drugset / Trial / NCT01905215

Study to Evaluate the Safety, Reactogenicity and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Investigational Respiratory Syncytial Virus (RSV) Vaccines

NCT01905215

Phase 1 Completed 128 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this first time in human (FTiH) study is to evaluate the safety, reactogenicity and immunogenicity of several formulations of Respiratory Syncytial Virus (RSV) investigational vaccines in healthy men.

Timeline

Start
2013-07-22
Primary completion
2014-04-09
Completion
2015-03-16

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK3003892A Vaccine Intramuscular
Subject GSK3003893A Vaccine Intramuscular
Subject GSK3003895A Vaccine Intramuscular
Subject GSK3003896A Vaccine Intramuscular
Subject GSK3003898A Vaccine Intramuscular
Subject GSK3003899A Vaccine Intramuscular