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iShares Health Innovation Active ETF
33.56
0.0000
成交量:
69
成交額:
2,349.44
市值:
1,342.44萬
市盈率:
- -
高:
33.56
開:
33.56
低:
33.56
收:
33.56
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:
0.13
換手率:
0.02%
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...
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公司
新聞資訊
公告
特朗普政府宣佈撥款1.493億美元,用於在阿肯色州農村地區擴展遠程醫療,並增加專科護理和預防性篩查的可及性。
智通财经
·
09/01
衞材宣佈:加拿大藥品管理局最終推薦侖卡奈單抗(Leqembi)在早期阿爾茨海默病中獲得報銷資格
美股速递
·
09/01
長春高新(000661.SZ)子公司GenSci161注射液臨床試驗申請獲受理
智通财经
·
08/31
石藥集團(01093.HK):SYH2092注射液用於成人超重或肥胖患者體重管理的I期臨床試驗在中國首個研究中心正式啓動
智通财经
·
08/31
石藥集團(01093):SYH2092注射液用於成人超重或肥胖患者體重管理的I期臨床試驗在中國首個研究中心正式啓動
智通财经
·
08/31
長春高新:子公司GenSci161注射液境內生產藥品註冊臨床試驗申請獲受理
智通财经
·
08/31
石藥創新:控股子公司SYH2092注射液啓動Ⅰ期臨床試驗
智通财经
·
08/31
歐康維視生物-B(01477):OT-202 III期臨床試驗完成首例患者入組
智通财经
·
08/31
ST百靈(002424.SZ)子公司創新藥吸入用BD77臨床試驗申請獲批
智通财经
·
08/31
ST百靈:全資子公司吸入用BD77獲臨床試驗批准
智通财经
·
08/31
樂意保®(侖卡奈單抗)皮下自動注射劑型LEQEMBI IQLIK®在美上市,適用於早期阿爾茨海默病的初始治療
美通社
·
08/31
港股異動 | 和譽-B(02256)高開逾6% ABSK211的I期臨床試驗完成首例患者給藥
智通财经
·
08/31
和譽-B(02256):新型pan-KRAS抑制劑ABSK211I期臨床試驗完成首例患者給藥
智通财经
·
08/31
和譽-B(02256.HK):新型pan-KRAS抑制劑ABSK211I期臨床試驗完成首例患者給藥
智通财经
·
08/31
BioNTech在進行安全性審查後終止了mRNA結直腸癌疫苗的臨床試驗
路透中文
·
08/28
美股生物醫藥股盤初走低,BioNTech跌超9%、Moderna跌近5%
老虎资讯综合
·
08/28
BioNTech美股盤前跌約10%,公司宣佈終止二期結直腸癌臨床試驗。
智通财经
·
08/28
BIONTECH結束二期結直腸癌臨床試驗。
智通财经
·
08/28
台裕製藥提交針對HER2陽性乳腺癌的抗體藥物偶聯物生物類似藥TSY-110的臨床試驗申請。
智通财经
·
08/28
焦點-歷經一個世紀的失敗後終於取得成功:揭秘莫德納和默克癌症疫苗的突破
路透中文
·
08/28
更多
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02:08","pubTimestamp":1788199690,"startTime":"0","endTime":"0","summary":"卫材今日宣布,加拿大药品管理局已就仑卡奈单抗在早期阿尔茨海默病治疗中的报销事宜发布最终积极推荐。这一决定意味着,符合条件的加拿大患者将有望获得这一创新疗法的公共资金支持。加拿大药品管理局经过严谨的临床证据评估后,最终给出了肯定意见。卫材公司表示,将继续与加拿大各省及地区的卫生部门密切协作,推动报销政策的实际落地。","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":"","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4585","BMED","BK4532","BIIB","IE00B894F039.SGD","IE00B19Z9P08.USD","IE00B19Z9Z06.USD","LU0109394709.USD","LU0234570918.USD","BK4139","LU0320765992.SGD","BK4533","BK4588","LU0889565916.HKD","PBE"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2663003390","title":"長春高新(000661.SZ)子公司GenSci161注射液臨床試驗申請獲受理","url":"https://stock-news.laohu8.com/highlight/detail?id=2663003390","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2663003390?lang=zh_tw&edition=fundamental","pubTime":"2026-08-31 20:25","pubTimestamp":1788179110,"startTime":"0","endTime":"0","summary":"智通财经APP讯,长春高新(000661.SZ)发布公告,近日,公司控股子公司长春金赛药业有限责任公司(简称“金赛药业”)收到国家药品监督管理局核准签发的《受理通知书》,金赛药业GenSci161注射液的境内生产药品注册临床试验申请获得受理。GenSci161注射液是金赛药业自主研发的一款治疗用生物制品1类药物,拟用于治疗结缔组织病相关间质性肺疾病。","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/1489784.html","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":"stock_zhitongcaijing","symbols":["000661","PSYK","BK0057","MDTX","BK0075","BK0046","IBBQ","BK0239","BMED","BK0028","BK0188","IBBJ"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2663359008","title":"石藥集團(01093.HK):SYH2092注射液用於成人超重或肥胖患者體重管理的I期臨床試驗在中國首個研究中心正式啓動","url":"https://stock-news.laohu8.com/highlight/detail?id=2663359008","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2663359008?lang=zh_tw&edition=fundamental","pubTime":"2026-08-31 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19:58","pubTimestamp":1788177490,"startTime":"0","endTime":"0","summary":"智通财经APP讯,石药集团 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19:29","pubTimestamp":1788175748,"startTime":"0","endTime":"0","summary":null,"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://www.zhitongcaijing.com/immediately.html?type=usstock","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":"live_zhitongcaijing","symbols":["MDTX","IBBQ","PSYK","IBBJ","BMED"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2663077697","title":"石藥創新:控股子公司SYH2092注射液啓動Ⅰ期臨床試驗","url":"https://stock-news.laohu8.com/highlight/detail?id=2663077697","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2663077697?lang=zh_tw&edition=fundamental","pubTime":"2026-08-31 19:08","pubTimestamp":1788174515,"startTime":"0","endTime":"0","summary":null,"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://www.zhitongcaijing.com/immediately.html?type=usstock","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":"live_zhitongcaijing","symbols":["IBBJ","IBBQ","MDTX","PSYK","BMED"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2663074148","title":"歐康維視生物-B(01477):OT-202 III期臨床試驗完成首例患者入組","url":"https://stock-news.laohu8.com/highlight/detail?id=2663074148","media":"智通财经","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2663074148?lang=zh_tw&edition=fundamental","pubTime":"2026-08-31 18:26","pubTimestamp":1788171975,"startTime":"0","endTime":"0","summary":"智通财经APP讯,欧康维视生物-B 发布公告,用于治疗干眼症的 OT-202于中国进行的III期临床试验已完成首例患者入组。首例患者成功入组标志着OT-202在中国临床开发的一项重要里程碑,并体现集团为干眼症患者推进创新疗法的承诺。OT-202的II期临床试验,已于2023年11月于中国完成合共213名患者的II期临床试验入组。OT-202的II期临床试验结果已在国际顶尖眼科期刊《Ophthalmology》发表。2024年3月,OT-202的II期临床试验达到其主要终点。","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://www.zhitongcaijing.com/content/detail/1489598.html","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":"stock_zhitongcaijing","symbols":["PSYK","BK1191","BMED","BK1574","MDTX","01477","IBBQ","IBBJ"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2663079555","title":"ST百靈(002424.SZ)子公司創新藥吸入用BD77臨床試驗申請獲批","url":"https://stock-news.laohu8.com/highlight/detail?id=2663079555","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2663079555?lang=zh_tw&edition=fundamental","pubTime":"2026-08-31 17:29","pubTimestamp":1788168556,"startTime":"0","endTime":"0","summary":"智通财经APP讯,ST百灵 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