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Trials / Completed

CompletedNCT02580539

A Study of the Safety and Efficacy of EBV Specific T-cell Lines

A Phase I/II Open-label Study of the Safety and Efficacy of Epstein-Barr Virus Specific T-cell Lines for the Treatment of EBV Infection or EBV-related Lymphoproliferative Diseases

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
12 (estimated)
Sponsor
Dr. Jean-Sebastien Delisle, MD, PhD · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This study evaluates the safety and efficacy of EBV-specific T-cell lines to treat patients suffering from high EBV viral titers not responding to standard of care therapies and to treat EBV-related lymphoma. The study will recruit 6 patients to receive autologous T cells or a T cell line derived from the patient's allogeneic donor (in the case of stem cell transplant recipients), and 6 patients to receive a T-cell line prepared from a matched or partially matched related donor.

Detailed description

Epstein-Barr virus (EBV) is a member of the herpes virus family and infects up to 95% of individuals over their lifetime. Most initial infections occur in childhood and after a brief flu-like illness, the virus enters a phase of latency. Patients who receive a bone marrow transplant or an organ transplant take medications drugs that weaken their immune systems. In these contexts, the virus can "reactivate" and cause very serious problems, such as lymphoma. For unknown reasons, people with a normal immune system can also develop lymphoma due to EBV. The purpose of this study is to test the safety and efficacy of immune cells (T lymphocytes) that are specifically "taught" to recognize the virus-infected cells and to eliminate them. This "education" occurs is done over during a 2 weeks period (approximately), in the research laboratory. The cells are then transfused into the patient.

Conditions

Interventions

TypeNameDescription
BIOLOGICALGroup APeptide-stimulated T cells 2 x 10\^7/m\^2
BIOLOGICALGroup BPeptide-stimulated T cells per dose-escalation protocol

Timeline

Start date
2015-11-01
Primary completion
2025-05-01
Completion
2025-05-01
First posted
2015-10-20
Last updated
2025-05-14

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT02580539. Inclusion in this directory is not an endorsement.

A Study of the Safety and Efficacy of EBV Specific T-cell Lines (NCT02580539) · Clinical Trials Directory