Sichuan KelunBiotech Biopharmaceutical receives NMPA approval for sacituzumab tirumotecan in EGFR mutant NSCLC after EGFR TKI therapy

Reuters

10/12

Sichuan KelunBiotech Biopharmaceutical receives NMPA approval for sacituzumab tirumotecan in EGFR mutant NSCLC after EGFR TKI therapy

Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. announced that its core product, sacituzumab tirumotecan (sac-TMT, also known as SKB264/MK-2870), has been approved for marketing by the National Medical Products Administration (NMPA) in China. This approval covers a third indication: the treatment of adult patients with epidermal growth factor receptor (EGFR) mutant-positive locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) who have progressed after EGFR-tyrosine kinase inhibitor (TKI) therapy. The company continues to pursue regulatory review for additional indications, with several clinical studies ongoing. No grant or funding by multiple organizations was mentioned in the announcement.

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. Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. published the original content used to generate this news brief on October 12, 2025, and is solely responsible for the information contained therein.

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This approval covers a third indication: the treatment of adult patients with epidermal growth factor receptor (EGFR) mutant-positive locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) who have progressed after EGFR-tyrosine kinase inhibitor (TKI) therapy. The company continues to pursue regulatory review for additional indications, with several clinical studies ongoing. No grant or funding by multiple organizations was mentioned in the announcement.\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. 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This approval covers a third indication: the treatment of adult patients with epidermal growth factor receptor (EGFR) mutant-positive locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) who have progressed after EGFR-tyrosine kinase inhibitor (TKI) therapy. The company continues to pursue regulatory review for additional indications, with several clinical studies ongoing. No grant or funding by multiple organizations was mentioned in the announcement.\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. Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. published the original content used to generate this news brief on October 12, 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":"BK1161","symbol_name":"生物科技","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251012:nNDLc6tMLH:1","article_id":"2574492655","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2574492655","pubTimestamp":1760265675,"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":"Sichuan KelunBiotech Biopharmaceutical receives NMPA approval for sacituzumab tirumotecan in EGFR mutant NSCLC after EGFR TKI therapy. Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd. announced that its core product, sacituzumab tirumotecan , has been approved for marketing by the National Medical Products Administration  in China. This approval covers a third indication: the treatment of adult patients with epidermal growth factor receptor  mutant-positive locally advanced or metastatic non-squamous non-small cell lung cancer  who have progressed after EGFR-tyrosine kinase inhibitor  therapy. The company continues to pursue regulatory review for additional indications, with several clinical studies ongoing. No grant or funding by multiple organizations was mentioned in the announcement.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. 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This approval covers a third indication: the treatment of adult patients with epidermal growth factor receptor (EGFR) mutant-positive locally advanced or metastatic non-squamous non-small cell lung cancer (NSCLC) who have progressed after EGFR-tyrosine kinase inhibitor (TKI) therapy. The company continues to pursue regulatory review for additional indications, with several clinical studies ongoing. No grant or funding by multiple organizations was mentioned in the announcement.\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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