Monte Rosa Therapeutics Announces Updated Phase 1/2 Study Results for MRT-2359 in mCRPC

Reuters

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<a href="https://laohu8.com/S/GLUE">Monte Rosa Therapeutics</a> Announces Updated Phase 1/2 Study Results for MRT-2359 in mCRPC

Monte Rosa Therapeutics Inc. announced that it will present updated interim clinical results from its ongoing Phase 1/2 study of MRT-2359, a GSPT1-directed molecular glue degrader, in heavily pretreated, metastatic castration-resistant prostate cancer (mCRPC) patients. The results will be presented during a live conference call and webcast scheduled for December 16, 2025, at 8:00 a.m. ET. The webcast will be accessible via the "Events & Presentations" section of the company's website, with an archived version available for 30 days following the presentation.

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. Monte Rosa Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9602325-en) on December 15, 2025, and is solely responsible for the information contained therein.

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The results will be presented during a live conference call and webcast scheduled for December 16, 2025, at 8:00 a.m. ET. The webcast will be accessible via the \"Events &amp; Presentations\" section of the company's website, with an archived version available for 30 days following the presentation.\n      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. Monte Rosa Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9602325-en) on December 15, 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":"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:20251215:nNDL2FRszm:1","article_id":"2591621292","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2591621292","pubTimestamp":1765832471,"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":"Monte Rosa Therapeutics Inc. announced that it will present updated interim clinical results from its ongoing Phase 1/2 study of MRT-2359, a GSPT1-directed molecular glue degrader, in heavily pretreated, metastatic castration-resistant prostate cancer  patients. 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The results will be presented during a live conference call and webcast scheduled for December 16, 2025, at 8:00 a.m. ET. The webcast will be accessible via the \"Events & Presentations\" section of the company's website, with an archived version available for 30 days following the presentation.\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. Monte Rosa Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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