Influenza Clinical Trial
Official title:
A Phase 2 Randomized Double Blind Parallel-Group Comparative Study to Evaluate the Immunogenicity and Safety of a Single Subcutaneous Injection of Trivalent Inactivated Influenza Virus Vaccine (TIV), TAK-850 (Cell-culture Derived) to TIV (Egg-derived) in Healthy Adults Aged 20-49 Years
The purpose of this study is to evaluate the immunogenicity and safety of TAK-850 administered subcutaneously as a single dose versus influenza HA vaccination in an exploratory manner.
This study is a phase 2, single dose study of TAK-850 (cell-culture derived TIV) administered subcutaneously in healthy Japanese adults, designed as a randomized, double-blind, parallel-group, comparative study to evaluate the immunogenicity and safety compared to an egg -derived TIV. ;
Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
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