drugset / Trial / NCT05517642

IH Convidecia as Second Booster Dose Against Breakthrough Infections

NCT05517642

Phase 3 Completed 540 enrolled CanSino Biologics Inc.
RandomizedParallel-groupSingle-blindPrevention

Summary

This will be a randomized single-blind controlled trial to determine the immunogenicity, efficacy and safety of IH Convidecia (CanSino), as a second booster vaccination against Omicron and other emerging VOCs to prevent breakthrough infections among people with a sub-optimal immune response to the first booster dose. These subjects will be randomized in a ratio of 1:1 to receive a second booster dose of IH Convidecia vaccine (treatment arm), or a second booster dose of mRNA vaccine BNT162b2 (Pfizer).

Timeline

Start
2022-09-20
Primary completion
2023-05-02
Completion
2023-05-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Ad5-nCoV-IH Vaccine Inhaled
Comparator BNT162b2 Messenger RNA (mRNA) Intramuscular

Indications