%0 Journal Article
%T A randomized, double-blind, placebo-controlled study of rapid-acting intramuscular olanzapine in Japanese patients for schizophrenia with acute agitation
%A Hideaki Katagiri
%A Shinji Fujikoshi
%A Takuya Suzuki
%A Kiyoshi Fujita
%A Naoya Sugiyama
%A Michihiro Takahashi
%A Juan-Carlos Gomez
%J BMC Psychiatry
%D 2013
%I BioMed Central
%R 10.1186/1471-244x-13-20
%X We conducted a placebo-controlled, randomized, double-blind, parallel-group study in Japanese patients diagnosed with schizophrenia according to the diagnostic criteria specified in the DSM-IV-TR. Patients were randomized to 2 treatment groups: IM olanzapine (10 mg) or IM placebo. The primary efficacy outcome was the change in PANSS-EC from baseline to 2 hours after the first IM injection. Treatment groups were compared with an analysis of variance model which included treatment and site as factors. During the 24-hour treatment period, safety was assessed by clinical examination and laboratory investigations, electrocardiograms, extrapyramidal symptoms scales, and recording spontaneously reported adverse events.Of the 91 randomized patients, 90 patients (45 IM olanzapine-group; 45 IM placebo-group) were in the full analysis set. The mean change of PANSS-EC total score from baseline to 2 hours after the first IM injection (mean¡Àstandard deviation) was £¿9.2¡À4.5 for the IM olanzapine group and £¿2.8¡À5.6 for the IM placebo group. The difference between treatment groups was statistically significant (p<.001). There were no deaths, serious adverse events, treatment-emergent adverse events (TEAEs) leading to discontinuation, severe TEAEs, or instances of oversedation in this study. There were no statistically significant differences between treatment groups in the proportion of patients with potentially clinically significant changes in laboratory tests, vital signs (blood pressure and pulse rate), electrocardiograms, and treatment-emergent extrapyramidal symptoms.The efficacy of IM olanzapine 10 mg in patients with exacerbation of schizophrenia with acute psychotic agitation was greater than IM placebo in the primary efficacy measure, PANSS-EC. Intramuscular olanzapine 10 mg was shown to be generally safe and tolerable, and could be a new option for treatment of schizophrenia in Japan.NCT00970281Schizophrenia is a chronic disease, but in the acute phase agitation is common
%K Rapid-acting intramuscular olanzapine
%K Schizophrenia
%K Acute psychotic agitation
%K Japanese
%U http://www.biomedcentral.com/1471-244X/13/20