drugset / Trial / NCT00436007

Safety and Immunogenicity Study of GSK Biologicals' Malaria Vaccine 257049, When Incorporated Into an EPI Regimen

NCT00436007

Phase 2 Completed 511 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

This study is being done to assess the possibility of the potential integration of malaria vaccine into the EPI regimen. It will evaluate whether the malaria vaccine is safe and immunogenic in infants aged 6 to 10 weeks at first dose, when co-administered with other EPI vaccine antigens. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.

Timeline

Start
2007-04-30
Primary completion
2008-09-15
Completion
2009-10-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK257049 Vaccine Intramuscular
Background Polio Sabin Vaccine Oral
Background Rouvax Vaccine Intramuscular
Background Tritanrix™ HepB/Hib Vaccine Intramuscular
Background Yellow Fever Vaccine Vaccine Intramuscular

Indications