King Chadwick Terence, Gegg Colin V, Hu Sylvia Nai-Yu, Sen Lu Hsieng, Chan Brian M, Berry Kelly A, Brankow David W, Boone Tom J, Kezunovic Nebojsa, Kelley Matt R, Shi Licheng, Xu Cen
Amgen Research, 1 Amgen Center Drive, Thousand Oaks, California 91320-1799, United States.
ACS Pharmacol Transl Sci. 2019 Sep 3;2(6):485-490. doi: 10.1021/acsptsci.9b00061. eCollection 2019 Dec 13.
In 2018, the United States Food and Drug Administration (FDA) approved Aimovig (erenumab) for the prevention of migraine. Erenumab is the first FDA approved antibody therapeutic against a G-protein-coupled receptor, the canonical receptor of calcitonin gene related peptide (CGRP-R). A novel, epitope-focused antigen was created to reconstruct the extracellular domains of the CGRP-R in a stable conformation. Successful inoculation of XenoMouse animals and careful screening yielded multiple candidate molecules for high potency and exquisite selectivity toward the CGRP-R over related receptors. These efforts led to the discovery of erenumab which has demonstrated the desired efficacy and safety profiles in multiple clinical studies for the prevention of migraine. The innovation developed in the discovery of erenumab furthers the ability to target G-coupled protein receptors using antibody approaches.
2018年,美国食品药品监督管理局(FDA)批准了Aimovig(erenumab)用于预防偏头痛。Erenumab是首个获FDA批准的针对G蛋白偶联受体(降钙素基因相关肽的经典受体,CGRP-R)的抗体疗法。通过构建一种新型的、聚焦表位的抗原,以稳定构象重建CGRP-R的胞外结构域。对XenoMouse动物的成功接种及仔细筛选,产生了多个对CGRP-R比对相关受体具有高效力和高选择性的候选分子。这些努力促成了erenumab的发现,其在多项预防偏头痛的临床研究中展现出了预期的疗效和安全性。在erenumab发现过程中所取得的创新,进一步提升了使用抗体方法靶向G蛋白偶联受体的能力。