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Regeneron (REGN), Sanofi (SNY) Announces Dupixent Recommended for EU Approval by the CHMP for the Treatment of Eosinophilic Esophagitis
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Dupixent® (dupilumab) Recommended for EU Approval by the CHMP for the Treatment of Eosinophilic Esophagitis
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Regeneron (REGN) and Sanofi (SNY) Announce EU Approval of Dupixent for Prurigo Nodularis
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Dupixent® (dupilumab) Approved by European Commission as the First and Only Targeted Medicine Indicated for Prurigo Nodularis
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Odronextamab (CD20xCD3) Demonstrates High and Durable Complete Response Rate among Patients with Relapsed/Refractory Follicular Lymphoma in Pivotal Phase 2 Trial
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Regeneron (REGN) Announces Linvoseltamab Initial Pivotal Phase 2 Data Show Clinically Meaningful Responses in Patients with Heavily Pre-treated Multiple Myeloma
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Linvoseltamab (BCMAxCD3) Initial Pivotal Phase 2 Data Show Clinically Meaningful Responses in Patients with Heavily Pre-treated Multiple Myeloma
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Regeneron Named on Dow Jones Sustainability World Index for Fourth Consecutive Year
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Regeneron (REGN) announces positive early trial of data of odronextamab in patients with relapsed/refractory diffuse large B-cell lymphoma at ASH
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Pivotal Odronextamab (CD20xCD3) Phase 2 Data in Patients with Relapsed/Refractory Diffuse Large B-cell Lymphoma Debut at ASH
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Regeneron ESMO IO Presentations Highlight Potential of Fianlimab and Libtayo® (cemiplimab) in Multiple Solid Tumor Types
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Regeneron (REGN) Announces Evkeeza sBLA for Children with Ultra-rare Inherited Form of High Cholesterol Accepted for FDA Priority Review
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Evkeeza® (evinacumab-dgnb) sBLA for Children with Ultra-rare Inherited Form of High Cholesterol Accepted for FDA Priority Review
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Regeneron (REGN) Announces Libtayo Approved in EU for Metastatic Cervical Cancer Irrespective of PD-L1 Expression Level or Tumor Histology
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Libtayo® (cemiplimab) Approved by the European Commission as the First Immunotherapy in Second Line Recurrent or Metastatic Cervical Cancer Irrespective of PD-L1 Expression Level or Tumor Histology
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Regeneron (REGN) and CytomX (CTMX) Announce Strategic Research Collaboration in the Field of Conditional Bispecific Therapeutics for the Treatment of Cancer
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CytomX and Regeneron Announce Strategic Research Collaboration in the Field of Conditional Bispecific Therapeutics for the Treatment of Cancer
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Regeneron and CytomX Announce Strategic Research Collaboration in the Field of Conditional Bispecific Therapeutics for the Treatment of Cancer
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Regeneron (REGN) Announces Dupixent Recommended for EU Approval by the CHMP
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Dupixent® (dupilumab) Recommended for EU Approval by the CHMP for the Treatment of Prurigo Nodularis
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Regeneron (REGN) Announces FDA Approval of Libtay in Combination with Chemotherapy for Treatment for Advanced Non-small Cell Lung Cancer (NSCLC)
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Libtayo® (cemiplimab-rwlc) in Combination with Chemotherapy Approved by the FDA as First-line Treatment for Advanced Non-small Cell Lung Cancer (NSCLC)
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Aflibercept 8 mg Late-breaking Data Presented at Retina Society in Diabetic Macular Edema and Wet Age-related Macular Degeneration
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Regeneron Announces Investor Conference Presentations
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Regeneron Presents New Data at ASH from Advancing Hematology Pipeline across Multiple Blood Cancers and Disorders
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Regeneron Reports Third Quarter 2022 Financial and Operating Results
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Regeneron's (REGN) Inmazeb Wins 2022 Prix Galien USA Best Biotechnology Product Award
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Inmazeb™ (atoltivimab, maftivimab, and odesivimab-ebgn) Wins Prestigious 2022 Prix Galien USA Best Biotechnology Product Award
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Regeneron (REGN) Granted Six Month US Pediatric Exclusivity for EYLEA
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Regeneron Receives Six Months of U.S. Pediatric Exclusivity for EYLEA® (aflibercept) Injection
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Immune-Onc Therapeutics Initiates Expansion Cohorts for IO-108 and Enters into Clinical Supply Agreement with Regeneron (REGN)
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Immune-Onc Therapeutics Initiates Expansion Cohorts for IO-108 and Enters into Clinical Supply Agreement with Regeneron
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Regeneron (REGN) Announces Positive CHMP Opinion for Libtayo
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Libtayo® (cemiplimab) Receives Positive CHMP Opinion Recommending Approval to Treat Advanced Cervical Cancer
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Regeneron (REGN) Announces EYLEA Injection sBLA for Treatment of Retinopathy of Prematurity Accepted for FDA Priority Review
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EYLEA® (aflibercept) Injection sBLA for Treatment of Retinopathy of Prematurity (ROP) Accepted for FDA Priority Review
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Dupixent® (dupilumab) Late-Breaking Phase 3 Data Presented at UEG Week 2022 Showed Significant Histological Remission of Eosinophilic Esophagitis (EoE) in Children 1 to 11 Years Old
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Regeneron to Report Third Quarter 2022 Financial and Operating Results and Host Conference Call and Webcast on November 3, 2022
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Regeneron (REGN) Appoints Craig B. Thompson to its Board
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Regeneron Elects Dr. Craig B. Thompson to Board of Directors
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Aflibercept 8 mg Positive Pivotal Results in Diabetic Macular Edema and Wet Age-Related Macular Degeneration Presented at AAO
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Regeneron (REGN), Sanofi (SNY) Announce FDA Approval for Dupixent to Treat Prurigo Nodularis
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Dupixent® (dupilumab) Approved by FDA as the First and Only Treatment Indicated for Prurigo Nodularis
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Regeneron (REGN) and Intellia (NTLA) Report Initial Data from the Cardiomyopathy Arm of Ongoing Phase 1 Study of NTLA-2001
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Intellia and Regeneron Announce Initial Data from the Cardiomyopathy Arm of Ongoing Phase 1 Study of NTLA-2001, an Investigational CRISPR Therapy for the Treatment of Transthyretin (ATTR) Amyloidosis
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Intellia and Regeneron Announce Initial Data from the Cardiomyopathy Arm of Ongoing Phase 1 Study of NTLA-2001, an Investigational CRISPR Therapy for the Treatment of Transthyretin (ATTR) Amyloidosis
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Regeneron (REGN) Reports Publication of Positive Dupixent Data in Children 6 Month - 5 Years Old
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Positive Dupixent® (dupilumab) Phase 3 Data in Children Aged 6 Months to 5 Years with Moderate-to-severe Atopic Dermatitis Published in The Lancet
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Regeneron (REGN) and Alnylam (ALNY) Report Strong Data from Ongoing Phase 1 Study of ALN-HSD
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Alnylam and Regeneron Report Promising Data from Ongoing Phase 1 Study of ALN-HSD in NASH Patients and Healthy Volunteers

