Wuhan YZY Biopharma Receives NMPA IND Approval for Y225 Emicizumab Injection

Reuters

2025/12/24

Wuhan YZY Biopharma Receives NMPA IND Approval for Y225 Emicizumab Injection

Wuhan YZY Biopharma Co., Ltd. has announced that its Y225 "Emicizumab Injection" has received Investigational New Drug $(IND)$ approval from the National Medical Products Administration (NMPA) of China. The approved clinical trial will evaluate the bioequivalence of Hemlibra® and Y225 in healthy adult male subjects. This milestone positions Y225 as a potential first biosimilar of Hemlibra® to be launched in China, aiming to address the domestic gap in high-barrier bispecific monoclonal antibody biosimilars.

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. Wuhan Yzy Biopharma Co. Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20251224-11967270), on December 24, 2025, and is solely responsible for the information contained therein.

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The approved clinical trial will evaluate the bioequivalence of Hemlibra® and Y225 in healthy adult male subjects. This milestone positions Y225 as a potential first biosimilar of Hemlibra® to be launched in China, aiming to address the domestic gap in high-barrier bispecific monoclonal antibody biosimilars.\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. Wuhan Yzy Biopharma Co. Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. ID: HKEX-EPS-20251224-11967270), on December 24, 2025, 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":"02496","symbol_name":"友芝友生物-B","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251224:nNDL2hMmWX:1","article_id":"2593713404","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2593713404","pubTimestamp":1766576009,"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":"Wuhan YZY Biopharma Co., Ltd. has announced that its Y225 \"Emicizumab Injection\" has received Investigational New Drug  approval from the National Medical Products Administration  of China. 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Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange  , on December 24, 2025, a","collect":0,"end_time":0,"defaultTopTitle":"","property":[],"viewcount":null,"language":"en","relate_stocks":{"02496":"友芝友生物-B","BK1161":"生物科技"},"translate_title":"Y225依米珠单抗注射液获NMPA IND批件","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"02496":0.9},"content_text":"Wuhan YZY Biopharma Receives NMPA IND Approval for Y225 Emicizumab Injection\n    \n\n        Wuhan YZY Biopharma Co., Ltd. has announced that its Y225 \"Emicizumab Injection\" has received Investigational New Drug $(IND)$ approval from the National Medical Products Administration (NMPA) of China. The approved clinical trial will evaluate the bioequivalence of Hemlibra® and Y225 in healthy adult male subjects. This milestone positions Y225 as a potential first biosimilar of Hemlibra® to be launched in China, aiming to address the domestic gap in high-barrier bispecific monoclonal antibody biosimilars.\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. Wuhan Yzy Biopharma Co. Ltd. published the original content used to generate this news brief via IIS, the Issuer Information Service operated by the Hong Kong Stock Exchange (HKex) (Ref. 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