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PagerDuty, Inc.
18.31
-0.0700
-0.38%
盤前:
17.40
-0.9100
-4.97%
04:31 EDT
成交量:
101.38萬
成交額:
1,854.43萬
市值:
16.68億
市盈率:
-30.93
高:
18.51
開:
18.16
低:
18.00
收:
18.38
資料載入中...
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公司
新聞
公告
【默沙東PD-1抑制劑可瑞達在華獲批局部晚期或轉移性尿路上皮癌治療適應證】默沙東宣佈,其PD-1抑制劑帕博利珠單抗已獲得中國國家藥品監督管理局批准,聯合注射用維恩妥尤單抗用於治療局部晚期或轉移性尿路上皮癌成人患者。此次新適應證獲批是基於全球III期臨牀試驗KEYNOTE-A39研究數據。
金融界
·
01-09
【君實生物:特瑞普利單抗二線及以上治療黑色素瘤獲國家藥監局常規批准】金融界1月6日消息,近日,君實生物的特瑞普利單抗(商品名:拓益®,產品代號:JS001)用於既往接受全身系統治療失敗的不可切除或轉移性黑色素瘤的治療適應症,由附條件批准轉為常規批准。該藥是中國首個批准上市的以PD-1為靶點的國產單抗藥物,至今已在全球開展了超過15個適應症的40多項臨牀研究。其10項適應症已在中國內地獲批,已全部納入《國家醫保目錄(2024年)》。2024年10月,用於復發/轉移性鼻咽癌治療的適應症在中國香港獲批。在國際化佈局方面,該藥已在美國、歐盟等多地獲批上市,澳大利亞和新加坡也分別受理了相關上市許可申請。但醫藥產品具高科技、高風險、高附加值特點,商業化情況存在不確定性。
金融界
·
01-06
金十數據整理:每日美股市場要聞速遞(1月3日 週五)
美港电讯
·
01-03
阿斯利康(AZN.US)PD-1/TIGIT雙抗啓動III期臨牀
智通财经
·
01-03
首個國產幹細胞注射液附條件批准上市,科倫博泰抗PD-L1單抗新藥獲批上市,禮來替爾泊肽在華上市,賽諾菲BTK抑制劑在中國申報上市
医药经济报
·
01-02
科倫博泰PD-L1單抗科泰萊獲批上市 適應症為鼻咽癌
中国网财经
·
01-02
科倫藥業:控股子公司抗PD-L1塔戈利單抗獲批上市
美港电讯
·
01-01
【科倫藥業:控股子公司抗PD-L1塔戈利單抗獲批上市】 科倫藥業1月1日晚間公告,公司控股子公司四川科倫博泰生物醫藥股份有限公司用於治療既往接受過2線及以上化療失敗的復發或轉移性鼻咽癌患者的靶向程序性細胞死亡配體1的創新人源化單克隆抗體塔戈利單抗已獲國家藥監局批准於中國上市。
金融界
·
01-01
【科倫博泰生物-B(06990.HK):抗PD-L1塔戈利單抗獲國家藥監局批准上市】科倫博泰生物-B(06990.HK)發佈公告,公司用於治療既往接受過2線及以上化療失敗的復發或轉移性鼻咽癌患者的靶向程序性細胞死亡配體1(PD-L1)的創新人源化單克隆抗體(單抗)塔戈利單抗(前稱KL-A167)(科泰萊®)已獲中國國家藥品監督管理局(NMPA)批准於中國上市。
金融界
·
2024-12-31
【研報掘金丨浙商證券:首予恆瑞醫藥“買入”評級,2025年開始創新+國際化加速】浙商證券研報指出,歷史上中國醫藥行業經歷多次政策變化,恆瑞醫藥(600276.SH)一直保持相對穩健的增速,充分顯示公司在政策演變中較強韌性。我們看好在2019-2024 年經歷了集採、醫保談判價格波動影響後,公司2025年開始創新+國際化加速,CDK4/6、PD-L1、海曲泊帕、JAK、HER2 ADC、IL-4R、GLP-1等大單品/適應症陸續商業化,驅動公司進入收入增長新一輪加速期,首次覆蓋並給予“買入”評級。
金融界
·
2024-12-25
【富滿微:公司PD類芯片大部分為ASIC架構】富滿微12月23日在互動平台表示,公司PD類芯片大部分為ASIC架構,適用於適配器、充電器等,PD類產品系公司主力產品之一。
金融界
·
2024-12-23
【百利天恆:GNC-038 四特異性抗體注射液項目治療系統性紅斑狼瘡、類風濕關節炎獲臨牀試驗批准】金融界12月23日消息,百利天恆近日收到國家藥品監督管理局正式批准簽發的《藥物臨牀試驗批准通知書》,其自主研發的創新生物藥GNC-038的藥物臨牀試驗獲得批准。GNC-038是一種靶向CD3、4-1BB、PD-L1和CD19的創新重組人源化四特異性抗體,是全球首個進入臨牀開發的四特異性治療性抗體。除新獲批的2個適應症外,目前已開展了1個Ia/Ib期和4個Ib/II期臨牀研究,適應症為急性淋巴細胞白血病和非霍奇金淋巴瘤等血液系統腫瘤。但藥品在獲得批准通知書後,尚需開展臨牀試驗並經批准方可生產上市,具有不確定性。
金融界
·
2024-12-23
基石藥業(02616)重磅產品CS2009(PD-1/VEGF/CTLA-4三抗)在澳大利亞遞交臨牀試驗申請
智通财经
·
2024-12-23
默沙東完成關於在研PD-1/VEGF雙特異性抗體LM-299的全球獨家許可協議
界面
·
2024-12-20
中穎電子12月18日在互動平台上表示,中穎PD協議芯片將在明年啓動市場推廣。
美港电讯
·
2024-12-18
日本國立材料研究所廖梅勇團隊實現金剛石DUV探測器低電壓高增益新突破!
市场资讯
·
2024-12-17
21健訊Daily|兩部門發文完善醫藥集中帶量採購和執行工作機制;默沙東PD-1抑制劑帕博利珠單抗新適應症獲批
21综合
·
2024-12-11
和譽-B(02256):口服PD-L1小分子抑制劑ABSK043聯合伏美替尼治療非小細胞肺癌的 II期臨牀研究完成首例患者給藥
智通财经
·
2024-12-11
默沙東PD-1抑制劑可瑞達在華獲批局部晚期宮頸癌治療適應證
每日经济新闻
·
2024-12-10
默沙東PD-1抑制劑可瑞達在華獲批局部晚期宮頸癌治療適應證
美港电讯
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2024-12-10
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21:19","pubTimestamp":1735910370,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,1月3日,药物临床试验登记与信息公示平台官网显示,阿斯利康(AZN.US)登记了一项 Rilvegostomig 或帕博利珠单抗联合化疗一线治疗转移性非鳞状非小细胞肺癌的全球 III 期研究(CTR20244980)。截图来源:药物临床试验登记与信息公示平台这是一项随机、双盲、多中心、全球、III 期研究,旨在评估 Rilvegostomig 联合化疗与帕博利珠单抗联合化疗相比一线治疗肿瘤表达 PD-L1(TC≥1%)的非鳞状非小细胞肺癌参与者的有效性和安全性。主要终点是 OS 和 PFS。该试验共有 250 家机构参与,国内计划入组132名受试者,国际878名受试者。","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/1233372.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":["III","LU0109394709.USD","AZN","BK4134","LU1169590202.USD","LU2417539215.USD","LU0889565916.HKD","BK4588","PD","BK4585","LU2236285917.USD","BK4023","LU2462157665.USD","LU1829250122.USD","LU1169589451.USD","BK4007","LU0320765992.SGD","LU2456880835.USD","BK4568"],"gpt_icon":0},{"id":"2500784928","title":"首個國產幹細胞注射液附條件批准上市,科倫博泰抗PD-L1單抗新藥獲批上市,禮來替爾泊肽在華上市,賽諾菲BTK抑制劑在中國申報上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2500784928","media":"医药经济报","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2500784928?lang=zh_tw&edition=fundamental","pubTime":"2025-01-02 20:25","pubTimestamp":1735820715,"startTime":"0","endTime":"0","summary":"今日该药获批上市,成为国内同类疗法的一大里程碑。根据科伦博泰公开资料,这是一款抗PD-L1单抗,本次获批的适应症为单药用于既往接受过二线及以上化疗失败的复发或转移性鼻咽癌患者的治疗。赛诺菲BTK抑制剂在中国申报上市!赛诺菲此前新闻稿表示,rilzabrutinib有希望成为首个治疗ITP适应症的BTK抑制剂。","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=nesSN20250102202931a212e27e&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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適應症為鼻咽癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2500137969","media":"中国网财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2500137969?lang=zh_tw&edition=fundamental","pubTime":"2025-01-02 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科倫藥業1月1日晚間公告,公司控股子公司四川科倫博泰生物醫藥股份有限公司用於治療既往接受過2線及以上化療失敗的復發或轉移性鼻咽癌患者的靶向程序性細胞死亡配體1的創新人源化單克隆抗體塔戈利單抗已獲國家藥監局批准於中國上市。","url":"https://stock-news.laohu8.com/highlight/detail?id=2500409604","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2500409604?lang=zh_tw&edition=fundamental","pubTime":"2025-01-01 16:42","pubTimestamp":1735720972,"startTime":"0","endTime":"0","summary":"科伦药业1月1日晚间公告,公司控股子公司四川科伦博泰生物医药股份有限公司用于治疗既往接受过2线及以上化疗失败的复发或转移性鼻咽癌患者的靶向程序性细胞死亡配体1的创新人源化单克隆抗体塔戈利单抗已获国家药监局批准于中国上市。","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/2025/01/01164247020312.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":["PD","BK0060","LU1169590202.USD","BK4023","002422","LU1169589451.USD","161726","LU1064130708.USD","BK0239","LU2148510915.USD","LU1064131003.USD","399441"],"gpt_icon":0},{"id":"2495664072","title":"【科倫博泰生物-B(06990.HK):抗PD-L1塔戈利單抗獲國家藥監局批准上市】科倫博泰生物-B(06990.HK)發佈公告,公司用於治療既往接受過2線及以上化療失敗的復發或轉移性鼻咽癌患者的靶向程序性細胞死亡配體1(PD-L1)的創新人源化單克隆抗體(單抗)塔戈利單抗(前稱KL-A167)(科泰萊®)已獲中國國家藥品監督管理局(NMPA)批准於中國上市。","url":"https://stock-news.laohu8.com/highlight/detail?id=2495664072","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2495664072?lang=zh_tw&edition=fundamental","pubTime":"2024-12-31 18:06","pubTimestamp":1735639600,"startTime":"0","endTime":"0","summary":"科伦博泰生物-B(06990.HK)发布公告,公司用于治疗既往接受过2线及以上化疗失败的复发或转移性鼻咽癌患者的靶向程序性细胞死亡配体1(PD-L1)的创新人源化单克隆抗体(单抗)塔戈利单抗(前称KL-A167)(科泰莱®)已获中国国家药品监督管理局(NMPA)批准于中国上市。","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/2024/12/31180646994450.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":["06990","LU0196878994.USD","BK1161","LU1169589451.USD","PD","BK4023","LU1169590202.USD"],"gpt_icon":0},{"id":"2494097688","title":"【研報掘金丨浙商證券:首予恆瑞醫藥“買入”評級,2025年開始創新+國際化加速】浙商證券研報指出,歷史上中國醫藥行業經歷多次政策變化,恆瑞醫藥(600276.SH)一直保持相對穩健的增速,充分顯示公司在政策演變中較強韌性。我們看好在2019-2024 年經歷了集採、醫保談判價格波動影響後,公司2025年開始創新+國際化加速,CDK4/6、PD-L1、海曲泊帕、JAK、HER2 ADC、IL-4R、GLP-1等大單品/適應症陸續商業化,驅動公司進入收入增長新一輪加速期,首次覆蓋並給予“買入”評級。","url":"https://stock-news.laohu8.com/highlight/detail?id=2494097688","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2494097688?lang=zh_tw&edition=fundamental","pubTime":"2024-12-25 13:50","pubTimestamp":1735105819,"startTime":"0","endTime":"0","summary":"浙商证券研报指出,历史上中国医药行业经历多次政策变化,恒瑞医药(600276.SH)一直保持相对稳健的增速,充分显示公司在政策演变中较强韧性。我们看好在2019-2024 年经历了集采、医保谈判价格波动影响后,公司2025年开始创新+国际化加速,CDK4/6、PD-L1、海曲泊帕、JAK、HER2 ADC、IL-4R、GLP-1等大单品/适应症陆续商业化,驱动公司进入收入增长新一轮加速期,首次覆盖并给予“买入”评级。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":["rate"],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://24h.jrj.com.cn/2024/12/25135046788128.shtml","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":"jinrongjie_stock","symbols":["ADC","600056","600276","601878","PD","GLP"],"gpt_icon":0},{"id":"2493754039","title":"【富滿微:公司PD類芯片大部分為ASIC架構】富滿微12月23日在互動平台表示,公司PD類芯片大部分為ASIC架構,適用於適配器、充電器等,PD類產品系公司主力產品之一。","url":"https://stock-news.laohu8.com/highlight/detail?id=2493754039","media":"金融界","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493754039?lang=zh_tw&edition=fundamental","pubTime":"2024-12-23 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四特異性抗體注射液項目治療系統性紅斑狼瘡、類風濕關節炎獲臨牀試驗批准】金融界12月23日消息,百利天恆近日收到國家藥品監督管理局正式批准簽發的《藥物臨牀試驗批准通知書》,其自主研發的創新生物藥GNC-038的藥物臨牀試驗獲得批准。GNC-038是一種靶向CD3、4-1BB、PD-L1和CD19的創新重組人源化四特異性抗體,是全球首個進入臨牀開發的四特異性治療性抗體。除新獲批的2個適應症外,目前已開展了1個Ia/Ib期和4個Ib/II期臨牀研究,適應症為急性淋巴細胞白血病和非霍奇金淋巴瘤等血液系統腫瘤。但藥品在獲得批准通知書後,尚需開展臨牀試驗並經批准方可生產上市,具有不確定性。","url":"https://stock-news.laohu8.com/highlight/detail?id=2493734438","media":"金融界","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493734438?lang=zh_tw&edition=fundamental","pubTime":"2024-12-23 17:56","pubTimestamp":1734947804,"startTime":"0","endTime":"0","summary":"金融界12月23日消息,百利天恒近日收到国家药品监督管理局正式批准签发的《药物临床试验批准通知书》,其自主研发的创新生物药GNC-038的药物临床试验获得批准。GNC-038是一种靶向CD3、4-1BB、PD-L1和CD19的创新重组人源化四特异性抗体,是全球首个进入临床开发的四特异性治疗性抗体。除新获批的2个适应症外,目前已开展了1个Ia/Ib期和4个Ib/II期临床研究,适应症为急性淋巴细胞白血病和非霍奇金淋巴瘤等血液系统肿瘤。但药品在获得批准通知书后,尚需开展临床试验并经批准方可生产上市,具有不确定性。","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/2024/12/23175646706774.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":["159839","BK1576","688506","BK1141","LU1169589451.USD","LU1169590202.USD","PD","BK4023","BK0239","BK1583","03347"],"gpt_icon":0},{"id":"2493271642","title":"基石藥業(02616)重磅產品CS2009(PD-1/VEGF/CTLA-4三抗)在澳大利亞遞交臨牀試驗申請","url":"https://stock-news.laohu8.com/highlight/detail?id=2493271642","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2493271642?lang=zh_tw&edition=fundamental","pubTime":"2024-12-23 08:41","pubTimestamp":1734914492,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,基石药业今日宣布,公司用于治疗多种实体瘤的管线2.0重磅产品CS2009已在澳大利亚递交临床试验申请。此外,基石药业计划于2025年初首先在澳洲启动CS2009的全球多中心、首次人体研究,未来将陆续扩展至中国及美国。CS2009是一款具有创新结构设计的、同时靶向PD-1、VEGFA及CTLA-4的三特异性抗体。CS2009还可以诱导高效内化,从而减少双阳性TILs细胞表面免疫抑制性分子PD-1和CTLA-4的表达。临床前数据显示,CS2009具有明显优于潜在竞品的抗肿瘤活性。","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/1228187.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":["BK1576","PD","BK1574","BK1161","03347","LU1169589451.USD","02616","BK4023","LU1169590202.USD","BK1583","BK1141"],"gpt_icon":0},{"id":"2492126744","title":"默沙東完成關於在研PD-1/VEGF雙特異性抗體LM-299的全球獨家許可協議","url":"https://stock-news.laohu8.com/highlight/detail?id=2492126744","media":"界面","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2492126744?lang=zh_tw&edition=fundamental","pubTime":"2024-12-20 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II期臨牀研究完成首例患者給藥","url":"https://stock-news.laohu8.com/highlight/detail?id=2490078184","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2490078184?lang=zh_tw&edition=fundamental","pubTime":"2024-12-11 07:04","pubTimestamp":1733871884,"startTime":"0","endTime":"0","summary":"智通财经APP讯,和誉-B 发布公告,公司附属和誉医药宣布已完成“一项评估ABSK043联合伏美替尼治疗 EGFR突变阳性的局部晚期或转移性非小细胞肺癌患者的有效性和安全性的II期开放性临床研究”的首例患者给药。ABSK043是由和誉医药自主研发的一款口服生物利用度好、高选择性、高活性的小分子PD-L1 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