drugset / Trial / NCT00896064

Evaluation of a Booster Dose of Pneumococcal Vaccine Formulations in Young Adults

NCT00896064

Phase 2 Completed 43 enrolled GlaxoSmithKline
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this study is to evaluate the safety, reactogenicity and immunogenicity of a booster dose of pneumococcal vaccines (GSK 2189242A) in young adults. This protocol posting deals with objectives \& outcome measures of the booster phase. The objectives \& outcome measures of the primary phase are presented in a separate protocol posting (NCT 00707798)

Timeline

Start
2009-05-18
Primary completion
2009-08-05
Completion
2009-08-05

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK2189242A Vaccine Intramuscular