Background: Treatment-resistance in schizophrenia remains a public health p
roblem. Clozapine has been shown to be effective in about one third of this
population, but carries with it medical risks and weekly blood draws. As o
lanzapine is a drug with a very similar biochemical profile to clozapine, i
t is important to evaluate whether non-response to olanzapine predicts cloz
apine non-response.
Methods: Forty-four treatment-resistant patients received eight weeks of ol
anzapine, either in a double-blind trial or subsequent open treatment at a
mean daily dose of 25 mg/day. Two of 44 patients (5%) responded to olanzapi
ne treatment. Patients who did not respond could then receive clozapine. Tw
enty-seven subsequently received an 8-week open trial of clozapine.
Results: Patients who did and did not receive clozapine did not differ demo
graphically or in psychopathology. Eleven of 27 (41%) met a priori response
criteria during clozapine treatment (mean dose 693 mg/day) after failing t
o respond to olanzapine.
Conclusions: This study demonstrates that failure to respond to olanzapine
treatment does not predict failure to clozapine. Treatment-resistant patien
ts who fail on olanzapine may benefit from a subsequent trial of clozapine.
(C) 1999 Society of Biological Psychiatry.