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.
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.
MetroHealth System, Cleveland, Ohio, United States
Atlantic Health System, Cedar Knolls, New Jersey, United States
Brigham and Women's Hospital, Boston, Massachusetts, United States
Regeneron Investigational Site, Seattle, Washington, United States
University of California San Diego (UCSD), San Diego, California, United States
University of California Los Angeles (UCLA), Los Angeles, California, United States
Sean N. Parker Center for Allergy & Asthma Research at Stanford University, Palo Alto, California, United States
Northwestern Medicine Digestive Health Center, Chicago, Illinois, United States
Icahn School of Medicine at Mount Sinai, New York, New York, United States
Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, United States
Brigham and Women's Hospital, Boston, Massachusetts, United States
UCSF Psoriasis and Skin Treatment Center, San Francisco, California, United States
Regeneron Study Site, Barnsley, Yorkshire, United Kingdom
Regeneron Study Site #2, Chicago, Illinois, United States
Regeneron Study Site #1, Chicago, Illinois, United States
Investigational Site Number :032002, La Plata, Buenos Aires, Argentina
Investigational Site Number :032005, Rosario, Santa Fe, Argentina
Investigational Site Number :032003, Ciudad Autonoma Bs As, Argentina
Rochester Regional Health - Allergy/Immunology, Rochester, New York, United States
Investigational Site Number : 6430005, St Petersburg, Russian Federation
Investigational Site Number : 6430003, St. Petersburg, Russian Federation
Investigational Site Number : 7100001, Cape Town, South Africa
Stay informed with timely notifications on clinical trials, regulatory changes, and research advancements related to this medication.