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Dupixent® (dupilumab) Approved by European Commission as the First and Only Targeted Medicine Indicated for Prurigo Nodularis

Approval based on direct-to-Phase 3 program showing more than three times as many Dupixent patients (60% and 58%) experienced clinically meaningful itch.

France generalGeorged yancopoulosNaimish patelRegeneron velocimmunePrnewswire regeneron pharmaceuticals incRegeneron pharmaceuticals incRegeneron genetics centerEuropean commissionDupilumab development programRegeneron velocimmune technologyExchange commissionEuropean unionMd head of global developmentChief scientific officerGlobal developmentDupixent prurigo nodularis

Positive Dupixent® (dupilumab) Phase 3 Data in Children Aged 6 Months to 5 Years with Moderate-to-severe Atopic Dermatitis Published in The Lancet

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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France generalWalterj hamlinRegeneron velocimmune technologyregeneronGeorged yancopoulosAmys pallerPrnewswire regeneron pharmaceuticals incRegeneron pharmaceuticals incRegeneron genetics centerDrug administrationNorthwestern university feinberg school of medicineTeva pharmaceutical industries ltdExchange commissionEuropean unionEuropean medicines agencyDupilumab development programdupilumabEuropean medicines

Positive Dupixent® (dupilumab) Phase 3 Data in Children Aged 6 Months to 5 Years with Moderate-to-severe Atopic Dermatitis Published in The Lancet

/PRNewswire/ Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) and Sanofi today announced that The Lancet has published positive results from a Phase 3.

France generalWalterj hamlinGeorged yancopoulosAmys pallerRegeneron velocimmunePrnewswire regeneron pharmaceuticals incRegeneron pharmaceuticals incRegeneron genetics centerDrug administrationDupilumab development programRegeneron velocimmune technologyNorthwestern university feinberg school of medicineTeva pharmaceutical industries ltdExchange commissionEuropean unionEuropean medicines agency

Positive Dupixent® (dupilumab) Phase 3 Data in Children Aged 6 Months to 5 Years with Moderate-to-severe Atopic Dermatitis Published in The Lancet

/PRNewswire/ Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) and Sanofi today announced that The Lancet has published positive results from a Phase 3.

France generalWalterj hamlinGeorged yancopoulosAmys pallerRegeneron velocimmunePrnewswire regeneron pharmaceuticals incRegeneron pharmaceuticals incRegeneron genetics centerDrug administrationDupilumab development programRegeneron velocimmune technologyNorthwestern university feinberg school of medicineTeva pharmaceutical industries ltdExchange commissionEuropean unionEuropean medicines agency

FDA Accepts Dupixent® (dupilumab) for Priority Review in Adults with Prurigo Nodularis

/PRNewswire/ Dupixent would be the first and only medicine specifically indicated to treat prurigo nodularis in the U.S., if approved Regeneron.

France generalPrnewswire dupixentGeorged yancopoulosRegeneron velocimmuneRegeneron pharmaceuticals incRegeneron genetics centerDrug administrationDupilumab development programRegeneron velocimmune technologyTeva pharmaceutical industries ltdExchange commissionEuropean unionPriority reviewBiologics license applicationChief scientific officer georgePrescribing informationincluding patient