drugset / Trial / NCT00453570

Immunogenicity and Safety of Pentaxim as 3 Doses Primary Vaccination Followed by a Booster Dose at 18 Months

NCT00453570

Phase 3 Completed 792 enrolled Sanofi
RandomizedParallel-groupOpen-labelPrevention

Summary

As per request by the Heath Authorities, the present clinical study will assess the immunogenicity and safety of sanofi pasteur's DTacP-IPV// PRP\~T combined vaccine (PENTAXIM™) as a three-dose primary vaccination at 2, 3, and 4 months of age or 3, 4 and 5 months of age followed by a booster dose at 18-20 months of age as compared to commercially available DTacP, Hib conjugate (Act-HIB™) and IPV (IMOVAX Polio™) monovalent vaccines in order to meet the requirements for registration of the product in People's Republic of China.

Timeline

Start
2007-03
Primary completion
2008-12
Completion
2009-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator ActHIB Vaccine 0.5 ml Intramuscular
Comparator DTaP Unknown 0.5 ml Intramuscular
Subject DTaP-IPV//PRP∼T Vaccine 0.5 ml Intramuscular
Comparator Imovax(®) Polio Unknown 0.5 ml Intramuscular