MBCOV-22
MBCOV-22
MBCOV-22

Immunogenicity and Safety Study of Half Dose of Moderna COVID-19 Vaccine Booster Heterologous in Adult Subjects in Indonesia. To compare the immunogenicity after booster dose between AstraZeneca and Sinovac priming group

Outcome

To evaluate the antibody titres before and 28 days (+7 days) after booster dose with half booster dose of mRNA-1273

Sponsor

Kementerian Kesehatan Republik Indonesia

Date

-

Subjects

200 subjects