The pharmacology, pharmacokinetics, clinical efficacy, adverse effects, and dosage and administration of
almotriptan are reviewed.
Migraine is a common disorder with a serious impact on quality of life. Newer
serotonin-receptor agonists have been developed with the aim of improving pharmacokinetic characteristics.
Almotriptan, a selective agonist of
serotonin receptors 1B and 1D, carries FDA-approved labeling for use in the management of
migraine with or without
aura in adults. The efficacy and receptor affinity resemble those of
sumatriptan, but
almotriptan has a more favorable pharmacokinetic profile. It has a rapid onset of action, an oral bioavailability of 70-80%, and a longer half-life than
sumatriptan. In clinical trials,
almotriptan has been significantly more effective than placebo and as effective as
sumatriptan. However, it has been associated with better tolerability and greater patient satisfaction. In clinical trials, the most commonly reported adverse effects were
nausea, dry mouth,
dizziness,
somnolence,
fatigue,
vomiting, and
paresthesia.
Almotriptan is contraindicated in patients with known
ischemic heart disease,
coronary vasospasm, and other significant cardiovascular disorders.
Almotriptan has a lower acquisition cost than other
triptans and possibly lower overall health care costs because of a lower frequency of cardiovascular adverse effects. The recommended dose of
almotriptan is one 6.25- or 12.5-mg
tablet given at the onset of symptoms.
Almotriptan is effective for the management of
migraine and offers the potential for fewer adverse effects than other agents in its class.