drugset / Trial / NCT01030822

Booster and Catch-up Vaccination With Vaccine GSK1024850A

NCT01030822

Phase 3 Completed 282 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate the immunogenicity, safety and reactogenicity of a booster dose of pneumococcal vaccine GSK1024850A administered either at 9-18 months or 15-18 months of age in children primed in primary study NCT00814710. This study also aims to assess the persistence of antibodies induced following primary vaccination with pneumococcal vaccine GSK1024850A in primary study NCT00814710 prior to booster vaccination and following vaccination in the present study at approximately 24 months of age. The study is also designed to evaluate the immunogenicity, safety and reactogenicity of pneumococcal vaccine GSK1024850A when administered as a catch-up vaccination (2+1) in the second year of life in children unprimed with vaccine GSK1024850A in study NCT00814710.

Timeline

Start
2010-04-02
Primary completion
2011-08-19
Completion
2011-08-19

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK1024850A Vaccine Intramuscular