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在 galcanezumab 预防阵发性和慢性偏头痛的 3 期安慰剂对照研究的亚组分析中,药物过度使用。

Medication overuse in a subgroup analysis of phase 3 placebo-controlled studies of galcanezumab in the prevention of episodic and chronic migraine.

机构信息

Department of Neurology, Mayo Clinic, Phoenix, AZ, USA.

Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN, USA.

出版信息

Cephalalgia. 2021 Mar;41(3):340-352. doi: 10.1177/0333102420966658. Epub 2020 Nov 3.

Abstract

INTRODUCTION

Acute medication overuse is prevalent in patients with migraine.

METHODS

In three phase 3, double-blind, randomized, placebo-controlled studies, patients with episodic migraine (EVOLVE-1 and EVOLVE-2) or chronic migraine (REGAIN) were randomized 2:1:1 to monthly subcutaneous injections of placebo or galcanezumab 120 or 240 mg for 3 or 6 months. This subgroup analysis evaluated mean changes in the number of monthly migraine headache days in each treatment among patients with versus without baseline acute medication overuse via mixing modelling with repeated measures.

RESULTS

The percentages of patients with baseline medication overuse in placebo, galcanezumab 120-mg and 240-mg groups, respectively, were 19.4%, 17.3%, and 19.3% for EVOLVE-1/-2 (pooled; ), and 63.4%, 64.3%, and 64.1% for REGAIN (). Both galcanezumab doses demonstrated significant improvement compared with placebo for overall least squares mean change in monthly migraine headache days in patients with baseline medication overuse in both the episodic and chronic migraine studies ( ≤ 0.001). Furthermore, both galcanezumab doses reduced average monthly medication overuse rates compared to placebo ( < 0.001) in both patient populations with medication overuse at baseline.

CONCLUSIONS

Galcanezumab appears to be effective for the preventive treatment of episodic and chronic migraine in patients who overuse acute medications. ClinicalTrials.gov Identifiers: NCT02614183, NCT02614196, and NCT02614261.

摘要

简介

急性药物过度使用在偏头痛患者中很常见。

方法

在三项 3 期、双盲、随机、安慰剂对照研究中,发作性偏头痛(EVOLVE-1 和 EVOLVE-2)或慢性偏头痛(REGAIN)患者以 2:1:1 的比例随机分配至每月皮下注射安慰剂或加奈珠单抗 120 或 240mg,治疗 3 或 6 个月。本亚组分析通过重复测量混合模型评估基线时有急性药物过度使用的患者中,与安慰剂相比,每月偏头痛头痛天数的平均变化。

结果

安慰剂、加奈珠单抗 120mg 和 240mg 组基线时有药物过度使用的患者比例分别为 EVOLVE-1/-2(合并)的 19.4%、17.3%和 19.3%,REGAIN 的 63.4%、64.3%和 64.1%()。在基线时有药物过度使用的发作性和慢性偏头痛研究患者中,与安慰剂相比,加奈珠单抗的两种剂量在每月偏头痛头痛天数的总体最小二乘均数变化方面均显示出显著改善( ≤ 0.001)。此外,与安慰剂相比,在基线时有药物过度使用的两种患者人群中,加奈珠单抗的两种剂量均降低了平均每月药物过度使用率( < 0.001)。

结论

加奈珠单抗似乎对急性药物过度使用的发作性和慢性偏头痛患者的预防性治疗有效。

临床试验注册号

NCT02614183、NCT02614196 和 NCT02614261。

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