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Regeneron (REGN) and Sanofi (SNY) to Present New Analyses from Praluent Injection ODYSSEY Clinical Trial Program at AHA
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Regeneron and Sanofi to Present New Analyses from the Praluent® (alirocumab) Injection ODYSSEY Clinical Trial Program at the AHA Scientific Sessions 2017
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Regeneron to Share Clinical Progress of REGN1979 and Cemiplimab (REGN2810) in B-Cell Lymphomas at the 2017 ASH Annual Meeting
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Sanofi (SNY) Says Dupilumab Significantly Reduced Steroid Use, Asthma Attacks, and Improved Lung Function in Phase 3 Study of People with Severe Steroid-Dependent Asthma
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Dupilumab Significantly Reduced Steroid Use, Asthma Attacks, and Improved Lung Function in Phase 3 Study of People with Severe Steroid-Dependent Asthma
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Sanofi : Dupilumab Significantly Reduced Steroid Use, Asthma Attacks, and Improved Lung Function in a Phase 3 Study of People with Severe Steroid-Dependent Asthma
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Regeneron's First Global Day of Service Supports Over 100 Non-Profit and Community Organizations
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Science Magazine Ranks Regeneron #1 Biopharma Employer for Fifth Time
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Sanofi (SNY), Regeneron (REGN) Phase 2 Study Results for Dupilumab Shows Significant Improvement Versus Placebo
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Sanofi and Regeneron Announce Positive Phase 2 Study Results for Dupilumab in Patients With Active Moderate-to-Severe Eosinophilic Esophagitis
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Regeneron and Sanofi Announce Positive Phase 2 Study Results for Dupilumab in Patients With Active Moderate-to-Severe Eosinophilic Esophagitis
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Regeneron to Report Third Quarter 2017 Financial and Operating Results and Host Conference Call and Webcast on November 8, 2017
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Internationally Acclaimed Writer and Executive Producer of HBO's The Night Of Reveals His Personal Story Detailing the Harsh Realities of Atopic Dermatitis
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Sanofi (SNY) Confirms Appellate Court Ordered New Trial and Vacated Permanent Injunction in Patent Case Regarding Praluent
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Regeneron (REGN) Confirms Appellate Court Ordered New Trial and Vacated Permanent Injunction in Patent Case Regarding Praluent
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Appellate Court Orders a New Trial and Vacates Permanent Injunction in Ongoing Patent Case Regarding Praluent® (alirocumab)
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Appellate Court Orders a New Trial and Vacates Permanent Injunction in Ongoing Patent Case Regarding Praluent® (alirocumab)
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Sanofi : Appellate Court Orders a New Trial and Vacates Permanent Injunction in Ongoing Patent Case Regarding Praluent® (alirocumab)
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Regeneron (REGN) Reports New Collaborations with HHS & BARDA to Develop New Treatments Against Ebola, Influenza and Multiple Other Emerging Pathogens
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Regeneron Announces New Collaborations with HHS to Develop Antibodies Against Ebola, Influenza and Multiple Other Emerging Pathogens
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Sanofi (SNY) & Regeneron (REGN) Report Approval of Dupixent (Dupilumab) in European Union to Treat Adult Patients with Moderate-to-Severe Atopic Dermatitis
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Sanofi and Regeneron Announce Approval of Dupixent® (dupilumab) to Treat Adult Patients with Moderate-to-Severe Atopic Dermatitis in the European Union
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Regeneron and Sanofi Announce Approval of DUPIXENT® (dupilumab) to Treat Adult Patients with Moderate-to-Severe Atopic Dermatitis in the European Union
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Sanofi (SNY) & Regeneron Pharmaceuticals (REGN) Report Positive Study Results for Dupixent (Dupilumab)
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Sanofi and Regeneron Announce Positive Study Results for Dupixent® (dupilumab) in Patients With Moderate-to-Severe Atopic Dermatitis
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Regeneron and Sanofi Announce Positive Study Results for DUPIXENT® (dupilumab) in Patients With Moderate-to-Severe Atopic Dermatitis
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Regeneron (REGN) & Sanofi (SNY) Report Positive Dupilumab Topline Results from Phase 3 Trial in Uncontrolled Persistent Asthma
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Regeneron and Sanofi Announce Positive Dupilumab Topline Results from Phase 3 Trial in Uncontrolled Persistent Asthma
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Sanofi, Regeneron: Dupilumab Hits Main Objectives in Late-Stage Asthma Trial
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Regeneron (REGN) & Sanofi (SNY) Granted FDA Breakthrough Designation for Cemiplimab (REGN2810), Advanced Cutaneous Squamous Cell Carcinoma
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Regeneron and Sanofi Announce Cemiplimab (REGN2810) Has Received FDA Breakthrough Therapy Designation for Advanced Cutaneous Squamous Cell Carcinoma
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Sanofi, Regeneron: Cemiplimab Receives FDA Breakthrough Designation for Advanced Cutaneous Squamous Cell Carcinoma
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Regeneron Announces Upcoming Investor Conference Presentations
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Regeneron and Sanofi to Present New Analyses from Praluent® (alirocumab) Injection Trials at the ESC Congress 2017
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Regeneron to Discontinue Development of Suptavumab for Respiratory Syncytial Virus
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Accessing the Regeneron Second Quarter 2017 Financial and Operating Results Webcast
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Regeneron Reports Second Quarter 2017 Financial and Operating Results
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Sanofi (SNY) and Regeneron (REGN) Receive Positive CHMP Opinion for Dupixent to Treat Adult Patients with Moderate-to-Severe Atopic Dermatitis
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Sanofi and Regeneron Receive Positive CHMP Opinion for Dupixent® (dupilumab) to Treat Adult Patients with Moderate-to-Severe Atopic Dermatitis
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Regeneron and Sanofi Receive Positive CHMP Opinion for Dupixent® (dupilumab) to Treat Adult Patients with Moderate-to-Severe Atopic Dermatitis
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Regeneron to Report Second Quarter 2017 Financial and Operating Results and Host Conference Call and Webcast on August 3, 2017
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Regeneron Announces the 2017 Winners of the Regeneron Prize for Creative Innovation
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Sanofi (SNY) & Regeneron (REGN) Granted EU Marketing Approval from Kevzara (sarilumab) in Combination with Methotrexate
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Sanofi and Regeneron Announce Approval of Kevzara® (sarilumab) to Treat Adult Patients with Moderately to Severely Active Rheumatoid Arthritis in the European Union
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Regeneron and Sanofi Announce Approval of Kevzara® (sarilumab) to Treat Adult Patients with Moderately to Severely Active Rheumatoid Arthritis in the European Union
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Regeneron (REGN) Details Royalty Agreement with Novartis for ACZ885
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Regeneron Details Royalty Agreement with Novartis for Canakinumab (ACZ885)
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Regeneron Recognized on "The Civic 50" List of the Most Community-Minded Companies in the United States
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Veeva Systems (VEEV) Reports 99% of Clinical Operations Leaders Report the Need to Unify Their Clinical Applications; Regeneron Pharmaceuticals (REGN) Standardizing on Veeva Vault Submissions
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Standardizing on Veeva Vault Enhances Regeneron’s Clinical and Regulatory Operations Processes

