Y. Lecrubier, MILNACIPRAN - THE CLINICAL PROPERTIES OF A SELECTIVE SEROTONIN AND NORADRENALINE REUPTAKE INHIBITOR (SNRI), Human psychopharmacology, 12, 1997, pp. 127-134
Milnacipran is a novel antidepressant agent which selectively inhibits
the reuptake of serotonin and noradrenaline without directly affectin
g postsynaptic receptor sites. The biochemical and pharmacological pro
file of milnacipran suggested that the drug would be therapeutically e
ffective and well tolerated. This has been borne out by the results of
placebo-controlled and open label trials of the antidepressant effica
cy of milnacipran, as well as of comparative trials with tricyclic ant
idepressants (TCAs) and selective serotonin reuptake inhibitors (SSRIs
). The designs and results of these studies are reviewed in this paper
. Milnacipran is more effective than placebo in the treatment of major
depressive episodes. It is equally effective as TCAs, but better tole
rated. Milnacipran appears to be superior in efficacy to the SSRIs, pa
rticularly in patients with severe depression, and is equally well tol
erated. The efficacy and tolerance profile of milnacipran reflects its
specific pharmacological activity. The effects of milnacipran are con
fined to the inhibition of serotonin and noradrenaline reuptake. There
is no activity on postsynaptic receptors. Overall, milnacipran offers
a beneficial combination of good efficacy and tolerability in patient
s with major depression. (C) 1997 John Wiley & Sons, Ltd.