Sanofi And Regeneron's Dupixent Meets Endpoints, Accepted For Priority Review By FDA

Reuters

2025/11/07

Nov 7 (Reuters) - Sanofi SA ::
*ACAAI: SANOFI AND REGENERON’S DUPIXENT PIVOTAL STUDY MET ALL PRIMARY AND SECONDARY ENDPOINTS, REDUCING SIGNS AND SYMPTOMS OF ALLERGIC FUNGAL RHINOSINUSITIS; SBLA ACCEPTED FOR FDA PRIORITY REVIEW
*PHASE 3 DATA SHOW DUPIXENT REDUCED NASAL SIGNS AND SYMPTOMS
*MEDICINE ACCEPTED FOR PRIORITY REVIEW BY US FDA WITH A TARGET ACTION DATE OF FEBRUARY 28, 2026

((Reuters Investor Briefs; email: reutersinvestor.briefs@thomsonreuters.com))
Source Date/Time = 07-NOV-202513:00:00.943 GMT

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