Tonabersat, a gap-junction modulator: efficacy and safety in two randomized, placebo-controlled, dose-ranging studies of acute migraine

被引:41
作者
Silberstein, S. D. [1 ]
Schoenen, J. [2 ]
Goebel, H. [3 ]
Diener, H. C. [4 ]
Elkind, A. H. [5 ]
Klapper, J. A. [6 ]
Howard, R. A. [7 ]
机构
[1] Jefferson Headache Ctr, Philadelphia, PA 19107 USA
[2] Univ Liege, Headache Res Unit, Dept Neurol & GIGA Neurosci, Liege, Belgium
[3] Kiel Pain & Headache Ctr Neurol & Behav Med, Kiel, Germany
[4] Univ Essen Gesamthsch, Essen, Germany
[5] Elkind Headache Ctr, Mt Vernon, NY USA
[6] Mile High Res Ctr, Denver, CO USA
[7] St Joseph Reg Hlth Ctr, College Stn, TX USA
关键词
Acute migraine; gap junction; migraine prophylaxis; cortical spreading depression; tonabersat; HEADACHE;
D O I
10.1111/j.1468-2982.2009.01974.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Tonabersat is a novel benzopyran derivative that blocks the cortical spreading depression proposed to be associated with migraine attacks. The ability of single oral doses of 15, 25, 40 and 80 mg of tonabersat to relieve the symptoms of moderate to severe migraine was evaluated in 859 migraineurs enrolled in two dose-ranging, double-blind, randomized, placebo-controlled, parallel-group trials, one international and the other North American. In the international study, significantly more patients given tonabersat than given placebo experienced relief of headache pain at 2 h (15 mg, 36.8%; 40 mg, 40.7%), the principal efficacy variable, and at 4 h (40 mg, 63.0%) and complete abolition of headache at 4 h (40 mg, 34.3%). None of the primary or secondary efficacy variables indicated significant differences between tonabersat and placebo in the North American study. Tonabersat was generally well tolerated, with dizziness and nausea the most common side-effects. Serious adverse events were uncommon, and no patient withdrew from either study because of adverse events. These results suggest a possible interplay between tonabersat pharmacokinetics (the relatively long time required to reach maximum plasma concentrations) and patient characteristics (previous triptan exposure) in the management of acute migraine attacks. Based on the pharmacokinetics and actions on cortical spreading depression, tonabersat may have potential value in migraine prophylaxis.
引用
收藏
页码:17 / 27
页数:11
相关论文
共 14 条
[1]   Gastric stasis in migraine: More than just a paroxysmal abnormality during a migraine attack [J].
Aurora, SK ;
Kori, SH ;
Barrodale, P ;
McDonald, SA ;
Haseley, D .
HEADACHE, 2006, 46 (01) :57-63
[2]   Progress report on new antiepileptic drugs: A summary of the Ninth Eilat Conference (EILAT IX) [J].
Bialer, Meir ;
Johannessen, Svein I. ;
Levy, Rene H. ;
Perucca, Emilio ;
Tomsone, Torbjorn ;
White, H. Steve .
EPILEPSY RESEARCH, 2009, 83 (01) :1-43
[3]   Intrinsic brain activity triggers trigeminal meningeal afferents in a migraine model [J].
Bolay, H ;
Reuter, U ;
Dunn, AK ;
Huang, ZH ;
Boas, DA ;
Moskowitz, MA .
NATURE MEDICINE, 2002, 8 (02) :136-142
[4]   EFNS guideline on the drug treatment of migraine -: report of an EFNS task force [J].
Evers, S. ;
Afra, J. ;
Frese, A. ;
Goadsby, P. J. ;
Linde, M. ;
May, A. ;
Sandor, P. S. .
EUROPEAN JOURNAL OF NEUROLOGY, 2006, 13 (06) :560-572
[5]   Oral triptans (serotonin 5-HT1B/1D agonists) in acute migraine treatment:: a meta-analysis of 53 trials [J].
Ferrari, MD ;
Roon, KI ;
Lipton, RB ;
Goadsby, PJ .
LANCET, 2001, 358 (9294) :1668-1675
[6]   Investigation of the role of mGluR5 inhibition in migraine: a proof of concept study of ADX10059 in acute treatment of migraine [J].
Goadsby, P. J. ;
Keywood, C. .
CEPHALALGIA, 2009, 29 :7-7
[7]   Drug therapy: Migraine - Current understanding and treatment. [J].
Goadsby, PJ ;
Lipton, RB ;
Ferrari, MD .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (04) :257-270
[8]   Mechanisms of migraine aura revealed by functional MRI in human visual cortex [J].
Hadjikhani, N ;
del Rio, MS ;
Wu, O ;
Schwartz, D ;
Bakker, D ;
Fischl, B ;
Kwong, KK ;
Cutrer, FM ;
Rosen, BR ;
Tootell, RBH ;
Sorensen, AG ;
Moskowitz, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (08) :4687-4692
[9]  
Kalra Arun A, 2007, Ther Clin Risk Manag, V3, P449
[10]   The potential anti-migraine compound SB-220453 does not contract human isolated blood vessels or myocardium; a comparison with sumatriptan [J].
MaassenVanDenBrink, A ;
van den Broek, RWM ;
de Vries, R ;
Upton, N ;
Parsons, AA ;
Saxena, PR .
CEPHALALGIA, 2000, 20 (06) :538-545