The purpose of this study is to investigate and valuate the immunogenicity and safety of the 13-valent pneumococcal polysaccharide conjugate vaccine in 2-71 months old healthy infants and toddlers (the youngest could be 6 weeks old)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
2,760
positive rate after infant doses
the rate of the immunoglobulin G ≥0.35μg/ml after infant doses
Time frame: 30 days after infant doses
GMC after infant doses
geometrical mean concentration of immunoglobulin G after infant doses
Time frame: 30 days after infant doses
positive rate after booster dose
the rate of the immunoglobulin G ≥0.35μg/ml after booster dose
Time frame: 30 days after booster dose
GMC after booster dose
geometrical mean concentration of immunoglobulin G after booster dose
Time frame: 30 days after booster dose
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