Kymera Therapeutics Doses First Patient in Phase 2b Asthma Trial of KT-621

Reuters

01/29

Kymera <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Doses First Patient in Phase 2b Asthma Trial of KT-621

Kymera Therapeutics Inc. has announced the initiation of dosing in its BREADTH Phase 2b clinical trial evaluating KT-621, a first-in-class oral STAT6 degrader, in patients with moderate to severe eosinophilic asthma. The company expects to report data from the BREADTH trial in late 2027. Additionally, data from the ongoing BROADEN2 Phase 2b trial of KT-621 in moderate to severe atopic dermatitis is anticipated by mid-2027. The results from these studies have not yet been presented and are expected in the future.

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. Kymera Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9644716-en) on January 29, 2026, and is solely responsible for the information contained therein.

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The company expects to report data from the BREADTH trial in late 2027. Additionally, data from the ongoing BROADEN2 Phase 2b trial of KT-621 in moderate to severe atopic dermatitis is anticipated by mid-2027. The results from these studies have not yet been presented and are expected in the future.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n<i>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. Kymera Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9644716-en) on January 29, 2026, and is solely responsible for the information contained therein.</span></i>\n</p>\n</div></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"KYMR","symbol_name":"Kymera Therapeutics, Inc.","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260129:nNDL3SQ8sc:1","article_id":"2607081694","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2607081694","pubTimestamp":1769688034,"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":"Kymera Therapeutics Inc. has announced the initiation of dosing in its BREADTH Phase 2b clinical trial evaluating KT-621, a first-in-class oral STAT6 degrader, in patients with moderate to severe eosinophilic asthma. 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The company expects to report data from the BREADTH trial in late 2027. Additionally, data from the ongoing BROADEN2 Phase 2b trial of KT-621 in moderate to severe atopic dermatitis is anticipated by mid-2027. The results from these studies have not yet been presented and are expected in the future.\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. Kymera Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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