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复宏汉霖

32.000

+0.1500.47%

成交量：417.30万

成交额：1.36亿

市值：173.92亿

市盈率：19.94

高：34.050

开：31.850

低：30.750

收：31.850

数据加载中...

总览公司新闻公告

复宏汉霖04月08日遭主力抛售9万元

复宏汉霖04月07日遭主力抛售627万元

复宏汉霖盘中异动早盘股价大跌12.56%

复宏汉霖“贝伐珠单抗”眼科III期研究成功

Golden Valley Value Select Master Fund增持复宏汉霖(02696)51.09万股每股作价34.817港元

亿胜生物科技（1061.HK）公布与复宏汉霖就渗出性（湿性）老年性黄斑部病变治疗三期临床研究达到主要研究终点

复宏汉霖盘中异动早盘股价大跌5.15%

金十数据整理：每日港股市场要闻速递（4月3日周四）

复宏汉霖HLX04-O临床试验达主要研究终点

复宏汉霖(02696)重组抗VEGF人源化单克隆抗体注射液HLX04-O三期临床研究达到主要研究终点

复宏汉霖(02696.HK)HLX04-O治疗黄斑变性3期临床研究达主要研究终点

阿斯达克财经

复宏汉霖(02696)：重组抗VEGF人源化单克隆抗体注射液HLX04-O 用于湿性年龄相关性黄斑变性(wAMD)治疗的3期临床研究达到主要研究终点

郭广昌回应复宏汉霖私有化被否：小股东们的眼光很好

复宏汉霖03月31日主力净流出205万元散户资金买入

复宏汉霖：帕妥珠单抗生物类似药HLX11(抗HER2结构域II人源化单克隆抗体注射液)的上市许可申请(MAA)获欧洲药品管理局(EMA)受理

复宏汉霖(02696)：帕妥珠单抗生物类似药HLX11 (抗HER2结构域II人源化单克隆抗体注射液)的上市许可申请(MAA)获欧洲药品管理局(EMA)受理

复宏汉霖03月28日获主力加仓1095万元

港股异动 | 生物医药板块持续走高，再鼎医药绩后涨超12%，康方生物涨近5%

老虎资讯综合

异动解读 | 复宏汉霖盘中大涨5.14%，HLX22临床进展及业绩增长提振股价

港股异动 | 复宏汉霖(02696)午后涨超4% HLX22联合治疗胃癌3期临床研究完成日本首例患者给药

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18:49","pubTimestamp":1743763784,"startTime":"0","endTime":"0","summary":"4月2日，复宏汉霖宣布HLX04-O治疗湿性年龄相关性黄斑变性中国患者的III期HLX04-O-wAMD-CN研究已成功达到预设的主要研究终点。HLX04-O有望成为中国首个获批用于眼科相关疾病治疗的贝伐珠单抗制剂。此外，HLX04-O和雷珠单抗对wAMD患者人群整体、眼部、非眼部的安全性特征均相似，且安全性良好。随着眼底治疗方法的突破与发展，抗VEGF药物已成为wAMD的一线疗法，贝伐珠单抗玻璃体注射治疗wAMD的有效性和安全性也已在多项临床研究中得到验证。","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=nesSN20250405001622a6afd38e&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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Fund增持复宏汉霖(02696)51.09万股，每股作价34.817港元，总金额约为1778.8万港元。增持后最新持股数目约为1187万股，最新持股比例为7.26%。本交易涉及其他关联方：LVC Management Holdings Limited、Vistra Trust (Singapore) Pte. Limited和LVC SG MANAGEMENT PTE. 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10:51","pubTimestamp":1743648699,"startTime":"0","endTime":"0","summary":"2025年04月03日早盘10时51分，复宏汉霖股票出现异动，股价大幅下跌5.15%。资金方面，该股资金流入323.09万港元，流出791.75万港元。机构评级方面，在所有1家参与评级的机构中，100%的券商给予持有建议，无券商给予买入、卖出建议。复宏汉霖股票所在的生物技术行业中，整体跌幅为1.50%。复宏汉霖公司简介：上海复宏汉霖生物技术股份有限公司是一家主要从事单克隆抗体产品的研发、生产及销售业务的中国公司。","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=nesSN20250403105140972d0349&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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09:06","pubTimestamp":1743642385,"startTime":"0","endTime":"0","summary":"4月2日，复宏汉霖（02696）发布公告，近日其重组抗VEGF人源化单克隆抗体注射液HLX04-O在一项针对湿性年龄相关性黄斑变性(wAMD)的3期临床研究中达到了主要研究终点。这项研究是多中心、随机、双盲的非劣效试验，旨在比较HLX04-O与雷珠单抗的有效性和安全性。","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://finance.eastmoney.com/a/202504033364345892.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":["BK1161","BK1141","BK1583","02696","03347","BK1576"],"gpt_icon":0},{"id":"2524422165","title":"复宏汉霖(02696)重组抗VEGF人源化单克隆抗体注射液HLX04-O三期临床研究达到主要研究终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2524422165","media":"金吾财讯","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524422165?lang=zh_cn&edition=fundamental","pubTime":"2025-04-03 09:00","pubTimestamp":1743642004,"startTime":"0","endTime":"0","summary":"金吾财讯 | 复宏汉霖(02696)公布，近日，重组抗VEGF人源化单克隆抗体注射液HLX04-O(\"HLX04-O\")在一项于湿性年龄相关性黄斑变性(wetage-related macular degeneration,wAMD)中国患者中开展的3期临床研究达到主要研究终点。HLX04-O是在公司自主研发的汉贝泰(贝伐珠单抗注射液)的基础上，根据眼科用药的需求对汉贝泰(贝伐珠单抗注射液)的处方、规格和生产工艺进行优化，保持活性成分不变，而开发的新的眼科制剂产品，拟用于湿性年龄相关性黄斑变性(wAMD)的治疗。","market":"nz","thumbnail":"https://static.szfiu.com/news/20250106/NjM1YWNhMGUzZGNhNThhMTg4MzM5MDkyOTUwOA==.jpg","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20250106/NjM1YWNhMGUzZGNhNThhMTg4MzM5MDkyOTUwOA==.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"1956542","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":null,"symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2524418185","title":"复宏汉霖(02696.HK)HLX04-O治疗黄斑变性3期临床研究达主要研究终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2524418185","media":"阿斯达克财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524418185?lang=zh_cn&edition=fundamental","pubTime":"2025-04-02 23:18","pubTimestamp":1743607080,"startTime":"0","endTime":"0","summary":"复宏汉霖(02696.HK) 公布，近日，重组抗VEGF人源化单克隆抗体注射液HLX04-O在一项于湿性年龄相关性黄斑变性中国患者中开展的3期临床研究达到主要研究终点。结果显示，HLX04-O组第48周最佳矫正视力较基线改善的平均字母数变化结果非劣于雷珠单抗组。HLX04-O是在公司自主研发的汉贝泰的基础上开发的新的眼科制剂产品。2020年10月，公司将汉贝泰于全球范围眼科治疗用途和/或疗法的独家权利许可给亿胜生物科技(01061.HK) ，双方并约定共同开发相关产品。(de/d)(港股报价延迟最少十五分钟。沽空资料截至 2025-04-02 16:25。)AASTOCKS新闻","market":"fut","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.1431404/latest-news/AAFN","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":"aastocks_highlight","symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2524496130","title":"复宏汉霖(02696)：重组抗VEGF人源化单克隆抗体注射液HLX04-O 用于湿性年龄相关性黄斑变性(wAMD)治疗的3期临床研究达到主要研究终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2524496130","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524496130?lang=zh_cn&edition=fundamental","pubTime":"2025-04-02 21:13","pubTimestamp":1743599621,"startTime":"0","endTime":"0","summary":"智通财经APP讯，复宏汉霖 发布公告，近日，重组抗VEGF人源化单克隆抗体注射液HLX04-O在一项于湿性年龄相关性黄斑变性中国患者中开展的3期临床研究达到主要研究终点。研究结果显示，HLX04-O组第48周BCVA较基线改善的平均字母数变化结果非劣于雷珠单抗组，达到主要研究终点。此外，HLX04-O和雷珠单抗对湿性年龄相关性黄斑变性患者人群整体、眼部、非眼部的安全性特征均相似，且安全性良好。","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/1273523.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1161","02696"],"gpt_icon":0},{"id":"2524276132","title":"郭广昌回应复宏汉霖私有化被否：小股东们的眼光很好","url":"https://stock-news.laohu8.com/highlight/detail?id=2524276132","media":"新浪财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2524276132?lang=zh_cn&edition=fundamental","pubTime":"2025-04-01 13:06","pubTimestamp":1743483962,"startTime":"0","endTime":"0","summary":"复星国际 董事长郭广昌在复星国际2024年业绩会上谈及 复宏汉霖 私有化被否事件，直言自认为当初给的价格还不错，但最终被小股东否决。他说感到遗憾，但也要感谢小股东，说明他们愿意与公司共同成长。“现在已经到35块了，说明小股东的眼光也是很好的”，“我们努力为他们赚钱”。","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=nesSN20250401132132a6ab6f23&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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复宏汉霖股价跌0.87%，报收34.35元，成交金额2688万元，换手率0.48%，振幅4.91%，量比0.40。复宏汉霖今日主力资金（超大单+大单）净流出205万元，上一交易日主力净流入1095万元。该股近5个交易日上涨8.70%，主力资金累计净流入1502万元；近20日主力资金累计净流入8478万元，其中净流入天数为11日。该股主力净额占比0.04%（主力资金净额/流通市值），港股市场排名2457/2651。（以上内容为腾讯自选股基于公开消息，由程序或算法智能生成，仅作为用户看盘参考，不作为投资建议或交易依据。股市有风险，请谨慎决策。）","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=nesSN20250331165731a448557f&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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17:36","pubTimestamp":1743154616,"startTime":"0","endTime":"0","summary":"HLX11是本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/或与原研药药品标签相符的其他适应症。2024年12月，HLX11的上市注册申请获国家药品监督管理局受理。2025年1月，HLX11的生物制品许可申请获美国食品药品管理局受理。本次向EMA提交的MAA基于HLX11对比其原研Perjeta产生的数据，包括分析相似性研究、药代动力学相似性研究及3期临床比对研究，申请Perjeta在欧盟已获批上市的所有适应症。","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=nesSN20250328173656972667e2&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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17:31","pubTimestamp":1743154290,"startTime":"0","endTime":"0","summary":"智通财经APP讯，复宏汉霖(02696)发布公告，近日，公司自主研发的Perjeta®(帕妥珠单抗)生物类似药候选药HLX11(重组抗HER2结构域II人源化单克隆抗体注射液)的上市许可申请获欧洲药品管理局受理，本次申请涉及的适应症如下：(1)与曲妥珠单抗和化疗联合：用于 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