drugset / Trial / NCT05329038

Immunogenicity,Safety and Cross - Immune Response With Mutant Strains of a Third Dose of an Inactivated COVID-19 Vaccine

NCT05329038

Phase 4 Unknown 180 enrolled Sinovac Life Sciences Co., Ltd.
RandomizedParallel-groupOpen-labelPrevention

Summary

This is a phase Ⅳ follow-up clinical trial based on the previous Phase Ⅳ clinical trial of an inactivated COVID-19 vaccine (CoronaVac) manufactured by Sinovac Life Sciences Co., Ltd.The purpose of this study is to evaluate the immunogenicity,safety and cross-immune response of booster immunization using COVID-19 vaccine,to compare the similarities and differences of immune responses between primary immunization and booster immunization and to detect antibody against hepatitis A and evaluate the immune persistence of the one dose immunization schedule of hepatitis A vaccine in healthy population aged 18 years and older.

Timeline

Start
2022-04-19
Primary completion
2022-06-19
Completion
2024-02-20

Drugs

EvaluationDrugModalityDoseRoute
Subject CoronaVac Vaccine 600 unknown

Indications