drugset / Trial / NCT07688369
Safety and Immunogenicity of a Recombinant Poliomyelitis Vaccine (rPV) in Comparison With IPOL Vaccine in Healthy Adults
RandomizedParallel-groupQuadruple-blindPrevention
Summary
The primary purpose of this study is to test a new experimental recombinant Poliomyelitis vaccine (rPV) in comparison to the commercially available inactivated poliovirus vaccine. The design of the study is double-blinded, randomised and active controlled. The active controlled product is considered the commercially available vaccine (IPOL).
Timeline
- Start
- 2026-07
- Primary completion
- 2026-11
- Completion
- 2027-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Inactivated Poliomyelitis Vaccine | Vaccine | — | — |
| Subject | Recombinant Poliomyelitis Vaccine | Vaccine | — | Intramuscular |