drugset / Trial / NCT05568797

A Study on the Immune Response and Safety of a Vaccine Against Respiratory Syncytial Virus (RSV) When Given Alone or Co-administered With an Adjuvanted Vaccine Against Influenza in Adults Aged 65 Years and Above

NCT05568797

Phase 3 Completed 1045 enrolled GlaxoSmithKline
RandomizedParallel-groupOpen-labelPrevention

Summary

The aim of this study is to assess the immunogenicity, safety and reactogenicity of the RSV PreFusion protein 3 older adult (RSVPreF3 OA) investigational vaccine when co-administered with an adjuvanted quadrivalent influenza (FLU aQIV) vaccine, in adults aged 65 years of age (YOA).

Timeline

Start
2022-10-14
Primary completion
2023-02-17
Completion
2023-07-17

Drugs

EvaluationDrugModalityDoseRoute
Subject RSVPreF3 OA vaccine Vaccine Intramuscular
Background Influenza Virus Vaccine Vaccine Intramuscular