Doods Henri, Arndt Kirsten, Rudolf Klaus, Just Stefan
Boehringer Ingelheim Pharma GmbH & Co. KG, 88397 Biberach, Germany.
Trends Pharmacol Sci. 2007 Nov;28(11):580-7. doi: 10.1016/j.tips.2007.10.005. Epub 2007 Oct 25.
Migraine is a complex, debilitating neurovascular disorder. Although knowledge on the main molecular players is still incomplete, recent preclinical and clinical findings indicate that there is a clear correlation between migraine-associated headache and the release of the neuropeptide calcitonin gene-related peptide (CGRP). BIBN4096 was the first CGRP antagonist to be tested in clinical trials for the treatment of migraine. The proven efficacy of this agent, and also the CGRP antagonist MK-0974, to alleviate acute migraine headache provided significant support for the hypothesis that CGRP has an important role in migraine pathophysiology. Moreover, the recently published results from Phase II trials are encouraging and suggest that this new type of drug might offer advantages over existing therapies for patients suffering from migraine and related headaches.
偏头痛是一种复杂的、使人衰弱的神经血管疾病。尽管关于主要分子参与者的知识仍不完整,但最近的临床前和临床研究结果表明,偏头痛相关头痛与神经肽降钙素基因相关肽(CGRP)的释放之间存在明显关联。BIBN4096是首个在偏头痛治疗临床试验中进行测试的CGRP拮抗剂。该药物以及CGRP拮抗剂MK - 0974缓解急性偏头痛头痛的已证实疗效,为CGRP在偏头痛病理生理学中起重要作用这一假说提供了重要支持。此外,最近发表的II期试验结果令人鼓舞,表明这种新型药物可能比现有疗法为偏头痛及相关头痛患者带来更多优势。