美股詳情

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PagerDuty, Inc.

18.27

-0.5000-2.66%

盤後：18.270.00000.00%19:13 EDT

成交量：94.12萬

成交額：1,719.37萬

市值：16.64億

市盈率：-30.86

高：18.45

開：18.45

低：18.03

收：18.77

資料載入中...

總覽公司新聞資訊公告

美國研究綜述-Advanced Flower Capital、BRT Apartments、Xponential Fitness

PagerDuty：2025年Q4財報實現營收1.214億美元，前值為1.111億美元

PagerDuty Inc 報告截至 1 月 31 日的季度業績 - 收益摘要

PagerDuty 2025 財年第四季度調整後每股收益 $0.22 高於預期 $0.16，銷售額 $121.40百萬高於預期 $119.77百萬

輝瑞(PFE)PD-L1靶向ADC新藥在華獲批臨牀

美國研究綜述-Beam Therapeutics、Lennar、Redfin

輝瑞(PFE.US)PD-L1靶向ADC新藥在華獲批臨牀擬治療晚期實體瘤

阿斯利康PD-L1在中國獲批第4項適應證 AI醫療概念股集體走強丨醫藥早參

每日经济新闻

阿斯利康PD-L1腫瘤藥在中國獲批第四項適應證

阿斯利康(AZN.US)胃癌圍手術期PD-L1聯合療法優於標準治療

【康方生物：依沃西頭對頭帕博利珠單抗Ⅲ期臨牀研究結果在《柳葉刀》發表】近日，康方生物自主研發的全球首創PD-1/VEGF雙特異性抗體新藥依沃西單藥對比帕博利珠單抗單藥一線治療PD-L1表達陽性的局部晚期或轉移性非小細胞肺癌的註冊性Ⅲ期臨牀研究(HARMONi-2/AK112-303）的研究數據，在國際頂級醫學期刊《柳葉刀》發表。

【基石藥業-B(02616.HK)在澳大利亞遞交CS5001(ROR1 ADC)聯合標準治療用於一線瀰漫大B細胞淋巴瘤的臨牀試驗申請】基石藥業-B(02616.HK)發佈公告，公司已在澳大利亞成功遞交CS5001(ROR1 ADC)聯合標準治療用於一線瀰漫大B細胞淋巴瘤(DLBCL)的Ib期臨牀試驗申請。此外 CS5001單藥及聯合PD-L1單抗治療晚期實體瘤的全球多中心臨牀試驗也在同步開展。

【百濟神州：百澤安在美國獲批用於晚期食管鱗狀細胞癌聯合化療的一線治療】3月4日，百濟神州宣佈，美國食品藥品監督管理局已批准百澤安®聯合含鉑化療用於腫瘤表達PD-L1的不可切除或轉移性食管鱗狀細胞癌成人患者一線治療。百澤安®已在美國獲批作為單藥用於治療既往接受過系統化療後不可切除或轉移性ESCC的成人患者，以及聯合化療用於胃和胃食管結合部癌成人患者的一線治療。

基石藥業PD-1/VEGF/CTLA-4三抗CS2009全球多中心I期臨牀試驗完成首例患者給藥

每日经济新闻

交銀國際：升百濟神州目標價至208.8港元維持買入評級

【基石藥業-B(02616.HK)：PD-1/VEGF/CTLA-4三特異性抗體CS2009全球多中心I期臨牀試驗順利完成首例患者給藥】基石藥業-B(02616.HK)發佈公告，公司自主研發的PD-1/VEGF/CTLA-4三特異性抗體CS2009的全球多中心I期臨牀試驗順利完成首例患者給藥，未發生輸液反應或其他不良事件。

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The company reported quarterly sales of $121.40 million which beat the analyst consensus estimate of $119.77 ","market":"us","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":"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","news_tag":"express","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["PD"],"gpt_icon":0},{"id":"2518797147","title":"輝瑞(PFE)PD-L1靶向ADC新藥在華獲批臨牀","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_tw&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 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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":["SG9999002224.SGD","LU0170899867.USD","LU0321505868.SGD","BK4581","LU0225284248.USD","IE00B19Z3581.USD","IE00BLSP4452.SGD","IE00BBT3K403.USD","ADC","LU1894683348.USD","BK4007","LU0058720904.USD","IE0002270589.USD","SG9999001176.USD","SG9999013999.USD","LU0122379950.USD","LU0321505439.SGD","LU1057294990.SGD","LU1169590202.USD","LU0985481810.HKD","SG9999002232.USD","SGXZ57979304.SGD","LU1066053197.SGD","LU0306807586.USD","IE00B19Z3B42.SGD","LU1169589451.USD","LU1883839398.USD","SG9999001176.SGD","BK4592","BK4534","LU0306806265.USD","LU0289739699.SGD","BK4231","LU1894683264.USD","BK4080","BK4550","LU0234572021.USD","LU1023059063.AUD","BK4533","BK4585","PFE","BK4588","SG9999003800.SGD","BK4599","SG9999011175.SGD","LU0868494617.USD","BK4023","LU0225771236.USD","LU1066051498.USD","PD"],"gpt_icon":1},{"id":"2518787053","title":"阿斯利康PD-L1在中國獲批第4項適應證 AI醫療概念股集體走強丨醫藥早參","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_tw&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":["LU0889565916.HKD","AZN","BK4007","BK1515","LU0320765992.SGD","LU2417539215.USD","LU2462157665.USD","LU1169589451.USD","09939","BK1574","LU2236285917.USD","BK4585","LU2456880835.USD","LU0109394709.USD","LU1829250122.USD","PD","BK4023","BK4568","LU1169590202.USD","BK4588","BK1161"],"gpt_icon":0},{"id":"2518248700","title":"阿斯利康PD-L1腫瘤藥在中國獲批第四項適應證","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_tw&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":"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/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":["BK4588","PD","LU2417539215.USD","BK4007","BK4585","LU0889565916.HKD","LU2462157665.USD","LU1169589451.USD","LU0320765992.SGD","LU1829250122.USD","LU2236285917.USD","LU2456880835.USD","AZN","LU0109394709.USD","LU1169590202.USD","BK4023","BK4568"],"gpt_icon":0},{"id":"2517122840","title":"【康方生物：依沃西頭對頭帕博利珠單抗Ⅲ期臨牀研究結果在《柳葉刀》發表】 近日，康方生物自主研發的全球首創PD-1/VEGF雙特異性抗體新藥依沃西單藥對比帕博利珠單抗單藥一線治療PD-L1表達陽性的局部晚期或轉移性非小細胞肺癌的註冊性Ⅲ期臨牀研究(HARMONi-2/AK112-303）的研究數據，在國際頂級醫學期刊《柳葉刀》發表。","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_tw&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":["LU2488822045.USD","IE00BPRC5H50.USD","PD","IE00B543WZ88.USD","LU1169589451.USD","LU0348784397.USD","LU0417516571.SGD","LU1169590202.USD","BK4023","BK1161","LU1720050803.USD","09926","IE00B5MMRT66.SGD","BK1574","LU0348783233.USD","LU1794554557.SGD"],"gpt_icon":0},{"id":"2517497936","title":"【基石藥業-B(02616.HK)在澳大利亞遞交CS5001(ROR1 ADC)聯合標準治療用於一線瀰漫大B細胞淋巴瘤的臨牀試驗申請】基石藥業-B(02616.HK)發佈公告，公司已在澳大利亞成功遞交CS5001(ROR1 ADC)聯合標準治療用於一線瀰漫大B細胞淋巴瘤(DLBCL)的Ib期臨牀試驗申請。此外 CS5001單藥及聯合PD-L1單抗治療晚期實體瘤的全球多中心臨牀試驗也在同步開展。","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_tw&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":"sh","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":["BK1161","BK4023","BK1583","BK4080","03347","BK4231","BK1576","BK1574","ADC","LU1169590202.USD","PD","02616","BK1141","LU1169589451.USD"],"gpt_icon":0},{"id":"2517802379","title":"【百濟神州：百澤安在美國獲批用於晚期食管鱗狀細胞癌聯合化療的一線治療】3月4日，百濟神州宣佈，美國食品藥品監督管理局已批准百澤安®聯合含鉑化療用於腫瘤表達PD-L1的不可切除或轉移性食管鱗狀細胞癌成人患者一線治療。百澤安®已在美國獲批作為單藥用於治療既往接受過系統化療後不可切除或轉移性ESCC的成人患者，以及聯合化療用於胃和胃食管結合部癌成人患者的一線治療。","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_tw&edition=fundamental","pubTime":"2025-03-05 07:10","pubTimestamp":1741129814,"startTime":"0","endTime":"0","summary":"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。","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/2025/03/05071048524623.shtml","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":"jinrongjie_stock","symbols":["LU0307460666.USD","LU1169589451.USD","BK4139","688235","LU1169590202.USD","BK0239","ONC","BK1500","BK1161","BK4023","LU0588546209.SGD","BK1583","BK1588","LU1969619763.USD","PD","06160","LU2328871848.SGD"],"gpt_icon":0},{"id":"2516690737","title":"基石藥業PD-1/VEGF/CTLA-4三抗CS2009全球多中心I期臨牀試驗完成首例患者給藥","url":"https://stock-news.laohu8.com/highlight/detail?id=2516690737","media":"每日经济新闻","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2516690737?lang=zh_tw&edition=fundamental","pubTime":"2025-03-04 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":"hk","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":["03347","LU1169589451.USD","BK4023","BK1576","PD","BK1141","BK1583","LU1169590202.USD"],"gpt_icon":0},{"id":"2516697852","title":"交銀國際：升百濟神州目標價至208.8港元 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