Entrada Therapeutics Advances ELEVATE-44-201 Study to Higher Dose for Duchenne Muscular Dystrophy

Reuters

Feb 17

Entrada <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Advances ELEVATE-44-201 Study to Higher Dose for Duchenne Muscular Dystrophy

Entrada Therapeutics Inc. announced that an independent Data Monitoring Committee has recommended the initiation of Cohort 2 at a 12 mg/kg dose in the ELEVATE-44-201 Phase 1/2 clinical trial of ENTR-601-44 for Duchenne muscular dystrophy patients amenable to exon 44 skipping. The company has completed dosing for Cohort 1 at 6 mg/kg, with data from this cohort expected in the second quarter of 2026. Data from Cohort 2 are anticipated by the end of the year. No clinical results have been presented yet.

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. Entrada Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9655691-en) on February 17, 2026, and is solely responsible for the information contained therein.

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ID: GNW9655691-en) on February 17, 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":"NDAQ","symbol_name":"纳斯达克OMX交易所","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260217:nNDL3bxBHw:1","article_id":"2612451369","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2612451369","pubTimestamp":1771329643,"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":"Entrada Therapeutics Inc. announced that an independent Data Monitoring Committee has recommended the initiation of Cohort 2 at a 12 mg/kg dose in the ELEVATE-44-201 Phase 1/2 clinical trial of ENTR-601-44 for Duchenne muscular dystrophy patients amenable to exon 44 skipping. 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