically remains under 6-9 months. Venetoclax (VEN) combined with hypomethylating agents (azacitidine or decitabine(DEC)) has emerged as a first-line therapy for these patients, significantly improving response rates and survival. However, challenges persist, including suboptimal complete remission (CR) rates, low Measurable Residual Disease(MRD) negativity, and tolerability issues with prolonged use. Recent studies suggest that a 3-day decitabine regimen combined with VEN may enhance efficacy and tolerability. Building on prior evidence and our institutional experience, we propose this study to evaluate an optimized dosing strategy of VEN plus decitabine in treatment-naïve elderly or chemotherapy-ineligible AML patients, aiming to further improve clinical outcomes.

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

Talk to the study team

LING XI GUO  ·  13932113351  ·  guoxiaoling@hebmu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

The Second Hospital of Hebei Medical UniversityHebei, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07117422