Sumatriptan, a 5HT1-like receptor agonist, is a completely new treatme
nt principle for migraine. In an extensive international programme of
controlled clinical trials, sumatriptan, 6 mg subcutaneously and 100 m
g orally, was superior to placebo in reducing headache and associated
symptoms. The response rate for subcutaneous sumatriptan (70-84% after
1 h and 81-87% after 2 h) was higher than for oral sumatriptan (50-67
% after 2 h). Additional doses did not increase efficacy. Oral sumatri
ptan was superior to Cafergot (2 mg ergotamine plus 200 mg caffeine) a
nd somewhat better than aspirin (900 mg) plus metoclopramide (10 mg).
Recurrence of migraine occurred in approximately 40% of attacks. Side
effects were generally mild and short-lived in the controlled clinical
trials. However, in clinical practice sumatriptan has subsequently ca
used rare cases of heart ischemia and sumatriptan is contraindicated i
n patients with a history of ischemic heart disease.