drugset / Trial / NCT00622232

A Rollover Study for Subjects Who Completed Participation in the VRX496-USA-05-002 Trial

NCT00622232 ↗

Phase 2 Unknown 40 enrolled VIRxSYS Corporation
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The objective of this study is to determine the long term safety and tolerability of an additional infusion of 10 billion VRX496 gene-modified CD4 T cells with a focus on evaluating additional therapeutic benefits with respect to viral load and CD4 counts.

Timeline

Start
2007-12
Primary completion
2009-01
Completion
2023-06

Drugs

EvaluationDrugModalityDoseRoute
Subject VRX496-transduced autologous CD4 T cells Cell therapy 1e+10 cells —