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Dupilumab - Regeneron/Sanofi

Drug Profile

Dupilumab - Regeneron/Sanofi

Alternative Names: Dupilumab-Sanofi/Regeneron; Dupixent; REGN-668; SAR-231893

Latest Information Update: 11 Mar 2024

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At a glance

  • Originator Regeneron Pharmaceuticals; sanofi-aventis
  • Developer Aimmune Therapeutics; Mayo Clinic; Regeneron Pharmaceuticals; Sanofi; Sanofi-Aventis GmbH
  • Class Anti-inflammatories; Antiallergics; Antiasthmatics; Antineoplastics; Immunotherapies; Monoclonal antibodies; Skin disorder therapies
  • Mechanism of Action Interleukin 13 receptor antagonists; Interleukin 4 receptor antagonists
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Bullous pemphigoid; Eosinophilic oesophagitis
  • New Molecular Entity Yes

Highest Development Phases

  • Marketed Asthma; Atopic dermatitis; Chronic urticaria; Eosinophilic oesophagitis; Prurigo nodularis; Rhinosinusitis
  • Preregistration Chronic obstructive pulmonary disease
  • Phase III Bullous pemphigoid; Pruritus; Wheezing
  • Phase II/III Eosinophilic gastroenteritis
  • Phase II Aspergillosis; Eczema; Milk hypersensitivity; Prostate cancer; Ulcerative colitis; Urticaria
  • No development reported Allergic asthma
  • Discontinued Grass pollen hypersensitivity; Peanut hypersensitivity

Most Recent Events

  • 05 Mar 2024 Regeneron and Sanofi plan a phase III trial in Prurigo nodularis (In infants, In children, In adolescents) (SC) in February 2024 (NCT06293053)
  • 04 Mar 2024 Discontinued - Phase-II for Rhinosinusitis (Treatment-experienced) in Spain, Russia, Portugal, South Korea, Hungary, China, Chile, Belgium, Argentina, United Kingdom, Sweden (SC)
  • 23 Feb 2024 Launched for Eosinophilic oesophagitis (In adolescents, In adults) in Canada (SC)
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