Goldstein D J, Wang O, Saper J R, Stoltz R, Silberstein S D, Mathew N T
Lilly Research Laboratories, Indianapolis, IN 46285-0532, USA.
Cephalalgia. 1997 Nov;17(7):785-90. doi: 10.1046/j.1468-2982.1997.1707785.x.
Lanepitant is a high-affinity, selective neurokinin-1 receptor (NK-1) and is effective in the dural inflammation model of acute migraine. Lanepitant 30, 80, and 240 mg given orally was evaluated in a double-blind, placebo-controlled crossover study to determine its effect in reducing migraine pain and severity of associated symptoms. Outpatients treated four migraine headaches of moderate or severe pain intensity with study drug according to a randomization schedule. They recorded their pain intensity and severity of migraine-associated symptoms at 30, 60, 90, and 120 min. Although 53 patients were randomly allocated to a treatment sequence, only 40 patients completed all treatments. There was no statistically significant difference in improvement in migraine pain at any time for any of the treatments. Additionally, there was no change in severity of migraine-associated symptoms associated with lanepitant therapy. No adverse events could be attributed to lanepitant. Lanepitant was ineffective orally in treating acute migraine in this trial. This may be due to poor bioavailability during a migraine attack. Alternatively, the neurogenic inflammation hypothesis may not apply to migraine.
兰尼泮是一种高亲和力的选择性神经激肽-1受体(NK-1)拮抗剂,在急性偏头痛的硬脑膜炎症模型中有效。在一项双盲、安慰剂对照的交叉研究中,评估了口服30、80和240毫克兰尼泮对减轻偏头痛疼痛及相关症状严重程度的效果。门诊患者根据随机分组方案,使用研究药物治疗4次中度或重度疼痛强度的偏头痛。他们在30、60、90和120分钟时记录疼痛强度和偏头痛相关症状的严重程度。虽然53名患者被随机分配到一个治疗序列,但只有40名患者完成了所有治疗。任何一种治疗在任何时间对偏头痛疼痛的改善均无统计学显著差异。此外,兰尼泮治疗相关的偏头痛相关症状严重程度没有变化。没有不良事件可归因于兰尼泮。在该试验中,兰尼泮口服治疗急性偏头痛无效。这可能是由于偏头痛发作期间生物利用度差。或者,神经源性炎症假说可能不适用于偏头痛。