Clinical Trial

Prophylactic Intervention for Relapse Prevention Post-Allogeneic Transplantation in Very High-Risk MDS Patients Based on IPSS-M Stratification

Recruiting Phase 2
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Summary
By collecting interventional clinical data to assess the survival and relapse conditions of patients post-transplantation and comparing them with historical data, the primary study endpoint is the 1-year and 2-year relapse-free survival (RFS) post-transplantation. This includes the time from the start of treatment until the documentation of disease progression (bone marrow smear blast cells \> 5% or extramedullary relapse) or death due to any cause, whichever occurs first. This experiment aims to improve the post-transplant survival rates of MDS patients classified as very high risk under the IPSS-M stratification and to explore pathways to prevent relapse.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-09-23; most recent amendment 2024-11-19.
Status change: Not Yet Recruiting → Recruiting 2024-11-19
Trial Details
NCT Number NCT06612944
Lead Sponsor Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
Conditions Myelodysplastic Syndromes, Adult
Enrollment 40 participants
Start Date 2024-11-12
Primary Completion 2027-11-12 (estimated)
Study Completion 2028-11-12 (estimated)
Updated on ClinicalTrials.gov 2024-11-26