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Dupilumab

Generic Name
Dupilumab
Brand Names
Dupixent
Drug Type
Biotech
Chemical Formula
-
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

Treatment of Alopecia Areata (AA) With Dupilumab in Patients With and Without Atopic Dermatitis (AD)

Phase 2
Completed
Conditions
Alopecia Areata
Interventions
Drug: Dupilumab
Drug: Placebo
First Posted Date
2017-12-02
Last Posted Date
2022-09-13
Lead Sponsor
Icahn School of Medicine at Mount Sinai
Target Recruit Count
60
Registration Number
NCT03359356
Locations
🇺🇸

The Rockefeller University Laboratory for Investigative Dermatology, New York, New York, United States

🇺🇸

Icahn School of Medicine at Mount Sinai, New York, New York, United States

Molecular Signatures in Inflammatory Skin Disease

First Posted Date
2017-11-30
Last Posted Date
2024-12-04
Lead Sponsor
Prof. Dr. Stephan Weidinger
Target Recruit Count
300
Registration Number
NCT03358693
Locations
🇩🇪

Department of Dermatology, University Hospital Schleswig Holstein, Campus Kiel, Kiel, Germany

Safety, Pharmacokinetics and Efficacy of Dupilumab in Patients ≥6 Months to <6 Years With Moderate-to-Severe Atopic Dermatitis (Liberty AD PRESCHOOL)

Phase 2
Completed
Conditions
Dermatitis, Atopic
Interventions
Drug: Dupilumab
Drug: Matching placebo
First Posted Date
2017-11-17
Last Posted Date
2022-07-28
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
202
Registration Number
NCT03346434
Locations
🇩🇪

Regeneron Investigational site, Muenchen, Germany

🇬🇧

Regeneron Investigational Site, Sheffield, South Yorkshire, United Kingdom

Study to Investigate the Efficacy and Safety of Dupilumab Administered With Topical Corticosteroids (TCS) in Participants ≥6 to <12 Years With Severe Atopic Dermatitis (AD)

Phase 3
Completed
Conditions
Dermatitis, Atopic
Interventions
Drug: Matching Placebo
Drug: Dupilumab
First Posted Date
2017-11-17
Last Posted Date
2020-08-13
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
367
Registration Number
NCT03345914
Locations
🇬🇧

Regeneron Research Site, Sheffield, United Kingdom

Immunogenetic Profiling of Dupilumab for the Treatment of Atopic Dermatitis

Phase 4
Completed
Conditions
Atopic Dermatitis
Eczema
Atopic Dermatitis Eczema
Atopic Dermatitis and Related Conditions
Interventions
First Posted Date
2017-09-26
Last Posted Date
2024-06-18
Lead Sponsor
University of California, San Francisco
Target Recruit Count
18
Registration Number
NCT03293030
Locations
🇺🇸

UCSF Psoriasis and Skin Treatment Center, San Francisco, California, United States

Study of REGN3500 and Dupilumab in Patients With Asthma

Phase 1
Completed
Conditions
Asthma, Allergic
Interventions
First Posted Date
2017-04-13
Last Posted Date
2020-01-18
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
32
Registration Number
NCT03112577
Locations
🇺🇸

WCCT Global, Cypress, California, United States

🇬🇧

Celerion, Belfast, United Kingdom

🇬🇧

Hammersmith Medicine Research, London, United Kingdom

and more 2 locations

Efficacy and Safety of Dupilumab in Participants ≥12 to <18 Years of Age, With Moderate-to-severe Atopic Dermatitis

Phase 3
Completed
Conditions
Dermatitis, Atopic
Dermatitis, Dermatitis Atopic
Diseases Genetic, Genetic
Hypersensitivity, Immune System Diseases
Eczema, Skin Diseases, Skin
Disease, Eczematous Skin
Hypersensitivity, Immediate
Moderate-to-Severe Atopic Dermatitis
Diseases Inborn, Skin
Interventions
Drug: Dupilumab
Drug: Placebo
First Posted Date
2017-02-15
Last Posted Date
2019-07-23
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
251
Registration Number
NCT03054428
Locations
🇨🇦

Regeneron Investigational Site, Windsor, Ontario, Canada

🇨🇦

Regeneron Research Site, Richmond Hill, Ontario, Canada

Study of Dupilumab Auto-injector Device When Used by Patients With Atopic Dermatitis

Phase 1
Completed
Conditions
Atopic Disorders
Eczema, Atopic
Interventions
Drug: Dupilumab
Device: Auto-injector Device
Device: Prefilled syringe
First Posted Date
2017-02-10
Last Posted Date
2018-08-01
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
176
Registration Number
NCT03050151
Locations
🇺🇸

Regeneron Investigational Site, Tacoma, Washington, United States

Dupilumab Compassionate Use Study

Conditions
Asthma
First Posted Date
2017-01-13
Last Posted Date
2018-03-07
Lead Sponsor
Sally E. Wenzel MD
Registration Number
NCT03020810

Evaluation of Dupilumab in Children With Uncontrolled Asthma

Phase 3
Completed
Conditions
Asthma
Interventions
Drug: Placebo
Drug: Dupilumab
Drug: Asthma Controller Therapies
Drug: Asthma Reliever Therapies
First Posted Date
2016-10-31
Last Posted Date
2022-03-28
Lead Sponsor
Sanofi
Target Recruit Count
408
Registration Number
NCT02948959
Locations
🇺🇸

Investigational Site Number 840012, Tucson, Arizona, United States

🇺🇸

Investigational Site Number 840001, Rolling Hills Estates, California, United States

🇺🇸

Investigational Site Number 840016, Ann Arbor, Michigan, United States

and more 96 locations
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