drugset / Trial / NCT00316524

A Randomized, Double-blind, Placebo-controlled Study on Immunogenicity and Safety of MVA-BN (IMVAMUNE™) Smallpox Vaccine in Healthy Subjects

NCT00316524

RandomizedParallel-groupQuadruple-blindPrevention

Summary

The primary objective of this study is to evaluate the immune response after a single vaccination of pre-immune subjects compared to two vaccinations in naive subjects. In addition the study further investigates the cardiac safety profile of MVA-BN® in a healthy population compared to placebo.

Timeline

Start
2006-04
Primary completion
2007-02
Completion
2007-08

Drugs

EvaluationDrugModalityDoseRoute
Subject IMVAMUNE Vaccine 1e+08 unknown Subcutaneous

Indications