drugset / Trial / NCT05517642
IH Convidecia as Second Booster Dose Against Breakthrough Infections
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ad5-nCoV-IH | Vaccine | — | Inhaled |
| Comparator | BNT162b2 | Messenger RNA (mRNA) | — | Intramuscular |