FDA Approves Milestone Pharmaceuticals’ CARDAMYST Nasal Spray for PSVT

Reuters

2025/12/13

FDA Approves Milestone Pharmaceuticals' CARDAMYST Nasal Spray for PSVT

Milestone Pharmaceuticals Inc. has received FDA approval for CARDAMYST™ (etripamil) nasal spray, marking the first self-administered treatment for adults with paroxysmal supraventricular tachycardia (PSVT). This is the first FDA-approved treatment for PSVT in over 30 years, offering more than two million Americans a rapid-acting option that can be used outside of healthcare settings. The approval is supported by robust clinical data, including the successful Phase 3 RAPID trial. CARDAMYST is expected to be available in retail pharmacies in the first quarter of 2026.

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. Milestone Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9601755) on December 13, 2025, and is solely responsible for the information contained therein.

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This is the first FDA-approved treatment for PSVT in over 30 years, offering more than two million Americans a rapid-acting option that can be used outside of healthcare settings. The approval is supported by robust clinical data, including the successful Phase 3 RAPID trial. CARDAMYST is expected to be available in retail pharmacies in the first quarter of 2026.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>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. Milestone Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9601755) on December 13, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"BK4588","symbol_name":"碎股","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251213:nNDL6wl3Wr:1","article_id":"2591068041","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2591068041","pubTimestamp":1765587622,"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":"Milestone Pharmaceuticals Inc. has received FDA approval for CARDAMYST  nasal spray, marking the first self-administered treatment for adults with paroxysmal supraventricular tachycardia . 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This is the first FDA-approved treatment for PSVT in over 30 years, offering more than two million Americans a rapid-acting option that can be used outside of healthcare settings. The approval is supported by robust clinical data, including the successful Phase 3 RAPID trial. CARDAMYST is expected to be available in retail pharmacies in the first quarter of 2026.\n      \n\nDisclaimer: 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. Milestone Pharmaceuticals Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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