Dupilumab - Regeneron/Sanofi
Alternative Names: Dupilumab-Sanofi/Regeneron; Dupixent; REGN-668; SAR-231893Latest Information Update: 25 Jun 2025
At a glance
- Originator Regeneron Pharmaceuticals; sanofi-aventis
- Developer Aimmune Therapeutics; Mayo Clinic; Regeneron Pharmaceuticals; Sanofi; Sanofi-Aventis GmbH
- Class Anti-inflammatories; Antiallergics; Antiasthmatics; Antifungals; Antineoplastics; Antipruritics; Immunotherapies; Monoclonal antibodies; Skin disorder therapies
- Mechanism of Action Interleukin 13 receptor antagonists; Interleukin 4 receptor antagonists
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Orphan Drug Status
Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.
- New Molecular Entity Yes
Highest Development Phases
- Marketed Asthma; Atopic dermatitis; Chronic obstructive pulmonary disease; Chronic urticaria; Eosinophilic oesophagitis; Prurigo nodularis; Rhinosinusitis
- Registered Bullous pemphigoid
- Phase III Pruritus; Wheezing
- Phase II/III Eosinophilic gastroenteritis
- Phase II Aspergillosis; Eczema; Prostate cancer; Ulcerative colitis; Urticaria
- No development reported Allergic asthma
- Discontinued Grass pollen hypersensitivity; Peanut hypersensitivity
Most Recent Events
- 20 Jun 2025 Preregistration for Bullous pemphigoid in Japan (SC) before June 2025
- 20 Jun 2025 Registered for Bullous pemphigoid (In adults) in USA (SC)
- 20 Jun 2025 Efficacy and adverse events data rom the phase II/III LIBERTY-BP ADEPT trial in bullous pemphigoid released by Regeneron Pharmaceuticals