drugset / Trial / NCT05156632

Efficacy,Immunogenicity and Safety of COVID-19 Vaccine , Inactivated Booster Dose in Adults Aged 18 Years and Above

NCT05156632

RandomizedParallel-groupDouble-blindPrevention

Summary

This is a multi-center, case-driven, randomized, double-blinded, and placebo-controlled Phase Ⅲb clinical trial of COVID-19 Vaccine manufactured by Sinovac Research \& Development Co., Ltd.The purpose of this study is to evaluate the efficacy of the booster dose after two doses of CoronaVac® against RT-PCR confirmed symptomatic COVID-19 cases in participants aged 18 years and above.

Timeline

Start
2023-02-20
Primary completion
2023-02-20
Completion
2023-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject CoronaVac Vaccine 600 unknown
Subject CoronaVac Vaccine 1200 unknown

Indications