drugset / Trial / NCT03308825

Safety and Immunogenicity of Fluzone® Quadrivalent and Fluzone® High-Dose, Influenza Vaccines

NCT03308825

Phase 4 Completed 240 enrolled Sanofi Pasteur, a Sanofi Company
Non-randomizedParallel-groupOpen-labelPrevention

Summary

The aim of the study was to describe the safety and immunogenicity of the 2017-2018 formulation of Fluzone Quadrivalent vaccine in children 6 months to \< 9 years of age, and in adults 18 to \< 65 years of age, and to describe the safety and immunogenicity of the 2017-2018 formulation of Fluzone High-Dose vaccine in adults ≥ 65 years of age.

Timeline

Start
2017-09-11
Primary completion
2017-11-22
Completion
2017-11-22

Drugs

EvaluationDrugModalityDoseRoute
Subject Fluzone High-Dose vaccine Vaccine 0.5 ml Intramuscular
Subject Fluzone Quadrivalent vaccine Vaccine 0.25 ml Intramuscular
Subject Fluzone Quadrivalent vaccine Vaccine 0.5 ml Intramuscular

Indications