The tolerability and pharmacokinetics of the novel antimigraine compound 311C90 in healthy male volunteers

被引:60
作者
Seaber, E
On, N
Phillips, S
Churchus, R
Posner, J
Rolan, P
机构
[1] Department of Clinical Pharmacology, Glaxo Wellcome, Beckenham, Kent, BR3 3BS, South Eden Park Road
[2] Medeval Ltd., University of Manchester, Skelton House, Manchester, M15 4SH, Manchester Sci. Pk., Lloyd St. North
关键词
311C90; tolerability; pharmacokinetics; first administration;
D O I
10.1111/j.1365-2125.1996.tb00172.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
1 311C90 is a novel and selective agonist at 5-HT1D receptors, with central and peripheral actions, currently in development for the acute oral treatment of migraine. 2 The pharmacokinetic and tolerability profiles of single oral doses from 1-50 mg 311C90 were investigated in 12 healthy male volunteers in a double-blind, placebo-controlled, dose-escalating study. 3 311C90 was well tolerated with most adverse experiences of mild and transient nature. 4 Absorption was rapid with dose-independent kinetics. Median t(max) was 2-4 h although 50-85% of eventual C-max was attained within 1 h. The t(1/2) was 2.5-3 h with a high apparent plasma clearance (CL/F > 2000 ml min(-1)) and apparent volume of distribution (V-z/F) of 400-500 l. 5 Three metabolites were detected in plasma and urine, one of which, the N-desmethyl metabolite, has 5-HT1D agonist activity. 6 311C90 showed no clinically significant effects on blood pressure, heart rate, ECG or laboratory variables at any dose and demonstrated a tolerability and pharmacokinetic profile compatible with an acute oral migraine treatment.
引用
收藏
页码:141 / 147
页数:7
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