A Phase 3 Trial of Brepocitinib in Dermatomyositis

皮肌炎 医学 肌炎 多发性肌炎 结缔组织病 内科学 皮肤病科 自身免疫性疾病 糖皮质激素 相(物质) 免疫病理学 全身性疾病 病理 临床研究阶段 胃肠病学 免疫学 疾病 肌肉疾病 临床试验 间质性肺病 炎性肌病 自身免疫
作者
Ruth Ann Vleugels,Julie J. Paik,Iazsmin Bauer Ventura,Aaron R. Mangold,Prateek C. Gandiga,Anna Haemel,Hector Chinoy,Yessar M. Hussain,Kumaraswamy Sivakumar,Zoltán Griger,Eun Bong Lee,F. Bozán,Chung-Yuan Hsu,Alisa N. Femia,Mazen M. Dimachkie,Michelle S. Min,Tahseen Mozaffar,C. Charles-Schoeman,David Fernández,Oluwakemi Onajin
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:394 (19): 1883-1893 被引量:8
标识
DOI:10.1056/nejmoa2503531
摘要

BACKGROUND: Brepocitinib is a first-in-class, oral, selective TYK2-JAK1 inhibitor that blocks cytokine signaling, which has been implicated in dermatomyositis. METHODS: In this phase 3, double-blind, randomized, placebo-controlled trial, adults with dermatomyositis were assigned in a 1:1:1 ratio to receive once-daily oral brepocitinib at a dose of 30 mg, brepocitinib at a dose of 15 mg, or placebo for 52 weeks. Standard therapies were continued, and glucocorticoids were tapered. The primary end point was the Total Improvement Score, a validated composite myositis index (with scores ranging from 0 to 100 and higher scores indicating greater improvement) at week 52. Key secondary end points, including skin disease activity, glucocorticoid tapering, and physical function, were tested in a multiplicity-controlled sequence. RESULTS: A total of 241 patients underwent randomization: 81 to receive brepocitinib 30 mg, 81 to receive brepocitinib 15 mg, and 79 to receive placebo. At week 52, the mean Total Improvement Score was 46.5, 37.5, and 31.2, respectively (difference with brepocitinib 30 mg vs. placebo, 15.3; 95% confidence interval [CI], 6.7 to 24.0; P<0.001; difference with brepocitinib 15 mg vs. placebo, 6.3; 95% CI, -2.4 to 14.9). Brepocitinib 30 mg was superior to placebo across all nine key secondary end points, including skin disease activity, systemic glucocorticoid tapering, and functional disability, with improvements observed as early as week 4. Serious infections were more frequent in the brepocitinib 30-mg group than in the placebo group (10% vs. 1%). No deaths occurred during the trial. CONCLUSIONS: In adults with dermatomyositis that was resistant to previous therapy, the use of brepocitinib at a dose of 30 mg (but not at a dose of 15 mg) resulted in significant benefits with respect to a composite myositis index, skin disease severity, glucocorticoid tapering, and functional disability. (Funded by Priovant Therapeutics; ClinicalTrials.gov number, NCT05437263.).
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