drugset / Trial / NCT04683224

A Study to Evaluate the Safety, Immunogenicity, and Efficacy of UB-612 COVID-19 Vaccine

NCT04683224

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

EvaluationDrugModalityDoseRoute
Subject UB-612 Vaccine 100 ug Intramuscular

Indications