John R. Sims, Eli Lilly and Company, Lilly Corporate Center, Indianapolis, IN 46285,
J Prev Alzheimers Dis. 2017;4(4):247-254. doi: 10.14283/jpad.2017.38.
Several ongoing clinical development programs are investigating potential disease-modifying treatments for Alzheimer's disease (AD), including lanabecestat (AZD3293/LY3314814). Lanabecestat is a brain-permeable oral inhibitor of human beta-site amyloid (Aβ) precursor protein-cleaving enzyme 1 (BACE1) that reduces Aβ production. As a potent BACE1 inhibitor, lanabecestat significantly reduced soluble Aβ species and soluble amyloid precursor proteins (sAPPβ) in mouse, guinea pig, and dog in a time- and dose-dependent manner. Significant reductions in plasma and cerebrospinal fluid (CSF) Aβ1-40 and Aβ1-42 were observed in Phase 1 studies of healthy subjects and AD patients treated with lanabecestat. Three lanabecestat trials are ongoing and intended to support registration in Early AD: (1) Phase 2/3 study in patients with mild cognitive impairment (MCI) due to AD and mild AD dementia (AMARANTH, NCT02245737); (2) Delayed-start extension study (AMARANTH-EXTENSION, NCT02972658) for patients who have completed treatment in the AMARANTH Study; and (3) Phase 3 study in mild AD dementia (DAYBREAK-ALZ, NCT02783573). This review will discuss the development of lanabecestat, results from the completed nonclinical and clinical studies, as well as describe the ongoing Phase 3 clinical trials.
目前有几个正在进行的临床开发项目正在研究阿尔茨海默病(AD)的潜在疾病修饰治疗方法,包括 lanabecestat(AZD3293/LY3314814)。Lanabecestat 是一种可透过血脑屏障的人β-位淀粉样前体蛋白裂解酶 1(BACE1)的口服抑制剂,可减少 Aβ 的产生。作为一种强效的 BACE1 抑制剂,Lanabecestat 可显著减少小鼠、豚鼠和狗中可溶性 Aβ 物种和可溶性淀粉样前体蛋白(sAPPβ)的产生,且具有时间和剂量依赖性。在健康受试者和 AD 患者接受 Lanabecestat 治疗的 1 期研究中,观察到血浆和脑脊液(CSF)中 Aβ1-40 和 Aβ1-42 的显著减少。正在进行三项 Lanabecestat 试验,旨在支持早期 AD 的注册:(1)在 AD 导致的轻度认知障碍(MCI)和轻度 AD 痴呆患者中的 2/3 期研究(AMARANTH,NCT02245737);(2)已完成 AMARANTH 研究治疗的患者的延迟开始扩展研究(AMARANTH-EXTENSION,NCT02972658);(3)在轻度 AD 痴呆患者中的 3 期研究(DAYBREAK-ALZ,NCT02783573)。本文将讨论 Lanabecestat 的开发情况、已完成的非临床和临床研究结果,并描述正在进行的 3 期临床试验。