drugset / Trial / NCT01214889

Study of PENTAXIM™ Vaccine Versus TETRAXIM™ Vaccine Given With ACTHIB™ Vaccine in South Korean Infants.

NCT01214889

Phase 3 Completed 370 enrolled Sanofi
RandomizedParallel-groupOpen-labelPrevention

Summary

This study is designed to assess the immunogenicity and safety of PENTAXIM™ combined vaccine versus TETRAXIM™ vaccine to support registration of PENTAXIM™ in South Korea. Primary Objective: To demonstrate the non-inferiority in terms of seroprotection rates (Diphtheria, Tetanus, Polio types 1, 2 and 3, Polyribosyl Ribitol Phosphate \[PRP\]) and vaccine response rates to acellular Pertussis antigens of sanofi pasteur's PENTAXIM™ vaccine versus sanofi pasteur's TETRAXIM™ and Act (Haemophilus influenzae type b) HIB™ vaccines, one month after the three-dose primary vaccination.

Timeline

Start
2010-09
Primary completion
2011-11
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator ActHIB Vaccine 0.5 ml Intramuscular
Subject PENTAXIM™ Vaccine 0.5 ml Intramuscular
Comparator TETRAXIM™ Vaccine 0.5 ml Intramuscular