Sanders-Brown Center on Aging, University of Kentucky, Lexington, Kentucky, USA.
Department of Neuroscience, University of Kentucky, Lexington, Kentucky, USA.
Clin Pharmacol Drug Dev. 2021 Feb;10(2):131-143. doi: 10.1002/cpdd.795. Epub 2020 Apr 7.
MW01-6-189WH (MW189) is a novel central nervous system-penetrant small-molecule drug candidate that selectively attenuates stressor-induced proinflammatory cytokine overproduction and is efficacious in intracerebral hemorrhage and traumatic brain injury animal models. We report first-in-human, randomized, double-blind, placebo-controlled phase 1 studies to evaluate the safety, tolerability, and pharmacokinetics (PK) of single and multiple ascending intravenous doses of MW189 in healthy adult volunteers. MW189 was safe and well tolerated in single and multiple doses up to 0.25 mg/kg, with no clinically significant concerns. The most common drug-related treatment-emergent adverse event was infusion-site reactions, likely related to drug solution acidity. No clinically concerning changes were seen in vital signs, electrocardiograms, physical or neurological examinations, or safety laboratory results. PK analysis showed dose-proportional increases in plasma concentrations of MW189 after single or multiple doses, with approximately linear kinetics and no significant drug accumulation. Steady state was achieved by dose 3 for all dosing cohorts. A pilot pharmacodynamic study administering low-dose endotoxin to induce a systemic inflammatory response was done to evaluate the effects of a single intravenous dose of MW189 on plasma cytokine levels. MW189 treatment resulted in lower levels of the proinflammatory cytokine TNF-α and higher levels of the anti-inflammatory cytokine IL-10 compared with placebo treatment. The outcomes are consistent with the pharmacological mechanism of MW189. Overall, the safety profile, PK properties, and pharmacodynamic effect support further development of MW189 for patients with acute brain injury.
MW01-6-189WH(MW189)是一种新型的中枢神经系统穿透性小分子药物候选物,可选择性减弱应激诱导的促炎细胞因子过度产生,并在脑出血和创伤性脑损伤动物模型中有效。我们报告了首次人体、随机、双盲、安慰剂对照的 I 期研究,以评估健康成年志愿者单次和多次递增静脉注射 MW189 的安全性、耐受性和药代动力学(PK)。MW189 在单剂量和多剂量高达 0.25mg/kg 时安全且耐受良好,无临床显著问题。最常见的与药物相关的治疗后出现的不良事件是输注部位反应,可能与药物溶液的酸度有关。生命体征、心电图、体格或神经检查或安全实验室结果均未见临床相关变化。PK 分析显示,单次或多次给药后 MW189 的血浆浓度呈剂量比例增加,具有近似线性动力学,无明显药物蓄积。所有给药队列在第 3 剂量时达到稳态。进行了一项低剂量内毒素给药的初步药效学研究,以评估单次静脉注射 MW189 对血浆细胞因子水平的影响。与安慰剂治疗相比,MW189 治疗导致促炎细胞因子 TNF-α水平降低,抗炎细胞因子 IL-10 水平升高。这些结果与 MW189 的药理学机制一致。总体而言,安全性、PK 特性和药效学效应支持进一步开发 MW189 用于急性脑损伤患者。