Kotian Pravin L, Wu Minwan, Vadlakonda Satish, Chintareddy Venkat, Lu Pengcheng, Juarez Luis, Kellogg-Yelder Debra, Chen Xilin, Muppa Saritha, Chambers-Wilson Ramanda, Davis Parker Cynthia, Williams Jason, Polach Kevin J, Zhang Weihe, Raman Krishnan, Babu Yarlagadda S
J Med Chem. 2021 Sep 9;64(17):12453-12468. doi: 10.1021/acs.jmedchem.1c00511. Epub 2021 Aug 26.
Hereditary angioedema (HAE) is a rare and potentially life-threatening disease that affects an estimated 1 in 50 000 individuals worldwide. Until recently, prophylactic HAE treatment options were limited to injectables, a burdensome administration route that has driven the need for an oral treatment. A substantial body of evidence has shown that potent and selective plasma kallikrein inhibitors that block the generation of bradykinin represent a promising approach for the treatment of HAE. Berotralstat (BCX7353, discovered by BioCryst Pharmaceuticals using a structure-guided drug design strategy) is a synthetic plasma kallikrein inhibitor that is potent and highly selective over other structurally related serine proteases. This once-daily, small-molecule drug is the first orally bioavailable prophylactic treatment for HAE attacks, having successfully completed a Phase III clinical trial (meeting its primary end point) and recently receiving the U.S. Food and Drug Administration's approval for the prophylactic treatment of HAE attacks in patients 12 years and older.
遗传性血管性水肿(HAE)是一种罕见且可能危及生命的疾病,全球估计每5万人中就有1人受其影响。直到最近,HAE的预防性治疗选择仅限于注射剂,这种给药途径很麻烦,因此催生了对口服治疗的需求。大量证据表明,阻断缓激肽生成的强效且选择性的血浆激肽释放酶抑制剂是一种很有前景的HAE治疗方法。贝罗他司他(BCX7353,由BioCryst制药公司采用结构导向药物设计策略发现)是一种合成血浆激肽释放酶抑制剂,对其他结构相关的丝氨酸蛋白酶具有强效和高度选择性。这种每日一次的小分子药物是首个口服生物可利用的预防HAE发作的治疗药物,已成功完成III期临床试验(达到其主要终点),最近获得美国食品药品监督管理局批准,用于12岁及以上患者HAE发作的预防性治疗。