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Emera Inc.

49.06

+0.19000.39%

Post-market: 49.060.00000.00%17:33 EST

Volume:419.09K

Turnover:20.53M

Market Cap:14.80B

PE:18.50

High:49.25

Open:48.91

Low:48.44

Close:48.87

52wk High:50.86

52wk Low:43.90

Shares:301.75M

Float Shares:298.86M

Volume Ratio:0.96

T/O Rate:0.14%

Dividend:2.14

Dividend Rate:4.35%

EPS(TTM):2.65

EPS(LYR):1.19

ROE:9.07%

ROA:3.07%

PB:1.67

PE(LYR):41.34

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Overview Company News Filings

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

Nanoscope Secures Japan MHLW Sakigake and Orphan Drug Designations Across Inherited Retinal Diseases - A First for a Retinal Gene Therapy

Rein Therapeutics receives orphan drug designation from EMA for LTI-03

EMA validates Type II Variation MAA for AstraZeneca, Daiichi’s Enhertu

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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":["BK4156","EMA","BK4081"],"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":"fut","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","BK4081","EMA"],"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":["BK4081","EMA"],"gpt_icon":0},{"id":"2607045311","title":"CMS (867.HK/8A8.SG): Ruxolitinib 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Maurice Choy from RBC Capital maintained a Buy rating on Emera, with a price target of C$76.00. The company’s s...","market":"fut","thumbnail":null,"type":0,"news_type":0,"thumbnails":[],"rights":{"source":"tipranks_highlight","url":"https://www.tipranks.com/news/blurbs/emera-ema-gets-a-buy-from-rbc-capital-blurbs?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/blurbs/emera-ema-gets-a-buy-from-rbc-capital-blurbs?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":["EMA","LU0128525929.USD","BK4081","LU0708994859.HKD","LU1267930573.SGD","LU0029864427.USD","BK4207","LU0310800379.SGD"],"gpt_icon":0},{"id":"2605144430","title":"Nanoscope Secures Japan MHLW Sakigake and Orphan Drug Designations Across Inherited Retinal Diseases - A First for a Retinal Gene Therapy","url":"https://stock-news.laohu8.com/highlight/detail?id=2605144430","media":"prnewswire","labels":["productRelease"],"top":-1,"itemType":null,"share":"https://ttm.financial/m/news/2605144430?lang=en_us&edition=fundamental","pubTime":"2026-01-21 06:00","pubTimestamp":1768946400,"startTime":"0","endTime":"0","summary":"Japan's Ministry of Health, Labour and Welfare  grants MCO-010 Sakigake  and Orphan Drug designations, enabling an accelerated regulatory pathway for patients with severe inherited retinal diseases. Enhances strong global regulatory momentum, including multiple FDA expedited programs and five EMA Orphan designations. FDA, EMA and PMDA conditionally approve the MOGENRY brand name. Strengthens global pre-commercialization readiness and reinforces leadership in optogenetic therapy. DALLAS, Jan. 21, 2026 /PRNewswire/ -- Nanoscope Therapeutics, Inc., a biotechnology company developing disease-agnostic therapies for vision loss caused by retinal degeneration, today announced that Japan's Ministry of Health, Labour and Welfare  has granted both Sakigake  and Orphan Drug designations to MCO-010, its lead optogenetic therapy for patients with severe vision loss from inherited retinal dystrophies . 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