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LABU 三倍做多标普生物-Direxion
交易中 10-01 14:35:05 EDT
259.13
-6.66
-2.50%
最高
271.77
最低
254.77
成交量
32.37万
今开
261.76
昨收
265.79
日振幅
6.40%
总市值
5.89亿
流通市值
5.89亿
总股本
227.45万
成交额
8,448万
换手率
14.23%
流通股本
227.45万
市净率
--
ROE
--
每股收益
0.00
52周最高
--
52周最低
--
市盈率
--
股息
--
股息收益率
--
ROA
--
分时
五日
日K
周K
月K
数据加载中...
北京优虎网络科技有限公司
资讯
新帖
简况
ADP报告:自5月以来,招聘活动首次加速,其中教育、医疗保健以及休闲和酒店行业引领增长。金融活动以及专业和商业服务行业则
格隆汇 · 09-30 20:21
ADP报告:自5月以来,招聘活动首次加速,其中教育、医疗保健以及休闲和酒店行业引领增长。金融活动以及专业和商业服务行业则
罗氏(RHHBY)推出三合一新生儿遗传病筛查试剂盒 多发性硬化症口服新药芬布替尼获FDA优先审评
金吾财讯 · 09-30 16:45
罗氏(RHHBY)推出三合一新生儿遗传病筛查试剂盒 多发性硬化症口服新药芬布替尼获FDA优先审评
亿帆医药:Ryzneuta增加中国境内生产场地获得美国FDA批准
智通财经 · 09-30 14:43
亿帆医药:Ryzneuta增加中国境内生产场地获得美国FDA批准
港股异动 | 和黄医药(00013)涨超3% 宣布向FDA提交沃瑞沙®联合泰瑞沙®联合疗法的新药上市申请
智通财经 · 09-30 10:50
港股异动 | 和黄医药(00013)涨超3% 宣布向FDA提交沃瑞沙®联合泰瑞沙®联合疗法的新药上市申请
健友股份:阿达木单抗40mg/0.4mL获FDA批准
智通财经 · 09-29 16:01
健友股份:阿达木单抗40mg/0.4mL获FDA批准
艾伯维(ABBV)旗下创新帕金森病治疗药物Juvmo片剂上市申请获FDA正式批准
金吾财讯 · 09-28
艾伯维(ABBV)旗下创新帕金森病治疗药物Juvmo片剂上市申请获FDA正式批准
美国食品药品监督管理局(FDA)批准艾伯维的JUVMO™(tavapadon)用于治疗帕金森病。
格隆汇 · 09-28
美国食品药品监督管理局(FDA)批准艾伯维的JUVMO™(tavapadon)用于治疗帕金森病。
德展健康(000813.SZ)子公司创新药WYY026B注射液获得美国FDA新药临床试验批准
智通财经 · 09-28
德展健康(000813.SZ)子公司创新药WYY026B注射液获得美国FDA新药临床试验批准
健友股份(603707.SH)子公司产品维生素B1注射液获得美国FDA批准
智通财经 · 09-28
健友股份(603707.SH)子公司产品维生素B1注射液获得美国FDA批准
信达生物:IBI363临床研究获美国FDA批准新增非鳞状非小细胞肺癌研究人群
智通财经 · 09-28
信达生物:IBI363临床研究获美国FDA批准新增非鳞状非小细胞肺癌研究人群
Prime Medicine(PRME)盘前涨10.45% FDA批准其PM647的新药临床试验申请
金吾财讯 · 09-25
Prime Medicine(PRME)盘前涨10.45% FDA批准其PM647的新药临床试验申请
夏邑人速看!延续实施扩大社会保险补贴范围政策,直补个人,最长可领12个月!
掌握夏邑 · 09-25
夏邑人速看!延续实施扩大社会保险补贴范围政策,直补个人,最长可领12个月!
兰州市自明年起不再向用人单位收取退休人员大额医疗保险费
中国兰州网 · 09-25
兰州市自明年起不再向用人单位收取退休人员大额医疗保险费
美国 FDA 批准一款肾病药物后,默沙东股价持平但成交量激增,最新上涨 0.50%,报 148.81 美元。
智通财经 · 09-25
美国 FDA 批准一款肾病药物后,默沙东股价持平但成交量激增,最新上涨 0.50%,报 148.81 美元。
遭FDA进口禁令,圣诺生物美国业务亮起红灯
新浪证券 · 09-24
遭FDA进口禁令,圣诺生物美国业务亮起红灯
全球多癌早筛闯过FDA专家这一关,华大基因早筛业务迎来下一轮产品兑现窗口
新浪财经 · 09-24
全球多癌早筛闯过FDA专家这一关,华大基因早筛业务迎来下一轮产品兑现窗口
晶泰向美国FDA提交KQTD-126新药临床试验申请
智通财经 · 09-24
晶泰向美国FDA提交KQTD-126新药临床试验申请
医疗保健板块市场快讯汇总
投资观察 · 09-23
医疗保健板块市场快讯汇总
医疗保健板块市场快讯综述
投资观察 · 09-23
医疗保健板块市场快讯综述
健友股份:子公司获美国FDA硫酸阿米卡星注射液生产场地批件
同花顺 · 09-22
健友股份:子公司获美国FDA硫酸阿米卡星注射液生产场地批件
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公司概况
公司名称:
三倍做多标普生物-Direxion
所属市场:
ARCA
上市日期:
--
主营业务:
发行价格:
--
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16:45","pubTimestamp":1790757948,"startTime":"0","endTime":"0","summary":"金吾财讯 | 罗氏 宣布,其诊断业务旗下子公司TIB MOLBIOL正式在认可欧盟CE标志的国家推出LightMix Newborn TREC/SMN1/HBB基因检测试剂盒。该产品已获得体外诊断医疗器械法规认证,标志着罗氏在早期诊断与新生儿筛查领域的进一步拓展。此外,罗氏同时宣布,美国食品药品监督管理局已正式受理其在研药物芬布替尼的新药申请,并授予优先审评资格。","market":"sh","thumbnail":"https://static.szfiu.com/news/20250107/MWM3M2E1ZjMzOTEwODk1MDE=.png","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20250107/MWM3M2E1ZjMzOTEwODk1MDE=.png"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"299f0a9977df499f8ead781071e5e5e7","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"306639","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease,policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["CANC","HRTS","BK4585","BK4588","RHHBY","LABU","03165","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2671506275","title":"亿帆医药:Ryzneuta增加中国境内生产场地获得美国FDA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2671506275","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2671506275?lang=zh_cn&edition=full","pubTime":"2026-09-30 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10:50","pubTimestamp":1790736612,"startTime":"0","endTime":"0","summary":"消息面上,9月29日,和黄医药发布公告,阿斯利康已向美国食品药品监督管理局提交沃瑞沙 和泰瑞沙 的联合疗法的新药上市申请,用于治疗接受一种表皮生长因子受体酪氨酸激酶抑制剂治疗期间或之后出现疾病进展的伴有MET过表达或扩增的局部晚期或转移性非小细胞肺癌患者。SAFFRON全球III期研究的数据支持了该项新药上市申请。据悉,沃瑞沙由阿斯利康与和黄医药共同开发,并由阿斯利康商业化。","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/1502493.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":["VXUS","BK1191","BK1588","BK4588","IPOS","KCAI","BK4585","00013","LABU","BK1587"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2671294611","title":"健友股份:阿达木单抗40mg/0.4mL获FDA批准","url":"https://stock-news.laohu8.com/highlight/detail?id=2671294611","media":"智通财经","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2671294611?lang=zh_cn&edition=full","pubTime":"2026-09-29 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21:15","pubTimestamp":1790601343,"startTime":"0","endTime":"0","summary":"此次获批基于成功的3期TEMPO临床项目。艾伯维官方表示,计划于2026年10月正式将Juvmo投放美国市场,供帕金森病患者使用。据介绍,该药是艾伯维此前斥资87亿美元收购Cerevel Therapeutics公司后迎来的首个重大研发成果落地,进一步夯实了其在神经科学领域的全球领先地位。","market":"sg","thumbnail":"https://static.szfiu.com/news/20250107/ZWE1ODViOTJlYWU0Yzg0YTU1MDJhZDdhZjY5ZjlmNDM0MDU5MzAwNzIw.png","type":0,"news_type":0,"thumbnails":["https://static.szfiu.com/news/20250107/ZWE1ODViOTJlYWU0Yzg0YTU1MDJhZDdhZjY5ZjlmNDM0MDU5MzAwNzIw.png"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"306564","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":["LU1720051108.HKD","SG9999001440.SGD","LU2087621335.USD","LU0882574055.USD","LU0211327993.USD","LU0289739343.SGD","ABBV","GLAM","LU0289961442.SGD","IE00BSNM7G36.USD","IXJ","LU1929549753.HKD","LU1720051017.SGD","LU1093756168.USD","TRUH","LU1037948897.HKD","LU0942090050.USD","LU1718418525.SGD","LU1244550577.SGD","VHT","XLV","PPH","MEDX","RXL","IE0002141913.USD","BK4533","BK4581","FHLC","LU0203347892.USD","IE0009355771.USD","LU1267930573.SGD","LU1934455863.HKD","IPOS","IYH","PJP","FTXH","LABU","LU2125909247.SGD","LU1496350502.SGD","LU1989772923.USD","AGNG","LU1839511570.USD","LU0203345920.USD","LU1934455277.USD","LU0124676726.USD","IE00B19Z3B42.SGD","LU0128525929.USD","IBRN","LU0738911758.USD","JDOC"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2670232662","title":"美国食品药品监督管理局(FDA)批准艾伯维的JUVMO™(tavapadon)用于治疗帕金森病。","url":"https://stock-news.laohu8.com/highlight/detail?id=2670232662","media":"格隆汇","labels":[],"top":-1,"itemType":null,"share":"https://www.laohunote.com/m/news/2670232662?lang=zh_cn&edition=full","pubTime":"2026-09-28 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17:08","pubTimestamp":1790586484,"startTime":"0","endTime":"0","summary":"智通财经APP讯,德展健康 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