The purpose of this study is to demonstrate that V181 is safe and well tolerated, elicits an immune response, and reduces the frequency of virologically confirmed dengue (VCD) of any severity, due to any of the 4 dengue serotypes, regardless of dengue serostatus at baseline in children 2 to 17 years of age.
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Percentage of Participants Experiencing a Medically Attended Adverse Event (MAAE)
Timeframe: Up to approximately 6 months postvaccination
Percentage of Participants Experiencing a Serious Adverse Event (SAE)
Timeframe: Up to approximately 5 years postvaccination
Reactogenicity and Immunogenicity Subset: Percentage of Participants Experiencing Solicited Injection-site AEs
Timeframe: Up to approximately 5 days postvaccination
Reactogenicity and Immunogenicity Subset: Percentage of Participants Experiencing Solicited Systemic AEs
Timeframe: Up to approximately 28 days postvaccination
Percentage of Participants Experiencing Symptomatic (Requiring Fever on at Least 2 of 3 Consecutive Days) VCD of Any Severity, Due to Any of the 4 Dengue Serotypes, Regardless of Dengue Serostatus at Baseline
Timeframe: Up to approximately 3 years postvaccination