drugset / Trial / NCT00829010

Primary and Booster Vaccination Study With a Pneumococcal Vaccine in HIV Infected, HIV Exposed Uninfected and HIV Uninfected Children 6 to 10 Weeks of Age.

NCT00829010

Phase 3 Completed 489 enrolled GlaxoSmithKline
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The purposes of this study: * To evaluate the immunogenicity, safety and reactogenicity of pneumococcal vaccine GSK1024850A in HIV infected infants, HIV exposed uninfected infants and HIV unexposed uninfected infants following a 3-dose primary vaccination at 6, 10 and 14 weeks of age and following booster vaccination at 9-10 months of age. * To evaluate the immunogenicity, safety and reactogenicity of pneumococcal vaccine GSK1024850A in HIV unexposed uninfected infants receiving either a 3-dose primary vaccination according to the EPI vaccination schedule at 6, 10 and 14 weeks of age with or without booster vaccination at 9-10 months of age or a 2-dose primary vaccination at 6 and 14 weeks of age followed by booster vaccination at 9-10 months of age. * This study also aims to assess the impact of the pneumococcal vaccine GSK1024850A on nasopharyngeal carriage of S. pneumoniae and H. influenzae up to 24 months of age in all study participants.

Timeline

Start
2009-02-17
Primary completion
2011-06-13
Completion
2012-06-27

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK1024850A Vaccine Intramuscular
Background M-M-R II Vaccine Intramuscular
Background Oral Poliovirus Vaccine Vaccine Oral
Background Rotarix Vaccine Oral
Background Tritanrix-HepB/Hib Vaccine Intramuscular