MedPath

Dupilumab

Generic Name
Dupilumab
Brand Names
Dupixent
Drug Type
Biotech
CAS Number
1190264-60-8
Unique Ingredient Identifier
420K487FSG
Background

Dupilumab is a fully human monoclonal antibody of the immunoglobulin G4 subclass that binds to the interleukin-4 (IL-4) receptor, inhibiting the receptor signaling pathways. As an interleukin-4 receptor alpha antagonist, dupilumab inhibits the signaling of pro-inflammatory cytokines, called interleukins (IL), that induce inflammatory and immunological reactions in several atopic or allergic conditions, such as eczema, allergic reaction, and rhinosinusitis. Dupilumab was generated by recombinant DNA technology in Chinese Hamster Ovary cell suspension culture.

Dupilumab is commonly marketed as Dupixent, which is available as a formulation for subcutaneous injection. It was first approved by the FDA in 2017. It is currently used to treat atopic dermatitis, asthma as an add-on maintenance treatment, chronic rhinosinusitis with nasal polyposis, and eosinophilic esophagitis. It is used as monotherapy or in combination with other drugs, such as corticosteroids. Dupilumab is currently under investigations for potential therapeutic use in diseases driven by allergic reactions or type 2 inflammation, such as pediatric atopic dermatitis, and chronic obstructive pulmonary disease. It is also being studied in combination with another antibody that which targets IL-33.

Indication

In the US, dupilumab is indicated for the treatment of patients aged six months and older with moderate-to-severe atopic dermatitis whose disease is not adequately controlled with topical prescription therapies or when those therapies are not advisable. In Europe and Canada, the drug for this indication is approved for patients aged six years and older. In Europe, patients six to 11 years of age should have severe atopic dermatitis and be candidates for systemic therapy. Dupilumab can be used with or without topical corticosteroids for this condition.

Dupilumab is indicated as an add-on maintenance treatment of patients aged six years and older with moderate-to-severe asthma characterized by an eosinophilic phenotype or with oral corticosteroid dependent asthma. However, the drug is not indicated for relief of acute bronchospasm or status asthmaticus.

Dupilumab is indicated as an add-on maintenance treatment in adult patients with inadequately controlled chronic rhinosinusitis with nasal polyposis. In Canada and Europe, it is used with intranasal corticosteroids.

In the US and Europe, dupilumab is also indicated for the treatment of adults and children aged 12 years and older weighing at least 40 kg with eosinophilic esophagitis (EoE), and adults with prurigo nodularis.

Associated Conditions
Chronic Rhinosinusitis Phenotype With Nasal Polyps (CRSwNP), Eosinophilic Esophagitis, Moderate to Severe Asthma, Moderate to Severe Atopic Dermatitis, Oral Steroid-Dependent Asthma (Disorder), Prurigo Nodularis, Severe Asthma, Severe Atopic Dermatitis, Moderate Atopic dermatitis, Moderate Prurigo Nodularis, Severe Prurigo Nodularis
Associated Therapies
Add-on therapy, Maintenance therapy

Replication of the Heads Up Atopic Dermatitis Trial With Registry Data

Active, not recruiting
Conditions
Atopic Dermatitis
Interventions
First Posted Date
2025-04-22
Last Posted Date
2025-04-22
Lead Sponsor
Technische Universität Dresden
Target Recruit Count
240
Registration Number
NCT06937788
Locations
🇩🇪

Center for Evidence Based Health Care, Dresden, Saxony, Germany

Olfactory Cleft Obstruction and Electrophysiological Field Potentials Predict Olfactory Restoration by Dupilumab in CRSwNP Patients.

Recruiting
Conditions
Chronic Rhinosinusitis Phenotype With Nasal Polyps (CRSwNP)
Smell Loss
Interventions
First Posted Date
2025-03-25
Last Posted Date
2025-05-14
Lead Sponsor
Northwestern University
Target Recruit Count
30
Registration Number
NCT06892704
Locations
🇺🇸

Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States

A Phase Ⅲ Comparative Study of QL2108 to Dupixent®

Phase 3
Not yet recruiting
Conditions
Atopic Dermatitis
Interventions
Drug: QL2108 injection
First Posted Date
2025-03-19
Last Posted Date
2025-03-21
Lead Sponsor
Qilu Pharmaceutical Co., Ltd.
Target Recruit Count
520
Registration Number
NCT06884891

A Study of JNJ-95475939 in the Treatment of Participants With Moderate to Severe Atopic Dermatitis (AD)

Phase 2
Recruiting
Conditions
Dermatitis, Atopic
Interventions
Drug: JNJ-95475939
Drug: Placebo
First Posted Date
2025-03-18
Last Posted Date
2025-04-27
Lead Sponsor
Janssen Research & Development, LLC
Target Recruit Count
240
Registration Number
NCT06881251
Locations
🇯🇵

Sapporo Skin Clinic, Sapporo shi, Japan

🇯🇵

Jitaikai Tachikawa dermatology clinic, Tachikawa, Japan

🇯🇵

Shirasaki Dermatology Clinic, Takaoka shi, Japan

and more 20 locations

A Study to Evaluate Efficacy of Remibrutinib Compared to Dupilumab at Early Timepoints in Adults With Chronic Spontaneous Urticaria Inadequately Controlled by Second Generation H1-antihistamines

Phase 3
Not yet recruiting
Conditions
Chronic Spontaneous Urticaria (CSU)
Interventions
Drug: Remibrutinib matching placebo
Drug: Placebo solution for injection
First Posted Date
2025-03-10
Last Posted Date
2025-03-10
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
400
Registration Number
NCT06868212

The Effectiveness and Safety of Dupilumab in Children with Asthma in China: a Real-world Study

Conditions
Asthma in Children
Interventions
First Posted Date
2025-02-28
Last Posted Date
2025-02-28
Lead Sponsor
Guangzhou Institute of Respiratory Disease
Target Recruit Count
213
Registration Number
NCT06851403
Locations
🇨🇳

Guangzhou institute of respiratory disease, Guangzhou, Guangdong, China

Dupixent Study for Alternate Administration

Phase 4
Active, not recruiting
Conditions
Nasal Polyps
Sinusitis
Chronic Disease
Interventions
First Posted Date
2024-12-27
Last Posted Date
2025-01-17
Lead Sponsor
Madigan Army Medical Center
Target Recruit Count
30
Registration Number
NCT06750471
Locations
🇺🇸

Madigan Army Medical Center, Tacoma, Washington, United States

Phase I/II Study of Neoadjuvant Cemiplimab and Dupilumab in Early-Stage Non-Small Cell Lung Cancer

Not Applicable
Not yet recruiting
Conditions
Non-Small Cell Lung Cancer
Immunotherapy
Neoadjuvant Therapy
Interventions
First Posted Date
2024-12-20
Last Posted Date
2024-12-20
Lead Sponsor
Centre hospitalier de l'Université de Montréal (CHUM)
Target Recruit Count
24
Registration Number
NCT06743581
Locations
🇨🇦

Centre hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec, Canada

Dupilumab Versus Topical Corticosteroid Effectiveness - Comparison in the Treatment of Stenotic EoE

Phase 2
Recruiting
Conditions
Eosinophilic Esophagitis
Interventions
First Posted Date
2024-11-26
Last Posted Date
2025-03-14
Lead Sponsor
University of Colorado, Denver
Target Recruit Count
72
Registration Number
NCT06705387
Locations
🇺🇸

Children's Hospital Colorado/University of Colorado School of Medicine, Aurora, Colorado, United States

A Non-interventional Observational Study to Assess Long-term Efficacy and Safety of Dupilumab for the Treatment of Patients (>= 12 Years) With Eosinophilic Esophagitis Under Real-world-conditions in Germany

Recruiting
Conditions
Eosinophilic Esophagitis
Interventions
First Posted Date
2024-11-19
Last Posted Date
2025-05-09
Lead Sponsor
Sanofi
Target Recruit Count
150
Registration Number
NCT06695897
Locations
🇩🇪

Investigational Site Number: 0000001, Dachau, Bayern, Germany

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