drugset / Trial / NCT03282240

Safety and Immunogenicity of High-Dose Quadrivalent Influenza Vaccine in Participants ≥65 Years in the US

NCT03282240

Phase 3 Completed 2670 enrolled Sanofi Pasteur, a Sanofi Company
RandomizedParallel-groupDouble-blindPrevention

Summary

This randomized, modified double-blind, active-controlled, multi-center trial assessed the safety and immunogenicity of the high-dose quadrivalent influenza vaccine (QIV-HD) compared to either the licensed or investigational high-dose trivalent influenza vaccine (TIV-HD) in adults.

Timeline

Start
2017-09-08
Primary completion
2017-11-02
Completion
2018-04-19

Drugs

EvaluationDrugModalityDoseRoute
Comparator Investigational TIV-HD2 Vaccine 0.5 ml Intramuscular
Comparator Licensed TIV-HD1 Vaccine 0.5 ml Intramuscular
Subject QIV-HD Vaccine 0.7 ml Intramuscular

Indications