Zolmitriptan:a new acute treatment for migraine
- 1 April 1998
- journal article
- Published by Informa Healthcare in Expert Opinion on Investigational Drugs
- Vol. 7 (4) , 633-652
- https://doi.org/10.1517/13543784.7.4.633
Abstract
Zolmitriptan is a new oral acute treatment for migraine. It is a selective and potent agonist at the serotonin (5-HT)1B/1D receptor and was developed to improve on the oral bioavailability, tissue selectivity and CNS penetration of earlier compounds. Animal studies confirmed that these objectives had been attained. In man, zolmitriptan is rapidly absorbed after oral administration, with at least 75% of the eventual Cmax reached within 1 h. Oral bioavailability is approximately 40%. The elimination half-life of zolmitriptan is approximately 2.5 h and the primary route of elimination is metabolism, with one of the metabolites being pharmacologically active. A consistent 2-h headache response rate of 60 - 70% was observed at doses of 2.5 mg and above. Long-term treatment response is high (> 80%) and consistent. In addition, there is evidence from electrophysiology in migraineurs that zolmitriptan has a central action not shared by sumatriptan. Zolmitriptan is well-tolerated. The nature and incidence of the m...Keywords
This publication has 39 references indexed in Scilit:
- The interaction between propranolol and the novel antimigraine agent zolmitriptan (311C90)British Journal of Clinical Pharmacology, 1997
- Lack of Interaction Between Pizotifen and the Novel Antimigraine Compound Zolmitriptan in Healthy VolunteersClinical Drug Investigation, 1997
- The pharmacokinetics and effects on blood pressure of multiple doses of the novel anti‐migraine drug zolmitriptan (311C90) in healthy volunteersBritish Journal of Clinical Pharmacology, 1997
- Sumatriptan can inhibit trigeminal afferents by an exclusively neural mechanismBrain, 1996
- The tolerability and pharmacokinetics of the novel antimigraine compound 311C90 in healthy male volunteersBritish Journal of Clinical Pharmacology, 1996
- The trigeminovascular system and migraine: Studies characterizing cerebrovascular and neuropeptide changes seen in humans and catsAnnals of Neurology, 1993
- Vasoactive peptide release in the extracerebral circulation of humans during migraine headacheAnnals of Neurology, 1990
- Ergot alkaloids block neurogenic extravasation in dura mater: Proposed action in vascular headachesAnnals of Neurology, 1988
- Release of vasoactive peptides in the extracerebral circulation of humans and the cat during activation of the trigeminovascular systemAnnals of Neurology, 1988
- Biochemical Investigations in Headache: Increase in the Hydroxyindoleacetic Acid Excretion During Migraine AttacksInternational Archives of Allergy and Immunology, 1961