Topical tofacitinib for atopic dermatitis: a phase II a randomized trial

托法替尼 湿疹面积及严重程度指数 耐受性 医学 Janus激酶抑制剂 特应性皮炎 不利影响 随机对照试验 临床终点 内科学 药效学 药代动力学 皮肤病科 类风湿性关节炎
作者
Robert Bissonnette,Kim Papp,Yves Poulin,Melinda Gooderham,Maitreyi Raman,Lotus Mallbris,C. Wang,Vivek S. Purohit,Carla Mamolo,Jocelyne Papacharalambous,William C. Ports
出处
期刊:British Journal of Dermatology [Wiley]
卷期号:175 (5): 902-911 被引量:357
标识
DOI:10.1111/bjd.14871
摘要

Despite unmet need, 15 years have passed since a topical therapy with a new mechanism of action for atopic dermatitis (AD) has been approved. Janus kinase (JAK) inhibitor treatment effect via topical application in patients with AD is unknown.Tofacitinib, a small-molecule JAK inhibitor, was investigated for the topical treatment of AD.In this 4-week, phase IIa, randomized, double-blind, vehicle-controlled study (NCT02001181), 69 adults with mild-to-moderate AD were randomized 1:1 to 2% tofacitinib or vehicle ointment twice daily. Percentage change from baseline (CFB) in Eczema Area and Severity Index (EASI) score at week 4 was the primary end point. Secondary efficacy end points included percentage CFB in body surface area (BSA), CFB in EASI Clinical Signs Severity Sum Score, proportion of patients with Physician's Global Assessment (PGA) response and CFB in patient-reported pruritus. Safety, local tolerability and pharmacokinetics were monitored.The mean percentage CFB at week 4 in EASI score was significantly greater (P < 0·001) for tofacitinib (-81·7%) vs. vehicle (-29·9%). Patients treated with tofacitinib showed significant (P < 0·001) improvements vs. vehicle across all prespecified efficacy end points and for pruritus at week 4. Significant improvements in EASI, PGA and BSA were observed by week 1 and improvements in pruritus were observed by day 2. Safety/local tolerability were generally similar for both treatments, although more adverse events were observed for vehicle vs. tofacitinib.Tofacitinib ointment showed significantly greater efficacy vs. vehicle across end points, with early onset of effect and comparable safety/local tolerability to vehicle. JAK inhibition through topical delivery is potentially a promising therapeutic target for AD.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI

祝大家在新的一年里科研腾飞
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
科研通AI2S应助张大宝采纳,获得10
2秒前
快乐滑板应助pz采纳,获得10
3秒前
好吃完成签到 ,获得积分10
3秒前
所所应助哭泣的采波采纳,获得10
7秒前
10秒前
Ava应助艺霖大王采纳,获得10
11秒前
快乐科研完成签到,获得积分10
12秒前
Wang完成签到,获得积分10
14秒前
pz完成签到,获得积分10
16秒前
18秒前
麻雀发布了新的文献求助10
21秒前
传奇3应助快乐科研采纳,获得10
21秒前
hxx完成签到,获得积分10
22秒前
yry发布了新的文献求助10
23秒前
26秒前
sissiarno应助qianduo采纳,获得50
27秒前
。。完成签到,获得积分10
27秒前
无花果应助复杂的鑫磊采纳,获得30
29秒前
29秒前
bkagyin应助lx采纳,获得10
29秒前
30秒前
敏er好学完成签到,获得积分10
31秒前
orixero应助yry采纳,获得10
31秒前
谢紫玲发布了新的文献求助10
33秒前
尤小玉完成签到,获得积分10
33秒前
诚心问玉完成签到,获得积分10
33秒前
Hello应助wenlin采纳,获得10
34秒前
winni完成签到,获得积分10
36秒前
失眠的蓝完成签到,获得积分10
37秒前
Lynn完成签到,获得积分10
38秒前
40秒前
43秒前
李盈盈完成签到,获得积分10
50秒前
50秒前
LLSN完成签到 ,获得积分10
50秒前
51秒前
XylonYu完成签到,获得积分10
55秒前
Rita发布了新的文献求助10
55秒前
华仔应助人间小阿姨采纳,获得10
55秒前
伯赏孱发布了新的文献求助10
56秒前
高分求助中
Востребованный временем 2500
Les Mantodea de Guyane 1000
Very-high-order BVD Schemes Using β-variable THINC Method 950
Field Guide to Insects of South Africa 660
The Three Stars Each: The Astrolabes and Related Texts 500
The Collected Works of Jeremy Bentham: Rights, Representation, and Reform: Nonsense upon Stilts and Other Writings on the French Revolution 320
SAS, Python and R: A Cross-Reference Guide for Data Science 300
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 细胞生物学 免疫学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3385461
求助须知:如何正确求助?哪些是违规求助? 2999103
关于积分的说明 8783292
捐赠科研通 2684734
什么是DOI,文献DOI怎么找? 1470606
科研通“疑难数据库(出版商)”最低求助积分说明 679845
邀请新用户注册赠送积分活动 672281