Sanofi SA and Regeneron Pharmaceuticals said the US Food and Drug Administration approved Dupixent (dupilumab) to treat allergic fungal rhinosinusitis in adults and children aged 6 years and older who have a history of sino-nasal surgery. The approval was supported by the phase 3 LIBERTY-AFRS-AIMS study and was reviewed under the FDA’s priority review program.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Sanofi SA published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202602240930OMX_____CNEWS_EN_GNW1001166459_en) on February 24, 2026, and is solely responsible for the information contained therein.
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