The purpose of this study is to determine if a Vero cell-derived trivalent seasonal influenza vaccine produced by the modified manufacturing process: 1. induces immune responses comparable to that produced by the current manufacturing process 2. has an acceptable safety profile compared to a licensed trivalent seasonal influenza vaccine 3. demonstrates consistency of immune response among three different lots.
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Hemagglutination Inhibition Antibody (HIA) Titer for Each of the Three Antigens Contained in the Vaccine
Timeframe: 21 days post vaccination
Non-inferiority of Modified Manufacturing Process Compared to the Current Process
Timeframe: 21 days post vaccination
Lot Consistency of the Three Modified Manufacturing Process Lots
Timeframe: 21 days post vaccination
Percentage of Participants With Fever
Timeframe: onset within 7 days post vaccination