美股詳情

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iShares Health Innovation Active ETF

33.32

+0.10420.31%

成交量：583

成交額：1.94萬

市值：1,332.60萬

市盈率：- -

高：33.32

開：33.23

低：33.23

收：33.21

52周最高：34.86

52周最低：25.79

股本：40.00萬

流通股本：40.00萬

量比：0.29

換手率：0.15%

股息：0.08

股息率：0.24%

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

Assembly Biosciences旗下Gs-1179預計2026年底前將推進至生殖器皰疹二期臨床試驗階段

Assembly Biosciences：吉利德獨享HSV HPI項目臨床開發與商業化權利

Assembly Biosciences行使與吉利德關於HSV解旋酶-引物酶抑制劑項目的美國利潤分成選擇權

吉利德科學(GILD)股票9月8日盤中下跌3.26%：釋放什麼信號？

TradingKey中文

阿斯利康慢阻肺藥物兩項晚期臨床試驗取得成功

环球市场播报

DELPHI‑305 三期臨床試驗達到主要終點。

Tozorakimab在OBERON和TITANIA兩項Ⅲ期臨床試驗中，在降低慢阻肺病急性加重方面均顯示出統計學和臨床意義上的顯著改善

禮邦醫藥-B(09637)：AP308治療IgA腎病的新藥臨床試驗申請獲美國食品藥品監督管理局批准

PHARVARIS的3期臨床試驗達到全部主要及次要終點。

石藥集團：SYH2083滴眼液獲臨床試驗批准

羅兵咸永道、默克與哈希圖集團試點可可溯源系統

膽固醇藥物臨床試驗受挫，數十億美元研發競賽蒙上陰影

环球市场播报

復星醫藥(600196.SH)子公司FXS5626片獲臨床試驗批准

製藥巨頭諾華股價大跌近10%，遭遇三項藥物臨床試驗受挫

环球市场播报

安進股價盤前下跌5.4%；競爭對手諾華的膽固醇藥物後期臨床試驗失敗。

邁普醫學(301033.SZ)：「可吸收止血流體明膠」進入臨床試驗階段

邁普醫學：可吸收止血流體明膠作為第三類醫療器械進入臨床試驗

諾華DM1藥物III期臨床試驗未達到主要終點

石藥集團(01093)：SYH2085片用於治療成人單純性流感的II期臨床試驗在中國正式啓動

石藥集團：SYH2085片II期臨床試驗在中國正式啓動

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21:45","pubTimestamp":1788875100,"startTime":"0","endTime":"0","summary":"阿斯利康周二公布慢阻肺在研药物两项成功的晚期临床试验完整结果，市场对该药创造数十亿美元营收的预期进一步升温。据阿斯利康数据，美国确诊及未确诊慢阻肺患者合计约 1600 万2600 万人，慢阻肺位列美国第五大死亡原因。阿斯利康近期将该药物销售峰值预期上调至50 亿美元以上，助力公司冲刺 2030 年整体 800 亿美元营收目标。两项临床试验同时纳入现吸烟者、既往吸烟者，覆盖全部嗜酸粒细胞水平、全部肺功能严重程度分级的患者。","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":"https://finance.sina.com.cn/stock/usstock/c/2026-09-08/doc-inircrns9296776.shtml","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":"sina","symbols":["BMED","IBBQ","PSYK","MDTX","IBBJ"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2665373053","title":"DELPHI‑305 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是首个在广泛慢阻肺病患者人群中显示出减少气道黏液栓堵塞作用的生物制剂3。Tozorakimab总体耐受性和安全性良好，唯一报告的药物不良反应为注射部位反应1,2。目前，tozorakimab已在欧盟、中国等主要市场进入上市许可审评阶段，用于治疗慢性阻塞性肺疾病。","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"prnasia","url":"http://wwwold.prnasia.com/story/archive/5042444_ZH42444_1","rn_cache_url":null,"directOrigin":true},"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://wwwold.prnasia.com/story/archive/5042444_ZH42444_1","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":"prnasia","symbols":["LU2236285917.USD","AZNH","LU1829250122.USD","BK4568","LU2089984988.USD","LU2237443549.SGD","LU0708994859.HKD","LU2237443895.HKD","LU2237443382.USD","LU2237443465.HKD","BMED","LU2456880835.USD","BK4585","LU0289739699.SGD","IBBJ","BK4588","AZN","LU0029864427.USD","LU2462157665.USD","LU2468319806.SGD","LU0432979614.USD","LU1267930573.SGD","LU0128525929.USD","LU0058720904.USD","IE00B3T34201.USD","IBBQ","LU2237443978.SGD","LU2417539215.USD","LU0310800379.SGD","LU0320765992.SGD","BK4007","LU2237443622.USD","LU0109394709.USD","LU0889565916.HKD","PSYK","MDTX"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2665320617","title":"禮邦醫藥-B(09637)：AP308治療IgA腎病的新藥臨床試驗申請獲美國食品藥品監督管理局批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2665320617","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2665320617?lang=zh_tw&edition=fundamental","pubTime":"2026-09-08 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Hashgraph Group 与默克公司（Merck）在普华永道德国（PwC Germany）的咨询与实施支持下，正试点一套可可溯源解决方案。该方案将默克的 M-Trust 物理认证技术与基于 Hedera 网络的 TrackTrace 数字产品护照平台相结合，旨在验证可可从农场到消费者的产地、真实性、质量、召回需求及合规数据。可可属于欧盟《反毁林法规》（EUDR）覆盖的七种商品之一。根据 2025 年 12 月达成的再次延期安排，大型运营商和贸易商须自 2026 年 12 月 30 日起履行相关义务，微型和小型运营商则从 2027 年 6 月 30 日起适用。该方案还对标欧盟《可持续产品生态设计法规》（ESPR）下数字产品护照的推进方向，不过食品和饲料目前被明确排除在 ESPR 范围之外，对可可而言，EUDR 尽职调查仍是近期约束性要求。合作伙伴表示，该架构不限于可可，未来可扩展至药品、奢侈品和工业组件等领域。普华永道德国企业区块链业务负责人 Husen Kapasi 指出，该方案具备可验证性，在食品召回或合规调查中能够发挥关键作用。 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