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Study identifier: NCT06612944 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Myelodysplastic Syndromes, Adult  ·  Sponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine

PhasePhase 2
Planned participants40
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

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.

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

Talk to the study team

Xianmin Song, MD  ·  +8613501672508  ·  shongxm@139.com

Always discuss trial participation with your own doctor first.

Locations (1)

Shanghai General HospitalShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06612944