drugset / Trial / NCT00529321

Immunotherapy With TG4040 in Treatment-naïve Patients Chronically Infected With Hepatitis C Virus

NCT00529321 ↗

Phase 1 Completed 42 enrolled Transgene
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objective is to determine the safety of sub-cutaneous (SC) injections of TG4040 in non-cirrhotic, treatment-naïve patients chronically infected with HCV (genotype 1). Patients will be sequentially treated at an escalting dose of TG4040. All patients will be followed up to at least 6 months after his/her first injection. In addition, all patients treated at the highest dose will receive a TG4040 boost injection 6 months after the first injection, and will be followed up during an additional 6-month period.

Timeline

Start
2006-12
Primary completion
2009-09
Completion
2010-09

Drugs

EvaluationDrugModalityDoseRoute
Subject TG4040 Vaccine 1e+06 unknown Subcutaneous
Subject TG4040 Vaccine 1e+07 unknown Subcutaneous
Subject TG4040 Vaccine 1e+08 unknown Subcutaneous