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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | RSVPreF3 OA vaccine | Vaccine | — | Intramuscular |
| Background | Influenza Virus Vaccine | Vaccine | — | Intramuscular |