Charité Universitätsmedizin Berlin, Berlin, Germany.
Hôpital Salengro, CHU de Lille, Lille, France.
Adv Ther. 2021 Nov;38(11):5465-5483. doi: 10.1007/s12325-021-01911-7. Epub 2021 Sep 20.
Results from the open-label extension of the phase 3b CONQUER trial are presented to evaluate the effectiveness and safety of galcanezumab, a monoclonal antibody targeting calcitonin gene-related peptide, for up to 6 months in patients with multiple prior migraine preventive treatment failures.
Patients were 18-75 years old with episodic or chronic migraine and 2-4 standard-of-care migraine preventive medication category failures. After 3 months of randomized treatment with galcanezumab (120 mg/month with 240 mg loading dose; n = 232) or placebo (n = 230), patients entered a 3-month open-label extension (120 mg/month galcanezumab with a blinded 240 mg loading dose for previous-placebo patients). Primary efficacy measure was mean change from double-blind baseline in monthly migraine headache days.
A total of 432/449 patients (96%) who entered open-label treatment completed the study. Mean change in monthly migraine headache days in the total population, which was - 1.3 for placebo and - 4.4 for galcanezumab patients at the end of double-blind treatment (p < 0.001), was - 5.2 and - 5.6, respectively, at the end of open-label treatment with galcanezumab. Among patients with episodic migraine, mean change in monthly migraine headache days had been - 0.6 for placebo and - 2.8 for galcanezumab after double-blind treatment (p < 0.001) and was - 4.5 and - 3.8, respectively, after open-label treatment. Among patients with chronic migraine, mean change in monthly migraine headache days had been - 2.5 for placebo and - 6.6 for galcanezumab after double-blind treatment (p < 0.001) and was - 6.5 and - 8.2, respectively, after open-label treatment. Adverse events were similar to those observed during double-blind placebo treatment. Review of data in elderly patients (65-75 years of age) indicated that galcanezumab was well tolerated in this age group, with no safety issues identified.
Galcanezumab was effective and safe during open-label treatment in patients who had experienced failures of previous migraine preventives.
ClinicalTrials.gov identifier NCT03559257.
本文呈现了 3b 期 CONQUER 试验的开放标签扩展部分的结果,旨在评估降钙素基因相关肽单克隆抗体加奈珠单抗在多达 6 个月的时间内对多种先前偏头痛预防治疗失败患者的有效性和安全性。
入组患者年龄 18-75 岁,患有发作性或慢性偏头痛,且在标准偏头痛预防治疗方案中失败 2-4 次。在随机接受 3 个月加奈珠单抗(120mg/月,负荷剂量 240mg;n=232)或安慰剂(n=230)治疗后,患者进入为期 3 个月的开放标签扩展期(120mg/月加奈珠单抗,之前接受安慰剂的患者接受盲法 240mg 负荷剂量)。主要疗效指标为双盲基线至每月偏头痛头痛天数的平均变化。
共有 432/449 名(96%)进入开放标签治疗的患者完成了研究。在总体人群中,安慰剂组每月偏头痛头痛天数的平均变化为-1.3,加奈珠单抗组为-4.4,这是在双盲治疗结束时(p<0.001)的结果,在开放标签治疗结束时,加奈珠单抗组分别为-5.2 和-5.6。在发作性偏头痛患者中,安慰剂组每月偏头痛头痛天数的平均变化为-0.6,加奈珠单抗组为-2.8,这是在双盲治疗结束时(p<0.001)的结果,在开放标签治疗结束时,加奈珠单抗组分别为-4.5 和-3.8。在慢性偏头痛患者中,安慰剂组每月偏头痛头痛天数的平均变化为-2.5,加奈珠单抗组为-6.6,这是在双盲治疗结束时(p<0.001)的结果,在开放标签治疗结束时,加奈珠单抗组分别为-6.5 和-8.2。不良反应与双盲安慰剂治疗期间观察到的不良反应相似。对老年患者(65-75 岁)数据的审查表明,加奈珠单抗在该年龄组中耐受性良好,未发现安全性问题。
在经历了先前偏头痛预防治疗失败的患者中,加奈珠单抗在开放标签治疗期间是有效且安全的。
ClinicalTrials.gov 标识符 NCT03559257。