A placebo controlled, randomized clinical trial of galcanezumab for vestibular migraine: The INVESTMENT study.

IF 5.4 2区 医学 Q1 CLINICAL NEUROLOGY Headache Pub Date : 2024-11-01 Epub Date: 2024-09-30 DOI:10.1111/head.14835
Jeffrey D Sharon, Roseanne Krauter, Ricky Chae, Adam Gardi, Maxwell Hum, Isabel Allen, Morris Levin
{"title":"A placebo controlled, randomized clinical trial of galcanezumab for vestibular migraine: The INVESTMENT study.","authors":"Jeffrey D Sharon, Roseanne Krauter, Ricky Chae, Adam Gardi, Maxwell Hum, Isabel Allen, Morris Levin","doi":"10.1111/head.14835","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To study if galcanezumab is effective for vestibular migraine (VM).</p><p><strong>Background: </strong>There are currently no placebo-controlled trials showing that treatment is effective for VM. Therefore, we performed the first placebo controlled, randomized clinical trial of a calcitonin gene-related peptide-targeted monoclonal antibody for VM.</p><p><strong>Methods: </strong>This was a single site, prospective, double-blind placebo controlled randomized clinical trial. Key inclusion criteria were as follows: participants aged 18-75 years with a diagnosis of VM or probable VM per Barany Society criteria. The primary outcome was change in VM-PATHI (Vestibular Migraine Patient Assessment Tool and Handicap Inventory) score, and secondary outcomes included change in DHI (Dizziness Handicap Inventory) score, and count of definite dizzy days (DDDs). Participants were randomized 1:1 to 3 months of treatment with galcanezumab or placebo via subcutaneous injection with a pre-filled syringe, 240 mg the first month, and 120 mg for the second and third months.</p><p><strong>Results: </strong>Forty participants were randomized, and 38 participants were in the modified intent to treat analysis. VM-PATHI score was reduced 5.1 points (95% confidence interval [CI] -13.0 to 2.7) for placebo (N = 21), and 14.8 points (95% CI -23.0 to -6.5) for galcanezumab (N = 17), a difference of -9.6 (95% CI -20.7 to 1.5, p = 0.044). DHI dropped 8.3 points in the placebo arm (95% CI -15.0 to 1.6), and 22.0 points in the galcanezumab arm (95% CI -31.9 to -12.1), a difference of -13.7 (95% CI -20.4 to -8.5, p = 0.018). The count of DDDs per month dropped from 18 days (standard deviation [SD] 7.6) in the baseline month to 12.5 days (SD 11.2) in month 4 for those in the placebo arm, and from 17.9 days (SD 7.9) in the baseline month to 6.6 days (SD 7.3) in month 4 for those in the galcanezumab arm, a difference of -5.7 days (95% CI -10.7 to -0.7, p = 0.026). No serious adverse events were observed.</p><p><strong>Conclusions: </strong>In this pilot study, galcanezumab was effective in treating VM.</p>","PeriodicalId":12844,"journal":{"name":"Headache","volume":" ","pages":"1264-1272"},"PeriodicalIF":5.4000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Headache","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1111/head.14835","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/9/30 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective: To study if galcanezumab is effective for vestibular migraine (VM).

Background: There are currently no placebo-controlled trials showing that treatment is effective for VM. Therefore, we performed the first placebo controlled, randomized clinical trial of a calcitonin gene-related peptide-targeted monoclonal antibody for VM.

Methods: This was a single site, prospective, double-blind placebo controlled randomized clinical trial. Key inclusion criteria were as follows: participants aged 18-75 years with a diagnosis of VM or probable VM per Barany Society criteria. The primary outcome was change in VM-PATHI (Vestibular Migraine Patient Assessment Tool and Handicap Inventory) score, and secondary outcomes included change in DHI (Dizziness Handicap Inventory) score, and count of definite dizzy days (DDDs). Participants were randomized 1:1 to 3 months of treatment with galcanezumab or placebo via subcutaneous injection with a pre-filled syringe, 240 mg the first month, and 120 mg for the second and third months.

Results: Forty participants were randomized, and 38 participants were in the modified intent to treat analysis. VM-PATHI score was reduced 5.1 points (95% confidence interval [CI] -13.0 to 2.7) for placebo (N = 21), and 14.8 points (95% CI -23.0 to -6.5) for galcanezumab (N = 17), a difference of -9.6 (95% CI -20.7 to 1.5, p = 0.044). DHI dropped 8.3 points in the placebo arm (95% CI -15.0 to 1.6), and 22.0 points in the galcanezumab arm (95% CI -31.9 to -12.1), a difference of -13.7 (95% CI -20.4 to -8.5, p = 0.018). The count of DDDs per month dropped from 18 days (standard deviation [SD] 7.6) in the baseline month to 12.5 days (SD 11.2) in month 4 for those in the placebo arm, and from 17.9 days (SD 7.9) in the baseline month to 6.6 days (SD 7.3) in month 4 for those in the galcanezumab arm, a difference of -5.7 days (95% CI -10.7 to -0.7, p = 0.026). No serious adverse events were observed.

Conclusions: In this pilot study, galcanezumab was effective in treating VM.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
安慰剂对照随机临床试验:加坎珠单抗治疗前庭性偏头痛:INVESTMENT 研究。
目的:研究加康珠单抗对前庭性偏头痛(VM)是否有效:研究 galcanezumab 是否对前庭性偏头痛(VM)有效:背景:目前还没有安慰剂对照试验显示治疗前庭性偏头痛有效。因此,我们对降钙素基因相关肽靶向单克隆抗体治疗前庭性偏头痛进行了首次安慰剂对照随机临床试验:这是一项单点、前瞻性、双盲安慰剂对照随机临床试验。主要纳入标准如下:年龄在18-75岁之间,根据巴拉尼学会标准诊断为VM或可能患有VM的参与者。主要结果是 VM-PATHI(前庭性偏头痛患者评估工具和障碍量表)评分的变化,次要结果包括 DHI(头晕障碍量表)评分的变化和确诊头晕天数(DDDs)的计数。参与者按1:1的比例随机接受为期3个月的galcanezumab或安慰剂治疗,使用预充注射器皮下注射,第一个月240毫克,第二和第三个月120毫克:40名参与者接受了随机治疗,38名参与者接受了修改后的意向治疗分析。安慰剂(21 人)的 VM-PATHI 评分降低了 5.1 分(95% 置信区间 [CI] -13.0 至 2.7),加仑珠单抗(17 人)的 VM-PATHI 评分降低了 14.8 分(95% 置信区间 [CI] -23.0 至 -6.5),差异为 -9.6(95% 置信区间 [CI] -20.7 至 1.5,p = 0.044)。安慰剂治疗组的DHI下降了8.3点(95% CI -15.0至1.6),加卡尼珠单抗治疗组的DHI下降了22.0点(95% CI -31.9至-12.1),差异为-13.7(95% CI -20.4至-8.5,p = 0.018)。安慰剂组患者的每月DDD次数从基线月的18天(标准差[SD]7.6)降至第4个月的12.5天(标准差11.2),而加坎珠单抗组患者的每月DDD次数从基线月的17.9天(标准差7.9)降至第4个月的6.6天(标准差7.3),差异为-5.7天(95% CI -10.7至-0.7,p = 0.026)。未观察到严重不良事件:在这项试点研究中,加卡尼珠单抗对治疗血管瘤有效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Headache
Headache 医学-临床神经学
CiteScore
9.40
自引率
10.00%
发文量
172
审稿时长
3-8 weeks
期刊介绍: Headache publishes original articles on all aspects of head and face pain including communications on clinical and basic research, diagnosis and management, epidemiology, genetics, and pathophysiology of primary and secondary headaches, cranial neuralgias, and pains referred to the head and face. Monthly issues feature case reports, short communications, review articles, letters to the editor, and news items regarding AHS plus medicolegal and socioeconomic aspects of head pain. This is the official journal of the American Headache Society.
期刊最新文献
Safety and tolerability of ubrogepant for the acute treatment of migraine in participants taking atogepant for the preventive treatment of episodic migraine: Results from the TANDEM study. Anxiety, depression, and headache-related disability in a large pediatric clinic-based sample. Associations of comorbid headache disorders and depression with leisure-time physical activity among 14,088 adults in The Brazilian Longitudinal Study of Adult Health. Magnetoencephalography studies in migraine and headache disorders: A systematic review. Comparative bioavailability of single-dose zavegepant during and between migraine attacks: A phase 1, randomized, open-label, fixed-sequence, two-period study.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1