特应性皮炎
医学
杜皮鲁玛
湿疹面积及严重程度指数
不利影响
安慰剂
皮肤病科
药理学
临床试验
内科学
病理
替代医学
作者
Ana Maria Lé,Melinda Gooderham,Tiago Torres
出处
期刊:Immunotherapy
[Future Medicine]
日期:2023-09-05
卷期号:15 (16): 1351-1362
被引量:9
标识
DOI:10.2217/imt-2023-0057
摘要
Abrocitinib is an oral small molecule which selectively inhibits JAK1, modulating multiple cytokine pathways involved in atopic dermatitis. Both abrocitinib 200 mg and 100 mg reached efficacy results comparable to dupilumab and superior to placebo. Abrocitinib 200 mg was superior to dupilumab in some trials, consistently providing a faster response and itch relief from week 2 to 26. Continuous abrocitinib 200 mg is the most effective at controlling this disease, but with an induction-maintenance approach with abrocitinib 200 mg followed by 100 mg, over 55% of patients did not flare for 40 weeks. Abrocitinib common adverse effects are nonserious. A self-limited dose-related decrease in platelet counts was consistently observed, without clinical repercussion. Abrocitinib demonstrated high efficacy and a favorable safety profile.
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