佐米曲普坦鼻喷雾剂急性治疗偏头痛的起效速度、疗效及耐受性:一项随机、双盲、安慰剂对照研究

Speed of onset, efficacy and tolerability of zolmitriptan nasal spray in the acute treatment of migraine: a randomised, double-blind, placebo-controlled study.

作者信息

Dodick David, Brandes Jan, Elkind Arthur, Mathew Ninan, Rodichok Lawrence

机构信息

Department of Neurology, Mayo Clinic College of Medicine, Scottsdale, Arizona 85259, USA.

出版信息

CNS Drugs. 2005;19(2):125-36. doi: 10.2165/00023210-200519020-00003.

Abstract

INTRODUCTION

Migraine is a common, disabling condition that has a significant impact on patients and relatives, and is a considerable economic burden on society. Migraine patients want fast-acting treatments with high efficacy. Previous studies have demonstrated that orally administered formulations of zolmitriptan are rapidly and highly effective in the acute treatment of migraine. The objective of this study was to assess the efficacy, speed of onset and tolerability of the nasal spray formulation of zolmitriptan in migraine treatment.

METHODS

This multicentre, randomised, double-blind study recruited 2122 patients (aged 18-65 years) who had an established diagnosis of migraine (according to International Headache Society criteria), with or without aura. Patients were randomised to receive zolmitriptan 5mg nasal spray or placebo to treat up to two migraine attacks within 15 minutes of headache pain becoming moderate or severe. The primary endpoint was headache response (reduction in migraine pain from severe/moderate to mild/none) at 2 hours, 1 hour, 30 minutes and 15 minutes post-dose (analysed using a step-down approach). Secondary endpoints included headache response at 4 hours, pain-free rates at 30 minutes and 1, 2 and 4 hours, and sustained headache response and pain-free status at 24 hours post-dose.

RESULTS

The headache response rate at 2 hours post-dose was 66.2% for the zolmitriptan group, compared with 35.0% for the placebo group (p < 0.001). Zolmitriptan nasal spray also produced significantly higher headache response rates than placebo at all earlier timepoints assessed, starting as early as 15 minutes post-dose (p < 0.001). Similar results were obtained for the analysis of the first attack. Significantly higher pain-free rates were obtained with zolmitriptan nasal spray, compared with placebo, from 15 minutes post-dose onward (p < 0.005). Zolmitriptan nasal spray was also significantly superior to placebo for headache response at 4 hours, sustained headache response at 24 hours and sustained pain-free rate at 24 hours. Zolmitriptan nasal spray was well tolerated, with most adverse events being of short duration and mild or moderate intensity.

CONCLUSIONS

Zolmitriptan nasal spray is highly effective in the acute treatment of migraine and has a very fast onset of action, producing significant headache response and pain-free rates as early as 15 minutes post-dose (the earliest assessment in this study). In addition to the very fast onset of action, zolmitriptan nasal spray produced significantly higher sustained headache response and pain-free rates at 24 hours post-dose compared with placebo. These desirable efficacy outcomes were combined with good tolerability.

摘要

引言

偏头痛是一种常见的致残性疾病,对患者及其亲属有重大影响,也是社会相当大的经济负担。偏头痛患者希望获得起效快且疗效高的治疗方法。先前的研究表明,口服佐米曲普坦制剂在偏头痛的急性治疗中起效迅速且疗效显著。本研究的目的是评估佐米曲普坦鼻喷雾剂在偏头痛治疗中的疗效、起效速度和耐受性。

方法

这项多中心、随机、双盲研究招募了2122名年龄在18至65岁之间、已确诊为偏头痛(根据国际头痛协会标准)、有无先兆的患者。患者被随机分配接受5毫克佐米曲普坦鼻喷雾剂或安慰剂,以在头痛疼痛变得中度或重度后的15分钟内治疗多达两次偏头痛发作。主要终点是给药后2小时、1小时、30分钟和15分钟时的头痛反应(偏头痛疼痛从重度/中度减轻至轻度/无)(采用逐步法分析)。次要终点包括给药后4小时的头痛反应、30分钟以及1、2和4小时时的无痛率,以及给药后24小时的持续头痛反应和无痛状态。

结果

佐米曲普坦组给药后2小时的头痛反应率为66.2%,而安慰剂组为35.0%(p<0.001)。在所有更早评估的时间点,佐米曲普坦鼻喷雾剂产生的头痛反应率也显著高于安慰剂,最早在给药后15分钟(p<0.001)。首次发作的分析也得到了类似结果。与安慰剂相比,佐米曲普坦鼻喷雾剂从给药后15分钟起无痛率显著更高(p<0.005)。佐米曲普坦鼻喷雾剂在给药后4小时的头痛反应、24小时的持续头痛反应以及24小时的持续无痛率方面也显著优于安慰剂。佐米曲普坦鼻喷雾剂耐受性良好,大多数不良事件持续时间短,强度为轻度或中度。

结论

佐米曲普坦鼻喷雾剂在偏头痛的急性治疗中非常有效,起效非常快,给药后15分钟(本研究中的最早评估时间)就产生显著的头痛反应和无痛率。除了起效非常快之外, 与安慰剂相比,佐米曲普坦鼻喷雾剂在给药后24小时产生的持续头痛反应和无痛率显著更高。这些理想的疗效结果与良好的耐受性相结合。

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