drugset / Trial / NCT05879107
Study to Assess the Immune Response, the Safety and the Reactogenicity of Respiratory Syncytial Virus (RSV) Prefusion Protein 3 Older Adult (OA) (RSVPreF3 OA) Investigational Vaccine When co Administered With PCV20 in Older Adults
RandomizedParallel-groupOpen-labelPrevention
Summary
The purpose of this study is to assess the ability of RSVPreF3 OA investigational vaccine to generate an immune response when given in combination with PCV20 and its safety in older adults, aged ≥60 years of age.
Timeline
- Start
- 2023-05-26
- Primary completion
- 2023-12-06
- Completion
- 2024-05-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PCV20 | Vaccine | — | Intramuscular |
| Subject | RSVPreF3 OA | Vaccine | — | Intramuscular |