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This combination refers to the co-administration or co-formulation of a tetravalent dengue vaccine and a hepatitis A vaccine. The dengue component is designed to provide protection against all four serotypes of the dengue virus (DENV-1, DENV-2, DENV-3, and DENV-4), typically utilizing a live-attenuated viral platform such as the chimeric yellow fever-dengue virus (CYD-TDV). The hepatitis A component is an inactivated whole-virus vaccine intended to prevent infection by the hepatitis A virus. Clinical studies, such as those conducted by Sanofi Pasteur, have evaluated the safety and immunogenicity of these vaccines when administered concomitantly to simplify immunization schedules in regions where both diseases are endemic. The combination aims to maintain the high seroconversion rates of the individual vaccines while reducing the number of clinical visits required for full immunization.
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