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艾格里房产
75.31
+0.8050
1.08%
成交量:
50.50万
成交额:
3,769.55万
市值:
82.69亿
市盈率:
42.58
高:
75.31
开:
74.59
低:
74.21
收:
74.50
数据加载中...
总览
公司
新闻
公告
【新股IPO】据报宜联生物寻求ADC药物YL201授权合作 为公司最快2026年在港上市铺路
金吾财讯
·
03-12
新股消息 | 传宜联生物考虑最快明年在港上市
智通财经
·
03-12
Nuvation Bio Inc.盘中异动 股价大涨5.32%报1.98美元
市场透视
·
03-12
药明合联与AbTis宣布达成战略合作,共同推进新一代ADC药物研发
美通社
·
03-11
辉瑞(PFE)PD-L1靶向ADC新药在华获批临床
金吾财讯
·
03-11
辉瑞(PFE.US)PD-L1靶向ADC新药在华获批临床 拟治疗晚期实体瘤
智通财经
·
03-11
基石药业-B(02616):迈向管线2.0,ROR1 ADC潜力十足
智通财经网
·
03-11
Nuvation Bio Inc.盘中异动 股价大跌10.84%
市场透视
·
03-10
美国研究综述-芝商所、Docusign、Paycom Software
路透中文
·
03-10
科伦博泰生物核心产品获批新增适应症
财中社
·
03-10
映恩生物二战港交所:尚无商业化产品累亏超17亿元 强力竞品已纳入医保降价超60%
新浪证券
·
03-07
第一三共(DSNKY.US)ADC癌症新药在中国获批临床
智通财经
·
03-06
【基石药业-B(02616.HK)在澳大利亚递交CS5001(ROR1 ADC)联合标准治疗用于一线弥漫大B细胞淋巴瘤的临床试验申请】基石药业-B(02616.HK)发布公告,公司已在澳大利亚成功递交CS5001(ROR1 ADC)联合标准治疗用于一线弥漫大B细胞淋巴瘤(DLBCL)的Ib期临床试验申请。此外 CS5001单药及联合PD-L1单抗治疗晚期实体瘤的全球多中心临床试验也在同步开展。
金融界
·
03-06
基石药业-B(02616)在澳大利亚递交CS5001(ROR1 ADC)联合标准治疗用于一线弥漫大B细胞淋巴瘤的临床试验申请
智通财经
·
03-06
第一三共/阿斯利康(AZN.US)重磅抗体偶联药物(ADC)Enhertu在3期临床试验中获得积极结果
智通财经
·
03-05
石药预付款助力康宁杰瑞首次盈利,ADC管线成股价催涨剂丨看财报
钛媒体
·
03-05
Nuvation Bio Inc.盘中异动 早盘股价大跌5.22%报1.73美元
市场透视
·
03-04
巴克莱:上调Agree Realty(ADC.US)评级,由减持调整至持股观望评级, 目标价由74.00美元调整至75.00美元。
金融界
·
03-04
丽珠集团:已终止HER2-ADC项目后续推进,聚焦优势项目研发进展
金融界
·
03-04
一款重磅ADC药物上市申请延迟 乐普生物股价大跌逾10%
第一财经
·
03-04
更多
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为公司最快2026年在港上市铺路","url":"https://stock-news.laohu8.com/highlight/detail?id=2518058979","media":"金吾财讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518058979?lang=zh_cn&edition=fundamental","pubTime":"2025-03-12 14:54","pubTimestamp":1741762478,"startTime":"0","endTime":"0","summary":"金吾财讯 | 有报道引述中国宜联生物公司(MediLink Therapeutics Ltd)正寻求就旗下抗体偶联药物(ADC)YL201,与一家全球制药公司达成授权协议,这将为公司最快2026年在香港上市铺路。消息指,目前的协商仍在进行当中,最终是否能够达成协议还无法确定。据悉,宜联生物总部位于苏州,于2020年7月8日成立,是一家专注于ADC(抗体偶联药物)及相关技术创新药物开发的企业,并且在上海和波士顿设置了研发中心。YL201是一款靶向B7H3的ADC药物。目前,YL201正在全球范围内开展针对多种实体瘤的探索性研究。","market":"sh","thumbnail":"https://static.szfiu.com/news/20250107/MWIxNzM2MjE4MjI2OTA1.png","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20250107/MWIxNzM2MjE4MjI2OTA1.png"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"1954895","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":null,"symbols":["BK4080","BK4231","ADC"],"gpt_icon":0},{"id":"2518854058","title":"新股消息 | 传宜联生物考虑最快明年在港上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2518854058","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518854058?lang=zh_cn&edition=fundamental","pubTime":"2025-03-12 14:48","pubTimestamp":1741762116,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,据媒体消息称,宜联生物正寻求就旗下抗体偶联药物(ADC)YL201,与一家全球制药公司达成授权协议,这将为公司最快2026年在香港上市铺路。消息指,蹉商仍在进行中,未必可以达成协议。据了解,宜联生物是一家专注于ADC和相关技术的创新药物开发公司。公司在上海和波士顿设有研发中心。YL201是一款靶向B7H3的ADC药物。目前,YL201正在全球范围内开展针对多种实体瘤的探索性研究。其中,小细胞肺癌、鼻咽癌适应症在中国已进入关键临床III期研究阶段。同时,YL201也在积极开展多种联用试验,探索其在多种实体瘤的前线治疗潜力。","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/1260825.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_zhitongcaijing","symbols":["ADC","BK4080","BK4231"],"gpt_icon":0},{"id":"2518721237","title":"Nuvation Bio Inc.盘中异动 股价大涨5.32%报1.98美元","url":"https://stock-news.laohu8.com/highlight/detail?id=2518721237","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518721237?lang=zh_cn&edition=fundamental","pubTime":"2025-03-12 00:22","pubTimestamp":1741710121,"startTime":"0","endTime":"0","summary":"北京时间2025年03月12日00时22分,Nuvation Bio Inc.股票出现波动,股价大幅上涨5.32%。截至发稿,该股报1.98美元/股,成交量136.184万股,换手率0.40%,振幅7.98%。Nuvation Bio Inc.股票所在的生物技术行业中,整体跌幅为2.37%。Nuvation Bio Inc.公司简介:Nuvation Bio Inc 是一家生物制药公司,致力于通过开发差异化的新型治疗候选药物来解决肿瘤学领域未满足的需求。值得注意的是,BET 蛋白具有重要的生物学功能,并且被发现在许多人类癌症中发生了改变。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250312002201ab5e2706&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description 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21:17","pubTimestamp":1741699020,"startTime":"0","endTime":"0","summary":"药明合联将依托其广泛的全球客户网络,全力推动AbTis技术的广泛应用,助力双方在生物偶联药领域的深度合作与共赢。此次合作将AbTis的先进ADC技术与药明合联的专业开发及生产能力深度融合,将为我们的客户提供更广泛先进的生物偶联技术选择和定制化解决方案,加速新一代 ADC 和生物偶联药物的研发进程。","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":"https://wwwold.prnasia.com/story/archive/4638419_ZH38419_1","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":"prnasia","symbols":["BK1141","SG9999014674.SGD","LU2488822045.USD","BK4231","02268","ADC","BK4080"],"gpt_icon":0},{"id":"2518797147","title":"辉瑞(PFE)PD-L1靶向ADC新药在华获批临床","url":"https://stock-news.laohu8.com/highlight/detail?id=2518797147","media":"金吾财讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518797147?lang=zh_cn&edition=fundamental","pubTime":"2025-03-11 17:07","pubTimestamp":1741684053,"startTime":"0","endTime":"0","summary":"金吾财讯 | 中国国家药监局药品审评中心 3月10日公示,辉瑞与Seagen联合开发的1类新药PF-08046054获得临床试验默示许可,拟开展转移性或不可切除晚期实体瘤适应症研究。该药物是辉瑞研发管线中首款靶向PD-L1的抗体偶联药物,具有\"first-in-class\"潜力。PF-08046054采用独特的抗PD-L1抗体-药物偶联设计,由抗PD-L1单抗、可裂解连接子及微管抑制剂MMAE组成。相较于传统PD-1/PD-L1抑制剂,该药物通过结合ADC的双重作用机制,可能为PD-L1表达不足或耐药的实体瘤患者提供新治疗选择。","market":"sh","thumbnail":"https://static.szfiu.com/news/20210625/ZGFjNmMxNjJiOWZlZTExMTI2OTIxOTcyMDA=.jpg","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20210625/ZGFjNmMxNjJiOWZlZTExMTI2OTIxOTcyMDA=.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"286261","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":null,"symbols":["BK4568","LU1883839398.USD","LU0985481810.HKD","LU1169589451.USD","SG9999002232.USD","SG9999002224.SGD","BK4007","BK4534","BK4581","IE00BBT3K403.USD","LU1023059063.AUD","LU1057294990.SGD","LU1894683264.USD","SG9999013999.USD","SG9999001176.SGD","SGXZ57979304.SGD","BK4080","BK4550","BK4592","LU0306806265.USD","LU1066053197.SGD","LU0225771236.USD","IE000M9KFDE8.USD","BK4585","IE00B19Z3581.USD","LU0321505439.SGD","BK4588","LU0289739699.SGD","SG9999001176.USD","PFE","LU1066051498.USD","ADC","LU0868494617.USD","LU0456855351.SGD","LU0321505868.SGD","LU1894683348.USD","BK4023","LU0170899867.USD","LU0306807586.USD","BK4533","IE00BLSP4239.USD","LU0122379950.USD","LU0058720904.USD","LU0225284248.USD","SG9999003800.SGD","IE00B19Z3B42.SGD","LU1169590202.USD","PD","BK4231","IE00BLSP4452.SGD"],"gpt_icon":1},{"id":"2518980763","title":"辉瑞(PFE.US)PD-L1靶向ADC新药在华获批临床 拟治疗晚期实体瘤","url":"https://stock-news.laohu8.com/highlight/detail?id=2518980763","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518980763?lang=zh_cn&edition=fundamental","pubTime":"2025-03-11 14:10","pubTimestamp":1741673430,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,3月10日,中国国家药监局药品审评中心官网最新公示,辉瑞公司旗下Seagen申报的1类新药PF-08046054获得临床试验默示许可,拟开发治疗转移性或不可切除的晚期实体瘤。公开资料显示,这是辉瑞在研的一款潜在“first-in-class”PD-L1靶向抗体偶联药物。截图来源:CDE官网根据辉瑞公开资料介绍,PF-08046054是一款靶向PD-L1的ADC,由抗PD-L1抗体、连接子和微管破坏剂MMAE组成,可通过直接细胞毒性、旁观者杀伤、免疫原性细胞死亡来发挥抗肿瘤活性。","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://www.zhitongcaijing.com/content/detail/1260252.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":["SG9999001176.SGD","LU0985481810.HKD","BK4588","LU1169589451.USD","BK4592","BK4533","IE00B19Z3581.USD","LU1057294990.SGD","SG9999001176.USD","LU1169590202.USD","SG9999002232.USD","LU0122379950.USD","LU1066051498.USD","LU0306806265.USD","LU0321505439.SGD","SG9999011175.SGD","IE00BLSP4452.SGD","LU0225771236.USD","LU1066053197.SGD","BK4534","LU0289739699.SGD","BK4007","IE00BBT3K403.USD","LU0058720904.USD","LU0170899867.USD","LU0225284248.USD","PD","BK4585","SG9999002224.SGD","LU1883839398.USD","PFE","LU0234572021.USD","LU1023059063.AUD","SG9999003800.SGD","LU1894683348.USD","BK4023","BK4080","LU0868494617.USD","LU1894683264.USD","BK4599","BK4581","BK4231","LU0321505868.SGD","SGXZ57979304.SGD","BK4550","SG9999013999.USD","LU0306807586.USD","IE0002270589.USD","IE00B19Z3B42.SGD","ADC"],"gpt_icon":1},{"id":"2518732608","title":"基石药业-B(02616):迈向管线2.0,ROR1 ADC潜力十足","url":"https://stock-news.laohu8.com/highlight/detail?id=2518732608","media":"智通财经网","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518732608?lang=zh_cn&edition=fundamental","pubTime":"2025-03-11 09:59","pubTimestamp":1741658376,"startTime":"0","endTime":"0","summary":"基石药业是一家专注于抗肿瘤药物研发的创新驱动型生物医药企业,截至2025年2月,公司已成功上市4款创新药、获批16项新药上市申请(NDA以及9项适应症。","market":"us","thumbnail":"https://img.zhitongcaijing.com/image/20250311/20250311100302_75957.png?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250","type":0,"news_type":0,"thumbnails":["https://img.zhitongcaijing.com/image/20250311/20250311100302_75957.png?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/1260169.html","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":"highlight_zhitongcaijin","symbols":["BK4080","BK1161","ADC","02616","BK1574","BK4231"],"gpt_icon":0},{"id":"2518303271","title":"Nuvation Bio Inc.盘中异动 股价大跌10.84%","url":"https://stock-news.laohu8.com/highlight/detail?id=2518303271","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518303271?lang=zh_cn&edition=fundamental","pubTime":"2025-03-10 21:33","pubTimestamp":1741613585,"startTime":"0","endTime":"0","summary":"北京时间2025年03月10日21时33分,Nuvation Bio Inc.股票出现波动,股价急速下跌10.84%。截至发稿,该股报1.80美元/股,成交量4.4904万股,换手率0.01%,振幅3.17%。Nuvation Bio Inc.股票所在的生物技术行业中,整体跌幅为0.08%。Nuvation Bio Inc.公司简介:Nuvation Bio Inc 是一家生物制药公司,致力于通过开发差异化的新型治疗候选药物来解决肿瘤学领域未满足的需求。值得注意的是,BET 蛋白具有重要的生物学功能,并且被发现在许多人类癌症中发生了改变。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250310213305abf2fcdb&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description 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20:49","pubTimestamp":1741610952,"startTime":"0","endTime":"0","summary":"美国研究综述-芝商所、Docusign、Paycom Software路透3月10日 - 华尔街证券分析师周一调整了对几家美国上市公司的评级和目标价,其中包括 芝商所、Docusign 和 Paycom Software。* Docusign Inc DOCU.O:摩根大通将其评级从 \"减持 \"上调至 \"中性\"。* Paycom Software, Inc:Keybanc将其评级从行业权重上调至增持 * Samsara Inc IOT.N:Piper Sandler 将评级从中性上调至增持以下是路透周一报导的美国公司研究报告摘要。","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":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250310:nL4T3PT0YS:1","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":["ASB","LU2430703095.HKD","AESI","ABNB","ADC","AMT","CPT","DVN","LU1989764664.SGD","LU0742537680.HKD","CDXC","APEI","CYH","ASTH","CHPT","CME","EQR","CDTX","DXPE","CTRE","XYZ","LU1934455277.USD","GTLS","AARD","LU1718418525.SGD","LU0472753341.HKD","BKSY","ALTG","LU0128525689.USD","ESS","APA","LU0444973449.USD","EQIX","DLR","COLD","EPR","DOCU","AVB","BK4595","BK4542","EPRT","LU1244550577.SGD","BLMN","AEP","ELME","CBRL","DD"],"gpt_icon":1},{"id":"2518319245","title":"科伦博泰生物核心产品获批新增适应症","url":"https://stock-news.laohu8.com/highlight/detail?id=2518319245","media":"财中社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518319245?lang=zh_cn&edition=fundamental","pubTime":"2025-03-10 17:55","pubTimestamp":1741600521,"startTime":"0","endTime":"0","summary":"3月10日,科伦博泰生物-B(06990)发布公告,公司的核心产品芦康沙妥珠单抗(sac-TMT)近日获得国家药品监督管理局批准,新增适应症用于EGFR突变非小细胞肺癌的治疗。这一批准使得芦康沙妥珠单抗成为全球首个在肺癌适应症获批上市的TROP2抗体药物偶联物(ADC),标志着公司在抗癌药物领域的重要进展。","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/202503103341366183.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":["BK1161","LU0196878994.USD","ADC","06990","BK4231","BK4080"],"gpt_icon":0},{"id":"2517610941","title":"映恩生物二战港交所:尚无商业化产品累亏超17亿元 强力竞品已纳入医保降价超60%","url":"https://stock-news.laohu8.com/highlight/detail?id=2517610941","media":"新浪证券","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517610941?lang=zh_cn&edition=fundamental","pubTime":"2025-03-07 17:10","pubTimestamp":1741338600,"startTime":"0","endTime":"0","summary":"炒股就看金麒麟分析师研报,权威,专业,及时,全面,助您挖掘潜力主题机会! 2月27日,映恩生物向港交所提交上市申请,拟通过上市规则18A寻求在联交所主板上市,摩根士丹利、杰弗瑞、中信证券为其联席保荐人。这是继其于2024年8月26日递表失效后的再一次申请。截至2024年9月末,公司累亏超17亿元。招股书显示,2022年5月26日,映恩生物与药明生物间接全资附属公司WuXi Biologics订立许可协议,获得了B7-H3抗体。","market":"sg","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/observe/2025-03-07/doc-inenvmwf5759065.shtml","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":"sina","symbols":["BK4585","BK4118","BK4566","BK4588","BK4231","DB","BK4080","ADC","BK4552"],"gpt_icon":0},{"id":"2517815279","title":"第一三共(DSNKY.US)ADC癌症新药在中国获批临床","url":"https://stock-news.laohu8.com/highlight/detail?id=2517815279","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517815279?lang=zh_cn&edition=fundamental","pubTime":"2025-03-06 21:20","pubTimestamp":1741267210,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,3月6日,中国国家药监局药品审评中心官网公示,第一三共申报的1类新药DS-3939a获批临床,拟开发治疗实体瘤。公开资料显示,DS-3939a是一种靶向肿瘤相关MUC1的抗体偶联药物,正在全球范围内处于1/2期临床研究阶段。根据CDE官网查询,本次为该产品首次在中国获批临床。本次这款创新ADC在中国获批临床,意味着其将在中国进入临床研究阶段。","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/1258792.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":["BK4080","DSNKY","BK4007","ADC","BK4231"],"gpt_icon":0},{"id":"2517497936","title":"【基石药业-B(02616.HK)在澳大利亚递交CS5001(ROR1 ADC)联合标准治疗用于一线弥漫大B细胞淋巴瘤的临床试验申请】基石药业-B(02616.HK)发布公告,公司已在澳大利亚成功递交CS5001(ROR1 ADC)联合标准治疗用于一线弥漫大B细胞淋巴瘤(DLBCL)的Ib期临床试验申请。此外 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CS5001单药及联合PD-L1单抗治疗晚期实体瘤的全球多中心临床试验也在同步开展。","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/2025/03/06081348552983.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":"jinrongjie_stock","symbols":["BK4231","PD","BK1583","LU1169589451.USD","LU1169590202.USD","ADC","BK4023","BK1574","BK1141","BK1161","02616","03347","BK1576","BK4080"],"gpt_icon":0},{"id":"2517763909","title":"基石药业-B(02616)在澳大利亚递交CS5001(ROR1 ADC)联合标准治疗用于一线弥漫大B细胞淋巴瘤的临床试验申请","url":"https://stock-news.laohu8.com/highlight/detail?id=2517763909","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517763909?lang=zh_cn&edition=fundamental","pubTime":"2025-03-06 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21:15","pubTimestamp":1741180517,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,阿斯利康和第一三共公司日前宣布,双方联合开发的重磅抗体偶联药物Enhertu,在3期临床试验DESTINY-Gastric04中获得积极结果。新闻稿表示,Enhertu是首个在随机3期临床试验中,作为二线疗法显著改善HER2阳性胃癌患者总生存期的HER2靶向疗法。新闻稿指出,转移性HER2阳性胃癌一线治疗出现疾病进展后,历史上在随机临床试验中,尚未有HER2靶向药物在二线治疗中展示出生存获益。","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/1258239.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":["AZN","03347","LU1829250122.USD","LU2417539215.USD","BK1583","BK4231","BK1141","LU0889565916.HKD","ADC","BK4585","LU2456880835.USD","LU2236285917.USD","BK4568","LU0320765992.SGD","BK4080","BK1576","LU2462157665.USD","BK4007","LU0109394709.USD","BK4588"],"gpt_icon":1},{"id":"2517916826","title":"石药预付款助力康宁杰瑞首次盈利,ADC管线成股价催涨剂丨看财报","url":"https://stock-news.laohu8.com/highlight/detail?id=2517916826","media":"钛媒体","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517916826?lang=zh_cn&edition=fundamental","pubTime":"2025-03-05 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