drugset / Trial / NCT00287092

Comparison of Safety and Immunogenicity of Pediacel™ and Infanrix™ IPV+Hib (Penta) Given in a 3 Dose Schedule in Infants

NCT00287092

Phase 3 Completed 807 enrolled Sanofi Pasteur, a Sanofi Company
RandomizedParallel-groupQuadruple-blindPrevention

Summary

Pediacel™ is currently licensed in the UK for use as a 3 dose regimen for the active immunisation of infants against Diphtheria, Tetanus, Pertussis, Poliomyelitis and invasive infections caused by Haemophilus influenzae type b. However there are currently no clinical data supporting the use of Pediacel™ using a 3, 5, and 12 months of age vaccination schedule. This study is designed to provide safety and immunogenicity data to support the use of Pediacel™ according to a 3, 5, and 12 months schedule.

Timeline

Start
2006-02
Primary completion
2007-05
Completion
2008-09

Drugs

EvaluationDrugModalityDoseRoute
Comparator Infanrix® -IPV+Hib Unknown 0.5 ml Intramuscular
Subject Pediacel® Vaccine 0.5 ml Intramuscular