OhioHealth Multiple Sclerosis Center, Riverside Methodist Hospital, 3535 Olentangy River Rd., Suite 1501, Columbus, OH 43214, USA.
Corinne Goldsmith Dickinson Center for Multiple Sclerosis, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Mult Scler Relat Disord. 2023 Jul;75:104745. doi: 10.1016/j.msard.2023.104745. Epub 2023 May 1.
To provide a comprehensive assessment of the treatment effects of nabiximols oromucosal spray on multiple sclerosis spasticity in two clinical trials, GWSP0604 and SAVANT.
Both studies enriched for responders before randomization, defined by a ≥20% improvement in Spasticity 0-10 numeric rating scale (NRS) score. Additionally, SAVANT used randomized re-titration following washout. Spasticity NRS outcomes, spasm count, and modified Ashworth scale (MAS) scores were analyzed.
Mean change from baseline in average daily Spasticity NRS scores was significantly larger for nabiximols than placebo at all postbaseline timepoints, ranging from -0.36 to -0.89 in GWSP0604 and -0.52 to -1.96 in SAVANT. Percent reduction in geometric mean change from baseline in average daily spasm count for nabiximols ranged from 19-35% versus placebo. A treatment difference favoring nabiximols was observed in overall MAS scores during the randomized part of each study. Treatment effect was larger for combinations of lower limb muscle groups (ranging between -0.16 and -0.37).
Nabiximols leads to improvement in spasticity that was sustained over the 12-week treatment period as measured by average daily Spasticity NRS scores, daily spasm counts, and MAS scores for combinations of muscle groups, especially the combination of the 6 key muscle groups in the lower limbs in NRS responders to nabiximols treatment.
为了全面评估纳比西莫司口腔喷雾剂在两项临床试验 GWSP0604 和 SAVANT 中对多发性硬化痉挛的治疗效果。
这两项研究均在随机分组前对应答者进行了富集,定义为痉挛 0-10 数字评定量表(NRS)评分至少改善 20%。此外,SAVANT 在洗脱后使用随机滴定重新滴定。分析了痉挛 NRS 结果、痉挛次数和改良 Ashworth 量表(MAS)评分。
纳比西莫司组与安慰剂组相比,在所有基线后时间点的平均每日痉挛 NRS 评分的平均变化均显著更大,GWSP0604 为 -0.36 至 -0.89,SAVANT 为 -0.52 至 -1.96。纳比西莫司组与安慰剂组相比,平均每日痉挛次数的几何均数变化从基线的降低幅度在 19%至 35%之间。在每项研究的随机部分观察到纳比西莫司有利于总体 MAS 评分的治疗差异。对于下肢肌肉群的组合(范围在 -0.16 至 -0.37 之间),治疗效果更大。
纳比西莫司可改善痉挛,在 12 周治疗期间,通过平均每日痉挛 NRS 评分、每日痉挛次数和 MAS 评分的组合(尤其是下肢 6 个关键肌肉群的组合),痉挛 NRS 应答者对纳比西莫司治疗的反应,持续改善。