drugset / Trial / NCT01436357

Staged Phase I/II Hepatitis C Prophylactic Vaccine

NCT01436357

RandomizedParallel-groupTriple-blindPrevention

Summary

A two stage, phase I/II, double-blinded, randomized, placebo-controlled study of hepatitis C virus (HCV)uninfected male and female injection drug users (IDU) aged 18 to 45. AdCh3NSmut1 and MVA-NSMut HCV vaccine will be administered to 68 (+/-4) volunteers in stage 1. A planned interim analysis of safety and immunogenicity will be conducted. If no safety signal is detected and there is evidence of a measurable immune response to HCV then 472 (+/-4) volunteers will be enrolled in stage 2. Primary objectives are to 1) assess the safety of AdCh3NSmut1 and MVA-NSmut compared to placebo when administered to HCV-uninfected IDUs and 2) determine if AdCh3NSmut1 and MVA-NSmut HCV vaccines will reduce incidence of chronic HCV infection compared to placebo among HCV-uninfected IDUs. Planned study duration is approx 63 months (accrual time, 2 months vaccination, 18 months follow-up, and 9 months extended observation for subjects becoming viremic in the last month of follow-up).

Timeline

Start
2012-03-06
Primary completion
2018-05-25
Completion
2018-05-25

Drugs

EvaluationDrugModalityDoseRoute
Subject AdCh3NSmut1 Vaccine 2.5e+10 unknown Intramuscular
Subject MVA-NSmut Vaccine 1.8e+08 unknown Intramuscular