美股详情

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PagerDuty, Inc.

18.38

+0.11000.60%

盘后：18.380.00000.00%18:37 EDT

成交量：69.24万

成交额：1,264.28万

市值：16.74亿

市盈率：-31.05

高：18.41

开：18.30

低：17.85

收：18.27

数据加载中...

总览公司新闻资讯公告

美国研究综述-Advanced Flower Capital、BRT Apartments、Xponential Fitness

PagerDuty：2025年Q4财报实现营收1.214亿美元，前值为1.111亿美元

PagerDuty Inc 报告截至 1 月 31 日的季度业绩 - 收益摘要

PagerDuty 2025 财年第四季度调整后每股收益 $0.22 高于预期 $0.16，销售额 $121.40百万高于预期 $119.77百万

辉瑞(PFE)PD-L1靶向ADC新药在华获批临床

美国研究综述-Beam Therapeutics、Lennar、Redfin

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

阿斯利康PD-L1在中国获批第4项适应证 AI医疗概念股集体走强丨医药早参

每日经济新闻

阿斯利康PD-L1肿瘤药在中国获批第四项适应证

阿斯利康(AZN.US)胃癌围手术期PD-L1联合疗法优于标准治疗

【康方生物：依沃西头对头帕博利珠单抗Ⅲ期临床研究结果在《柳叶刀》发表】近日，康方生物自主研发的全球首创PD-1/VEGF双特异性抗体新药依沃西单药对比帕博利珠单抗单药一线治疗PD-L1表达阳性的局部晚期或转移性非小细胞肺癌的注册性Ⅲ期临床研究(HARMONi-2/AK112-303）的研究数据，在国际顶级医学期刊《柳叶刀》发表。

【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。

【百济神州：百泽安在美国获批用于晚期食管鳞状细胞癌联合化疗的一线治疗】3月4日，百济神州宣布，美国食品药品监督管理局已批准百泽安®联合含铂化疗用于肿瘤表达PD-L1的不可切除或转移性食管鳞状细胞癌成人患者一线治疗。百泽安®已在美国获批作为单药用于治疗既往接受过系统化疗后不可切除或转移性ESCC的成人患者，以及联合化疗用于胃和胃食管结合部癌成人患者的一线治疗。

基石药业PD-1/VEGF/CTLA-4三抗CS2009全球多中心I期临床试验完成首例患者给药

每日经济新闻

交银国际：升百济神州目标价至208.8港元维持买入评级

【基石药业-B(02616.HK)：PD-1/VEGF/CTLA-4三特异性抗体CS2009全球多中心I期临床试验顺利完成首例患者给药】基石药业-B(02616.HK)发布公告，公司自主研发的PD-1/VEGF/CTLA-4三特异性抗体CS2009的全球多中心I期临床试验顺利完成首例患者给药，未发生输液反应或其他不良事件。

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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":"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/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","LU0306807586.USD","BK4581","BK4592","LU0170899867.USD","LU0306806265.USD","LU1883839398.USD","BK4588","LU0225284248.USD","LU1057294990.SGD","BK4007","LU1066053197.SGD","IE0002270589.USD","SG9999002224.SGD","SGXZ57979304.SGD","LU0321505439.SGD","BK4599","SG9999003800.SGD","SG9999013999.USD","IE00BBT3K403.USD","PFE","LU0058720904.USD","LU1894683264.USD","LU0234572021.USD","LU1066051498.USD","LU1894683348.USD","BK4585","SG9999002232.USD","LU1169589451.USD","PD","SG9999011175.SGD","BK4080","IE00B19Z3B42.SGD","IE00B19Z3581.USD","ADC","BK4023","LU0289739699.SGD","LU1169590202.USD","BK4550","LU0985481810.HKD","LU0122379950.USD","LU0321505868.SGD","LU0225771236.USD","LU0868494617.USD","LU1023059063.AUD","SG9999001176.USD","BK4534","BK4231","IE00BLSP4452.SGD","BK4533"],"gpt_icon":1},{"id":"2518787053","title":"阿斯利康PD-L1在中国获批第4项适应证 AI医疗概念股集体走强丨医药早参","url":"https://stock-news.laohu8.com/highlight/detail?id=2518787053","media":"每日经济新闻","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518787053?lang=zh_cn&edition=fundamental","pubTime":"2025-03-11 07:33","pubTimestamp":1741649613,"startTime":"0","endTime":"0","summary":"阿斯利康PD-L1在中国获批第4项适应证 AI医疗概念股集体走强丨医药早参","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202503113341709854.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/202503113341709854.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":["LU0320765992.SGD","BK4588","LU1169590202.USD","09939","BK4007","BK4585","LU2456880835.USD","AZN","BK4568","LU2236285917.USD","LU0109394709.USD","LU2462157665.USD","BK1515","LU0889565916.HKD","LU2417539215.USD","PD","BK4023","LU1169589451.USD","LU1829250122.USD","BK1574","BK1161"],"gpt_icon":0},{"id":"2518248700","title":"阿斯利康PD-L1肿瘤药在中国获批第四项适应证","url":"https://stock-news.laohu8.com/highlight/detail?id=2518248700","media":"美港电讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2518248700?lang=zh_cn&edition=fundamental","pubTime":"2025-03-10 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21:20","pubTimestamp":1741353606,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，3月7日，阿斯利康宣布III期MATTERHORN研究结果显示，Imfinzi联合标准治疗FLOT化疗作为可切除的早期和局部晚期的胃癌和胃食管交界处癌患者围手术期治疗方案，主要终点无事件生存期具有统计学意义和临床意义的改善。MATTERHORN是首个证明免疫疗法联合治疗优于标准治疗的全球随机III期临床研究。","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/1259345.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":"stock_zhitongcaijing","symbols":["LU1829250122.USD","PD","AZN","LU1169589451.USD","LU2417539215.USD","LU1169590202.USD","LU0109394709.USD","BK4023","BK4585","BK4588","BK4007","LU2456880835.USD","LU2462157665.USD","BK4568","LU0320765992.SGD","LU0889565916.HKD","LU2236285917.USD"],"gpt_icon":0},{"id":"2517122840","title":"【康方生物：依沃西头对头帕博利珠单抗Ⅲ期临床研究结果在《柳叶刀》发表】 近日，康方生物自主研发的全球首创PD-1/VEGF双特异性抗体新药依沃西单药对比帕博利珠单抗单药一线治疗PD-L1表达阳性的局部晚期或转移性非小细胞肺癌的注册性Ⅲ期临床研究(HARMONi-2/AK112-303）的研究数据，在国际顶级医学期刊《柳叶刀》发表。","url":"https://stock-news.laohu8.com/highlight/detail?id=2517122840","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517122840?lang=zh_cn&edition=fundamental","pubTime":"2025-03-07 13:57","pubTimestamp":1741327045,"startTime":"0","endTime":"0","summary":"近日，康方生物自主研发的全球首创PD-1/VEGF双特异性抗体新药依沃西单药对比帕博利珠单抗单药一线治疗PD-L1表达阳性的局部晚期或转移性非小细胞肺癌的注册性Ⅲ期临床研究(HARMONi-2/AK112-303）的研究数据，在国际顶级医学期刊《柳叶刀》发表。","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/2025/03/07135748586398.shtml","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":"jinrongjie_stock","symbols":["BK1574","PD","IE00BPRC5H50.USD","LU0348783233.USD","BK1161","LU0348784397.USD","09926","LU1169589451.USD","LU0417516571.SGD","LU1720050803.USD","LU1794554557.SGD","LU1169590202.USD","IE00B543WZ88.USD","LU2488822045.USD","IE00B5MMRT66.SGD","BK4023"],"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 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。","url":"https://stock-news.laohu8.com/highlight/detail?id=2517497936","media":"金融界","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517497936?lang=zh_cn&edition=fundamental","pubTime":"2025-03-06 08:13","pubTimestamp":1741220034,"startTime":"0","endTime":"0","summary":"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。","market":"us","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":["BK1583","BK4231","BK1161","BK1141","LU1169589451.USD","PD","03347","BK4080","02616","BK1574","BK4023","ADC","LU1169590202.USD","BK1576"],"gpt_icon":0},{"id":"2517802379","title":"【百济神州：百泽安在美国获批用于晚期食管鳞状细胞癌联合化疗的一线治疗】3月4日，百济神州宣布，美国食品药品监督管理局已批准百泽安®联合含铂化疗用于肿瘤表达PD-L1的不可切除或转移性食管鳞状细胞癌成人患者一线治疗。百泽安®已在美国获批作为单药用于治疗既往接受过系统化疗后不可切除或转移性ESCC的成人患者，以及联合化疗用于胃和胃食管结合部癌成人患者的一线治疗。","url":"https://stock-news.laohu8.com/highlight/detail?id=2517802379","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2517802379?lang=zh_cn&edition=fundamental","pubTime":"2025-03-05 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10:43","pubTimestamp":1741056197,"startTime":"0","endTime":"0","summary":"每经AI快讯，基石药业今日宣布，公司自主研发的PD-1/VEGF/CTLA-4三特异性抗体CS2009的全球多中心I期临床试验顺利完成首例患者给药，未发生输液反应或其他不良事件。该试验将深入评估CS2009在多种晚期实体瘤中的临床应用价值，包括非小细胞肺癌、肝癌、胃癌、子宫内膜癌、卵巢癌、肾细胞癌及宫颈癌等，进而推动肿瘤免疫疗法的创新与发展。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202503043335813894.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/202503043335813894.html","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":"stock_eastmoney","symbols":["LU1169590202.USD","BK1583","LU1169589451.USD","BK1141","BK1576","03347","BK4023","PD"],"gpt_icon":0},{"id":"2516697852","title":"交银国际：升百济神州目标价至208.8港元 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