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PagerDuty, Inc.

15.91

+0.24001.53%

盤後：15.910.00000.00%17:17 EDT

成交量：126.84萬

成交額：2,000.21萬

市值：14.49億

市盈率：-26.88

高：16.00

開：15.77

低：15.61

收：15.67

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總覽公司新聞資訊公告

阿斯利康PD-L1單抗一項III期研究成功

從PD-1跟隨到多款ADC領先，樂普生物-B（02157）迎價值重估？

【加科思-B(01167.HK)：SHP2抑制劑SITNEPROTAFIB聯用研究數據發表於學術期刊】加科思-B(01167.HK)發佈公告，公司自主研發的SHP2抑制劑sitneprotafib (JAB-3312)相關研究見刊Clinical Cancer Research(《臨牀腫瘤研究》)。文章公佈了SHP2抑制劑與PD-1抗體以及靶向RTK/RAS/MAPK通路的聯合療法中的臨牀前體內外數據和對聯合療法有回應的代表性患者病例。

百濟神州一季度虧損大幅收窄國內BTK抑制劑銷售加速、PD-1銷售減速

每日经济新闻

基石藥業(02616)重磅發佈CS2009(PD-1/VEGF/CTLA-4)最新臨牀前研究結果

港股異動 | 三生製藥(01530)再漲超9% 抗VEGF/PD-1雙特異性抗體707被納入突破性治療品種

康方生物依沃西獲批用於PD-L1陽性肺癌治療

【康方生物(09926.HK)：依達方®(依沃西，PD-1/VEGF)第二個適應症上市申請獲得NMPA批准用於一線治療PD-L1陽性NSCLC】康方生物(09926.HK)發佈公告，由公司自主研發的全球首創雙特異性抗體依達方®(依沃西，PD-1/VEGF)單藥用於PD-L1陽性(TPS≥1%)的表皮生長因子受體(EGFR)基因突變陰性和間變性淋巴瘤激酶(ALK)陰性的局部晚期或轉移性非小細胞肺癌(NSCLC)的一線治療的新藥上市申請(sNDA)，已獲得中國國家藥品監督管理局(NMPA)批准上市。這是依沃西獲批上市的第二個適應症，讓中國患者“率先用上全球最優治療方案”成為現實。

康方生物(09926.HK)：依達方®(依沃西，PD-1/VEGF)第二個適應症上市申請獲得NMPA批准，用於一線治療PD-L1陽性NSCLC

【康方生物(09926.HK)安尼可®（派安普利，PD -1）獲美國食品藥品監督管理局批准兩項適應症用於治療晚期鼻咽癌】康方生物(09926.HK)發佈公告，安尼可®(派安普利，PD-1)已獲得美國食品藥品監督管理局(FDA)批准上市，用於治療復發或轉移性鼻咽癌的一線治療和以鉑類為基礎的至少一線化療治療失敗後治療的2項適應症。派安普利由公司自主研發並由正大天晴康方負責後續開發和商業化，也是公司第一個獲得美國FDA批准上市的自主研發創新生物藥。

康方生物(09926)安尼可®（派安普利，PD -1）獲美國食品藥品監督管理局批准兩項適應症用於治療晚期鼻咽癌

港股異動 | 信達生物(01801)漲超5% IBI363（PD-1/IL-2α-bias）等多款管線將亮相2025 ASCO

港股異動 | 基石藥業-B(02616)最高漲超7% 三抗CS2009（PD-1/VEGF/CTLA-4）即將在AACR更新更多數據

榮獲七項ASCO口頭報告：信達生物IBI363（PD-1/IL-2α-bias）領銜多款管線亮相美國臨牀腫瘤學會2025年大會

Pagerduty, Inc.盤中異動早盤股價大漲5.08%

又一次“頭對頭”勝出！康方生物雙抗藥物療效“擊敗”百濟神州PD-1

康方生物在一項臨牀三期試驗中贏了百濟神州的PD-1抗體聯合療法

每日经济新闻

港股異動 | 康方生物(09926)漲超13%創歷史新高康方PD-1/VEGF雙抗首次戰勝PD-1+化療

百時美施貴寶（BMY.US）PD-1抑制劑在中國獲批新適應症

智通财经网

港股異動 | 三生製藥(01530)漲超3% 抗VEGF/PD-1雙特異性抗體獲國家藥監局突破性療法認定

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Research(《临床肿瘤研究》)。文章公布了SHP2抑制剂与PD-1抗体以及靶向RTK/RAS/MAPK通路的联合疗法中的临床前体内外数据和对联合疗法有回应的代表性患者病例。","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/2025/05/09064650243257.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":["PD","LU1169590202.USD","BK1574","BK4023","BK1161","LU1169589451.USD","01167"],"gpt_icon":0},{"id":"2533932462","title":"百濟神州一季度虧損大幅收窄 國內BTK抑制劑銷售加速、PD-1銷售減速","url":"https://stock-news.laohu8.com/highlight/detail?id=2533932462","media":"每日经济新闻","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2533932462?lang=zh_tw&edition=fundamental","pubTime":"2025-05-07 22:41","pubTimestamp":1746628873,"startTime":"0","endTime":"0","summary":"作为国内创新药龙头企业，百济神州目前有3款主要自研产品，分别为BTK抑制剂泽布替尼、PD-1单抗替雷利珠单抗和PARP抑制剂帕米帕利。对于一季度的产品收入增长，公司归因于百悦泽、百泽安及安进授权产品的销售增长。具体来说，今年第一季度，百悦泽全球销售额总计56.92亿元，同比增长63.7%。而在竞争更为激烈的国内PD-1单抗市场中，百泽安实现销售额12.45亿元，同比增长19.3%。","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=nesSN2025050722420597521340&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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抗VEGF/PD-1雙特異性抗體707被納入突破性治療品種","url":"https://stock-news.laohu8.com/highlight/detail?id=2532724863","media":"智通财经","labels":["productRelease","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2532724863?lang=zh_tw&edition=fundamental","pubTime":"2025-05-02 11:48","pubTimestamp":1746157731,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，三生制药再涨超9%，截至发稿，涨9.53%，报13.1港元，成交额1.22亿港元。消息面上，三生制药发布公告，该公司自主研发的抗VEGF/PD-1双特异性抗体于2025年4月17日获国家药品监督管理局纳入突破性治疗品种，适应症为一线治疗PD-L1表达阳性的局部晚期或转移性非小细胞肺癌。关注三生制药等。","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/1288917.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease,movement","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1593","LU1169590202.USD","BK4023","LU1169589451.USD","BK1583","01530","BK1161","PD"],"gpt_icon":0},{"id":"2530549955","title":"康方生物依沃西獲批用於PD-L1陽性肺癌治療","url":"https://stock-news.laohu8.com/highlight/detail?id=2530549955","media":"财中社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530549955?lang=zh_tw&edition=fundamental","pubTime":"2025-04-28 09:32","pubTimestamp":1745803955,"startTime":"0","endTime":"0","summary":"4月27日，康方生物（09926）发布公告，宣布其自主研发的双特异性抗体依达方?（依沃西，PD-1/VEGF）获得中国国家药品监督管理局（NMPA）批准，用于一线治疗PD-L1阳性非小细胞肺癌（NSCLC）。这是依沃西获得的第二个适应症，标志着中国患者能够率先使用全球最优治疗方案。","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://finance.eastmoney.com/a/202504283390722024.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":["LU2488822045.USD","09926","LU1169589451.USD","BK1574","IE00B5MMRT66.SGD","LU0348783233.USD","IE00B543WZ88.USD","BK1161","BK4023","LU1720050803.USD","LU0348784397.USD","LU1169590202.USD","LU1794554557.SGD","PD","IE00BPRC5H50.USD","LU0417516571.SGD"],"gpt_icon":0},{"id":"2530343711","title":"【康方生物(09926.HK)：依達方®(依沃西，PD-1/VEGF)第二個適應症上市申請獲得NMPA批准 用於一線治療PD-L1陽性NSCLC】康方生物(09926.HK)發佈公告，由公司自主研發的全球首創雙特異性抗體依達方®(依沃西，PD-1/VEGF)單藥用於PD-L1陽性(TPS≥1%)的表皮生長因子受體(EGFR)基因突變陰性和間變性淋巴瘤激酶(ALK)陰性的局部晚期或轉移性非小細胞肺癌(NSCLC)的一線治療的新藥上市申請(sNDA)，已獲得中國國家藥品監督管理局(NMPA)批准上市。這是依沃西獲批上市的第二個適應症，讓中國患者“率先用上全球最優治療方案”成為現實。","url":"https://stock-news.laohu8.com/highlight/detail?id=2530343711","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530343711?lang=zh_tw&edition=fundamental","pubTime":"2025-04-27 20:01","pubTimestamp":1745755264,"startTime":"0","endTime":"0","summary":"康方生物(09926.HK)发布公告，由公司自主研发的全球首创双特异性抗体依达方®(依沃西，PD-1/VEGF)单药用于PD-L1阳性(TPS≥1%)的表皮生长因子受体(EGFR)基因突变阴性和间变性淋巴瘤激酶(ALK)阴性的局部晚期或转移性非小细胞肺癌(NSCLC)的一线治疗的新药上市申请(sNDA)，已获得中国国家药品监督管理局(NMPA)批准上市。这是依沃西获批上市的第二个适应症，让中国患者“率先用上全球最优治疗方案”成为现实。","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/2025/04/27200149930796.shtml","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"jinrongjie_stock","symbols":["BK4585","IE00BPRC5H50.USD","LU1794554557.SGD","LU0348784397.USD","BK1161","BK4008","09926","IE00B543WZ88.USD","IE00B5MMRT66.SGD","LU1169589451.USD","LU0348783233.USD","BK4500","LU1169590202.USD","BK1574","BK4023","LU2488822045.USD","PD","ALK","LU1720050803.USD","LU0417516571.SGD","BK4588"],"gpt_icon":0},{"id":"2530379034","title":"康方生物(09926.HK)：依達方®(依沃西，PD-1/VEGF)第二個適應症上市申請獲得NMPA批准，用於一線治療PD-L1陽性NSCLC","url":"https://stock-news.laohu8.com/highlight/detail?id=2530379034","media":"格隆汇","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530379034?lang=zh_tw&edition=fundamental","pubTime":"2025-04-27 19:58","pubTimestamp":1745755137,"startTime":"0","endTime":"0","summary":"格隆汇4月27日丨康方生物宣布，由公司自主研发的全球首创双特异性抗体依达方单药用于PD-L1阳性的表皮生长因子受体基因突变阴性和间变性淋巴瘤激酶阴性的局部晚期或转移性非小细胞肺癌的一线治疗的新药上市申请，已获得中国国家药品监督管理局批准上市。这是依沃西获批上市的第二个适应症，让中国患者‘‘率先用上全球最优治疗方案’’成为现实。依沃西是全球首个在头对头帕博利珠单抗的III期临床研究中获得显著阳性结果的药物。","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://finance.jrj.com.cn/2025/04/27195849930778.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":["BK4023","IE00B543WZ88.USD","PD","09926","BK1574","IE00B5MMRT66.SGD","LU1169589451.USD","LU1169590202.USD","LU2488822045.USD","LU0348784397.USD","LU0417516571.SGD","LU1794554557.SGD","LU0348783233.USD","IE00BPRC5H50.USD","LU1720050803.USD","BK1161"],"gpt_icon":1},{"id":"2530916455","title":"【康方生物(09926.HK)安尼可®（派安普利，PD -1）獲美國食品藥品監督管理局批准 兩項適應症用於治療晚期鼻咽癌】康方生物(09926.HK)發佈公告，安尼可®(派安普利，PD-1)已獲得美國食品藥品監督管理局(FDA)批准上市，用於治療復發或轉移性鼻咽癌的一線治療和以鉑類為基礎的至少一線化療治療失敗後治療的2項適應症。派安普利由公司自主研發並由正大天晴康方負責後續開發和商業化，也是公司第一個獲得美國FDA批准上市的自主研發創新生物藥。","url":"https://stock-news.laohu8.com/highlight/detail?id=2530916455","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530916455?lang=zh_tw&edition=fundamental","pubTime":"2025-04-25 08:18","pubTimestamp":1745540328,"startTime":"0","endTime":"0","summary":"康方生物(09926.HK)发布公告，安尼可®(派安普利，PD-1)已获得美国食品药品监督管理局(FDA)批准上市，用于治疗复发或转移性鼻咽癌的一线治疗和以铂类为基础的至少一线化疗治疗失败后治疗的2项适应症。派安普利由公司自主研发并由正大天晴康方负责后续开发和商业化，也是公司第一个获得美国FDA批准上市的自主研发创新生物药。","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/2025/04/25081849860793.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":["IE00BPRC5H50.USD","09926","IE00B5MMRT66.SGD","LU1169590202.USD","LU0348783233.USD","IE00B543WZ88.USD","LU0417516571.SGD","LU1169589451.USD","LU1720050803.USD","LU2488822045.USD","PD","BK1161","159839","BK4023","LU0348784397.USD","BK1574","LU1794554557.SGD"],"gpt_icon":0},{"id":"2530191575","title":"康方生物(09926)安尼可®（派安普利，PD -1）獲美國食品藥品監督管理局批准 兩項適應症用於治療晚期鼻咽癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2530191575","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2530191575?lang=zh_tw&edition=fundamental","pubTime":"2025-04-25 08:13","pubTimestamp":1745539980,"startTime":"0","endTime":"0","summary":"智通财经APP讯，康方生物 发布公告，安尼可已获得美国食品药品监督管理局批准上市，用于治疗复发或转移性鼻咽癌的一线治疗和以铂类为基础的至少一线化疗治疗失败后治疗的2项适应症。派安普利由公司自主研发并由正大天晴康方负责后续开发和商业化，也是公司第一个获得美国FDA批准上市的自主研发创新生物药。派安普利本次在美国获批上市，为全球的晚期鼻咽癌患者提供了免疫治疗新选择。","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/1284598.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1574","LU0417516571.SGD","LU0348783233.USD","09926","LU0348784397.USD","LU1720050803.USD","LU2488822045.USD","IE00B543WZ88.USD","IE00B5MMRT66.SGD","LU1794554557.SGD","LU1169590202.USD","PD","IE00BPRC5H50.USD","BK1161","BK4023","LU1169589451.USD"],"gpt_icon":0},{"id":"2529640246","title":"港股異動 | 信達生物(01801)漲超5% IBI363（PD-1/IL-2α-bias）等多款管線將亮相2025 ASCO","url":"https://stock-news.laohu8.com/highlight/detail?id=2529640246","media":"智通财经","labels":["conferences","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529640246?lang=zh_tw&edition=fundamental","pubTime":"2025-04-24 14:37","pubTimestamp":1745476662,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，信达生物涨超5%，截至发稿，涨5.05%，报54.05港元，成交额15.91亿港元。消息面上，4月24日，信达生物宣布将在美国临床肿瘤学会年会上展示肿瘤创新管线的一系列临床数据。其中，IBI363在黑色素瘤、肠癌、非小细胞肺癌的临床研究，以及 IBI343在胰腺癌研究方面均有口头报告。本届 ASCO 年会将于当地时间2025年5月30日-6月3日在美国芝加哥举办。","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/1283860.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"conferences,movement","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["LU2328871848.SGD","LU1169590202.USD","BK1589","LU1969619763.USD","PD","BK1161","LU2488822045.USD","BK1583","BK4023","01801","LU1169589451.USD"],"gpt_icon":0},{"id":"2529617317","title":"港股異動 | 基石藥業-B(02616)最高漲超7% 三抗CS2009（PD-1/VEGF/CTLA-4）即將在AACR更新更多數據","url":"https://stock-news.laohu8.com/highlight/detail?id=2529617317","media":"智通财经","labels":["dataReport","movement"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529617317?lang=zh_tw&edition=fundamental","pubTime":"2025-04-24 11:35","pubTimestamp":1745465743,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，基石药业-B早盘最高涨超7%，截至发稿，涨2.41%，报2.97港元，成交额1672.07万港元。基石药业5款自主研发创新药物的最新临床前研究成果将同时亮相这一国际顶级学术舞台，包括三抗CS2009、双抗CS2011及出自公司自有抗体偶联药物平台的三款创新ADC分子CS5006、CS5007与CS5005。其中90%用于与集团“管线2.0”中的资产，尤其是CS5001，以及CS2009有关的进一步研发；余下净额于适当时用于其他一般公司用途。","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/1283807.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"dataReport,movement","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["BK1161","02616","BK4023","PD","BK1574","LU1169590202.USD","LU1169589451.USD"],"gpt_icon":0},{"id":"2529693739","title":"榮獲七項ASCO口頭報告：信達生物IBI363（PD-1/IL-2α-bias）領銜多款管線亮相美國臨牀腫瘤學會2025年大會","url":"https://stock-news.laohu8.com/highlight/detail?id=2529693739","media":"美通社","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529693739?lang=zh_tw&edition=fundamental","pubTime":"2025-04-24 07:00","pubTimestamp":1745449200,"startTime":"0","endTime":"0","summary":"本届 ASCO 年会将于当地时间2025年5月30日-6月3日在美国芝加哥举办。信达生物制药集团高级副总裁周辉博士表示：\"很高兴在本次ASCO大会上，IBI363开发的第一批三大适应症黑色素瘤、肠癌、非小细胞肺癌的临床研究均被接收为口头报告，代表了下一代PD-1双抗肿瘤免疫疗法引起了全球的广泛关注。同时IBI343胰腺癌研究继去年12月ESMO Asia口头报告之后，再次以口头报告登上ASCO舞台。","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":"https://wwwold.prnasia.com/story/archive/4671176_ZH71176_1","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":"prnasia","symbols":["LU2328871848.SGD","BK4139","IVBIY","01801","LU1169589451.USD","BK1589","LU1169590202.USD","LU2488822045.USD","BK4023","BK1583","LU1969619763.USD","BK1161","PD"],"gpt_icon":1},{"id":"2529687522","title":"Pagerduty, Inc.盤中異動 早盤股價大漲5.08%","url":"https://stock-news.laohu8.com/highlight/detail?id=2529687522","media":"市场透视","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2529687522?lang=zh_tw&edition=fundamental","pubTime":"2025-04-23 21:40","pubTimestamp":1745415624,"startTime":"0","endTime":"0","summary":"北京时间2025年04月23日21时40分，Pagerduty, Inc.股票出现异动，股价大幅上涨5.08%。Pagerduty, Inc.股票所在的软件服务行业中，整体涨幅为3.35%。其相关个股中，Pegasystems Inc.、Apptech Payments Corp C/Wts 04/01/2027 、Triller Group Inc C/Wts 15/03/2027 涨幅较大，Femto Technologies Inc.、Microalgo, Inc.、Oblong Inc.较为活跃，换手率分别为15.88%、12.57%、11.91%，振幅较大的相关个股有Triller Group Inc C/Wts 15/03/2027 、Femto Technologies Inc.、百家云，振幅分别为18.07%、15.28%、13.36%。Pagerduty, Inc.公司简介：PagerDuty 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