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HENLIUS

76.600

+0.7000.92%

Volume:3.17M

Turnover:237.51M

Market Cap:41.59B

PE:44.61

High:78.600

Open:76.000

Low:74.100

Close:75.900

52wk High:92.000

52wk Low:23.000

Shares:543.00M

HK Float Shares:346.07M

Volume Ratio:1.81

T/O Rate:0.92%

Dividend:- -

Dividend Rate:- -

EPS(LYR):1.717

ROE:23.72%

ROA:4.45%

PB:9.23

PE(LYR):44.61

PS:5.48

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Overview Company News Filings

Taikang Insurance Group, Inc. Increases Stake in HENLIUS (02696) by 518,500 Shares at HK$67.07 per Share

Shanghai Henlius Biotech (2696) Announces First Patient Dosed in Phase 1 Trial of HLX13 for Unresectable HCC

Bulletin Express

HENLIUS (02696): First Patient Dosed in China for International Phase 1 Clinical Study of HLX13 (Ipilimumab Biosimilar) in First-Line Treatment of Unresectable Hepatocellular Carcinoma (HCC)

HK Stock Movement | HENLIUS (02696) Rises Over 6% in Afternoon Session as Serplulimab Included in NMPA's Breakthrough Therapy List

US September Nonfarm Payrolls Exceed Expectations, Third Rate Cut This Year Unlikely

HENLIUS (02696): Hansizhuang® (Serplulimab Injection) Combined with Chemotherapy for Gastric Cancer Neoadjuvant/Adjuvant Therapy Officially Included in NMPA's Breakthrough Therapy Designation Program

Shanghai Henlius Biotech Receives Breakthrough Therapy Designation for HANSIZHUANG in Gastric Cancer

Shanghai Henlius Biotech - Hansizhuang Granted Breakthrough Therapy Designation for Gastric Cancer by Nmpa

THOMSON REUTERS

Hong Kong Stocks Movement | HENLIUS (02696) Rises Over 4% as POHERDY Gains U.S. Approval, Covering All Indications of Reference Product

Organon, Shanghai Henlius Biotech Says FDA Clears Poherdy as Pertuzumab Biosimilar

MT Newswires Live

BUZZ-Organon rises after US FDA clears first biosimilar for breast cancer

FDA Approves Organon and Henlius' POHERDY as First Perjeta Biosimilar in US

Henlius Biotech Gets US FDA Nod for Breast Cancer Drug's Biologics License Application

MT Newswires Live

Shanghai Henlius Biotech (2696) Announces FDA Approval of HLX11 (Pertuzumab-dpzb) for Key Breast Cancer Treatments

Bulletin Express

HENLIUS (02696): FDA Approves HLX11 (Pertuzumab, US Brand Name: POHERDY®) for HER2-Positive Early Breast Cancer Neoadjuvant/Adjuvant and Metastatic Breast Cancer Treatment

Shanghai Henlius Biotech Inc - Approval Letter From FDA for Poherdy

THOMSON REUTERS

HK Stock Movement | HENLIUS (02696) Rises Over 4% as Denosumab Biosimilars BILDYOS and BILPREVDA Gain UK Approval

Boyu Capital Opportunities Master Fund Increases Stake in HENLIUS (02696) by 262,500 Shares at Average Price of HK$61.28 per Share

Boyu Capital Group Holdings Ltd. Increases Stake in HENLIUS (02696) by 80,000 Shares at Average Price of HK$61.78 per Share

Hong Kong Stock Short Interest Data as of November 7

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Increases Stake in HENLIUS (02696) by 518,500 Shares at HK$67.07 per Share","url":"https://stock-news.laohu8.com/highlight/detail?id=1192467692","media":"Stock News","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1192467692?lang=en_us&edition=fundamental","pubTime":"2025-11-25 19:06","pubTimestamp":1764068787,"startTime":"0","endTime":"0","summary":"According to the latest disclosure from the Hong Kong Stock Exchange, Taikang Insurance Group, Inc. acquired an additional 518,500 shares of HENLIUS (02696) on November 20 at HK$67.0678 per share,...","market":"other","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1161","02696","HK0000165453.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1122838052","title":"Shanghai Henlius Biotech (2696) Announces First Patient Dosed in Phase 1 Trial of HLX13 for Unresectable HCC","url":"https://stock-news.laohu8.com/highlight/detail?id=1122838052","media":"Bulletin Express","labels":["productRelease","SGX"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1122838052?lang=en_us&edition=fundamental","pubTime":"2025-11-25 16:44","pubTimestamp":1764060247,"startTime":"0","endTime":"0","summary":"On 25 November 2025, Shanghai Henlius Biotech (2696) announced that the first patient in Mainland China had been dosed in an international multicenter Phase 1 clinical study of HLX13 (Ipilimumab...","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease,SGX","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["02696"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1118435898","title":"HENLIUS (02696): First Patient Dosed in China for International Phase 1 Clinical Study of HLX13 (Ipilimumab Biosimilar) in First-Line Treatment of Unresectable Hepatocellular Carcinoma (HCC)","url":"https://stock-news.laohu8.com/highlight/detail?id=1118435898","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1118435898?lang=en_us&edition=fundamental","pubTime":"2025-11-25 16:36","pubTimestamp":1764059807,"startTime":"0","endTime":"0","summary":"HENLIUS (02696) announced that the first patient in China has been dosed in its international multicenter Phase 1 clinical study for HLX13 (recombinant fully human anti-CTLA-4 monoclonal antibody...","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["HCC","BK4006","HK0000165453.HKD","BK1161","02696"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1153166979","title":"HK Stock Movement | HENLIUS (02696) Rises Over 6% in Afternoon Session as Serplulimab Included in NMPA's Breakthrough Therapy List","url":"https://stock-news.laohu8.com/highlight/detail?id=1153166979","media":"Stock News","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1153166979?lang=en_us&edition=fundamental","pubTime":"2025-11-24 15:14","pubTimestamp":1763968458,"startTime":"0","endTime":"0","summary":"HENLIUS (02696) surged more than 6% in the afternoon session, with gains narrowing to 4.94% by the time of writing, trading at HK$66.95 and recording a turnover of HK$63.14 million. The company...","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1161","HK0000165453.HKD","02696"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1157079242","title":"US September Nonfarm Payrolls Exceed Expectations, Third Rate Cut This Year Unlikely","url":"https://stock-news.laohu8.com/highlight/detail?id=1157079242","media":"Stock News","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1157079242?lang=en_us&edition=fundamental","pubTime":"2025-11-21 07:50","pubTimestamp":1763682632,"startTime":"0","endTime":"0","summary":"【Top Story】Innovent Biologics (01801): Obesity Drug Meets Primary Endpoint in Phase 3 Trial, Plans to Submit MASHITIDE 9mg for Approval   Innovent Biologics announced that its global first-in-class...","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"3d776d860091c121dc4a4735cfb272f5","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["GCmain","MGCmain","159934","IAU","SImain","02565","GDX","BK1161","DUST","518880","02696","GLD","SGUmain","NUGT","SGCmain","HK0000165453.HKD"],"isVideo":false,"video":null,"gpt_icon":1},{"id":"1125215211","title":"HENLIUS (02696): Hansizhuang® (Serplulimab Injection) Combined with Chemotherapy for Gastric Cancer Neoadjuvant/Adjuvant Therapy Officially Included in NMPA's Breakthrough Therapy Designation Program","url":"https://stock-news.laohu8.com/highlight/detail?id=1125215211","media":"Stock News","labels":["productRelease","policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1125215211?lang=en_us&edition=fundamental","pubTime":"2025-11-20 16:56","pubTimestamp":1763628982,"startTime":"0","endTime":"0","summary":"HENLIUS (02696) announced that Hansizhuang® (Serplulimab Injection) combined with chemotherapy for neoadjuvant/adjuvant treatment of gastric cancer has been officially included in the Breakthrough...","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease,policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["HK0000165453.HKD","BK1161","02696"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2584956181","title":"Shanghai Henlius Biotech Receives Breakthrough Therapy Designation for HANSIZHUANG in Gastric Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2584956181","media":"Reuters","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2584956181?lang=en_us&edition=fundamental","pubTime":"2025-11-20 16:50","pubTimestamp":1763628629,"startTime":"0","endTime":"0","summary":"Shanghai Henlius Biotech Inc. announced that its product HANSIZHUANG , in combination with chemotherapy, has been officially granted Breakthrough Therapy Designation by the Center for Drug Evaluation of the National Medical Products Administration  for the neo-/adjuvant treatment of gastric cancer. This designation is expected to accelerate the regulatory review and market approval process for HANSIZHUANG. As of the announcement date, no other monoclonal antibody drug targeting PD-1 has received global approval for this indication. There is no indication that this grant was obtained by multiple organizations; it is specific to Shanghai Henlius Biotech Inc.Disclaimer: This news brief was created by Public Technologies  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. Shanghai Henlius Biotech Inc. pub","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251120:nNDL7CTkYn:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1230","HK0000165453.HKD","00656","02696","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2584181568","title":"Shanghai Henlius Biotech - Hansizhuang Granted Breakthrough Therapy Designation for Gastric Cancer by Nmpa","url":"https://stock-news.laohu8.com/highlight/detail?id=2584181568","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2584181568?lang=en_us&edition=fundamental","pubTime":"2025-11-20 16:47","pubTimestamp":1763628439,"startTime":"0","endTime":"0","summary":null,"market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251120:nFWN3WV1GE:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"reuters_en_live","symbols":["BK1161","02696","HK0000165453.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1138286818","title":"Hong Kong Stocks Movement | HENLIUS (02696) Rises Over 4% as POHERDY Gains U.S. Approval, Covering All Indications of Reference Product","url":"https://stock-news.laohu8.com/highlight/detail?id=1138286818","media":"Stock News","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1138286818?lang=en_us&edition=fundamental","pubTime":"2025-11-20 11:00","pubTimestamp":1763607621,"startTime":"0","endTime":"0","summary":"HENLIUS (02696) surged over 4%, reaching HK$67.1 by the time of writing, with a trading volume of HK$31.4 million. The company, in collaboration with Organon, announced that the Biologics License...","market":"other","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["HK0000165453.HKD","02696","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2584408076","title":"Organon, Shanghai Henlius Biotech Says FDA Clears Poherdy as Pertuzumab Biosimilar","url":"https://stock-news.laohu8.com/highlight/detail?id=2584408076","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2584408076?lang=en_us&edition=fundamental","pubTime":"2025-11-17 19:44","pubTimestamp":1763379894,"startTime":"0","endTime":"0","summary":"Organon  and Shanghai Henlius Biotech said Monday that the US Food and Drug Administration has approved the biologics license application for Poherdy as an \"interchangeable biosimilar\" to Perjeta, also known as pertuzumab.The companies said Poherdy is indicated for use in combination with trastuzumab and docetaxel for the treatment of adults with HER2-positive metastatic breast cancer, and in combination with trastuzumab and chemotherapy as a neoadjuvant treatment for adults with HER2-positive, locally advanced, inflammatory, or early stage breast cancer.Organon has a 2022 license deal with Shanghai Henlius Biotech, covering exclusive commercialization rights to Poherdy and other biosimilars, according to the statement.","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["HK0000165453.HKD","OGN","02696","BK4585","BK4588","LU2065170008.USD","LU2065171311.SGD","BK4559","BK1161","BK4007","LU2065169927.USD","LU2065171402.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2584429376","title":"BUZZ-Organon rises after US FDA clears first biosimilar for breast cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2584429376","media":"Reuters","labels":["shareholding","productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2584429376?lang=en_us&edition=fundamental","pubTime":"2025-11-17 19:08","pubTimestamp":1763377714,"startTime":"0","endTime":"0","summary":"BUZZ-Organon rises after US FDA clears first biosimilar for breast cancer** Shares of healthcare firm Organon OGN.N rise 4.65% to $7.88 premarket** Co and Shanghai Henlius Biotech say US FDA approves their breast cancer drug Poherdy** The two companies' Poherdy first biosimilar to rival Roche's ROG.S Perjeta for HER2-positive breast cancer - OGN** Co says drug to be used with other therapies for advanced or early-stage breast cancer; Organon to market in U.S - OGN** Poherdy carries warnings for heart issues and birth defects; doctors advised to monitor patients, co says** Up to last close, stock down ~50% YTD  ","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251117:nL4N3WT0P0:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"shareholding,productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["00656","LU2065171311.SGD","BK1161","BK4559","02696","LU2065170008.USD","HK0000165453.HKD","BK4585","LU2065169927.USD","BK4007","LU2065171402.SGD","OGN","BK4588","BK1230"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2584010641","title":"FDA Approves Organon and Henlius' POHERDY as First Perjeta Biosimilar in US","url":"https://stock-news.laohu8.com/highlight/detail?id=2584010641","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2584010641?lang=en_us&edition=fundamental","pubTime":"2025-11-17 18:30","pubTimestamp":1763375433,"startTime":"0","endTime":"0","summary":"Organon & Co. and Shanghai Henlius Biotech, Inc. have announced that the US Food and Drug Administration  has approved the Biologics License Application for POHERDY , an interchangeable biosimilar to PERJETA . POHERDY is the first and only approved pertuzumab biosimilar in the US and is indicated for all uses of the reference product, expanding access to potentially more affordable biologic therapies for patients with certain HER2-positive breast cancers. This approval follows an agreement between Henlius and Organon granting Organon exclusive global commercialization rights to POHERDY, except in China.Disclaimer: This news brief was created by Public Technologies  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. Organon & Co. published the original content used to generate this news brief via Busin","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251117:nNDL7M1FWn:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["02696","BK4585","LU2065171402.SGD","BK4007","LU2065170008.USD","BK1161","HK0000165453.HKD","LU2065169927.USD","LU2065171311.SGD","OGN","00656","BK4588","BK1230","BK4559"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2583574990","title":"Henlius Biotech Gets US FDA Nod for Breast Cancer Drug's Biologics License Application","url":"https://stock-news.laohu8.com/highlight/detail?id=2583574990","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2583574990?lang=en_us&edition=fundamental","pubTime":"2025-11-14 18:07","pubTimestamp":1763114852,"startTime":"0","endTime":"0","summary":"Shanghai Henlius Biotech  obtained approval for the biologics license application of POHERDY injection for intravenous use from the US Food and Drug Administration , a Friday Hong Kong bourse filing said.The approved indications include use in combination with trastuzumab and chemotherapy in the treatment of adults with breast cancer.","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["02696","HK0000165453.HKD","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1153639262","title":"Shanghai Henlius Biotech (2696) Announces FDA Approval of HLX11 (Pertuzumab-dpzb) for Key Breast Cancer Treatments","url":"https://stock-news.laohu8.com/highlight/detail?id=1153639262","media":"Bulletin Express","labels":["productRelease","SGX"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1153639262?lang=en_us&edition=fundamental","pubTime":"2025-11-14 16:44","pubTimestamp":1763109854,"startTime":"0","endTime":"0","summary":"Shanghai Henlius Biotech, Inc. 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