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Clinical Trial Summary

The objective of study is to evaluate the immunogenicity and safety of SCTV01C or SCTV01E as booster compared with Sinopharm inactivated COVID-19 vaccine as booster. The study will also evaluate the immunogenicity and safety of 2-dose vaccinations.


Clinical Trial Description

The study is a randomized, double-blind, and approved vaccine-controlled Phase II booster study. It will evaluate the immunogenicity and safety of one dose of SCTV01C or SCTV01E as booster compared with one dose of Sinopharm inactivated COVID-19 vaccine or one dose of Commirnaty as booster. The study will also evaluate the immunogenicity and safety of 2-dose vaccinations (1-dose of SCTV01C and 1-dose of SCTV01E, or 2-dose of SCTV01E, or 1-dose of Sinopharm inactivated COVID-19 vaccine and 1-dose of SCTV01E, 1-dose of Comirnaty and 1-dose of SCTV01E). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05239806
Study type Interventional
Source Sinocelltech Ltd.
Contact Min Ke
Phone +86 18501160269
Email min_ke@sinocelltech.com
Status Not yet recruiting
Phase Phase 2
Start date April 1, 2022
Completion date August 1, 2023

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