Antengene Corporation Ltd. Secures Regulatory Approval for XPOVIO® in China for Second-Line Treatment of Multiple Myeloma

Reuters

Jul 28

Antengene Corporation Ltd. Secures Regulatory Approval for XPOVIO® in China for Second-Line Treatment of Multiple Myeloma

Antengene Corporation Ltd. has announced that the China National Medical Products Administration (NMPA) has approved XPOVIO® (selinexor) for a new indication in the treatment of multiple myeloma. The approval is for its use in combination with bortezomib and dexamethasone (XVd) for adult patients who have received at least one prior therapy. This marks a significant milestone for Antengene, enhancing their pipeline of oncology assets and expanding their presence in the Asia Pacific market.

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. Antengene Corporation Ltd. published the original content used to generate this news brief on July 28, 2025, and is solely responsible for the information contained therein.

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Secures Regulatory Approval for XPOVIO® in China for Second-Line Treatment of Multiple Myeloma","media":"Reuters","content":"<html xmlns=\"http://www.w3.org/1999/xhtml\" xmlns:newsg2=\"http://iptc.org/std/nar/2006-10-01/\" xmlns:xhtml=\"http://www.w3.org/1999/xhtml\"><head><title>\n      Antengene Corporation Ltd. Secures Regulatory Approval for XPOVIO® in China for Second-Line Treatment of Multiple Myeloma\n    </title></head><body><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n        Antengene Corporation Ltd. has announced that the <a href=\"https://laohu8.com/S/688128\">China National</a> Medical Products Administration (NMPA) has approved XPOVIO® (selinexor) for a new indication in the treatment of multiple myeloma. The approval is for its use in combination with bortezomib and dexamethasone (XVd) for adult patients who have received at least one prior therapy. 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Secures Regulatory Approval for XPOVIO® in China for Second-Line Treatment of Multiple Myeloma\n</h2>\n\n<h4 class=\"meta\">\n\n\n<a class=\"head\" href=\"https://laohu8.com/wemedia/1032215980\">\n\n\n<div class=\"h-thumb\" style=\"background-image:url(https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48);background-size:cover;\"></div>\n\n<div class=\"h-content\">\n<p class=\"h-name\">Reuters </p>\n<p class=\"h-time\">2025-07-28 16:54</p>\n</div>\n\n</a>\n\n\n</h4>\n\n</header>\n<article>\n<html xmlns=\"http://www.w3.org/1999/xhtml\" xmlns:newsg2=\"http://iptc.org/std/nar/2006-10-01/\" xmlns:xhtml=\"http://www.w3.org/1999/xhtml\"><head><title>\n      Antengene Corporation Ltd. 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