drugset / Trial / NCT00343889

Comparison of DTaP-HB-PRP~T Combined Vaccine to Tritanrix-HepB/Hib™, Both Given Concomitantly With Oral Polio Vaccine

NCT00343889

Phase 3 Completed 379 enrolled Sanofi Pasteur, a Sanofi Company
RandomizedParallel-groupSingle-blindPrevention

Summary

The purpose of this study is to support the registration of the pentavalent DTaP-HB-PRP\~T vaccine in countries that follow the World Health Organization-Expanded Program of Immunization (WHO-EPI) schedule. The primary objective is: * To demonstrate that the pentavalent DTaP-HB-PRP\~T combined vaccine does not induce a lower immune response than Tritanrix-HepB/Hib™ in terms of the seroprotection rate to hepatitis B (HB) one month after a 3-dose primary series at 6, 10, and 14 weeks of age. The secondary objectives are: * To describe in each group the immunogenicity parameters one month after the 3-dose primary series at 6, 10, and 14 weeks of age; and * To evaluate the overall safety in terms of any adverse events in the first 28 days after each injection and any serious adverse events during the entire trial.

Timeline

Start
2006-08
Primary completion
2007-11
Completion
2008-04

Drugs

EvaluationDrugModalityDoseRoute
Subject DTaP-HB-PRP~T Vaccine 0.5 ml Intramuscular
Comparator Tritanrix-HepB/Hib™ Vaccine 0.5 ml Intramuscular
Background Oral Polio Vaccine Vaccine Oral