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Standardizing on Veeva Vault Enhances Regeneron’s Clinical and Regulatory Operations Processes
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Industry Survey Reveals 99% of Clinical Operations Leaders Report the Need to Unify Their Clinical Applications
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Industry Survey Reveals 99% of Clinical Operations Leaders Report the Need to Unify Their Clinical Applications
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Sanofi (SNY) & Regeneron (REGN) Presents Positive Results on Praluent (alirocumab) for Patients with Diabetes & Hypercholesterolemia
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Sanofi and Regeneron Announce Positive Results from First Dedicated Studies Evaluating Praluent® (alirocumab) in Individuals with Diabetes and Hypercholesterolemia
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Sanofi and Regeneron Announce Positive Results from First Dedicated Studies Evaluating Praluent® (alirocumab) in Individuals with Diabetes and Hypercholesterolemia
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Regeneron and Sanofi Announce Positive Results from First Dedicated Studies Evaluating Praluent® (alirocumab) in Individuals with Diabetes and Hypercholesterolemia
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Regeneron (REGN) & Sanofi (SNY) Initial Clinical Trial Data from Phase 1/2 trial of Cabiralizumab in Pigmented Villonodular Synovitis (PVNS) at ASCO Meetings
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Sanofi and Regeneron Present Positive Study Results for Investigational PD-1 Antibody REGN2810 at American Society of Clinical Oncology (ASCO) Annual Meeting
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Regeneron and Sanofi Present Positive Study Results for Investigational PD-1 Antibody REGN2810 at American Society of Clinical Oncology (ASCO) Annual Meeting
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Regeneron (REGN) Says Data on ANGPTL3/Evinacumab Published in NEJM
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Regeneron Announces ANGPTL3/Evinacumab Publication in New England Journal of Medicine and Positive Phase 2 Data in People with HoFH
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Sanofi and Regeneron Announce FDA Approval of Kevzara® (sarilumab) for the Treatment of Moderately to Severely Active Rheumatoid Arthritis in Adult Patients
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Sanofi and Regeneron Announce FDA Approval of Kevzara® (sarilumab) for the Treatment of Moderately to Severely Active Rheumatoid Arthritis in Adult Patients
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Regeneron (REGN), Sanofi (SNY) Announce FDA Approval of Kevzara for RA
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Regeneron and Sanofi Announce FDA Approval of Kevzara® (sarilumab) for the Treatment of Moderately to Severely Active Rheumatoid Arthritis in Adult Patients
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Regeneron Announces Upcoming Investor Conference Presentations
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Regeneron and SillaJen Announce Immuno-Oncology Clinical Study Agreement for Combination Treatment in Kidney Cancer
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Regeneron (REGN), Inovio (INO) Enter Agreement for Glioblastoma Combination Therapy
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Inovio & Regeneron Enter Immuno-Oncology Clinical Study Agreement for Glioblastoma Combination Therapy
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Regeneron and Inovio Enter Immuno-Oncology Clinical Study Agreement for Glioblastoma Combination Therapy
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Regeneron Announces Upcoming Investor Conference Presentations
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Regeneron Reports First Quarter 2017 Financial and Operating Results
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Survey Results Show Eighty Percent of Rheumatoid Arthritis Patients Report Life-Altering Pain Daily or Multiple Times a Week, Despite Treatment
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Survey Results Show Eighty Percent of Rheumatoid Arthritis Patients Report Life-Altering Pain Daily or Multiple Times a Week, Despite Treatment
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Sanofi (SNY) & Regeneron (REGN) Report Kevzara® (sarilumab) Biologics License Application Resubmission Accepted for Review by FDA
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Regeneron and Sanofi Announce Kevzara® (sarilumab) Biologics License Application Resubmission Accepted for Review by U.S. FDA
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Regeneron (REGN), Sanofi (SNY) Announce FDA Approval of sBLA for Once-Monthly Dosing Option for Praluent
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Sanofi (SNY) & Regeneron Pharmaceuticals (REGN) Report FDA Approval of a New Once-Monthly Dosing Option for Praluent® (Alirocumab) Injection
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Sanofi and Regeneron Announce FDA Approval of a New Once-Monthly Dosing Option for Praluent® (alirocumab) Injection
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Regeneron and Sanofi Announce FDA Approval of a New Once-Monthly Dosing Option for Praluent® (alirocumab) Injection
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Regeneron (REGN) & Sanofi (SNY) Announce Positive CHMP Opinion on Kevzara® (sarilumab) from European Medicine Agency
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Regeneron and Sanofi Receive Positive CHMP Opinion for Kevzara® (sarilumab) to Treat Adult Patients with Moderately to Severely Active Rheumatoid Arthritis
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Regeneron to Report First Quarter 2017 Financial and Operating Results and Host Conference Call and Webcast on May 4, 2017
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Regeneron Science Talent Search to Ring The Nasdaq Stock Market Closing Bell
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Regeneron (REGN) Reports Evinacumab has Received FDA Breakthrough Therapy Designation for Homozygous Familial Hypercholesterolemia (HoFH)
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Regeneron Announces Evinacumab has Received FDA Breakthrough Therapy Designation for Homozygous Familial Hypercholesterolemia (HoFH)
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Regeneron and Sanofi to Host Investor Conference Call to Discuss DUPIXENT® (dupilumab) Approval
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Sanofi and Regeneron Announce FDA Approval of Dupixent® (dupilumab), the First Targeted Biologic Therapy for Adults with Moderate-to-Severe Atopic Dermatitis
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Regeneron (REGN) and Sanofi (SNY) Announce FDA Approval of DUPIXENT to Treat Moderate-to-Severe Atopic Dermatitis
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Sanofi and Regeneron Announce FDA Approval of Dupixent® (dupilumab), the First Targeted Biologic Therapy for Adults with Moderate-to-Severe Atopic Dermatitis
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Regeneron and Sanofi Announce FDA Approval of DUPIXENT® (dupilumab), the First Targeted Biologic Therapy for Adults with Moderate-to-Severe Atopic Dermatitis
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Regeneron (REGN), U.K. Biobank and GSK to Launch DNA Sequencing Database Initiative from 500K U.K. Volunteers
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U.K. Biobank, Regeneron and GSK Announce Largest Gene Sequencing Initiative on World's Most Detailed Health Database to Improve Drug Discovery and Disease Diagnosis
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Teen Scientist Researches New Approach to Neurological Damage; Wins Regeneron Science Talent Search 2017
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Teen Scientist Researches New Approach to Neurological Damage; Wins Regeneron Science Talent Search 2017
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Regeneron (REGN), Sanofi (SNY) to Present New Phase 3 Praluent Injection Trial Analyses at ACC
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Regeneron and Sanofi to Present New Phase 3 Praluent® (alirocumab) Injection Clinical Trial Analyses at ACC.17 Scientific Sessions
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Sanofi and Regeneron Announce Presentation of Positive Data from Long-Term Pivotal Phase 3 CHRONOS Study of Dupixent® (dupilumab) in Moderate-to-Severe Atopic Dermatitis
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Regeneron and Sanofi Announce Presentation of Positive Data from Long-Term Pivotal Phase 3 CHRONOS Study of DUPIXENT® (dupilumab) in Moderate-to-Severe Atopic Dermatitis

