Janssen Research and Development, LLC, Titusville, NJ, USA.
Janssen Research and Development, LLC, Fremont, CA, USA.
Curr Med Res Opin. 2019 Dec;35(12):2117-2127. doi: 10.1080/03007995.2019.1653068. Epub 2019 Sep 13.
To evaluate the safety and efficacy of fulranumab as adjunct or monotherapy in patients with knee or hip pain related to moderate-to-severe osteoarthritis. Osteoarthritic patients (aged ≥18 years) from four phase 3 randomized, double-blind (DB), placebo-controlled studies were randomized to receive placebo, fulranumab 1 mg every 4 weeks (Q4wk), or 3 mg Q4wk in 16-week DB phase, followed by a 52-week post-treatment follow-up phase. Safety assessments included treatment-emergent adverse events (TEAEs), and neurological, sympathetic, and joint-related events of interest. Efficacy assessments included pain and physical function sub-scales of Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) scores. Of 245 patients from the ITT set (median age = 64 years; 62% women), 84 (34%) completed the DB phase; the majority of discontinuations (57%) were due to early study termination. In the DB phase, the incidence of TEAEs in fulranumab 3 mg (57.8%) and 1 mg (56.8%) was similar to placebo (56.8%). Two events adjudicated as joint-related events of interest include rapidly progressive osteoarthritis and fracture of unknown etiology. There were no new neurological TEAEs. Fulranumab showed evidence of efficacy in improving pain and physical function based on WOMAC sub-scale scores. Due to premature study termination, the number of patients enrolled were too small to make any definitive efficacy claims. Treatment with fulranumab was generally tolerated with no new safety signals. Within the limited sample analyzed, fulranumab showed evidence of improvement of pain and function in patients with moderate-to-severe osteoarthritis who had failed prior therapy and were candidates for joint replacement surgery. NCT02336685; NCT02336698; NCT02289716; NCT02301234KEY POINTSFulranumab as adjuvant or monotherapy was well tolerated with no new safety signalsFulranumab demonstrated evidence suggestive of efficacy in osteoarthritic pain of hip and kneeFulranumab demonstrated evidence suggestive of improvement of pain and physical function in osteoarthritis.
评估富鲁单抗作为辅助或单药治疗与中重度骨关节炎相关的膝或髋疼痛患者的安全性和疗效。来自四项 3 期随机、双盲(DB)、安慰剂对照研究的骨关节炎患者(年龄≥18 岁)按 1:1:1 比例随机分配至安慰剂、富鲁单抗 1mg 每 4 周(Q4wk)或 3mg Q4wk 治疗组,在 16 周的 DB 阶段后,进入 52 周的治疗后随访阶段。安全性评估包括治疗中出现的不良事件(TEAEs)以及神经系统、交感神经和关节相关的关注事件。疗效评估包括 Western Ontario and McMaster Universities Osteoarthritis Index(WOMAC)评分的疼痛和身体功能子量表。在意向治疗人群(ITT 人群)中,245 例患者(中位年龄=64 岁,62%为女性)中,有 84 例(34%)完成了 DB 阶段;大多数停药(57%)是由于研究提前终止。在 DB 阶段,富鲁单抗 3mg(57.8%)和 1mg(56.8%)组的 TEAEs 发生率与安慰剂组(56.8%)相似。2 例关节相关关注事件的裁定包括进展迅速的骨关节炎和病因不明的骨折。无新的神经系统 TEAEs。富鲁单抗显示出改善 WOMAC 子量表评分的疼痛和身体功能的疗效证据。由于研究提前终止,纳入的患者数量太少,无法做出任何明确的疗效结论。富鲁单抗治疗具有良好的耐受性,没有新的安全性信号。在有限的分析样本中,富鲁单抗在先前治疗失败且有接受关节置换手术候选资格的中重度骨关节炎患者中显示出改善疼痛和功能的疗效证据。NCT02336685;NCT02336698;NCT02289716;NCT02301234