Sarepta Therapeutics Receives MHRA Approval to Continue Dosing in Phase 3 Study of ELEVIDYS for Duchenne Muscular Dystrophy

Reuters

05-21

<a href="https://laohu8.com/S/SRPT">Sarepta Therapeutics</a> Receives MHRA Approval to Continue Dosing in Phase 3 Study of ELEVIDYS for Duchenne Muscular Dystrophy

Sarepta Therapeutics Inc. announced an update regarding its ongoing regulatory review for ELEVIDYS, a gene therapy for Duchenne muscular dystrophy. The Medicines & Healthcare products Regulatory Agency (MHRA) in the United Kingdom has given the green light for dosing to continue uninterrupted in the ENVISION study, which is a global Phase 3 trial. This study involves both non-ambulatory and older ambulatory individuals with Duchenne and is designed as a randomized, double-blind, placebo-controlled trial. Sarepta, a leader in precision genetic medicine for rare diseases, emphasized the significance of this approval as it continues to advance its treatment for Duchenne muscular dystrophy.

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. Sarepta Therapeutics Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20250521736806) on May 21, 2025, and is solely responsible for the information contained therein.

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The Medicines &amp; Healthcare products Regulatory Agency (MHRA) in the United Kingdom has given the green light for dosing to continue uninterrupted in the ENVISION study, which is a global Phase 3 trial. This study involves both non-ambulatory and older ambulatory individuals with Duchenne and is designed as a randomized, double-blind, placebo-controlled trial. Sarepta, a leader in precision genetic medicine for rare diseases, emphasized the significance of this approval as it continues to advance its treatment for Duchenne muscular dystrophy.\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. 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The Medicines &amp; Healthcare products Regulatory Agency (MHRA) in the United Kingdom has given the green light for dosing to continue uninterrupted in the ENVISION study, which is a global Phase 3 trial. This study involves both non-ambulatory and older ambulatory individuals with Duchenne and is designed as a randomized, double-blind, placebo-controlled trial. Sarepta, a leader in precision genetic medicine for rare diseases, emphasized the significance of this approval as it continues to advance its treatment for Duchenne muscular dystrophy.\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. Sarepta Therapeutics Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20250521736806) on May 21, 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":"BK4585","symbol_name":"ETF&股票定投概念","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250521:nNDL43Vp5v:1","article_id":"2537938236","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2537938236","pubTimestamp":1747830679,"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":"Sarepta Therapeutics Inc. announced an update regarding its ongoing regulatory review for ELEVIDYS, a gene therapy for Duchenne muscular dystrophy. The Medicines & Healthcare products Regulatory Agency  in the United Kingdom has given the green light for dosing to continue uninterrupted in the ENVISION study, which is a global Phase 3 trial. This study involves both non-ambulatory and older ambulatory individuals with Duchenne and is designed as a randomized, double-blind, placebo-controlled trial. Sarepta, a leader in precision genetic medicine for rare diseases, emphasized the significance of this approval as it continues to advance its treatment for Duchenne muscular dystrophy.Disclaimer: This news brief was created by Public Technologies  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. 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The Medicines & Healthcare products Regulatory Agency (MHRA) in the United Kingdom has given the green light for dosing to continue uninterrupted in the ENVISION study, which is a global Phase 3 trial. This study involves both non-ambulatory and older ambulatory individuals with Duchenne and is designed as a randomized, double-blind, placebo-controlled trial. Sarepta, a leader in precision genetic medicine for rare diseases, emphasized the significance of this approval as it continues to advance its treatment for Duchenne muscular dystrophy.\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. Sarepta Therapeutics Inc. published the original content used to generate this news brief via Business Wire (Ref. 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