Publication date: Jul 16, 2026
This phase 1 clinical trial will evaluate the safety, reactogenicity, and immunogenicity of RVX-sCPD9, given Intranasally (IN), as a booster dose to previously vaccinated healthy adults. The study is designed as a non-randomized, open-label, dose-escalation clinical trial evaluating four dose levels of RVX-sCPD9 administered IN (10^2, 10^3, 10^4, 5 x 10^4 FFU). A sample size of 80 participants (20 participants in each cohort). The primary objective is to evaluate the safety and reactogenicity of a single IN administration of 4 ascending dosages of RVX-sCPD9 in previously vaccinated healthy adults.
| Concepts | Keywords |
|---|---|
| Boost | |
| Boster | |
| Coronavirus | |
| COVID | |
| Intranasal | |
| Next Generation | |
| Phase 1 | |
| RVX-sCPD9 | |
| SARS-CoV-2 | |
| Vaccine |
Semantics
Original Article
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