Galcanezumab Effects on Migraine Severity and Symptoms in Japanese Patients with Episodic Migraine: Secondary Analysis of a Phase 2 Randomized Trial

被引:3
|
作者
Igarashi, Hisaka [1 ]
Shibata, Mamoru [2 ]
Ozeki, Akichika [3 ]
Matsumura, Taka [3 ,4 ]
机构
[1] Fujitsu Clin, Dept Internal Med, Kawasaki, Kanagawa, Japan
[2] Tokyo Dent Coll, Dept Neurol, Ichikawa Gen Hosp, Ichikawa, Japan
[3] Eli Lilly Japan KK, Tokyo, Japan
[4] Eli Lilly Japan KK, Japan Drug Dev & Med Affairs, 4-15-1 Akasaka,Akasaka Garden City 13F, Tokyo 1070052, Japan
关键词
Galcanezumab; Japan; Menstruation; Migraine disorders; Prodromal symptoms; Randomized controlled trial; Aura; Episodic migraine; Migraine severity; Migraine symptoms; MENSTRUAL MIGRAINE; POST-HOC; HEADACHE; FREQUENCY; PREVALENCE; DISABILITY; NAUSEA; WOMEN; SCORE; 1ST;
D O I
10.1007/s40120-022-00410-3
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction Galcanezumab, a humanized monoclonal antibody against calcitonin gene-related peptide, is a preventive migraine treatment. In global, randomized, placebo-controlled trials, galcanezumab reduced migraine headache severity and the frequency of migraine headaches associated with nausea and/or vomiting, photophobia and phonophobia, prodromal symptoms, or aura. We report secondary analyses from a Japanese phase 2 trial that assessed the effect of galcanezumab on migraine headache severity, frequency of migraine-associated symptoms, and frequency of migraine headaches during menstrual periods in Japanese patients with episodic migraine. Methods Adults with migraine (International Classification of Headache Disorders, 3rd edition; 4-14 migraine headache days/month) were randomized (2:1:1) to a monthly placebo (n = 230), 120 mg galcanezumab (240 mg loading dose; n = 115), or 240 mg galcanezumab (n = 114) for 6 months (double-blind). Patients recorded migraine headache days, severity, and symptoms in an electronic diary. Changes from baseline were analyzed (mixed model for repeated measures). Results Both galcanezumab doses significantly reduced the number of monthly moderate-to-severe and severe migraine headache days compared with placebo, overall (difference in least-squares mean change from baseline, 120 mg/240 mg versus placebo: moderate-to-severe, -1.9/-1.8 days; severe: -0.4/-0.4 days) and in each month; mean severity score was significantly reduced in the 240 mg group. Both galcanezumab doses significantly reduced the number of migraine headache days with nausea/vomiting (-1.1/-1.0 days), photophobia/phonophobia (-2.3/-1.7 days), prodromal symptoms (-0.7/-0.8 days), and aura (-0.7/-0.7 days). In most cases, the proportion of migraine headache days with these symptoms was reduced by galcanezumab. Both galcanezumab doses reduced the number of migraine headache days occurring during menstrual periods (n = 269; -0.8/-0.9 days). Conclusion Once-monthly galcanezumab significantly reduced the frequency of migraine headache days with moderate-to-severe or severe headache, migraine headache days with migraine-associated symptoms, and migraine headache days during menstrual periods in Japanese patients with episodic migraine, consistent with results from global studies. Trial Registration: ClinicalTrials.gov (NCT02959177).
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收藏
页码:73 / 87
页数:15
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