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EMA Emera Inc.
未开盘 04-14 16:00:00 EDT
52.46
-0.04
-0.08%
盘后
52.46
+0.00
0.00%
19:47 EDT
最高
52.74
最低
52.10
成交量
123.48万
今开
52.64
昨收
52.50
日振幅
1.23%
总市值
160.41亿
流通市值
160.00亿
总股本
3.06亿
成交额
6,473万
换手率
0.40%
流通股本
3.05亿
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
港股异动 | 和誉-B(02256)盘中涨近10% FGFR4抑制剂依帕戈替尼获EMA授予孤儿药资格
智通财经 · 04-01
港股异动 | 和誉-B(02256)盘中涨近10% FGFR4抑制剂依帕戈替尼获EMA授予孤儿药资格
和誉-B(02256):FGFR4抑制剂依帕戈替尼获EMA授予孤儿药资格,用于治疗肝细胞癌
智通财经 · 03-31
和誉-B(02256):FGFR4抑制剂依帕戈替尼获EMA授予孤儿药资格,用于治疗肝细胞癌
韩国与新加坡启动自贸协定升级谈判并签署核电合作备忘录
核电网 · 03-03
韩国与新加坡启动自贸协定升级谈判并签署核电合作备忘录
百奥泰:Usymro(乌司奴单抗注射液)获得英国 MHRA 上市批准
格隆汇 · 03-03
百奥泰:Usymro(乌司奴单抗注射液)获得英国 MHRA 上市批准
复宏汉霖(02696):帕妥珠单抗生物类似药HLX11(重组抗HER2结构域II人源化单克隆抗体注射液)获欧洲药品管理局(EMA)人用医药产品委员会(CHMP)积极审评意见
智通财经 · 02-27
复宏汉霖(02696):帕妥珠单抗生物类似药HLX11(重组抗HER2结构域II人源化单克隆抗体注射液)获欧洲药品管理局(EMA)人用医药产品委员会(CHMP)积极审评意见
百奥泰(688177)披露Gotenfia(戈利木单抗注射液)获欧洲EMA上市批准的公告,2月24日股价下跌0.68%
中金财经 · 02-24
百奥泰(688177)披露Gotenfia(戈利木单抗注射液)获欧洲EMA上市批准的公告,2月24日股价下跌0.68%
财报前瞻|Emera Inc.本季度营收预计降52.39%,机构观点偏谨慎
财报Agent · 02-16
财报前瞻|Emera Inc.本季度营收预计降52.39%,机构观点偏谨慎
乐城引进帕西生长激素注射液 为GHD患儿提供新选择
智通财经网 · 2025-12-08
乐城引进帕西生长激素注射液 为GHD患儿提供新选择
港股异动 | 亚盛医药-B(06855)涨超6% 耐立克®POLARIS-1研究获美国FDA和欧洲EMA批准
智通财经 · 2025-12-05
港股异动 | 亚盛医药-B(06855)涨超6% 耐立克®POLARIS-1研究获美国FDA和欧洲EMA批准
亚盛医药-B(06855)耐立克®一线治疗Ph+ ALL的全球注册III期临床研究获美国FDA和欧洲EMA批准
智通财经 · 2025-12-05
亚盛医药-B(06855)耐立克®一线治疗Ph+ ALL的全球注册III期临床研究获美国FDA和欧洲EMA批准
EMA十月药品审评会议:赛诺菲(SNY.US)、Insmed(INSM.US)等公司新药获上市推荐
智通财经 · 2025-10-17
EMA十月药品审评会议:赛诺菲(SNY.US)、Insmed(INSM.US)等公司新药获上市推荐
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公司概况
公司名称:
Emera Inc.
所属市场:
NYSE
上市日期:
--
主营业务:
Emera Inc.于1998年7月23日在加拿大注册成立,是一家北美能源服务提供商,拥有并经营服务成本、费率管制的电力和天然气公用事业组合。该公司最大的业务在佛罗里达州,并在加拿大大西洋省、新墨西哥州和加勒比地区增加了业务。Emera总部位于新斯科舍省哈利法克斯,其业务战略侧重于对其受监管的公用事业、卓越运营和效率进行持续投资,以便为其270万客户可靠地提供能源。公司在受监管公用事业的盈利机会取决于净投资规模、资本结构权益和目标回报,这些都是通过监管建立起来的。
发行价格:
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15:57","pubTimestamp":1775030256,"startTime":"0","endTime":"0","summary":"消息面上,和誉宣布,其自主研发的高选择性小分子FGFR4抑制剂依帕戈替尼已获得欧洲药品管理局授予的孤儿药资格,用于治疗肝细胞癌。目前,依帕戈替尼正在全球多地开展临床研究,此次获EMA授予ODD,将为该产品在欧洲的临床开发、注册申报与商业化进程提供有力支持。除本次获得EMA孤儿药资格外,依帕戈替尼此前还分别获得了美国食品药品监督管理局授予的ODD和快速通道资格认定,以及中国国家药品监督管理局授予的突破性疗法认定。","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":"http://www.zhitongcaijing.com/content/detail/1423918.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":["IE00BPRC5H50.USD","LU2476274720.SGD","BK4585","BK4588","VXUS","BK1161","LU2778985437.USD","IE00B543WZ88.USD","IE00B5MMRT66.SGD","02256","LU2476274308.USD","EMA","BK4081","LU2488822045.USD"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2623581546","title":"和誉-B(02256):FGFR4抑制剂依帕戈替尼获EMA授予孤儿药资格,用于治疗肝细胞癌","url":"https://stock-news.laohu8.com/highlight/detail?id=2623581546","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2623581546?lang=zh_cn&edition=full","pubTime":"2026-03-31 20:32","pubTimestamp":1774960347,"startTime":"0","endTime":"0","summary":"智通财经APP讯,和誉-B 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18:22","pubTimestamp":1772533330,"startTime":"0","endTime":"0","summary":"近日,韩国总统李在明对新加坡进行了国事访问,两国就升级韩-兴自由贸易协定及核电合作达成重要共识。韩国产业通商资源部长官与新加坡贸工部代表于3月2日共同签署了《关于启动韩新自贸协定升级谈判的联合宣言》。与此同时,韩国水电与核电公司和新加坡能源市场厅也签署了关于小型模块化反应堆合作的谅解备忘录,这标志着韩国核电企业首次与新加坡政府机构在核电领域建立正式合作关系。","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=nesSN20260303202141a69d90f6&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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批准上市,美国注册商品名称为STARJEMZA,欧洲注册商品名称为 Usymro;已向中国 NMPA 递交上市许可申请,目前正在评审中。Usymro获得英国 MHRA 上市批准后可在英国进行销售,公司海外销售产品品类得到进一步扩充,将进一步提升公司产品的国际影响力,有望对公司长期经营业绩产生积极影响。","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=nesSN20260303163601a445ce72&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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发布公告,近日,HLX11获EMA人用医药产品委员会积极审评意见,推荐批准HLX11的上市许可申请。倘若获得EC批准,HLX11的集中上市许可将在所有欧盟成员国及欧洲经济区国家冰岛、列支敦士登和挪威生效。HLX11是本公司自主研发的帕妥珠单抗生物类似药。2024年12月,HLX11的上市注册申请获国家药品监督管理局受理。2025年3月,HLX11的上市许可申请获欧洲药品管理局受理。","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":"http://www.zhitongcaijing.com/content/detail/1408509.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":["BK1161","159938","BK4081","BK1515","CHMP","HK0000320264.USD","HK0000306701.USD","BK1574","BK4087","HK0000165453.HKD","02696","HK0000320223.HKD","EMA","HK0000306685.HKD","09939"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2613797244","title":"百奥泰(688177)披露Gotenfia(戈利木单抗注射液)获欧洲EMA上市批准的公告,2月24日股价下跌0.68%","url":"https://stock-news.laohu8.com/highlight/detail?id=2613797244","media":"中金财经","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2613797244?lang=zh_cn&edition=full","pubTime":"2026-02-24 18:41","pubTimestamp":1771929669,"startTime":"0","endTime":"0","summary":"百奥泰生物制药股份有限公司近日披露公告,公司收到欧洲药品管理局通知,其开发的戈利木单抗注射液已获EMA上市批准。BAT2506是依据NMPA、FDA和EMA指导原则开发的生物类似药,目前上市申请已获NMPA、FDA及巴西国家卫生监督局受理。该批准有望对公司长期经营业绩产生积极影响,但未来可能面临激烈市场竞争。","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://sc.stock.cnfol.com/gushiyaowen/20260224/32024193.shtml","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":"zhongjincaijing_highlight","symbols":["BK0239","688177","BK4081","EMA"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"1189502436","title":"财报前瞻|Emera Inc.本季度营收预计降52.39%,机构观点偏谨慎","url":"https://stock-news.laohu8.com/highlight/detail?id=1189502436","media":"财报Agent","labels":["earningPreview"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/1189502436?lang=zh_cn&edition=full","pubTime":"2026-02-16 10:14","pubTimestamp":1771208088,"startTime":"0","endTime":"0","summary":"Emera Inc.将于2026年02月23日美股盘前发布最新季度财报,市场关注营收与每股收益的同比下滑幅度及业务结构变化。市场一致预期显示,本季度Emera Inc.营收预计为9.66亿美元,同比下降52.39%;调整后每股收益预计为0.56美元,同比下降27.14%;息税前利润预计为2.11亿美元,同比下降72.86%。上季度Emera Inc.营收21.06亿美元,同比增长16.87%;毛利率44.06%;归属母公司净利润2.47亿美元,净利率11.73%,净利润环比增长60.39%;调整后每股收益0.88美元,同比增长8.64%。","market":"sh","thumbnail":"","type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":"","theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":"财报前瞻|Emera 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21:29","pubTimestamp":1760707780,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,在本周召开的会议上,欧洲药品管理局的专家小组对赛诺菲与Insmed的两款新药做出了推荐在该地区上市的积极意见。除了推荐新药获批外,该委员会还否决了赛诺菲的一款新药,并推荐了8项新的药品适应症扩展申请。赛诺菲表示,这一决定基于该公司关键的LUNA 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