CARsgen's Zevor-Cel Approved in China for Relapsed/Refractory Multiple Myeloma

Reuters

2025/12/07

CARsgen's Zevor-Cel Approved in China for Relapsed/Refractory Multiple Myeloma

CARsgen Therapeutics Holdings Ltd. announced that its fully human BCMA-targeted CAR-T product, zevorcabtagene autoleucel (zevor-cel), has been included in China's Commercial Health Insurance Innovative Drug Catalogue (2025) following approval from the National Healthcare Security Administration (NHSA). Zevor-cel received marketing authorization from the National Medical Products Administration (NMPA) on February 23, 2024, for the treatment of adult patients with relapsed or refractory multiple myeloma who have progressed after at least three prior lines of therapy. This inclusion is expected to improve patient access to the therapy and reflects national support for innovative treatments.

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. CARsgen Therapeutics Holdings Ltd. published the original content used to generate this news brief via PR Newswire (Ref. ID: CN40954) on December 07, 2025, and is solely responsible for the information contained therein.

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Zevor-cel received marketing authorization from the National Medical Products Administration (NMPA) on February 23, 2024, for the treatment of adult patients with relapsed or refractory multiple myeloma who have progressed after at least three prior lines of therapy. This inclusion is expected to improve patient access to the therapy and reflects national support for innovative treatments.\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. CARsgen Therapeutics Holdings Ltd. published the original content used to generate this news brief via PR Newswire (Ref. 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Zevor-cel received marketing authorization from the National Medical Products Administration (NMPA) on February 23, 2024, for the treatment of adult patients with relapsed or refractory multiple myeloma who have progressed after at least three prior lines of therapy. This inclusion is expected to improve patient access to the therapy and reflects national support for innovative treatments.\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. CARsgen Therapeutics Holdings Ltd. published the original content used to generate this news brief via PR Newswire (Ref. ID: CN40954) on December 07, 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:20251207:nNDLy7y7N:1","article_id":"2589587181","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2589587181","pubTimestamp":1765099332,"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":"CARsgen Therapeutics Holdings Ltd. announced that its fully human BCMA-targeted CAR-T product, zevorcabtagene autoleucel , has been included in China's Commercial Health Insurance Innovative Drug Catalogue  following approval from the National Healthcare Security Administration . 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Zevor-cel received marketing authorization from the National Medical Products Administration (NMPA) on February 23, 2024, for the treatment of adult patients with relapsed or refractory multiple myeloma who have progressed after at least three prior lines of therapy. This inclusion is expected to improve patient access to the therapy and reflects national support for innovative treatments.\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. CARsgen Therapeutics Holdings Ltd. published the original content used to generate this news brief via PR Newswire (Ref. 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