Jefferson Headache Center, Thomas Jefferson University, Philadelphia, PA, USA.
Headache. 2019 Oct;59(9):1597-1608. doi: 10.1111/head.13661. Epub 2019 Sep 26.
To describe the new classes of medication for headache management and their roles in clinical practice.
Calcitonin gene-related peptide (CGRP) is a key component in the underlying pathophysiology of migraine. Research focused on targeting CGRP for headache treatment has led to the development of entirely new classes of medications - the gepants and the CGRP monoclonal antibodies (mAbs) - for both acute and preventive treatment. A third class, the ditans, is being developed to target the 5-HT receptor to provide acute treatment without vasoconstrictive effects.
This article reviews the pathophysiology of migraine that has led to these new pharmacologic developments. Available information from randomized controlled trials, abstracts, press releases, and relevant preclinical studies is summarized for each class of medications.
At the time of this writing, one ditan has been submitted to the U.S. Food and Drug Administration (FDA) for approval. One gepant is anticipated to be submitted within the first quarter of 2019, and others are in clinical trials. Three CGRP mAbs have been FDA approved and are now available in clinical practice, and a fourth was submitted in the first quarter of 2019.
The development of new migraine-specific classes of medications provides more treatment options for both acute and preventive treatment of migraine.
描述头痛管理的新类别的药物及其在临床实践中的作用。
降钙素基因相关肽(CGRP)是偏头痛潜在病理生理学的关键组成部分。针对 CGRP 进行头痛治疗的研究导致了完全新型药物类别的开发 - gepants 和 CGRP 单克隆抗体(mAbs) - 用于急性和预防性治疗。第三类 ditans 正在开发中,以靶向 5-HT 受体提供无血管收缩作用的急性治疗。
本文综述了导致这些新的药理发展的偏头痛病理生理学。对每个药物类别,从随机对照试验、摘要、新闻稿和相关的临床前研究中总结了可用信息。
在撰写本文时,一种 ditan 已提交给美国食品和药物管理局(FDA)批准。预计在 2019 年第一季度将提交一种 gepant,其他药物也正在临床试验中。三种 CGRP mAbs 已获得 FDA 批准,现已在临床实践中使用,第四种药物已于 2019 年第一季度提交。
新型偏头痛特异性药物类别的开发为偏头痛的急性和预防性治疗提供了更多的治疗选择。