美股詳情

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Militia Long/Short Equity ETF

38.99

+0.30000.78%

盤後：38.990.00000.00%16:10 EST

成交量：58.46萬

成交額：2,276.09萬

市值：4.51億

市盈率：- -

高：39.12

開：38.86

低：38.70

收：38.69

52周最高：39.12

52周最低：25.85

股本：1,157.00萬

流通股本：1,113.00萬

量比：1.65

換手率：5.25%

股息：- -

股息率：- -

淨資產收益率：--

總資產收益率：--

市淨率：--

市盈率(LYR):- -

資料載入中...

總覽公司新聞資訊公告

78億美金，跨國藥企達成閃電併購

药圈观察局

澤璟製藥-U事件點評：ZG006授權給艾伯維澤速寧獲批上市

甬兴证券有限公司

5000億！一戰封神，他是中國最成功的美國人

優赫得在華拓展第六個適應症，去年上半年銷售額突破22億美金

德曲妥珠單抗胃癌新適應證獲批，填補臨床治療空白

優赫得®在華獲批治療既往接受過一種含曲妥珠單抗治療方案的局部晚期或轉移性HER2陽性成人胃或胃食管結合部腺癌患者

向「領跑者」跨越！中國雙抗藥物再迎高光時刻

每日经济新闻

Rybrevant雙靶風暴來襲：強生重塑難治性結直腸癌治療天花板，51% ORR+11.3月肝轉移PFS，EGFR/MET雙鎖+免疫殺傷直擊耐藥痛點

医道社创新药新...

ORR高達89.5%！智翔金泰BCMA/CD3雙抗申報上市

全球首個HER2突變肺癌口服靶向藥上新，境外新藥加速入華新政助力藥品一年落地

君賽生物：聚焦實體瘤「免清淋」突破，GC101預計2026年提交上市申請

肺癌一線！「伏美替尼」新適應症擬納入突破性療法

優赫得®在華獲批為首個用於既往在轉移性疾病階段經一種或一種以上內分泌治療進展的HER2低表達或超低表達乳腺癌患者的HER2靶向療法

多個新藥或新適應症獲FDA批准，涉及腫瘤、肥胖、肺纖維化等領域

關注，又新增2款國產創新藥擬納入突破性療法

北京药研汇

君賽生物赴港IPO：核心產品數據平平且專利仍待審批遞表前股東要求回購或轉讓股權

新股前瞻|佈局TCE腫瘤療法千億藍海，時邁藥業能否博得市場青睞？

吉利德Anito-cel 神經毒性低，2年多發性骨髓瘤生存率高 | ASH25

iza-bren食管鱗癌Ⅲ期臨床期中分析迎關鍵突破

每日经济新闻

一哥新高，要起風了

CPHI制药在线

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08:34","pubTimestamp":1769301264,"startTime":"0","endTime":"0","summary":"文 | 华商韬略 韩翔州2010年，旧金山的一次私人聚会上，已在中国创业有成的美国人欧雷强，结识了已在美国功成名就的中国人王晓东。终于在年底，他们决定一起冒险：在中国建立一家世界级的生物科技公司，在中国做创新药卖给全世界。作为一名连续创业者，欧雷强的履历堪称完美。事实证明，中国没有辜负欧雷强的眼光。欧雷强预见到，中国的监管环境即将迎来一场有利于创新药的剧变。","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://www.lanjinger.com/d/1769137313695679325","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":["LU1719994722.HKD","BK4195","ASH","ORR","LU1969619763.USD","LU1251922891.USD","LU0588546209.SGD","BK1161","BK1583","06160","LU1770034418.SGD","LU2463526074.USD","LU1303224171.USD","BK1500","BMS","BK1588","LU2328871848.SGD","PFS","LU0307460666.USD","BK4211","BK4109"],"gpt_icon":0},{"id":"2605034473","title":"優赫得在華拓展第六個適應症，去年上半年銷售額突破22億美金","url":"https://stock-news.laohu8.com/highlight/detail?id=2605034473","media":"蓝鲸财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2605034473?lang=zh_tw&edition=fundamental","pubTime":"2026-01-23 17:13","pubTimestamp":1769159628,"startTime":"0","endTime":"0","summary":"2024 年全球已获批上市的 17 款 ADC 药物合计销售额达百亿美金，其中第一三共的德曲妥珠单抗表现尤为突出，2024 年销售额达到 34.8 亿美元、同比增长 52%。根据阿斯利康2025年上半年财报，其自身销售额为12.6亿美元，增长38%；包括合作伙伴第一三共报告的销售额在内，总销售额为22.9亿美元。","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://www.lanjinger.com/d/1769159310955231385","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":"lanjinger_stock","symbols":["BK4080","PFS","BK4195","BK4231","BK4211","OS","ORR","ADC","BK4097"],"gpt_icon":0},{"id":"2605989254","title":"德曲妥珠單抗胃癌新適應證獲批，填補臨床治療空白","url":"https://stock-news.laohu8.com/highlight/detail?id=2605989254","media":"上观新闻","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2605989254?lang=zh_tw&edition=fundamental","pubTime":"2026-01-22 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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":"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/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":["LU2506951958.HKD","ADC","LU2247934214.USD","BK4195","SG9999015978.USD","LU2237443622.USD","IE00BFMHRM44.USD","LU1571399168.USD","LU1046421795.USD","ORR","CSCO","LU0234572021.USD","LU2462157665.USD","IE00BKVL7J92.USD","SG9999001440.SGD","BK4579","LU2506952097.USD","LU2417539215.USD","SG9999015945.SGD","BK4080","BK4588","LU2237443549.SGD","LU0109394709.USD","LU1244550577.SGD","LU2237443895.HKD","OS","BK4585","LU1221951129.SGD","LU1244550494.USD","LU1196500208.SGD","LU1929549753.HKD","LU0868494617.USD","LU1894683348.USD","PFS","LU1066051498.USD","BK4231","IE000M9KFDE8.USD","LU0320765992.SGD","LU1880398471.USD","LU1880398554.USD","BK4560","AZN","BK4527","LU0792757196.USD","BK4612","LU1066053197.SGD","LU1221951046.USD","LU2506951875.HKD","BK4097","LU2237443382.USD"],"gpt_icon":0},{"id":"2603130816","title":"向「領跑者」跨越！ 中國雙抗藥物再迎高光時刻","url":"https://stock-news.laohu8.com/highlight/detail?id=2603130816","media":"每日经济新闻","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603130816?lang=zh_tw&edition=fundamental","pubTime":"2026-01-14 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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":"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":"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":["ORR","BK0239","688443"],"gpt_icon":0},{"id":"2601861815","title":"全球首個HER2突變肺癌口服靶向藥上新，境外新藥加速入華新政助力藥品一年落地","url":"https://stock-news.laohu8.com/highlight/detail?id=2601861815","media":"蓝鲸财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2601861815?lang=zh_tw&edition=fundamental","pubTime":"2026-01-06 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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":["TIL","BK4505","ORR","BK4139"],"gpt_icon":0},{"id":"2594965422","title":"肺癌一線！「伏美替尼」新適應症擬納入突破性療法","url":"https://stock-news.laohu8.com/highlight/detail?id=2594965422","media":"新浪医药","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2594965422?lang=zh_tw&edition=fundamental","pubTime":"2025-12-26 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成人患者的治疗。","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/2025-12-26/doc-inhecrxf2583740.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","symbols":["BK4211","PFS","ORR","BK4195"],"gpt_icon":0},{"id":"2594360732","title":"優赫得®在華獲批為首個用於既往在轉移性疾病階段經一種或一種以上內分泌治療進展的HER2低表達或超低表達乳腺癌患者的HER2靶向療法","url":"https://stock-news.laohu8.com/highlight/detail?id=2594360732","media":"美通社","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2594360732?lang=zh_tw&edition=fundamental","pubTime":"2025-12-25 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