Cue Biopharma Reports Positive Preclinical Safety Data for CUE-401

Reuters

Feb 17

<a href="https://laohu8.com/S/CUE">Cue Biopharma</a> Reports Positive Preclinical Safety Data for CUE-401

Cue Biopharma Inc. announced new preclinical safety and tolerability data for its lead autoimmune asset, CUE-401. In two non-GLP studies involving mice and non-human primates, CUE-401 was well tolerated with no adverse events observed at escalating dose levels. The company stated that further scientific data and details regarding its planned investigational new drug $(IND)$ filing for CUE-401 will be shared in the coming months. Results from these preclinical studies have been presented.

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. Cue Biopharma Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9654635-en) on February 17, 2026, and is solely responsible for the information contained therein.

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In two non-GLP studies involving mice and non-human primates, CUE-401 was well tolerated with no adverse events observed at escalating dose levels. The company stated that further scientific data and details regarding its planned investigational new drug <a href=\"https://laohu8.com/S/IND\">$(IND)$</a> filing for CUE-401 will be shared in the coming months. Results from these preclinical studies have been presented.\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. Cue Biopharma Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9654635-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:nNDL4MVx4V:1","article_id":"2612745268","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2612745268","pubTimestamp":1771333297,"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":"Cue Biopharma Inc. announced new preclinical safety and tolerability data for its lead autoimmune asset, CUE-401. In two non-GLP studies involving mice and non-human primates, CUE-401 was well tolerated with no adverse events observed at escalating dose levels. The company stated that further scientific data and details regarding its planned investigational new drug  filing for CUE-401 will be shared in the coming months. Results from these preclinical studies have been presented.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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In two non-GLP studies involving mice and non-human primates, CUE-401 was well tolerated with no adverse events observed at escalating dose levels. The company stated that further scientific data and details regarding its planned investigational new drug $(IND)$ filing for CUE-401 will be shared in the coming months. Results from these preclinical studies have been presented.\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. Cue Biopharma Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9654635-en) on February 17, 2026, and is solely responsible for the information contained therein.","kind":"highlight","is_publish_news":true,"is_publish_highlight":false,"is_publish_live":false,"is_publish_wemedia":null,"editions":null,"column":"","sentiment":"1","news_tag":"express","news_rank":0,"symbols":[],"gpt_button":0,"need_auth":false,"code":"91000000","status":"200"}}}