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U.S. FDA Extends Review of Biologics License Application for REGEN-COV® (casirivimab and imdevimab) for Treatment and Prophylaxis of COVID-19
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Regeneron (REGN) Announces Dupixent Approved in EU for Children Aged 6-11 with Severe Asthma with Type Inflammation
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Press Release: Dupixent® (dupilumab) approved by European Commission for children aged 6 to 11 years with severe asthma with type 2 inflammation
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Dupixent® (dupilumab) Approved by European Commission for Children Aged 6 to 11 Years with Severe Asthma with Type 2 Inflammation
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Regeneron to Report First Quarter 2022 Financial and Operating Results and Host Conference Call and Webcast on May 4, 2022
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Regeneron (REGN) and Sanofi (SNY) Announces FDA Acceptance of Dupixent for Priority Review in Patients Aged 12 Years and Older with Eosinophilic Esophagitis
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Press Release: FDA accepts Dupixent® (dupilumab) for Priority Review in patients aged 12 years and older with eosinophilic esophagitis
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FDA Accepts Dupixent® (dupilumab) for Priority Review in Patients Aged 12 Years and Older with Eosinophilic Esophagitis
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Press release: Late-breaking Phase 3 data at AAD 2022 show Dupixent® (dupilumab) significantly improved signs and symptoms of prurigo nodularis
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Late-breaking Phase 3 Data at AAD 2022 Show Dupixent® (dupilumab) Significantly Improved Signs and Symptoms of Prurigo Nodularis
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(REGN Alert) Long Term Holders of Regeneron Contact Johnson Fistel for Information Regarding Investigation
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Students Win $1.8 Million at Regeneron Science Talent Search 2022 for Exceptional Research on Neutron Star--Black Hole Systems, Narrowband Radar, and Ribosome Movement in Protein Translation
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Intellia Therapeutics (NTLA) and Regeneron (REGN) Report Updated Phase 1 Data Demonstrating a Single Dose of NTLA-2001, an Investigational CRISPR Therapy for Transthyretin (ATTR) Amyloidosis, Resulte
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Intellia and Regeneron Announce Updated Phase 1 Data Demonstrating a Single Dose of NTLA-2001, Investigational CRISPR Therapy for Transthyretin (ATTR) Amyloidosis, Resulted in Rapid, Deep and Sustaine
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Intellia and Regeneron Announce Updated Phase 1 Data Demonstrating a Single Dose of NTLA-2001, an Investigational CRISPR Therapy for Transthyretin (ATTR) Amyloidosis, Resulted in Rapid, Deep and Sus
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Regeneron (REGN) Reports Phase 3 Data Showing Dupixent Significantly Reduced Itch and Hives in Patients With Chronic Spontaneous Urticaria
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Late-breaking data at 2022 AAAAI Annual Meeting show Dupixent® (dupilumab) significantly improved signs and symptoms of eosinophilic esophagitis
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Late-breaking Data at 2022 AAAAI Annual Meeting Show Dupixent® (dupilumab) Significantly Improved Signs and Symptoms of Eosinophilic Esophagitis
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Late-breaking phase 3 data at 2022 AAAAI Annual Meeting show Dupixent® (dupilumab) significantly reduced itch and hives in patients with chronic spontaneous urticaria
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Late-breaking Phase 3 Data at 2022 AAAAI Annual Meeting Show Dupixent® (dupilumab) Significantly Reduced Itch and Hives in Patients with Chronic Spontaneous Urticaria
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Regeneron (REGN) and Sanofi (SNY) Announce CUPID STUDY B of Dupixent (dupilumab) Did Not Show Statistical Significance
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Update on ongoing Dupixent® (dupilumab) chronic spontaneous urticaria Phase 3 program
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Regeneron and Sanofi Provide Update on Ongoing Dupixent® (dupilumab) Chronic Spontaneous Urticaria Phase 3 Program
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Regeneron Announces Investor Conference Presentations
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Regeneron (REGN) Presents Encouraging Phase 2 Results for High-dose Aflibercept 8 mg in Wet Age-related Macular Degeneration
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Regeneron Presents Encouraging Phase 2 Results for High-dose Aflibercept 8 mg in Wet Age-related Macular Degeneration at Angiogenesis Meeting
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Regeneron (REGN) Announces FDA Accepts for Review Dupixent in Children with Moderate-to-Severe Atopic Dermatitis
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FDA accepts Dupixent® (dupilumab) for Priority Review in children aged 6 months to 5 years with moderate-to-severe atopic dermatitis
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FDA Accepts Dupixent® (dupilumab) for Priority Review in Children Aged 6 Months to 5 Years with Moderate-to-severe Atopic Dermatitis
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Regeneron Reports Fourth Quarter and Full Year 2021 Financial and Operating Results
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Regeneron (REGN) to Present Positive Dupixent Data Across Five Diseases with Underlying Type 2 Inflammation
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Positive Dupixent® (dupilumab) Data Across Five Diseases with Underlying Type 2 Inflammation to be Presented at 2022 AAAAI Annual Meeting
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Regeneron (REGN) Announces CHMP Recommends Approval of Dupixent for Children Aged 6 to 11
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CHMP recommends approval of Dupixent® (dupilumab) for children aged 6 to 11 years with severe asthma with type 2 inflammation
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CHMP Recommends Approval of Dupixent® (dupilumab) for Children Aged 6 to 11 Years with Severe Asthma with Type 2 Inflammation
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Regeneron (REGN), Sanofi (SNY) voluntary withdraw sBLA for Libtayo as second-line treatment for patients with advanced cervical cancer
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Regeneron and Sanofi Provide Regulatory Update on Libtayo® (cemiplimab-rwlc) in Advanced Cervical Cancer
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Forty Accomplished Young Scientists Named Finalists in the 2022 Regeneron Science Talent Search
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Forty Accomplished Young Scientists Named Finalists in the 2022 Regeneron Science Talent Search
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Regeneron (REGN) Announces FDA Accepts for Review Libtayo in Combination with Chemotherapy
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FDA Accepts for Review Libtayo® (cemiplimab-rwlc) in Combination with Chemotherapy for First-line Treatment of Advanced NSCLC
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Regeneron (REGN) Announces Phase 3 of Dupixent Met Primary and Secondary Endpoints
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Second positive Phase 3 Dupixent® (dupilumab) trial confirms significant improvements for patients with prurigo nodularis
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Second Positive Phase 3 Dupixent® (dupilumab) Trial Confirms Significant Improvements for Patients with Prurigo Nodularis
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Regeneron to Report Fourth Quarter and Full Year 2021 Financial and Operating Results and Host Conference Call and Webcast on
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Regeneron (REGN), Ultragenyx (RARE) Collaborate to Commercialize Evkeeza (evinacumab) Outside the United States
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Regeneron and Ultragenyx Collaborate to Commercialize Evkeeza® (evinacumab) Outside the United States
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Regeneron Announces Presentation at the 40th Annual J.P. Morgan Healthcare Conference
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Regeneron (REGN) Reports New REGN5458 Phase 1 Data Showing 75% Response Rate at Highest Dose Levels
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Regeneron (REGN) and Sanofi (SNY) Present Positive Phase 3 Dupixent Data in Children

