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Emera Inc.

50.10

+0.01000.02%

Volume:300.31K

Turnover:15.01M

Market Cap:15.32B

PE:22.47

High:50.39

Open:49.79

Low:49.70

Close:50.09

52wk High:55.49

52wk Low:45.77

Shares:305.78M

Float Shares:305.78M

Volume Ratio:0.95

T/O Rate:0.10%

Dividend:2.10

Dividend Rate:4.19%

EPS(TTM):2.23

EPS(LYR):2.47

ROE:7.56%

ROA:2.91%

PB:1.65

PE(LYR):20.32

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Overview Company News Filings

Zai Lab Receives EU Orphan Drug Designation for Lung Cancer Drug

MT Newswires Live

Press Release: GENFIT: June 15, 2026 Combined Shareholders Meeting Results

XRP Presents Strongest Move Since Dropping Below 50 EMA

GSK announces momelotinib granted ODD from U.S. FDA, EMA

Press Release: Cosmos Health Signs LOI to Acquire Doc Pharma S.A., a European GMP Pharmaceutical Manufacturer, a Transformative Step Expected to Boost Assets, Profitability, Production Capacity, and Product Portfolio

Oculis to Present Privosegtor at Upcoming Clinical Trials at the Summit 2026

Oculis to Present Privosegtor at Upcoming Clinical Trials at the Summit 2026

MAIA Biotechnology Activates and Opens Enrollment at Second U.S. Clinical Site for International Phase 2 THIO-101 Expansion Trial

Cosmos Health CEO Issues Letter to Shareholders: Building an Innovative AI-Driven Global Healthcare Platform — Record Growth with U.S. Expansion Underway

Longeveron Granted Small or Medium-sized Enterprise (SME) Status by the European Medicines Agency (EMA)

Oculis to Present at the 47th Annual Goldman Sachs Global Healthcare Conference

Cardano Price Hits All-Time Low: Why Charles Hoskinson's Project Failed

Cosmos Health Continues U.S. Expansion with Launch of Oliv18, Targeting Cardiovascular and Antioxidant Categories

Cosmos Health Identifies Approximately $20 Million in Non-Core Assets Available for Monetization to Accelerate Growth and Unlock Shareholder Value

Cosmos Health Enters $69 Billion Global Animal Health Industry with Veterinary C-Scrub Wash 4% Following Successful European Standard Testing Under EN 1656 and EN 1657

Ascentage Pharma Presents Data on Olverembatinib in CML-LBP and Ph+ BCP-ALL at ASCO 2026

Ascentage Pharma Presents Updated Clinical Data for Olverembatinib as Second-Line Therapy in CML-CP at ASCO 2026

Actinogen receives positive EMA scientific advice aligned with prior FDA guidance for its Alzheimer’s disease program

Ribo Announces Phase 2 Clinical Trial Submission to EMA, Further Advancing siRNA Therapeutics in Thromboembolic Disease

Actinogen Medical Reaches Common Understanding With European Regulator on Pathway to Marketing Approval for Alzheimers' Disease Program

MT Newswires Live

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Lille ; Cambridge, ; Zurich ; June 15, 2026 - GENFIT ,, a biopharmaceutical company dedicated to improving the lives of patients with rare and life-threatening liver diseases, today announced the results of the Combined Shareholders Meeting which took place on June 15, 2026. The quorum on first convening amounted to 32.13 % and shareholders approved all of the resolutions, with the exception of resolution ndeg26 which was rejected in accordance with the recommendations of the Board of Directors.The voting results, resolution by resolution, are available in the Investors & Media section of the Company's website .This press release contains certain forward-looking statements with respect to GENFIT. The use of certain words, such as \"believe\", \"potential\", \"expect\", \"target\", \"may\", \"will\", \"should\", \"could\", \"if\"","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://dowjonesnews.com/newdjn/logon.aspx?AL=N","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":null,"symbols":["BK4588","BK4604","BK4555","BK4099","BK4081","BK4022","BK4232","EMA","PBC","R","CCA","BK4132","HE","AD","TM","BK4585","USA","03160"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2643207889","title":"XRP Presents Strongest Move Since Dropping Below 50 EMA","url":"https://stock-news.laohu8.com/highlight/detail?id=2643207889","media":"utoday","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2643207889?lang=en_us&edition=fundamental","pubTime":"2026-06-15 10:33","pubTimestamp":1781490780,"startTime":"0","endTime":"0","summary":"After weeks of intense selling pressure, XRP is finally beginning to show signs of life.The asset experienced a severe correction that drove it toward the $1.10 region after breaking below the 50-day ","market":"hk","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"utodaynews_highlight","url":"https://u.today/xrp-presents-strongest-move-since-dropping-below-50-ema","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://u.today/xrp-presents-strongest-move-since-dropping-below-50-ema","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":"utodaynews_highlight","symbols":["XRPI","XRPK","BK7129","XRP","XRPZ","XRPR","XRPC","UXRP","BK4081","XRPT","TOXR","EMA","EMA.AU","XXRP","BITW"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642267278","title":"GSK announces momelotinib granted ODD from U.S. FDA, EMA","url":"https://stock-news.laohu8.com/highlight/detail?id=2642267278","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642267278?lang=en_us&edition=fundamental","pubTime":"2026-06-12 19:07","pubTimestamp":1781262453,"startTime":"0","endTime":"0","summary":"GSK (GSK) announced that momelotinib, a JAK inhibitor with a differentiated mechanism of action, has received Orphan Drug Designation, ODD, from th...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/the-fly/gsk-announces-momelotinib-granted-odd-from-u-s-fda-ema-thefly-news?utm_source=itigerup.com&utm_medium=referral","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.tipranks.com/news/the-fly/gsk-announces-momelotinib-granted-odd-from-u-s-fda-ema-thefly-news?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["BK4183","BK4585","ODD","BK4588","LU1829250122.USD","GSK","IE0009354923.USD","BK4081","EMA","GSK.UK","BK4532","LABU","GSKH","BK4007"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2642023976","title":"Press Release: Cosmos Health Signs LOI to Acquire Doc Pharma S.A., a European GMP Pharmaceutical Manufacturer, a Transformative Step Expected to Boost Assets, Profitability, Production Capacity, and Product Portfolio","url":"https://stock-news.laohu8.com/highlight/detail?id=2642023976","media":"Dow Jones","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2642023976?lang=en_us&edition=fundamental","pubTime":"2026-06-12 03:31","pubTimestamp":1781206260,"startTime":"0","endTime":"0","summary":"-- Doc Pharma financial profile: approximately $24 million asset base,approximately $6.7 million in average annual revenue and approximately. -- Immediately accretive: expected to support margin expansion,-- Deepens vertical integration: expected to drive synergies, optimized. production, economies of scale, expanded capacity, and a strengthened R&D. square feet, built to the highest European standards, providing a clear. -- Manufacturing excellence: a broad range of dosage forms, certified to GMP,ISO, Kosher, and Halal standards, with site registrations for the UAE,-- Boosts product portfolio: adds advanced and branded generics and OTC. 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Despite the widespread use of standard of care therapies, including antiplatelet and anticoagulant therapies, a substantial residual risk of thrombotic events remains in patients with stable CAD, even when treated with optimized treatment. Current therapies are further limited by an increased risk of bleeding, restricting their intensity and long-term use in many patients. Consequently, there is a significant unmet medical need for novel antithrombotic approaches that can provide effective and sustained protection against thrombosis while maintaining a favorable safety profile, particularly with respect to bleeding risk.\"We are very pleased to advance our anti-thrombotic siRNA programs into the next stage of clinical development in Europe. This milestone reflects ","market":"other","thumbnail":"https://mma.prnewswire.com/media/2804420/logo_Ribolia_Logo.jpg?w=300","type":0,"news_type":0,"thumbnails":["https://mma.prnewswire.com/media/2804420/logo_Ribolia_Logo.jpg?w=300"],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.prnewswire.com/apac/news-releases/ribo-announces-phase-2-clinical-trial-submission-to-ema-further-advancing-sirna-therapeutics-in-thromboembolic-disease-302783857.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":null,"symbols":["CTA","BK4007","EMA.AU","BK7129","BK7504","BK4539","BK4081","EMA","BK7095","BK4139","CAD.AU","LENZ"],"isVideo":false,"video":null,"gpt_icon":0},{"id":"2638653254","title":"Actinogen Medical Reaches Common Understanding With European Regulator on Pathway to Marketing Approval for Alzheimers' Disease Program","url":"https://stock-news.laohu8.com/highlight/detail?id=2638653254","media":"MT Newswires Live","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2638653254?lang=en_us&edition=fundamental","pubTime":"2026-05-28 09:53","pubTimestamp":1779933233,"startTime":"0","endTime":"0","summary":"Actinogen Medical  reached a common understanding of the pathway to marketing approval for its Alzheimer's disease program in its scheduled scientific advice meeting with the European Medicines Agency , according to a Thursday Australian bourse filing.The understanding includes the specification of regulatory starting materials for the commercial manufacturing of Xanamem  drug substance, design considerations for an additional pivotal clinical trial, as well as the limited number of ancillary clinical pharmacology trials and nonclinical studies required.The understandings also include ensuring the proposed makeup of the planned safety database is consistent with EMA and US Food and Drug Administration  guidelines.The firm said the understandings align closely with the guidance received at an earlier meeting with the US FDA's Neurology-I division.Actinogen Medical's shares rose nearly 3% in recent trading on Thursday.","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"corporation","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["ACW.AU","EMA","EPV","BK4081","EMA.AU","BK7508","BK7067","BK7129"],"isVideo":false,"video":null,"gpt_icon":0}],"pageSize":20,"totalPage":10,"pageCount":6,"totalSize":200,"code":"91000000","status":"200"}]}}