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FDA Suspends Valneva's Chikungunya Vaccine After Deaths

8/25/2025

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Story summary
  • The FDA suspended Valneva's chikungunya vaccine, Ixchiq, following serious adverse reactions, including one death from encephalitis.
  • This suspension halts all marketing and distribution of the vaccine in the U.S.
  • Valneva will evaluate the financial impact but maintains current revenue forecasts.
  • Ixchiq generated $10.2 million in sales, part of Valneva's total sales of $123 million in early 2025.