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

Pivotal Study to Assess the Efficacy, Safety and Tolerability of Dupilumab in Patients With Moderate-to-severe COPD With Type 2 Inflammation

Phase 3
Completed
Conditions
Chronic Obstructive Pulmonary Disease
Interventions
Drug: Inhaled Corticosteroid
Drug: Inhaled Long-Acting Beta Agonist
Drug: Placebo
Drug: Inhaled Long-Acting Muscarinic Antagonist
First Posted Date
2019-04-29
Last Posted Date
2024-02-28
Lead Sponsor
Sanofi
Target Recruit Count
939
Registration Number
NCT03930732
Locations
🇨🇦

Investigational Site Number :1240013, Windsor, Ontario, Canada

🇨🇦

Investigational Site Number :1240021, Edmonton, Alberta, Canada

🇨🇳

Investigational Site Number :1560037, Baotou, China

and more 272 locations

Evaluation of Dupilumab in Chinese Adult Patients With Moderate to Severe Atopic Dermatitis

Phase 3
Completed
Conditions
Atopic Dermatitis
Interventions
Drug: Placebo
Drug: Emollient (moisturizer)
First Posted Date
2019-04-11
Last Posted Date
2023-12-19
Lead Sponsor
Sanofi
Target Recruit Count
165
Registration Number
NCT03912259
Locations
🇨🇳

Investigational Site Number 1560006, Changsha, China

🇨🇳

Investigational Site Number 1560030, Lianyungang, China

🇨🇳

Investigational Site Number 1560021, Changchun, China

and more 24 locations

Neoadjuvant Dupilumab in Men With Localized High-Risk Prostate Cancer

Phase 2
Terminated
Conditions
Prostate Cancer
Interventions
First Posted Date
2019-03-22
Last Posted Date
2021-10-15
Lead Sponsor
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Target Recruit Count
7
Registration Number
NCT03886493
Locations
🇺🇸

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, United States

Efficacy and Safety of Dupilumab Chronic Hands Eczema Refractory to Highly Potent Topical Corticosteroids

Phase 2
Completed
Conditions
Chronic Hand Eczema
Interventions
Drug: placebo
First Posted Date
2019-03-04
Last Posted Date
2024-12-03
Lead Sponsor
University Hospital, Toulouse
Target Recruit Count
94
Registration Number
NCT03861455
Locations
🇫🇷

CHU Lyon-Sud Département d'allergologie et d'immunologie clinique, Pierre-Bénite, France

🇫🇷

Saint André Hospital, Bordeaux, France

🇫🇷

Hôpital Saint Eloi, Montpellier, France

and more 1 locations

Study to Evaluate Dupilumab Monotherapy in Pediatric Patients With Peanut Allergy

Phase 2
Completed
Conditions
Peanut Allergy
Interventions
First Posted Date
2019-01-04
Last Posted Date
2022-05-19
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
25
Registration Number
NCT03793608
Locations
🇨🇦

Regeneron Investigational Site, Montreal, Quebec, Canada

Efficacy and Safety Study of Dupilumab in Patients With Persistent Asthma

Phase 3
Completed
Conditions
Asthma
Interventions
Drug: Placebo
Drug: Asthma Controller Therapies (include prednisone/prednisolone)
Drug: Asthma Reliever Therapies
First Posted Date
2018-12-20
Last Posted Date
2022-12-28
Lead Sponsor
Sanofi
Target Recruit Count
486
Registration Number
NCT03782532
Locations
🇮🇳

Investigational Site Number :3560009, Pune, India

🇨🇳

Investigational Site Number :1560025, Chongqing, China

🇨🇳

Investigational Site Number :1560004, Guangzhou, China

and more 64 locations

Dupilumab in Chronic Spontaneous Urticaria

Phase 2
Completed
Conditions
Chronic Spontaneous Urticaria
Recurrent Angioedema
Interventions
Drug: Placebo
First Posted Date
2018-11-21
Last Posted Date
2022-02-02
Lead Sponsor
Charite University, Berlin, Germany
Target Recruit Count
72
Registration Number
NCT03749135
Locations
🇩🇪

Universitätsklinikum Carl Gustav Carus, Dresden, Sachsen, Germany

🇩🇪

Hautklinik der Universitätsmedizin Mainz Clinical Research Center, Mainz, Rheinland-Pfalz, Germany, Germany

🇩🇪

Universitätsklinikum Giessen und Marburg, Marburg, Hessen, Germany

and more 3 locations

Cholinergic Urticaria - Efficacy of Dupilumab

Phase 2
Completed
Conditions
Cholinergic Urticaria
Interventions
Drug: Placebo
First Posted Date
2018-11-21
Last Posted Date
2023-09-06
Lead Sponsor
Charite University, Berlin, Germany
Target Recruit Count
48
Registration Number
NCT03749148
Locations
🇩🇪

Universitätsklinikum Carl Gustav Carus, Dresden, Sachsen, Germany

🇩🇪

Charité-Universitätsmedizin Berlin, Berlin, Germany

🇩🇪

Hautklinik Universitätsklinikum Münster, Münster, Nordrhein-Westfalen, Germany

and more 5 locations

Efficacy and Safety of REGN3500 Monotherapy and Combination of REGN3500 Plus Dupilumab in Adult Patients With Moderate-to-Severe Atopic Dermatitis

Phase 2
Terminated
Conditions
Atopic Dermatitis
Interventions
First Posted Date
2018-11-09
Last Posted Date
2021-11-01
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
206
Registration Number
NCT03736967
Locations
🇪🇸

Regeneron Research Site, Santiago de Compostela, Spain

Study Evaluating Efficacy and Safety of PF-04965842 and Dupilumab in Adult Subjects With Moderate to Severe Atopic Dermatitis on Background Topical Therapy

Phase 3
Completed
Conditions
Dermatitis, Atopic
Eczema
Skin Diseases
Skin Diseases, Eczematous
Hypersensitivity, Immediate
Dermatitis
Hypersensitivity
Genetic Diseases, Inborn
Skin Diseases, Genetic
Immune System Diseases
Interventions
Drug: Injectable Placebo
Drug: Oral Placebo
First Posted Date
2018-10-25
Last Posted Date
2021-01-19
Lead Sponsor
Pfizer
Target Recruit Count
838
Registration Number
NCT03720470
Locations
🇺🇸

Moonshine Research Center, Inc., Doral, Florida, United States

🇺🇸

PMG Research of Raleigh, LLC d/b/a PMG Research of Cary, Cary, North Carolina, United States

🇨🇦

Toronto Research Centre, Toronto, Ontario, Canada

and more 210 locations
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