drugset / Trial / NCT01905215
Study to Evaluate the Safety, Reactogenicity and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Investigational Respiratory Syncytial Virus (RSV) Vaccines
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | GSK3003892A | Vaccine | — | Intramuscular |
| Subject | GSK3003893A | Vaccine | — | Intramuscular |
| Subject | GSK3003895A | Vaccine | — | Intramuscular |
| Subject | GSK3003896A | Vaccine | — | Intramuscular |
| Subject | GSK3003898A | Vaccine | — | Intramuscular |
| Subject | GSK3003899A | Vaccine | — | Intramuscular |