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Post-authorisation experience and reported adverse events following use of a virus-like particle chikungunya vaccine, United States and Germany, up to August 2025
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View Affiliations Hide AffiliationsCorrespondence:Benedetto Simonebesi bavarian-nordic.com
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Citation style for this article: . Post-authorisation experience and reported adverse events following use of a virus-like particle chikungunya vaccine, United States and Germany, up to August 2025. Euro Surveill. 2025;30(44):pii=2500792. https://doi.org/10.2807/1560-7917.ES.2025.30.44.2500792 Received: 15 Oct 2025; Accepted: 04 Nov 2025
Abstract
Older adults are at increased risk of severe chikungunya. Some countries advise against vaccinating ≥ 60 or ≥ 65-year-olds with the licenced live-attenuated vaccine (CHIKV LA, IXCHIQ), following severe adverse event (SAE) reports. A virus-like particle vaccine (CHIKV VLP, VIMKUNYA) is licensed in the United States (US), EU/EEA and the United Kingdom. Up to 31 August 2025, over 12,500 doses were administered in US and Germany; no SAEs in ≥ 65-year-olds were reported. Early post-authorisation data support its favourable safety profile in ≥ 65-year-olds.
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