Lowes Brian D, Shakar Simon F, Metra Marco, Feldman Arthur M, Eichhorn Eric, Freytag J William, Gerber Michael J, Liard Jean-Francois, Hartman Craig, Gorczynski Rick, Evans Gwyn, Linseman Jennifer V, Stewart Jennifer, Robertson Alastair D, Roecker Ellen B, Demets David L, Bristow Michael R
University of Colorado Health Sciences Center, Denver, Colorado 80262, USA.
J Card Fail. 2005 Dec;11(9):659-69. doi: 10.1016/j.cardfail.2005.10.013.
Chronic heart failure is a disease syndrome characterized in its advanced stages by a poor quality of life, frequent hospitalizations, and a high risk of mortality. In advanced and ultra-advanced chronic heart failure, many treatment options, such as cardiac transplantation and mechanical devices, are severely limited by availability and cost. Short-term Phase II clinical trials suggest that low-dose oral inotropic therapy with enoximone may improve hemodynamics and exercise capacity, without adversely affecting mortality, in selected subjects with advanced chronic heart failure. Based on these data, the ability of enoximone to deliver safe and efficacious palliative treatment of advanced/ultra-advanced chronic heart failure is being evaluated in Phase III clinical trials.
The Enoximone Clinical Trials Program is a series of 4 clinical trials designed to evaluate the safety and efficacy of oral enoximone in advanced chronic heart failure. ESSENTIAL I and II (The Studies of Oral Enoximone Therapy in Advanced Heart Failure) will investigate the effects of oral enoximone on all-cause mortality and cardiovascular hospitalization, submaximal exercise capacity, and quality of life in subjects with New York Heart Association Class III/IV chronic heart failure. EMOTE (Oral Enoximone in Intravenous Inotrope-Dependent Subjects) will evaluate the potential of oral enoximone to wean subjects with ultra-advanced chronic heart failure from chronic intravenous inotropic therapy to which they have been shown to be dependent. EMPOWER (Enoximone Plus Extended-Release Metoprolol Succinate in Subjects with Advanced Chronic Heart Failure) will explore the potential of enoximone to increase the tolerability of continuous release metoprolol in subjects shown previously to be hemodynamically intolerant to beta-blocker treatment.
These studies are Phase III, multicenter, randomized, double-blinded, placebo-controlled trials designed to test the general hypothesis that chronic oral administration of low doses of enoximone can produce beneficial effects in subjects with advanced or ultra-advanced chronic heart failure.
慢性心力衰竭是一种疾病综合征,在其晚期表现为生活质量差、频繁住院和高死亡风险。在晚期和超晚期慢性心力衰竭中,许多治疗选择,如心脏移植和机械装置,受到可用性和成本的严重限制。短期II期临床试验表明,对于选定的晚期慢性心力衰竭患者,使用依诺昔酮进行低剂量口服强心治疗可能改善血流动力学和运动能力,且不影响死亡率。基于这些数据,正在进行III期临床试验以评估依诺昔酮对晚期/超晚期慢性心力衰竭进行安全有效的姑息治疗的能力。
依诺昔酮临床试验项目是一系列4项临床试验,旨在评估口服依诺昔酮在晚期慢性心力衰竭中的安全性和有效性。ESSENTIAL I和II(晚期心力衰竭口服依诺昔酮治疗研究)将研究口服依诺昔酮对纽约心脏协会III/IV级慢性心力衰竭患者全因死亡率、心血管住院率、次极量运动能力和生活质量的影响。EMOTE(静脉注射强心剂依赖受试者的口服依诺昔酮)将评估口服依诺昔酮使超晚期慢性心力衰竭患者从已证明依赖的慢性静脉注射强心治疗中撤药的潜力。EMPOWER(晚期慢性心力衰竭患者中依诺昔酮加琥珀酸美托洛尔缓释片)将探索依诺昔酮提高先前对β受体阻滞剂治疗血流动力学不耐受的患者对美托洛尔持续释放耐受性的潜力。
这些研究是III期、多中心、随机、双盲、安慰剂对照试验,旨在检验以下总体假设:长期口服低剂量依诺昔酮可对晚期或超晚期慢性心力衰竭患者产生有益效果。