STEADY-STATE INVESTIGATION OF POSSIBLE PHARMACOKINETIC INTERACTIONS OF MOXONIDINE AND GLIBENCLAMIDE

被引:0
|
作者
MULLER, M
WEIMANN, HJ
EDEN, G
WEBER, W
MICHAELIS, K
DILGER, C
ACHTERT, G
机构
[1] KALI CHEM PHARM GMBH,D-30173 HANNOVER,GERMANY
[2] LAB GMBH & CO,W-7910 NEU ULM,GERMANY
关键词
MOXONIDINE; GLIBENCLAMIDE; ORAL ADMINISTRATION; HUMAN PHARMACOKINETICS; DRUG INTERACTION; STEADY STATE; HEALTHY VOLUNTEERS;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the study presented here was to determine possible pharmacokinetic interactions of moxonidine and glibenclamide at steady state in 18 healthy male volunteers. Multiple oral doses of 0.2 mg of moxonidine b.i.d. (q. 12 h) and of 2.5 mg of glibenclamide o.i.d. (q. 24 h) were administered alone and in combination in an open, non-randomized, three-treatment design. The preparations were given for 5 days in each of the 3 periods. The results of this multiple dose study did not indicate substantial pharmacokinetic interactions of the drugs. Regarding the influence of glibenclamide on the pharmacokinetics of moxonidine, no significant changes were seen at all In the presence of moxonidine, a minor decrease of bioavailability of glibenclamide was detectable, as could be derived from the AUC and clearance data. The actual differences were small and not considered to be of clinical significance.
引用
收藏
页码:277 / 283
页数:7
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