Effect of galcanezumab on severity and symptoms of migraine in phase 3 trials in patients with episodic or chronic migraine.

Michael Ament, Kathleen Day, Virginia L Stauffer, Vladimir Skljarevski, Mallikarjuna Rettiganti, Eric Pearlman, Sheena K Aurora
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引用次数: 15

Abstract

Background: Galcanezumab, a humanized monoclonal antibody that binds calcitonin gene-related peptide, has demonstrated a significant reduction in monthly migraine headache days compared with placebo. Here, we analyze data from 3 randomized clinical trials (2 episodic trials [EVOLVE-1, EVOLVE-2] and 1 chronic trial [REGAIN]), to examine if galcanezumab also alleviates the severity and symptoms of migraine.

Methods: The episodic migraine trials were 6-month, double-blind studies in patients with episodic migraine (4-14 monthly migraine headache days). The chronic migraine trial was a 3-month, double-blind study in patients with chronic migraine (≥ 15 headache days per month, where ≥ 8 met criteria for migraine). Patients (18-65 years) were randomized to placebo or galcanezumab 120 mg with a 240-mg loading dose or 240 mg. Patients recorded headache characteristics, duration, severity, and presence of associated symptoms with each headache. The outcomes analyzed were changes from baseline in number of monthly migraine headache days with nausea and/or vomiting, photophobia and phonophobia, aura, and prodromal symptoms other than aura. Additional outcomes analyzed included the number of moderate-to-severe monthly migraine headache days, number of severe migraine headache days, and mean severity of remaining migraine headache days. Change from baseline in the proportion of days with nausea and/or vomiting and the proportion of days with photophobia and phonophobia among the remaining monthly migraine headache days were also analyzed.

Results: Galcanezumab was superior to placebo in reducing the frequency of migraine headache days with associated symptoms of migraine such as nausea and/or vomiting, photophobia and phonophobia, and prodromal symptoms. Galcanezumab reduced the frequency of migraine headache days with aura in the episodic migraine studies. There was a significant reduction in the proportion of remaining migraine headache days with nausea and/or vomiting for the episodic and chronic migraine studies, and with photophobia and phonophobia for the episodic migraine studies. Galcanezumab was superior to placebo in reducing the number of monthly moderate-to-severe migraine headache days and the overall and monthly severe migraine headache days.

Conclusions: Galcanezumab reduces the frequency of migraine headache days and can alleviate potentially disabling non-pain symptoms on days when migraine is present in patients with episodic or chronic migraine.

Trial registration: NCT, NCT02614183 (EVOLVE-1), registered 25 November 2015; NCT, NCT02614196 , (EVOLVE-2), registered 25 November 2015; NCT, NCT02614261 (REGAIN), registered 25 November 2015.

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galcanezumab对发作性或慢性偏头痛患者严重程度和症状的影响
背景:Galcanezumab是一种结合降钙素基因相关肽的人源化单克隆抗体,与安慰剂相比,已证明可显著减少每月偏头痛天数。在这里,我们分析了3个随机临床试验的数据(2个发作性试验[EVOLVE-1, EVOLVE-2]和1个慢性试验[重新获得]),以检查galcanezumab是否也减轻了偏头痛的严重程度和症状。方法:发作性偏头痛试验为为期6个月的双盲研究,研究对象为发作性偏头痛患者(每月偏头痛天数4-14天)。慢性偏头痛试验是一项为期3个月的双盲研究,研究对象为慢性偏头痛患者(每月头痛天数≥15天,其中≥8天符合偏头痛标准)。患者(18-65岁)随机分为安慰剂组或galcanezumab 120 mg组,外加240 mg负荷组或240 mg负荷组。患者记录每次头痛的特征、持续时间、严重程度和相关症状。分析的结果是每月偏头痛伴有恶心和/或呕吐的天数、畏光和恐音、先兆和先兆以外的前驱症状的基线变化。分析的其他结果包括每月中度至重度偏头痛天数、重度偏头痛天数和平均剩余偏头痛天数。还分析了在每月剩余的偏头痛天数中,恶心和/或呕吐天数比例以及畏光和恐音天数比例的基线变化。结果:Galcanezumab在减少伴有偏头痛相关症状(如恶心和/或呕吐、畏光、恐音和前驱症状)的偏头痛天数频率方面优于安慰剂。在发作性偏头痛研究中,Galcanezumab降低了伴有先兆的偏头痛天数的频率。在发作性和慢性偏头痛研究中,伴有恶心和/或呕吐的偏头痛天数比例显著减少,在发作性偏头痛研究中伴有畏光和恐音的偏头痛天数比例显著减少。Galcanezumab在减少每月中度至重度偏头痛天数以及总体和每月重度偏头痛天数方面优于安慰剂。结论:Galcanezumab可减少偏头痛天数的频率,并可减轻发作性或慢性偏头痛患者出现偏头痛时的潜在致残性非疼痛症状。试验注册:NCT, NCT02614183 (EVOLVE-1),注册于2015年11月25日;NCT, NCT02614196, (EVOLVE-2), 2015年11月25日注册;NCT, NCT02614261(重获),注册于2015年11月25日。
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