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首页> 外文期刊>Emerging Topics in Life Sciences >Fremanezumab: a disease-specific option for the preventive treatment of migraine, including difficult-to-treat migraine
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Fremanezumab: a disease-specific option for the preventive treatment of migraine, including difficult-to-treat migraine

机译:Fremanezumab:针对偏头痛的预防性治疗的特定疾病选择,包括难以治疗的偏头痛

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Fremanezumab is a fully humanized monoclonal antibody (IgG2 Delta a) that targets calcitonin gene-related peptide (CGRP), a key neuropeptide involved in the pathophysiology of migraine. Fremanezumab is approved for quarterly and monthly subcutaneous dosing for the preventive treatment of migraine in adults. The phase 3 clinical development program for fremanezumab aimed to evaluate the efficacy of this preventive treatment across different patient populations, including those with difficult-to-treat migraine. Two pivotal 12-week, phase 3, placebo-controlled studies investigated quarterly and monthly dosing of fremanezumab in participants with chronic migraine (HALO CM) and episodic migraine (HALO EM). The efficacy of fremanezumab was further explored in individuals with difficult-to-treat chronic or episodic migraine in the 12-week FOCUS study, which enrolled participants who had previously experienced an inadequate response to 2-4 pharmacological classes of migraine preventive medications. The long-term efficacy of fremanezumab was assessed in a 12-month long-term study (HALO LTS), which enrolled participants completing the 12-week HALO studies and new participants. Across these studies, treatment with fremanezumab dosed quarterly or monthly provided significant reductions in the frequency of migraine days, headache days of at least moderate severity, and migraine- and headache-related disability compared with placebo. Sustained improvements were seen with long-term fremanezumab treatment. Subgroup analyses of participants with difficult-to-treat migraine (those with comorbid depression, overuse of acute headache medications, and concomitant use of other migraine preventive medications) demonstrated the effectiveness of quarterly or monthly fremanezumab in these populations. Ongoing studies are further exploring the potential benefits of fremanezumab in difficult-to-treat migraine and other headache and pain disorders.
机译:Fremanezumab是一种靶向降钙素基因相关肽(CGRP)的完全人性化的单克隆抗体(IgG2 delta A),这是一种参与偏头痛病理生理学的关键神经肽。 Fremanezumab被批准用于季度和每月皮下剂量,以预防成人偏头痛。 Fremanezumab的3阶段临床开发计划旨在评估不同患者人群(包括难以治疗偏头痛的患者)的预防治疗的功效。安慰剂对照研究的两次关键为12周,第3阶段研究研究了慢性偏头痛(Halo CM)和情节性偏头痛(Halo EM)的季度和每月给予Fremanezumab的剂量。在这项为期12周的焦点研究中,弗雷曼卫生酶的疗效进一步探讨了难以治疗的慢性或情节性偏头痛的个体,该研究招募了以前曾经历了对2-4药理学偏头痛预防药物的反应不足的参与者。在一项为期12个月的长期研究(HALO LTS)中评估了弗雷曼苏岛的长期疗效,该研究招募了完成为期12周的Halo研究和新参与者的参与者。在这些研究中,季刊或每月服用弗雷曼卫生的治疗可显着降低偏头痛天的频率,至少中度严重程度的头痛日以及与安慰剂相比,与偏头痛和头痛相关的残疾。长期的fremanezumab治疗可以看到持续的改善。对难以治疗偏头痛的参与者(患有合并症,急性头痛药物过度使用以及同时使用其他偏头痛药物的参与者)的亚组分析表明,在这些人群中季度或每月fremanezumab的有效性。正在进行的研究进一步探讨了弗雷曼武族蛋糕在难以治疗的偏头痛以及其他头痛和疼痛障碍中的潜在益处。

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