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Clinical Trial Summary

To evaluate the safety and tolerability of partial HLA-matched VSTs against both CMV and EBV viruses in recipients of allogeneic hematopoietic stem cells with refractory viral infections (CMV and/or EBV). Preliminary evaluation of the efficacy of partial HLA-matched VSTs against both CMV and EBV viruses in recipients of allogeneic hematopoietic stem cells with refractory viral infections (CMV and/or EBV); To monitor the duration and expansion of multi-virus VSTs cells after infusion.


Clinical Trial Description

This study consists of two parts: (1) The first stage is the safety evaluation of multi-virus VSTs and the exploration of DLT and MTD; (2) The second phase is to evaluate the safety and efficacy of multi-viral VSTs in selecting appropriate doses in the first phase. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06075927
Study type Interventional
Source Peking University People's Hospital
Contact Yuanjie Ding
Phone 010-88325948
Email rmkyc@163.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date November 1, 2023
Completion date October 30, 2025

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