drugset / Trial / NCT01353703

Immunogenicity and Safety Study in Infants of GlaxoSmithKline Biologicals' Infanrix Hexa™ (DTPa-HBV-IPV/Hib) Vaccine

NCT01353703

Phase 3 Completed 224 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

This study evaluates the immunogenicity and safety of Infanrix hexa™ (DTPa-HBV-IPV/Hib) when administered as a primary vaccination course to Indian infants according to a 6-10-14 weeks or a 2-4-6 months schedule.

Timeline

Start
2012-04-16
Primary completion
2013-02-25
Completion
2013-02-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Infanrix hexa Vaccine Intramuscular