http://www.twitter.comTwitter is a service for friends, family, and co-workers to communicate and stay connected through the exchange of quick, frequent answers to one simple question: What are you doing?
View Older Stories View More Recent Stories
-
Positive Phase 3 Dupixent® (dupilumab) data in children 6 months to 5 years with moderate-to-severe atopic dermatitis featured in RAD 2021 late-breaking session
-
Positive Phase 3 Dupixent® (dupilumab) Data in Children 6 Months to 5 Years with Moderate-to-severe Atopic Dermatitis Featured in RAD 2021 Late-breaking Session
-
New REGN5458 (BCMAxCD3) Phase 1 Data Show 75% Response Rate at Highest Dose Levels Studied in Patients with Heavily Pretreated Multiple Myeloma
-
Regeneron (REGN) Announces Publication of Positive Phase 3 Data of Dupixent in Children with Moderate-to-Severe Asthma
-
New England Journal of Medicine publishes positive Phase 3 Dupixent® (dupilumab) results in children with moderate-to-severe asthma
-
Regeneron (REGN) Announces NEJM Publishes Positive Phase 3 Dupixent Results in Children with Moderate-to-severe Asthma
-
New England Journal of Medicine Publishes Positive Phase 3 Dupixent® (dupilumab) Results in Children with Moderate-to-severe Asthma
-
Regeneron to Participate in H.C. Wainwright & Co. Virtual Event
-
Regeneron Announces Investor Conference Presentations
-
Regeneron Listed on Dow Jones Sustainability World Index for Third Consecutive Year
-
Regeneron (REGN) Announces $3 Billion Share Repurchase Program
-
Regeneron Announces $3 Billion Share Repurchase Program
-
Regeneron (REGN) Antibody Cocktail Approved by European Commission to Treat and Prevent COVID-19
-
Regeneron Antibody Cocktail Approved by European Commission to Treat and Prevent COVID-19
-
CHMP Recommends EU Approves Regeneron (REGN) Antibody Cocktail for Treatment and Prevention of COVID-19
-
CHMP Recommends EU Approval of Regeneron Antibody Cocktail to Treat and Prevent COVID-19
-
Pre-Open Stock Movers 11/08: (AUTL) (TTD) (BLNK) Higher; (EHTH) (BLUE) (TSLA) Lower (more...)
-
Regeneron (REGN) Announces New Phase 3 Analyses Show That Single Dose of REGEN-COV® (casirivimab and imdevimab) Provides Long-term Protection Against COVID-19
-
New Phase 3 Analyses Show That a Single Dose of REGEN-COV® (casirivimab and imdevimab) Provides Long-term Protection Against COVID-19
-
Regeneron Presentations at ASH Highlight Expanding Clinical Research in Blood Cancers and Disorders
-
Regeneron Reports Third Quarter 2021 Financial and Operating Results
-
Regeneron (REGN) and Sanofi (SNY) Report Second Dupixent Phase 3 Trial Achieves Primary Endpoints Demonstrating Significant Disease Improvements
-
Second Dupixent® (dupilumab) Phase 3 eosinophilic esophagitis trial to demonstrate significant disease improvements, underscoring role of type 2 inflammation in this complex disease
-
Second Dupixent® (dupilumab) Phase 3 Eosinophilic Esophagitis Trial to Demonstrate Significant Disease Improvements, Underscoring Role of Type 2 Inflammation in This Complex Disease
-
Regeneron's (REGN) Dupixent Significantly Reduces Itch and Skin Lesions in Phase 3 trial for prurigo nodularis
-
Dupixent® (dupilumab) is the first biologic to significantly reduce itch and skin lesions in Phase 3 trial for prurigo nodularis, demonstrating the role of type 2 inflammation in this disease
-
Dupixent® (dupilumab) is the First Biologic to Significantly Reduce Itch and Skin Lesions in Phase 3 Trial for Prurigo Nodularis, Demonstrating the Role of Type 2 Inflammation in this Disease
-
Regeneron (REGN) Announces FDA Expands Approval of Dupixent to Include Children Aged 6 to 11 Years with Moderate-to-severe Asthma
-
FDA expands approval of Dupixent® (dupilumab) to include children aged 6 to 11 years with moderate-to-severe asthma
-
FDA Expands Approval of Dupixent® (dupilumab) to Include Children Aged 6 to 11 Years with Moderate-to-severe Asthma
-
FDA Accepts Regeneron's (REGN) REGEN-COV for Priority Review for Treatment and Prophylaxis of COVID-19
-
FDA Accepts REGEN-COV® (casirivimab and imdevimab) for Priority Review for Treatment and Prophylaxis of COVID-19
-
Regeneron to Report Third Quarter 2021 Financial and Operating Results and Host Conference Call and Webcast on November 4, 2021
-
New REGEN-COV™ (casirivimab and imdevimab) Data Show Supportive Results in Patients Hospitalized with COVID-19
-
Regeneron (REGN) Announces NEJM Publishes Positive Phase 3 Trial Results for REGEN-COV to Treat COVID-19
-
New England Journal of Medicine Publishes Positive Phase 3 Trial Results for REGEN-COV™ (casirivimab and imdevimab) to Treat COVID-19
-
Regeneron (REGN) Announces FDA Accepts Libtayo for Priority Review for Advanced Cervical Cancer
-
FDA Accepts Libtayo® (cemiplimab-rwlc) for Priority Review for Advanced Cervical Cancer
-
Regeneron (REGN) and Sanofi (SNY) to Present New Dupixent® Data for Dermatitis in Children at WCPD and EADV
-
New Dupixent® (dupilumab) data in patients as young as 6 years old with moderate-to-severe atopic dermatitis to be presented at WCPD and EADV
-
New Dupixent® (dupilumab) Data in Patients as Young as Six Years Old With Moderate-to-Severe Atopic Dermatitis to Be Presented at WCPD and EADV
-
Regeneron's (REGN) Phase 3 Trial of Libtayo and Chemotherapy as First-line Treatment Met Primary and Secondary Endpoints
-
ESMO late-breaking data show Libtayo® (cemiplimab) and chemotherapy first-line treatment combination significantly improved overall survival in patients with advanced NSCLC
-
ESMO Late-breaking Data Show Libtayo® (cemiplimab) and Chemotherapy First-line Treatment Combination Significantly Improved Overall Survival in Patients with Advanced NSCLC
-
Regeneron (REGN) Announces New U.S. Government Agreement to Purchase Additional Doses of REGEN-COV Antibody Cocktail
-
Regeneron Announces New U.S. Government Agreement to Purchase Additional Doses of REGEN-COV™ (casirivimab and imdevimab) Antibody Cocktail
-
Regeneron Announces Investor Conference Presentations
-
Dupixent® (dupilumab) pivotal trial meets all primary and secondary endpoints becoming first biologic medicine to significantly reduce signs and symptoms of moderate-to-severe atopic dermatitis in ch
-
Dupixent® (dupilumab) Pivotal Trial Meets All Primary and Secondary Endpoints Becoming First Biologic Medicine to Significantly Reduce Signs and Symptoms of Moderate-to-severe Atopic Dermatitis in Ch
-
Regeneron (REGN) Announces Encouraging Topline Phase 2 Data of High-dose aflibercept in Wet Age-related Macular Degeneration

