Literature DB >> 12083998

Review of zolmitriptan and its clinical applications in migraine.

Andrew J Dowson1, Bruce Charlesworth.   

Abstract

Preclinical studies have shown that zolmitriptan is a selective serotonin 5-HT(1B/1D) receptor agonist (triptan). Randomised, placebo-controlled, double-blind trials in patients with migraine have shown that zolmitriptan has good efficacy measured using 2 h response and pain-free rates. Migraine-associated symptoms, including nausea, photophobia and phonophobia, are also improved with zolmitriptan. Oral zolmitriptan (2.5 and 5 mg) has an onset of action within 45 min and efficacy is sustained in most patients who respond at 2 h. The orally-disintegrating zolmitriptan tablet has the advantage that it may be taken immediately, without the need for additional fluids, any time a migraine headache occurs. Patients may benefit in terms of improved efficacy from the convenience of the disintegrating tablet, since there is evidence that taking triptan therapy as early as possible in an attack is advantageous. For similar reasons, as well as improved efficacy, a nasal spray formulation is in development. Zolmitriptan is effective in the treatment of migraine associated with menses and migraine with aura. There is no tachyphylaxis following repeated doses for multiple attacks of migraine over a prolonged period of time. Compared to placebo, the incidence of persistent migraine headache is reduced by zolmitriptan and recurrent migraine headache occurs less frequently. Zolmitriptan has also shown efficacy in the treatment of persistent and/or recurrent migraine headache. Comparative clinical studies have shown overall that zolmitriptan has similar or superior efficacy to sumatriptan in the treatment of migraine. Specifically, zolmitriptan 2.5 mg was significantly more effective than sumatriptan 25 or 50 mg according to a number of end points, including headache response at 2 h. Oral zolmitriptan is also effective in the acute treatment of cluster headache. Zolmitriptan is generally well tolerated, with most adverse events being mild-to-moderate, transient and resolving without intervention or the need for treatment withdrawal. The consistent efficacy in treating all types of migraine and the choice of available formulations make zolmitriptan acceptable to patients and a suitable first-line therapy for the treatment of migraine.

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Year:  2002        PMID: 12083998     DOI: 10.1517/14656566.3.7.993

Source DB:  PubMed          Journal:  Expert Opin Pharmacother        ISSN: 1465-6566            Impact factor:   3.889


  5 in total

1.  Frovatriptan versus zolmitriptan for the acute treatment of migraine: a double-blind, randomized, multicenter, Italian study.

Authors:  Vincenzo Tullo; Gianni Allais; Michel D Ferrari; Marcella Curone; Eliana Mea; Stefano Omboni; Chiara Benedetto; Dario Zava; Gennaro Bussone
Journal:  Neurol Sci       Date:  2010-06       Impact factor: 3.307

Review 2.  Newer formulations of the triptans: advances in migraine management.

Authors:  Jonathan Paul Gladstone; Marek Gawel
Journal:  Drugs       Date:  2003       Impact factor: 9.546

3.  EQ-5D™-derived utility values for different levels of migraine severity from a UK sample of migraineurs.

Authors:  Megan R Stafford; Asha Hareendran; Daisy S Ng-Mak; Ralph P Insinga; Ruifeng Xu; Donald E Stull
Journal:  Health Qual Life Outcomes       Date:  2012-06-12       Impact factor: 3.186

Review 4.  Solvent-free incorporation of CO2 into 2-oxazolidinones: a review.

Authors:  Sattar Arshadi; Alireza Banaei; Saeideh Ebrahimiasl; Aazam Monfared; Esmail Vessally
Journal:  RSC Adv       Date:  2019-06-21       Impact factor: 4.036

5.  Zolmitriptan: a novel portal hypotensive agent which synergizes with propranolol in lowering portal pressure.

Authors:  Mercedes Reboredo; Haisul C Y Chang; Roberto Barbero; Carlos M Rodríguez-Ortigosa; Francisco Pérez-Vizcaíno; Asunción Morán; Mónica García; Jesús M Banales; Norberto Carreño; Félix Alegre; Ignacio Herrero; Jorge Quiroga; Jesús Prieto; Bruno Sangro
Journal:  PLoS One       Date:  2013-01-16       Impact factor: 3.240

  5 in total

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