BioXcel Therapeutics Reports Phase 3 Study Results on BXCL501 for Agitation in Bipolar Disorder and Schizophrenia at Home

Reuters

Nov 10

BioXcel <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Reports Phase 3 Study Results on BXCL501 for Agitation in Bipolar Disorder and Schizophrenia at Home

BioXcel Therapeutics Inc. published a document detailing results from a Phase 3 study evaluating BXCL501 (sublingual dexmedetomidine) for the treatment of agitation associated with bipolar disorder or schizophrenia in the home setting. The document reports on the safety and efficacy of BXCL501, noting that the treatment was safe and well tolerated over a 12-week period, with consistent reduction in agitation symptoms and no increase in adverse events with repeat dosing. The full document can be accessed through the link below.

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. BioXcel Therapeutics Inc. published the original content used to generate this news brief on November 10, 2025, and is solely responsible for the information contained therein.

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BioXcel Therapeutics Inc. published the original content used to generate this news brief on November 10, 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":"BTAI","symbol_name":"Bioxcel Therapeutics Inc.","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251110:nNDL1LbWVt:1","article_id":"2582887040","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2582887040","pubTimestamp":1762786961,"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":"BioXcel Therapeutics Inc. published a document detailing results from a Phase 3 study evaluating BXCL501  for the treatment of agitation associated with bipolar disorder or schizophrenia in the home setting. The document reports on the safety and efficacy of BXCL501, noting that the treatment was safe and well tolerated over a 12-week period, with consistent reduction in agitation symptoms and no increase in adverse events with repeat dosing. The full document can be accessed through the link below.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 document reports on the safety and efficacy of BXCL501, noting that the treatment was safe and well tolerated over a 12-week period, with consistent reduction in agitation symptoms and no increase in adverse events with repeat dosing. The full document can be accessed through the link below.\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. 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