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EMA Emera Inc.
休市中 02-27 16:00:00 EST
52.04
+1.10
+2.16%
盘后
52.64
+0.60
+1.15%
17:21 EST
最高
52.29
最低
51.13
成交量
20.34万
今开
51.17
昨收
50.94
日振幅
2.27%
总市值
157.03亿
流通市值
155.53亿
总股本
3.02亿
成交额
1,059万
换手率
0.07%
流通股本
2.99亿
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
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 22:27
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
马斯克给出“AI能源”解决方案:电网夜间储能、白天放电,将使美国电力产出翻倍
华尔街见闻 · 2025-10-11
马斯克给出“AI能源”解决方案:电网夜间储能、白天放电,将使美国电力产出翻倍
选年薪百万还是985学历?研究发现收入管开心,教育管健康,两者在中上水平后均趋缓
尹哥聊基因 · 2025-10-03
选年薪百万还是985学历?研究发现收入管开心,教育管健康,两者在中上水平后均趋缓
路虎“卫士Defender运动版”纯电入门SUV路测图曝光
IT之家 · 2025-09-27
路虎“卫士Defender运动版”纯电入门SUV路测图曝光
IIgANN 2025:耐赋康®最新真实世界研究证实长期对因治疗持续展现良好有效性与安全性
智通财经 · 2025-09-18
IIgANN 2025:耐赋康®最新真实世界研究证实长期对因治疗持续展现良好有效性与安全性
欧洲药品管理局(EMA):诺和诺德(Novo Nordisk)将在2026年底前停止在欧盟/欧洲经济区(EEA)销售维格
智通财经 · 2025-09-05
欧洲药品管理局(EMA):诺和诺德(Novo Nordisk)将在2026年底前停止在欧盟/欧洲经济区(EEA)销售维格
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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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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":"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/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":["02696","HK0000165453.HKD","HK0000306685.HKD","HK0000320223.HKD","HK0000306701.USD","BK1161","BK1574","159938","BK1515","09939","BK4081","HK0000320264.USD","BK4087","EMA","CHMP"],"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","EMA","BK4081","688177"],"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":"us","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 Inc.本季度营收预计降52.39%,机构观点偏谨慎","news_tag":"earningPreview","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["EMA"],"gpt_icon":0},{"id":"2589334696","title":"乐城引进帕西生长激素注射液 为GHD患儿提供新选择","url":"https://stock-news.laohu8.com/highlight/detail?id=2589334696","media":"智通财经网","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2589334696?lang=zh_cn&edition=full","pubTime":"2025-12-08 18:40","pubTimestamp":1765190402,"startTime":"0","endTime":"0","summary":"今年1月,诺和诺德长效生长激素——帕西生长激素注射液作为临床急需药物被引入乐城博鳌未来医院(海南省妇女儿童医学中心乐城分院),并于5月正式投入临床。目前,该药已惠及20余例年龄在4.5至14.5岁之间的生长激素缺乏症(GHD)患儿,为我国GHD患儿提供了新的治疗选择。","market":"fut","thumbnail":"https://img.zhitongcaijing.com/image/20251208/20251208183409_27282.png?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250","type":0,"news_type":0,"thumbnails":["https://img.zhitongcaijing.com/image/20251208/20251208183409_27282.png?x-oss-process=image/format,jpg/quality,Q_80/resize,w_250"],"rights":null,"property":[],"language":"zh","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"http://www.zhitongcaijing.com/content/detail/1378903.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":"highlight_zhitongcaijin","symbols":["BK4208","IE00BMG7P694.USD","EMA","IE00BMG7P819.SGD","IE00BMG7P587.USD","IE00BD4GTV84.USD","BK4585","IE00BD4GTT62.SGD","IE00BMG7P926.USD","LU2346227817.USD","IE00BD4GTW91.USD","BK4588","BK4081","PEG"],"gpt_icon":0},{"id":"2589519008","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=2589519008","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2589519008?lang=zh_cn&edition=full","pubTime":"2025-12-05 09:33","pubTimestamp":1764898401,"startTime":"0","endTime":"0","summary":"智通财经APP获悉,亚盛医药-B涨超6%,截至发稿,涨5.67%,报64.2港元,成交额1993.31万港元。消息面上,12月5日,亚盛医药-B发布公告,公司原创1类新药奥雷巴替尼联合化疗治疗新诊断费城染色体阳性(Ph+)急性淋巴细胞白血病患者的全球注册III期临床研究获美国食品药品监督管理局和欧洲药品管理局同意开展。作为耐立克在欧美监管机构获批的第二个全球注册III期研究,POLARIS-1研究在多国家多中心同步入组,将加速耐立克全球特别是欧美市场的上市进程。","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/1377993.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":["BK4081","AAPG","EMA","BK1161","06855","BK4139","BK1574"],"gpt_icon":0},{"id":"2589985521","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=2589985521","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2589985521?lang=zh_cn&edition=full","pubTime":"2025-12-05 08:03","pubTimestamp":1764893004,"startTime":"0","endTime":"0","summary":"智通财经APP讯,亚盛医药-B 发布公告,公司原创1类新药奥雷巴替尼联合化疗治疗新诊断费城染色体阳性(Ph+)急性淋巴细胞白血病患者的全球注册III期临床研究获美国食品药品监督管理局和欧洲药品管理局同意开展。同时,耐立克在Ph+ ALL领域深度布局,针对Ph+ ALL领域的治疗已获《CSCO恶性血液病诊疗指南》连续推荐,并获CDE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/1377959.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":["LU1571399168.USD","LU2355687059.USD","III","BK4134","ALL","LU0985320562.USD","BK4533","BK1574","EMA","BK4585","BK4107","06855","BK4139","BK4081","BK4588","LU1699723380.USD","AAPG","BK1161"],"gpt_icon":0},{"id":"2576055837","title":"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","url":"https://stock-news.laohu8.com/highlight/detail?id=2576055837","media":"智通财经","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2576055837?lang=zh_cn&edition=full","pubTime":"2025-10-17 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 3期临床试验。该公司表示,CHMP的这一决定令人失望,并将寻求对该决定进行重新审查。","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/1356643.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":["LU0053671581.USD","EMA","INSM","BK4081","BK4007","BK4139","LU0889565916.HKD","SNY","BK4585","LU0109394709.USD","LU0320765992.SGD","IE00BFXG1179.USD","BK4588"],"gpt_icon":0},{"id":"2574545435","title":"马斯克给出“AI能源”解决方案:电网夜间储能、白天放电,将使美国电力产出翻倍","url":"https://stock-news.laohu8.com/highlight/detail?id=2574545435","media":"华尔街见闻","labels":[],"top":-1,"itemType":null,"share":"https://www.laohu8.com/m/news/2574545435?lang=zh_cn&edition=full","pubTime":"2025-10-11 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