遗传性血管水肿
激肽释放酶
蛋白酵素
药品
化学
生物利用度
Icatibant公司
预防性治疗
口服
C1抑制剂
药理学
血管性水肿
医学
缓激肽
内科学
免疫学
酶
生物化学
受体
作者
Pravin L. Kotian,Minwan Wu,Satish Vadlakonda,Venkat Chintareddy,Pengcheng Lu,Luis Juarez,Debra Kellogg-Yelder,Xilin Chen,Saritha Muppa,Ramanda Chambers-Wilson,Cynthia Parker,Jason H. Williams,Kevin J. Polach,Weihe Zhang,Krishnan Raman,Y.S. Babu
标识
DOI:10.1021/acs.jmedchem.1c00511
摘要
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.
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