美股詳情

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PagerDuty, Inc.

6.27

-0.3000-4.57%

成交量：185.25萬

成交額：1,165.33萬

市值：5.75億

市盈率：3.85

高：6.51

開：6.41

低：6.19

收：6.57

52周最高：19.70

52周最低：6.19

股本：9,177.68萬

流通股本：8,727.34萬

量比：0.60

換手率：2.12%

股息：- -

股息率：- -

每股收益(TTM):1.63

每股收益(LYR):-0.5920

淨資產收益率：66.13%

總資產收益率：-0.59%

市淨率：1.80

市盈率(LYR):-10.59

資料載入中...

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10:18","pubTimestamp":1771553881,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，基石药业-B宣布公司核心资产CS2009用于晚期实体瘤的II期临床试验IND申请已经获得FDA批准。CS2009用于晚期实体瘤的II期新药临床试验申请获美国食品药品监督管理局批准，标志着这一创新免疫疗法的全球开发取得重要进展。基石药业首席执行官、研发总裁及执行董事杨建新博士表示，非常高兴能够看到CS2009的全球多中心II期临床试验高效推进并获美国FDA批准开展。","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/1405983.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":["BK1161","LU1169589451.USD","BK1574","PD","BK4023","LU1169590202.USD","02616"],"gpt_icon":0},{"id":"2611171921","title":"基石藥業-B(02616)：CS2009(PD-1/VEGF/CTLA-4三特異性抗體)II期臨床試驗申請獲美國FDA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2611171921","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2611171921?lang=zh_tw&edition=fundamental","pubTime":"2026-02-16 08:08","pubTimestamp":1771200501,"startTime":"0","endTime":"0","summary":"智通财经APP讯，基石药业-B 发布公告，公司核心资产CS2009用于晚期实体瘤的II期新药临床试验申请已经获得美国食品药品监督管理局批准。CS2009的I期临床研究初步数据已在2025年欧洲肿瘤内科学会年会上公布，安全性与耐受性良好，抗肿瘤活性数据积极。更多I期和II期临床研究数据预计将在今年召开的美国临床肿瘤学会和ESMO会议上公布。","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/1405604.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_zhitongcaijing","symbols":["BK1574","PD","BK4023","LU1169590202.USD","BK1161","LU1169589451.USD","02616"],"gpt_icon":0},{"id":"2610670395","title":"Genprex在澳大利亞獲得Reqorsa基因療法與PD-L1抗體聯合用於癌症治療的專利保護Genprex Secures Australian Patent for Reqorsa Gene Therapy Combined with PD-L1 Antibodies in Cancer Treatment","url":"https://stock-news.laohu8.com/highlight/detail?id=2610670395","media":"动脉网","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610670395?lang=zh_tw&edition=fundamental","pubTime":"2026-02-10 22:40","pubTimestamp":1770734400,"startTime":"0","endTime":"0","summary":"The patent will provide coverage for the combination therapy across various types of cancers, including lung cancer and other solid tumors. Reqorsa is designed to deliver tumor suppressor genes directly to cancer cells, potentially enhancing the efficacy of existing immunotherapy treatments such as PD-L1 inhibitors.该专利将为包括肺癌和其他实体瘤在内的各种癌症的联合疗法提供保障。","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=nesSN20260210224223a4940e84&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, .wx-sou","directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://gu.qq.com/resources/shy/news/detail-v2/index.html#/?id=nesSN20260210224223a4940e84&s=b","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"tencent","symbols":["BK4023","GNPX","PD","BK4139","LU1169589451.USD","LU1169590202.USD"],"gpt_icon":0},{"id":"2609752625","title":"復宏漢霖PD-1新藥「出海」日本 最早將於2028年產生銷售提成","url":"https://stock-news.laohu8.com/highlight/detail?id=2609752625","media":"证券日报","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2609752625?lang=zh_tw&edition=fundamental","pubTime":"2026-02-08 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":["LU1169590202.USD","HK0000306701.USD","HK0000320223.HKD","HK0000306685.HKD","02696","HK0000165453.HKD","PD","BK4023","LU1169589451.USD","BK1161","HK0000320264.USD"],"gpt_icon":0},{"id":"2609375221","title":"復宏漢霖攜手衞材就抗PD-1單抗漢斯狀達成日本市場合作","url":"https://stock-news.laohu8.com/highlight/detail?id=2609375221","media":"南方财经网","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2609375221?lang=zh_tw&edition=fundamental","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","LU1169589451.USD","BK4588","LU1169590202.USD","PD","HK0000320264.USD","HK0000320223.HKD","BK1161","BK4585","HK0000165453.HKD","BK4023","EWJ","HK0000306701.USD"],"gpt_icon":0},{"id":"2609432256","title":"釋放pipeline in a drug潛力 NLRP3能否催生下一個「藥王」?","url":"https://stock-news.laohu8.com/highlight/detail?id=2609432256","media":"智通财经网","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2609432256?lang=zh_tw&edition=fundamental","pubTime":"2026-02-05 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":"hk","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":["IBD","BK4135","AD","PD","CNS","BBB","BK4023","LU1169590202.USD","BK4132","LU1169589451.USD"],"gpt_icon":0},{"id":"2605290194","title":"阿斯利康(AZN.US)宣佈PD-L1單抗在華獲批新適應症 針對子宮內膜癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2605290194","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2605290194?lang=zh_tw&edition=fundamental","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":"fut","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":["LU1169589451.USD","LU2236285917.USD","BK4568","LU0109394709.USD","LU0320765992.SGD","LU0889565916.HKD","AZN","LU2456880835.USD","BK4585","LU2462157665.USD","BK4588","LU1829250122.USD","PD","BK4023","LU2417539215.USD","BK4007","LU1169590202.USD"],"gpt_icon":0},{"id":"2603621919","title":"港股異動 | 維立志博-B(09887)升逾4% PD-L1/4-1BB雙抗獲FDA快速通道資格","url":"https://stock-news.laohu8.com/highlight/detail?id=2603621919","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603621919?lang=zh_tw&edition=fundamental","pubTime":"2026-01-15 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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":"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/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":["HK0000252152.HKD","HK0000500386.USD","HK0000252160.HKD","BK4023","09887","LU1169589451.USD","LU1169590202.USD","PD","BK1161"],"gpt_icon":1},{"id":"2603539575","title":"港股異動 | 復宏漢霖(02696)再升逾8% 廣譜抗腫瘤PD-L1 ADC HLX43末線食管鱗癌II期數據首次發布","url":"https://stock-news.laohu8.com/highlight/detail?id=2603539575","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603539575?lang=zh_tw&edition=fundamental","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":"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/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":["02696","BK4080","HK0000306685.HKD","HK0000320223.HKD","HK0000165453.HKD","PD","LU1169590202.USD","HK0000320264.USD","BK4023","LU1169589451.USD","ADC","HK0000306701.USD","BK4231","BK1161"],"gpt_icon":0},{"id":"2603357301","title":"PD-1/VEGF雙抗交易熱潮迴歸？榮昌生物簽下56億美元授權","url":"https://stock-news.laohu8.com/highlight/detail?id=2603357301","media":"第一财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603357301?lang=zh_tw&edition=fundamental","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":"other","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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適應症為活動性狼瘡腎炎等疾病","url":"https://stock-news.laohu8.com/highlight/detail?id=2601387879","media":"新浪财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2601387879?lang=zh_tw&edition=fundamental","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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08:01","pubTimestamp":1767571299,"startTime":"0","endTime":"0","summary":"此前，公司公布了芦康沙妥珠单抗联合帕博利珠单抗一线治疗PD-L1阳性NSCLC的3期OptiTROP-Lung05临床试验结果，其在主要终点无进展生存期显示出统计学意义和临床意义的显著改善，并在总生存期方面观察到获益趋势。OptiTROP-Lung05研究是首个免疫联合ADC在一线治疗NSCLC上达到主要终点的3期临床研究。此次在一线治疗PD-L1阳性NSCLC获得突破性疗法认定，将为加速芦康沙妥珠单抗在此适应症审评与上市进程提供助力。","market":"fut","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/1388399.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":["BK4080","BK4231","06990","LU1169589451.USD","LU0196878994.USD","LU1169590202.USD","PD","BK1161","BK4023","ADC"],"gpt_icon":0},{"id":"2600089095","title":"達伯舒新適應症醫保落地 系晚期pMMR子宮內膜癌唯一醫保抗PD-(L)1藥物","url":"https://stock-news.laohu8.com/highlight/detail?id=2600089095","media":"中国网财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2600089095?lang=zh_tw&edition=fundamental","pubTime":"2026-01-01 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建議謹慎申購","url":"https://stock-news.laohu8.com/highlight/detail?id=2592795703","media":"金吾财讯","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2592795703?lang=zh_tw&edition=fundamental","pubTime":"2025-12-17 10:55","pubTimestamp":1765940103,"startTime":"0","endTime":"0","summary":"2023 年5月获FDA批准开展 HX009 Ib/II 期治疗 DLBCL 研究。公司的管线有独特的竞争优势，截至2025年12 月 1 日，全球无已获批的 CD47/PD-1 双特异性抗体产品，HX009在该靶点组合中处于唯一性地位。上市后市值在 38.14-43.59 亿港元，但考虑到公司的 CD47/PD-1 双特异性抗体有一定的独特性，如果上市之后，产品有较大的潜力，建议谨慎申购。","market":"hk","thumbnail":"https://static.szfiu.com/news/20250107/NWEyNjUzNmNkZDE2ZjIxMDg2ODEwOTExNzY3Nw==.png","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20250107/NWEyNjUzNmNkZDE2ZjIxMDg2ODEwOTExNzY3Nw==.png"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"1971704","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":null,"symbols":["03378","BK1535","LU1169590202.USD","LU1169589451.USD","PD","BK4023","BK1173"],"gpt_icon":1},{"id":"2591164645","title":"康辰藥業(603590.SH)：KC1036聯合PD-1抗體和含鉑化療一線治療晚期復發或轉移性食管鱗癌Ⅱ期臨床研究完成首例受試者入組","url":"https://stock-news.laohu8.com/highlight/detail?id=2591164645","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2591164645?lang=zh_tw&edition=fundamental","pubTime":"2025-12-15 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FDA授予百時美施貴寶PD-1療法組合優先審評資格；創新帕金森病免疫療法積極試驗結果公布","url":"https://stock-news.laohu8.com/highlight/detail?id=2590504741","media":"药明康德","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590504741?lang=zh_tw&edition=fundamental","pubTime":"2025-12-12 08:00","pubTimestamp":1765497601,"startTime":"0","endTime":"0","summary":"FDA授予百时美施贵宝PD-1疗法组合优先审评资格百时美施贵宝今日宣布，美国FDA已受理Opdivo的补充生物制品许可申请，用于与多柔比星、长春花碱和达卡巴嗪联合，治疗既往未接受治疗的III期或IV期经典型霍奇金淋巴瘤成人及儿童患者。FDA授予该申请优先审评资格，并将PDUFA日期确定为2026年4月8日。此次FDA受理及优先审评的决定，主要基于3期SWOG S1826研究的积极结果。","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=nesSN20251212092546a443889e&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, 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