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

Evaluation of Dupilumab in Patients With Severe Steroid Dependent Asthma

Phase 3
Completed
Conditions
Asthma
Interventions
Drug: Placebo
Drug: Oral corticosteroid therapy (prednisone/prednisolone)
Drug: Inhaled corticosteroid (ICS) therapy
Drug: Albuterol/Salbutamol
Drug: Levalbuterol/Levosalbutamol
First Posted Date
2015-08-19
Last Posted Date
2019-10-01
Lead Sponsor
Sanofi
Target Recruit Count
210
Registration Number
NCT02528214
Locations
🇪🇸

Investigational Site Number 724014, Barcelona, Spain

🇪🇸

Investigational Site Number 724006, Pozuelo De Alarcón, Spain

🇦🇷

Investigational Site Number 032001, Caba, Argentina

and more 77 locations

Evaluation of Dupilumab in Patients With Persistent Asthma (Liberty Asthma Quest)

Phase 3
Completed
Conditions
Asthma
Interventions
Drug: Placebo
Drug: Inhaled corticosteroid (ICS) therapy
Drug: Albuterol/Salbutamol
Drug: Levalbuterol/Levosalbutamol
First Posted Date
2015-04-13
Last Posted Date
2018-10-23
Lead Sponsor
Sanofi
Target Recruit Count
1902
Registration Number
NCT02414854
Locations
🇯🇵

Investigational Site Number 392168, Uozu-Shi, Japan

🇺🇸

Investigational Site Number 840011, Los Angeles, California, United States

🇺🇸

Investigational Site Number 840021, San Jose, California, United States

and more 386 locations

A Study to Determine the Safety and Tolerability of Dupilumab (REGN668/SAR231893) in Patients Aged ≥6 to <18 Years With Atopic Dermatitis (Eczema)

Phase 2
Completed
Conditions
Atopic Dermatitis
Interventions
First Posted Date
2015-04-03
Last Posted Date
2020-11-27
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
78
Registration Number
NCT02407756

A Study to Confirm the Efficacy and Safety of Different Dupilumab Dose Regimens in Adults With Atopic Dermatitis (AD)

Phase 3
Completed
Conditions
Atopic Dermatitis
Interventions
Drug: Placebo
First Posted Date
2015-03-20
Last Posted Date
2020-03-11
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
422
Registration Number
NCT02395133

Study of Dupilumab in Adult Participants With Active Eosinophilic Esophagitis (EoE)

Phase 2
Completed
Conditions
Eosinophilic Esophagitis
Interventions
Drug: Placebo
First Posted Date
2015-03-04
Last Posted Date
2020-02-28
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
47
Registration Number
NCT02379052

Study of Dupilumab (REGN668/SAR231893) Monotherapy Administered to Adult Patients With Moderate-to-Severe Atopic Dermatitis

Phase 3
Completed
Conditions
Dermatitis, Atopic
Interventions
Drug: Placebo (for Dupilumab)
First Posted Date
2014-10-29
Last Posted Date
2020-06-02
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
708
Registration Number
NCT02277769

Study of Dupilumab Monotherapy Administered to Adult Patients With Moderate-to-Severe Atopic Dermatitis

Phase 3
Completed
Conditions
Dermatitis, Atopic
Interventions
Drug: Placebo (for Dupilumab)
First Posted Date
2014-10-29
Last Posted Date
2017-11-21
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
671
Registration Number
NCT02277743

Study to Assess the Efficacy and Long-term Safety of Dupilumab (REGN668/SAR231893) in Adult Participants With Moderate-to-Severe Atopic Dermatitis

Phase 3
Completed
Conditions
Atopic Dermatitis
Interventions
Drug: Placebo (for Dupilumab)
Other: Topical Corticosteroid (TCS)
First Posted Date
2014-10-09
Last Posted Date
2017-10-17
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
740
Registration Number
NCT02260986

Study of Dupilumab and Immune Responses in Adults With Atopic Dermatitis (AD)

Phase 2
Completed
Conditions
Atopic Dermatitis
Interventions
Drug: Placebo
First Posted Date
2014-08-07
Last Posted Date
2020-05-07
Lead Sponsor
Regeneron Pharmaceuticals
Target Recruit Count
194
Registration Number
NCT02210780

Long-Term Safety Evaluation of Dupilumab in Patients With Asthma (LIBERTY ASTHMA TRAVERSE)

Phase 3
Completed
Conditions
Asthma
Interventions
First Posted Date
2014-05-08
Last Posted Date
2022-03-28
Lead Sponsor
Sanofi
Target Recruit Count
2282
Registration Number
NCT02134028
Locations
🇺🇸

Investigational Site Number 840402, Tucson, Arizona, United States

🇺🇸

Investigational Site Number 840045, Long Beach, California, United States

🇺🇸

Investigational Site Number 840044, Newport Beach, California, United States

and more 362 locations
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