RecruitingPhase 4NCT07561892
Study of the Effectiveness and Safety of Daunorubicin /Idarubicin ± Silibinin in Treating Newly Diagnosed AML (Non-M3).
Studying Acute promyelocytic leukemia
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
- Fujian Medical University Union Hospital
- Principal Investigator
- Yuanzhong Chen, MDFujian Institute of Haematology, Fujian Medical University Union Hospital
- Intervention
- daunomycin/Idarubicin+ Silybinin(drug)
- Enrollment
- 100 target
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2022 – 2026
Study locations (1)
- Fujian Medical University Union Hospital, Fuzhou, Fujian, 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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