drugset / Trial / NCT02914275

A Study to Evaluate the Immunogenicity and Safety of Seqirus Quadrivalent Influenza Vaccine (QIV) in a Pediatric Population 6 Months Through 59 Months of Age.

NCT02914275

Phase 3 Completed 2250 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 2016/2017 Quadrivalent Influenza Vaccine (comparator QIV) in a healthy pediatric population 6 months through 59 months of age.

Timeline

Start
2016-09-27
Primary completion
2017-03-09
Completion
2017-08-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Comparator QIV Vaccine 60 ug Intramuscular
Comparator Influenza Virus Vaccine Vaccine Intramuscular

Indications