From initial FDA approvala
SINCE 2017, ≈221,000
PATIENTS HAVE FILLED AT
LEAST
1 DUPIXENT
PRESCRIPTIONb,c
a FDA approved since 2017 for adults, 2019 for adolescents (aged 12‑17 years) and 2020 for children (aged 6‑11 years)
with uncontrolled moderate‑to‑severe atopic dermatitis.
b IQVIA National Source of Business (NSOB) data as of December 2021.
c New adult and pediatric patients with uncontrolled moderate‑to‑severe atopic dermatitis.
In uncontrolled moderate-to-severe atopic dermatitis
DUPIXENT demonstrated rapid and sustained results in adults
and avoids broad immunosuppression1
- It is unknown if DUPIXENT will influence the immune response against helminth infections.
Demonstrated safety profile in patients as young as 6 years of age1
In patients aged 6 years and older, one dose every 2 or 4 weeks based on age and weight (after an initial loading dose of two subcutaneous injections). For patients aged 6 months to 5 years, one dose every 4 weeks based on weight, with no initial loading dose recommended.1
Explore appropriate dosing schedules and weight-tiered regimens for DUPIXENT, which does not require initial lab testing or ongoing lab monitoring according to the Prescribing Information.
DUPIXENT is available in a 200 mg or 300 mg pre-filled pen (for patients 12+ years of age) or pre-filled syringe (for 6+ months of age) for subcutaneous injection.
Samples may be available—speak with your DUPIXENT representative for more information, or click here to contact a representative.
See DosAGE and Administration for patients 6+ years of age See dosage and administration for patients 6 months to 5 years of age
DUPIXENT MyWay is a patient support program that can help enable access to DUPIXENT and offers financial assistance for eligible patients, one-on-one nursing support, and more.