In the study through 76 weeks, no new risks were observed with once-daily upadacitinib (15 mg or 30 mg).
In a study that assessed 3 randomized clinical trials of adolescents with moderate-to-severe atopic dermatitis (AD) who were treated with upadacitinib, results demonstrated sustained efficacy responses through 76 weeks to go along with a favorable safety profile. These results were published in JAMA Dermatology.
AD is a common, chronic inflammatory skin disease in which onset can occur at any point in life, with the highest incidence of onset in childhood, according to the study authors, led by Amy S. Paller, MD, of the Departments of Dermatology and Pediatrics in the Feinberg School of Medicine at Northwestern University, located in Chicago, Illinois.
"Upadacitinib is an oral, once-daily selective small-molecule JAK inhibitor with greater inhibitory potency for JAK1 than JAK2, JAK3, or tyrosine kinase 2," Paller and authors wrote. "It is approved in many jurisdictions, including the European Union, Japan, Canada, and the US, for the treatment of moderate to severe AD in patients 12 years and older."
In the Measure Up 1 (NCT03569293), Measure Up 2 (NCT03607422), and AD Up (NCT03568318) trials—ongoing, double-blind, placebo-controlled phase 3 randomized clinical trials featuring adolescents aged 12 to 17 years with moderate to severe AD—once-daily upadacitinib, 15 mg or 30 mg, was superior to placebo alone (Measure Up 1 and Measure Up 2 trials) or with topical corticosteroids (AD Up trial) through 16 weeks, and was sustained through 52 weeks during blinded extension phases of the studies.
To further evaluate the once-daily JAK inhibitor, the study investigators sought to assess the efficacy of upadacitinib, 15 mg and 30 mg, with or without topical corticosteroids, in the same patient population through 76 weeks.
"The Measure Up 1, Measure Up 2, and AD Up studies demonstrated the efficacy and adverse events of upadacitinib through 52 weeks in adults and adolescents with atopic dermatitis (AD); however, longer-term outcomes (longer than 1 year) in adolescents have not previously been available," stated the authors.
Data from the trio of randomized clinical trials were collected from August 2018 to April 2022, and were analyzed from June 2022 to September 2023. In the trials, adolescents were randomized 1:1:1 to receive once-daily upadacitinib 15 mg, 30 mg, or placebo alone (Measure Up 1 and Measure Up 2) or with topical corticosteroids (AD Up).
The study featured co-primary endpoints including:
A total of 542 adolescents across all 3 studies were included, of which 52.4% were female.
According to study results at week 76, EASI-75 among those who received a 15 mg dose of upadacitinib was achieved by 89.1%, 84.4%, and 87.8% in the Measure Up 1, Measure Up 2, and AD Up trials, respectively. Among the 30 mg cohort in each trial, EASI-75 was achieved by 96.1%, 93.6%, and 82.7% of adolescents, with results having indicated maintenance or improvement in EASI-75 across 76 weeks, respectively.
Similarly, efficacy measured by vIGA-AD score of 0 or 1 achievement and WP-NRS improvement of 4 points or more from baseline was either maintained or improved through 76 weeks of upadacitinib 15 mg or 30 mg treatment. Additionally, no new safety signals were observed with either dose through the extended evaluation period.
"In summary, these results through 76 weeks demonstrated that upadacitinib, with a favorable benefit-risk profile, was an effective long-term treatment option for adolescents with moderate to severe AD," stated the study authors.
Reference:
Paller AS, Mendes-Bastos P, Siegfried E, et al. Upadacitinib in Adolescents With Moderate to Severe Atopic Dermatitis: Analysis of 3 Phase 3 Randomized Clinical Trials Through 76 Weeks. JAMA Dermatol. Published online October 23, 2024. doi:10.1001/jamadermatol.2024.3696
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