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Clinical Trial Summary

This is a multi-center, single arm, open-label, phase I study to determine the safety and effectiveness of EBV-TCR-T cell immunotherapy in treating EBV virus infection after allogenic HSCT.


Clinical Trial Description

EB virus (EBV) infection after allogeneic hematopoietic stem cell transplantation (HSCT) is common and can be lethal without prompt treatment. In this prospective study, HLA-A*02:01/11:01/24:02-restricted EBV-specific T cell receptor (TCR) will be introduced into the T cells of HSCT donors by ex vivo lentiviral transduction to generate EBV-TCR-T cells. An escalated dose ranging from 3×10^5/kg to 1×10^6/kg of EBV-TCR-T cells will be infused into patients with EBV infection. The safety, efficacy, pharmacokinetics and cytokine levels of allogenic EBV-TCR-T cell therapy will be evaluated. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06119256
Study type Interventional
Source Chinese PLA General Hospital
Contact Daihong Liu, Doctor
Phone +86 18301339032
Email daihongrm@163.com
Status Recruiting
Phase Phase 1
Start date August 1, 2023
Completion date December 31, 2026