drugset / Trial / NCT05044195

A Clinical Study to Evaluate the Immunogenicity and Safety of an Adjuvanted Quadrivalent Influenza Vaccine Compared With a Licensed Quadrivalent Vaccine in Adults 50 to 64 Years of Age

NCT05044195

Phase 3 Completed 2044 enrolled Seqirus
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This Phase 3 study is a randomized, observer-blind immunogenicity and safety study of aQIV (an MF59-adjuvanted quadrivalent influenza vaccine) compared with a licensed quadrivalent influenza vaccine in adults 50 to 64 years of age.

Timeline

Start
2021-09-30
Primary completion
2022-01-18
Completion
2022-09-09

Drugs

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

Indications