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Valneva Announces Removal of FDA-Recommended Pause on Use of Chikungunya Vaccine IXCHIQ® in Elderly and Updates to the Prescribing Information

UNITED STATES, AUG 7 – The FDA updated the chikungunya vaccine label to warn of serious adverse events mainly in older adults with underlying conditions after reviewing 17 global cases, including two deaths.

Summary by Benzinga
Saint Herblain (France), August 7, 2025 – Valneva SE (NASDAQ:VALN, PARIS:VLA), a specialty vaccine company, today announced that the FDA has removed its recommended pause in the use of IXCHIQ® in individuals 60 years of age and older and has approved updates to the Prescribing Information (PI) for IXCHIQ®. IXCHIQ® remains indicated in the United States for the prevention of disease caused by the Chikungunya Virus (CHIKV) in individuals 18 years …

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L'AGEFI broke the news in on Thursday, August 7, 2025.
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