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港股
詳情
本頁面由Tiger Fintech (Singapore) Pte. Ltd.提供服務
復宏漢霖
33.950
+1.950
6.09%
手動刷新
成交量:
243.75萬
成交額:
8,264.40萬
市值:
184.52億
市盈率:
21.13
高:
35.450
開:
32.150
低:
32.000
收:
32.000
資料載入中...
總覽
公司
新聞
公告
復星醫藥子公司復宏漢霖簽署許可協議
北京商报
·
02-06
復宏漢霖與Dr.Reddy’s簽署HLX15獨家許可協議
财中社
·
02-06
Golden Valley Value Select Master Fund增持復宏漢霖(02696)63.1萬股 每股作價約17.39港元
智通财经
·
02-06
復宏漢霖(02696)就HLX15(重組抗CD38全人單克隆抗體注射液)與Dr. Reddy’s訂立許可協議
智通财经
·
02-06
復宏漢霖PD-1抑制劑獲歐盟批准一線治療肺癌,信達生物信迪利單抗聯合療法擬納入優先審評,德曲妥珠單抗補充申請獲FDA批准
医药经济报
·
02-06
【港股異動 | 復宏漢霖(02696.HK)盤中漲超3%】復宏漢霖(02696.HK)盤中漲超3%,截至發稿,漲2.9%,報18.48港元,成交額467.26萬港元。
金融界
·
02-06
港股異動 | 復宏漢霖(02696)盤中漲超3% H藥漢斯狀®於歐盟獲批上市 用於一線治療廣泛期小細胞肺癌
智通财经
·
02-06
金十數據整理:每日港股市場要聞速遞(2月6日 週四)
美港电讯
·
02-06
復宏漢霖(02696.HK)獲股東林利軍增持15.39萬股
格隆汇
·
02-06
復宏漢霖(02696.HK)單抗注射液漢斯狀獲歐盟批准上市
阿斯达克财经
·
02-06
復宏漢霖抗PD-1單抗H藥獲歐盟批准,為廣泛期小細胞肺癌患者帶來新希望
金融界
·
02-05
復宏漢霖獲批斯魯利單抗在歐盟上市
财中社
·
02-05
復宏漢霖(02696):歐盟委員會批准斯魯利單抗注射液聯合化療用於廣泛期小細胞肺癌成人患者的一線治療
智通财经网
·
02-05
【復星醫藥:控股子公司藥品獲歐盟上市批准】金融界2月5日消息,上海復星醫藥(集團)股份有限公司控股子公司復宏漢霖自主研發的斯魯利單抗注射液聯合卡鉑和依託泊苷適用於廣泛期小細胞肺癌成人患者的一線治療的上市許可申請近日獲歐盟委員會批准。該藥品為本集團自主研發的創新型抗PD-1單抗,在中國境內獲批多個適應症,在歐盟、印度尼西亞、柬埔寨、泰國已獲批上市。截至2024年12月,本集團針對該藥品累計研發投入約為人民幣298,271萬元。2023年,靶向PD-1的單克隆抗體藥品於全球範圍的銷售額約為399億美元。復宏漢霖已授予 Intas Pharmaceuticals Ltd.於許可區域及許可領域獨家商業化該藥品的權利許可。本次獲批將拓展該藥品全球市場區域,提升本集團產品國際影響力。但藥品銷售情況受多種因素影響具有較大不確定性。
金融界
·
02-05
林利軍增持復宏漢霖(02696)15.39萬股 每股作價約16.89港元
智通财经
·
02-05
復宏漢霖盤中漲超5% 帕妥珠單抗生物類似藥HLX11的生物製品許可申請獲FDA受理
新浪港股
·
02-04
港股異動 | 復宏漢霖(02696)現漲超4% 帕妥珠單抗生物類似藥HLX11的生物製品許可申請獲FDA受理
智通财经
·
02-04
復宏漢霖盤中異動 快速上漲5.30%
市场透视
·
02-04
復宏漢霖(02696.HK)帕妥珠單抗HLX11生物製品許可申請獲FDA受理
阿斯达克财经
·
02-02
【復宏漢霖(02696.HK):劉志勇獲選為職工代表監事】復宏漢霖(02696.HK)發佈公告,袁曄星先生(袁先生)因個人發展原因不再擔任本公司第三屆監事會的職工代表監事,自2025年1月31日起生效。
金融界
·
02-02
更多
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19:10","pubTimestamp":1738840257,"startTime":"0","endTime":"0","summary":"北京商报讯(记者丁宁)2月6日晚间,复星医药(600196)发布公告称,公司控股子公司复宏汉霖就在研产品HLX15(即重组抗CD38全人单克隆抗体注射液)的静脉注射制剂(IV)与皮下注射制剂(SC)剂型授予Dr.Reddys于许可区域(即美国及约定的欧洲地区)及许可领域(即各约定参比制剂于许可区域内各国家获批上市之适应症)内的开发、生产及商业化权利的许可。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202502063312456310.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202502063312456310.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["BK1593","02696","BK1515","02196","BK1191","BK1161"],"gpt_icon":0},{"id":"2509298052","title":"復宏漢霖與Dr.Reddy’s簽署HLX15獨家許可協議","url":"https://stock-news.laohu8.com/highlight/detail?id=2509298052","media":"财中社","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509298052?lang=zh_tw&edition=fundamental","pubTime":"2025-02-06 19:04","pubTimestamp":1738839873,"startTime":"0","endTime":"0","summary":"财中社2月6日电复宏汉霖(02696)发布公告,公司于2025年2月6日与Dr.Reddy‘sLaboratoriesSA签订了一份许可协议。根据该协议,公司将向Dr.Reddy’s授予在美国及约定的欧洲地区(包括英国、瑞士等42个国家)开发、生产和商业化HLX15(重组抗CD38全人单克隆抗体注射液)的独家许可。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202502063312453410.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2509226185","title":"Golden Valley Value Select Master Fund增持復宏漢霖(02696)63.1萬股 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Limited和LVC SG MANAGEMENT PTE. 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Reddy’s订立许可协议有助于深化公司产品的出海进程,进一步提升公司产品在国际市场的可及性和影响力,并有望为区域内患者提供更多治疗选择。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1246715.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["02696","BK1161"],"gpt_icon":0},{"id":"2509407182","title":"復宏漢霖PD-1抑制劑獲歐盟批准一線治療肺癌,信達生物信迪利單抗聯合療法擬納入優先審評,德曲妥珠單抗補充申請獲FDA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2509407182","media":"医药经济报","labels":["productRelease","policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509407182?lang=zh_tw&edition=fundamental","pubTime":"2025-02-06 17:53","pubTimestamp":1738835599,"startTime":"0","endTime":"0","summary":"与此同时,复宏汉霖同步在全球开展10余项以斯鲁利单抗为核心的免疫联合疗法临床研究。公开资料显示,这是信达生物在研的抗CTLA-4单抗IBI310与抗PD-1单抗信迪利单抗联合疗法,该联合疗法此前已经被CDE纳入突破性治疗品种。信迪利单抗是一种抗PD-1单抗,能够阻断导致肿瘤免疫耐受的PD-1/L1通路,重新启动淋巴细胞的抗肿瘤活性,从而达到治疗肿瘤的目的。本次IBI310联合信迪利单抗拟纳入优先审评,意味着这款联合疗法有望加速获批,惠及患者。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250206180205abc48936&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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11:12","pubTimestamp":1738811558,"startTime":"0","endTime":"0","summary":"复宏汉霖(02696.HK)盘中涨超3%,截至发稿,涨2.9%,报18.48港元,成交额467.26万港元。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://24h.jrj.com.cn/2025/02/06111247979757.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"movement","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["02696","BK1161"],"gpt_icon":0},{"id":"2509181299","title":"港股異動 | 復宏漢霖(02696)盤中漲超3% H藥漢斯狀®於歐盟獲批上市 用於一線治療廣泛期小細胞肺癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2509181299","media":"智通财经","labels":["productRelease","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509181299?lang=zh_tw&edition=fundamental","pubTime":"2025-02-06 11:07","pubTimestamp":1738811222,"startTime":"0","endTime":"0","summary":"消息面上,2月5日,复宏汉霖宣布,抗PD-1单抗H药汉斯状正式获得欧盟委员会批准,联合卡铂和依托泊苷用于广泛期小细胞肺癌成人患者的一线治疗,标志着H药成为首个且唯一在欧盟获批上市用于广泛期小细胞肺癌治疗的抗PD-1单抗。据了解,H药 汉斯状是全球首个获批一线治疗小细胞肺癌的PD-1抑制剂。复宏汉霖执行董事、首席执行官朱俊博士表示,H药在欧盟获批上市,标志着复宏汉霖在惠及全球患者的进程中再进一步。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1246423.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease,movement","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2509264719","title":"金十數據整理:每日港股市場要聞速遞(2月6日 週四)","url":"https://stock-news.laohu8.com/highlight/detail?id=2509264719","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509264719?lang=zh_tw&edition=fundamental","pubTime":"2025-02-06 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06:54","pubTimestamp":1738796084,"startTime":"0","endTime":"0","summary":"格隆汇2月6日丨根据联交所最新权益披露资料显示,2025年1月28日,复宏汉霖(02696.HK)获股东林利军在场内以每股均价16.8922港元增持15.39万股,涉资约259.97万港元。增持后,林利军最新持股数目为14,741,184股,持股比例由8.92%上升至9.02%。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/02/06065447975629.shtml","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":"jinrongjie_stock","symbols":["02696","BK1161"],"gpt_icon":0},{"id":"2509235479","title":"復宏漢霖(02696.HK)單抗注射液漢斯狀獲歐盟批准上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2509235479","media":"阿斯达克财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509235479?lang=zh_tw&edition=fundamental","pubTime":"2025-02-06 00:17","pubTimestamp":1738772220,"startTime":"0","endTime":"0","summary":"复宏汉霖(02696.HK) 公布,近日,欧盟委员会“EC”已批准公司自主研发的创新抗PD-1单抗斯鲁利单抗注射液(境内商品名:汉斯状)联合卡铂和依托泊苷适用于广泛期小细胞肺癌成人患者的一线治疗,其于欧盟获批的商品名为Hetronifly。此次获批意味汉斯状在所有欧盟成员国及冰岛、列支敦士登和挪威获得集中上市许可。据此,汉斯状成为公司第二个于欧盟获批上市的产品,也成为欧盟首个批准用于广泛期小细胞肺癌治疗的抗PD-1单抗药品。(de/d)(港股报价延迟最少十五分钟。沽空资料截至 2025-02-05 16:25。)AASTOCKS新闻","market":"sh","thumbnail":"https://plib.aastocks.com/aafnnews/image/medialib/20180119144849220_s.jpg","type":0,"news_type":0,"thumbnails":["https://plib.aastocks.com/aafnnews/image/medialib/20180119144849220_s.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.aastocks.com/tc/stocks/news/aafn-con/NOW.1415073/latest-news/AAFN","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":"aastocks_highlight","symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2509028463","title":"復宏漢霖抗PD-1單抗H藥獲歐盟批准,為廣泛期小細胞肺癌患者帶來新希望","url":"https://stock-news.laohu8.com/highlight/detail?id=2509028463","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509028463?lang=zh_tw&edition=fundamental","pubTime":"2025-02-05 22:18","pubTimestamp":1738765082,"startTime":"0","endTime":"0","summary":"2月5日,复宏汉霖宣布了一项重大突破:其自主研发的抗PD-1单抗H药——汉斯状正式获得欧盟委员会的批准,联合卡铂和依托泊苷用于广泛期小细胞肺癌成人患者的一线治疗。这一里程碑式的成就标志着H药成为首个且唯一在欧盟获批上市用于广泛期小细胞肺癌治疗的抗PD-1单抗,为全球小细胞肺癌患者带来了新的治疗曙光。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.jrj.com.cn/2025/02/05221847974225.shtml","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":"jinrongjie_stock","symbols":["BK1161","BK0196","BK0028","02696","BK0183","BK0238","000876","BK4023","PD","BK0012","BK0188","LU1169590202.USD","BK0187","LU1169589451.USD"],"gpt_icon":0},{"id":"2509400365","title":"復宏漢霖獲批斯魯利單抗在歐盟上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2509400365","media":"财中社","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509400365?lang=zh_tw&edition=fundamental","pubTime":"2025-02-05 20:09","pubTimestamp":1738757384,"startTime":"0","endTime":"0","summary":"财中社2月5日电复宏汉霖(02696)发布公告,近日,欧盟委员会批准公司自主研发的创新抗PD-1单抗斯鲁利单抗注射液(中国境内商品名:汉斯状?;欧盟商品名:Hetronifly?)联合化疗用于广泛期小细胞肺癌(ES-SCLC)成人患者的一线治疗。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202502053311272098.html","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":"stock_eastmoney","symbols":["02696","BK1161"],"gpt_icon":0},{"id":"2509407514","title":"復宏漢霖(02696):歐盟委員會批准斯魯利單抗注射液聯合化療用於廣泛期小細胞肺癌成人患者的一線治療","url":"https://stock-news.laohu8.com/highlight/detail?id=2509407514","media":"智通财经网","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509407514?lang=zh_tw&edition=fundamental","pubTime":"2025-02-05 20:02","pubTimestamp":1738756937,"startTime":"0","endTime":"0","summary":"复宏汉霖(02696)发布公告,近日,欧盟委员会(European \nCommis...","market":"sg","thumbnail":"https://img.zhitongcaijing.com/gonggao/ztcj_announce_10.jpeg?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250","type":0,"news_type":0,"thumbnails":["https://img.zhitongcaijing.com/gonggao/ztcj_announce_10.jpeg?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1246231.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":"复宏汉霖(02696):欧盟委员会批准斯鲁利单抗注射液联合化疗用于广泛期小细胞肺癌成人患者的一线治疗","news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"highlight_zhitongcaijin","symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2509069434","title":"【復星醫藥:控股子公司藥品獲歐盟上市批准】金融界2月5日消息,上海復星醫藥(集團)股份有限公司控股子公司復宏漢霖自主研發的斯魯利單抗注射液聯合卡鉑和依託泊苷適用於廣泛期小細胞肺癌成人患者的一線治療的上市許可申請近日獲歐盟委員會批准。該藥品為本集團自主研發的創新型抗PD-1單抗,在中國境內獲批多個適應症,在歐盟、印度尼西亞、柬埔寨、泰國已獲批上市。截至2024年12月,本集團針對該藥品累計研發投入約為人民幣298,271萬元。2023年,靶向PD-1的單克隆抗體藥品於全球範圍的銷售額約為399億美元。復宏漢霖已授予 Intas Pharmaceuticals Ltd.於許可區域及許可領域獨家商業化該藥品的權利許可。本次獲批將拓展該藥品全球市場區域,提升本集團產品國際影響力。但藥品銷售情況受多種因素影響具有較大不確定性。","url":"https://stock-news.laohu8.com/highlight/detail?id=2509069434","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509069434?lang=zh_tw&edition=fundamental","pubTime":"2025-02-05 18:52","pubTimestamp":1738752748,"startTime":"0","endTime":"0","summary":"截至2024年12月,本集团针对该药品累计研发投入约为人民币298,271万元。2023年,靶向PD-1的单克隆抗体药品于全球范围的销售额约为399亿美元。本次获批将拓展该药品全球市场区域,提升本集团产品国际影响力。但药品销售情况受多种因素影响具有较大不确定性。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://24h.jrj.com.cn/2025/02/05185247963837.shtml","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":"jinrongjie_stock","symbols":["BK0096","BK0188","BK1515","BK4023","BK0183","BK0239","BK0012","BK0187","600196","BK0060","BK1191","LU1169589451.USD","02696","02196","BK0196","LU1169590202.USD","BK1593","BK1161","BK0175","BK0028","PD"],"gpt_icon":0},{"id":"2509567406","title":"林利軍增持復宏漢霖(02696)15.39萬股 每股作價約16.89港元","url":"https://stock-news.laohu8.com/highlight/detail?id=2509567406","media":"智通财经","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2509567406?lang=zh_tw&edition=fundamental","pubTime":"2025-02-05 18:46","pubTimestamp":1738752379,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,香港联交所最新资料显示,1月28日,林利军增持复宏汉霖(02696)15.39万股,每股作价16.8922港元,总金额约为259.97万港元。增持后最新持股数目约为1474.12万股,最新持股比例为9.02%。","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1246150.html","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":"stock_zhitongcaijing","symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2508105577","title":"復宏漢霖盤中漲超5% 帕妥珠單抗生物類似藥HLX11的生物製品許可申請獲FDA受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2508105577","media":"新浪港股","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2508105577?lang=zh_tw&edition=fundamental","pubTime":"2025-02-04 09:52","pubTimestamp":1738633920,"startTime":"0","endTime":"0","summary":"热点栏目\n\n自选股\n数据中心\n行情中心\n资金流向\n模拟交易\n\n客户端\n\n\n 复宏汉霖(02696)盘中涨超5%,截至发稿,股价上涨3.42%,现报17.56港元,成交额413.68万港元。\n 消息面上,复宏汉霖公告,公司自主研发的Perjeta (帕妥珠单抗)生物类似药候选药HLX11的生物制品许可申请(BLA)获美国食品药品管理局(FDA)受理。据悉,HLX11是公司自主研发的帕妥珠单抗生物类似药,拟用于HER2阳性早期乳腺癌的新辅助/辅助治疗、HER2阳性转移性乳腺癌的治疗及与原研药药品标签相符的其他适应症。\n\n\n\n海量资讯、精准解读,尽在新浪财经APP\n\n责任编辑:卢昱君","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://finance.sina.com.cn/stock/hkstock/marketalerts/2025-02-04/doc-ineihqmc6398135.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"sina","symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2508103142","title":"港股異動 | 復宏漢霖(02696)現漲超4% 帕妥珠單抗生物類似藥HLX11的生物製品許可申請獲FDA受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2508103142","media":"智通财经","labels":["productRelease","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2508103142?lang=zh_tw&edition=fundamental","pubTime":"2025-02-04 09:40","pubTimestamp":1738633214,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,复宏汉霖现涨超4%,截至发稿,涨4.24%,报17.7港元,成交额365.55万港元。消息面上,复宏汉霖公告,公司自主研发的Perjeta 生物类似药候选药HLX11的生物制品许可申请获美国食品药品管理局受理。据悉,HLX11是公司自主研发的帕妥珠单抗生物类似药,拟用于HER2阳性早期乳腺癌的新辅助/辅助治疗、HER2阳性转移性乳腺癌的治疗及与原研药药品标签相符的其他适应症。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1245517.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease,movement","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["02696","BK1161"],"gpt_icon":0},{"id":"2508510587","title":"復宏漢霖盤中異動 快速上漲5.30%","url":"https://stock-news.laohu8.com/highlight/detail?id=2508510587","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2508510587?lang=zh_tw&edition=fundamental","pubTime":"2025-02-04 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