🇪🇺 IXCHIQ in European Union

EMA authorised IXCHIQ on 28 June 2024

Marketing authorisation

EMA — authorised 28 June 2024

  • Application: EMEA/H/C/005797
  • Marketing authorisation holder: Valneva Austria GmbH
  • Local brand name: Ixchiq
  • Indication: Ixchiq is indicated for active immunisation for the prevention of disease caused by chikungunya virus (CHIKV) in individuals between 12 years older. The use of this vaccine should be in accordance with official recommendations. 
  • Pathway: PRIME
  • Status: approved

The European Medicines Agency (EMA) approved IXCHIQ, a vaccine for active immunisation against chikungunya virus (CHIKV) disease. This approval was granted on 28 June 2024, under the PRIME expedited pathway. The vaccine is indicated for individuals aged 12 years and above, and its use should follow official recommendations.

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IXCHIQ in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Other Other approved in European Union

Frequently asked questions

Is IXCHIQ approved in European Union?

Yes. EMA authorised it on 28 June 2024.

Who is the marketing authorisation holder for IXCHIQ in European Union?

Valneva Austria GmbH holds the EU marketing authorisation.