美股詳情

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安進

377.35

-5.1200-1.34%

盤後：377.950.6000+0.16%19:59 EDT

成交量：227.29萬

成交額：8.61億

市值：2,031.96億

市盈率：23.44

高：386.99

開：386.14

低：377.22

收：382.47

52周最高：447.03

52周最低：269.77

股本：5.38億

流通股本：5.37億

量比：0.68

換手率：0.42%

股息：9.80

股息率：2.60%

每股收益(TTM):16.10

每股收益(LYR):14.23

淨資產收益率：91.47%

總資產收益率：8.67%

市淨率：17.38

市盈率(LYR):26.52

資料載入中...

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21:00","pubTimestamp":1775480413,"startTime":"0","endTime":"0","summary":"安进公司宣布，其Tepezza皮下注射剂针对中重度活动性甲状腺眼病成人患者的三期临床试验取得积极顶线结果。","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":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU2089984988.USD","IE00BFTCPJ56.SGD","LU0058720904.USD","LU0122379950.USD","LU1057294990.SGD","LU2468319806.SGD","LU0289739699.SGD","IE00BJJMRZ35.SGD","AMGN","IE0002141913.USD","LU1571399168.USD","IE00B2B36J28.USD","BK4139","IE00BJT1NW94.SGD","BK4585","LU1061106388.HKD","BK4588","LU1023059063.AUD","LU2112291526.USD","BK4534","LU2242646821.SGD","LU0320765992.SGD","SG9999001440.SGD","BK4566","BK4599","IE0009355771.USD","LU0109394709.USD","BK4581","BK4533","LU1983299246.USD","LU2242652126.USD","IE00B4R5TH58.HKD","LU0889565916.HKD","LU0868494617.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1151218584","title":"安進：Tepezza三期試驗總體安全性結果與靜脈注射Tepezza已知安全性特徵基本一致","url":"https://stock-news.laohu8.com/highlight/detail?id=1151218584","media":"美股速递","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1151218584?lang=zh_tw&edition=fundamental","pubTime":"2026-04-06 21:00","pubTimestamp":1775480413,"startTime":"0","endTime":"0","summary":"安进公司公布的最新数据显示，其Tepezza药物在三期临床试验中的总体安全性结果，与静脉注射Tepezza已知的安全性特征大体相符。","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":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IE00B2B36J28.USD","LU1983299246.USD","AMGN","BK4581","LU2468319806.SGD","LU2242646821.SGD","LU0289739699.SGD","IE00BFTCPJ56.SGD","LU0889565916.HKD","IE0002141913.USD","LU1057294990.SGD","LU2089984988.USD","LU2112291526.USD","BK4588","LU2242652126.USD","LU1061106388.HKD","BK4566","IE00BJJMRZ35.SGD","LU0320765992.SGD","LU0058720904.USD","LU1571399168.USD","IE00BJT1NW94.SGD","BK4139","LU0868494617.USD","LU1023059063.AUD","SG9999001440.SGD","BK4534","BK4599","LU0109394709.USD","LU0122379950.USD","BK4533","IE0009355771.USD","BK4585","IE00B4R5TH58.HKD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624524927","title":"再鼎醫藥午前漲近5% 與安進公司達成一項全球臨床研究合作","url":"https://stock-news.laohu8.com/highlight/detail?id=2624524927","media":"新浪港股","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624524927?lang=zh_tw&edition=fundamental","pubTime":"2026-04-02 11:37","pubTimestamp":1775101020,"startTime":"0","endTime":"0","summary":"　　再鼎医药午前涨超4%，截至发稿，股价上涨4.82%，现报15.88港元，成交额2.88亿港元。　　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":"other","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/hkstock/marketalerts/2026-04-02/doc-inhtaraa1102717.shtml","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":"sina","symbols":["BK4588","09688","LU0122379950.USD","SG9999001440.SGD","BK1574","LU0289739699.SGD","IE00B2B36J28.USD","BK4585","BK4533","BK4534","LU0320765992.SGD","LU2242646821.SGD","AMGN","BK4531","BK1161","BK4548","LU0058720904.USD","LU0109394709.USD","IE00BFTCPJ56.SGD","LU1023059063.AUD","LU1983299246.USD","BK4139","BK1588","LU2468319806.SGD","LU1061106388.HKD","BK4566","LU2488822045.USD","BK4526","IE00B4R5TH58.HKD","LU2242652126.USD","BK4581","IE0002141913.USD","LU1571399168.USD","IE00BJJMRZ35.SGD","ZLAB","LU2089984988.USD","LU0868494617.USD","LU1057294990.SGD","LU2112291526.USD","BK4599","IE00BJT1NW94.SGD","LU0889565916.HKD","IE0009355771.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624490526","title":"港股異動 | 再鼎醫藥(09688)升逾4% 與安進就zoci聯合塔拉妥單抗用於小細胞肺癌達成全球臨床合作","url":"https://stock-news.laohu8.com/highlight/detail?id=2624490526","media":"智通财经","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624490526?lang=zh_tw&edition=fundamental","pubTime":"2026-04-02 09:48","pubTimestamp":1775094517,"startTime":"0","endTime":"0","summary":"消息面上，4月1日，再鼎医药宣布，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":"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/1424380.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":["IE00BFTCPJ56.SGD","BK1574","BK1588","BK4566","IE00BJJMRZ35.SGD","LU0122379950.USD","LU0289739699.SGD","LU2089984988.USD","LU1057294990.SGD","BK4588","AMGN","LU2468319806.SGD","SG9999001440.SGD","LU2242646821.SGD","LU2242652126.USD","LU0320765992.SGD","IE00B2B36J28.USD","BK4139","LU0109394709.USD","IE0002141913.USD","09688","LU2112291526.USD","BK4526","LU2488822045.USD","LU0889565916.HKD","BK4531","BK4581","VXUS","LU1983299246.USD","BK4533","BK4585","LU1061106388.HKD","LU1571399168.USD","LU0058720904.USD","LU0868494617.USD","BK4599","BK4534","BK4548","LU1023059063.AUD","ZLAB","IE00B4R5TH58.HKD","IE0009355771.USD","BK1161","IE00BJT1NW94.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2624518223","title":"BUZZ-Zai Lab股價上漲，因與安進合作進行肺癌藥物試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2624518223","media":"路透中文","labels":["shareholding","corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2624518223?lang=zh_tw&edition=fundamental","pubTime":"2026-04-01 19:57","pubTimestamp":1775044650,"startTime":"0","endTime":"0","summary":"** Zai Lab表示，早期研究显示其药物效果良好，包括对癌细胞扩散到大脑的情况，且副作用可控。** Zai Lab称其药物已获得美国FDA孤儿药和快速通道资格** 安进公司股价盘前小幅上涨 ** 截至上一交易日收盘，ZLAB 股价上涨约 7%，AMGN 股价年初至今上涨约 8%。由于自动化翻译可能有误，或未能包含所需语境，路透不保证自动化翻译文本的准确性，仅是为了便利读者而提供自动化翻译。对于因为使用自动化翻译功能而造成的任何损害或损失，路透不承担任何责任。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260401:nL4S40K10S:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"shareholding,corporation","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU2112291526.USD","LU0889565916.HKD","LU0122379950.USD","IE00BFTCPJ56.SGD","LU0320765992.SGD","LU2242646821.SGD","BK4534","09688","BK1574","LU0289739699.SGD","LU1061106388.HKD","IE0002141913.USD","BK4566","LU0868494617.USD","BK4526","BK4581","LU1983299246.USD","ZLAB","IE00B4R5TH58.HKD","LU2242652126.USD","AMGN","LU0109394709.USD","LU1023059063.AUD","BK1161","BK4139","IE0009355771.USD","LU2488822045.USD","BK4585","BK4531","BK4548","LU2089984988.USD","LU2468319806.SGD","LU1057294990.SGD","BK1588","BK4533","IE00B2B36J28.USD","IE00BJJMRZ35.SGD","LU1571399168.USD","LU0058720904.USD","SG9999001440.SGD","IE00BJT1NW94.SGD","BK4599","BK4588"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623538013","title":"重發-美國 FDA 就與安進公司罕見病藥物有關的肝損傷病例發出警告","url":"https://stock-news.laohu8.com/highlight/detail?id=2623538013","media":"路透中文","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2623538013?lang=zh_tw&edition=fundamental","pubTime":"2026-03-31 23:05","pubTimestamp":1774969529,"startTime":"0","endTime":"0","summary":"重发-美国 FDA 就与安进公司罕见病药物有关的肝损伤病例发出警告更正第1段中的日期路透3月31日 - 美国食品和药物管理局周二表示， 已发现服用安进公司AMGN.O治疗一组罕见自身免疫性疾病的药物的患者出现肝损伤病例，并敦促医疗服务提供者密切监测患者，一旦怀疑出现肝损伤，应立即停止治疗。这项安全警告使得Tavneos面临的监管审查日益增加。FDA 表示，药物引起的肝损伤发病的中位时间是开始治疗后的 46 天。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260331:nL4S40J1LB:1","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU0320765992.SGD","IE0002141913.USD","LU0889565916.HKD","LU1061106388.HKD","IE00B4R5TH58.HKD","IE00B2B36J28.USD","LU1023059063.AUD","AMGN","LU2242646821.SGD","SG9999001440.SGD","BK4581","LU0058720904.USD","LU1057294990.SGD","LU1571399168.USD","BK4585","BK4566","LU2089984988.USD","BK4534","LU2242652126.USD","IE00BFTCPJ56.SGD","IE00BJT1NW94.SGD","LU2468319806.SGD","BK4139","IE00BJJMRZ35.SGD","BK4599","LU0868494617.USD","LU1983299246.USD","LU0122379950.USD","LU2112291526.USD","BK4533","IE0009355771.USD","BK4588","LU0289739699.SGD","LU0109394709.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1179256799","title":"FDA警示：Tavneos出現膽管消失綜合徵及致死性藥物性肝損傷病例 構成新安全隱患","url":"https://stock-news.laohu8.com/highlight/detail?id=1179256799","media":"美股速递","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1179256799?lang=zh_tw&edition=fundamental","pubTime":"2026-03-31 21:10","pubTimestamp":1774962657,"startTime":"0","endTime":"0","summary":"美国食品药品监督管理局（FDA）近期发布安全警示，抗炎药物Tavneos（avacopan）在临床使用中出现了胆管消失综合征及致死性药物性肝损伤的病例报告，这些严重不良反应构成了该药物新的安全性隐忧。\n胆管消失综合征是一种罕见的严重肝损伤，其特征为肝内胆管进行性破坏消失。而此次报告的药物性肝损伤病例已出现致命后果。监管机构指出，医疗专业人员需对接受Tavneos治疗的患者保持高度警惕，密切监测其肝功能指标。\n此次安全信号的浮现，为Tavneos的风险效益评估增添了新的考量维度。临床医生在处方时应充分权衡其治疗潜力与潜在的严重肝毒性风险。","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":"-2","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["IE00BJT1NW94.SGD","IE00BJJMRZ35.SGD","LU0122379950.USD","BK4533","LU1061106388.HKD","LU1023059063.AUD","LU1983299246.USD","LU0320765992.SGD","BK4581","BK4588","BK4585","LU2089984988.USD","IE0002141913.USD","IE00B4R5TH58.HKD","LU0289739699.SGD","IE00B2B36J28.USD","LU1571399168.USD","BK4599","SG9999001440.SGD","LU2242646821.SGD","LU0109394709.USD","LU0889565916.HKD","LU2112291526.USD","LU0058720904.USD","LU2242652126.USD","LU1057294990.SGD","IE00BFTCPJ56.SGD","BK4534","LU2468319806.SGD","AMGN","IE0009355771.USD","BK4139","LU0868494617.USD","BK4566"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623930813","title":"重發-焦點-製藥商推遲在歐洲上市，警惕特朗普的定價政策","url":"https://stock-news.laohu8.com/highlight/detail?id=2623930813","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2623930813?lang=zh_tw&edition=fundamental","pubTime":"2026-03-31 14:00","pubTimestamp":1774936846,"startTime":"0","endTime":"0","summary":"重发-焦点-制药商推迟在欧洲上市，警惕特朗普的定价政策更正第 15 段中抗炎药物名称 Brinsupri 的排印错误特朗普最惠国待遇引发定价不确定性数据显示欧洲新药上市量下降 35%公司表示希望首先明确美国的价格 美国作为首选市场的地位得到加强游说团体称欧洲需要重新考虑药品定价以保持竞争力Maggie Fick/Bhanvi Satija/Dominique Patton. 该药物于 11 月获得欧洲批准，但尚未在该地区上市。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260331:nL4T40J0GP:1","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":null,"symbols":["AZN.UK","LU0310799852.SGD","LU0211326839.USD","LU0889566641.SGD","LU2089984988.USD","LU2242646821.SGD","LU0211326755.USD","LU0526926950.USD","BK4139","LU2539964713.USD","LU1019632923.USD","LU0889565080.SGD","LU0575583348.USD","LU0114720955.EUR","LU0889565916.HKD","AMGN","IE00BJT1NW94.SGD","LU0289739699.SGD","LU0827474353.SGD","LU0053671581.USD","LU2125909247.SGD","LU0969580561.USD","IE00B3T34201.USD","LU0310800379.SGD","LU1153585028.USD","INSM","IE0034235188.USD","LU1061106388.HKD","LU0499090636.EUR","BK4588","LU0708994859.HKD","IE00BJJMRZ35.SGD","LU0976567544.SGD","LU0784385840.USD","IE00BFTCPJ56.SGD","LU0957799991.USD","INDV","LU0211327993.USD","LU1273509221.SGD","LU1119994496.HKD","BK4533","SG9999001176.SGD","LU0823399737.USD","LU2433249047.HKD","IE00BKPKM643.USD","03165","LU1267930490.SGD","LU1153584641.USD","LU0949170426.SGD","LU2091194634.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623314391","title":"儘管試驗成功，但眼病藥物療效令人失望，Viridian 下挫","url":"https://stock-news.laohu8.com/highlight/detail?id=2623314391","media":"路透中文","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2623314391?lang=zh_tw&edition=fundamental","pubTime":"2026-03-30 19:18","pubTimestamp":1774869502,"startTime":"0","endTime":"0","summary":"更新版 3-尽管试验成功，但眼病药物疗效令人失望，Viridian 下挫更新股份，改写第 1 段，在第 9 段增加分析师评论，在第 7 段增加公司评论Siddhi Mahatole路透3月30日 - Viridian Therapeutics VRDN.O的股价周一暴跌34%，创八个月新低，因为该公司在一项晚期研究中对甲状腺眼病的实验性治疗虽然达到了减少眼球突出的主要目标，但在疗效上却落后于竞争对手。Viridian的股价最后下跌32%，报18.66美元。Viridian公司预计将于2027年第一季度提交美国上市申请。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260330:nL4S40I0XR:1","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":null,"symbols":["LU1057294990.SGD","IE00BJJMRZ35.SGD","LU0320765992.SGD","LU0868494617.USD","LU1571399168.USD","BK4585","LU0109394709.USD","IE00B4R5TH58.HKD","LU0058720904.USD","IE0009355771.USD","BK4534","BK4533","LU2242652126.USD","BK4139","BK4581","LU1983299246.USD","BK4599","VRDN","IE00BFTCPJ56.SGD","SG9999001440.SGD","LU2242646821.SGD","IE00BJT1NW94.SGD","LU0289739699.SGD","LU2112291526.USD","AMGN","IE0002141913.USD","LU1061106388.HKD","LU1023059063.AUD","LU0889565916.HKD","BK4566","BK4588","IE00B2B36J28.USD","LU0122379950.USD","LU2468319806.SGD","LU2089984988.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1150502063","title":"安進Repatha可將高風險無顯著動脈粥樣硬化患者首次主要心血管事件風險降低31%","url":"https://stock-news.laohu8.com/highlight/detail?id=1150502063","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1150502063?lang=zh_tw&edition=fundamental","pubTime":"2026-03-29 04:46","pubTimestamp":1774730777,"startTime":"0","endTime":"0","summary":"安进公司宣布，其降胆固醇药物Repatha在针对未确诊明显动脉粥样硬化但具有高风险因素的患者群体中，展现出显著疗效——能够将首次发生主要心血管事件的风险降低达31%。这一突破性数据为心血管疾病预防领域提供了新的临床依据，尤其为尚未出现明显血管病变的高危人群带来了更前沿的干预方案。","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":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["AMGN","LU0868494617.USD","BK4585","LU0889565916.HKD","IE0002141913.USD","LU1983299246.USD","IE00BJJMRZ35.SGD","LU2468319806.SGD","LU2242646821.SGD","BK4588","LU2242652126.USD","LU2089984988.USD","BK4581","IE00B2B36J28.USD","LU0058720904.USD","SG9999001440.SGD","LU1023059063.AUD","IE00B4R5TH58.HKD","BK4566","BK4599","LU1061106388.HKD","BK4534","LU0109394709.USD","IE00BFTCPJ56.SGD","BK4533","LU2112291526.USD","LU0320765992.SGD","IE00BJT1NW94.SGD","BK4139","LU0289739699.SGD","LU1571399168.USD","IE0009355771.USD","LU0122379950.USD","LU1057294990.SGD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1192752433","title":"安進公布Vesalius-Cv三期臨床試驗結果：Repatha顯著降低心肌梗死、冠心病死亡及缺血性卒中風險","url":"https://stock-news.laohu8.com/highlight/detail?id=1192752433","media":"美股速递","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1192752433?lang=zh_tw&edition=fundamental","pubTime":"2026-03-29 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日本武田药品4502.TTAK.N周六称，在两项后期试验中，其试验性银屑病药片帮助约70%的患者皮肤症状达到清除或基本清除，从而有望成为注射疗法的便捷替代品。武田公司表示，在第40周有反应并继续服药的患者中，90%以上的患者在第60周保持了好转。武田表示，该公司有望在今年向美国食品和药物管理局及其他监管机构提交上市申请。","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://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260328:nL4T40G03T:1","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":null,"symbols":["LU0225284248.USD","LU1868837136.USD","LU1989771016.USD","LU1023059063.AUD","BK4585","LU1074936037.SGD","LU0889565916.HKD","BK4581","LU1868836591.USD","LU2089984988.USD","IE00B4R5TH58.HKD","LU2125154778.USD","LU0320765992.SGD","LU2468319806.SGD","LU1883839398.USD","LU2242652126.USD","LU0061475181.USD","BMY","BK4532","BK4139","LU1670711040.USD","LU0456855351.SGD","LU0306807586.USD","AMGN","IE00BSNM7G36.USD","LU2112291526.USD","LU1585245621.USD","LU0237698245.USD","LU1571399168.USD","LU0868494617.USD","LU1868837300.USD","LU1670710588.SGD","BK4007","LU1093756168.USD","BK4559","LU1670711123.USD","LU1868836757.USD","LU1868836914.USD","IE0002141913.USD","LU0267386448.USD","LU0321505439.SGD","BK4566","LU1430594728.SGD","LU0114720955.EUR","LU2360032135.SGD","SG9999001440.SGD","LU2242646821.SGD","BK4599","LU0109394709.USD","BK4533"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1146126461","title":"EMA人用藥品委員會：Joenja（Leniolisib）獲特殊情況下上市許可積極意見","url":"https://stock-news.laohu8.com/highlight/detail?id=1146126461","media":"美股速递","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/1146126461?lang=zh_tw&edition=fundamental","pubTime":"2026-03-27 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19:43","pubTimestamp":1774611797,"startTime":"0","endTime":"0","summary":"欧洲药品管理局人用医药产品委员会（CHMP）近日发布积极意见，建议授予安进公司开发的靶向疗法Imdylltra（Tarlatamab）上市许可。该药物拟用于治疗既往接受过系统性治疗的复发广泛期小细胞肺癌患者。\n此次推荐基于关键临床研究数据，显示Tarlatamab作为双特异性T细胞衔接抗体，能显著激活患者自身免疫系统攻击肿瘤细胞。若最终获欧盟委员会批准，这将成为首款针对该适应症的靶向免疫疗法，为预后极差的晚期肺癌群体提供新的治疗选择。","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":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["LU2112291526.USD","SG9999001440.SGD","LU1057294990.SGD","LU2468319806.SGD","IE0009355771.USD","LU2089984988.USD","BK4588","LU0289739699.SGD","LU1061106388.HKD","LU0320765992.SGD","IE0002141913.USD","IE00BFTCPJ56.SGD","IE00B4R5TH58.HKD","LU2242652126.USD","LU0122379950.USD","BK4581","IE00BJJMRZ35.SGD","BK4139","BK4599","BK4533","LU2242646821.SGD","LU0889565916.HKD","LU1983299246.USD","LU1571399168.USD","BK4585","LU0109394709.USD","LU0868494617.USD","LU1023059063.AUD","IE00B2B36J28.USD","IE00BJT1NW94.SGD","AMGN","LU0058720904.USD","BK4534","BK4566"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":9,"pageCount":9,"totalSize":175,"code":"91000000","status":"200"}]}}