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地夸磷索钠滴眼液治疗干眼病的有效性和安全性的 Meta 分析

Delgocitinib ointment, a topical Janus kinase inhibitor, in adult patients with moderate to severe atopic dermatitis: A phase 3, randomized, double-blind, vehicle-controlled study and an open-label, long-term extension study.

机构信息

Jikei University School of Medicine, Tokyo, Japan.

Kojinkai Sapporo Skin Clinic, Hokkaido, Japan.

出版信息

J Am Acad Dermatol. 2020 Apr;82(4):823-831. doi: 10.1016/j.jaad.2019.12.015. Epub 2020 Feb 3.

Abstract

BACKGROUND

Previous studies showed the potential effectiveness of delgocitinib ointment, a novel topical Janus kinase inhibitor, in atopic dermatitis (AD).

OBJECTIVE

This study aimed to evaluate the efficacy and safety of delgocitinib 0.5% ointment.

METHODS

In part 1, a 4-week double-blind period, Japanese patients aged 16 years or older with moderate or severe AD were randomly assigned in a 2:1 ratio to delgocitinib 0.5% ointment or vehicle ointment. Eligible patients entered part 2, a 24-week extension period, to receive delgocitinib 0.5% ointment.

RESULTS

At the end of treatment in part 1, the least-squares mean percent changes from baseline in the modified Eczema Area and Severity Index score, the primary efficacy endpoint, were significantly greater in the delgocitinib group than in the vehicle group (-44.3% vs 1.7%, P < .001). The improvement in modified Eczema Area and Severity Index score was maintained in part 2. Most adverse events were mild and unrelated to delgocitinib across the study periods.

LIMITATIONS

Only Japanese patients were included. The vehicle-controlled period lasted only 4 weeks. In part 2, topical corticosteroids were allowed for the treatment of worsening of AD.

CONCLUSION

Delgocitinib ointment was effective and well tolerated in Japanese adult patients with moderate to severe AD for up to 28 weeks.

摘要

背景

先前的研究表明,新型局部 Janus 激酶抑制剂地洛替尼软膏在特应性皮炎(AD)方面具有潜在疗效。

目的

本研究旨在评估地洛替尼 0.5%软膏的疗效和安全性。

方法

在第 1 部分的 4 周双盲期内,16 岁及以上患有中度或重度 AD 的日本患者以 2:1 的比例随机分配至地洛替尼 0.5%软膏或赋形剂软膏组。符合条件的患者进入第 2 部分的 24 周扩展期,接受地洛替尼 0.5%软膏治疗。

结果

在第 1 部分的治疗结束时,主要疗效终点改良 Eczema Area and Severity Index 评分的最小二乘均数自基线的变化率在地洛替尼组显著大于赋形剂组(-44.3%对 1.7%,P<.001)。在第 2 部分,改良 Eczema Area and Severity Index 评分的改善得以维持。整个研究期间,大多数不良事件为轻度,且与地洛替尼无关。

局限性

仅纳入了日本患者。赋形剂对照期仅持续 4 周。在第 2 部分,允许使用局部皮质类固醇治疗 AD 恶化。

结论

地洛替尼软膏在日本中重度 AD 成年患者中使用长达 28 周时具有疗效且耐受性良好。

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