Probity Medical Research, 135 Union Street East, Waterloo, ON, N2J 1C4, Canada.
Comprehensive Center for Inflammation Medicine, University Medical School Schleswig-Holstein, University of Lübeck, Lübeck, Germany.
Br J Dermatol. 2015 Oct;173(4):930-9. doi: 10.1111/bjd.13932. Epub 2015 Oct 15.
Tildrakizumab is a high-affinity, humanized, IgG1/κ, anti-interleukin (IL)-23p19 monoclonal antibody that does not bind human IL-12 or p40 is being developed for the treatment of chronic plaque psoriasis.
To evaluate the safety and efficacy of subcutaneous tildrakizumab in patients with moderate-to-severe chronic plaque psoriasis.
A three-part, randomized, double-blind, phase IIb trial was conducted in 355 adults with chronic plaque psoriasis. Participants were randomized to receive subcutaneous tildrakizumab (5, 25, 100, 200 mg) or placebo at weeks 0 and 4 (part I) and every 12 weeks thereafter until week 52 (part II). Study drug was discontinued at week 52 and participants were followed through week 72 (part III). Primary efficacy end point was Psoriasis Area and Severity Index (PASI) 75 response at week 16. Adverse events (AEs) and vital signs were monitored throughout the study.
At week 16, PASI 75 responses were 33·3% (n = 14), 64·4% (n = 58), 66·3% (n = 59), 74·4% (n = 64) and 4·4% (n = 2) in the 5-, 25-, 100- and 200-mg tildrakizumab and placebo groups, respectively (P ≤ 0·001 for each tildrakizumab dose vs. placebo). PASI 75 response was generally maintained through week 52; only eight of 222 participants who achieved PASI 75 response at week 52 and continued to part III relapsed following discontinuation up to week 72. Possible drug-related serious AEs included bacterial arthritis and lymphoedema (part I), and melanoma, stroke, epiglottitis and knee infection (part II).
Tildrakizumab had treatment effects that were superior to placebo, maintained for 52 weeks of treatment, and persisted for 20 weeks after cessation. Tildrakizumab was generally safe and well tolerated. These results suggest that IL-23p19 is a key target for suppressing psoriasis.
替度鲁单抗是一种高亲和力的人源化 IgG1/κ 型抗白细胞介素(IL)-23p19 单克隆抗体,它不与人类 IL-12 或 p40 结合,目前正在开发用于治疗慢性斑块型银屑病。
评估皮下注射替度鲁单抗治疗中重度慢性斑块型银屑病的安全性和疗效。
这是一项三部分、随机、双盲、Ⅱb 期临床试验,共纳入 355 例慢性斑块型银屑病成人患者。患者被随机分配至接受皮下注射替度鲁单抗(5、25、100、200mg)或安慰剂,分别于第 0 周和第 4 周(第 1 部分)以及此后每 12 周一次,直至第 52 周(第 2 部分)。第 52 周时停止研究药物治疗,所有患者继续随访至第 72 周(第 3 部分)。主要疗效终点为第 16 周时的银屑病面积与严重程度指数(PASI)75 应答。整个研究过程中监测不良事件(AE)和生命体征。
第 16 周时,5、25、100、200mg 替度鲁单抗组的 PASI 75 应答率分别为 33.3%(n=14)、64.4%(n=58)、66.3%(n=59)、74.4%(n=64)和 4.4%(n=2),安慰剂组为 2%(n=1)(各剂量组替度鲁单抗与安慰剂相比,P均≤0.001)。第 52 周时,PASI 75 应答仍基本维持;在第 52 周达到 PASI 75 应答且继续进入第 3 部分的 222 例患者中,仅 8 例在停药后 72 周时出现复发。可能与药物相关的严重 AE 包括细菌性关节炎和淋巴水肿(第 1 部分)、黑色素瘤、卒中和会厌炎(第 2 部分)以及膝部感染(第 2 部分)。
替度鲁单抗的治疗效果优于安慰剂,在 52 周的治疗期间持续存在,停药后 20 周仍持续存在。替度鲁单抗总体上安全且耐受良好。这些结果表明,白细胞介素-23p19 是抑制银屑病的关键靶点。