Goldstein D J, Offen W W, Klein E G, Phebus L A, Hipskind P, Johnson K W, Ryan R E
Neuroscience Research, Lilly Research Laboratories, Department of Pharmacology and Toxicology, Indiana University Medical School, Indianapolis, IN 46285-2033, USA.
Cephalalgia. 2001 Mar;21(2):102-6. doi: 10.1046/j.1468-2982.2001.00161.x.
Lanepitant, a potent non-peptide neurokinin-1 receptor antagonist, inhibits neurogenic dural inflammation, and may have a role in migraine therapy. This study evaluated the effect of lanepitant taken daily for migraine prevention. Patients with migraine headaches with and without aura by International Headache Society classification criteria were enrolled in a 12-week double-blind, parallel design study comparing the effect of 200 mg qd lanepitant (n = 42) and placebo (n = 42) on reduction of migraine frequency. The primary outcome measure was response rate, i.e. the proportion of patients with a 50% reduction in days of headache. Of the 84 patients enrolled, 90.5% were female. The endpoint response rate for lanepitant-treated patients (41.0%) was not statistically significantly (P = 0.065) greater than that for placebo-treated patients (22.0%). No efficacy variables differed significantly between treatments, except for response rates at month 3 (P = 0.045). Higher plasma concentrations were no more effective than lower concentrations. In this study lanepitant was not effective in preventing migraine, but was well tolerated. These results do not support a role for NK-1 antagonism in migraine prevention.
兰尼地坦是一种强效非肽类神经激肽-1受体拮抗剂,可抑制神经源性硬脑膜炎症,可能在偏头痛治疗中发挥作用。本研究评估了每日服用兰尼地坦预防偏头痛的效果。按照国际头痛协会分类标准,有无先兆偏头痛患者参加了一项为期12周的双盲、平行设计研究,比较200 mg每日一次兰尼地坦(n = 42)和安慰剂(n = 42)对降低偏头痛发作频率的效果。主要结局指标为缓解率,即头痛天数减少50%的患者比例。在纳入的84例患者中,90.5%为女性。兰尼地坦治疗患者的终点缓解率(41.0%)高于安慰剂治疗患者(22.0%),但差异无统计学意义(P = 0.065)。除第3个月的缓解率外(P = 0.045),各治疗组间的疗效变量无显著差异。较高的血浆浓度并不比较低浓度更有效。在本研究中,兰尼地坦预防偏头痛无效,但耐受性良好。这些结果不支持NK-1拮抗剂在偏头痛预防中的作用。