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阿斯利康

79.54

+0.42000.53%

盘后：79.890.3500+0.44%19:50 EDT

成交量：368.99万

成交额：2.93亿

市值：2,466.83亿

市盈率：29.97

高：79.80

开：79.33

低：79.22

收：79.12

52周最高：87.68

52周最低：61.24

股本：31.01亿

流通股本：30.88亿

量比：0.86

换手率：0.12%

股息：1.57

股息率：1.97%

每股收益(TTM):2.65

每股收益(LYR):2.27

净资产收益率：19.67%

总资产收益率：8.28%

市净率：5.52

市盈率(LYR):35.05

数据加载中...

总览公司新闻公告

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阿斯利康盘中异动早盘股价大跌3.00%报74.30美元

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3 款创新药在中国获批，来自强生、阿斯利康、李氏大药厂

Insight数据库

增长11%！阿斯利康2025H1财报：营收280亿美元，Enhertu大卖22.89亿美元

阿斯利康放弃3款细胞疗法

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21:31","pubTimestamp":1753968698,"startTime":"0","endTime":"0","summary":"北京时间2025年07月31日21时31分，阿斯利康股票出现波动，股价急速下跌3.00%。截至发稿，该股报74.30美元/股，成交量70.4185万股，换手率0.02%，振幅0.46%。阿斯利康股票所在的制药行业中，整体跌幅为0.96%。该信息摘要如下：二季度阿斯利康核心每股收益达2.17美元，同比增长10%，略超市场预期。据阿斯利康周二发布的业绩显示，二季度公司收入达到144.6亿美元，同比增长12%，超过分析师预期的141.5亿美元。","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=nesSN20250731213138972a4bdd&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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Vaccine","url":"https://stock-news.laohu8.com/highlight/detail?id=2555354748","media":"动脉网","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2555354748?lang=zh_cn&edition=fundamental","pubTime":"2025-07-31 21:05","pubTimestamp":1753967100,"startTime":"0","endTime":"0","summary":"This achievement underscores Symbiosis’s role in supporting critical medical advancements. The completion of 1,000 batches highlights the company’s capacity for large-scale production and its involvement in high-profile projects such as the AstraZeneca vaccine. Symbiosis continues to play a key part in addressing public health challenges through its expertise in injectable drug manufacturing..这一成就突显了共生公司在支持关键医疗进步方面的作用。完成1000批次的生产彰显了该公司的大规模生产能力，以及其参与阿斯利康疫苗等高知名度项目的能力。共生公司通过其在注射药物制造方面的专业知识，继续在应对公共卫生挑战中发挥重要作用。","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=nesSN2025073121071694c652c9&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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20:20","pubTimestamp":1753964453,"startTime":"0","endTime":"0","summary":"根据 Insight 数据库，7 月份，有 24 款新药向 NMPA 递交上市申请，包括 12 个首次上市申请和 12 个新适应症申请。从注册分类来看，24 款药中，国产药有 15 款，进口药有 9 款。今年 6 月，维迪西妥单抗的第 4 项适应症上市申请也已获得 CDE 受理，用于HER2 低表达乳腺癌的二线治疗。2024 年 7 月，CDE 已受理这两款药物联合用于治疗既往内分泌经治的 HR+/HER2-局部晚期或转移性乳腺癌的上市申请。","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250731211811a46dad09&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, .recom-box, 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期临床告捷！头对头击败“药王”伊布替尼","url":"https://stock-news.laohu8.com/highlight/detail?id=2555241077","media":"药事纵横","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2555241077?lang=zh_cn&edition=fundamental","pubTime":"2025-07-31 10:04","pubTimestamp":1753927461,"startTime":"0","endTime":"0","summary":"7月30日，礼来公司宣布，其非共价BTK抑制剂吡妥布替尼在关键性三期临床试验BRUIN CLL-314中取得突破性成果。这是首个纳入初治患者、针对共价BTK抑制剂的头对头III期研究。作用机制创新吡妥布替尼作为首个也是目前唯一获批的非共价可逆BTK抑制剂，吡妥布替尼通过全新的机制克服了现有治疗的局限性。BTK抑制剂市场一直是肿瘤治疗领域的重要竞争赛道。目前，多家制药巨头在BTK抑制剂领域布局。","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=nesSN20250731121022a6cacbd1&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, body","filters":".relate-stock, .hot-list, 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款创新药在中国获批，来自强生、阿斯利康、李氏大药厂","url":"https://stock-news.laohu8.com/highlight/detail?id=2555680075","media":"Insight数据库","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2555680075?lang=zh_cn&edition=fundamental","pubTime":"2025-07-31 08:09","pubTimestamp":1753920565,"startTime":"0","endTime":"0","summary":"2025 年 4 月 15 日，该药在中国首次获批上市，与常规治疗药物联合用于治疗抗乙酰胆碱受体抗体阳性的成人全身型重症肌无力患者。本次获批的是瑞利珠单抗在华申报的第二项适应症。2022 年 10 月，阿斯利康公布该试验的阳性结果。Insight 数据库显示，此前国内仅有 3 款新药获批用于 NMOSD，除阿斯利康的依库珠单抗之外，还有翰森制药引进的的 CD19 单抗“伊奈利珠单抗”和罗氏制药的 IL6R 单抗“萨特利珠单抗”。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tencent","url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20250731082915a46c52b2&s=b","rn_cache_url":null,"customStyle":"body{padding-top:10px;}#news_title{font-weight:bold;#titleStyle#;}#news_description span{font-size:12px;#descriptionStyle#;}.footer-note{#statement#}","selectors":".mod-LoadTzbdNews, 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