EMA Accepts Milestone Pharmaceuticals' Application for Etripamil Nasal Spray in PSVT

Reuters

Jan 06

EMA Accepts Milestone Pharmaceuticals' Application for Etripamil Nasal Spray in PSVT

Milestone Pharmaceuticals Inc. announced that the European Medicines Agency $(EMA)$ has accepted its Marketing Authorization Application for etripamil nasal spray, branded as TACHYMIST™ in Europe, for the treatment of paroxysmal supraventricular tachycardia (PSVT). The application is supported by clinical data from over 1,800 participants, including results from the pivotal Phase 3 RAPID trial. If approved, etripamil would become the first self-administered therapy for PSVT available to patients outside of a healthcare setting. A decision from the EMA is expected by the first quarter of 2027.

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: 9620218) on January 06, 2026, and is solely responsible for the information contained therein.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

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ID: 9620218) on January 06, 2026, and is solely responsible for the information contained therein.</span></i>\n</p>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"LU2210149790.SGD","symbol_name":"Natixis Thematics Subscription Economy R/A SGD-H","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260106:nNDL8kxr0c:1","article_id":"2601989711","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2601989711","pubTimestamp":1767704573,"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. announced that the European Medicines Agency  has accepted its Marketing Authorization Application for etripamil nasal spray, branded as TACHYMIST in Europe, for the treatment of paroxysmal supraventricular tachycardia . 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The application is supported by clinical data from over 1,800 participants, including results from the pivotal Phase 3 RAPID trial. If approved, etripamil would become the first self-administered therapy for PSVT available to patients outside of a healthcare setting. A decision from the EMA is expected by the first quarter of 2027.\n      \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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