California Medical Research Associates, Northridge.
University of Belgrade School of Medicine, Belgrade, Serbia.
Arthritis Rheumatol. 2020 Oct;72(10):1621-1631. doi: 10.1002/art.41316. Epub 2020 Sep 7.
To evaluate the efficacy and safety of PF-06651600 (ritlecitinib), an irreversible inhibitor of JAK3 and the tyrosine kinase expressed in hepatocellular carcinoma (TEC) kinase family, in comparison with placebo in patients with rheumatoid arthritis (RA).
An 8-week, phase II, double-blind, parallel-group study was conducted. Seventy patients who were seropositive for anti-citrullinated protein antibodies and/or rheumatoid factor were randomized 3:2 to receive oral PF-06651600 (200 mg once daily) or placebo for 8 weeks. Eligible patients had an inadequate response to methotrexate, and the study design allowed up to 50% of patients to have previously received 1 tumor necrosis factor inhibitor that was inadequately effective and/or not tolerated. The primary end point was change from baseline in the Simplified Disease Activity Index (SDAI) score at week 8, assessed by Bayesian analysis using an informative prior distribution for placebo response.
Mean change from baseline in the SDAI score at week 8 was greater in the PF-06651600 group (-26.1 [95% credible interval -29.7, -22.4]) than in the placebo group (-16.8 [95% credible interval -20.9, -12.7]; P < 0.001). Most adverse events (AEs) were mild in severity, and no treatment-related serious AEs, severe AEs, or deaths were reported. The most common classes of AE were infections and infestations as well as skin and subcutaneous tissue disorders; there was 1 mild case of herpes simplex in the PF-06651600 group that was considered to be treatment related, which resolved within 3 days without study treatment discontinuation or antiviral therapy.
Treatment with the oral JAK3/TEC inhibitor PF-06651600 (200 mg once daily) was associated with significant improvements in RA disease activity and was generally well-tolerated in this small 8-week study.
评估 PF-06651600(ritlecitinib),一种 JAK3 不可逆抑制剂和酪氨酸激酶受体表达于肝细胞癌(TEC)激酶家族,在与安慰剂比较时对类风湿关节炎(RA)患者的疗效和安全性。
这是一项为期 8 周的、Ⅱ期、双盲、平行分组研究。70 名抗瓜氨酸化蛋白抗体和/或类风湿因子阳性的患者被随机分为 3:2 组,分别接受口服 PF-06651600(200mg,每日 1 次)或安慰剂治疗 8 周。符合条件的患者对甲氨蝶呤治疗反应不足,且研究设计允许多达 50%的患者之前曾接受过 1 种肿瘤坏死因子抑制剂,其疗效不足且/或不耐受。主要终点是 8 周时简化疾病活动指数(SDAI)评分的基线变化,采用贝叶斯分析,使用安慰剂反应的信息先验分布进行评估。
8 周时 PF-06651600 组 SDAI 评分的平均基线变化大于安慰剂组(-26.1[95%可信区间-29.7,-22.4] vs -16.8[95%可信区间-20.9,-12.7];P<0.001)。大多数不良事件(AE)为轻度,无治疗相关严重 AE、严重 AE 或死亡报告。最常见的 AE 类别为感染和寄生虫感染以及皮肤和皮下组织疾病;PF-06651600 组有 1 例轻度单纯疱疹病例,被认为与治疗相关,该病例在 3 天内自行消退,无需停止研究治疗或使用抗病毒治疗。
口服 JAK3/TEC 抑制剂 PF-06651600(200mg,每日 1 次)治疗与 RA 疾病活动的显著改善相关,在这项为期 8 周的小型研究中总体耐受性良好。