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韦那克林(HP 029)在健康老年受试者中的多剂量药代动力学、安全性及耐受性:一种潜在的阿尔茨海默病治疗药物。

Multiple dose pharmacokinetics, safety, and tolerance of velnacrine (HP 029) in healthy elderly subjects: a potential therapeutic agent for Alzheimer's disease.

作者信息

Puri S K, Ho I, Hsu R, Lassman H B

机构信息

Clinical Pharmacology Section, Hoechst-Roussel Pharmaceuticals Inc., Somerville, NJ 08876.

出版信息

J Clin Pharmacol. 1990 Oct;30(10):948-55. doi: 10.1002/j.1552-4604.1990.tb03576.x.

Abstract

The pharmacokinetics, safety, and tolerance of 1,2,3,4-tetrahydro-9-aminoacridin-1-olmaleate (HP 029) a potential therapeutic agent for Alzheimer's disease, were assessed after multiple oral doses in a randomized double-blind, placebo controlled, ascending dose study in 56 healthy elderly men (14 per dose group). The subjects in the first three groups received 25, 50, or 100 mg two times a day and a fourth group was administered 100 mg velnacrine tid for 28 days. All subjects received a final dose on day 29. Subjects were confined for continuous observation during the 36-day study period. Blood and urine samples were collected for the pharmacokinetic assessment. There were no clinically important changes in the safety variables in both age groups after any dose. There was no evidence of hepatotoxicity when elderly men were given 100 mg tid for 28 days. Nine subjects reported one or two episodes of gastrointestinal (diarrhea) side effects (6 in the 100 mg bid group and 3 in the 100 mg tid dose group) during a 29-day trial. None required treatment or were discontinued from study. These results indicate that the safety and tolerance up to 100 mg tid for 28 days in healthy elderly men are acceptable. Velnacrine was rapidly absorbed after oral administration. There were dose-related increases in Cmax, AUCs, and amount of drug excreted in urine. During multiple dosing, the Cmax increased as a function of dose. The tmax and t1/2 were not affected by dosage nor multiple dosing. Steady state levels of velnacrine were reached between days 2 and 3 with no evidence of further accumulation of velnacrine thereafter. Approximately 11-30% of the administered dose was excreted in the urine over the course of the study. The favorable pharmacokinetic characteristics and acceptable safety and tolerance of multiple dosing oral doses of velnacrine support further testing of this compound for efficacy and safety in Alzheimer's patients.

摘要

1,2,3,4-四氢-9-氨基吖啶-1-醇马来酸盐(HP 029)是一种潜在的阿尔茨海默病治疗药物,在一项随机双盲、安慰剂对照、剂量递增研究中,对56名健康老年男性(每组14人)多次口服给药后,评估了其药代动力学、安全性和耐受性。前三组受试者每天两次分别接受25、50或100毫克药物,第四组受试者每天三次接受100毫克韦纳克林,持续28天。所有受试者在第29天接受最后一剂药物。在为期36天的研究期间,受试者被限制进行连续观察。采集血液和尿液样本进行药代动力学评估。任何剂量后,两个年龄组的安全变量均无临床重要变化。老年男性每天三次服用100毫克,持续28天,未发现肝毒性证据。在为期29天的试验中,9名受试者报告了一或两次胃肠道(腹泻)副作用(100毫克每日两次组6例,100毫克每日三次剂量组3例)。无人需要治疗或退出研究。这些结果表明,健康老年男性每天三次服用高达100毫克,持续28天,其安全性和耐受性是可以接受的。韦纳克林口服给药后迅速吸收。Cmax、AUCs和尿中排泄的药物量呈剂量相关增加。多次给药期间,Cmax随剂量增加而增加。tmax和t1/2不受剂量和多次给药的影响。韦纳克林在第2天至第3天达到稳态水平,此后没有进一步蓄积的证据。在研究过程中,约11%-30%的给药剂量经尿液排泄。多次口服韦纳克林良好的药代动力学特征以及可接受的安全性和耐受性,支持对该化合物在阿尔茨海默病患者中的疗效和安全性进行进一步测试。

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