drugset / Trial / NCT04683224
A Study to Evaluate the Safety, Immunogenicity, and Efficacy of UB-612 COVID-19 Vaccine
RandomizedParallel-groupQuadruple-blindPrevention
Summary
This is a Phase 2/3, randomized, multicenter, double-blind, dose-response study to evaluate the safety, immunogenicity, and efficacy of UB 612 in 2 age groups, adults 18 to 59 and ≥60 years of age with or without comorbidities.
Timeline
- Start
- 2021-02-01
- Primary completion
- 2023-03-22
- Completion
- 2023-03-22
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | UB-612 | Vaccine | 100 ug | Intramuscular |