FDA Accepts IND Application for Boundless Bio's BBI-940

Reuters

Jan 20

FDA Accepts IND Application for <a href="https://laohu8.com/S/BOLD">Boundless Bio</a>'s BBI-940

Boundless Bio Inc. announced that the U.S. Food and Drug Administration (FDA) has accepted its Investigational New Drug $(IND)$ application for its novel Kinesin oral degrader program, BBI-940. This regulatory acceptance enables Boundless Bio to proceed with the initiation of a first-in-human clinical trial, which is on track to begin in the first half of 2026.

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. Boundless Bio Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9628134-en) on January 20, 2026, and is solely responsible for the information contained therein.

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This regulatory acceptance enables Boundless Bio to proceed with the initiation of a first-in-human clinical trial, which is on track to begin in the first half of 2026.\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. Boundless Bio Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9628134-en) on January 20, 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":"BK4588","symbol_name":"碎股","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260120:nNDL3fH6SH:1","article_id":"2604919707","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2604919707","pubTimestamp":1768910424,"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":"Boundless Bio Inc. announced that the U.S. Food and Drug Administration  has accepted its Investigational New Drug  application for its novel Kinesin oral degrader program, BBI-940. 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This regulatory acceptance enables Boundless Bio to proceed with the initiation of a first-in-human clinical trial, which is on track to begin in the first half of 2026.\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. Boundless Bio Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9628134-en) on January 20, 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":"executive","news_rank":0,"symbols":[],"gpt_button":0,"need_auth":false,"code":"91000000","status":"200"}}}