drugset / Trial / NCT03020628

Immunogenicity and Safety of Quadrivalent Influenza Vaccine in Children Aged 6~35 Months

NCT03020628

Phase 3 Completed 171 enrolled SK Chemicals Co., Ltd.
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This study is a multi-center, randomized, double-blind Phase III Clinical trial. The purpose of this study is to assess the immunogenicity and safety of the quadrivalent cell culture-derived influenza vaccine compare to the trivalent cell culture-derived influenza vaccine in children aged 6\~35 months.

Timeline

Start
2016-10
Primary completion
2017-03
Completion
2017-06

Drugs

EvaluationDrugModalityDoseRoute
Subject NBP607-QIV Vaccine 0.5 ml Intramuscular
Comparator NBP607-TIV Vaccine 0.25 ml Intramuscular

Indications