阿斯利康(AZN)_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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AZN 阿斯利康

休市中 09-25 16:00:00 EDT

166.58

+2.02

+1.23%

盘后166.58

+0.000.00%

19:50 EDT

最高166.81	最低164.60	成交量206.79万
今开166.16	昨收164.56	日振幅1.34%
总市值2,584亿	流通市值2,497亿	总股本15.51亿
成交额3.43亿	换手率0.14%	流通股本14.99亿
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

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III期临床研究中国人群亚组OS数据显示 泰瑞沙联合化疗一线治疗EGFR突变晚期非小细胞肺癌总生存期获益趋势与全球保持一致","url":"https://stock-news.laohu8.com/highlight/detail?id=2668504920","media":"美通社","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2668504920?lang=zh_cn&edition=full","pubTime":"2026-09-18 21:48","pubTimestamp":1789739280,"startTime":"0","endTime":"0","summary":"OS是评估肿瘤患者生存获益的\"金标准\"，此次中国人群OS数据的公布，为该方案在中国EGFR突变晚期肺癌患者中的长生存获益提供了循证依据，进一步证实奥希替尼联合化疗可成为一线标准治疗选择。晚期患者中，奥希替尼在FLAURA III期研究中作为单药疗法，以及在FLAURA2 III期研究中联合化疗，均显示出临床结局改善。作为阿斯利康持续承诺治疗早期肺癌的重要组成部分，ADAURA2 III期临床研究正在进行中，评估奥希替尼用于早期可切除EGFRm 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20:33","pubTimestamp":1789734792,"startTime":"0","endTime":"0","summary":"金吾财讯 | 9月18日消息，欧洲药品管理局 人用药品委员会出具积极意见，推荐批准由第一三共与阿斯利康联合开发的ADC药物Enhertu，用于新辅助治疗后仍有残留浸润性病灶的高危HER2阳性早期乳腺癌成年患者的辅助治疗。结果显示，与现有标准疗法T-DM1相比，Enhertu将患者的浸润性疾病复发或死亡风险大幅降低了53%，三年无浸润性疾病生存率达到92.4%。目前该意见已提交欧盟委员会进行最终上市许可审批，若顺利获批，Enhertu有望重塑欧洲早期乳腺癌术后治疗标准。","market":"nz","thumbnail":"https://static.szfiu.com/news/20250107/NTkwMTRiMmRhYjljZTk4MGRjMGViZTQ1NDI1NzQxMTc4OQ==.png","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20250107/NTkwMTRiMmRhYjljZTk4MGRjMGViZTQ1NDI1NzQxMTc4OQ==.png"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"306231","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":["FSXEmain","LU0708994859.HKD","LU0320765992.SGD","LU2456880835.USD","LU0109394709.USD","LU0889565916.HKD","LU2237443382.USD","LU2237443549.SGD","BK4588","LU2468319806.SGD","LU0289739699.SGD","BK4585","LU0432979614.USD","LU2089984988.USD","LU2417539215.USD","LU2237443465.HKD","AZN","IE00B3T34201.USD","LU2237443978.SGD","LU0029864427.USD","LU2462157665.USD","FESXmain","LU0058720904.USD","LU0310800379.SGD","LU0128525929.USD","BK4568","AZNH","LU2237443622.USD","LU1267930573.SGD","LU2236285917.USD","BK4087","LU2237443895.HKD","CHMP","LU1829250122.USD","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1115044656","title":"异动解读｜阿斯利康盘后下跌3.65%，报154.61美元","url":"https://stock-news.laohu8.com/highlight/detail?id=1115044656","media":"行情直击","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/1115044656?lang=zh_cn&edition=full","pubTime":"2026-09-12 04:33","pubTimestamp":1789158806,"startTime":"0","endTime":"0","summary":"9月12日，阿斯利康盘后下跌3.65%，报154.61美元/股，成交额244.99万美元。阿斯利康所在的制药行业中，个股中，礼来涨0.11%，默沙东跌0.02%，强生涨0.34%，辉瑞跌0.1%，诺和诺德持平。阿斯利康股份有限公司于1992年根据《公司法》在英格兰和威尔士注册成立，1999年与瑞典Astra公司合并。公司主营业务覆盖肿瘤、呼吸、罕见病等多个治疗领域，2007年收购美国生物制剂企业MedImmune，2021年收购罕见病企业Alexion。（以上内容均基于市场公开消息，由程序或算法智能生成，仅作为股价异动提醒，不作为投资建议或交易依据。）","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":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["AZN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2666712586","title":"安进（AMGN）联合疗法III期临床达主要终点","url":"https://stock-news.laohu8.com/highlight/detail?id=2666712586","media":"金吾财讯","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2666712586?lang=zh_cn&edition=full","pubTime":"2026-09-09 16:59","pubTimestamp":1788944360,"startTime":"0","endTime":"0","summary":"金吾财经 | 安进公布，双特异性T细胞衔接器Imdelltra联合阿斯利康PD-L1抑制剂英飞凡，在广泛期小细胞肺癌的后期临床试验中实现总生存期延长。这家加州生物制药企业披露III期DeLLphi-305研究中期数据，该试验达成广泛期小细胞肺癌患者总生存期主要终点。该项全球试验评估该组合作为一线维持治疗，受试者既往接受过包含英飞凡的治疗且病情未发生进展。研究同时达成无进展生存期、客观缓解率两项次要终点。","market":"us","thumbnail":"https://static.szfiu.com/news/20210810/NjNkZWQ4NGZiN2I3MDYxNDlhOTlmZGM4ZTUwODkzNDUzNTE2.jpg","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20210810/NjNkZWQ4NGZiN2I3MDYxNDlhOTlmZGM4ZTUwODkzNDUzNTE2.jpg"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"305840","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":["BK4566","LU2242646821.SGD","IE00BFTCPJ56.SGD","BK4599","LU2242652126.USD","LU2462157665.USD","LU2456880835.USD","LU2468319806.SGD","SG9999001440.SGD","LU2112291526.USD","LU1829250122.USD","BIB","BBH","LU0029864427.USD","LU1023059063.AUD","BK4585","PBE","BK4139","PJP","AMGN","LU2237443622.USD","LU0889565916.HKD","LU0708994859.HKD","LU1571399168.USD","LU0128525929.USD","LU2237443895.HKD","LU2236285917.USD","IE00B2B36J28.USD","IE0002141913.USD","LU1267930573.SGD","TBXU","BK4568","AZN","IBB","IE00B4R5TH58.HKD","LU2237443978.SGD","IBBQ","BK4581","LU2237443382.USD","AZNH","LU0122379950.USD","BK4533","BK4534","LU0289739699.SGD","LU2089984988.USD","LU0432979614.USD","IE00BJJMRZ35.SGD","LU0868494617.USD","LU0058720904.USD","LU0109394709.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2665968376","title":"Tozorakimab在OBERON和TITANIA两项Ⅲ期临床试验中，在降低慢阻肺病急性加重方面均显示出统计学和临床意义上的显著改善","url":"https://stock-news.laohu8.com/highlight/detail?id=2665968376","media":"美通社","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2665968376?lang=zh_cn&edition=full","pubTime":"2026-09-08 21:18","pubTimestamp":1788873480,"startTime":"0","endTime":"0","summary":"OBERON和TITANIA两项Ⅲ期试验的结果令人鼓舞，证实tozorakimab在广泛患者人群中均能降低急性加重风险，有望帮助患者摆脱反复急性加重的困扰，获得全新的治疗选择。Tozorakimab 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