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Long-term open-label study of tanezumab for moderate to severe osteoarthritic knee pain.

机译:tanezumab用于中度至重度骨关节炎膝盖疼痛的长期开放标签研究。

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OBJECTIVE: This study was designed to evaluate the long-term safety and effectiveness of repeated doses of the humanized anti-nerve growth factor antibody, tanezumab, during open-label treatment of patients with OA knee pain. DESIGN: The current study (clinicaltrials.gov identifier: NCT00399490) was a multicenter, phase II, open-label, multiple-dose extension of an earlier randomized clinical trial. All patients (N=281) received infusions of tanezumab 50mug/kg on Days 1 and 56 with subsequent doses administered at 8-week intervals (up to a total of eight infusions). The primary endpoint of this study was safety. Effectiveness evaluations included overall knee pain, Western Ontario and McMaster Universities Osteoarthritis (WOMAC) index subscales, and subject global assessment (SGA) of response to therapy on 0-100 point visual analog scales. RESULTS: Repeated administration of tanezumab resulted in a low incidence of treatment-related adverse events (AEs; 7.5%). The rate of serious AEs was also low (2.8%) with none considered treatment-related. Few AEs of abnormal peripheral sensation were reported; hypoesthesia was reported by nine patients (3.2%), paresthesia by seven patients (2.5%), and hyperesthesia, peripheral neuropathy, and sensory disturbance were each reported by one patient (0.4% for each). Most AEs of abnormal peripheral sensation were rated as mild (95%) and the majority (65%) resolved before study completion. At Week 8, overall knee pain and SGA improved from baseline by a mean (+/- standard error) of -12.8 (+/-1.78) and 8.0 (+/-1.66), respectively. Similar improvements occurred for WOMAC subscales. CONCLUSIONS: Repeated injections of tanezumab in patients with moderate to severe knee OA provide continued pain relief and improved function with a low incidence of side effects. Additional studies to define the efficacy and duration of pain reduction and to provide a more complete assessment of long-term safety are warranted.
机译:目的:本研究旨在评估在开放标签治疗OA膝关节疼痛患者中重复剂量的人源化抗神经生长因子抗体tanezumab的长期安全性和有效性。设计:当前研究(clinicaltrials.gov标识符:NCT00399490)是早期随机临床试验的多中心,II期,开放标签,多剂量扩展方案。在第1天和第56天,所有患者(N = 281)均接受tanezumab 50mug / kg的输注,并以8周为间隔进行后续剂量(总共输注8次)。这项研究的主要终点是安全性。有效性评估包括总体膝关节疼痛,安大略省西部和麦克马斯特大学骨关节炎(WOMAC)指数子量表,以及以0-100点视觉模拟量表对治疗反应的受试者总体评估(SGA)。结果:重复给予tanezumab导致与治疗相关的不良事件发生率低(AEs; 7.5%)。严重的不良事件发生率也很低(2.8%),没有与治疗有关的事件。很少有异常周围感觉的不良事件报道。 9例患者(3.2%)报告感觉异常,7例患者(2.5%)报告感觉异常,1例患者分别报告感觉异常,周围神经病变和感觉障碍(0.4%)。在研究完成之前,大多数异常周围感觉的不良事件被定为轻度(95%),大多数(65%)已解决。在第8周,总体膝关节疼痛和SGA与基线相比分别改善了-12.8(+/- 1.78)和8.0(+/- 1.66)的平均值(+/-标准误差)。 WOMAC分量表也发生了类似的改进。结论:中度至重度膝骨关节炎患者反复注射tanezumab可持续缓解疼痛,改善功能,副作用发生率低。必须进行其他研究来确定疼痛减轻的功效和持续时间,并提供对长期安全性的更完整评估。

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