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A Multicenter, Randomized, Placebo-Controlled, Double-Blinded Pivotal Study To Evaluate Safety And Immunogenicity Of A Live-Attenuated Chikungunya Virus Vaccine Candidate In Adults Aged 18 Years And Above

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Trial Profile

A Multicenter, Randomized, Placebo-Controlled, Double-Blinded Pivotal Study To Evaluate Safety And Immunogenicity Of A Live-Attenuated Chikungunya Virus Vaccine Candidate In Adults Aged 18 Years And Above

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 07 Feb 2025

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At a glance

  • Drugs VLA 1553 (Primary)
  • Indications Chikungunya virus infections
  • Focus Adverse reactions; Pharmacodynamics; Registrational
  • Sponsors Valneva

    • Most Recent Events

    • 05 Feb 2025 According to a Valneva media release, company expects to receive marketing approval in Brazil in the first quarter of 2025, which would represent the first approval in an endemic country.
    • 05 Feb 2025 According to a Valneva media release, company announced that the Medicines and Healthcare products Regulatory Agency (MHRA) has granted marketing authorization in the United Kingdom (UK) for the world's first and only chikungunya vaccine, IXCHIQ based on the data of this study.
    • 01 Jul 2024 According to Valneva media release, company announced that the European Commission (EC) has granted marketing authorization in Europe for Valneva's single-dose vaccine, based on data from this trial.

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