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美股
詳情
本頁面由Tiger Fintech (Singapore) Pte. Ltd.提供服務
阿斯利康
79.54
+0.4200
0.53%
盤後:
79.80
0.2600
+0.33%
18:53 EDT
成交量:
368.96萬
成交額:
2.93億
市值:
2,466.83億
市盈率:
29.97
高:
79.80
開:
79.33
低:
79.22
收:
79.12
52周最高:
87.68
52周最低:
61.24
股本:
31.01億
流通股本:
30.88億
量比:
0.86
換手率:
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
淨資產收益率:
19.67%
總資產收益率:
8.28%
市淨率:
5.52
市盈率(LYR):
35.05
資料載入中...
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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_tw&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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13:57","pubTimestamp":1753941423,"startTime":"0","endTime":"0","summary":"近日,阿斯利康宣布终止三项细胞疗法合作管线,分别是通过收购得到的TCR-T疗法NT-125,以及两款CAR-T疗法AZD5851和AZD6422。无独有偶,专注于TCR-T细胞疗法的Biotech公司Adaptimmune近日也宣布将一系列TCR-T疗法打包出售,这一举措导致公司股价以71%的断崖式暴跌震惊市场。这表明,阿斯利康等大药企并非放弃细胞疗法,而是在进行战略调整,淘汰那些前景不够明朗或与公司整体发展战略不符的项目,将资源集中到更具竞争力和发展潜力的管线中。","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=nesSN2025073113572094c56f5e&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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12:00","pubTimestamp":1753934458,"startTime":"0","endTime":"0","summary":"庞大的市场规模,使精神类药物市场开始成为全球药企新的竞争焦点,同时也带起了该赛道的风口。据悉,Gilgamesh专注于开发用于治疗抑郁症、焦虑症、药物成瘾及其他精神疾病的疗法。2024年8月1日,艾伯维发布公告,其将以87亿美元完成对神经科学生物技术公司Cerevel Therapeutics的收购。除了艾伯维,近年来还有不少大型药企也正在通过高额并购与合作抢占神经药物领域赛道制高点。据了解,阿斯利康在神经科学领域的撤离并非突然之举。","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=nesSN2025073112014897292f84&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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期臨牀告捷!頭對頭擊敗“藥王”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_tw&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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款創新藥在中國獲批,來自強生、阿斯利康、李氏大藥廠","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_tw&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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