REGN - Regeneron Pharmaceuticals, Inc.

NasdaqGS - NasdaqGS Real Time Price. Currency in USD
390.19
+2.28 (+-0.02%)
At close: 4:00PM EDT
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Previous Close390.28
Open387.29
Bid390.19 x 1000
Ask395.00 x 1000
Day's Range385.95 - 393.80
52 Week Range281.89 - 477.00
Volume366,160
Avg. Volume744,426
Market Cap42.119B
Beta1.77
PE Ratio (TTM)28.33
EPS (TTM)13.77
Earnings DateNov 6, 2018 - Nov 12, 2018
Forward Dividend & YieldN/A (N/A)
Ex-Dividend DateN/A
1y Target Est406.05
Trade prices are not sourced from all markets
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  • The Zacks Analyst Blog Highlights: Regeneron Pharmaceuticals, Celgene, Sanofi and Gilead Sciences
    Zacks5 days ago

    The Zacks Analyst Blog Highlights: Regeneron Pharmaceuticals, Celgene, Sanofi and Gilead Sciences

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  • Biotech Stock Roundup: CELG, REGN Present Data, VKTX Soars on Drug's Success
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    Biotech Stock Roundup: CELG, REGN Present Data, VKTX Soars on Drug's Success

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  • Regeneron Gains on Eylea, Dupixent and Pipeline Progress
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    Solid performance of approved drugs like Eylea and Dupixent along with an encouraging pipeline progress improve Regeneron's (REGN) market position.

  • Reuters7 days ago

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  • Regeneron-Sanofi Report Data on Dupixent in Atopic Dermatitis
    Zacks8 days ago

    Regeneron-Sanofi Report Data on Dupixent in Atopic Dermatitis

    Regeneron (REGN) and partner Sanofi present encouraging data from a late-stage trial on dermatitis drug Dupixent in adolescents.

  • Time to Focus on Regeneron Pharmaceuticals (REGN) for Strong Earnings Growth Potential
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    Time to Focus on Regeneron Pharmaceuticals (REGN) for Strong Earnings Growth Potential

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  • See what the IHS Markit Score report has to say about Regeneron Pharmaceuticals Inc.
    Markit10 days ago

    See what the IHS Markit Score report has to say about Regeneron Pharmaceuticals Inc.

    Regeneron Pharmaceuticals Inc NASDAQ/NGS:REGN

  • GlobeNewswire10 days ago

    Sanofi: Positive Phase 3 results presented for Dupixent® (dupilumab)

    September 15, 2018 - Detailed results from a pivotal Phase 3 trial showed Dupixent® (dupilumab) monotherapy demonstrated a significant improvement in signs and symptoms of atopic dermatitis and certain quality of life measures in adolescent patients (12-17 years) with moderate-to-severe atopic dermatitis, whose disease was inadequately controlled with topical therapies or for whom topical treatment was medically inadvisable. There continues to be a significant unmet need for adolescents with moderate-to-severe atopic dermatitis, whose disease cannot be controlled with topical treatments. Dupixent is currently approved for use in certain adult patients with moderate-to-severe atopic dermatitis in countries including the U.S., European Union, Canada and Japan.

  • PR Newswire10 days ago

    Positive Phase 3 Results Presented for Dupixent® (dupilumab) Show Significant Improvement on Multiple Measures of Disease Severity in Adolescents with Moderate-to-Severe Atopic Dermatitis

    Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) and Sanofi today presented detailed results from a pivotal Phase 3 trial showing Dupixent® (dupilumab) monotherapy demonstrated a significant improvement in signs and symptoms of atopic dermatitis and certain quality of life measures in adolescent patients (12-17 years) with moderate-to-severe atopic dermatitis, whose disease was inadequately controlled with topical therapies or for whom topical treatment was medically inadvisable. There continues to be a significant unmet need for adolescents with moderate-to-severe atopic dermatitis, whose disease cannot be controlled with topical treatments. Dupixent is currently approved for use in certain adult patients with moderate-to-severe atopic dermatitis in countries including the U.S., European Union, Canada and Japan.

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  • PR Newswire12 days ago

    FDA to Review EYLEA (aflibercept) Injection for the Treatment of Diabetic Retinopathy

    TARRYTOWN, N.Y., Sept. 13, 2018 /PRNewswire/ -- Regeneron Pharmaceuticals, Inc. (REGN) today announced that the U.S. Food and Drug Administration (FDA) has accepted for review the supplemental Biologics License Application (sBLA) of EYLEA® (aflibercept) Injection for the treatment of diabetic retinopathy (DR), the leading cause of vision loss for patients with diabetes. The sBLA submission is based on results from the Phase 3 PANORAMA trial investigating EYLEA as a treatment for patients with moderately severe to severe non-proliferative diabetic retinopathy (NPDR) without diabetic macular edema (DME).

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  • Regeneron/Sanofi's sBLA for Praluent to be Reviewed by FDA
    Zacks13 days ago

    Regeneron/Sanofi's sBLA for Praluent to be Reviewed by FDA

    The FDA will review Regeneron (REGN) and Sanofi's sBLA for its PCSK9 Inhibitor Praluent to reduce risk of major adverse cardiovascular events.

  • PR Newswire13 days ago

    FDA to review supplemental Biologics License Application for Praluent® (alirocumab) Injection as potential treatment to reduce major adverse cardiovascular events

    /PRNewswire/ -- Sanofi and Regeneron Pharmaceuticals, Inc. announced that the U.S. Food and Drug Administration (FDA) has accepted a supplemental Biologics License Application (sBLA) for Praluent® (alirocumab) Injection, a PCSK9 inhibitor. The sBLA outlines a proposed update to the Prescribing Information to include the effect of Praluent in reducing the overall risk of major adverse cardiovascular events (MACE).

  • GlobeNewswire13 days ago

    FDA to review supplemental Biologics License Application for Praluent® (alirocumab) Injection as potential treatment to reduce major adverse cardiovascular events

    September 12, 2018 - Sanofi and Regeneron Pharmaceuticals, Inc. announced that the U.S. Food and Drug Administration (FDA) has accepted a supplemental Biologics License Application (sBLA) for Praluent® (alirocumab) Injection, a PCSK9 inhibitor. The sBLA outlines a proposed update to the Prescribing Information to include the effect of Praluent in reducing the overall risk of major adverse cardiovascular events (MACE).