British Journal of Clinical Pharmacology · 1992 · 19 citations · 5 references
MedicinePharmacokineticsPharmacologyClinical PharmacologyGeneral PharmacologyPharmacodynamicsPharmacokinetics In Children With CancerPopulation Pharmacokinetic-pharmacodynamic ModelingBlood Pressure
Twenty-four healthy subjects completed a double-blind, placebo controlled, parallel group study to evaluate the effect of treatment with flunarizine on the pharmacokinetics and pharmacodynamics of sumatriptan, a 5HT1-like agonist. Subjects received a single oral 200 mg dose of sumatriptan on the eighth day of a once daily treatment with either flunarizine 10 mg or matching placebo. There were no significant differences between treatments in relation to Cmax (82.3 ng ml-1 in the absence and 81.4 ng ml-1 in the presence of flunarizine), AUC (368 ng ml-1 h in the absence and 360 ng ml-1 in the presence) and elimination half-life (2.2 h in the absence and 2.4 h in the presence of flunarizine) of sumatriptan. Similarly pretreatment with flunarizine was not found to have any clinically significant effect on the pharmacodynamics of sumatriptan as measured by pulse rate, blood pressure and ECG.
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The Clinical Pharmacology, Pharmacokinetics and Metabolism of Sumatriptan
Paul Fowler, LF Lacey, M L Thomas et al. · European Neurology · 2008 · 248 citations
Overview of initial clinical studies with intravenous and oral GR43175 in acute migraine.
V.L. Perrin, Martti Färkkilâ, J Goasguen et al. · PubMed · 1989 · 57 citations
Lack of an interaction between propranolol and sumatriptan.
AK Scott, T Walley, AM Breckenridge et al. · British Journal of Clinical Pharmacology · 1991 · 32 citations · Full text
Early studies with the novel 5-HT 1-like agonist GR43175 in healthy volunteers.
P.A. Fowler, M L Thomas, LF Lacey et al. · PubMed · 1989 · 25 citations