drugset / Trial / NCT05188677

Immunogenicity and Safety Study of SCB-2019 Vaccine as a Booster to COVID-19 Vaccine in Adults

NCT05188677

Phase 3 Completed 1831 enrolled Clover Biopharmaceuticals AUS Pty
RandomizedParallel-groupQuadruple-blindPrevention

Summary

The purpose of this study is to assess the immunogenicity and safety of the investigational SCB-2019 vaccine, administered as a booster dose, to adults who: * Received primary series with one of the selected authorized or investigational COVID-19 vaccines at least 3 months prior to enrollment. * Received primary series and a booster dose of CoronaVac at least 3 months prior to enrollment.

Timeline

Start
2022-06-13
Primary completion
2023-06-06
Completion
2023-06-06

Drugs

EvaluationDrugModalityDoseRoute
Comparator AZD1222 Vaccine Intramuscular
Comparator BNT162b2 Messenger RNA (mRNA) Intramuscular
Comparator CoronaVac Vaccine Intramuscular
Subject SCB-2019 Vaccine Intramuscular

Indications