Lurasidone in the treatment of schizophrenia: Results of a double-blind, placebo-controlled trial in Asian patients.

Abstract

To evaluate efficacy and safety of lurasidone for the treatment of Asian patients with schizophrenia. Patients with schizophrenia from Japan, South Korea, Malaysia, and Taiwan were randomly assigned to 6weeks of double-blind treatment with 40 or 80mg/d of lurasidone or placebo. The primary efficacy measure was change from baseline to week 6 on the Positive and Negative Syndrome Scale (PANSS) total score. Efficacy was evaluated using a mixed-model repeated-measures (MMRM) analysis in the modified intention-to-treat (mITT) population. On the basis of the analysis for the mITT population, the estimated difference score for lurasidone 40 and 80mg/d vs placebo was -4.8 (P=0.050) and -4.2 (P=0.080). For the full intention-to-treat (ITT) population, the difference score for lurasidone 40 and 80mg/d vs placebo was -5.8 (P=0.017) and -4.2 (P=0.043). The most frequent adverse events in the lurasidone 40 and 80mg/d and placebo groups, respectively, were akathisia (7.3%, 10.4%, 3.3%), somnolence (6.0%, 2.6%, 0.7%), and vomiting (6.0%, 5.8%, 2.0%). The proportion of patients experiencing clinically significant weight gain (≥7%) was 5.3% for lurasidone 40mg/d, 1.3% for 80mg/d, and 1.4% for placebo. End point changes in metabolic parameters and prolactin were comparable for both lurasidone groups and placebo. In the ITT (but not the mITT) population, treatment with lurasidone was associated with significant improvement in the PANSS total score in patients with schizophrenia. Lurasidone was generally well tolerated with minimal impact on weight and metabolic parameters.