Nanjing Leads Biolabs Doses First Patient in Phase II Trial of LBL-024 for Liver Cancer

Reuters

11/10

Nanjing Leads Biolabs Doses First Patient in Phase II Trial of LBL-024 for Liver Cancer

Nanjing Leads Biolabs Co. Ltd. has announced the initiation of a Phase II clinical trial for Opamtistomig (LBL-024), a PD-L1/4-1BB bispecific antibody, as a first-line treatment for hepatocellular carcinoma. The first patient has been successfully dosed in this open-label, multi-center study, which is led by Professor Jian Zhou of Zhongshan Hospital, Fudan University, and is being conducted across multiple hospitals in China. The company previously received approval from the National Medical Products Administration for a single-arm registrational trial in April 2024, as well as Breakthrough Therapy Designation for LBL-024 in late-line advanced EP-NEC and Orphan Drug Designation from the U.S. FDA for neuroendocrine carcinoma. Results from this trial have not yet 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. Nanjing Leads Biolabs Co. Ltd. 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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Ltd. has announced the initiation of a Phase II clinical trial for Opamtistomig (LBL-024), a PD-L1/4-1BB bispecific antibody, as a first-line treatment for hepatocellular carcinoma. The first patient has been successfully dosed in this open-label, multi-center study, which is led by Professor Jian Zhou of Zhongshan Hospital, Fudan University, and is being conducted across multiple hospitals in China. The company previously received approval from the National Medical Products Administration for a single-arm registrational trial in April 2024, as well as Breakthrough Therapy Designation for LBL-024 in late-line advanced EP-NEC and Orphan Drug Designation from the U.S. FDA for neuroendocrine carcinoma. 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Ltd. 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":"09887","symbol_name":"维立志博-B","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251110:nNDL8z7m1q:1","article_id":"2582825908","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2582825908","pubTimestamp":1762764115,"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":"Nanjing Leads Biolabs Co. 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