Department of Dermatology, The Jikei University School of Medicine, Tokyo, Japan.
Kojinkai Sapporo Skin Clinic, Hokkaido, Japan.
Br J Dermatol. 2018 Feb;178(2):424-432. doi: 10.1111/bjd.16014. Epub 2018 Jan 15.
JTE-052 is a novel Janus kinase inhibitor presently under clinical development for the topical treatment of atopic dermatitis (AD).
To evaluate the efficacy and safety of JTE-052 ointment in Japanese adult patients with AD.
Patients with moderate-to-severe AD were randomized (2: 2: 2: 2: 1: 1) to receive JTE-052 ointment at 0·25%, 0·5%, 1% or 3%, the vehicle ointment or tacrolimus 0·1% ointment (reference) twice daily for 4 weeks. The primary efficacy end point was the percentage change in modified Eczema Area Severity Index (mEASI) score from baseline at the end of treatment (EOT). Secondary efficacy end points included change from baseline in the pruritus numerical rating scale (NRS) score.
In total, 327 patients were enrolled. At EOT, the least-squares mean percentage changes from baseline in mEASI score for JTE-052 at 0·25%, 0·5%, 1% and 3% and the vehicle ointment were -41·7%, -57·1%, -54·9%, -72·9% and -12·2%, respectively. All JTE-052 groups showed significant reductions of mEASI score vs. the vehicle group (P < 0·001 for all). In the tacrolimus group, the mean percentage change in mEASI score was -62·0%. The JTE-052 groups also showed significant improvement in other parameters; notably, the pruritus NRS score was reduced as early as day 1 night-time. JTE-052 ointment at doses up to 3% was safe and well tolerated.
Topical JTE-052 markedly and rapidly improved clinical signs and symptoms in Japanese adult patients with moderate-to-severe AD, with a favourable safety profile. The study results indicate that topical JTE-052 is a promising therapeutic option for AD. The trial registration number is JapicCTI-152887.
JTE-052 是一种新型的 Janus 激酶抑制剂,目前正在开发用于治疗特应性皮炎(AD)的局部治疗。
评估 JTE-052 软膏在日本成年 AD 患者中的疗效和安全性。
中重度 AD 患者随机(2:2:2:2:1:1)接受 JTE-052 软膏 0.25%、0.5%、1%或 3%、赋形剂软膏或他克莫司 0.1%软膏(参比),每日 2 次,共 4 周。主要疗效终点为治疗结束时(EOT)与基线相比改良 Eczema Area Severity Index(mEASI)评分的变化百分比。次要疗效终点包括瘙痒数字评分量表(NRS)评分从基线的变化。
共纳入 327 例患者。EOT 时,JTE-052 0.25%、0.5%、1%和 3%及赋形剂软膏组 mEASI 评分较基线的最小二乘均数百分比变化分别为-41.7%、-57.1%、-54.9%、-72.9%和-12.2%。与赋形剂组相比,所有 JTE-052 组 mEASI 评分均显著降低(均<0.001)。他克莫司组 mEASI 评分的平均百分比变化为-62.0%。JTE-052 组其他参数也有显著改善;值得注意的是,瘙痒 NRS 评分在第 1 天夜间即可降低。JTE-052 软膏剂量高达 3%时安全且耐受良好。
JTE-052 软膏可显著且迅速改善日本中重度 AD 成年患者的临床体征和症状,安全性良好。研究结果表明,JTE-052 软膏是治疗 AD 的一种有前途的治疗选择。试验注册号为 JapicCTI-152887。