drugset / Trial / NCT01988857

Safety of a Booster Dose of GlaxoSmithKline (GSK) Biologicals' Boostrix™ Vaccine in Healthy Vietnamese Children

NCT01988857

Phase 3 Completed 302 enrolled GlaxoSmithKline
NaSingle-groupOpen-labelPrevention

Summary

This study will evaluate the safety and reactogenicity of GSK Biologicals' combined reduced-antigen-content diphtheria-tetanus-acellular pertussis (dTpa) vaccine, Boostrix™ when given as a single injection to 6-10 year old children. Data that are available globally on the age group from four to six years of age will be used to bridge the age gap in this study and aid in the registration of the vaccine for children from the age of four years.

Timeline

Start
2014-02-22
Primary completion
2014-05-10
Completion
2014-05-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Boostrix Vaccine Intramuscular

Indications