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Measures of Functioning in Patients With Episodic Migraine: Findings From a Double-Blind, Randomized, Placebo-Controlled Phase 2b Trial With Galcanezumab

机译:偏振术患者的功能措施:从加仑南巴马布进行双盲,随机,安慰剂对照期2B试验的研究结果

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Objective - To evaluate 12-week changes from baseline of 2 disease-specific patient-reported outcome (PRO) measures in adults with migraine treated with galcanezumab, an investigational humanized antibody binding calcitonin gene-related peptide (CGRP), or placebo. Background - Preventing headache-related functional impairment is an important goal of migraine preventive treatment and a measurement target for PROs. Understanding which drugs have the potential to improve patient functioning in addition to preventing migraine headaches is vital to lessening patient burden. Design/Methods - This Phase 2b double-blind, randomized, placebo-controlled study enrolled adults with episodic migraine. Galcanezumab (120 mg subcutaneous injection; n=60) or placebo (n=127) was administered every 28 days for 12 weeks. Post hoc secondary analyses were conducted for those who completed 12 weeks of treatment on 2 PROs: The Migraine-Specific Quality of Life Questionnaire (MSQ) v2.1 and the Headache Impact Test (HIT-6). Results - Analysis of covariance revealed significant differences in least square mean changes from baseline between galcanezumab and placebo for all MSQ domains including total mean change placebo of 18.63, galcanezumab of 27.36 (95% CI 2.449, 15.008; P-value of .0067); Role Function-Restrictive mean change placebo of 22.40, galcanezumab of 31.92 (95% CI 2.636, 16.518; P-value of .0071); Role Function-Preventive mean change placebo of 13.43, galcanezumab of 19.76 (95% CI 0.476, 12.185; P-value of .0342); and Emotional Function mean change placebo of 16.88, galcanezumab of 26.61 (95% CI 2.789, 16.674; P-value of .0063). At baseline, mean number of migraine headache days (MHDs) did not correlate with MSQ total scores or HIT-6. At 12 weeks post-treatment, MHD correlated with MSQ and HIT-6 scores (all P.0001). Change in MHD was associated with change in MSQ domains and change in HIT-6 scores (all P.0001). Conclusions - In comparison with placebo, treatment with galcanezumab was associated with significant functional improvements as reflected by changes in MSQ scores. Change in MHD was associated with improvements in MSQ and reductions in HIT-6 scores, indicating the clinical importance of these changes in relation to PROs that measure function.
机译:目的 - 评估与用Galcanezumab治疗的偏头痛的成人患者的2例疾病特异性患者报告的结果(Pro)措施的12周变化,研究人源化结合降钙素基因相关肽(CGRP)或安慰剂。背景 - 预防头痛相关的功能障碍是偏头痛预防治疗和专业人士的测量目标的重要目标。了解哪些药物潜力可以改善患者的功能,除了预防偏头痛头痛对减少患者负担至关重要。设计/方法 - 该阶段2B双盲,随机,安慰剂对照研究招收成年人与巨型偏头痛。每28天施用Galcanezumab(120mg皮下注射; n = 60)或安慰剂(n = 127),持续12周。为2个优点完成12周的人进行后次级分析:偏头痛特异性生活质量问卷(MSQ)V2.1和头痛冲击试验(HIT-6)。结果 - 协方差分析揭示了全部MSQ域与Alloble之间的基线基线的显着差异,包括27.36(95%Ci 2.449,15.008; P值为.0067)的全部MSQ结构的基准组合和安慰剂。角色函数限制性平均改变安慰剂22.40,Galcanezumab为31.92(95%Ci 2.636,16.518; P值为.0071);作用功能预防性平均变化安慰剂为19.76(95%CI 0.476,12.185; 0342)的Galcanezumab。和情绪函数意味着改变安慰剂16.88,Galcanezumab为26.61(95%CI 2.789,16.674; P值为.0063)。在基线时,偏头痛的平均数量(MHD)与MSQ总分数或HIT-6没有相关。在治疗后12周,MHD与MSQ和HIT-6分数相关(所有P& .0001)。 MHD的变化与MSQ域的变化相关联,并在HIN-6分数中的变化(所有P& .0001)。结论 - 与安慰剂相比,随着MSQ分数的变化反映,与Galcanezumab的治疗与显着的功能改进有关。 MHD的变化与MSQ的改进相关,并在HIT-6分数减少,表明这些变化与衡量功能的专业人员的临床重要性。

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