drugset / Trial / NCT04545749

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

NCT04545749

Non-randomizedSequentialOpen-labelPrevention

Summary

This is a phase I, open-label, dose-escalation clinical study to evaluate the safety, tolerability and immunogenicity of 3 ascending doses of UB-612 COVID-19 vaccine in healthy adults, aged from 20 to 55 years old.

Timeline

Start
2020-09-25
Primary completion
2021-01-18
Completion
2021-05-24

Drugs

EvaluationDrugModalityDoseRoute
Subject UB-612 Vaccine 10 ug
Subject UB-612 Vaccine 30 ug
Subject UB-612 Vaccine 100 ug

Indications