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ORR Militia Long/Short Equity ETF
未开盘 06-09 16:00:00 EDT
35.55
-0.04
-0.13%
盘后
35.55
+0.00
0.00%
16:10 EDT
最高
36.00
最低
35.38
成交量
16.48万
今开
35.61
昨收
35.59
日振幅
1.74%
总市值
3.55亿
流通市值
3.55亿
总股本
998.00万
成交额
587.49万
换手率
1.65%
流通股本
998.00万
市净率
--
ROE
--
每股收益
0.00
52周最高
--
52周最低
--
市盈率
--
股息
--
股息收益率
--
ROA
--
分时
五日
日K
周K
月K
数据加载中...
北京优虎网络科技有限公司
资讯
新帖
简况
核心管线数据利空 基石药业股价大跌
21世纪经济报道 · 06-03
核心管线数据利空 基石药业股价大跌
劲方医药-B公布GFH375治疗癌症疗效数据 ORR达40%
财中社 · 06-02
劲方医药-B公布GFH375治疗癌症疗效数据 ORR达40%
核心管线数据利空,基石药业股价大跌超32%
21世纪经济报道 · 06-01
核心管线数据利空,基石药业股价大跌超32%
核药“狂飙”:2026年中外巨头激战300亿美元蓝海
21世纪经济报道 · 04-14
核药“狂飙”:2026年中外巨头激战300亿美元蓝海
营收同比下降33.8%,基石药业押注三抗管线进展如何?
21世纪经济报道 · 04-01
营收同比下降33.8%,基石药业押注三抗管线进展如何?
科赛优®在华获批用于治疗伴有症状、无法手术的丛状神经纤维瘤的1型神经纤维瘤病(NF1-PN)儿童及成人患者
美通社 · 03-30
科赛优®在华获批用于治疗伴有症状、无法手术的丛状神经纤维瘤的1型神经纤维瘤病(NF1-PN)儿童及成人患者
Pan-KRAS赛道的新变量:JAB-23E73的胰腺癌ORR 38.5%背后的估值差
智通财经 · 03-11
Pan-KRAS赛道的新变量:JAB-23E73的胰腺癌ORR 38.5%背后的估值差
达唯珂折戟,创新药研发安全红线再敲警钟
21世纪经济报道 · 03-10
达唯珂折戟,创新药研发安全红线再敲警钟
78亿美金,跨国药企达成闪电并购
药圈观察局 · 02-23
78亿美金,跨国药企达成闪电并购
德曲妥珠单抗胃癌新适应证获批,填补临床治疗空白
上观新闻 · 01-22
德曲妥珠单抗胃癌新适应证获批,填补临床治疗空白
优赫得®在华获批治疗既往接受过一种含曲妥珠单抗治疗方案的局部晚期或转移性HER2阳性成人胃或胃食管结合部腺癌患者
美通社 · 01-22
优赫得®在华获批治疗既往接受过一种含曲妥珠单抗治疗方案的局部晚期或转移性HER2阳性成人胃或胃食管结合部腺癌患者
ORR高达89.5%!智翔金泰BCMA/CD3双抗申报上市
医药魔方 · 01-08
ORR高达89.5%!智翔金泰BCMA/CD3双抗申报上市
君赛生物:聚焦实体瘤“免清淋”突破,GC101预计2026年提交上市申请
新浪科技 · 2025-12-30
君赛生物:聚焦实体瘤“免清淋”突破,GC101预计2026年提交上市申请
多个新药或新适应症获FDA批准,涉及肿瘤、肥胖、肺纤维化等领域
制药网 · 2025-12-24
多个新药或新适应症获FDA批准,涉及肿瘤、肥胖、肺纤维化等领域
KRAS G12D先驱都扛不住了
蓝鲸财经 · 2025-03-10
KRAS G12D先驱都扛不住了
东方亮,西方不亮:出海管线之殇
蓝鲸财经 · 2025-02-19
东方亮,西方不亮:出海管线之殇
DLL3领域的中国时刻
蓝鲸财经 · 2025-02-17
DLL3领域的中国时刻
信达生物与奥赛康药业宣布第三代EGFR TKI 肺癌靶向药物奥壹新®(利厄替尼片)获批上市
美通社 · 2025-01-17
信达生物与奥赛康药业宣布第三代EGFR TKI 肺癌靶向药物奥壹新®(利厄替尼片)获批上市
公司概况
公司名称:
Militia Long/Short Equity ETF
所属市场:
NASDAQ
上市日期:
--
主营业务:
发行价格:
--
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09:14","pubTimestamp":1780362840,"startTime":"0","endTime":"0","summary":"6月2日,劲方医药-B(02595)发布公告,宣布其GFH375单药治疗KRASG12D突变型胆管癌和结直肠癌的初步疗效数据已于6月1日的ASCO年会上进行口头报告。报告显示,20名KRASG12D突变型胆管癌患者的总体客观缓解率(ORR)为40%,疾病控制率(DCR)为95%。在600mgQD(RP2D)剂量水平的18名患者中,ORR为44.4%,DCR为94.4%。","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/202606023756897496.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_eastmoney","symbols":["BK1515","BK1574","09939","02595","ORR","159938","BK1161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2640438958","title":"核心管线数据利空,基石药业股价大跌超32%","url":"https://stock-news.laohu8.com/highlight/detail?id=2640438958","media":"21世纪经济报道","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2640438958?lang=zh_cn&edition=full","pubTime":"2026-06-01 18:05","pubTimestamp":1780308300,"startTime":"0","endTime":"0","summary":"21世纪经济报道记者韩利明6月1日盘前,基石药业(2616.HK)宣布核心资产CS2009(PD-1/VEGF/CTLA-4三特异性抗体)的多项关键临床进展,于美国临床肿瘤学会(ASCO)年会上通过两份壁报正式发布,涵盖一线及后线非小细胞肺癌(NSCLC)及结直肠癌(CRC)患者I/II期临床试验数据,以及晚期实体瘤患者更长随访后的成熟I期临床数据。","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202606013756146980.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/202606013756146980.html","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"stock_eastmoney","symbols":["LU0456854461.SGD","BK4213","LU0266512127.USD","CRC","ORR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2627491097","title":"核药“狂飙”:2026年中外巨头激战300亿美元蓝海","url":"https://stock-news.laohu8.com/highlight/detail?id=2627491097","media":"21世纪经济报道","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2627491097?lang=zh_cn&edition=full","pubTime":"2026-04-14 12:54","pubTimestamp":1776142440,"startTime":"0","endTime":"0","summary":"21世纪经济报道记者季媛媛2026年的春天,核药赛道没有一丝“倒春寒”的迹象。4月中旬,两则消息几乎同时引爆了全球核医学圈。一则是关于“中国原创”的崛起:百洋医药集团孵化企业瑞迪奥研发的99mTc-3PRGD2(吉伦泰)正式获批,这是全球首个用于SPECT显像的广谱肿瘤显像剂,打破了PET技术近30年的垄断。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202604143704207863.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/202604143704207863.html","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":"stock_eastmoney","symbols":["BK4006","CR","ORR","HCC","RDC","BK4161"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624601597","title":"营收同比下降33.8%,基石药业押注三抗管线进展如何?","url":"https://stock-news.laohu8.com/highlight/detail?id=2624601597","media":"21世纪经济报道","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2624601597?lang=zh_cn&edition=full","pubTime":"2026-04-01 18:50","pubTimestamp":1775040648,"startTime":"0","endTime":"0","summary":"继2024年上半年首次实现盈利、全年财务业绩持续改善后,基石药业(2616.HK)2025年业绩再度下滑。年报显示,公司2025年实现收入2.7亿元,同比下降33.8%;年内亏损扩大至4.37亿元,较2024年的0.91亿元亏损增加3.46亿元。在业绩承压的背景下,基石药业同步披露了PD-1/VEGF/CTLA-4三特异性抗体CS2009的最新开发进展及I/II期关键临床数据。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202604013692073178.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/202604013692073178.html","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":"stock_eastmoney","symbols":["LU0053666078.USD","BK4588","BK4585","ORR","BK4107","L","LU0210528500.USD","LU2487616109.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623539793","title":"科赛优®在华获批用于治疗伴有症状、无法手术的丛状神经纤维瘤的1型神经纤维瘤病(NF1-PN)儿童及成人患者","url":"https://stock-news.laohu8.com/highlight/detail?id=2623539793","media":"美通社","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2623539793?lang=zh_cn&edition=full","pubTime":"2026-03-30 15:46","pubTimestamp":1774856760,"startTime":"0","endTime":"0","summary":"成为国内首个且唯一*获批用于3岁及3岁以上该患者人群的治疗药物 上海2026年3月30日 /美通社/ -- 阿斯利康宣布,中国国家药品监督管理局已正式批准科赛优,一种选择性、口服MEK抑制剂,用于3岁及3岁以上伴有症状、无法手术的丛状神经纤维瘤的1型神经纤维瘤病儿童及成人患者的治疗[1]。司美替尼已在美国、欧盟、日本、中国及其他国家/地区获批,用于治疗特定伴有症状且无法手术切除PN的 NF1 儿童患者。","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://wwwold.prnasia.com/story/archive/4922084_ZH22084_1","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":"prnasia","symbols":["LU0109394709.USD","LU1829250122.USD","LU2456880835.USD","LU2462157665.USD","BK4568","BK4588","IE00B3T34201.USD","BK4096","BK4007","LU2417539215.USD","ORR","LU0320765992.SGD","BK4585","LU0289739699.SGD","LU0058720904.USD","LU0889565916.HKD","AZN","LU2236285917.USD","PN"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2618995755","title":"Pan-KRAS赛道的新变量:JAB-23E73的胰腺癌ORR 38.5%背后的估值差","url":"https://stock-news.laohu8.com/highlight/detail?id=2618995755","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2618995755?lang=zh_cn&edition=full","pubTime":"2026-03-11 09:20","pubTimestamp":1773192006,"startTime":"0","endTime":"0","summary":"Pan-KRAS赛道最近披露了一组很值得细看的数据。加科思公布了JAB-23E73在胰腺癌患者中的一期研究结果。目前披露的JAB-23E73安全性数据来自42例患者。RMC-6236的血液及肝肾毒性三级治疗相关不良事件为4%-7%,综合来看JAB-23E73安全性更优。JAB-23E73在160mg以上治疗组中,在可评估的13例KRAS突变胰腺癌患者中,有2例是二线治疗,剩下11例都是三线或三线以上的患者。","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/1412427.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":["ORR","BK1574","BK1161","01167"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2618987798","title":"达唯珂折戟,创新药研发安全红线再敲警钟","url":"https://stock-news.laohu8.com/highlight/detail?id=2618987798","media":"21世纪经济报道","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2618987798?lang=zh_cn&edition=full","pubTime":"2026-03-10 09:14","pubTimestamp":1773105251,"startTime":"0","endTime":"0","summary":"达唯珂由法国药企益普生旗下Epizyme开发,为全球同类首创的EZH2甲基转移酶抑制剂。达唯珂是全球首个且唯一获批用于滤泡性淋巴瘤的口服EZH2抑制剂。此次产品撤市、相关临床试验全面终止后,该细分领域精准治疗方案的空白将再次凸显,临床未满足需求亟待新一代创新药填补。2025年4月,公司以6.085亿美元现金出售上海和黄药业45%股权,仅保留5%股权,全面聚焦创新药研发。","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=nesSN20260310091707a45cda1c&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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19:18","pubTimestamp":1769080687,"startTime":"0","endTime":"0","summary":"由阿斯利康和第一三共共同开发与商业化的优赫得(英文商品名:Enhertu,通用名:注射用德曲妥珠单抗)今天获中国国家药品监督管理局(NMPA)批准,本品单药适用于治疗既往接受过一种含曲妥珠单抗治疗方案的局部晚期或转移性HER2阳性成人胃或胃食管结合部腺癌患者。德曲妥珠单抗是由阿斯利康和第一三共联合开发和商业化的一款独特设计靶向HER2的抗体偶联药物(ADC)。","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/202601223627553572.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":["ORR","BK4195","OS","BK4211","PFS","BK4231","BK4097","BK4080","ADC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2605495703","title":"优赫得®在华获批治疗既往接受过一种含曲妥珠单抗治疗方案的局部晚期或转移性HER2阳性成人胃或胃食管结合部腺癌患者","url":"https://stock-news.laohu8.com/highlight/detail?id=2605495703","media":"美通社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2605495703?lang=zh_cn&edition=full","pubTime":"2026-01-22 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MM的I期研究数据。结果显示,在至少接受了一次疗效评估的57例患者中,客观缓解率为89.5%。","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/stock/relnews/cn/2026-01-08/doc-inhfqyhi5239845.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":["BK0239","688443","ORR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2595412750","title":"君赛生物:聚焦实体瘤“免清淋”突破,GC101预计2026年提交上市申请","url":"https://stock-news.laohu8.com/highlight/detail?id=2595412750","media":"新浪科技","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2595412750?lang=zh_cn&edition=full","pubTime":"2025-12-30 10:41","pubTimestamp":1767062460,"startTime":"0","endTime":"0","summary":"新浪科技讯 12月30日上午消息,日前,聚焦实体瘤创新细胞疗法与创新药开发的上海君赛生物股份有限公司 正式向港交所递交招股书,拟依据港股18A章登陆生物科技板块。 目前,GC101用于治疗黑色素瘤的临床试验正在开展关键II期临床试验,预计将于2026年提交生物制品许可申请;GC101用于治疗非小细胞肺癌的临床管线目前处于Ib期临床。 按照计划,GC101预计2026年提交上市申请,若成功获批,将成为国内首个上市的TIL疗法。","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":"https://finance.sina.com.cn/stock/newstock/2025-12-30/doc-inhepszw4394800.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":"sina","symbols":["BK4139","BK4505","ORR","TIL"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2593176440","title":"多个新药或新适应症获FDA批准,涉及肿瘤、肥胖、肺纤维化等领域","url":"https://stock-news.laohu8.com/highlight/detail?id=2593176440","media":"制药网","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2593176440?lang=zh_cn&edition=full","pubTime":"2025-12-24 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G12D领域敲响了警钟,尤其是对于处在跟随阶段的国内药企来说。很显然,这些国内跟随的选手需要进一步审视其KRAS G12D分子的结构。","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://www.lanjinger.com/d/252604","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":"lanjinger_stock","symbols":["ORR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2512794661","title":"东方亮,西方不亮:出海管线之殇","url":"https://stock-news.laohu8.com/highlight/detail?id=2512794661","media":"蓝鲸财经","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2512794661?lang=zh_cn&edition=full","pubTime":"2025-02-19 17:18","pubTimestamp":1739956689,"startTime":"0","endTime":"0","summary":"海外的临床结果,能否达到中国早期试验的承诺?但很遗憾,结果并不是那么让人满意。最新给出回答的是Corbus 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