Karttunen P, Uusitupa M, Helin M, Tukiainen H, Silvasti M
Orion Corporation Ltd., Orion Pharmaceutica, Medical Department, Kuopio, Finland.
Arzneimittelforschung. 1988 Apr;38(4A):642-6.
Vadocaine hydrochloride (2',4'-dimethyl-6'-methoxy-3-(2-methylpiperidyl)propionanilide+ ++ hydrochloride, OR K-242-HCl; INN: vadocaine) is an anilide derivative with antitussive and local anaesthetic action. The safety of this new compound was studied in 8 healthy male volunteers in a Phase I clinical trial. Vadocaine was administered orally as a single dose of 50, 100, 200, 300, 400 and 500 mg. At the two highest dose levels used, 400 and 500 mg, vadocaine induced side-effects originating in the central nervous system; ECG analysis revealed small prolongations in the P-Q interval and QRS complex after 400 and 500 mg. At a dose of 500 mg the P-Q interval was prolonged by a maximum of 38% (184 ms at 0.5 h; 134 ms pre-dose). The compound had no effect on blood and urinary parameters measured for safety evaluation. On the basis of these results, a 300 mg dose of vadocaine appears to be safe in man in all respects. This dose level is 10 times the therapeutic dose (30 mg). Vadocaine is sufficiently safe for future clinical trials in patients with cough.
盐酸瓦多卡因(2',4'-二甲基-6'-甲氧基-3-(2-甲基哌啶基)丙酰苯胺盐酸盐,即K-242-HCl;国际非专利药品名称:瓦多卡因)是一种具有镇咳和局部麻醉作用的酰苯胺衍生物。在一项I期临床试验中,对8名健康男性志愿者研究了这种新化合物的安全性。瓦多卡因以50、100、200、300、400和500毫克的单剂量口服给药。在使用的两个最高剂量水平,即400毫克和500毫克时,瓦多卡因引发了源自中枢神经系统的副作用;心电图分析显示,服用400毫克和500毫克后,P-Q间期和QRS复合波略有延长。在500毫克剂量时,P-Q间期最长延长38%(给药后0.5小时为184毫秒;给药前为134毫秒)。该化合物对为安全性评估而测量的血液和尿液参数没有影响。基于这些结果,300毫克剂量的瓦多卡因在各方面对人体似乎都是安全的。这个剂量水平是治疗剂量(30毫克)的10倍。瓦多卡因对于未来咳嗽患者的临床试验来说足够安全。