Trial ChiCTR2000034825 ; NCT04523571
Publication Li J, Nature Medicine, 2021
Primary outcome on the report: The primary endpoints for the safety evaluation were the incidence of solicited local reactions at the injection site or systemic adverse reactions in the 14 d after the prime or boost dose, and adverse events after the full immunization in the 28 d after receiving the boost dose.

Note: The risk of bias by domain corresponds to the highest risk of bias among outcomes by domain.
The overall risk of bias corresponds to the overall highest risk of bias assessed among outcomes.