复宏汉霖(02696)_个股概要_股票价格_最新资讯_行情走势_历史数据 - 老虎社区

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02696 复宏汉霖

休市中 05-22 16:08:22

70.750

+0.600

+0.86%

最高73.000	最低69.350	成交量35.67万
今开71.000	昨收70.150	日振幅5.20%
总市值384.17亿	流通市值244.85亿	总股本5.43亿
成交额2,504万	换手率0.10%	流通股本3.46亿
市净率--	ROE--	每股收益0.00
52周最高--	52周最低--	市盈率--
股息--	股息收益率--	ROA--

数据加载中...

北京优虎网络科技有限公司

免责声明:香港交易所资讯服务有限公司、其控股公司及／或该等控股公司的任何附属公司均竭力确保所提供信息的准确和可靠度，但不能保证其绝对准确和可靠，且亦不会承担因任何不准确或遗漏而引起的任何损失或损害的责任（不管是否侵权法下的责任或合约责任又或其它责任）

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发布公告，近日，公司自主开发的斯鲁利单抗注射液获欧洲药品管理局人用医药产品委员会积极审评意见，推荐批准斯鲁利单抗联合卡铂和白蛋白紫杉醇适用于不可手术切除的局部晚期或转移性鳞状非小细胞肺癌成人患者的一线治疗。一旦获得EC批准，斯鲁利单抗的集中上市许可将在所有欧盟成员国及欧洲经济区国家冰岛、列支敦士登和挪威生效。此次CHMP的积极意见主要是基于一项随机、双盲、国际多中心3期临床研究。","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/1445327.html","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":"stock_zhitongcaijing","symbols":["HK0000320264.USD","HK0000320223.HKD","BK1515","02696","HK0000165453.HKD","HK0000306685.HKD","159938","09939","HK0000306701.USD","BK1161","BK1574"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1197788354","title":"复宏汉霖Serplulimab获欧盟CHMP积极意见，用于鳞状非小细胞肺癌一线治疗","url":"https://stock-news.laohu8.com/highlight/detail?id=1197788354","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1197788354?lang=zh_cn&edition=full","pubTime":"2026-05-22 21:49","pubTimestamp":1779457773,"startTime":"0","endTime":"0","summary":"上海复宏汉霖生物技术股份有限公司宣布，其核心产品Serplulimab用于联合化疗一线治疗鳞状非小细胞肺癌的上市许可申请，已获得欧洲药品管理局人用药品委员会的积极意见。该结果表明，与单纯化疗相比，Serplulimab联合化疗方案能显著延长患者的无进展生存期和总生存期，且安全性可控。若最终获得批准，这将是Serplulimab在欧盟市场取得的首个适应症，标志着该药物在国际化征程中迈出坚实一步。Serplulimab若成功获批，将为欧盟地区的该类肺癌患者提供新的重要治疗选择。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","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","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK1161","HK0000320264.USD","HK0000306685.HKD","02696","HK0000320223.HKD","HK0000165453.HKD","HK0000306701.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2637397692","title":"复宏汉霖：注射用HLX316的1期临床于中国境内完成首例给药","url":"https://stock-news.laohu8.com/highlight/detail?id=2637397692","media":"财中社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2637397692?lang=zh_cn&edition=full","pubTime":"2026-05-22 17:02","pubTimestamp":1779440520,"startTime":"0","endTime":"0","summary":"5月22日，复宏汉霖（02696）发布公告，近日注射用HLX316（靶向B7-H3的唾液酸酶Fc融合蛋白）在晚期/转移性实体瘤患者中的1期临床研究于中国境内完成首例患者给药。本研究是一项评估HLX316在晚期/转移性实体瘤患者中的安全性、耐受性、药代动力学特征以及初步疗效的开放性、首次人体1期临床研究，研究分为两个阶段：1a期剂量递增及回填阶段和1b期剂量扩展阶段。","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://finance.eastmoney.com/a/202605223746786796.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["HK0000306685.HKD","HK0000165453.HKD","HK0000320223.HKD","HK0000306701.USD","HK0000320264.USD","BK1161","02696"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2637860753","title":"复宏汉霖(02696)自主研发的注射用HLX48用于晚期/转移性实体瘤治疗的1期临床试验申请获批","url":"https://stock-news.laohu8.com/highlight/detail?id=2637860753","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2637860753?lang=zh_cn&edition=full","pubTime":"2026-05-21 17:15","pubTimestamp":1779354954,"startTime":"0","endTime":"0","summary":"智通财经APP讯，复宏汉霖 公布，近日，公司自主研发的注射用HLX48 用于晚期/转移性实体瘤治疗的1期临床试验申请获国家药品监督管理局批准。因此，HLX48有望实现靶向治疗与免疫调节的双重增效，抑制肿瘤生长并兼具良好安全性。临床前研究显示，HLX48抗肿瘤疗效及安全性良好，其有望获得临床获益。2026年5月，HLX48用于晚期/转移性实体瘤治疗的1期临床试验已获得相关人类研究伦理委员会的批准，并通过澳大利亚药品管理局的临床试验备案。","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/1444517.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":"复宏汉霖(02696)自主研发的注射用HLX48用于晚期/转移性实体瘤治疗的1期临床试验申请获批","news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["HK0000320223.HKD","HK0000306701.USD","HK0000320264.USD","02696","HK0000306685.HKD","HK0000165453.HKD","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1125498263","title":"复宏汉霖获NMPA批准开展HLX48用于晚期/转移性实体瘤的I期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=1125498263","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1125498263?lang=zh_cn&edition=full","pubTime":"2026-05-21 17:15","pubTimestamp":1779354912,"startTime":"0","endTime":"0","summary":"复宏汉霖宣布，其创新药HLX48已获得中国国家药品监督管理局的临床试验默示许可，将针对晚期或转移性实体瘤患者开展I期临床研究。该批准标志着公司在肿瘤治疗领域的研发管线取得又一重要进展。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","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":["HK0000306701.USD","02696","BK1161","HK0000165453.HKD","HK0000320264.USD","HK0000320223.HKD","HK0000306685.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2637802772","title":"复宏汉霖在南京成立新生物技术公司","url":"https://stock-news.laohu8.com/highlight/detail?id=2637802772","media":"每日经济新闻","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2637802772?lang=zh_cn&edition=full","pubTime":"2026-05-21 14:30","pubTimestamp":1779345031,"startTime":"0","endTime":"0","summary":"天眼查App显示，近日，复星汉霖（南京）生物技术有限公司成立，法定代表人为余诚，注册资本5000万元人民币，经营范围为技术服务、技术开发、技术咨询、技术交流、技术转让、技术推广，由复宏汉霖（02696.HK）全资持股。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202605213744976962.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/202605213744976962.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":["HK0000165453.HKD","BK1161","HK0000306701.USD","HK0000320223.HKD","HK0000320264.USD","02696","HK0000306685.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2636272044","title":"港股异动 | 复宏汉霖(02696)午后涨超4% 近日H药汉斯状®日本一线治疗小细胞肺癌桥接试验完成入组","url":"https://stock-news.laohu8.com/highlight/detail?id=2636272044","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2636272044?lang=zh_cn&edition=full","pubTime":"2026-05-18 14:00","pubTimestamp":1779084010,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，复宏汉霖午后涨超4%，截至发稿，涨3.19%，报69.65港元，成交额3725.2万港元。消息面上，近日，据复宏汉霖官微消息，公司宣布，其自主研发的创新型抗PD-1单抗H药汉斯状联合化疗一线治疗广泛期小细胞肺癌适应症的日本桥接试验已顺利完成全部受试者入组。NCT06812260以及支持ES-SCLC在中国和欧洲等地获批的ASTRUM-005研究结果，将共同构成支持H药在日本市场注册申报的关键临床数据，并计划携手日本合作伙伴卫材于其2026财年期间递交上市申请。","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/1442808.html","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":"stock_zhitongcaijing","symbols":["VXUS","BK1161","HK0000165453.HKD","HK0000306685.HKD","HK0000320223.HKD","HK0000320264.USD","BK4585","02696","HK0000306701.USD","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635908882","title":"复星医药：目前控股子公司复宏汉霖已收到与Eisai合作项下的首付现金款","url":"https://stock-news.laohu8.com/highlight/detail?id=2635908882","media":"每日经济新闻","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2635908882?lang=zh_cn&edition=full","pubTime":"2026-05-15 17:47","pubTimestamp":1778838457,"startTime":"0","endTime":"0","summary":"每经AI快讯，有投资者在投资者互动平台提问：董秘您好，请问：复宏汉霖2026年2月授权卫材的7500万美元首付款，在复星医药2026年一季度合并报表中，是否已确认为当期收入？谢谢。复星医药（600196.SH）5月15日在投资者互动平台表示，截至目前，控股子公司复宏汉霖已收到与Eisai合作项下的首付现金款，并根据会计准则进行会计处理。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202605153739043716.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/202605153739043716.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","BK0096","BK1191","BK0028","BK1593","HK0000320223.HKD","BK0239","HK0000306685.HKD","HK0000306701.USD","BK0187","BK0060","600196","BK0188","HK0000165453.HKD","BK0012","BK1161","BK0183","BK0175","HK0000320264.USD","BK0196","BK1515","02196"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635200887","title":"复宏汉霖： HLX48获澳洲临床备案 填补同类药物市场空白","url":"https://stock-news.laohu8.com/highlight/detail?id=2635200887","media":"财中社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2635200887?lang=zh_cn&edition=full","pubTime":"2026-05-13 17:38","pubTimestamp":1778665080,"startTime":"0","endTime":"0","summary":"5月13日，复宏汉霖（02696）发布公告，公司自主研发的注射用HLX48（靶向EGFR和c-MET的抗体偶联药物）用于晚期/转移性实体瘤治疗的1期临床试验已获得相关人类研究伦理委员会的批准，并通过澳大利亚药品管理局的临床试验备案。HLX48是一款靶向c-MET和EGFR的双特异性抗体偶联药物，旨在通过诱导受体介导的内吞作用来实现肿瘤细胞的靶向治疗，并具备良好的安全性。","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://finance.eastmoney.com/a/202605133736002952.html","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":"stock_eastmoney","symbols":["HK0000165453.HKD","HK0000306701.USD","02696","HK0000306685.HKD","HK0000320264.USD","HK0000320223.HKD","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635202592","title":"复宏汉霖(02696)：HLX97在晚期/转移性实体瘤患者中的1期临床研究于中国境内完成首例患者给药","url":"https://stock-news.laohu8.com/highlight/detail?id=2635202592","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2635202592?lang=zh_cn&edition=full","pubTime":"2026-05-13 17:03","pubTimestamp":1778663020,"startTime":"0","endTime":"0","summary":"智通财经APP讯，复宏汉霖 发布公告，近日，本公司自主研发的HLX97 在晚期/转移性实体瘤患者中的1期临床研究于中国境内完成首例患者给药。Part 2在HR 阳性HER2阴性局部晚期或转移性乳腺癌患者中开展，其中两个组是不同剂量的HLX97联合氟维司群的联合治疗组，一个组为氟维司群单药治疗组。2026 年3月，HLX97在晚期/转移性实体瘤患者中的1期临床试验申请获国家药品监督管理局批准。","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/1441210.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":"复宏汉霖(02696)：HLX97在晚期/转移性实体瘤患者中的1期临床研究于中国境内完成首例患者给药","news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["HK0000320264.USD","BK1161","HK0000306685.HKD","HK0000320223.HKD","HK0000165453.HKD","02696","HK0000306701.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634557442","title":"复宏汉霖(02696)：西妥昔单抗注射液生物类似药HLX05-N用于转移性结直肠癌(mCRC)治疗的 1期临床试验申请获美国FDA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2634557442","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2634557442?lang=zh_cn&edition=full","pubTime":"2026-05-10 18:31","pubTimestamp":1778409109,"startTime":"0","endTime":"0","summary":"智通财经APP讯，复宏汉霖 发布公告，近日，本公司自主研发的西妥昔单抗注射液生物类似药HLX05-N用于转移性结直肠癌治疗的1期临床试验申请获美国药品监督管理局批准。本公司拟于条件具备后于美国开展相关1期临床试验。西妥昔单抗能与正常和肿瘤细胞中的EGFR特异性结合，竞争性抑制EGF等配体的结合。此外，西妥昔单抗还可通过抗体依赖的细胞毒性对部分肿瘤发挥抗肿瘤作用。经药学和非临床比对研究证明，HLX05-N与原研西妥昔单抗注射液相似。","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/1439907.html","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":"stock_zhitongcaijing","symbols":["BK1161","HK0000165453.HKD","HK0000306685.HKD","HK0000320223.HKD","HK0000320264.USD","BK4585","02696","HK0000306701.USD","LABU","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634423354","title":"复宏汉霖(02696)：欧盟委员会(EC)批准斯鲁利单抗注射液两项新增适应症","url":"https://stock-news.laohu8.com/highlight/detail?id=2634423354","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2634423354?lang=zh_cn&edition=full","pubTime":"2026-05-10 18:20","pubTimestamp":1778408419,"startTime":"0","endTime":"0","summary":"智通财经APP讯，复宏汉霖 发布公告，近日，欧盟委员会已批准本公司自主开发的斯鲁利单抗注射液两项新增适应症。此次获批意味着斯鲁利单抗两项新增适应症在所有欧盟成员国及冰岛、列支敦士登和挪威获得批准。此次EC批准主要是基于两项随机、双盲、多中心3期临床研究。此外，2026年3月，斯鲁利单抗获欧洲药品管理局人用药品委员会积极审评意见，推荐批准本次两项新增适应症。","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/1439905.html","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":"stock_zhitongcaijing","symbols":["EC","BK4201","HK0000320223.HKD","HK0000165453.HKD","HK0000306701.USD","BK1161","HK0000306685.HKD","HK0000320264.USD","02696"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1144584436","title":"复宏汉霖更新4月股份变动月报表，股本维持稳定","url":"https://stock-news.laohu8.com/highlight/detail?id=1144584436","media":"公告速递","labels":["SGX"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1144584436?lang=zh_cn&edition=full","pubTime":"2026-05-07 16:53","pubTimestamp":1778144012,"startTime":"0","endTime":"0","summary":"上海复宏汉霖生物技术股份有限公司于2026年5月7日发布截至2026年4月30日的股份变动月报表。公告显示，公司本月末法定注册股本总额为人民币543,494,853元，较上月保持不变。具体来看，H股已发行股份及非上市股份的数量分别为346,074,397股和197,420,456股，月内无新增发行、回购或注销活动。本月月底，共有7,722,000份股份期权处于获授未失效状态。截至月末，7,742,000份受限制股份单位已授出且未失效，但并未导致公司当月实质新增发行股份或库藏股变动。","market":"hk","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"SGX","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["02696"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1162320541","title":"复宏汉霖获准在日启动HLX43治疗晚期鳞状非小细胞肺癌的II/III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=1162320541","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1162320541?lang=zh_cn&edition=full","pubTime":"2026-05-04 17:06","pubTimestamp":1777885593,"startTime":"0","endTime":"0","summary":"上海复宏汉霖生物技术股份有限公司近日宣布，其研发的创新药HLX43已获得日本监管机构批准，将正式启动针对晚期鳞状非小细胞肺癌的II/III期临床试验。该试验旨在评估HLX43在晚期鳞状非小细胞肺癌患者中的疗效与安全性，标志着复宏汉霖在肿瘤免疫治疗领域的全球化布局取得重要进展。随着试验的逐步开展，HLX43的临床数据将为后续注册申报奠定基础，助力公司拓展海外市场。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","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":["HK0000320264.USD","HK0000306685.HKD","HK0000320223.HKD","BK1161","02696","HK0000306701.USD","HK0000165453.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2632931566","title":"复宏汉霖(02696)：注射用HLX43单药或联合PIMURUTAMAB HLX07于日本获许可开展用于晚期鳞状非小细胞肺癌治疗的国际多中心2/3期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2632931566","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2632931566?lang=zh_cn&edition=full","pubTime":"2026-05-04 17:02","pubTimestamp":1777885322,"startTime":"0","endTime":"0","summary":"智通财经APP讯，复宏汉霖(02696)发布公告，近日，向日本药品医疗器械综合机构(PMDA)提交的注射用HLX43(靶向PD-L1抗体偶联药物)(“HLX43”)单药或联合pimurutamab HLX07(重组抗EGFR人源化单克隆抗体注射液)(“HLX07”)对比多西他赛用于晚期鳞状非小细胞肺癌(NSCLC)治疗的国际多中心2/3期临床试验通知获得默示许可。根据有关规定，相关临床试验可以在日本开展。公司拟于条件具备后在日本开展相关临床研究。","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/1437852.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":"复宏汉霖(02696)：注射用HLX43单药或联合PIMURUTAMAB HLX07于日本获许可开展用于晚期鳞状非小细胞肺癌治疗的国际多中心2/3期临床试验","news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["HK0000320223.HKD","HK0000165453.HKD","HK0000306701.USD","BK1161","HK0000306685.HKD","HK0000320264.USD","02696"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1198057523","title":"欧盟委员会批准复宏汉霖与Organon的Poherdy®（帕妥珠单抗） 成为欧洲首个获准的Perjeta（帕妥珠单抗）生物类似药","url":"https://stock-news.laohu8.com/highlight/detail?id=1198057523","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1198057523?lang=zh_cn&edition=full","pubTime":"2026-04-29 17:31","pubTimestamp":1777455074,"startTime":"0","endTime":"0","summary":"欧盟委员会正式批准了复宏汉霖与Organon公司联合开发的Poherdy®（帕妥珠单抗），该药物成为欧洲地区首个获得上市许可的Perjeta（帕妥珠单抗）生物类似药。这一批准标志着两家公司在生物制药领域取得重要突破，将为欧洲市场提供更多治疗选择。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","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":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["HK0000306701.USD","02696","BK1161","HK0000165453.HKD","HK0000320264.USD","BK4585","BK4588","HK0000320223.HKD","OGN","LU2065171311.SGD","BK4007","HK0000306685.HKD","LU2065169927.USD","BK4559","LU2065170008.USD","LU2065171402.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2630309173","title":"复宏汉霖(02696)自主研发的POHERDY®于欧盟获批上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2630309173","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2630309173?lang=zh_cn&edition=full","pubTime":"2026-04-28 19:50","pubTimestamp":1777377048,"startTime":"0","endTime":"0","summary":"智通财经APP讯，复宏汉霖 发布公告，近日，公司自主研发的POHERDY 420mg/14mL注射液的上市许可申请 已获欧盟委员会批准，该商品名由N.V. Organon于欧盟注册商标。此次获批意味着POHERDY 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。继于美国获批上市之后，此次POHERDY于欧盟获批上市，是集团产品在国际主流市场获得的又一认可，将进一步推进公司国际化布局的进程，提升公司产品的国际影响力。","market":"fut","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/1435508.html","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":"stock_zhitongcaijing","symbols":["IPOS","HK0000306701.USD","HK0000320264.USD","HK0000306685.HKD","HK0000320223.HKD","BK1161","FESXmain","FSXEmain","02696","HK0000165453.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1128740396","title":"复宏汉霖旗下汉曲优®获欧盟批准用于治疗HER2阳性早期及转移性乳腺癌","url":"https://stock-news.laohu8.com/highlight/detail?id=1128740396","media":"美股速递","labels":["corporation"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1128740396?lang=zh_cn&edition=full","pubTime":"2026-04-28 19:49","pubTimestamp":1777376981,"startTime":"0","endTime":"0","summary":"上海复宏汉霖生物技术股份有限公司近日宣布，其核心产品汉曲优®（通用名：曲妥珠单抗）已获得欧盟委员会批准，用于治疗HER2阳性早期乳腺癌及转移性乳腺癌。此项批准标志着公司创新研发成果获得国际主流市场认可，为欧洲患者提供了重要的治疗选择。\nHER2阳性乳腺癌是一种侵袭性较强的乳腺癌亚型，汉曲优®作为曲妥珠单抗的生物类似药，在疗效与安全性方面与原研药高度相似。此次获批将进一步提升复宏汉霖在全球生物药市场的竞争力，并为其国际化战略注入新动力。","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","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":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["HK0000165453.HKD","BK1161","HK0000306701.USD","HK0000320223.HKD","HK0000320264.USD","02696","HK0000306685.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1189910896","title":"复宏汉霖Hlx07联合汉斯状®治疗晚期鳞状非小细胞肺癌II/III期临床试验获准在澳大利亚启动","url":"https://stock-news.laohu8.com/highlight/detail?id=1189910896","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1189910896?lang=zh_cn&edition=full","pubTime":"2026-04-24 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