Headache Group, Basic and Clinical Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, King's College London, 125 Coldharbour Lane, London, UK.
NIHR-Wellcome Trust, King's Clinical Research Facility, King's College Hospital, London, UK.
Neurotherapeutics. 2018 Apr;15(2):304-312. doi: 10.1007/s13311-018-0617-4.
Migraine is a highly prevalent, severe, and disabling neurological condition with a significant unmet need for effective acute therapies. Patients (~50%) are dissatisfied with their currently available therapies. Calcitonin gene-related peptide (CGRP) has emerged as a key neuropeptide involved in the pathophysiology of migraines. As reviewed in this manuscript, a number of small molecule antagonists of the CGRP receptor have been developed for migraine therapy. Incredibly, the majority of the clinical trials conducted have proven positive, demonstrating the importance of this signalling pathway in migraine. Unfortunately, a number of these molecules raised liver toxicity concerns when used daily for as little as 7 days resulting in their discontinuation. Despite the clear safety concerns, clinical trial data suggests that their intermittent use remains a viable and safe alternative, with 2 molecules remaining in clinical development (ubrogepant and rimegepant). Further, these proofs of principle studies identifying CGRP as a viable clinical target have led to the development of several CGRP or CGRP receptor-targeted monoclonal antibodies that continue to show good clinical efficacy.
偏头痛是一种普遍存在、严重且致残的神经疾病,对于有效的急性治疗方法存在巨大的未满足需求。大约有 50%的患者对现有治疗方法不满意。降钙素基因相关肽(CGRP)已成为偏头痛发病机制中的关键神经肽。正如本文所综述的,已经开发出许多 CGRP 受体的小分子拮抗剂用于偏头痛治疗。令人惊讶的是,进行的大多数临床试验都证明了该信号通路在偏头痛中的重要性,结果为阳性。不幸的是,当这些分子每天使用仅 7 天时,就会引起肝毒性问题,导致它们被停用。尽管存在明显的安全问题,但临床试验数据表明,这些药物的间歇性使用仍然是一种可行且安全的替代方案,有 2 种药物仍处于临床开发阶段(ubrogepant 和 rimegepant)。此外,这些确定 CGRP 作为可行临床靶点的原理验证研究导致了几种 CGRP 或 CGRP 受体靶向单克隆抗体的开发,这些抗体继续显示出良好的临床疗效。