美股詳情

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信息服務

4.12

-0.1400-3.29%

盤後：4.120.00000.00%19:34 EDT

成交量：16.93萬

成交額：69.72萬

市值：1.97億

市盈率：19.62

高：4.26

開：4.26

低：4.06

收：4.26

52周最高：6.45

52周最低：3.74

股本：4,788.41萬

流通股本：3,498.93萬

量比：0.88

換手率：0.48%

股息：0.18

股息率：4.37%

每股收益(TTM):0.2100

每股收益(LYR):0.1900

淨資產收益率：11.17%

總資產收益率：5.99%

市淨率：2.09

市盈率(LYR):21.68

資料載入中...

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发布公告，本集团自主研发的创新药安奈拉唑钠肠溶片近日获得中国国家药品监督管理局药品审评中心批准，开展含安奈拉唑钠肠溶片的铋剂四联疗法根除幽门螺杆菌的III期临床研究。本次安奈拉唑钠新适应症III期临床试验申请获批，有助于拓展产品适应症范围，提升本公司在消化疾病治疗领域的影响力，对本公司长远发展及商业化布局具有重要意义。","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/1428565.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":["BK4134","III","BK1191","02575"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627498112","title":"港股異動 | 再鼎醫藥(09688)升逾3% 近日與安進達成全球臨床合作 Zoci正處於全球註冊性臨床III期階段","url":"https://stock-news.laohu8.com/highlight/detail?id=2627498112","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627498112?lang=zh_tw&edition=fundamental","pubTime":"2026-04-14 09:46","pubTimestamp":1776131184,"startTime":"0","endTime":"0","summary":"消息面上，近日，再鼎医药官微宣布，公司与安进公司达成一项全球临床研究合作，旨在评估再鼎医药处于临床阶段的靶向delta样配体3的抗体药物偶联物zocilurtatug pelitecan联合安进IMDELLTRA，一款靶向DLL3的双特异性T细胞衔接器疗法，用于治疗广泛期小细胞肺癌患者。作为该合作协议的一部分，安进将申办一项全球1b期研究，评估zoci联合IMDELLTRA在ES-SCLC患者中的安全性和有效性。再鼎医药将保留zoci的完整所有权，并将向安进提供临床研究用药。","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/1428082.html","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":"stock_zhitongcaijing","symbols":["LU1023059063.AUD","LU2112291526.USD","IE00B2B36J28.USD","ZLAB","BK4585","IE0009355771.USD","BK1161","BK4139","LU2468319806.SGD","IE00BFTCPJ56.SGD","LU0320765992.SGD","BK4534","LU0109394709.USD","LU1983299246.USD","BK4531","BK4533","BK4526","IE00BJJMRZ35.SGD","LU0058720904.USD","LU2242646821.SGD","SG9999001440.SGD","BK1574","BK4548","LU0289739699.SGD","LU1057294990.SGD","VXUS","III","BK4134","BK4566","IE00BJT1NW94.SGD","LU0889565916.HKD","BK4581","BK1588","LU1571399168.USD","IE00B4R5TH58.HKD","AMGN","LU2242652126.USD","09688","LU1061106388.HKD","LU2488822045.USD","LU0868494617.USD","BK4588","BK4599","LU0122379950.USD","LU2089984988.USD","IE0002141913.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627481537","title":"港股異動 | 科笛-B(02487)升逾3%  CU-20101（注射用A型肉毒毒素）完成中國III期臨床試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2627481537","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627481537?lang=zh_tw&edition=fundamental","pubTime":"2026-04-13 13:37","pubTimestamp":1776058657,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，科笛-B(02487)涨超3%，截至发稿，涨3.25%，报4.76港元，成交额40.99万港元。消息面上，科笛今日宣布，集团完成CU-20101（注射用A型肉毒毒素）用于改善中度至重度眉间纹的中国III期临床试验。该临床试验旨在评估CU-20101单次及重复注射治疗中重度眉间纹的有效性和安全性。该临床试验以参比制剂保妥适®注射用A型肉毒毒素（“BOTOX®”）作为对照。该临床试验于2025年11月完成所有受试者出组，并于2026年1月完成数据库锁定且取得积极的顶线结果。","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/1427621.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":["BK4588","BK4134","BK4585","III","02487","BK1161","VXUS"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627629100","title":"做好信息服務破解人崗錯配","url":"https://stock-news.laohu8.com/highlight/detail?id=2627629100","media":"滚动播报","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627629100?lang=zh_tw&edition=fundamental","pubTime":"2026-04-13 09:10","pubTimestamp":1776042600,"startTime":"0","endTime":"0","summary":"解决这些问题，关键是建立一个统一、智能的就业信息服务平台。鼓励市场化人力资源服务机构参与公益性信息服务，给予税收优惠等支持。以精准信息服务打通毕业生就业“最后一公里”，让人才与岗位在透明、高效的信息环境中精准匹配，是以数字赋能提升人力资源配置效率的有益探索。","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":"https://finance.sina.com.cn/jjxw/2026-04-13/doc-inhuihzn4873373.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":"2627102514","title":"科笛-B(02487)：CU-20101(注射用A型肉毒毒素)用於改善中度至重度眉間紋完成中國III期臨床試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2627102514","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2627102514?lang=zh_tw&edition=fundamental","pubTime":"2026-04-13 08:18","pubTimestamp":1776039501,"startTime":"0","endTime":"0","summary":"智通财经APP讯，科笛-B 发布公告，本集团完成CU-20101用于改善中度至重度眉间纹的中国III期临床试验。在安全性方面，CU-20101的整体安全性良好，未发生导致提前煺出试验或导致死亡的不良事件，且未发生治疗有关的严重不良事件。CU-20101与BOTOX的安全性评估情况相近，未出现新的安全性信号。CU-20101多次重复注射给药后的有效性及安全性表现与单次用药相似。CU-20101将进一步丰富本集团的皮肤产品矩阵，并有利于与本集团现有产品形成协同效应。","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/1427503.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":["BK4134","02487","III","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2626188654","title":"深桑達Ａ：公司研發重點圍繞數字與信息服務業務中的「雲數智」相關產品","url":"https://stock-news.laohu8.com/highlight/detail?id=2626188654","media":"中金财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626188654?lang=zh_tw&edition=fundamental","pubTime":"2026-04-09 17:33","pubTimestamp":1775727194,"startTime":"0","endTime":"0","summary":"证券之星消息，深桑达Ａ04月09日在投资者关系平台上答复投资者关心的问题。公司研发重点围绕数字与信息服务业务中的“云数智”相关产品、产业服务业务中的洁净室和智能运维等相关产品及工艺展开，具体情况请关注公司将披露的2025年年度报告。","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://sc.stock.cnfol.com/gushiyaowen/20260409/32134181.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":"zhongjincaijing_highlight","symbols":["III","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2626975845","title":"開山股份(300257.SZ)肯尼亞Menengai III 35兆瓦地熱電站投入商業運營","url":"https://stock-news.laohu8.com/highlight/detail?id=2626975845","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2626975845?lang=zh_tw&edition=fundamental","pubTime":"2026-04-09 07:54","pubTimestamp":1775692490,"startTime":"0","endTime":"0","summary":"智通财经APP讯，开山股份(300257.SZ)公告，公司下属公司Orpower Twenty Two Limited公司(简称“Orpower22”)顺利完成了肯尼亚Menengai III 35兆瓦地热电站的可靠性测试，该电站机组调试、测试工作已圆满结束。Menengai III 35兆瓦地热电站已于2026年3月10日正式投入商业运营。","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/1426300.html","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":"stock_zhitongcaijing","symbols":["300257","BK0117","BK0188","BK4134","BK0196","BK0259","III","BK0070"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1105607138","title":"眾議院民主黨人要求緊急投票以阻止「第三次世界大戰」","url":"https://stock-news.laohu8.com/highlight/detail?id=1105607138","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1105607138?lang=zh_tw&edition=fundamental","pubTime":"2026-04-08 02:02","pubTimestamp":1775584951,"startTime":"0","endTime":"0","summary":"众议院民主党高层呼吁议员立即返回华盛顿，就终止伊朗战争进行投票。由纽约州民主党领袖哈基姆·杰弗里斯及其他众议院民主党主要议员联合签署的声明指出，特朗普总统已“完全失控”，必须通过投票阻止其“将国家拖入第三次世界大战”。\n目前众议院休会至下周一。今年三月，一项反对伊朗战争的两党《战争权力决议案》曾以212票赞成、219票反对的结果在众议院被否决，当时议员投票结果基本按党派划线划分。\n（本文结束）道琼斯通讯社\n2026年4月7日 14:01 ET（18:01 GMT）\n版权所有（c）2026 道琼斯公司","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":"","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":["III","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1175143092","title":"美國對失蹤飛行員信息泄露事件展開調查","url":"https://stock-news.laohu8.com/highlight/detail?id=1175143092","media":"投资观察","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1175143092?lang=zh_tw&edition=fundamental","pubTime":"2026-04-07 01:34","pubTimestamp":1775496862,"startTime":"0","endTime":"0","summary":"美国总统特朗普表示，当局已启动调查程序，追查有关失踪飞行员的信息如何被泄露给媒体。\"我们正在全力追查泄密者，\"他表态称。特朗普指责相关报道危及了在伊朗开展的救援行动。\n特朗普透露，计划要求首家报道救援行动的媒体公司公开其消息来源，但未具体点名涉事机构。\"要么交出线人，要么面临牢狱之灾，\"总统警告称，\"他们的行为不仅将那名飞行员置于险境，更连累了数百名参与搜救的人员。\"\n（本文源自道琼斯通讯社实时报道合集，完整内容可通过检索代码P/WSJL获取）\n（报道截止时间：2026年4月6日13:32美国东部时间/17:32格林威治时间）","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":"","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":["III","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624017509","title":"西藏自治區互聯網新聞信息服務單位許可信息","url":"https://stock-news.laohu8.com/highlight/detail?id=2624017509","media":"中国西藏新闻网","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624017509?lang=zh_tw&edition=fundamental","pubTime":"2026-04-02 20:35","pubTimestamp":1775133300,"startTime":"0","endTime":"0","summary":"截至2026年3月31日，经西藏自治区互联网信息办公室审批的互联网新闻信息服务单位总计86家，具体服务形式包括：互联网站19个、应用程序14个、公众账号440个，共计473个服务项。","market":"sg","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/jjxw/2026-04-02/doc-inhtcnfv4278286.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":["159792","III","160636","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624123594","title":"百利天恒：iza-bren聯合用藥獲2個II/III期臨床試驗批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2624123594","media":"每日经济新闻","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624123594?lang=zh_tw&edition=fundamental","pubTime":"2026-04-01 18:06","pubTimestamp":1775038011,"startTime":"0","endTime":"0","summary":"每经AI快讯，4月1日，百利天恒(688506.SH)公告称，公司近日收到国家药监局签发的2个《药物临床试验批准通知书》，公司自主研发的创新生物药iza-bren(EGFR×HER3双抗ADC)的2个联合用药方案获得批准。获批适应症包括：联合阿比特龙±奥拉帕利、联合奥拉帕利用于去势抵抗性前列腺癌；联合贝伐珠单抗±化疗、联合奥拉帕利±贝伐珠单抗±化疗用于晚期卵巢癌。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202604013692048171.html","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://finance.eastmoney.com/a/202604013692048171.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":["BK0239","91194","BK4134","III","02615","688506"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624562436","title":"港股異動 | 歐康維視生物-B(01477)午後升逾16% OT-211治療乾眼症III期臨床試驗完成首例患者入組","url":"https://stock-news.laohu8.com/highlight/detail?id=2624562436","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624562436?lang=zh_tw&edition=fundamental","pubTime":"2026-04-01 14:26","pubTimestamp":1775024786,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，欧康维视生物-B午后涨超16%，截至发稿，涨15.33%，报8.5港元，成交额2606.87万港元。消息面上，欧康维视生物发布公告称，OT-211在中国开展的III期临床试验已完成首例患者入组。首例患者成功入组标志着OT-211在中国的临床开发取得重要里程碑进展，并体现了集团致力于为DED患者推进创新疗法。公开资料显示，Alcon Inc.开发出AR-15512的0.003%浓度滴眼液配方，并完成一项IIb期及三项III期临床试验。OT-211已于2025年5月28日获FDA批准用于治疗DED的体征及症状。","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/1423857.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":["BK4588","VXUS","BK1191","III","BK1574","01477","BK4134","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623583940","title":"康寧傑瑞製藥-B(09966)：KN026新輔助治療HER2陽性乳腺癌III期臨床研究達到主要終點","url":"https://stock-news.laohu8.com/highlight/detail?id=2623583940","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2623583940?lang=zh_tw&edition=fundamental","pubTime":"2026-03-31 19:03","pubTimestamp":1774955020,"startTime":"0","endTime":"0","summary":"BC是中国女性发病率最高的恶性肿瘤，其中HER2阳性亚型约占20%至30%。该研究旨在比较KN026联合HB1801±卡铂对比曲妥珠单抗联合帕妥珠单抗和多西他赛±卡铂新辅助治疗早期和局部晚期HER2阳性BC的有效性及安全性。","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/1423118.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":["III","BK1574","BK1161","09966","BK4134"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623347904","title":"宜明昂科-B(01541)：IMM0306治療複發性╱難治性濾泡性淋巴瘤的III期臨床試驗完成首例患者給藥","url":"https://stock-news.laohu8.com/highlight/detail?id=2623347904","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2623347904?lang=zh_tw&edition=fundamental","pubTime":"2026-03-31 00:28","pubTimestamp":1774888085,"startTime":"0","endTime":"0","summary":"智通财经APP讯，宜明昂科-B 发布公告，IMM0306联合来那度胺治疗复发性╱难治性滤泡性淋巴瘤的III期临床试验顺利完成首例患者给药。由本集团独立研发的IMM0306是一种靶向分化簇47 及分化簇20 的双特异性分子，是全球首个进入临床阶段的CD47和CD20双靶向双特异性分子。截至本公告日期，本集团拥有IMM0306的全球知识产权及商业化权利。","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/1422402.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":["BK4134","III","BK1161","01541"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623346987","title":"歐康維視生物-B(01477)：OT-211 III期臨床試驗完成首例患者入組","url":"https://stock-news.laohu8.com/highlight/detail?id=2623346987","media":"智通财经","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2623346987?lang=zh_tw&edition=fundamental","pubTime":"2026-03-30 22:05","pubTimestamp":1774879506,"startTime":"0","endTime":"0","summary":"智通财经APP讯，欧康维视生物-B 发布公告，OT-211 在中国开展的III期临床试验已完成首例患者入组。OT-211 为一种 0.003%浓度滴眼液配方，亦为首款获美国食品药品监督管理局批准用于治疗干眼症的TRPM8激动剂。首例患者成功入组标志着OT-211在中国的临床开发取得重要里程碑进展，并体现了集团致力于为DED患者推进创新疗法。OT-211 已于2025年5月 28日获FDA批准用于治疗DED的体征及症状。","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/1422176.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"0","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":"stock_zhitongcaijing","symbols":["01477","BK4134","BK1191","III","BK1574"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2622830947","title":"益方生物(688382.SH)：D-2570治療銀屑病註冊性III期臨床試驗完成全部受試者入組","url":"https://stock-news.laohu8.com/highlight/detail?id=2622830947","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2622830947?lang=zh_tw&edition=fundamental","pubTime":"2026-03-26 16:48","pubTimestamp":1774514885,"startTime":"0","endTime":"0","summary":"智通财经APP讯，益方生物(688382.SH)公告，公司自主研发的TYK2抑制剂D-2570用于治疗中重度斑块状银屑病(PsO)的注册性III期临床试验已于近日完成全部受试者入组。公告显示，D-2570是公司自主研发的一款靶向酪氨酸激酶2(TYK2)的新型口服选择性抑制剂，用于治疗银屑病等自身免疫性疾病。D-2570通过选择性结合TYK2假激酶域JH2部位，抑制TYK2激酶的活性，进而阻断TYK2依赖性的细胞因子信号传导介导的STAT蛋白的磷酸化，抑制炎症因子释放，参与免疫调节。","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/1419477.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":["688382","BK4134","BK0239","III"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2622881272","title":"港股異動 | 軒竹生物-B(02575)早盤升逾18% 吡洛西利III期BRIGHT-2臨床研究結果於國際醫學頂刊發表","url":"https://stock-news.laohu8.com/highlight/detail?id=2622881272","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2622881272?lang=zh_tw&edition=fundamental","pubTime":"2026-03-26 09:47","pubTimestamp":1774489669,"startTime":"0","endTime":"0","summary":"智通财经APP获悉，轩竹生物-B早盘涨超18%，截至发稿，涨11.85%，报40.58港元，成交额1886.4万港元。消息面上，3月24日，轩竹生物-B发布公告，公司自主研发的新型CDK2/4/6抑制剂吡洛西利的III期BRIGHT-2临床研究最终分析结果，已于近日在国际顶尖医学期刊《美国医学会杂志·肿瘤学》正式在线全文发表。公司曾于2025年4月在《Nature Communications》期刊上公布BRIGHT-2研究的中期分析结果。","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/1419250.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":["BK0114","BK4588","BK1191","VXUS","BK4134","000516","BK0042","02575","BK0046","BK0146","BK0181","BK0096","BK0236","III","BK0188","BK0077","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2622292100","title":"基石藥業-B(02616)：舒格利單抗再獲ESMO指南【I， A】推薦 ——用於III期非小細胞肺癌鞏固治療","url":"https://stock-news.laohu8.com/highlight/detail?id=2622292100","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2622292100?lang=zh_tw&edition=fundamental","pubTime":"2026-03-25 17:20","pubTimestamp":1774430400,"startTime":"0","endTime":"0","summary":"智通财经APP讯，基石药业-B 发布公告，公司核心商业化产品舒格利单抗获得欧洲肿瘤内科学会指南的级推荐。2025年2月，舒格利单抗联合化疗已获得ESMO《非驱动基因阳性转移性非小细胞肺癌动态临床指南》的推荐，用于鳞状及非鳞状IV期非小细胞肺癌双适应症的一线治疗。至此，舒格利单抗在欧盟及英国获批的两项肺癌适应症均已被纳入ESMO指南，充分体现了其临床价值。","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/1418760.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":["BK4134","BK1161","III","02616","BK1574"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2621206968","title":"軒竹生物-B(02575)：吡洛西利聯合氟維司群治療HR+/HER2-晚期乳腺癌III期臨床研究最終分析結果於國際頂尖期刊《JAMA Oncology》發表","url":"https://stock-news.laohu8.com/highlight/detail?id=2621206968","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2621206968?lang=zh_tw&edition=fundamental","pubTime":"2026-03-24 19:12","pubTimestamp":1774350738,"startTime":"0","endTime":"0","summary":"智通财经APP讯，轩竹生物-B 发布公告，公司自主研发的新型CDK2/4/6抑制剂吡洛西利的III期BRIGHT-2临床研究最终分析结果，已于近日在国际顶尖医学期刊《美国医学会杂志·肿瘤学》正式在线全文发表。BRIGHT-2研究最终分析结果显示，吡洛西利联合氟维司群为患者带来了具有临床意义且持久稳健的获益。","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/1418161.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":["02575","BK4203","BK4134","BK1191","BK4225","III","HR"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":9,"pageCount":6,"totalSize":167,"code":"91000000","status":"200"}]}}