Efficacy, Safety, and Tolerability of ONO-4474, an Orally Available Pan-Tropomyosin Receptor Kinase Inhibitor, in Japanese Patients With Moderate to Severe Osteoarthritis of the Knee: A Randomized, Placebo-Controlled, Double-Blind, Parallel-Group Comparative Study.

IF 2.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Journal of clinical pharmacology Pub Date : 2020-01-01 Epub Date: 2019-07-08 DOI:10.1002/jcph.1470
Naoki Ishiguro, Shusuke Oyama, Ryunosuke Higashi, Kunio Yanagida
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引用次数: 6

Abstract

We examined the efficacy, safety, and tolerability of ONO-4474 in Japanese patients with osteoarthritis (OA) of the knee. In this multicenter, placebo-controlled, randomized, double-blind, parallel-group comparative study, patients with moderate to severe OA who were refractory to nonsteroidal anti-inflammatory drugs were orally administered 100 mg of ONO-4474 twice daily for 28 days. The primary end point was knee pain during walking, assessed by visual analog scale over 24 hours (VAS24 ). Treatment-emergent adverse events (TEAEs) and adverse drug reactions were reported for safety. In total, 110 patients were randomized (1:1) to receive placebo or ONO-4474. The mean (standard deviation) change in VAS24 scores at week 4 was -26.9 (25.0) mm in the ONO-4474 group and -19.5 (19.6) mm in the placebo group. The difference (ONO-4474 group - placebo group) in posterior mean change in VAS24 at week 4 was -5.8 (posterior standard deviation, 4.4; 95% confidence interval, -14.3 to 2.8) mm. TEAEs were reported in 41.8% of patients in the ONO-4474 group and 18.2% of patients in the placebo group. The most common TEAEs in the ONO-4474 group related to the musculoskeletal system and the peripheral and central nervous systems were myalgia (7.3%), arthralgia (5.5%), dizziness (3.6%), and hypoesthesia (3.6%). Four patients from the ONO-4474 group and 1 patient from the placebo group discontinued treatment because of AEs; however, none were judged to be serious, and all patients recovered or were recovering after discontinuation. ONO-4474 is a novel tropomyosin receptor kinase inhibitor that has an analgesic effect in patients with OA.

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口服泛原肌球蛋白受体激酶抑制剂ONO-4474在日本中度至重度膝关节骨关节炎患者中的疗效、安全性和耐受性:一项随机、安慰剂对照、双盲、平行组比较研究
我们研究了ONO-4474在日本膝关节骨关节炎(OA)患者中的有效性、安全性和耐受性。在这项多中心、安慰剂对照、随机、双盲、平行组比较研究中,对非甾体抗炎药难治的中重度OA患者口服ONO-4474 100 mg,每天两次,持续28天。主要终点是行走时的膝关节疼痛,通过24小时视觉模拟量表(VAS24)进行评估。报告了治疗中出现的不良事件(teae)和药物不良反应的安全性。总共有110名患者被随机分配(1:1)接受安慰剂或ONO-4474。第4周时,ONO-4474组VAS24评分的平均(标准差)变化为-26.9 (25.0)mm,安慰剂组为-19.5 (19.6)mm。ONO-4474组与安慰剂组在第4周VAS24后验平均变化的差异为-5.8(后验标准差,4.4;95%可信区间为-14.3 ~ 2.8)mm。ONO-4474组41.8%的患者和安慰剂组18.2%的患者报告了teae。ONO-4474组中最常见的与肌肉骨骼系统、外周和中枢神经系统相关的teae是肌痛(7.3%)、关节痛(5.5%)、头晕(3.6%)和感觉减退(3.6%)。ONO-4474组的4名患者和安慰剂组的1名患者因不良事件而停止治疗;然而,没有人被认为是严重的,所有患者都恢复或停药后正在恢复。ONO-4474是一种新型原肌球蛋白受体激酶抑制剂,对OA患者具有镇痛作用。
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来源期刊
CiteScore
5.10
自引率
3.40%
发文量
176
审稿时长
2 months
期刊介绍: The Journal of Clinical Pharmacology (JCP) is a Human Pharmacology journal designed to provide physicians, pharmacists, research scientists, regulatory scientists, drug developers and academic colleagues a forum to present research in all aspects of Clinical Pharmacology. This includes original research in pharmacokinetics, pharmacogenetics/pharmacogenomics, pharmacometrics, physiologic based pharmacokinetic modeling, drug interactions, therapeutic drug monitoring, regulatory sciences (including unique methods of data analysis), special population studies, drug development, pharmacovigilance, womens’ health, pediatric pharmacology, and pharmacodynamics. Additionally, JCP publishes review articles, commentaries and educational manuscripts. The Journal also serves as an instrument to disseminate Public Policy statements from the American College of Clinical Pharmacology.
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