FDA Accepts Valneva’s Chikungunya Vaccine License Application for Priority Review
By Dr. Matthew Watson
Saint-Herblain (France), February 20, 2023 – Valneva SE (Nasdaq: VALN; Euronext Paris: VLA), a specialty vaccine company, today announced that the U.S. Food and Drug Administration (FDA) has completed a filing review of its Biologics License Application for Valneva’s single-shot chikungunya vaccine candidate VLA1553 and has determined that the application is sufficiently complete to permit a substantive review. The review classification is Priority.
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FDA Accepts Valneva’s Chikungunya Vaccine License Application for Priority Review
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February 21st, 2023
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