Naratriptan HCL is the third oral 5-HT1 receptor agonist approved for
acute treatment of migraine. Compared with sumatriptan succinate, the
first oral 5-HT1 receptor agonist approved for this use, naratriptan h
as marked lipophilicity, a long half-life, and excellent bioavailabili
ty. In clinical trials, the approved doses of 1 mg and 2.5 mg have bee
n more effective than placebo, although 1 mg appeared to be less effec
tive than the higher dose. Direct comparative trials have shown sumatr
iptan to produce a higher 4-hour response rate than either 1 or 2.5 mg
of naratriptan. Moreover, no 2-hour response data are available for n
aratriptan. Headache recurrence rates, however, have been significantl
y lower with naratriptan than with sumatriptan. Adverse effects associ
ated with naratriptan have been consistent with those occurring with o
ther 5-HT1 agonists, although a lower incidence was observed with nara
triptan in direct com parative trials with sumatriptan.