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Proven effective in the treatment of atopic dermatitis (AD) and other allergic conditions, these study results confirm the ability of dupilumab to improve symptoms in children with other concurrent conditions.
New study results published in the journal Advances in Therapy show that dupilumab (Dupixent; Sanofi, Regeneron) treatment demonstrated improvement in signs and symptoms of atopic dermatitis (AD) in children aged 6 months to 5 years both with and without comorbidities such as food allergies, allergic rhinitis (AR), and asthma.1,2
Dupilumab, a fully human monoclonal antibody that inhibits the signaling of both IL-4 and IL-13, has numerous FDA-approved indications, including in patients with uncontrolled chronic spontaneous urticaria and other inflammatory conditions. For AD, it is approved for the treatment of adult and pediatric patients as young as 6 months with moderate-to-severe disease.1,3,4
Dozens of key clinical trials have indicated significant efficacy and safety in patients with AD treated with dupilumab. However, this new research is the first to analyze the drug’s effectiveness in children with both AD and comorbid type 2 conditions. Using a cohort from the LIBERTY AD PRESCHOOL part B clinical trial, which found that dupilumab and topical corticosteroids improved AD signs, the current investigators sought to evaluate this effectiveness in the presence of comorbidities.1,2
Efficacy end points included measurements of AD resolution assessed at week 16. Three measurements were used to evaluate the clearing of skin in patients: the Investigator’s Global Assessment (IGA); the Eczema Area and Severity Index (EASI-75); and the Worst Scratch Itch Numeric Rating Scale (WSI-NRS).1
At the 16-week follow-up point, the investigators found that significantly more patients being treated with dupilumab versus placebo—with or without asthma or AR—had an IGA score of 0 or 1. Furthermore, a much higher number of patients with comorbid food allergies achieved an IGA of 0 or 1.1
These positive scores continued to be reported. In the EASI, significantly more patients who received dupilumab versus placebo, regardless of the presence of comorbidities, had a 75% or greater improvement in their score. Lastly, a much higher proportion of patients who received dupilumab with or without AR or food allergies had a greater than 4-point reduction in weekly average daily score on the WSI-NRS.1
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Dupilumab provides a versatile treatment option for the millions of patients burdened with AD and the additional impacts that concurrent type 2 inflammatory conditions can have. Early treatment with the medicine is critical and could potentially offer a strategy for disease alternation by preventing the development of other allergic conditions. The manageable safety profile confirmed in this trial further incentivizes the use of dupilumab in these patients; pharmacists should be aware of evolving treatment guidelines for this patient population.1,4
“Many children suffer from multiple allergic conditions at the same time, so knowing that dupilumab can be used to safely and effectively treat their atopic dermatitis whether or not they have additional atopic diseases such as asthma or allergies is an important step forward,” Mark Boguniewicz, MD, pediatric allergist and lead author of the study, said in a news release.2