drugset / Trial / NCT02545543

A Study to Evaluate the Immunogenicity and Safety of Seqirus Quadrivalent Influenza Vaccine (QIV) in a Pediatric Population 5 Through 17 Years of Age

NCT02545543

Phase 3 Completed 2278 enrolled Seqirus
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is a study to assess the immune (antibody) response and safety of a Seqirus split virion, inactivated Quadrivalent Influenza Vaccine (Seqirus QIV), in comparison with a US licensed 2015/2016 Quadrivalent Influenza Vaccine (comparator QIV) in a healthy pediatric population 5 through 17 years of age.

Timeline

Start
2015-09
Primary completion
2016-01
Completion
2016-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator Comparator QIV Vaccine 0.5 ml Intramuscular
Subject Seqirus QIV Vaccine 0.5 ml Intramuscular

Indications