drugset / Trial / NCT01439360

An Efficacy Study of GlaxoSmithKline (GSK) Biologicals' Candidate Influenza Vaccine GSK2321138A in Children

NCT01439360 ↗

Phase 3 Completed 12046 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to evaluate the efficacy, immunogenicity and safety of GSK Biologicals' influenza candidate vaccine GSK2321138A when compared to non-influenza vaccine comparators in children 6 to 35 months of age. Recruitment will encompass at least 4 independent cohorts: a first cohort in the Northern Hemisphere (2011-2012), a second cohort in subtropical countries (2012), third cohort in the Northern Hemisphere (2012-2013) and a fourth cohort and additional independent cohorts possibly in NH countries (end 2013) and subtropical countries (beginning 2014).

Timeline

Start
2011-10-01
Primary completion
2014-10-31
Completion
2014-12-31

Outcome

Met primary endpoint

registry Vaccine efficacy (VE) 63.2 (97.5% CI 51.8 to 72.3) NCT01439360 ↗

registry Vaccine efficacy (VE) 49.8 (97.5% CI 41.8 to 56.8) NCT01439360 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject GSK2321138A Vaccine — Intramuscular
Comparator Havrix Junior Vaccine — Intramuscular
Comparator Prevenar 13 Vaccine — Intramuscular
Comparator Varilrix Vaccine — Subcutaneous
Comparator Varivax Vaccine — Intramuscular

Indications