Objective: To evaluate the efficacy and safety of divalproex sodium (D
VPX) when used as prophylactic monotherapy in patients with migraine.
Design: Multicenter, double-blind, placebo-controlled, parallel group.
Patients were previously untreated or had failed no more than two ade
quate trials of prophylactic therapy. During the 4-week (single-blind)
baseline, patients received placebo and completed a headache diary. P
atients with two or more migraine attacks during the baseline were ran
domized to receive a DVPX daily dose of 500, 1000, or 1500 mg, or to p
lacebo. The experimental phase (EP) lasted 12 weeks, the first 4 weeks
for dose escalation to randomized dose, and the remaining 8 weeks for
maintenance at that dose. The primary efficacy variable was 4-week mi
graine attack frequency during the EP. Results: One-hundred-and-sevent
y-six patients (44 placebo, 132 DVPX) were randomized; 171 provided ef
ficacy data and 137 completed the study. During the EP, after adjustme
nt for differences in baseline migraine attack frequencies, mean reduc
tions in the DVPX groups were 1.7 (500 mg), 2.0 (1000 mg) and 1.7 (150
0 mg) migraine attacks per 4 weeks compared to a mean reduction of 0.5
migraine attacks in the placebo group (p less than or equal to 0.05 v
s placebo). Forty-four to 45% of DVPX-treated patients compared to 21%
of patients in the placebo group achieved greater than or equal to 50
% reduction in their migraine attack frequencies (p less than or equal
to 0.05 vs placebo). The recommended initial dose of DVPX in migraine
prophylaxis is 500 mg per day, although some patients may benefit fro
m higher doses. Adverse events were similar in the DVPX and placebo tr
eatment groups except for nausea, dizziness and tremor, in which incid
ence rates were significantly higher in the DVPX 1500 mg group (nausea
was also higher in 500 mg group) than in the placebo group. Conclusio
n: Divalproex sodium is an effective prophylactic treatment in migrain
e and is generally well tolerated.