4.5 Article

Early onset of efficacy with fremanezumab in patients with episodic and chronic migraine: subanalysis of two phase 2b/3 trials in Japanese and Korean patients

期刊

JOURNAL OF HEADACHE AND PAIN
卷 23, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s10194-022-01393-0

关键词

Calcitonin gene-related peptide; Chronic migraine; Episodic migraine; Fremanezumab; Japanese; Korean; Early onset

资金

  1. Otsuka Pharmaceutical Co., Ltd.

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This study aimed to explore the onset of action of fremanezumab in Japanese and Korean migraine patients. The results showed that fremanezumab could reduce the frequency of migraine attacks from the first week after the initial injection, indicating an early onset of action.
Background: Early onset of action has become recognized as an important efficacy feature of preventive migraine treatment, which can help overcome adherence issues commonly associated with older medications. Preventive treatments that target the calcitonin gene-related peptide (CGRP) or the CGRP receptor have been previously shown to provide early onset of action. Methods: This subanalysis of primary endpoints of two separate phase 2b/3 studies sought to determine the onset of action of fremanezumab in Japanese and Korean patients with episodic migraine (EM) and chronic migraine (CM). Results: In EM patients (n = 357), both fremanezumab quarterly and fremanezumab monthly led to greater reductions in weekly migraine days (days/week) than placebo from the first week after the initial injection and thereafter during the remainder of the study period. Similarly, CM patients (n = 57 1) had a greater reduction in headache days of at least moderate severity (days/week) with fremanezumab (total) than placebo. The percentage of patients with a migraine day (EM) or headache day at least moderate severity (CM) was lower in those treated with fremanezumab than placebo and this effect was apparent from as early as Day 2 (1 day after first injection). Conclusions: These results suggest that fremanezumab has an early onset of action, as noted in previous post hoc analyses of anti-CGRP monoclonal antibodies.

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