JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY | 卷:85 |
Delgocitinib ointment in pediatric patients with atopic dermatitis: A phase 3, randomized, double-blind, vehicle-controlled study and a subsequent open-label, long-term study | |
Article | |
Nakagawa, Hidemi1  Nemoto, Osamu2  Igarashi, Atsuyuki3  Saeki, Hidehisa4  Kabashima, Kenji5  Nagata, Takeshi6  | |
[1] Jikei Univ, Sch Med, Tokyo, Japan | |
[2] Kojinkai Sapporo Skin Clin, Sapporo, Hokkaido, Japan | |
[3] NTT Med Ctr Tokyo, Dept Dermatol, Tokyo, Japan | |
[4] Nippon Med Sch, Dept Dermatol, Tokyo, Japan | |
[5] Kyoto Univ, Grad Sch Med, Dept Dermatol, Kyoto, Japan | |
[6] Japan Tobacco Inc, Pharmaceut Div, Tokyo, Japan | |
关键词: atopic dermatitis; delgocitinib; eczema; Janus kinase; JAK inhibitor; JTE-052; ointment; pediatric patients; pruritus; skin barrier; topical therapy; | |
DOI : 10.1016/j.jaad.2021.06.014 | |
来源: Elsevier | |
【 摘 要 】
Background: Delgocitinib 0.5% ointment, a topical Janus kinase inhibitor, has been approved in Japan for adult patients with atopic dermatitis (AD). Objective: To evaluate the efficacy and safety of delgocitinib ointment in pediatric patients with AD. Methods: Part 1 of this study was a 4-week double-blind period in which Japanese patients aged 2 through 15 years were randomized in a 1:1 ratio to delgocitinib 0.25% ointment or vehicle ointment. Part 2 was a 52 week extension period. Eligible patients entered part 2 to receive 0.25% or 0.5% delgocitinib ointment. Results: At the initiation of the study, approximately half of the patients had moderate AD. At the end of treatment in part 1, the least-squares mean percent change from baseline in modified Eczema Area and Severity Index score, the primary efficacy endpoint, was significantly greater for delgocitinib ointment than for vehicle (-39.3% vs +10.9%, P < .001). In part 2, improvements in AD were also seen through week 56. Most adverse events were mild and unrelated to delgocitinib across the study periods. Limitations: Only Japanese patients were included. In part 2, no control group was included and rescue therapy was allowed. Conclusion: Delgocitinib ointment was effective and well tolerated when applied to Japanese pediatric patients with AD for up to 56 weeks.
【 授权许可】
Free
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
10_1016_j_jaad_2021_06_014.pdf | 899KB | download |