This study will assess the immunogenicity and safety of booster vaccination with NBP606 compared to the existing commercial vaccine, when given concomitantly with routine pediatric vaccinations.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Enrollment
462
Clinical Research Center
Seoul, South Korea
Proportion of subjects with the targeted antibody concentration
Time frame: 1 month after the booster vaccination
Geometric mean concentration ratio
Time frame: 1 month after the booster vaccination
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