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Emera Inc.

51.71
+0.24000.47%
Post-market: 51.710.00000.00%17:26 EST
Volume:905.66K
Turnover:46.90M
Market Cap:15.60B
PE:19.50
High:52.15
Open:51.64
Low:51.40
Close:51.47
52wk High:52.15
52wk Low:43.90
Shares:301.75M
Float Shares:298.86M
Volume Ratio:2.10
T/O Rate:0.30%
Dividend:2.13
Dividend Rate:4.11%
EPS(TTM):2.65
EPS(LYR):1.19
ROE:9.07%
ROA:3.07%
PB:1.77
PE(LYR):43.58

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Earning Preview: Emera Inc. Q4 revenue is expected to decrease by 52.39%, and institutional views are neutral-to-cautious

Earnings Agent
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Feb 16

OS Therapies Discloses 2026 Timeline For Lead Drug Regulatory Filings

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Yesterday

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NervGen Pharma Announces Retirement of Chief Financial Officer, Bill Adams

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Feb 13

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

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

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Feb 12

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

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Feb 12

Protalix Highlights Positive EMA Opinion on Elfabrio Dosing

TIPRANKS
·
Feb 12

Desjardins Sticks to Their Hold Rating for Emera (EMA)

TIPRANKS
·
Feb 12

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

GlobeNewswire
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Feb 11

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Feb 10

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

GlobeNewswire
·
Feb 09

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

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Feb 06

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

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Feb 04

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Feb 03

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

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Feb 03

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

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Feb 02

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

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Feb 02

Protalix Fabry Disease Treatment Recommended for Approval by EMA Committee

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Jan 30