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本页面由Tiger Trade Technology Pte. Ltd.提供服务
Militia Long/Short Equity ETF
38.69
-0.0900
-0.23%
盘后:
38.98
0.2900
+0.75%
19:45 EST
成交量:
45.35万
成交额:
1,743.78万
市值:
4.48亿
市盈率:
- -
高:
38.83
开:
38.83
低:
38.10
收:
38.78
52周最高:
39.04
52周最低:
25.85
股本:
1,157.00万
流通股本:
1,113.00万
量比:
1.41
换手率:
4.07%
股息:
- -
股息率:
- -
净资产收益率:
--
总资产收益率:
--
市净率:
--
市盈率(LYR):
- -
数据加载中...
总览
公司
新闻资讯
公告
78亿美金,跨国药企达成闪电并购
药圈观察局
·
02/23
泽璟制药-U事件点评:ZG006授权给艾伯维 泽速宁获批上市
甬兴证券有限公司
·
01/25
5000亿!一战封神,他是中国最成功的美国人
蓝鲸财经
·
01/25
优赫得在华拓展第六个适应症,去年上半年销售额突破22亿美金
蓝鲸财经
·
01/23
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
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
向“领跑者”跨越! 中国双抗药物再迎高光时刻
每日经济新闻
·
01/14
Rybrevant双靶风暴来袭:强生重塑难治性结直肠癌治疗天花板,51% ORR+11.3月肝转移PFS,EGFR/MET双锁+免疫杀伤直击耐药痛点
医道社创新药新...
·
01/13
ORR高达89.5%!智翔金泰BCMA/CD3双抗申报上市
医药魔方
·
01/08
全球首个HER2突变肺癌口服靶向药上新,境外新药加速入华新政助力药品一年落地
蓝鲸财经
·
01/06
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
肺癌一线!“伏美替尼”新适应症拟纳入突破性疗法
新浪医药
·
2025/12/26
优赫得®在华获批为首个用于既往在转移性疾病阶段经一种或一种以上内分泌治疗进展的HER2低表达或超低表达乳腺癌患者的HER2靶向疗法
美通社
·
2025/12/25
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
关注,又新增2款国产创新药拟纳入突破性疗法
北京药研汇
·
2025/12/19
君赛生物赴港IPO:核心产品数据平平且专利仍待审批 递表前股东要求回购或转让股权
新浪证券
·
2025/12/17
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
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
iza-bren食管鳞癌Ⅲ期临床期中分析迎关键突破
每日经济新闻
·
2025/11/19
一哥新高,要起风了
CPHI制药在线
·
2025/11/13
更多
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20:03","pubTimestamp":1771848202,"startTime":"0","endTime":"0","summary":"2023年6月,因一名患者死亡,FDA暂停了anito-cel的关键II期临床试验。然而,仅两个月后,FDA经审查解除了搁置,试验重回正轨。同年11月,Kite进一步扩大合作,支付2.85亿美元以获得Arcellx另一条管线ACLX-001的权益,并将对Arcellx的股权投资增至2亿美元,持股比例达到约13%。其市值在不到三年内从不足4亿美元飙升至收购前的数十亿美元,堪称“十倍股”。据悉,此次收购的灵魂是Arcellx的两大核心资产。市场方面,多发性骨髓瘤CAR-T市场预计在2030年达到120亿美元。","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=nesSN202602232009079541ac53&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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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":["ASH","LU2463526074.USD","BMS","06160","LU0588546209.SGD","BK1583","BK1588","BK4109","LU1969619763.USD","LU2328871848.SGD","BK4195","LU1303224171.USD","BK1161","LU0307460666.USD","LU1719994722.HKD","BK4211","BK1500","PFS","LU1770034418.SGD","LU1251922891.USD","ORR"],"gpt_icon":0},{"id":"2605034473","title":"优赫得在华拓展第六个适应症,去年上半年销售额突破22亿美金","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_cn&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":"德曲妥珠单抗胃癌新适应证获批,填补临床治疗空白","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_cn&edition=fundamental","pubTime":"2026-01-22 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":"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://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":["BK4080","BK4231","OS","BK4195","ORR","PFS","ADC","BK4211","BK4097"],"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://ttm.financial/m/news/2605495703?lang=zh_cn&edition=fundamental","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":["IE000M9KFDE8.USD","LU0868494617.USD","LU1221951129.SGD","BK4612","ADC","SG9999015978.USD","LU2417539215.USD","BK4080","IE00BKVL7J92.USD","IE00BFMHRM44.USD","LU1066051498.USD","LU1221951046.USD","LU1929549753.HKD","SG9999001440.SGD","LU1196500208.SGD","LU2506951958.HKD","SG9999015945.SGD","LU0320765992.SGD","LU2506952097.USD","BK4579","LU1571399168.USD","CSCO","LU2462157665.USD","LU1046421795.USD","LU1880398554.USD","LU0109394709.USD","LU2237443382.USD","PFS","AZN","BK4560","ORR","BK4195","LU1894683348.USD","BK4585","LU0792757196.USD","LU2237443622.USD","LU2247934214.USD","LU1880398471.USD","LU2506951875.HKD","BK4527","BK4588","BK4097","LU2237443895.HKD","OS","LU1066053197.SGD","BK4231","LU1244550494.USD","LU1244550577.SGD","LU2237443549.SGD","LU0234572021.USD"],"gpt_icon":0},{"id":"2603130816","title":"向“领跑者”跨越! 中国双抗药物再迎高光时刻","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_cn&edition=fundamental","pubTime":"2026-01-14 20:14","pubTimestamp":1768392877,"startTime":"0","endTime":"0","summary":"2026年1月12日,第四十四届摩根大通医疗健康大会在美国旧金山召开,当全球生物医药界的目光聚焦于该会议时,大洋彼岸的中国接连传来重磅消息。","market":"sh","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"stock_eastmoney","url":"http://finance.eastmoney.com/a/202601143619177920.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/202601143619177920.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":["LU1720050803.USD","BK4195","LU2778985437.USD","ORR","LU1969619763.USD","LU0561508036.HKD","LU0348766576.USD","BK4588","BK1161","LU0417516902.SGD","LU0540923850.HKD","LU0417516738.SGD","LU0348825331.USD","LU2399975544.HKD","BK1583","LU1794554557.SGD","LU0053666078.USD","LU2476274308.USD","LU0417516571.SGD","L","IE00B5MMRT66.SGD","LU0348827113.USD","09995","BK4585","LU1829250122.USD","LU0348767384.USD","GSK.UK","BK4107","LU0210528500.USD","LU2476274720.SGD","LU2488822045.USD","BMS","BK1574","LU2487616109.SGD","09926","BK4007","LU0348783233.USD","BK4532","LU0348784397.USD","LU0634319403.HKD","LU2328871848.SGD","PFS","LU1961090484.USD","IE00BPRC5H50.USD","BK4211","IE00B543WZ88.USD","GSK","LU0348735423.USD"],"gpt_icon":0},{"id":"2603985636","title":"Rybrevant双靶风暴来袭:强生重塑难治性结直肠癌治疗天花板,51% ORR+11.3月肝转移PFS,EGFR/MET双锁+免疫杀伤直击耐药痛点","url":"https://stock-news.laohu8.com/highlight/detail?id=2603985636","media":"医道社创新药新...","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2603985636?lang=zh_cn&edition=fundamental","pubTime":"2026-01-13 20:22","pubTimestamp":1768306935,"startTime":"0","endTime":"0","summary":"可Rybrevant联合化疗,在OrigAMI-1研究中直接打出51%总体ORR、一线亚组73%、肝转移PFS 11.3个月!Rybrevant单药ORR 22%,PFS 3.7个月;联合化疗ORR 43%,PFS 7.4个月,DCR 86%。传统单抗易逃逸,Rybrevant加持Fc介导ADCC/ADCP,激活NK/巨噬细胞“围剿”癌细胞。ctDNA研究证实,停药后耐药克隆消退,Rybrevant清除残留,恢复敏感性。","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=nesSN20260113220712a7162b63&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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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":"全球首个HER2突变肺癌口服靶向药上新,境外新药加速入华新政助力药品一年落地","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_cn&edition=fundamental","pubTime":"2026-01-06 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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":"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/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","BK4139","ORR","BK4505"],"gpt_icon":0},{"id":"2594965422","title":"肺癌一线!“伏美替尼”新适应症拟纳入突破性疗法","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_cn&edition=fundamental","pubTime":"2025-12-26 19:30","pubTimestamp":1766748600,"startTime":"0","endTime":"0","summary":"12 月 25 日,CDE 官网显示,艾力斯医药伏美替尼的一项新适应症拟纳入突破性治疗品种,适应症为用于具有 EGFR PACC 突变的局部晚期或转移性非小细胞肺癌成人患者的一线治疗。今年 7 月,伏美替尼的第 3 项适应症上市申请获得 CDE 受理,并被纳入优先审评,用于既往经含铂化疗治疗时或治疗后出现疾病进展或不耐受含铂化疗并且存在EGFR 20 外显子插入突变的局部晚期或转移性 NSCLC 成人患者的治疗。","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/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":["BK4195","BK4211","ORR","PFS"],"gpt_icon":0},{"id":"2594360732","title":"优赫得®在华获批为首个用于既往在转移性疾病阶段经一种或一种以上内分泌治疗进展的HER2低表达或超低表达乳腺癌患者的HER2靶向疗法","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_cn&edition=fundamental","pubTime":"2025-12-25 15:30","pubTimestamp":1766647800,"startTime":"0","endTime":"0","summary":"在对HER2超低表达患者进行的探索性分析中,显示HER2超低表达患者群体的试验结果和HER2低表达试验群体的结果具有一致性。经筛查,约85%的HR阳性、HER2阴性转移性乳腺癌患者被检测出有HER2低表达或HER2超低表达3。目前,对于HR阳性转移性乳腺癌患者,不论HER2表达水平如何,内分泌治疗仍被广泛用于早期治疗方案。基于德曲妥珠单抗已取得的临床实践改变,此次获批将为更广泛的HER2表达转移性乳腺癌患者带来亟需的靶向治疗选择。","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/4853703_ZH53703_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":["BK4588","BK4231","BK4568","LU2417539215.USD","LU0889565916.HKD","BK4007","ORR","ADC","BK4585","HR","LU2456880835.USD","LU0109394709.USD","BK4195","BK4203","LU0320765992.SGD","BK4225","BK4162","BK4211","BK4080","PFS","LU2462157665.USD","AZN","LU1829250122.USD","LU2236285917.USD","IHC"],"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://ttm.financial/m/news/2593176440?lang=zh_cn&edition=fundamental","pubTime":"2025-12-24 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递表前股东要求回购或转让股权","url":"https://stock-news.laohu8.com/highlight/detail?id=2592502964","media":"新浪证券","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2592502964?lang=zh_cn&edition=fundamental","pubTime":"2025-12-17 15:10","pubTimestamp":1765955400,"startTime":"0","endTime":"0","summary":"炒股就看金麒麟分析师研报,权威,专业,及时,全面,助您挖掘潜力主题机会! 近日,上海君赛生物股份有限公司正式向港交所递交招股说明书。招股书显示,公司专注于实体瘤创新细胞疗法的生物科技公司,其核心产品GC101为全球首款无需高强度清淋化疗及IL-2给药的肿瘤浸润淋巴细胞疗法,承载着成为国内首个获批TIL疗法的期望。 TIL细胞疗法是指通过离体激活来源于肿瘤组织内部的TIL细胞、规模扩增并注入患者体内发挥疗效。","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/observe/2025-12-17/doc-inhcavhm7560592.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":["BK4107","LU2487616109.SGD","BK4585","PFS","L","LU0210528500.USD","ORR","LU0053666078.USD","BK4195","BK4139","BK4505","BK4211","BK4588","TIL"],"gpt_icon":0},{"id":"2590394122","title":"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?","url":"https://stock-news.laohu8.com/highlight/detail?id=2590394122","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2590394122?lang=zh_cn&edition=fundamental","pubTime":"2025-12-09 13:05","pubTimestamp":1765256702,"startTime":"0","endTime":"0","summary":"近日,又一创新药企正式向港交所提交上市申请。在此背景下,作为一家专注于实体瘤TCE疗法、且具备多款全球前列临床管线的企业,时迈药业的上市进程亦自然备受瞩目。布局TCE疗法 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":["BK4585","BK4588","IE0031619046.USD","BK4080","BK4107","LU0963586101.USD","IE00B66KJ199.SGD","LU2487616109.SGD","LU0210528500.USD","CRS","L","BK4231","IE00B19Z4B17.USD","IE00B7SZL793.SGD","LU0053666078.USD","ADC","BK4006","ORR","LU2065731478.USD","BK4187"],"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://ttm.financial/m/news/2590451393?lang=zh_cn&edition=fundamental","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 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