CSL Behring, Pasadena, CA, USA.
CSL Behring, King of Prussia, PA, USA.
J Clin Pharmacol. 2019 Mar;59(3):427-436. doi: 10.1002/jcph.1337. Epub 2018 Nov 19.
CSL112 (apolipoprotein A-I [human]) is a novel intravenous formulation of plasma-derived apolipoprotein A-I (apoA-I) that enhances cholesterol efflux capacity. Renal impairment is a common comorbidity in acute myocardial infarction patients and is associated with impaired lipid metabolism. The aim of this phase 1 study was to assess the impact of moderate renal impairment on the pharmacokinetic and pharmacodynamic profile of CSL112. Sixteen subjects with moderate renal impairment and 16 age-, sex-, and weight-matched subjects with normal renal function participated in the study. Within each renal function cohort, subjects were randomized 3:1 to receive a single intravenous infusion of CSL112 2 g (n = 6) or placebo (n = 2) or CSL112 6 g (n = 6) or placebo (n = 2). At baseline, subjects with moderate renal impairment versus normal renal function had higher total cholesterol efflux, ABCA1-dependent cholesterol efflux capacity, and pre-β1-high-density lipoprotein (HDL) levels. Infusing CSL112 resulted in similar, immediate, robust, dose-dependent elevations in apoA-I and cholesterol efflux capacity in both renal function cohorts and significantly greater elevations in pre-β1-HDL (P < .05) in moderate renal impairment. Lecithin-cholesterol acyltransferase activity, demonstrated by a time-dependent change in the ratio of unesterified to esterified cholesterol, did not differ by renal function. No meaningful changes in proatherogenic lipid levels were observed. Moderate renal impairment did not impact the ability of CSL112 to enhance cholesterol efflux capacity. CSL112 may represent a novel therapy to reduce the risk of early recurrent cardiovascular events following acute myocardial infarction in patients with or without moderate renal impairment.
CSL112(载脂蛋白 A-I[人])是一种新型的静脉内制剂,来源于人血浆载脂蛋白 A-I(apoA-I),可增强胆固醇外排能力。急性心肌梗死患者常合并肾功能损害,且与脂质代谢受损有关。这项 1 期研究旨在评估中度肾功能损害对 CSL112 药代动力学和药效学特征的影响。16 名中度肾功能损害患者和 16 名年龄、性别和体重匹配的肾功能正常患者参与了这项研究。在每个肾功能队列中,受试者随机分为 3:1 接受 CSL112 2 g(n=6)或安慰剂(n=2)或 CSL112 6 g(n=6)或安慰剂(n=2)静脉输注。与肾功能正常者相比,中度肾功能损害者的总胆固醇外排率、ABCA1 依赖性胆固醇外排能力和前-β1-高密度脂蛋白(HDL)水平更高。CSL112 输注可导致两个肾功能队列中即刻、迅速、剂量依赖性升高 apoA-I 和胆固醇外排能力,且在中度肾功能损害者中前-β1-HDL 显著升高(P<.05)。通过未酯化胆固醇与酯化胆固醇之比的时间依赖性变化来表示的卵磷脂胆固醇酰基转移酶活性不受肾功能影响。未观察到致动脉粥样硬化脂质水平发生有意义的变化。中度肾功能损害并不影响 CSL112 增强胆固醇外排能力的能力。CSL112 可能为一种新型治疗药物,可降低伴有或不伴有中度肾功能损害的急性心肌梗死后早期复发性心血管事件的风险。