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Study identifier: NCT06529250 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Intermediate-dose HAD Regimen for CEBPA Double-mutated AML

Condition: AML  ·  Sponsor: Institute of Hematology & Blood Diseases Hospital, China

PhaseNA
Planned participants148
Who can joinAll sexes, 14 Years to 54 Years
Healthy volunteersNo

About this study

AML is highly heterogeneous in pathogenesis, and CEBPA double-mutated (CEBPAdm) AML is a common type of leukemia in China. Currently, no targeted therapies for CEBPAdm, and chemotherapy and transplantation are still the treatment options for CEBPA double-mutated AML. At present, the "3+7" treatment induction regimen of cytarabine combined with anthracyclines is still the first-line recommended regimen. In our retrospective study, the intermediate dose HAD regimen produced a 3-year RFS of 84.7% and a 3-year OS of 92.8% in CEBPAdm AML. Therefore, this project intends to confirm the efficacy of intermediate-dose HAD in the treatment of CEBPA double-mutated AML is superior to the conventional treatment regimen through the multi-center RCT study.

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

Talk to the study team

Hui Wei, MD  ·  13132507161  ·  weihui@ihcams.ac.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Blood HospitalTianjin, Tianjin Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06529250