RecruitingNot applicableNCT07183878
Venetoclax-Enhanced BUCY vs. Standard BUCY Conditioning in High-Risk AML and MDS Patients Undergoing Allo-HSCT (Ven-BUCY Study)
Studying Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13)
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
- First Affiliated Hospital of Zhejiang University
- Principal Investigator
- Yanmin Zhao, MDBone Marrow Transplantation Center, The First Affiliated Hospital, Zhejiang University School Of Medicine
- Intervention
- Venetoclax(drug)
- Enrollment
- 138 enrolled
- Eligibility
- 12-60 years · All sexes
- Timeline
- 2025 – 2028
Study locations (1)
- The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, China
Collaborators
The First Affiliated Hospital of Zhengzhou University · Union Hospital, Tongji Medical College, Huazhong University of Science and Technology · Tongji Hospital · The Children's Hospital of Zhejiang University School of Medicine · Ruijin Hospital North Shanghai Jiao Tong University School of Medicine
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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