BCOV-21
BCOV-21
BCOV-21
BCOV-21
BCOV-21

Immunogenicity and Safety Study of Half and Full Dose of Heterologous and Homologous COVID-19 Vaccine Booster in Adult Subjects in Indonesia (Bcov 21)

Outcome

To evaluate the antibody titres before and one month (+7 days) after booster dose with full and half booster dose of ChAdOx1;S, Comirnaty®, or CoronaVac®

Sponsor

Badan Penelitian dan Pengembangan Kesehatan

Date

-

Subjects

715 (329 primary astrazeneca + 386 primary Sinovac) subjects