drugset / Trial / NCT00601770

Virological Response Study of the HCV Vaccine IC41

NCT00601770 ↗

Phase 2 Completed 71 enrolled Valneva Austria GmbH
NaSingle-groupOpen-labelTreatment

Summary

The objective is to investigate the virological (HCV-RNA) responses following biweekly immunization with IC41. Treatment phase 14 weeks, total study duration including follow-up period 38 weeks.

Timeline

Start
2006-02
Primary completion
2008-07
Completion
2008-07

Drugs

EvaluationDrugModalityDoseRoute
Subject IC41 Vaccine 0.125 ml Other