drugset / Trial / NCT00148941

Immune Response and Safety Comparison of 3 Lots of GSK Biologicals' DTaP-IPV Candidate Vaccine to DTaP + IPV Vaccines

NCT00148941

Phase 3 Completed 4209 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

The aims of this trial are to demonstrate the consistency of three manufacturing lots of GSK Biologicals' DTaP-IPV candidate vaccine in terms of immunogenicity and to evaluate the non-inferiority of GSK Biologicals' DTaP-IPV vaccine with respect to immunogenicity and safety compared to the control vaccines (separate injections of GSK Biologicals' DTaP vaccine \[Infanrix\] and Aventis Pasteur's IPV vaccine \[IPOL\]) when administered as a 5th dose of DTaP and a 4th dose of inactivated poliovirus vaccine in subjects 4 to 6 years of age. Vaccines will be co-administered with the second dose of M-M-RII, which is recommended at this age. Concomitant administration of a US-licensed influenza vaccine will be allowed according to seasonal availability of vaccine and at the discretion of the investigator.

Timeline

Start
2005-01-06
Primary completion
2006-11-01
Completion
2006-12-04

Drugs

EvaluationDrugModalityDoseRoute
Comparator Adacel Vaccine Intramuscular
Comparator IPOL Vaccine Subcutaneous
Subject SB213503 Vaccine Intramuscular
Background M-M-R II Vaccine Subcutaneous

Indications