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The Efficacy and Safety of Abrocitinib as a Treatment Option for Atopic Dermatitis: A Short Report of the Clinical Data

Journal

DRUG DESIGN DEVELOPMENT AND THERAPY
Volume 15, Issue -, Pages 1135-1147

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/DDDT.S240866

Keywords

atopic dermatitis; abrocitinib; JAK inhibitors; JAK-STAT

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Atopic dermatitis (AD) is a chronic inflammatory skin disease that affects children and adults, with dysfunction of the epidermal barrier and immune dysregulation playing key roles in its pathogenesis. Recent studies have highlighted the importance of Janus kinase (JAK) enzymes in AD, leading to the emergence of oral and topical JAK inhibitors as new treatment options. Abrocitinib, an oral JAK1 inhibitor, has shown promising results in reducing the severity of moderate-to-severe AD with minimal adverse events, comparable to established treatments like dupilumab.
Atopic dermatitis (AD) is a chronic, pruritic, inflammatory skin disease that predominantly affects children. However, it can persist in adulthood and/or start at older ages. Both dysfunction of the epidermal barrier and immune dysregulation are known to play a role in the pathogenesis of AD. In the last years, numerous studies showed that Janus kinase (JAK) enzymes have a key role in AD pathogenesis. Therefore, oral and topical JAK inhibitors are new emerging treatments for AD. We report the data relating to abrocitinib, an oral JAK1 inhibitor. For this purpose, we examined articles already published concerning, in particular, concluded clinical trials. Furthermore, we also report the design of current ongoing clinical trials. The search was carried out considering the main search engines relating to medical literature and clinical trials. From all the data we collected, abrocitinib proved to be an effective drug in significantly reducing the severity of moderate-to-severe AD when compared to placebo. Furthermore, the efficacy was similar to other well-established treatment for AD, such as dupilumab. Adverse events were generally mild; indeed, the drug was definitively suspended only in few patients.

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