Influenza Clinical Trial
Official title:
Evaluation of Safety and Immunogenicity Among Different Age-groups Receiving Different Split Influenza Vaccines
The purpose of this study is to observe the adverse reaction ratio and hemagglutination inhibition (HI) antibody positive rate, Geometric mean titer (GMT) of three brands split influenza virus vaccine in different population.
Observational Objectives:
To describe the safety of evaluated vaccine, given in the two-dose schedule in accordance
with the Package Insert, in children aged ≥ 6 months to ≤ 36 months,6th to 12th birthday and
≥ 60th birthday.
To describe the immunogenicity of evaluated vaccine, given in the two-dose schedule in
accordance with the Package Insert, in children aged ≥ 6 months to ≤ 36 months, 6th to 12th
birthday and ≥ 60rd birthday.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention
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