drugset / Trial / NCT00548171

Immunogenicity & Reactogenicity of Boostrix 10 Years After Previous Booster Vaccination in Study NCT01267058

NCT00548171

Phase 4 Completed 203 enrolled GlaxoSmithKline
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this study is to assess the efficacy and safety of repeating dTpa booster in adults 10 years after previous booster vaccination with dTpa in a previous clinical study (NCT01267058). Only subjects who received the booster vaccination in a previous clinical study are eligible for participation in this study. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007. No new recruitment will be performed in this booster phase (see inclusion criteria).

Timeline

Start
2007-11-05
Primary completion
2008-04-30
Completion
2008-04-30

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Boostrix Vaccine Intramuscular

Indications