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  2. Dengue vaccine - Wikipedia

    en.wikipedia.org/wiki/Dengue_vaccine

    In December 2018, Dengvaxia was approved in the European Union. [7]In May 2019, Dengvaxia was approved in the United States as the first vaccine approved for the prevention of dengue disease caused by all dengue virus serotypes (1, 2, 3, and 4) in people ages nine through 16 who have laboratory-confirmed previous dengue infection and who live in endemic areas.

  3. WHO clears Takeda's dengue vaccine - AOL

    www.aol.com/news/clears-takedas-dengue-vaccine...

    French giant Sanofi's Dengvaxia is the other available dengue vaccine, having received approval in several countries in the Americas, the EU and Asia starting in 2015.

  4. Dengue virus - Wikipedia

    en.wikipedia.org/wiki/Dengue_virus

    The 2016 vaccine Dengvaxia is only recommended in individuals who have been previously infected, or in populations with a high rate of prior infection by age nine. [80] [58] Dengvaxia has been approved in 11 countries (Mexico, the Philippines, Indonesia, Brazil, El Salvador, Costa Rica, Paraguay, Guatemala, Peru, Thailand, and Singapore). [81 ...

  5. Dengue fever - Wikipedia

    en.wikipedia.org/wiki/Dengue_fever

    Dengvaxia (formerly CYD-TDV) became available in 2015, and is approved for use in the US, EU and in some Asian and Latin American countries. [54] It is an attenuated virus, is suitable for individuals aged 6–45 years and protects against all four serotypes of dengue. [ 55 ]

  6. Takeda withdraws US application for dengue vaccine candidate

    www.aol.com/news/takeda-withdraws-us-application...

    The Japan-based company cited data collection issues, which cannot be addressed within the current review cycle. Sanofi's Dengvaxia, the world's first dengue vaccine, was licensed in 2015. Takeda ...

  7. List of stringent regulatory authorities - Wikipedia

    en.wikipedia.org/wiki/List_of_stringent...

    The idea is that countries with non-SRA drug authorities can use accelerated process to facilitate approval (registration or marketing authorization) of medicines, including vaccines and biologics, which have already been approved by SRAs. [1] As of 2022, the national regulatory authorities of 36 countries are considered SRAs: [2]

  8. Flavivirus - Wikipedia

    en.wikipedia.org/wiki/Flavivirus

    CYD-TDV, sold under the trade name Dengvaxia, is a tetravalent chimeric vaccine that splices structural genes of the four dengue viruses onto a 17D yellow fever backbone. [50] [51] Dengvaxia is approved in five countries. [52] An alternate approach to the development of flavivirus vaccine vectors is based on the use of viruses that infect insects.

  9. Mosquito-borne disease - Wikipedia

    en.wikipedia.org/wiki/Mosquito-borne_disease

    Dengvaxia, developed by Sanofi-Pasteur, was the first dengue vaccine available in the United States. [ 49 ] Dengvaxia (CYD-TVD) is a live attenuated vaccine , meaning it consists of a less severe pathogen which helps provide the human immune system with protective antigens and greater long term immunity.