美股詳情

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信息服務

5.19

-0.0900-1.70%

盤後：5.200.0101+0.19%19:30 EDT

成交量：57.40萬

成交額：299.42萬

市值：2.51億

市盈率：21.64

高：5.34

開：5.26

低：5.18

收：5.28

52周最高：6.45

52周最低：3.74

股本：4,841.35萬

流通股本：3,555.23萬

量比：3.02

換手率：1.61%

股息：0.18

股息率：3.47%

每股收益(TTM):0.2399

每股收益(LYR):0.1900

淨資產收益率：12.30%

總資產收益率：6.36%

市淨率：2.62

市盈率(LYR):27.32

資料載入中...

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III熒光檢測器，實現UHPLC速度下的高信度痕量分析","url":"https://stock-news.laohu8.com/highlight/detail?id=2637334485","media":"环球市场播报","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2637334485?lang=zh_tw&edition=fundamental","pubTime":"2026-05-21 22:07","pubTimestamp":1779372420,"startTime":"0","endTime":"0","summary":"安捷伦科技公司宣布推出Agilent 1290 Infinity III荧光检测器。这款新型检测器专为现代超高效液相色谱工作流程设计，将荧光检测技术带入UHPLC时代，为实验室提供痕量分析所需的更高置信度。传统荧光检测器并非为UHPLC方法的窄峰和快速分离而设计。1290 Infinity III FLD通过专为现代UHPLC优化的设计填补了这一空白。","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://finance.sina.com.cn/stock/usstock/c/2026-05-21/doc-inhysnxc6275941.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":"sina","symbols":["III","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2637336990","title":"思路迪醫藥股份(01244)：恩維達®非小細胞肺癌新輔助╱輔助治療III期臨床研究提前完成入組","url":"https://stock-news.laohu8.com/highlight/detail?id=2637336990","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2637336990?lang=zh_tw&edition=fundamental","pubTime":"2026-05-21 20:43","pubTimestamp":1779367407,"startTime":"0","endTime":"0","summary":"智通财经APP讯，思路迪医药股份 发布公告，本公司与康宁杰瑞生物制药共同开发的恩维达用于可切除非小细胞肺癌患者新辅助╱辅助治疗的随机、对照、双盲、多中心III期临床研究已提前完成入组。本次III期临床研究由天津医科大学肿瘤医院王长利教授担任主要研究者，在全国约60家临床研究中心开展，计划入组约390例可切除III期非小细胞肺癌患者，实际入组人数符合研究方案要求，已提前完成入组工作。","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/1444708.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","BK1161","01244","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2636285087","title":"Bimzelx頭對頭III期研究告捷，斑塊狀銀屑病關節炎指標顯著優於Skyrizi","url":"https://stock-news.laohu8.com/highlight/detail?id=2636285087","media":"环球市场播报","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2636285087?lang=zh_tw&edition=fundamental","pubTime":"2026-05-19 23:01","pubTimestamp":1779202886,"startTime":"0","endTime":"0","summary":"　　比利时生物制药企业优时比公布了其IL-17A/IL-17F抑制剂Bimzelx的III期BE BOLD研究详细数据。结果显示，Bimzelx在治疗活动性银屑病关节炎患者的关键指标上，击败了艾伯维的重磅IL-23抑制剂Skyrizi。早在治疗第4周，Bimzelx组达到ACR50的患者比例便显著高于Skyrizi组。Bimzelx治疗组念珠菌感染的发生率较高，但均为轻中度，未导致停药。","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://finance.sina.com.cn/stock/usstock/c/2026-05-19/doc-inhymytc2158400.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":"sina_us","symbols":["BK4134","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2636863428","title":"港股異動 | 維立志博-B(09887)早盤升逾4% 維利信™治療晚期肺外神經內分泌癌III期臨床研究獲批","url":"https://stock-news.laohu8.com/highlight/detail?id=2636863428","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2636863428?lang=zh_tw&edition=fundamental","pubTime":"2026-05-19 09:53","pubTimestamp":1779155590,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，维立志博-B早盘涨超4%，截至发稿，涨3.21%，报64.35港元，成交额897.51万港元。消息面上，5月19日，维立志博-B发布公告，中华人民共和国国家药品监督管理局药品审评中心已批准开展评价维利信联合含铂化疗作为一线治疗在晚期肺外神经内分泌癌患者中的确证性III期临床研究。该研究获批是基于奥帕替苏米单抗在Ib/II期概念验证性研究中所展现的突破性疗效与良好安全性。","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/1443260.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":["BK4585","BK4588","VXUS","III","BK1161","BK4134","HK0000252152.HKD","09887","HK0000252160.HKD","HK0000500386.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2636022270","title":"維立志博-B(09887)：維利信™(PD-L1/4-1BB雙特異性抗體奧帕替蘇米單抗，LBL-024)治療晚期肺外神經內分泌癌的III期臨床研究獲得CDE批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2636022270","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2636022270?lang=zh_tw&edition=fundamental","pubTime":"2026-05-19 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期临床试验中展示出全球首创或同类最优潜力。","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/1443206.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":["LU1223082196.USD","LU1169590202.USD","09887","BK4017","HK0000500386.USD","BK4134","BK4023","BK1161","CDE","III","LU1223082519.USD","HK0000252160.HKD","HK0000252152.HKD","LU1169589451.USD","LU1223083913.SGD","PD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635761328","title":"港股異動 | 來凱醫藥-B(02105)午前升逾5% LAE002 III期臨床到達終點 將提交上市申請","url":"https://stock-news.laohu8.com/highlight/detail?id=2635761328","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2635761328?lang=zh_tw&edition=fundamental","pubTime":"2026-05-14 11:58","pubTimestamp":1778731118,"startTime":"0","endTime":"0","summary":"消息面上，来凯医药核心产品AKT抑制剂LAE002治疗乳腺癌的III期临床试验已于4月15日宣布达到主要终点。根据公司计划，将协同合作伙伴齐鲁制药于近期向国家药监局提交新药上市申请。齐鲁制药也于4月30日宣布将推进该药的国内上市申请。作为回报，若LAE002在中国获批首个适应症，来凯医药有权获得5.3亿元不可退还的首付款与总计最高20.45亿元的里程碑款项。","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/1441599.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","VXUS","IPOS","BK4588","BK4134","BK4585","02105","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635750797","title":"眾生藥業：公司正在積極推進RAY1225注射液的III期臨床試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2635750797","media":"中金财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2635750797?lang=zh_tw&edition=fundamental","pubTime":"2026-05-14 08:51","pubTimestamp":1778719865,"startTime":"0","endTime":"0","summary":"证券之星消息，众生药业(002317)05月13日在投资者关系平台上答复投资者关心的问题。投资者提问：公司的RAY1225创新三期试验进展如何？减重版三期试验什么时间全部结束？读取数据大概需要多长时间？众生药业回复：您好！公司正在积极推进RAY1225注射液的III期临床试验，有关创新药的进展情况请以公司公告为准。谢谢！为证券之星据公开信息整理，由AI算法生成(网信算备310104345710301240019号)，不构成投资建议。","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://sc.stock.cnfol.com/gushiyaowen/20260514/32223258.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":"zhongjincaijing_highlight","symbols":["BK4134","002317","BK0239","BK0077","III","BK0188"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2635278901","title":"新股前瞻|大單品進入III期臨床，現金流告急的質肽生物就差臨門一腳？","url":"https://stock-news.laohu8.com/highlight/detail?id=2635278901","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2635278901?lang=zh_tw&edition=fundamental","pubTime":"2026-05-13 10:23","pubTimestamp":1778639015,"startTime":"0","endTime":"0","summary":"目前，该药物正在中国开展减重II期临床，有望填补口服多肽GLP-1市场空白。公司已于2026年1月在中国完成了ZT002用于肥胖症治疗的III期临床试验的首例患者入组。","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/1441033.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":["159399","BK4134","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2634476449","title":"港股異動 | 銀諾醫藥-B(02591)午前升逾43% Suba的III期減重數據預計2026年年底前公布","url":"https://stock-news.laohu8.com/highlight/detail?id=2634476449","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2634476449?lang=zh_tw&edition=fundamental","pubTime":"2026-05-11 11:37","pubTimestamp":1778470647,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，银诺医药-B午前涨超43%，截至发稿，涨42.21%，报17.99港元，成交额1.73亿港元。消息面上，银诺医药年度业绩显示，2025 年实现收入1.32亿元，亏损3.41亿元。值得注意的是，银诺医药基石投资者的禁售期将于2026年5月14日届满，相关股份将于5月15日正式解禁流通。Suba的III期减重数据预计2026年年底前公布。治疗肥胖及超重的III期临床研究，已于2025年完成患者入组。","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/1440054.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"2","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["02591","BK4588","BK4134","BK1161","VXUS","BK4585","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2633182090","title":"翰宇藥業(300199.SZ)：司美格魯肽注射液減重及降糖兩項國內適應症的III期臨床試驗均獲得達到等效標準","url":"https://stock-news.laohu8.com/highlight/detail?id=2633182090","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2633182090?lang=zh_tw&edition=fundamental","pubTime":"2026-05-06 19:13","pubTimestamp":1778065991,"startTime":"0","endTime":"0","summary":"智通财经APP讯，翰宇药业(300199.SZ)发布公告，近日，公司司美格鲁肽注射液取得了III期临床数据，数据显示，该药物的减重及降糖两项国内适应症的III期临床试验均获得了达到等效标准。公司司美格鲁肽注射液在国内进行了两项临床试验，分别是：一项在二甲双胍单药治疗血糖控制不佳的2型糖尿病患者中比较HY310注射液与诺和泰®治疗32周的疗效和安全性的多中心、随机、开放设计的III期临床研究。一项在肥胖患者中比较HY310注射液与诺和盈®治疗44周的疗效和安全性的多中心、随机、开放设计的III期临床研究。","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/1438679.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":["BK0070","300199","BK4134","BK0239","III","BK0028","BK0077","BK0188"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":9,"pageCount":7,"totalSize":172,"code":"91000000","status":"200"}]}}