McNeill Eileen
University of Oxford, Department of Cardiovascular Medicine, John Radcliffe Hospital, Headley Way, Headington, Oxford OX39DU, UK.
Curr Opin Investig Drugs. 2010 Mar;11(3):357-64.
RVX-208 (RVX-000222) is a first-in-class, orally active, small-molecule stimulator of apolipoprotein (APO)AI gene expression, which is being developed by Resverlogix Corp for the potential treatment of cardiovascular diseases, in particular atherosclerosis and coronary artery disease. In vitro, RVX-208 stimulated APOAI transcription and was associated with dose-dependent increases in apoAI mRNA and protein. Toxicity studies in animals and phase I/II clinical trials have indicated that RVX-208 is safe and well tolerated in multiple dosing regimens. Plasma exposure to RVX-208 was dose-dependent following single or multiple oral doses and the drug was readily absorbed. In healthy volunteers and patients with low HDL-cholesterol levels, RVX-208 increased total HDL as well as the alpha- and pre-beta HDL fractions that are important substrates in the reverse cholesterol transport pathway. The results of further phase II trials are eagerly awaited to determine whether RVX-208 can deliver plaque regression via improvements in the plasma HDL profile of patients. In addition, a phase I trial indicated that RVX-208 may have potential for the removal of beta-amyloid plaques in Alzheimer's disease and this will be further assessed in an ongoing phase I/II clinical trial.
RVX-208(RVX-000222)是一种一流的、口服活性的载脂蛋白(APO)AI基因表达小分子刺激剂,由Resverlogix公司开发,用于潜在治疗心血管疾病,特别是动脉粥样硬化和冠状动脉疾病。在体外,RVX-208刺激APOAI转录,并与载脂蛋白AI mRNA和蛋白质的剂量依赖性增加相关。动物毒性研究和I/II期临床试验表明,RVX-208在多种给药方案中安全且耐受性良好。单次或多次口服给药后,RVX-208的血浆暴露呈剂量依赖性,且该药物易于吸收。在健康志愿者和低高密度脂蛋白胆固醇水平的患者中,RVX-208增加了总高密度脂蛋白以及α-和前β-高密度脂蛋白组分,这些是逆向胆固醇转运途径中的重要底物。人们急切期待进一步II期试验的结果,以确定RVX-208是否能通过改善患者的血浆高密度脂蛋白水平实现斑块消退。此外,一项I期试验表明,RVX-208可能具有清除阿尔茨海默病中β-淀粉样斑块的潜力,这将在正在进行的I/II期临床试验中进一步评估。