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ORR Militia Long/Short Equity ETF
盘后交易 05-26 19:02:41 EDT
36.41
+0.19
+0.52%
盘后
36.41
+0.00
0.00%
16:10 EDT
最高
36.50
最低
36.07
成交量
9.83万
今开
36.20
昨收
36.22
日振幅
1.19%
总市值
3.70亿
流通市值
3.70亿
总股本
1,015万
成交额
357.33万
换手率
0.97%
流通股本
1,015万
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
新股前瞻|布局TCE肿瘤疗法千亿蓝海,时迈药业能否博得市场青睐?
智通财经 · 2025-12-09
新股前瞻|布局TCE肿瘤疗法千亿蓝海,时迈药业能否博得市场青睐?
吉利德Anito-cel 神经毒性低,2年多发性骨髓瘤生存率高 | ASH25
Minhua笔记 · 2025-12-08
吉利德Anito-cel 神经毒性低,2年多发性骨髓瘤生存率高 | ASH25
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
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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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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":["BK4585","LU0053666078.USD","ORR","LU0210528500.USD","BK4588","BK4107","LU2487616109.SGD","L"],"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":"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://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":["LU0320765992.SGD","LU1829250122.USD","LU2417539215.USD","BK4007","BK4585","LU2462157665.USD","AZN","BK4588","LU0889565916.HKD","LU2456880835.USD","LU0058720904.USD","BK4096","PN","BK4568","ORR","LU0289739699.SGD","IE00B3T34201.USD","LU2236285917.USD","LU0109394709.USD"],"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":"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/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":["BK1574","01167","ORR","BK1161"],"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":["BK4097","BK4211","ORR","PFS","BK4080","ADC","BK4231","OS","BK4195"],"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 18:38","pubTimestamp":1769078280,"startTime":"0","endTime":"0","summary":"研究显示,对于局部晚期或转移性HER2阳性成人胃或胃食管结合部腺癌患者,与雷莫西尤单抗+紫杉醇相比,德曲妥珠单抗带来具有显著统计学差异和临床意义的总生存期改善。自一年多前首次在中国获批用于HER2阳性局部晚期或转移性胃癌以来,德曲妥珠单抗仅可用于三线及后线治疗。","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/4868984_ZH68984_1","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":"prnasia","symbols":["CSCO","LU1244550494.USD","IE00BFMHRM44.USD","BK4579","LU1880398554.USD","LU2237443622.USD","LU2506952097.USD","OS","BK4097","LU0109394709.USD","IE000M9KFDE8.USD","BK4612","ORR","LU1929549753.HKD","LU2237443382.USD","AZN","LU0234572021.USD","LU1244550577.SGD","BK4588","LU1066051498.USD","LU2247934214.USD","LU1571399168.USD","LU0868494617.USD","BK4195","LU2506951875.HKD","LU1196500208.SGD","LU2506951958.HKD","LU2417539215.USD","SG9999015978.USD","LU1066053197.SGD","LU0792757196.USD","BK4527","LU2462157665.USD","LU0320765992.SGD","LU1894683348.USD","BK4231","LU1046421795.USD","LU1221951046.USD","SG9999001440.SGD","LU2237443895.HKD","IE00BKVL7J92.USD","ADC","BK4080","LU1880398471.USD","BK4560","PFS","LU1221951129.SGD","LU2237443549.SGD","SG9999015945.SGD","BK4585"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2601490365","title":"ORR高达89.5%!智翔金泰BCMA/CD3双抗申报上市","url":"https://stock-news.laohu8.com/highlight/detail?id=2601490365","media":"医药魔方","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2601490365?lang=zh_cn&edition=full","pubTime":"2026-01-08 19:01","pubTimestamp":1767870060,"startTime":"0","endTime":"0","summary":"1月8日,智翔金泰宣布双抗药物GR1803的附条件上市申请已获得国家药监局受理,用于治疗既往至少接受过三线治疗的复发或难治性多发性骨髓瘤成人患者。GR1803是智翔金泰自主研发的一款BCMA/CD3双抗药物,其结合BCMA的亲和力较结合CD3的亲和力高两个数量级。2025年11月,智翔金泰在ASH 2025年会上公布了GR1803治疗R/R 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":"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/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":["688443","ORR","BK0239"],"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":"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/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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四款创新药物处于临床阶段智通财经APP了解到,时迈药业目前仍处于临床研发阶段,并无产品商业化。根据时迈药业招股书披露,当前仅有两款用于实体瘤的TCE药物获得全球批准,市场存在大量空白,这为具备相关布局能力的创新药企提供了结构性机遇。","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/1379203.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":["BK4231","BK4588","BK4187","BK4080","LU0053666078.USD","IE00B19Z4B17.USD","L","BK4585","IE00B7SZL793.SGD","IE0031619046.USD","BK4006","IE00B66KJ199.SGD","LU0963586101.USD","BK4107","LU2065731478.USD","CRS","LU2487616109.SGD","ADC","LU0210528500.USD","ORR"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2590451393","title":"吉利德Anito-cel 神经毒性低,2年多发性骨髓瘤生存率高 | ASH25","url":"https://stock-news.laohu8.com/highlight/detail?id=2590451393","media":"Minhua笔记","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2590451393?lang=zh_cn&edition=full","pubTime":"2025-12-08 11:58","pubTimestamp":1765166299,"startTime":"0","endTime":"0","summary":"在ASH 2025年会上,吉利德旗下Kite Pharma公布Anito-cel在iMMagine-1 II期试验中的更新数据,该靶向BCMA的CAR-T疗法在复发/难治性多发性骨髓瘤患者中显示96% ORR、74% sCR/CR率、95% MRD阴性率,中位随访15.9个月,缓解持续。III期iMMagine-3试验正在招募中,该研究将Anito-cel与标准治疗比较,预计2026年获得数据;该药物获FDA快速通道、孤儿药和RMAT资格。ICANS 发生率为 8%,其中 1 例为 3 级;其余均为 2 级或更低。","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=nesSN20251208144817a43ac231&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, 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