drugset / Trial / NCT01195480

Summary

The aim of this clinical trial is to evaluate the feasibility, safety and biological effect of adoptive transfer of CD19ζ chimaeric receptor transduced donor-derived EBV-specific cytotoxic T-lymphocytes (EBV-CTL) in patients with high-risk or relapsed B cell precursor ALL after allogeneic Haematopoietic Stem Cell Transplantation (HSCT).

Timeline

Start
2012-05
Primary completion
2015-11
Completion
2015-11

Outcome

Outcome not reported

Stopped: “Due to lack of biological efficacy and CD19 CAR CTL persistence”

Drugs

EvaluationDrugModalityDoseRoute
Subject donor-derived EBV-specific cytotoxic T-cells (EBV-CTL) Cell therapy 2e+08 unknown —
Subject donor-derived Lymphoblastoid Cell Line Vaccine 5e+06 cells Subcutaneous