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France generalUnited statesArnaud delepineEva schaefer jansenRegeneron velocimmuneSharon chenVesna tosicGeorged yancopoulosCorentine driancourtSally bainSurya bhattNathalie phamFelix lauscherTarik elgoutniTrial programExchange commission

Dupixent® (dupilumab) Late-breaking Phase 3 COPD Results Presented at ATS and Simultaneously Published in the New England Journal of Medicine

Dupixent is the first and only investigational biologic for COPD that has demonstrated a significant reduction in moderate or severe acute exacerbations by 30% compared to placebo Dupixent is the. | June 11, 2023

United statesFrance generalSurya bhattGeorged yancopoulosRegeneron velocimmuneAmerican thoracic societyTrial programDupilumab development programRegeneron velocimmune technologyClinical research programPulmonary researchRegeneron genetics centerRegeneron pharmaceuticals incInternational conferenceExchange commissionDupixent phase

Dupixent® (dupilumab) Approved by European Commission as First and Only Targeted Medicine for Children as Young as Six Months Old with Severe Atopic Dermatitis

Approximately seven times as many patients aged 6 months to 5 years with severe atopic dermatitis treated with Dupixent experienced clear or almost clear skin and reduced overall disease. | March 21, 2023

France generalKorey capozzaGeorged yancopoulosNaimish patelRegeneron velocimmuneGlobal parents for eczema researchRegeneron pharmaceuticals incGlobal developmentRegeneron genetics centerEuropean commissionDupilumab development programRegeneron velocimmune technologyExchange commissionEuropean unionExecutive directorGlobal parents

Dupixent® (dupilumab) Late-Breaking Data at AAD Show

More than twice as many patients on Dupixent achieved clear or almost clear skin compared to placebo at 16 weeks Nearly four times as many patients on.

United statesFrance generalEricl simpsonGeorged yancopoulosFrancesj storrsScience universityRegeneron pharmaceuticals incRegeneron genetics centerOregon healthDupilumab development programRegeneron velocimmune technologyExchange commissionAmerican academy of dermatologyEuropean unionAmerican academyMedical dermatology

Dupixent® (dupilumab) Application for Treatment of Chronic Spontaneous Urticaria (CSU) in Adults and Adolescents Aged 12 Years and Older Accepted for FDA Review

Dupixent® (dupilumab) Application for Treatment of Chronic Spontaneous Urticaria (CSU) in Adults and Adolescents Aged 12 Years and Older Accepted for FDA Review
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France generalGeorged yancopoulosRegeneron velocimmune technologyRegeneron pharmaceuticals incRegeneron genetics centerDrug administrationExchange commissionDupilumab development programdupilumabBiologics license applicationTrial programtheVelocimmune technology regeneronChief scientific officer georgeDevelopment programdupilumabForward looking statementsDigital mediathisRegeneron pharmaceuticals