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

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: 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
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: 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

A Controlled Clinical Study of Dupilumab in Patients With Bilateral Nasal Polyps

Phase 3
Completed
Conditions
Chronic Rhinosinusitis Phenotype With Nasal Polyps (CRSwNP)
Interventions
First Posted Date
2016-09-23
Last Posted Date
2019-07-25
Lead Sponsor
Sanofi
Target Recruit Count
276
Registration Number
NCT02912468
Locations
🇫🇷

Investigational Site Number 2500001, Montpellier, France

🇫🇷

Investigational Site Number 2500003, Lyon, France

🇺🇸

Investigational Site Number 8400020, Medford, Oregon, United States

and more 73 locations

Controlled Clinical Study of Dupilumab in Patients With Nasal Polyps

Phase 3
Completed
Conditions
Chronic Rhinosinusitis Phenotype With Nasal Polyps (CRSwNP)
Interventions
First Posted Date
2016-09-13
Last Posted Date
2019-10-23
Lead Sponsor
Sanofi
Target Recruit Count
448
Registration Number
NCT02898454
Locations
🇺🇸

Investigational Site Number 8400011, Fresno, California, United States

🇦🇷

Investigational Site Number 0320005, Caba, Argentina

🇦🇷

Investigational Site Number 0320004, Buenos Aires, Argentina

and more 120 locations

A Study to Assess the Efficacy and Safety of Dupilumab in Participants With Severe Atopic Dermatitis (AD) That Are Not Controlled With Oral Cyclosporine A (CSA) or for Those Who Cannot Take Oral CSA Because it is Not Medically Advisable

Phase 3
Completed
Conditions
Atopic Dermatitis
Interventions
Drug: Matching Placebo
First Posted Date
2016-04-29
Last Posted Date
2020-08-20
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
325
Registration Number
NCT02755649
Locations
🇩🇪

Site 7, Berlin, Germany

🇩🇪

Site 5, Berlin, Germany

🇬🇧

Site 1, London, United Kingdom

and more 4 locations

Open Label, Drug-Drug Interaction (DDI) Study of Dupilumab (REGN668/SAR231893) in Patients With Moderate to Severe Atopic Dermatitis (AD)

First Posted Date
2016-01-06
Last Posted Date
2016-08-22
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
14
Registration Number
NCT02647086
Locations
🇺🇸

Regeneron Study Site, Raleigh, North Carolina, United States

Study to Assess the Long-term Safety of Dupilumab Administered in Participants ≥6 Months to <18 Years of Age With Atopic Dermatitis (AD)

Phase 3
Active, not recruiting
Conditions
Atopic Dermatitis
Interventions
First Posted Date
2015-11-23
Last Posted Date
2024-06-10
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
880
Registration Number
NCT02612454
Locations
🇬🇧

Regeneron Investigational Site, Sheffield, South Yorkshire, United Kingdom

🇩🇪

Regeneron Study Site, Muenchen, Germany

🇺🇸

Regeneron Investigational site, Philadelphia, Pennsylvania, United States

Evaluation of Dupilumab's Effects on Airway Inflammation in Patients With Asthma

First Posted Date
2015-10-09
Last Posted Date
2022-04-04
Lead Sponsor
Sanofi
Target Recruit Count
42
Registration Number
NCT02573233
Locations
🇨🇦

Investigational Site Number 124012, Montreal, Canada

🇺🇸

Investigational Site Number 840028, Pittsburgh, Pennsylvania, United States

🇸🇪

Investigational Site Number 752001, Lund, Sweden

and more 13 locations
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