Background: This multicenter, open-label study evaluated the efficacy and safety of olanzapine in patients with schizophrenia who had been nonresponsive or intolerant to a course of risperidone (mean duration of risperidone treatment = 46.3 days).
Method: A total of 34 patients with DSM-III-R and ICD-9 schizophrenia entered this trial.
Objective: This multicenter, open-label study was designed to assess the efficacy and tolerability of olanzapine in patients with chronic schizophrenia who are resistant to therapy with classic neuroleptic agents and are either not responsive to or unable to tolerate clozapine.
Methods: Patients received olanzapine orally once daily for 18 weeks at doses ranging from 5 to 25 mg. The primary efficacy measure was change in the total score on the Positive and Negative Syndrome Scale (PANSS) from baseline to end point.
Sb Ved Pr Lek Fak Karlovy Univerzity Hradci Kralove
December 1996
Beitr Klin Tuberk Spezif Tuberkuloseforsch
July 2000