The purpose of this study is to describe the immunogenicity and safety of IMOJEVĀ® in adult and pediatric populations in Vietnam and serve a bridging study to compare immunogenicity, reactogenicity, and safety data obtained with IMOJEVĀ® in the Vietnamese population with data from other Asian pediatric populations. Primary objective: \- To describe the safety profile of a single dose of IMOJEVĀ®. Secondary objectives: * To evaluate the immune response to JE 28 days after the administration of a single dose of IMOJEVĀ® in healthy Vietnamese subjects aged from 9 months to 60 years.
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Number of Participants With Solicited Injection Site Reactions and Systemic Events Following a Single Primary Dose of a Live Attenuated Japanese Encephalitis Chimeric Virus Vaccine (IMOJEVĀ®)
Timeframe: Day 0 up to Day 14 post-vaccination
Percentage of Participants With Japanese Encephalitis Seroprotection Following a Single Primary Dose of a Live Attenuated Japanese Encephalitis Chimeric Virus Vaccine (IMOJEVĀ®)
Timeframe: Day 0 (pre-vaccination) and Day 28 post-vaccination
Percentage of Participants With Japanese Encephalitis Seroconversion Following a Single Primary Dose of a Live Attenuated Japanese Encephalitis Chimeric Virus Vaccine (IMOJEVĀ®)
Timeframe: Day 0 (pre-vaccination) and Day 28 post-vaccination
Summary of Geometric Mean Titers of Japanese Encephalitis Antibodies Following a Single Primary Dose of a Live Attenuated Japanese Encephalitis Chimeric Virus Vaccine (IMOJEVĀ®)
Timeframe: Day 0 (pre-vaccination) and Day 28 post-vaccination