美股详情

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信息服务

4.12

-0.1400-3.29%

盘后：4.120.00000.00%19:34 EDT

成交量：16.93万

成交额：69.72万

市值：1.97亿

市盈率：19.62

高：4.26

开：4.26

低：4.06

收：4.26

52周最高：6.45

52周最低：3.74

股本：4,788.41万

流通股本：3,498.93万

量比：0.88

换手率：0.48%

股息：0.18

股息率：4.37%

每股收益(TTM):0.2100

每股收益(LYR):0.1900

净资产收益率：11.17%

总资产收益率：5.99%

市净率：2.09

市盈率(LYR):21.68

数据加载中...

总览公司新闻公告

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沃森生物：公司四价流脑结合疫苗目前处于III期临床研究阶段

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21世纪经济报道

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瞄准数字资产与AI赛道，Dune Acquisition III递交1.5亿美元SPAC IPO申请

港股异动 | 基石药业-B(02616)再涨超6% 月内涨超25% 舒格利单抗III期NSCLC获英国正式批准

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百利天恒(688506.SH)：iza-bren(EGFR×HER3双抗ADC)用于局部晚期或转移性三阴乳腺癌III期临试期中分析达到主要终点

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智通财经网

倍择瑞®治疗未控制哮喘的KALOS与LOGOS III期试验取得具有临床意义的阳性结果相关成果发表于《柳叶刀-呼吸病学杂志》

对外投资合作信息服务

商务部网站

沃森生物：公司九价HPV疫苗目前处于III期临床研究阶段

中国生物制药(01177)升5% TQB2102 III期临床完成入组此前Ib期ASCO数据良好

中国生物制药(01177)：TQB2102“HER2双抗ADC”HER2低表达乳腺癌III期临床试验完成受试者入组

中国生物制药(01177)：维特柯妥拜单抗“CLDN18.2 ADC”III期临床试验完成受试者入组

众生药业(002317.SZ)：创新药昂拉地韦项目两项III期临床试验获顶线分析数据结果

南京软件和信息服务业产业集群收入突破万亿元

恒丰银行广州分行被罚25万，涉投融资信息服务收费质价不符

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16:00","pubTimestamp":1772438425,"startTime":"0","endTime":"0","summary":"证券之星消息，沃森生物03月02日在投资者关系平台上答复投资者关心的问题。康希诺 ACYW135 群脑膜炎球菌多糖结合疫苗临床启动晚于公司，却已于2021 年 12 月获批上市。而公司同款疫苗进入三期临床多年，至今仅披露 “撰写报告”，无明确上市时间表。公司四价流脑结合疫苗目前处于III期临床研究阶段，公司在研疫苗的研发若有实质性和阶段性进展公司会及时披露，后续进展情况请关注公司披露的相关信息。","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://sc.stock.cnfol.com/gushiyaowen/20260302/32037575.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":"zhongjincaijing_highlight","symbols":["BK0077","159646","BK0070","300142","BK0046","BK0239","III","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2616877702","title":"瑞博生物-B(06938)：RBD7022注射液即将于中国启动用于治疗高血脂症适应症的 III期临床试验","url":"https://stock-news.laohu8.com/highlight/detail?id=2616877702","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2616877702?lang=zh_cn&edition=fundamental","pubTime":"2026-03-02 08:11","pubTimestamp":1772410260,"startTime":"0","endTime":"0","summary":"智通财经APP讯，瑞博生物-B(06938)公布，集团自主研发的RBD7022注射液已由合作方齐鲁制药有限公司(齐鲁制药)完成III期临床试验登记公示，即将启动III期临床试验。RBD7022注射液是一款靶向PCSK9的siRNA药物。PCSK9是一种酶，在调节体内胆固醇，尤其是通常被称为“LDL-C”或“坏胆固醇”的低密度脂蛋白(LDL)胆固醇的水平方面起关键作用，可作为管理高胆固醇血症的一种治疗选择，旨在降低与高胆固醇水平相关的心血管疾病风险。2023年12月，公司将RBD7022注射液在中国内地、中国香港和中国澳门开发、生产和商业化的独家权利授予齐鲁制药。","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/1408738.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":["BK4134","III","BK1161","06938"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2614289542","title":"iza-bren公告III期结果；君实生物等药企发布业绩快报 | 健讯Daily","url":"https://stock-news.laohu8.com/highlight/detail?id=2614289542","media":"21世纪经济报道","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2614289542?lang=zh_cn&edition=fundamental","pubTime":"2026-02-28 08:06","pubTimestamp":1772237206,"startTime":"0","endTime":"0","summary":"国家药监局：2025年共收到创新医疗器械特别审批申请457项近日，国家药监局发布2025年度创新医疗器械等产品注册审批情况。2025年，国家药监局按照《创新医疗器械特别审查程序》《医疗器械优先审批程序》继续做好相关产品的审查工作，共收到创新医疗器械特别审批申请457项，其中104项获准进入创新医疗器械特别审查程序；收到优先申请38项，其中26项获准优先审批。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202602283657320729.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/202602283657320729.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":["III","01877","BK1515","688180","BK0239","BK1161","BK1583","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2614882728","title":"港股异动 | 基石药业-B(02616)尾盘涨超8% 舒格利单抗III期非小细胞肺癌新适应症获英国MHRA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2614882728","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2614882728?lang=zh_cn&edition=fundamental","pubTime":"2026-02-27 15:54","pubTimestamp":1772178879,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，基石药业-B尾盘涨超8%，截至发稿，涨6.73%，报6.66港元，成交额9312.3万港元。消息面上，基石药业此前宣布，舒格利单抗的新适应症申请已获英国MHRA批准单药用于治疗肿瘤细胞PD-L1表达≥1%、无表皮生长因子受体敏感突变或ALK、ROS1基因组变异、在含铂放化疗后未出现疾病进展的、不可切除的III期NSCLC成人患者。","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/1408123.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":["BK4134","BK4585","VT","BK1161","III","02616","VXUS","BK1574","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1128180907","title":"美联储鲍曼：巴塞尔III终版提案将于下月出炉——市场快讯","url":"https://stock-news.laohu8.com/highlight/detail?id=1128180907","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1128180907?lang=zh_cn&edition=fundamental","pubTime":"2026-02-27 02:44","pubTimestamp":1772131472,"startTime":"0","endTime":"0","summary":"美联储负责监管事务的副主席米歇尔·鲍曼在听证会上向参议员们表示，旨在使美国银行监管与国际巴塞尔III标准接轨的提案将在三月底前公布。鲍曼指出，三大联邦银行监管机构——美联储、联邦存款保险公司（FDIC）和货币监理署（OCC）——已就该提案达成共识。\n南达科他州共和党参议员迈克·朗兹指出，该项目酝酿已久。此前由前副主席迈克尔·巴尔推动的巴塞尔III改革尝试未能成功。鲍曼谈及自己及其同由特朗普任命的FDIC和OCC负责人时表示：\"我认为我们正在以创纪录的速度推进工作。\"\n（完）","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":"","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":null,"symbols":["US6M.BOND","TMF","TLT","III","BK4585","BIL","BK4134","US2Y.BOND","BK4588","US12M.BOND","US5Y.BOND","US7Y.BOND","US10Y.BOND","US30Y.BOND","US3Y.BOND","TLTW"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2614670859","title":"瞄准数字资产与AI赛道，Dune Acquisition III递交1.5亿美元SPAC IPO申请","url":"https://stock-news.laohu8.com/highlight/detail?id=2614670859","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2614670859?lang=zh_cn&edition=fundamental","pubTime":"2026-02-25 14:52","pubTimestamp":1772002329,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，专注于数字资产、体育娱乐、软件即服务及人工智能领域的特殊目的收购公司Dune Acquisition III，于周二向美国证券交易委员会递交文件，计划通过首次公开募股筹资至多1.5亿美元。Dune Acquisition III由首席执行官兼董事长Carter Glatt领导，他曾任GTY公司企业发展主管兼高级副总裁。管理层的过往SPAC项目包括：于2023年上市并完成与氢气供应商Global Gas业务合并的Dune Acquisition，以及于2025年上市的Dune Acquisition II。Dune Acquisition III已于2025年11月6日以保密方式递交申请。","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/1407059.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":["III","BK4134","DUNEU"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2614777939","title":"港股异动 | 基石药业-B(02616)再涨超6% 月内涨超25% 舒格利单抗III期NSCLC获英国正式批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2614777939","media":"智通财经","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2614777939?lang=zh_cn&edition=fundamental","pubTime":"2026-02-25 14:04","pubTimestamp":1771999477,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，基石药业-B再涨超6%，月内累计涨幅已超25%。消息面上，2月23日，基石药业宣布，其PD-L1抗体舒格利单抗针对III期非小细胞肺癌的新适应症，已正式取得英国药品和医疗保健用品管理局的批准。此外，基石药业核心资产CS2009用于晚期实体瘤的II期临床试验IND申请近期获得FDA批准。CS2009用于晚期实体瘤的II期新药临床试验申请获美国食品药品监督管理局批准，标志着这一创新免疫疗法的全球开发取得重要进展。","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/1407038.html","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":"stock_zhitongcaijing","symbols":["BK4134","III","BK4585","BK1574","VXUS","02616","BK4588","BK1161","VT"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2613750586","title":"港股异动 | 基石药业-B(02616)涨超5% 舒格利单抗III期非小细胞肺癌新适应症获英国MHRA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2613750586","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2613750586?lang=zh_cn&edition=fundamental","pubTime":"2026-02-24 10:30","pubTimestamp":1771900210,"startTime":"0","endTime":"0","summary":"消息面上，基石药业昨日公布，舒格利单抗的新适应症申请已获英国药品和医疗保健用品管理局批准单药用于治疗肿瘤细胞PD-L1表达≥1%、无表皮生长因数受体敏感突变或ALK、ROS1基因组变异、在含铂放化疗后未出现疾病进展的、不可切除的III期小细胞肺癌成人患者。继欧盟委员会批准后，舒格利单抗III期NSCLC新适应症再获英国MHRA批准，这是该产品在英国获得的第二个适应症批准。","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/1406514.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":["III","02616","BK4585","BK4134","BK1161","VT","BK1574","VXUS","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2613820071","title":"百利天恒(688506.SH)：iza-bren(EGFR×HER3双抗ADC)用于局部晚期或转移性三阴乳腺癌III期临试期中分析达到主要终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2613820071","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2613820071?lang=zh_cn&edition=fundamental","pubTime":"2026-02-23 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披露公告，关于iza-bren用于局部晚期或转移性三阴乳腺癌III期临床试验的期中分析达到主要终点的事项，该III期临床研究独立数据监查委员会，在预设的期中分析中，建议：“基于现有的分析结果，与监管沟通提前申报，同时继续对受试者进行随访”。","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/1406323.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":["BK4134","91194","688506","BK4080","ADC","III","02615","BK4231","BK0239"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2613027209","title":"基石药业-B(02616)：舒格利单抗III期小细胞肺癌新适应症获英国MHRA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2613027209","media":"智通财经网","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2613027209?lang=zh_cn&edition=fundamental","pubTime":"2026-02-23 08:17","pubTimestamp":1771805849,"startTime":"0","endTime":"0","summary":"基石药业-B(02616)发布公告，舒格利单抗的新适应症申请已获英国药品和医疗保健用品管理局(MHRA)批准单药用于治疗肿瘤细胞PD-L1表达≥1%、无表皮生长因数受体(EGFR)敏感突变或ALK、ROS1基因组变异、在含铂放化疗(CRT)后未出现疾病进展的、不可切除的III期小细胞肺癌(NSCLC)成人患者。","market":"fut","thumbnail":"https://img.zhitongcaijing.com/gonggao/ztcj_announce_48.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_48.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/1406210.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":"highlight_zhitongcaijin","symbols":["BK1574","BK1161","BK4134","02616","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2611713190","title":"倍择瑞®治疗未控制哮喘的KALOS与LOGOS III期试验取得具有临床意义的阳性结果 相关成果发表于《柳叶刀-呼吸病学杂志》","url":"https://stock-news.laohu8.com/highlight/detail?id=2611713190","media":"美通社","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2611713190?lang=zh_cn&edition=fundamental","pubTime":"2026-02-13 15:43","pubTimestamp":1770968580,"startTime":"0","endTime":"0","summary":"完整结果可查阅《柳叶刀-呼吸病学杂志》。KALOS与LOGOS试验表明，布地格福固定三联吸入疗法能够同时发挥ICS、LAMA和LABA的疗效，改善肺功能。KALOS与LOGOS研究结果有力地证实，布地格福固定三联吸入疗法有望为该类型哮喘患者带来健康获益。\" 在KALOS与LOGOS试验中，布地格福吸入气雾剂未出现新的安全性或耐受性问题。KALOS与LOGOS研究共纳入约4300名随机分组患者。KALOS和LOGOS试验的主要终点和治疗比较方案因监管申报途径的不同而有所差异。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"prnasia","url":"http://wwwold.prnasia.com/story/archive/4887756_ZH87756_1","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://wwwold.prnasia.com/story/archive/4887756_ZH87756_1","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":"prnasia","symbols":["LU0889565916.HKD","AZN","BK4007","LU0320765992.SGD","LU2462157665.USD","LU0109394709.USD","LU2236285917.USD","III","BK4588","BK4585","LU2417539215.USD","LU0058720904.USD","BK4134","LU0289739699.SGD","LU2456880835.USD","LU1829250122.USD","BK4568"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2611915245","title":"对外投资合作信息服务","url":"https://stock-news.laohu8.com/highlight/detail?id=2611915245","media":"商务部网站","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2611915245?lang=zh_cn&edition=fundamental","pubTime":"2026-02-13 14:11","pubTimestamp":1770963060,"startTime":"0","endTime":"0","summary":"关于公布对外劳务合作企业名单的说明根据《对外劳务合作管理条例》第五条，从事对外劳务合作，应当按照盛自治区、直辖市人民政府的规定，经省级或者设区的市级人民政府商务主管部门批准，取 ...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tonghuashun_highlight","url":"http://news.10jqka.com.cn/20260213/c674792752.shtml","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://news.10jqka.com.cn/20260213/c674792752.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":"tonghuashun_highlight","symbols":["BK4134","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2610161154","title":"沃森生物：公司九价HPV疫苗目前处于III期临床研究阶段","url":"https://stock-news.laohu8.com/highlight/detail?id=2610161154","media":"中金财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610161154?lang=zh_cn&edition=fundamental","pubTime":"2026-02-10 15:25","pubTimestamp":1770708314,"startTime":"0","endTime":"0","summary":"证券之星消息，沃森生物(300142)02月09日在投资者关系平台上答复投资者关心的问题。投资者提问：公司九价HPV疫苗目前III期临床、数据统计、申报准备的最新节点是否顺利？预计提交上市申请的时间窗口与后续规划如何？相比同类产品的临床优势、产能规划、市场定位有哪些积极亮点？沃森生物回复：尊敬的投资者，您好！公司九价HPV疫苗目前处于III期临床研究阶段，公司在研疫苗的研发若有实质性和阶段性进展公司会及时披露，后续进展情况请关注公司披露的相关信息。谢谢！为证券之星据公开信息整理，由AI算法生成(网信算备310104345710301240019号)，不构成投资建议。","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://sc.stock.cnfol.com/gushiyaowen/20260210/32009687.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":"zhongjincaijing_highlight","symbols":["300142","BK4134","III","BK0046","BK0077","BK0239","BK0070","159646"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2610699154","title":"中国生物制药(01177)升5% TQB2102 III期临床完成入组 此前Ib期ASCO数据良好","url":"https://stock-news.laohu8.com/highlight/detail?id=2610699154","media":"金吾财讯","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610699154?lang=zh_cn&edition=fundamental","pubTime":"2026-02-10 10:52","pubTimestamp":1770691959,"startTime":"0","endTime":"0","summary":"金吾财讯 | 中国生物制药(01177)短线拉高，截止发稿， 升5.15%，报6.94港元，成交额1.94亿港元。公司公告公布，集团自主研发的国家1类创新药TQB2102“HER2双抗ADC”正在开展一项“评价注射用TQB2102对比研究者选择的化疗在HER2低表达复发╱转移性乳腺癌中有效性和安全性的随机、开放、平行对照的III期临床试验(TQB2102-III-01)”，近期已完成全部受试者入组。在2025年美国临床肿瘤学会(ASCO)年会上，集团公布了TQB2102用于HER2低表达晚期乳腺癌的 Ib期临床研究结果，显示出良好的疗效与安全性。","market":"sh","thumbnail":"https://static.szfiu.com/news/20241108/ODBhOTU0MzI3NjMwOTM5MjE=.jpg","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20241108/ODBhOTU0MzI3NjMwOTM5MjE=.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"1974849","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":["BK4134","IE00BZ08YS42.EUR","BK1521","IE00BZ08YT58.USD","BK1515","BK1589","BK1191","III","IE00BZ08YR35.GBP","01177","HK0000165453.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2610661036","title":"中国生物制药(01177)：TQB2102“HER2双抗ADC”HER2低表达乳腺癌III期临床试验完成受试者入组","url":"https://stock-news.laohu8.com/highlight/detail?id=2610661036","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610661036?lang=zh_cn&edition=fundamental","pubTime":"2026-02-10 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发布公告，集团自主研发的国家1类创新药TQB2102“HER2双抗ADC”正在开展一项“评价注射用TQB2102对比研究者选择的化疗在HER2低表达复发╱转移性乳腺癌中有效性和安全性的随机、开放、平行对照的III期临床试验”，近期已完成全部受试者入组。以上核心技术的结合，突破了传统HER2单抗及单靶点ADC的局限，使TQB2102在HER2低表达肿瘤治疗中展现出显著潜力。","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/1403406.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":["BK1521","BK1191","IE00BZ08YS42.EUR","BK1515","BK4231","BK1589","BK4134","III","ADC","IE00BZ08YR35.GBP","HK0000165453.HKD","IE00BZ08YT58.USD","01177","BK4080"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2610503880","title":"中国生物制药(01177)：维特柯妥拜单抗“CLDN18.2 ADC”III期临床试验完成受试者入组","url":"https://stock-news.laohu8.com/highlight/detail?id=2610503880","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610503880?lang=zh_cn&edition=fundamental","pubTime":"2026-02-09 06:15","pubTimestamp":1770588951,"startTime":"0","endTime":"0","summary":"智通财经APP讯，中国生物制药 发布公告，集团全资附属公司礼新医药科技(上海)有限公司自主研发的国家1类创新药维特柯妥拜单抗“CLDN18.2 ADC”正在开展用于治疗三线及以上CLDN18.2阳性的局部晚期或转移性胃及胃食管交界部腺癌的III期注册临床试验，已顺利完成患者入组。其中，LM302是全球首款完成注册III期临床试验入组的CLDN18.2 ADC药物。该研究表明，LM302联合治疗方案在CLDN18.2阳性患者中展现出显著的抗肿瘤活性和可管理的安全性特征。","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/1402910.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":["ADC","BK1515","IE00BZ08YT58.USD","III","IE00BZ08YR35.GBP","BK4231","01177","BK4080","BK4134","HK0000165453.HKD","BK1589","BK1191","BK1521","IE00BZ08YS42.EUR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2609243573","title":"众生药业(002317.SZ)：创新药昂拉地韦项目两项III期临床试验获顶线分析数据结果","url":"https://stock-news.laohu8.com/highlight/detail?id=2609243573","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2609243573?lang=zh_cn&edition=fundamental","pubTime":"2026-02-08 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