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Emera Inc.

50.43

+1.372.79%

Volume:98.84K

Turnover:4.94M

Market Cap:15.22B

PE:19.01

High:50.43

Open:49.27

Low:49.27

Close:49.06

52wk High:50.86

52wk Low:43.90

Shares:301.75M

Float Shares:298.86M

Volume Ratio:0.37

T/O Rate:0.03%

Dividend:2.13

Dividend Rate:4.22%

EPS(TTM):2.65

EPS(LYR):1.19

ROE:9.07%

ROA:3.07%

PB:1.72

PE(LYR):42.50

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Overview Company News Filings

Press Release: ORYZON Announces Appointment of Rolando Gutierrez-Esteinou, M.D., as Chief Medical Officer for CNS

Press Release: Celyad Oncology Announces the Sale of C-CATHez (R) Catheter

Press Release: Ipsen delivers strong results in 2025, driven by solid execution across all therapeutic areas, and provides 2026 guidance

Protalix Highlights Positive EMA Opinion on Elfabrio Dosing

Desjardins Sticks to Their Hold Rating for Emera (EMA)

NervGen Pharma to Present at Unite2Fight Paralysis’ 20th Annual Science and Advocacy Symposium

Enlivex Treasury Portfolio Update: New Listing of the RAIN Token on Kraken, the Second-Largest U.S. Cryptocurrency Exchange

NervGen Pharma Appoints Adam Rogers as Chief Executive Officer to Continue Leading the Company’s Growth and Execution of Its Mission in Spinal Cord Injury

Neuren's Regulatory Hurdles for Trofinetide May Push Back EU Royalties, Says Jefferies

MT Newswires Live

Neuren Pharmaceuticals (ASX:NEU) Is Down 16.1% After EMA Setback on Trofinetide Approval Prospects

Simply Wall St.

Dogecoin Death Cross Countdown: Why This Chart Pattern Is Red Flag for DOGE Price

Neuren Faces EU Setback as EMA Panel Issues Negative Trend Vote on Trofinetide for Rett Syndrome

Aquestive Therapeutics Announces FDA Issuance of Complete Response Letter for Anaphylm™

Argenica Wins EMA Paediatric Waiver, Streamlining EU Pathway for Stroke Drug ARG-007

Protalix Fabry Disease Treatment Recommended for Approval by EMA Committee

MT Newswires Live

Protalix Wins EMA Panel Backing for New Elfabrio Dosing

CMS (867.HK/8A8.SG): Ruxolitinib Phosphate Cream Obtained China NDA Approval, Becoming The First and Only Targeted Drug for Vitiligo in China

Interim Results for the six months ended 31 October 2025

Enlivex Therapeutics Shares to Trade Exclusively on Nasdaq

Emera (EMA) Gets a Buy from RBC Capital

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Release: ORYZON Announces Appointment of Rolando Gutierrez-Esteinou, M.D., as Chief Medical Officer for CNS","url":"https://stock-news.laohu8.com/highlight/detail?id=2610929187","media":"Dow Jones","labels":["executive"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610929187?lang=en_us&edition=fundamental","pubTime":"2026-02-12 21:00","pubTimestamp":1770901200,"startTime":"0","endTime":"0","summary":"-- Based in New Jersey , to lead ORYZON's CNS clinical development. MADRID and CAMBRIDGE, Mass., Feb. 12, 2026  -- Oryzon Genomics, S.A. , a clinical-stage biopharmaceutical company and global leader in epigenetics, today announced the appointment of Rolando Gutierrez-Esteinou, M.D., as Chief Medical Officer, CNS Programs. Dr. Gutierrez-Esteinou is a Harvard-trained psychiatrist and an accomplished global clinical development executive with more than 20 years of leadership experience advancing neuroscience and psychiatry-focused drug development programs. He brings deep expertise in late-stage clinical execution, regulatory strategy, and pathways to market approval.\"It is a privilege to join Oryzon as Chief Medical Officer and help advance vafidemstat, the onl","market":"hk","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":"1","news_top_title":null,"news_tag":"executive","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4081","BK4090","USA","CNS","BK4022","BK4156","EMA","ORR","CMT","R","BK4135","BK4232"],"gpt_icon":0},{"id":"2610913763","title":"Press Release: Celyad Oncology Announces the Sale of C-CATHez (R) Catheter","url":"https://stock-news.laohu8.com/highlight/detail?id=2610913763","media":"Dow Jones","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610913763?lang=en_us&edition=fundamental","pubTime":"2026-02-12 14:00","pubTimestamp":1770876000,"startTime":"0","endTime":"0","summary":"Celyad Oncology  , today announced the acquisition by CellProthera of C-Cath  , the transendocardial catheter originally developed by Celyad Oncology. The acquisition is a decisive step for CellProthera as it prepares to enter Phase 3 clinical trial, with the transendocardial catheter as a cornerstone of its therapeutic approach, enabling targeted delivery of stem cells directly into damaged cardiac tissue. The transaction relates to all intellectual property rights and associated technical documentation.This release may contain forward-looking statements, including, without limitation, statements regarding beliefs about and expectations for the Company's updated strategic business model, including associated potential benefits, transactions and partnerships, statements regarding the potential value of the Company's IP, statements regarding the Company's financial statements and cash runway, statements regarding the Company's future fundraising plans, statements regarding the Company's","market":"sg","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":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4232","R","EMA","BK4081","BK4022"],"gpt_icon":0},{"id":"2610137659","title":"Press Release: Ipsen delivers strong results in 2025, driven by solid execution across all therapeutic areas, and provides 2026 guidance","url":"https://stock-news.laohu8.com/highlight/detail?id=2610137659","media":"Dow Jones","labels":["dataReport"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610137659?lang=en_us&edition=fundamental","pubTime":"2026-02-12 14:00","pubTimestamp":1770876000,"startTime":"0","endTime":"0","summary":"-- FY 2025 sales growth of 10.9% at CER1, or 8.1% as reported, driven by. growth of the three therapeutic areas of Oncology , Rare Disease.  and Neuroscience ; Somatuline sales growth of 4.3%1,with all other products, excluding Somatuline, achieving double-digit. -- FY 2025 core operating income of EUR1,294m, growing by 16.7% as reported,with a core operating margin of 35.2% of total sales, increasing by. -- 2025 continued pipeline expansion, driven by significant regulatory and. clinical milestones, integration of multiple preclinical assets with. global rights and innovative approaches, and a mid-stage candidate from. addition to the full data readout for IPN10200 in an aesthetics. PARIS, FRANCE, 12 February 2026 - Ipsen , a global specialty-care biopharmaceutical company, today presents its financial results for the full year  2025 and for the fourth quarter of 2025.\"In 2025, Ipsen delivered strong sales and profit growth,\" said David Loew, Chief Executive Officer, Ipsen. \"We contin","market":"sg","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":"1","news_top_title":null,"news_tag":"dataReport","news_rank":0,"length":0,"strategy_id":0,"source":null,"symbols":["BK4231","BK4232","EMA","BK4080","BK4081","ADC","R","BOLD","BK4022","BK4139"],"gpt_icon":0},{"id":"2610962722","title":"Protalix Highlights Positive EMA Opinion on Elfabrio Dosing","url":"https://stock-news.laohu8.com/highlight/detail?id=2610962722","media":"TIPRANKS","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610962722?lang=en_us&edition=fundamental","pubTime":"2026-02-12 06:28","pubTimestamp":1770848911,"startTime":"0","endTime":"0","summary":"Protalix ( ($PLX) ) just unveiled an announcement. On February 11, 2026, Protalix BioTherapeutics posted an updated corporate presentation outlinin...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/protalix-highlights-positive-ema-opinion-on-elfabrio-dosing?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/company-announcements/protalix-highlights-positive-ema-opinion-on-elfabrio-dosing?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["EMA","BK4081"],"gpt_icon":0},{"id":"2610295288","title":"Desjardins Sticks to Their Hold Rating for Emera (EMA)","url":"https://stock-news.laohu8.com/highlight/detail?id=2610295288","media":"TIPRANKS","labels":[],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2610295288?lang=en_us&edition=fundamental","pubTime":"2026-02-12 00:35","pubTimestamp":1770827716,"startTime":"0","endTime":"0","summary":"In a report released today, Brent Stadler from Desjardins maintained a Hold rating on Emera, with a price target of C$68.00. 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investment firm now expects royalties from EU sales of trofinetide to kick in the fourth quarter of fiscal 2026, and not second quarter.Meanwhile, it projects Neuren's experimental drug NNZ-2591 for treating Pitt-Hopkins Syndrome, a rare neurodevelopmental disorder, will receive reimbursement approval in the US in fiscal 2029.Jefferies lowered the company's fisca","market":"sg","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":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["CHMP","BK7508","EMA","EMA.AU","BK4087","BK7129","BK4156","NEU.AU","BK4081","BK7096"],"gpt_icon":0},{"id":"2608549573","title":"Neuren Pharmaceuticals (ASX:NEU) Is Down 16.1% After 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As of this week,DOGE is trading at just over $0.107 - barely holding above the Oct. 10 dump level of $0.0995, when $40 billion at least","market":"other","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"utodaynews_highlight","url":"https://u.today/dogecoin-death-cross-countdown-why-this-chart-pattern-is-red-flag-for-doge-price","rn_cache_url":null,"directOrigin":true},"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://u.today/dogecoin-death-cross-countdown-why-this-chart-pattern-is-red-flag-for-doge-price","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-1","news_top_title":null,"news_tag":"","news_rank":0,"length":0,"strategy_id":0,"source":"utodaynews_highlight","symbols":["GTLS","IE00B66KJ199.SGD","LU0823414478.USD","IE0031619046.USD","BK7129","EMA","BK4217","SMA","LU2249611893.SGD","LU2048586759.USD","LU1988902786.USD","LU2211815571.USD","LU2264538146.SGD","BK4161","IE00B7SZL793.SGD","LU1064131342.USD","IE00B19Z4B17.USD","DOGE.USD.HKCC","PEGI","LU2355687059.USD","IE00BFMHRM44.USD","EMA.AU","BK4081"],"gpt_icon":0},{"id":"2608628819","title":"Neuren Faces EU Setback as EMA Panel Issues Negative Trend Vote on Trofinetide for Rett Syndrome","url":"https://stock-news.laohu8.com/highlight/detail?id=2608628819","media":"TIPRANKS","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2608628819?lang=en_us&edition=fundamental","pubTime":"2026-02-03 07:48","pubTimestamp":1770076136,"startTime":"0","endTime":"0","summary":"Neuren Pharmaceuticals Limited ( ($AU:NEU) ) has provided an update. Neuren Pharmaceuticals disclosed that its licensee Acadia Pharmaceuticals has ...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/neuren-faces-eu-setback-as-ema-panel-issues-negative-trend-vote-on-trofinetide-for-rett-syndrome?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/company-announcements/neuren-faces-eu-setback-as-ema-panel-issues-negative-trend-vote-on-trofinetide-for-rett-syndrome?utm_source=itigerup.com&utm_medium=referral","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"-2","news_top_title":null,"news_tag":"policyRegulatory","news_rank":0,"length":0,"strategy_id":0,"source":"tipranks_highlight","symbols":["EMA","BK4081","BK4156"],"gpt_icon":0},{"id":"2608866509","title":"Aquestive Therapeutics Announces FDA Issuance of Complete Response Letter for Anaphylm™","url":"https://stock-news.laohu8.com/highlight/detail?id=2608866509","media":"GlobeNewswire","labels":["policyRegulatory"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2608866509?lang=en_us&edition=fundamental","pubTime":"2026-02-02 20:00","pubTimestamp":1770033600,"startTime":"0","endTime":"0","summary":"Deficiencies limited to packaging and administrationCompany believes it can rapidly resolve deficiencies and expects to resubmit as early as Q3 2026Remains well-capitalized and anticipates ending 2026","market":"hk","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.globenewswire.com/news-release/2026/02/02/3230115/0/en/Aquestive-Therapeutics-Announces-FDA-Issuance-of-Complete-Response-Letter-for-Anaphylm.html","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":null,"symbols":["BK4139","HF","PK","BK4181","EMA","IE00BFMHRM44.USD","CRL","LU0390134368.USD","LU0128526141.USD","LU1815336091.USD","LU0029874061.USD","BK4081","LENZ","AQST","BK4530","BK4007","BK4588","BK4539","LU0757428866.USD","BK4121","BK4585","BK4218"],"gpt_icon":0},{"id":"2608824758","title":"Argenica Wins EMA Paediatric Waiver, Streamlining EU Pathway for Stroke Drug ARG-007","url":"https://stock-news.laohu8.com/highlight/detail?id=2608824758","media":"TIPRANKS","labels":["corporation"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2608824758?lang=en_us&edition=fundamental","pubTime":"2026-02-02 07:17","pubTimestamp":1769987833,"startTime":"0","endTime":"0","summary":"Argenica Therapeutics Ltd ( ($AU:AGN) ) has issued an update. Argenica Therapeutics has secured a full product-specific paediatric waiver from the ...","market":"us","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/argenica-wins-ema-paediatric-waiver-streamlining-eu-pathway-for-stroke-drug-arg-007?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/company-announcements/argenica-wins-ema-paediatric-waiver-streamlining-eu-pathway-for-stroke-drug-arg-007?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["BK4156","EMA","BK4081"],"gpt_icon":0},{"id":"2607047855","title":"Protalix Fabry Disease Treatment Recommended for Approval by EMA Committee","url":"https://stock-news.laohu8.com/highlight/detail?id=2607047855","media":"MT Newswires Live","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2607047855?lang=en_us&edition=fundamental","pubTime":"2026-01-30 23:32","pubTimestamp":1769787142,"startTime":"0","endTime":"0","summary":"Protalix BioTherapeutics and Chiesi Global Rare Diseases said Friday that Elfabrio, an enzyme replacement therapy to treat Fabry disease, has received a positive opinion from the Committee for Medicinal Products for Human Use of the European Medicines Agency.Protalix will be eligible to receive a regulatory milestone payment of $25 million if the treatment is approved by the European Commission, the companies said.Protalix shares were more than 7% higher in recent trading.Price: 2.26, Change: +0.18, Percent Change: +8.41","market":"sg","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":null,"property":[],"language":"en","translate_title":"","themeId":null,"theme_name":"","theme_type":"","isJumpTheme":false,"source_url":"https://www.mtnewswires.com/","is_publish_highlight":false,"source_rank":0,"column":"","sentiment":"1","news_top_title":null,"news_tag":"productRelease","news_rank":0,"length":0,"strategy_id":0,"source":"mtnewswires_news","symbols":["BK4081","PLX","EMA","BK4139"],"gpt_icon":0},{"id":"2607899047","title":"Protalix Wins EMA Panel Backing for New Elfabrio Dosing","url":"https://stock-news.laohu8.com/highlight/detail?id=2607899047","media":"TIPRANKS","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2607899047?lang=en_us&edition=fundamental","pubTime":"2026-01-30 23:28","pubTimestamp":1769786915,"startTime":"0","endTime":"0","summary":"Protalix ( ($PLX) ) just unveiled an announcement. On January 30, 2026, Protalix BioTherapeutics and its partner Chiesi Global Rare Diseases announ...","market":"nz","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/company-announcements/protalix-wins-ema-panel-backing-for-new-elfabrio-dosing?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/company-announcements/protalix-wins-ema-panel-backing-for-new-elfabrio-dosing?utm_source=itigerup.com&utm_medium=referral","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":"tipranks_highlight","symbols":["EMA","BK4081"],"gpt_icon":0},{"id":"2607045311","title":"CMS (867.HK/8A8.SG): Ruxolitinib 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