drugset / Trial / NCT00322335

Long-term Persistence Study to Assess a Booster Dose of GSK Biologicals' Hib-MenC

NCT00322335

Phase 3 Completed 230 enrolled GlaxoSmithKline
Non-randomizedParallel-groupOpen-labelPrevention

Summary

This protocol posting deals with objectives \& outcome measures of the extension phase at Months 18, 30, 42, 54 and 66 post booster. The objectives \& outcome measures of the primary phase are presented in a separate protocol posting (NCT number = NCT00352963). The objectives \& outcome measures of the Booster phase/study are presented in a separate protocol posting (NCT number =NCT00323050). The purpose of this study is to evaluate the persistence of meningococcal serogroup C and Hib antibodies on a yearly basis for a period of 5.5 years after booster vaccination. The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.

Timeline

Start
2006-05
Primary completion
2006-07
Completion
2010-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Menitorix Vaccine Intramuscular
Comparator Engerix-B Vaccine Intramuscular
Comparator Infanrix hexa Vaccine Intramuscular
Comparator Infanrix™ IPV/HIB Unknown Intramuscular
Comparator Meningitec Vaccine Intramuscular
Comparator NeisVac-C Vaccine Intramuscular
Background Pediarix Vaccine Intramuscular