drugset / Trial / NCT00529321
Immunotherapy With TG4040 in Treatment-naïve Patients Chronically Infected With Hepatitis C Virus
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | TG4040 | Vaccine | 1e+06 unknown | Subcutaneous |
| Subject | TG4040 | Vaccine | 1e+07 unknown | Subcutaneous |
| Subject | TG4040 | Vaccine | 1e+08 unknown | Subcutaneous |