drugset / Trial / NCT01974895

Study to Evaluate Immunogenicity and Safety of GlaxoSmithKline (GSK) Biologicals' Quadrivalent Influenza Vaccine GSK2282512A When Administered to Children From 6 to 35 Months of Age

NCT01974895

Phase 2 Completed 316 enrolled GlaxoSmithKline
RandomizedParallel-groupTriple-blindPrevention

Summary

The purpose of this study is to evaluate the immunogenicity and safety of the new influenza vaccine GSK2282512A (FLU Q-QIV) and compare its activity to Sanofi Pasteur's Fluzone® (TIV) in children 6 to 35 months of age.

Timeline

Start
2013-10-23
Primary completion
2014-02-27
Completion
2014-07-03

Drugs

EvaluationDrugModalityDoseRoute
Subject FluLaval® Quadrivalent Vaccine Intramuscular
Comparator Influenza Virus Vaccine Vaccine Intramuscular

Indications