MHRA Approves ALK-Abelló A/S's EURneffy® as First Needle-Free Anaphylaxis Treatment in the UK

Reuters

07-18

MHRA Approves ALK-Abelló A/S's EURneffy® as First Needle-Free Anaphylaxis Treatment in the UK

ALK-Abelló A/S has announced that the Medicines and Healthcare Products Regulatory Agency (MHRA) has approved EURneffy® 2 mg in the United Kingdom for the treatment of anaphylaxis in adults and children weighing 30 kg or more. This marks the first approval of a needle-free adrenaline nasal spray for emergency allergic reaction treatment in the UK. Expected to launch in the market once access negotiations conclude, EURneffy® offers a longer shelf life and superior temperature stability compared to existing adrenaline auto-injectors. The approval was based on data from a development program involving over 700 participants, with no serious adverse events reported. This innovative product aims to transform the management of severe allergies, making adrenaline administration more accessible and reliable.

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. ALK-Abelló A/S published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW1001118621-en) on July 18, 2025, and is solely responsible for the information contained therein.

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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. ALK-Abelló A/S published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW1001118621-en) on July 18, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"IE00BKPKM429.USD","symbol_name":"NEUBERGER BERMAN GLOBAL SUSTAINABLE EQUITY \"A\" (USD) ACC","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250718:nNDLbdLtVP:1","article_id":"2552903467","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2552903467","pubTimestamp":1752840081,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"ALK-Abelló A/S has announced that the Medicines and Healthcare Products Regulatory Agency  has approved EURneffy 2 mg in the United Kingdom for the treatment of anaphylaxis in adults and children weighing 30 kg or more. 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