Ubrogepant users' real-world experience: Patients on ubrogepant, characteristics and outcomes (UNIVERSE) study

被引:1
作者
Shewale, Anand R. [1 ]
Poh, Weijie [2 ]
Reed, Michael L. [3 ]
Liu, Jinjie [4 ]
Cadiou, Francois [2 ]
Ezzati, Ali [5 ]
Burslem, Kate [1 ]
Manthena, Shivaji [1 ]
Lipton, Richard B. [6 ]
机构
[1] AbbVie, 1 N Waukegan Rd, N Chicago, IL 60064 USA
[2] Healint Pte Ltd, Singapore, Singapore
[3] Vedanta Res, Chapel Hill, NC USA
[4] Genesis Res, Hoboken, NJ USA
[5] Univ Calif Irvine, Dept Neurol, Irvine, CA USA
[6] Albert Einstein Coll Med, Saul R Korey Dept Neurol, Bronx, NY USA
来源
HEADACHE | 2024年 / 64卷 / 10期
关键词
calcitonin gene-related peptide; migraine; outcomes research; ubrogepant; OPIOID USE; MIGRAINE; DISCONTINUATION;
D O I
10.1111/head.14839
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectiveTo assess the real-world effectiveness of ubrogepant by evaluating self-reported satisfaction with pain relief, ability to think clearly, and return to normal function in individuals who had used ubrogepant to treat a migraine episode within the preceding 14 days.BackgroundUbrogepant is an oral calcitonin gene-related peptide receptor antagonist approved for the acute treatment of migraine in adults. Few studies have evaluated the real-world effectiveness of ubrogepant.MethodsThe UNIVERSE study was an observational, cross-sectional survey conducted between February 2021 and April 2021 in US adult Migraine Buddy application (app) users currently treated with ubrogepant. Individuals who were 18 years of age or older and reported at least one dose of ubrogepant in the previous 14 days completed a 30-question survey in the app. The survey assessed respondent demographics, migraine history, acute treatment patterns, and treatment satisfaction with ubrogepant. Respondents also reported prior acute medication use and reasons for switching to ubrogepant.ResultsOf the 1303 ubrogepant users contacted, 302 (23.2%; 50 mg, 120 participants; 100 mg, 182 participants) were included in this study. The mean (standard deviation) age was 41.9 (11.2) years, and 90.1% (272/302) were female. Satisfaction with migraine relief at 2, 4, and 24 h post-dose was reported by 75.8% (229/302), 83.4% (252/302), and 78.5% (237/302) of participants, respectively. Satisfaction with the ability to think clearly after taking ubrogepant was reported by 85.1% (257/302) of participants, and 83.8% (253/302) were satisfied with their ability to return to normal function. Furthermore, 90.7% (274/302) of participants reported that they were likely to continue using ubrogepant to treat their migraine. Most participants (n = 264 [87%]) reported switching to ubrogepant due to inadequate treatment response with their previous treatment. In this subgroup, comparable outcomes were observed with respect to satisfaction with migraine relief, ability to think clearly, and return to normal function.ConclusionsUbrogepant demonstrated real-world effectiveness in the acute treatment of migraine, as evidenced by high levels of treatment satisfaction and a strong indication of their intent to continue using the medication. Ubrogepant is approved for the acute treatment of migraine in adults. In this study, adults who had used ubrogepant to treat a migraine attack in the previous 14 days responded to survey questions regarding their satisfaction with pain relief, ability to think clearly, and return to normal function. Results indicated that the majority of participants experienced high levels of satisfaction with ubrogepant because most of them said that these areas of their life improved after treatment.
引用
收藏
页码:1244 / 1252
页数:9
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