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AKESO

92.500

-2.350-2.48%

Volume:9.44M

Turnover:868.22M

Market Cap:83.07B

PE:-139.77

High:95.300

Open:94.700

Low:90.050

Close:94.850

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Overview Company News Filings

Cadonilimab Receives Regulatory Approval from China's NMPA for First-Line Treatment of Advanced Cervical Cancer, Reports Akeso Inc

TransThera Sciences Launches Up to HK$201 Million IPO in Hong Kong

MT Newswires Live

Akeso's Pd-1/Ctla-4 Bispecific Antibody Cadonilimab Approved for First-Line Treatment of Cervical Cancer in All-Comer Populations--Third Approved Indication for Cadonilimab

THOMSON REUTERS

Akeso Inc. Receives NMPA Approval for Cadonilimab as First-Line Treatment for Cervical Cancer

Akeso - Nmpa Approved Snda for Cadonilimab as First-Line Treatment for Cervical Cancer

THOMSON REUTERS

Akeso Hits Snag with Less Favorable Clinical Trial Data for Lung Cancer Treatment; Shares Rise 7%

MT Newswires Live

Akeso Grants Share Options, Restricted Share Units

MT Newswires Live

Akeso Inc. Announces New Grant of Share Options and Restricted Share Units for Directors and Employees

Pfizer Is Jumping Into a Hot Cancer-Drug Race. It May Have Overpaid. -- Barrons.com

Nomura Downgrades Akeso to Neutral From Buy, Adjusts Price Target to HK$99.66 From HK$75.14

MT Newswires Live

Akeso Gets China Nod for Lung Cancer Drug Indication

MT Newswires Live

Ivonescimab Receives Nmpa Approval for First-Line Treatment of Pd-L1-Positive Nsclc, Based on Breakthrough Head to Head Phase Iii Trial Demonstrating Superior Efficacy Over Pembrolizumab

THOMSON REUTERS

US FDA Approves Nasopharyngeal Carcinoma Drug

MT Newswires Live

BRIEF-Akeso Says FDA Approved Anniko (Penpulimab-Kcqx, Pd-1) In Two Indications

Akeso Announces FDA Approval for Penpulimab-Kcqx in Two Bla Indications for Comprehensive Treatment of Advanced Nasopharyngeal Carcinoma

THOMSON REUTERS

Akeso - FDA Approved Anniko (Penpulimab-Kcqx, Pd-1) in Two Indications for Comprehensive Treatment of Advanced Nasopharyngeal Carcinoma

THOMSON REUTERS

FDA: on April 23, Approves Penpulimab-Kcqx for Non-Keratinizing Nasopharyngeal Carcinoma

THOMSON REUTERS

HK Movers | Biotech Stocks Jump With ImmuneOnco up 10%

Tiger Newspress

Akeso's Lung Cancer Drug Meets Primary Endpoints in China Phase 3 Trial; Shares Rise 5%

MT Newswires Live

HK Movers | Biotech Stocks Rally With Zai Lab up 8%

Tiger Newspress

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Akeso Inc. has announced a significant regulatory approval for their innovative treatment, cadonilimab. The China National Medical Products Administration  has approved the use of cadonilimab as a first-line treatment for advanced, recurrent, or metastatic cervical cancer as of May 2025. This approval marks an important milestone for Akeso, as cadonilimab, a first-in-class PD-1/CTLA-4 bispecific antibody, has shown significant improvements in progression-free survival and overall survival in various patient subgroups. This development highlights the ongoing impact of cadonilimab in transforming the treatment standards for advanced cervical cancer and underscores its potential global health benefits for women.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. While PUBT strives to provide accurate and t","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:20250616:nNDL83jy4r:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":"Cadonilimab Receives Regulatory Approval from China's NMPA for First-Line Treatment of Advanced Cervical Cancer, Reports Akeso Inc","news_tag":"corporation,express","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IE00BPRC5H50.USD","LU2488822045.USD","LU1794554557.SGD","LU1720050803.USD","LU0348784397.USD","LU0417516571.SGD","LU0348783233.USD","BK1574","IE00B543WZ88.USD","09926","IE00B5MMRT66.SGD","BK1161"],"gpt_icon":0},{"id":"2543579573","title":"TransThera Sciences Launches Up to HK$201 Million IPO in Hong Kong","url":"https://stock-news.laohu8.com/highlight/detail?id=2543579573","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2543579573?lang=en_us&edition=fundamental","pubTime":"2025-06-13 11:06","pubTimestamp":1749783992,"startTime":"0","endTime":"0","summary":"TransThera Sciences  launched its initial public offering in Hong Kong that seeks to raise up to HK$200.9 million, according to a Friday Hong Kong bourse filing.The clinical-stage biopharmaceutical firm is offering as much as 15,281,000 shares at an indicative price of HK$13.15 each.TransThera secured five cornerstone investors, including Jiangbei Pharmaceutical, Akeso , Sinohsc Honest, Pharmablock Horizon, and Kelingan, which committed to subscribe for a combined HK$130.0 million worth of IPO shares, representing around 64.1% of the offering.The issuer expects to determine its offer price and disclose the allocations on June 20. It will then start trading on the Hong Kong bourse on June 23, according to a prospectus filing.Proceeds from the deal will primarily fund a multiregional Phase III trial of its core product Tinengotinib, with remaining funds allocated to general working capital and corporate purposes.CLSA, Huatai Financial, BOCOM International, BOCI Asia, CMB International, S","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":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["09926","LU0348783233.USD","LU1794554557.SGD","LU0348784397.USD","LU2488822045.USD","IE00BPRC5H50.USD","BK1574","02617","LU1720050803.USD","LU0417516571.SGD","IE00B543WZ88.USD","IE00B5MMRT66.SGD","BK1161"],"gpt_icon":0},{"id":"2541981015","title":"Akeso's Pd-1/Ctla-4 Bispecific Antibody Cadonilimab Approved for First-Line Treatment of Cervical Cancer in All-Comer Populations--Third Approved Indication for Cadonilimab","url":"https://stock-news.laohu8.com/highlight/detail?id=2541981015","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2541981015?lang=en_us&edition=fundamental","pubTime":"2025-06-05 09:36","pubTimestamp":1749087418,"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:20250605:nTUACG1H0G: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":["IE00B543WZ88.USD","LU0417516571.SGD","IE00B5MMRT66.SGD","09926","LU1794554557.SGD","BK1574","IE00BPRC5H50.USD","LU0348783233.USD","LU0348784397.USD","LU2488822045.USD","LU1720050803.USD","BK1161"],"gpt_icon":0},{"id":"2541904690","title":"Akeso Inc. Receives NMPA Approval for Cadonilimab as First-Line Treatment for Cervical Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2541904690","media":"Reuters","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2541904690?lang=en_us&edition=fundamental","pubTime":"2025-06-05 08:19","pubTimestamp":1749082781,"startTime":"0","endTime":"0","summary":"Akeso Inc. has announced a significant regulatory milestone, as the National Medical Products Administration  of China has approved the supplemental New Drug Application  for cadonilimab . This approval allows the use of cadonilimab in combination with platinum-based chemotherapy, with or without bevacizumab, as a first-line treatment for persistent, recurrent, or metastatic cervical cancer. This marks the third approved indication for cadonilimab and addresses the critical unmet needs for immune-based therapies for cervical cancer patients in China. The approval is based on the successful results of the COMPASSION-16/AK104-303 study, which demonstrated significant improvements in progression-free survival and overall survival.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 ","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:20250605:nNDL3qpqQ3:1","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":["BK1574","IE00B543WZ88.USD","BK1161","LU1720050803.USD","IE00BPRC5H50.USD","LU2488822045.USD","IE00B5MMRT66.SGD","LU0348783233.USD","LU0417516571.SGD","LU0348784397.USD","09926","LU1794554557.SGD"],"gpt_icon":1},{"id":"2541090985","title":"Akeso -  Nmpa Approved Snda for Cadonilimab  as First-Line Treatment for Cervical Cancer","url":"https://stock-news.laohu8.com/highlight/detail?id=2541090985","media":"THOMSON REUTERS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2541090985?lang=en_us&edition=fundamental","pubTime":"2025-06-05 08:17","pubTimestamp":1749082675,"startTime":"0","endTime":"0","summary":null,"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:20250605:nFWN3S70DJ: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":["LU0348784397.USD","LU1794554557.SGD","IE00B543WZ88.USD","LU2488822045.USD","BK1161","IE00BPRC5H50.USD","IE00B5MMRT66.SGD","LU0348783233.USD","BK1574","09926","LU0417516571.SGD","LU1720050803.USD"],"gpt_icon":0},{"id":"2540478427","title":"Akeso Hits Snag with Less Favorable Clinical Trial Data for Lung Cancer Treatment; Shares Rise 7%","url":"https://stock-news.laohu8.com/highlight/detail?id=2540478427","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2540478427?lang=en_us&edition=fundamental","pubTime":"2025-06-03 14:41","pubTimestamp":1748932906,"startTime":"0","endTime":"0","summary":"Akeso  and Summit Therapeutics suffered a setback after less favorable clinical data for its ivonescimab lung cancer drug diminished hopes for approval, the South China Morning Post reported Monday.The US Food and Drug Administration indicated a \"statistically significant\" overall survival benefit, from start of treatment to death, not just delayed tumor progression, is needed for US approval, the report said, citing Summit.The drug showed progression-free survival but had not yet shown a good enough survival benefit for patients in its study for US approval, the report said.Shares in Akeso jumped 7% during afternoon trading on Tuesday.","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":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["LU0348784397.USD","LU1794554557.SGD","IE00B543WZ88.USD","LU2488822045.USD","BK1161","IE00BPRC5H50.USD","IE00B5MMRT66.SGD","LU0348783233.USD","BK1574","09926","LU0417516571.SGD","LU1720050803.USD"],"gpt_icon":1},{"id":"2538120705","title":"Akeso Grants Share Options, Restricted Share Units","url":"https://stock-news.laohu8.com/highlight/detail?id=2538120705","media":"MT Newswires Live","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2538120705?lang=en_us&edition=fundamental","pubTime":"2025-05-26 15:46","pubTimestamp":1748245608,"startTime":"0","endTime":"0","summary":"Akeso  granted 7,115,000 share options to 114 grantees under its share option scheme at an exercise price of HK$84.60 apiece, according to a Monday filing with the Hong Kong bourse.Chairperson Xia Yu is entitled to 3 million share options, the filing said.The biopharmaceutical company will also offer 3,420,000 restricted share units to 107 grantees, including Xia, who will be entitled to 2 million RSUs, and six other directors.The closing price of the shares is HK$83.15 per share, the filing said.","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":"0","news_top_title":null,"news_tag":"shareholding","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["09926","IE00BPRC5H50.USD","LU0348783233.USD","LU1720050803.USD","LU1794554557.SGD","IE00B543WZ88.USD","LU2488822045.USD","IE00B5MMRT66.SGD","LU0348784397.USD","BK1161","LU0417516571.SGD","BK1574"],"gpt_icon":0},{"id":"2538491911","title":"Akeso Inc. Announces New Grant of Share Options and Restricted Share Units for Directors and Employees","url":"https://stock-news.laohu8.com/highlight/detail?id=2538491911","media":"Reuters","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2538491911?lang=en_us&edition=fundamental","pubTime":"2025-05-26 07:41","pubTimestamp":1748216464,"startTime":"0","endTime":"0","summary":"Akeso Inc., a biopharmaceutical company incorporated in the Cayman Islands, announced on May 24, 2025, the grant of Share Options and Restricted Share Units  to recognize the contributions of its directors and existing employees. The announcement, made in compliance with the Listing Rules of the Stock Exchange of Hong Kong, disclosed the allocation of 4,080,000 Share Options to its board members, with Dr. XIA Yu, the chairwoman and executive director, receiving the largest portion of 3,000,000 options. Additionally, 3,035,000 Share Options were distributed among other company employees. The vesting of RSUs will be contingent upon individual performance targets, specifically tailored to the functions of each grantee, such as research and development, sales, and financial performance. This strategic move aims to align the interests of the company's leadership and staff with its operational and growth objectives.","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:20250525:nNDL4BqbR0:1","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":["LU2488822045.USD","BK1574","LU1794554557.SGD","LU0348783233.USD","09926","LU0348784397.USD","LU1720050803.USD","IE00B543WZ88.USD","BK1161","IE00B5MMRT66.SGD","IE00BPRC5H50.USD","LU0417516571.SGD"],"gpt_icon":0},{"id":"2536646754","title":"Pfizer Is Jumping Into a Hot Cancer-Drug Race. It May Have Overpaid. -- Barrons.com","url":"https://stock-news.laohu8.com/highlight/detail?id=2536646754","media":"Dow Jones","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2536646754?lang=en_us&edition=fundamental","pubTime":"2025-05-20 22:46","pubTimestamp":1747752360,"startTime":"0","endTime":"0","summary":"Pfizer has thrown itself into the fiercest horse race in biopharma, saying late Monday it had bought the rights to an experimental cancer drug in a competitive and promising category. Analysts say it may have overpaid.The big move in biotech for the past few years has been for global players in the industry to make deals with Chinese biopharma companies to license PD-1/VEGF bispecific antibodies, a new type of tumor-killing treatment. The race heated up last June, when the U.S.-based biotech Summit Therapeutics said that its PD-1/VEGF bispecific antibody, licensed from a Chinese company called Akeso, beat Merck's Keytruda in lung-cancer patients.Now, everyone seems to be piling into the race. Merck announced a deal to license a Chinese PD-1/VEGF in November. BioNTech has one, too.Pfizer does have a partnership with Summit, announced in February, where the companies are testing Summit's PD-1/VEGF in combination with some Pfizer cancer drugs. But that deal wouldn't gi","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://dowjonesnews.com/newdjn/logon.aspx?AL=N","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":["BK4007","LU1066053197.SGD","LU1894683264.USD","IE00BFTCPJ56.SGD","SG9999014575.USD","LU0965508806.USD","LU1941712348.USD","LU1116320901.HKD","LU1069347547.HKD","09926","BNTX","SG9999003800.SGD","BK4551","IE00B1BXHZ80.USD","LU1430594728.SGD","LU0203345920.USD","LU0208291251.USD","LU1035773651.USD","SG9999013999.USD","IE00B5MMRT66.SGD","IE00BBT3K403.USD","LU0211331839.USD","SMMT","LU1974910355.USD","LU0203347892.USD","LU1066051811.HKD","LU0321505439.SGD","BK4559","IE0009355771.USD","BK4535","LU1989772840.SGD","BK4568","BK4588","LU0265550946.USD","LU0965509010.AUD","LU0170899867.USD","LU0306806265.USD","LU1989772923.USD","LU0234572021.USD","LU1929549753.HKD","IE0002141913.USD","SG9999002224.SGD","IE00BPRC5H50.USD","PFE","BK1574","LU0225284248.USD","LU2361045086.USD","IE000M9KFDE8.USD","LU0106261372.USD"],"gpt_icon":1},{"id":"2530647914","title":"Nomura Downgrades Akeso to Neutral From Buy, Adjusts Price Target to HK$99.66 From HK$75.14","url":"https://stock-news.laohu8.com/highlight/detail?id=2530647914","media":"MT Newswires Live","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530647914?lang=en_us&edition=fundamental","pubTime":"2025-04-28 18:55","pubTimestamp":1745837736,"startTime":"0","endTime":"0","summary":"Akeso (HKG:9926) has an average rating of buy and mean price target of HK$103.34, according to analysts polled by FactSet.(MT Newswires covers equity, commodity and economic research from major banks ","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":["rate"],"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":"","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["09926"],"gpt_icon":0},{"id":"2530842448","title":"Akeso Gets China Nod for Lung Cancer Drug Indication","url":"https://stock-news.laohu8.com/highlight/detail?id=2530842448","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530842448?lang=en_us&edition=fundamental","pubTime":"2025-04-28 14:13","pubTimestamp":1745820829,"startTime":"0","endTime":"0","summary":"Akeso  obtained approval for a supplementary new drug application for ivonescimab to treat non-small cell lung cancer from China's National Medical Products Administration, an April 25 Hong Kong bourse filing said.The approval is for the indication of use of the drug as a monotherapy for the first-line treatment of PD-L1-positive  non-small cell lung cancer patients.This indication marks the second major approval for ivonescimab, according to the drug company.","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://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["IE00BPRC5H50.USD","LU1720050803.USD","LU0417516571.SGD","LU1794554557.SGD","LU2488822045.USD","09926","BK1574","LU0348784397.USD","BK1161","IE00B5MMRT66.SGD","LU0348783233.USD","IE00B543WZ88.USD"],"gpt_icon":1},{"id":"2530996168","title":"Ivonescimab Receives Nmpa Approval for First-Line Treatment of Pd-L1-Positive Nsclc, Based on Breakthrough Head to Head Phase Iii Trial Demonstrating Superior Efficacy Over Pembrolizumab","url":"https://stock-news.laohu8.com/highlight/detail?id=2530996168","media":"THOMSON 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