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ODYSSEY OUTCOMES Investigators Highlight at AHA that Praluent® (alirocumab) Injection Was Associated with Fewer Deaths from Any Cause
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Regeneron (REGN), Sanofi (SNY) announce NEJM published positive detailed results from Praluent cardiovascular outcomes trial
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New England Journal of Medicine publishes positive detailed results from Praluent® (alirocumab) cardiovascular outcomes trial
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New England Journal of Medicine publishes positive detailed results from Praluent® (alirocumab) cardiovascular outcomes trial
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New England Journal of Medicine Publishes Positive Detailed Results From Praluent® (alirocumab) Injection Cardiovascular Outcomes Trial
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New England Journal of Medicine publishes positive detailed results from Praluent® (alirocumab) Injection cardiovascular outcomes trial
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Sanofi (SNY), Regeneron (REGN) Report FDA Priority Review Acceptance of Supplemental Biologics License Application for Dupixent
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FDA grants priority review for Dupixent® (dupilumab) as potential treatment for adolescents with uncontrolled moderate-to-severe atopic dermatitis
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Regeneron Reports Third Quarter 2018 Financial and Operating Results
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FDA grants priority review for Dupixent® (dupilumab) as potential treatment for adolescents with uncontrolled moderate-to-severe atopic dermatitis
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FDA grants priority review for Dupixent® (dupilumab) as potential treatment for adolescents with uncontrolled moderate-to-severe atopic dermatitis
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FDA Grants Priority Review for Dupixent® (dupilumab) as Potential Treatment for Adolescents with Uncontrolled Moderate-to-Severe Atopic Dermatitis
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Regeneron Ranked #1 Biopharma Employer for Sixth Time by Science Magazine
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Regeneron (REGN) Says EYLEA Injection Improved Diabetic Retinopathy and Reduces Vision-Threatening Complications in Phase 3 Trial
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EYLEA® (aflibercept) Injection Improves Diabetic Retinopathy and Reduces Vision-Threatening Complications in Phase 3 Trial
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Regeneron (REGN) Announces FDA Approves Asthma Indication for Dupixent
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FDA Approves Asthma Indication for Dupixent® (dupilumab)
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Regeneron (REGN), Sanofi (SNY) Report FDA Approval of Asthma Indication for Dupixent (dupilumab)
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Sanofi: FDA approves asthma indication for Dupixent® (dupilumab)
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Sanofi: FDA approves asthma indication for Dupixent® (dupilumab)
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FDA approves asthsma indication for Dupixent® (dupilumab)
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FDA Approves Asthma Indication for Dupixent® (dupilumab)
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Kevzara® (sarilumab) Data at the 2018 ACR/ARHP Annual Meeting Provide Additional Insight on Safety and Efficacy in Rheumatoid Arthritis
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Dupixent® (dupilumab) showed positive topline results in two Phase 3 trials of patients with chronic rhinosinusitis with nasal polyps
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Regeneron (REGN) Reports Positive Topline Result in Two Phase 3 Trials Evaluating Dupixent (dupilumab) in Patients with Chronic Rhinosinusitis with Nasal Polyps
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Sanofi: Dupixent® (dupilumab) showed positive topline results in two Phase 3 trials of patients with chronic rhinosinusitis with nasal polyps
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Sanofi: Dupixent® (dupilumab) showed positive topline results in two Phase 3 trials of patients with chronic rhinosinusitis with nasal polyps
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Dupixent® (dupilumab) Showed Positive Topline Results in Two Phase 3 Trials of Patients with Chronic Rhinosinusitis with Nasal Polyps
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Libtayo® (cemiplimab-rwlc) Data at ESMO 2018 Congress Provide New Insights in Six Tumor Types Under Investigation
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Regeneron to Report Third Quarter 2018 Financial and Operating Results and Host Conference Call and Webcast on November 6, 2018
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Regeneron (REGN), Sanofi (SNY) Report Approcal of Libtayo (cemiplimab), the First and Only Treatment for Advanced Cutaneous Squamous Cell Carcinoma
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Sanofi : FDA approves Libtayo® (cemiplimab) as first and only treatment for advanced cutaneous squamous cell carcinoma
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Sanofi : FDA approves Libtayo® (cemiplimab) as first and only treatment for advanced cutaneous squamous cell carcinoma
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FDA approves Libtayo® (cemiplimab-rwlc) as first and only treatment for advanced cutaneous squamous cell carcinoma
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FDA Approves Libtayo® (cemiplimab-rwlc) as First and Only Treatment for Advanced Cutaneous Squamous Cell Carcinoma
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Regeneron (REGN), Sanofi (SNY) Highlight Positive Phase 3 Results Presented for Dupixent (dupilumab) at 2018 EADV Congress
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Sanofi: Positive Phase 3 results presented for Dupixent® (dupilumab)
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Sanofi: Positive Phase 3 results presented for Dupixent® (dupilumab)
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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
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Regeneron (REGN) Says FDA to Review EYLEA Injection for Treatment of Diabetic Retinopathy
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FDA to Review EYLEA (aflibercept) Injection for the Treatment of Diabetic Retinopathy
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FDA to review supplemental Biologics License Application for Praluent® (alirocumab) Injection as potential treatment to reduce major adverse cardiovascular events
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Sanofi (SNY) and Regeneron (REGN) Announce FDA to review sBLA for Praluent Injection as Potential Treatment to Reduce Major Adverse Cardiovascular Events
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FDA to review supplemental Biologics License Application for Praluent® (alirocumab) Injection as potential treatment to reduce major adverse cardiovascular events
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FDA to review supplemental Biologics License Application for Praluent® (alirocumab) Injection as potential treatment to reduce major adverse cardiovascular events
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FDA to Review Supplemental Biologics License Application for Praluent® (alirocumab)Injection as Potential Treatment to Reduce Major Adverse Cardiovascular Events
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Regeneron Announces Upcoming Investor Conference Presentation
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Regeneron (REGN) Reports FDA Approval of EYLEA (aflibercept) Injection sBLA in Wet Age-related Macular Degeneration
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FDA Approves EYLEA® (aflibercept) Injection sBLA in Wet Age-related Macular Degeneration
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Regeneron (REGN), Teva (TEVA) Announce Positive Topline Phase 3 Fasinumab Results in Patients with Chronic Pain from OA of Knee or Hip

