drugset / Trial / NCT01147900

Evaluation of Boostrix™10 Years After Previous Booster Vaccination

NCT01147900

Phase 4 Completed 180 enrolled GlaxoSmithKline
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The purpose of the study is to evaluate the immunogenicity, safety and reactogenicity of a dTpa (Boostrix™ vaccine) booster dose given 10 years after the previous vaccination with dTpa in GSK 263855/029 study. Only subjects who were part of the primary study will be invited to participate in this study.This protocol posting deals with objectives \& outcome measures of the booster phase. The objectives \& outcome measures of the primary phase are presented in a separate study (see reference).

Timeline

Start
2010-06-15
Primary completion
2012-05-08
Completion
2012-05-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Boostrix Vaccine Intramuscular

Indications