A Phase 1 interventional study of CMV-TCR-T cells in CMV Infection or Reactivation After Allogenic HSCT, sponsored by Hebei Yanda Ludaopei Hospital. Completed at 1 site in China. Open to participants aged 1 Year to 70 Years. Per ClinicalTrials.gov, last updated 2023-01-12.
Sponsored by Hebei Yanda Ludaopei Hospital · Phase 1, Interventional, and Treatment
This is a single cente, single arm, open-label, phase I study to evaluate the safety and effectiveness of CMV-TCR-T cell immunotherapy in treating CMV virus infection after HSCT.
CMV infection is a common virus infection of HSCT, and which is highly related with the failure of transplantation and survival time of transplant patients. To evaluate the safety and efficacy of allogenic CMV-TCR-T cell therapy in subjects with CMV infection, patients with CMV emias or deseases will be enrolled, and donor derived CMV-TCR-T(HLA-A*1101\0201\2402) cells will be intravenously infused with a escalated dose of 0.1-1×106 CMV-TCR-T cells. The CMV DNA copies and CMV-TCR-T cell proliferation will be monitored in the scheduled time (day 0, day 4, day 7, day 10, day 14, day 28).
6,687 studies on the registry are indexed under Infections; 807 are open to participants now.
This study's enrollment of 17 is below the median of 120 across 4,200 interventional studies indexed under Infections.
Browse Infections studies →Hebei Yanda Ludaopei Hospital is the lead sponsor of 15 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
At least one of the following conditions after allogeneic HSCT:
Exclusion Criteria:
patients with organ failure:
The patients will receive one dose of CMV-TCR-T.The dosage ranges from 0.1×10\^6 to 1×10\^6 TCR+T/Kg.
Biological: CMV-TCR-T cells
Patients with CMV emias or CMV disease will be enrolled, and donor derived CMV-TCR-T(HLA-A\*1101\\0201\\2402) cells will be intravenously infused with a escalated dose of 0.1-1×106 CMV-TCR-T cells. The CMV DNA copies and CMV-TCR-T cell proliferation will be monitored in the scheduled time (day 0, day 4, day 7, day 10, day 14,day 28).
Percentage of adverse events
Percentage of participants with adverse events.
Time frame: 3months
Persistence of TCR-T cells
Time frame: 3months
Changes of CMV-DNA copies number
Time frame: 3months
This study is completed, as verified in Nov 2022. You cannot join it, but the record below documents what was studied.
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Hebei Yanda Ludaopei Hospital