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PD PagerDuty, Inc.
交易中 02-27 15:45:59 EST
7.00
-0.08
-1.20%
最高
7.03
最低
6.74
成交量
208.33万
今开
6.88
昨收
7.08
日振幅
4.03%
总市值
6.42亿
流通市值
6.10亿
总股本
9,178万
成交额
1,442万
换手率
2.39%
流通股本
8,727万
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
--
分时
五日
日K
周K
月K
数据加载中...
北京优虎网络科技有限公司
资讯
新帖
简况
患者死亡引 FDA 出手 PD-1/CTLA-4 双抗临床试验遇阻
生物制品圈 · 02-25 11:54
患者死亡引 FDA 出手 PD-1/CTLA-4 双抗临床试验遇阻
君实生物与德琪医药达成战略合作,共同开展JS207(PD-1/VEGF双抗)与ATG-037(CD73口服小分子抑制剂)联合用药研究
美通社 · 02-25 08:30
君实生物与德琪医药达成战略合作,共同开展JS207(PD-1/VEGF双抗)与ATG-037(CD73口服小分子抑制剂)联合用药研究
Pagerduty, Inc.盘中异动 急速拉升5.19%报7.04美元
市场透视 · 02-20
Pagerduty, Inc.盘中异动 急速拉升5.19%报7.04美元
基石药业-B(02616)CS2009(PD-1/VEGF/CTLA-4三特异性抗体)II期临床试验申请获美国FDA批准
智通财经 · 02-20
基石药业-B(02616)CS2009(PD-1/VEGF/CTLA-4三特异性抗体)II期临床试验申请获美国FDA批准
基石药业-B(02616):CS2009(PD-1/VEGF/CTLA-4三特异性抗体)II期临床试验申请获美国FDA批准
智通财经 · 02-16
基石药业-B(02616):CS2009(PD-1/VEGF/CTLA-4三特异性抗体)II期临床试验申请获美国FDA批准
复宏汉霖PD-1新药“出海”日本 最早将于2028年产生销售提成
证券日报 · 02-08
复宏汉霖PD-1新药“出海”日本 最早将于2028年产生销售提成
复宏汉霖携手卫材就抗PD-1单抗汉斯状达成日本市场合作
南方财经网 · 02-05
复宏汉霖携手卫材就抗PD-1单抗汉斯状达成日本市场合作
释放pipeline in a drug潜力 NLRP3能否催生下一个“药王”?
智通财经网 · 02-05
释放pipeline in a drug潜力 NLRP3能否催生下一个“药王”?
阿斯利康(AZN.US)宣布PD-L1单抗在华获批新适应症 针对子宫内膜癌
智通财经 · 01-23
阿斯利康(AZN.US)宣布PD-L1单抗在华获批新适应症 针对子宫内膜癌
港股异动 | 维立志博-B(09887)涨超4% PD-L1/4-1BB双抗获FDA快速通道资格
智通财经 · 01-15
港股异动 | 维立志博-B(09887)涨超4% PD-L1/4-1BB双抗获FDA快速通道资格
维立志博-B(09887):维利信™(PD-L1/4-1BB双特异性抗体奥帕替苏米单抗,LBL-024)获美国FDA授予快速通道资格认定
智通财经 · 01-14
维立志博-B(09887):维利信™(PD-L1/4-1BB双特异性抗体奥帕替苏米单抗,LBL-024)获美国FDA授予快速通道资格认定
港股异动 | 复宏汉霖(02696)再涨超8% 广谱抗肿瘤PD-L1 ADC HLX43末线食管鳞癌II期数据首次发布
智通财经 · 01-13
港股异动 | 复宏汉霖(02696)再涨超8% 广谱抗肿瘤PD-L1 ADC HLX43末线食管鳞癌II期数据首次发布
PD-1/VEGF双抗交易热潮回归?荣昌生物签下56亿美元授权
第一财经 · 01-13
PD-1/VEGF双抗交易热潮回归?荣昌生物签下56亿美元授权
港股异动 | 复宏汉霖(02696)盘中涨超5% 公司首次公布PD-L1 ADC食管鳞状细胞癌Ⅱ期临床数据
智通财经 · 01-08
港股异动 | 复宏汉霖(02696)盘中涨超5% 公司首次公布PD-L1 ADC食管鳞状细胞癌Ⅱ期临床数据
维亚臻生物VSA012注射液启动II期临床 适应症为活动性狼疮肾炎等疾病
新浪财经 · 01-07
维亚臻生物VSA012注射液启动II期临床 适应症为活动性狼疮肾炎等疾病
天士力:PD-L1/VEGF双抗的实体瘤适应症IIa期、直肠癌适应症IIb期临床试验正在入组中
证券日报 · 01-05
天士力:PD-L1/VEGF双抗的实体瘤适应症IIa期、直肠癌适应症IIb期临床试验正在入组中
科伦博泰生物-B(06990)核心产品TROP2 ADC芦康沙妥珠单抗(SAC-TMT)联合免疫疗法帕博利珠单抗一线治疗PD-L1阳性局部晚期或转移性非小细胞肺癌获NMPA突破性疗法认定
智通财经 · 01-05
科伦博泰生物-B(06990)核心产品TROP2 ADC芦康沙妥珠单抗(SAC-TMT)联合免疫疗法帕博利珠单抗一线治疗PD-L1阳性局部晚期或转移性非小细胞肺癌获NMPA突破性疗法认定
达伯舒新适应症医保落地 系晚期pMMR子宫内膜癌唯一医保抗PD-(L)1药物
中国网财经 · 01-01
达伯舒新适应症医保落地 系晚期pMMR子宫内膜癌唯一医保抗PD-(L)1药物
【新股IPO】国元国际:瀚思艾泰-B(03378)CD47/PD-1双特异性抗体具备独特性 建议谨慎申购
金吾财讯 · 2025-12-17
【新股IPO】国元国际:瀚思艾泰-B(03378)CD47/PD-1双特异性抗体具备独特性 建议谨慎申购
康辰药业(603590.SH):KC1036联合PD-1抗体和含铂化疗一线治疗晚期复发或转移性食管鳞癌Ⅱ期临床研究完成首例受试者入组
智通财经 · 2025-12-15
康辰药业(603590.SH):KC1036联合PD-1抗体和含铂化疗一线治疗晚期复发或转移性食管鳞癌Ⅱ期临床研究完成首例受试者入组
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公司概况
公司名称:
PagerDuty, Inc.
所属市场:
NYSE
上市日期:
--
主营业务:
PagerDuty, Inc.于2010年5月根据特拉华州法律注册成立。PagerDuty是数字企业的中枢神经系统。PagerDuty利用几乎任何支持软件的系统或设备的数字信号,将其与人工响应数据相结合,并协调团队实时采取正确的行动。公司的产品可帮助组织改善运营,加速创新,增加收入,降低安全风险并提供出色的客户体验。
发行价格:
--
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17:39","pubTimestamp":1770543568,"startTime":"0","endTime":"0","summary":"日前,上海复宏汉霖生物技术股份有限公司(以下简称“复宏汉霖”)与卫材株式会社(以下简称“卫材”)共同宣布,双方已就抗PD-1单抗汉斯状(斯鲁利单抗,以下简称“PD-1新药”)在日本达成一项独家商业化及共同独家开发与生产许可协议。汉斯状是复宏汉霖自主研发的一款PD-1新药。根据协议,卫材将获得汉斯状在日本的独家商业化权益。","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://finance.eastmoney.com/a/202602083644840016.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":["LU1169589451.USD","HK0000306701.USD","HK0000306685.HKD","HK0000165453.HKD","BK4023","HK0000320223.HKD","LU1169590202.USD","PD","BK1161","HK0000320264.USD","02696"],"gpt_icon":0},{"id":"2609375221","title":"复宏汉霖携手卫材就抗PD-1单抗汉斯状达成日本市场合作","url":"https://stock-news.laohu8.com/highlight/detail?id=2609375221","media":"南方财经网","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2609375221?lang=zh_cn&edition=full","pubTime":"2026-02-05 18:33","pubTimestamp":1770287601,"startTime":"0","endTime":"0","summary":"南方财经2月5日电,卫材与复宏汉霖今日共同宣布,双方已就抗PD-1单抗H药汉斯状?(斯鲁利单抗,欧洲商品名:Hetronifly?)在日本达成一项独家商业化及共同独家开发与生产许可协议。根据协议,卫材将向复宏汉霖支付7,500万美元的首付款,并在此基础上,支付最高不超过8,001万美元的监管里程碑付款,以及最高不超过2.333亿美元的销售里程碑付款。","market":"sh","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://finance.eastmoney.com/a/202602053642892718.html","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":"stock_eastmoney","symbols":["02696","HK0000306685.HKD","HK0000320223.HKD","HK0000165453.HKD","PD","LU1169590202.USD","BK4585","EWJ","HK0000320264.USD","BK4588","BK4023","LU1169589451.USD","HK0000306701.USD","BK1161"],"gpt_icon":0},{"id":"2609432256","title":"释放pipeline in a drug潜力 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16:35","pubTimestamp":1770280559,"startTime":"0","endTime":"0","summary":"近期,英硅智能(03696)宣布提名靶向NLRP3的外周限制性抑制剂ISM5059,该候选药物具有新颖母核,由英硅智能自有Pharma.AI平台驱动设计。","market":"sg","thumbnail":"https://img.zhitongcaijing.com/image/20260205/20260205163220_51027.png?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250","type":0,"news_type":0,"thumbnails":["https://img.zhitongcaijing.com/image/20260205/20260205163220_51027.png?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1402047.html","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":"highlight_zhitongcaijin","symbols":["BK4132","BK4135","IBD","LU1169590202.USD","CNS","LU1169589451.USD","BBB","PD","AD","BK4023"],"gpt_icon":0},{"id":"2605290194","title":"阿斯利康(AZN.US)宣布PD-L1单抗在华获批新适应症 针对子宫内膜癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2605290194","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2605290194?lang=zh_cn&edition=full","pubTime":"2026-01-23 14:42","pubTimestamp":1769150545,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,1月22日,阿斯利康宣布,英飞凡已获中国国家药品监督管理局批准,与卡铂和紫杉醇联合用于错配修复缺陷的原发晚期或复发性子宫内膜癌成人患者的一线治疗,随后以本品单药维持治疗。截至目前该药已在美国获批 10 项适应症,在欧盟获批 11 项适应症,在国内获批 7 项。安全性方面,度伐利尤单抗联合化疗方案的总体安全性和耐受性良好,并且与此前临床试验结果总体一致,没有出现新的安全信号。","market":"sh","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/1396591.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":["LU2456880835.USD","LU0320765992.SGD","PD","BK4568","AZN","BK4588","LU0889565916.HKD","LU2236285917.USD","BK4585","LU1829250122.USD","LU2417539215.USD","LU2462157665.USD","LU0109394709.USD","BK4007","LU1169590202.USD","LU1169589451.USD","BK4023"],"gpt_icon":0},{"id":"2603621919","title":"港股异动 | 维立志博-B(09887)涨超4% 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22:52","pubTimestamp":1768402376,"startTime":"0","endTime":"0","summary":"智通财经APP讯,维立志博-B 发布公告,于2026年1月14日,PD-L1/4-1BB双特异性抗体维利信TM获美国食品药品监督管理局授予快速通道资格认定,用于治疗肺外神经内分泌癌。快速通道资格认定是FDA批准加速审查治疗严重或危及生命病情或解决未满足医疗需求的药物以助加快药物开发的方法。维利信TM是一种同时靶向PD-L1与4-1BB的双特异性抗体,为针对肺外神经内分泌癌的全球首款达到注册临床阶段的靶向4-1BB受体的疗法。","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/1393010.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":["HK0000500386.USD","PD","HK0000252160.HKD","BK1161","LU1169590202.USD","09887","LU1169589451.USD","BK4023","HK0000252152.HKD"],"gpt_icon":1},{"id":"2603539575","title":"港股异动 | 复宏汉霖(02696)再涨超8% 广谱抗肿瘤PD-L1 ADC HLX43末线食管鳞癌II期数据首次发布","url":"https://stock-news.laohu8.com/highlight/detail?id=2603539575","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603539575?lang=zh_cn&edition=full","pubTime":"2026-01-13 10:12","pubTimestamp":1768270333,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,复宏汉霖再涨超8%,截至发稿,涨8.05%,报69.8港元,成交额1864.08万港元。消息面上,1月9日,复宏汉霖在2026年美国临床肿瘤学会胃肠道肿瘤研讨会上,首度公布了其PD-L1 ADC HLX43治疗复发/转移性食管鳞癌的II期概念验证数据,本次发布的数据初步验证了HLX43在经治的晚期ESCC患者中的治疗潜力,展现出令人鼓舞的疗效及良好的安全性。","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/1392033.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_zhitongcaijing","symbols":["ADC","HK0000306685.HKD","HK0000306701.USD","PD","BK4023","02696","BK4080","HK0000165453.HKD","HK0000320223.HKD","LU1169589451.USD","BK1161","LU1169590202.USD","BK4231","HK0000320264.USD"],"gpt_icon":0},{"id":"2603357301","title":"PD-1/VEGF双抗交易热潮回归?荣昌生物签下56亿美元授权","url":"https://stock-news.laohu8.com/highlight/detail?id=2603357301","media":"第一财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2603357301?lang=zh_cn&edition=full","pubTime":"2026-01-13 10:03","pubTimestamp":1768269780,"startTime":"0","endTime":"0","summary":"艾伯维拿下荣昌生物的双抗授权。 1月12日晚间,中国生物医药企业荣昌生物宣布,与艾伯维达成一笔总金额高达56亿美元的授权合作。 RC148是荣昌生物研发的一款新型靶向PD-1/VEGF的双特异性抗体药物,其设计旨在激活抗肿瘤免疫反应的同时抑制肿瘤驱动的血管生成。通过同时靶向并抑制PD-1与VEGF通路,有望通过多机制增强免疫系统的抗肿瘤活性。 值得一提的是,康方生物PD-1/VEGF再度传来新的进展消息。","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"sina","url":"https://finance.sina.com.cn/roll/2026-01-13/doc-inhhcntx9294031.shtml","rn_cache_url":null,"customStyle":"body{padding-top:10px;}.art_tit_h1{#titleStyle#}a{#lv2TextColor#}.art_time, .art_cite{#sourceStyle#;} .art_cite{margin-left: 3px;}","selectors":".module-article, article","filters":"header, .voice2, .tags, #norm_qrcode_link_auto, .unfold-box, 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11:18","pubTimestamp":1767842338,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,复宏汉霖盘中涨超5%,截至发稿,涨4.39%,报66.65港元,成交额2390.53万港元。其中,复宏汉霖首次公布其PD-L1 ADC药物HLX43治疗复发/转移性食管鳞状细胞癌中的临床数据。HLX43是靶向PD-L1的新型ADC药物,兼具免疫检查点抑制与细胞毒性双重作用,其I期临床已证实对免疫治疗无效患者具有前景疗效和良好耐受性。本项Ⅱ期研究旨在评估HLX43用于经治复发 / 转移性食管鳞状细胞癌患者的疗效与安全性。","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/1390237.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_zhitongcaijing","symbols":["02696","PD","BK1161","BK4231","BK4080","LU1169590202.USD","LU1169589451.USD","BK4023","ADC","HK0000165453.HKD"],"gpt_icon":0},{"id":"2601387879","title":"维亚臻生物VSA012注射液启动II期临床 适应症为活动性狼疮肾炎等疾病","url":"https://stock-news.laohu8.com/highlight/detail?id=2601387879","media":"新浪财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2601387879?lang=zh_cn&edition=full","pubTime":"2026-01-07 18:03","pubTimestamp":1767780180,"startTime":"0","endTime":"0","summary":"药物临床试验登记与信息公示平台数据显示,维亚臻生物技术(苏州)有限公司的评估VSA012注射液在中国活动性狼疮肾炎患者、原发性IgA肾病患者、C3肾小球病患者和免疫复合物介导的膜增生性肾小球肾炎患者中的有效性和安全性的多中心、开放设计的II期临床研究已启动。这些疾病均属肾脏病症,会损害肾功能,引发蛋白尿、血尿等症状,诊断依赖肾活检及相关检验。","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=nesSN20260107185357a6fe6d42&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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1月5日,天士力在互动平台回答投资者提问时表示,根据公司《2025年半年度报告》,PD-L1/VEGF双抗的实体瘤适应症IIa期、直肠癌适应症IIb期临床试验正在入组中;培重组人成纤维细胞生长因子21注射液,临床试验已进入Ib期。后续研发进展公司会根据信息披露相关规定进行公告。(文章来源:证券日报)\n\n\n海量资讯、精准解读,尽在新浪财经APP","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"sina","url":"https://finance.sina.com.cn/stock/relnews/cn/2026-01-05/doc-inhfhpmh6572122.shtml","rn_cache_url":null,"customStyle":"body{padding-top:10px;}.art_tit_h1{#titleStyle#}a{#lv2TextColor#}.art_time, .art_cite{#sourceStyle#;} .art_cite{margin-left: 3px;}","selectors":".module-article, article","filters":"header, .voice2, .tags, #norm_qrcode_link_auto, .unfold-box, 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