drugset / Trial / NCT02858440

A Study to Assess the Immunogenicity and Safety of GSK Biologicals' Infanrix-IPV/Hib Vaccine Administered as a Three-dose Vaccination Course at 3, 4.5 and 6 Months of Age and a Booster Dose at 18 Months of Age in Healthy Infants in Russia

NCT02858440 ↗

Phase 3 Completed 235 enrolled GlaxoSmithKline
NaSingle-groupOpen-labelPrevention

Summary

The purpose of this study is to evaluate the immune response, safety and reactogenicity after receiving combined DTPa-IPV/Hib vaccine when administered as a three-dose primary vaccination course at 3, 4.5 and 6 months of age and as a booster dose at 18 months of age in Russian healthy children according to the Russian immunisation schedule

Timeline

Start
2016-09-13
Primary completion
2017-10-24
Completion
2018-11-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Infanrix-IPV/Hib Vaccine — Intramuscular