RecruitingNot applicableNCT06529250
Intermediate-dose HAD Regimen for CEBPA Double-mutated AML
Studying Acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Institute of Hematology & Blood Diseases Hospital, China
- Principal Investigator
- Hui Wei, MDBlood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College
- Intervention
- HAD(drug)
- Enrollment
- 148 enrolled
- Eligibility
- 14-54 years · All sexes
- Timeline
- 2024 – 2028
Study locations (1)
- Blood Hospital, Tianjin, Tianjin Municipality, China
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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