drugset / Trial / NCT02753413

Safety and Reactogenicity Study of GlaxoSmithKline (GSK) Biologicals' Investigational Respiratory Syncytial Virus (RSV) Vaccine (GSK3003891A) in Healthy Women

NCT02753413

Phase 2 Completed 102 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to assess the safety and reactogenicity of a single intramuscular dose of GSK Biologicals' investigational RSV vaccine, in healthy, non-pregnant women aged 18 to 45 years.

Timeline

Start
2016-04-01
Primary completion
2016-06-28
Completion
2016-06-28

Drugs

EvaluationDrugModalityDoseRoute
Comparator Boostrix Vaccine Intramuscular
Subject GSK3003891A Vaccine 60 ug Intramuscular