ARS Pharmaceuticals Inc. Secures UK Regulatory Approval for EURneffy, the First Needle-Free Adrenaline Treatment for Severe Allergies

Reuters
18 Jul
ARS Pharmaceuticals Inc. Secures UK Regulatory Approval for EURneffy, the First Needle-Free Adrenaline Treatment for Severe Allergies

SAN DIEGO, July 18, 2025 (GLOBE NEWSWIRE) -- ARS Pharmaceuticals, Inc. (Nasdaq: SPRY), a biopharmaceutical company focused on innovative treatments for allergic reactions, announced that the United Kingdom's Medicines and Healthcare products Regulatory Agency (MHRA) has granted approval for EURneffy, an adrenaline nasal spray, for the emergency treatment of allergic reactions (anaphylaxis) in adults and children over 30 kg. This marks the first and only needle-free emergency treatment available in the U.K. for severe allergies, offering a new delivery method for adrenaline. The approval is a significant milestone in ARS Pharma's collaboration with ALK-Abelló A/S, who will market EURneffy in the U.K., with expected availability in late Q3 2025.

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. ARS Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9496825-en) on July 18, 2025, and is solely responsible for the information contained therein.

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