Frank G J, Knapp L E, Olson S C, Phelps M C, Quade M M, Rieger M M, Sedman A J
Clinical Development, Parke-Davis Pharmaceutical Research Division, Warner-Lambert Company, Ann Arbor, Michigan 48105.
J Cardiovasc Pharmacol. 1990;15 Suppl 2:S14-23. doi: 10.1097/00005344-199000152-00004.
Quinapril has been extensively studied for efficacy and safety in patients with hypertension or congestive heart failure (CHF) in the United States and Europe. Thirty-nine clinical pharmacology studies involving 383 patients have been completed. Moreover, 12 controlled, multicenter clinical studies and 3 single-center studies involving 1,793 patients have been conducted in hypertension. Three hemodynamic trials, two of which included both acute and long-term phases, and one placebo-controlled, dose-response study have been conducted in 333 patients with CHF. An additional 519 patients who completed studies on comparative agents were started on quinapril at the initiation of six long-term, open-label trials, which extended for up to 3 years. Twelve of 15 hypertension trials evaluated quinapril as first-line monotherapy in 1,452 patients with hypertension. Comparative agents included placebo in five trials (524 patients), enalapril in three trials (339 patients), captopril in four trials (335 patients), and chlorthalidone in one trial (74 patients). A total of 510 patients received quinapril in addition to a diuretic in double-blind trials: 341 patients with moderate to severe hypertension participated in three trials, and 169 patients with CHF participated in one trial. Quinapril administered once daily (o.d.) was evaluated in four placebo-controlled studies and in two studies of o.d. vs. twice-daily doses. The safety of quinapril has been evaluated in almost 2,700 patients in controlled, double-blind studies or in open-label extensions, for a total of more than 1,600 patient-years of exposure to quinapril. More than one-half of all patients participated in long-term trials: 980 patients were studied for 1 year and 315 patients were studied for 2 years at the time of data analysis. Safety data are available for 451 older patients (aged greater than or equal to 65 years), and comparative safety data from other compounds in the controlled studies are available for 1,058 patients. Quinapril's efficacy is comparable to that of other angiotensin-converting enzyme (ACE) inhibitors, and it has a lower incidence of adverse events or withdrawals due to adverse events than has been associated with captopril or enalapril.
在美国和欧洲,喹那普利已针对高血压或充血性心力衰竭(CHF)患者的疗效和安全性进行了广泛研究。已完成39项涉及383名患者的临床药理学研究。此外,还针对高血压开展了12项对照多中心临床研究和3项涉及1793名患者的单中心研究。针对333名CHF患者开展了3项血流动力学试验,其中2项包括急性和长期阶段,以及1项安慰剂对照剂量反应研究。在6项长达3年的长期开放标签试验开始时,另外519名完成对照药物研究的患者开始服用喹那普利。15项高血压试验中的12项评估了喹那普利作为1452名高血压患者的一线单一疗法。对照药物在5项试验(524名患者)中为安慰剂,在3项试验(339名患者)中为依那普利,在4项试验(335名患者)中为卡托普利,在1项试验(74名患者)中为氯噻酮。在双盲试验中,共有510名患者除了服用利尿剂外还接受了喹那普利治疗:341名中度至重度高血压患者参与了3项试验,169名CHF患者参与了1项试验。在4项安慰剂对照研究以及2项每日一次与每日两次剂量对比研究中评估了每日一次(o.d.)服用喹那普利的情况。在对照双盲研究或开放标签扩展研究中,对近2700名患者评估了喹那普利的安全性,总共接触喹那普利的时间超过1600患者年。所有患者中超过一半参与了长期试验:在数据分析时,980名患者接受了1年研究,315名患者接受了2年研究。有451名老年患者(年龄大于或等于65岁)的安全数据,对照研究中1058名患者有其他化合物的比较安全数据。喹那普利的疗效与其他血管紧张素转换酶(ACE)抑制剂相当,与卡托普利或依那普利相比,其不良事件或因不良事件停药的发生率较低。