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艾格里房产

66.17

+0.22000.33%

成交量：265.36万

成交额：1.75亿

市值：82.30亿

市盈率：35.74

高：66.32

开：65.97

低：65.62

收：65.95

52周最高：82.08

52周最低：64.43

股本：1.24亿

流通股本：1.22亿

量比：1.56

换手率：2.17%

股息：3.14

股息率：4.75%

每股收益(TTM):1.85

每股收益(LYR):1.77

净资产收益率：3.70%

总资产收益率：2.40%

市净率：1.30

市盈率(LYR):37.38

数据加载中...

总览公司新闻资讯公告

中国生物制药(01177)：维特柯妥拜单抗“CLDN18.2 ADC”新药上市申请获得受理

国产创新药三箭齐发：全球首个双抗ADC、全球首个治疗实体瘤的CAR-T产品、全球首个狂犬病双抗同日获批

每日经济新闻

全球首个获批双抗ADC上市，百利天恒(688506.SH)加速向MNC跨代跃迁

港股ADC龙头映恩生物冲刺科创板：现金流与在研产品面临大考，创新药企“回A”趋势隐现

新诺威(300765.SZ)：SYS6041(叶酸受体ADC)获得药物临床试验批准

百利天恒：EGFR×HER3双抗ADC药品上市申请获受理

百利天恒：注射用BL-M14D1（DLL3 ADC）获临床试验批准

南方财经网

映恩生物(09606)上交所科创板IPO已受理深耕于抗体偶联药物(ADC)领域

港股异动 | 君实生物(01877)涨超5% 近日拟入股上海致域生物医药布局ADC与多特异抗体研发

【湾区早参】港珠澳大桥香港口岸本月25日将启用“无感通关”；深圳上榜毕业旅行十大热门城市

基石药业-B(02616)：CS5007(EGFR/HER3双特异性ADC)全球多中心I期临床试验启动

Immunome宣布IM-1617 ADC一期临床完成首例患者给药

环球市场播报

缇乐®（注射用维替索妥尤单抗）获国家药品监督管理局批准用于治疗复发或转移性宫颈癌成人患者

双抗ADC：中国Biotech滚石上山

君实生物(01877)拟以专利设备作价5308万元入股上海致域生物医药布局 ADC 与多特异抗体研发

晚间重要公告汇总

信达生物(01801): IBI343(CLDN18.2 ADC)治疗晚期胃癌的新药上市申请获国家药品监督管理局受理

中国生物制药双创新药闪耀ASCO：肺癌一线疗法PFS显著延长，全球首个EGFR/c-Met双抗ADC临床数据亮眼

中国生物制药(01177)：TQB6411“EGFR/C-MET ADC”于2026 ASCO公布I期临床数据

中国生物制药(01177)：维特柯妥拜单抗“CLDN18.2 ADC”于2026 ASCO公布一线胃癌II期临床数据

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发布公告，公司的控股子公司石药集团巨石生物制药有限公司于近日收到国家药品监督管理局核准签发关于SYS6041的《药物临床试验批准通知书》，将于近期开展临床试验。SYS6041是一种靶向叶酸受体α(FRα)的抗体-药物偶联物。SYS6041的潜在适应症为妇科肿瘤和肺癌等实体瘤。临床I期试验的现有数据显示，SYS6041在同类产品中具有竞争力。本次获批的SYS6041联合用药临床试验探索研究，将进一步拓展SYS6041的临床应用场景。","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/1454439.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":["BK4231","300765","BK4080","BK0226","ADC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2643981246","title":"百利天恒：EGFR×HER3双抗ADC药品上市申请获受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2643981246","media":"财中社","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2643981246?lang=zh_cn&edition=fundamental","pubTime":"2026-06-14 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ADC一期临床完成首例患者给药","url":"https://stock-news.laohu8.com/highlight/detail?id=2642280708","media":"环球市场播报","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642280708?lang=zh_cn&edition=fundamental","pubTime":"2026-06-11 22:26","pubTimestamp":1781187960,"startTime":"0","endTime":"0","summary":"生物技术公司Immunome周三宣布，其潜在首创新药抗体偶联药物IM-1617的一期临床试验已完成首例患者给药。该药物针对一种未公开的实体瘤靶点，用于治疗晚期实体瘤患者。　　IM-1617是一款靶向实体瘤的抗体偶联药物，其靶向的是一种促进肿瘤细胞存活并介导免疫细胞排斥的受体酪氨酸激酶。该药物搭载了Immunome专有的拓扑异构酶I抑制剂HC74作为有效载荷。公司计划分别于2026年中和2026年末提交另外两款抗体偶联药物IM-1340和IM-1335的新药临床试验申请。","market":"other","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/usstock/c/2026-06-11/doc-inicaenm0622024.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":"sina","symbols":["BK4231","BK4080","ADC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642523384","title":"缇乐®（注射用维替索妥尤单抗）获国家药品监督管理局批准用于治疗复发或转移性宫颈癌成人患者","url":"https://stock-news.laohu8.com/highlight/detail?id=2642523384","media":"美通社","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642523384?lang=zh_cn&edition=fundamental","pubTime":"2026-06-09 13:16","pubTimestamp":1780982160,"startTime":"0","endTime":"0","summary":"在接受维替索妥尤单抗治疗的中国亚组中，未发现新的安全信号。对于在系统治疗期间或治疗后疾病进展的复发或转移性宫颈癌患者，目前的治疗选择有限。维替索妥尤单抗有望为之前接受过治疗的晚期宫颈癌患者提供一种新的治疗选择。维替索妥尤单抗于2024年4月获得美国食品药品监督管理局完全批准。该药物在美国的首次获批可追溯至2021年9月，通过加速批准通道上市，用于治疗在化疗期间或化疗后疾病进展的复发或转移性宫颈癌成人患者。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"prnasia","url":"http://wwwold.prnasia.com/story/archive/4979181_ZH79181_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/4979181_ZH79181_1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"prnasia","symbols":["ITT","BK4527","LU1221951046.USD","LU0098860793.USD","LU1894683264.USD","BK4525","LU1244550577.SGD","IE000M9KFDE8.USD","LU1674673428.USD","LU1506573853.SGD","BK4161","LU0320765646.SGD","LU2236285917.USD","LU1162221912.USD","LU0053671581.USD","LU0731783394.SGD","LU1571399168.USD","IE00BFXG1179.USD","LU1430594728.SGD","LU1244550221.USD","LU0868494617.USD","IE00BZ1G4Q59.USD","LU2237443622.USD","IE00B3PB1722.GBP","LU1244550494.USD","IE00BSNM7G36.USD","SG9999001440.SGD","HK0000819398.USD","LU2417539215.USD","ADC","BK4515","LU1066051498.USD","LU1880398471.USD","LU0942090050.USD","LU2237443549.SGD","LU2462157665.USD","LU2102340556.USD","CSCO","ZLAB","L","SG9999015945.SGD","BK1574","09688","CSCS","LU1674673691.USD","BK4588","SG9999015952.SGD","LU1066051225.USD","LU2487616109.SGD","CSCL"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2641310850","title":"双抗ADC：中国Biotech滚石上山","url":"https://stock-news.laohu8.com/highlight/detail?id=2641310850","media":"蓝鲸财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2641310850?lang=zh_cn&edition=fundamental","pubTime":"2026-06-08 11:21","pubTimestamp":1780888916,"startTime":"0","endTime":"0","summary":"双抗ADC与双载荷ADC合计超100项。大会评选出的100个“重磅ADC”中，中国药企独占72席。在单抗ADC上，中国企业一直在追赶。在双抗ADC上，双方站在了同一条起跑线附近。TQB6411是全球首个公布人体临床数据的EGFR/c-Met双抗ADC。单抗ADC时代的中国药企，大多是在已验证的靶点上做工程化改良。双抗ADC的靶点组合需要从头设计，亲和力差异需要自主设定，这让中国企业第一次有机会在“原创靶点组合”这个维度上站到全球前排。","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://www.lanjinger.com/d/1779680903204339558","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":"lanjinger_stock","symbols":["ADC","BK4585","BK4231","BK4581","XBI","BK4080","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2641460591","title":"君实生物(01877)拟以专利设备作价5308万元入股上海致域生物医药 布局 ADC 与多特异抗体研发","url":"https://stock-news.laohu8.com/highlight/detail?id=2641460591","media":"智通财经","labels":["shareholding"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2641460591?lang=zh_cn&edition=fundamental","pubTime":"2026-06-05 22:52","pubTimestamp":1780671175,"startTime":"0","endTime":"0","summary":"作为前述者的代价，代价金额约为人民币5308万元，合资公司将向该公司发行新增注册资本人民币25万元。此外，合资公司拟与姚盛博士及天使轮投资人已订立增资协议，据此，合资公司有条件同意以总代价1500万美元认购合资公司新增注册资本合共人民币 46.875万元。","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/1451042.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","BK1515","399441","161726","BK4588","01877","ADC","BK4080","BK4231","BK4585","XBI","BK1583","BK4581"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2640157815","title":"晚间重要公告汇总","url":"https://stock-news.laohu8.com/highlight/detail?id=2640157815","media":"第一财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2640157815?lang=zh_cn&edition=fundamental","pubTime":"2026-06-04 19:53","pubTimestamp":1780574029,"startTime":"0","endTime":"0","summary":"晚间重要公告汇总","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202606043760585142.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/202606043760585142.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":["ADC","BK4080","BK4231"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2640153816","title":"信达生物(01801): IBI343(CLDN18.2 ADC)治疗晚期胃癌的新药上市申请获国家药品监督管理局受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2640153816","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2640153816?lang=zh_cn&edition=fundamental","pubTime":"2026-06-04 16:34","pubTimestamp":1780562045,"startTime":"0","endTime":"0","summary":"智通财经APP讯，信达生物 发布公告，IBI343用于晚期胃癌人群的国际III期临床研究按预设方案完成第一次期中分析，达到主要研究终点，IBI343在晚期胃癌治疗中展现出了卓越的疗效和良好的安全性和耐受性。基于这一积极的临床结果，公司已向中国国家药品监督管理局递交IBI343的新药上市申请。IBI343是全球首个获监管审评受理的CLDN18.2靶向ADC药物。","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/1450109.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":["01801","BK4231","BK1589","LU1969619763.USD","LU2328871848.SGD","LU0502904849.HKD","LU2097828631.EUR","LU2097828805.USD","LU2097828714.EUR","ADC","LU0455707207.USD","LU2097828557.USD","HK0000165453.HKD","BK1161","LU2097828474.EUR","LU2488822045.USD","BK1583","IPOS","LU2242644610.SGD","BK4080"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2640140982","title":"中国生物制药双创新药闪耀ASCO：肺癌一线疗法PFS显著延长，全球首个EGFR/c-Met双抗ADC临床数据亮眼","url":"https://stock-news.laohu8.com/highlight/detail?id=2640140982","media":"财中社","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2640140982?lang=zh_cn&edition=fundamental","pubTime":"2026-06-01 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ADC”于2026 ASCO公布I期临床数据","url":"https://stock-news.laohu8.com/highlight/detail?id=2640398600","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2640398600?lang=zh_cn&edition=fundamental","pubTime":"2026-06-01 06:53","pubTimestamp":1780267985,"startTime":"0","endTime":"0","summary":"智通财经APP讯，中国生物制药 发布公告，集团附属公司正大天晴药业集团股份有限公司自主研发的国家1类创新药TQB6411“EGFR/ c-Met ADC”于2026年美国临床肿瘤学会  大会上公布在晚期实体瘤患者中的首次人体I期临床研究数据。研究表明，TQB6411在有效剂量下呈现良好的安全性特征，尤其是血液学毒性较低。作为全球首批公布临床数据的EGFR/c-Met ADC，TQB6411凭借成熟的靶点组合及偏向c-Met端的亲和力设计，在降低研发风险的同时构建了差异化竞争优势。","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/1448217.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":["IE00BZ08YR35.GBP","BK1589","BK1521","LU1989772923.USD","LU1496350502.SGD","BK4080","BK4588","BK1191","01177","BK1515","LU1989771016.USD","LU1989772840.SGD","MET","BK4231","LU1291159041.SGD","IE00BZ08YS42.EUR","BK4585","ADC","BK4162","IE00BZ08YT58.USD","HK0000165453.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2640798605","title":"中国生物制药(01177)：维特柯妥拜单抗“CLDN18.2 ADC”于2026 ASCO公布一线胃癌II期临床数据","url":"https://stock-news.laohu8.com/highlight/detail?id=2640798605","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2640798605?lang=zh_cn&edition=fundamental","pubTime":"2026-06-01 06:47","pubTimestamp":1780267642,"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创新药维特柯妥拜单抗“CLDN18.2 ADC”于2026年美国临床肿瘤学会  大会上公布一线治疗胃或胃食管交界部腺癌的II期临床研究数据。结果显示，LM-302联合PD-1单抗  在CLDN18.2阳性晚期胃或胃食管结合部腺癌一线治疗中展现出令人鼓舞的抗肿瘤活性和可管理的安全性。治疗期间不良事件导致剂量降低的比例分别为17.9%和43.8%，导致治疗终止的比例分别为 23.1%和31.3%。","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/1448214.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":["BK4080","ADC","01177","IE00BZ08YT58.USD","BK1521","BK1589","IE00BZ08YR35.GBP","BK1515","BK4231","BK1191","HK0000165453.HKD","IE00BZ08YS42.EUR"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":5,"pageCount":4,"totalSize":99,"code":"91000000","status":"200"}]}}