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Review

Role of paliperidone extended-release in treatment of schizoaffective disorder

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Pages 667-679 | Published online: 28 Sep 2010
 

Abstract

Schizoaffective disorder is characterized by the presence of symptoms of both schizophrenia and a major mood disorder. The coexistence of these symptoms can be difficult to manage, and these patients are generally treated with antipsychotics as well as mood stabilizers and/or antidepressants. Additionally, no established treatment guidelines exist for this disorder. This review describes the combined results of two international, double-blind, placebo-controlled clinical studies of paliperidone extended-release (ER), an atypical antipsychotic recently approved in the US for the treatment of schizoaffective disorder. Subjects in these six-week trials were aged 18–65 years, had a diagnosis of schizoaffective disorder based on the Structural Clinical Interview for DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, 4th Edition) Disorders, and were experiencing an acute exacerbation. The subjects from these studies had significant symptomatology as evidenced by a mean (standard deviation) baseline Positive and Negative Syndrome Scale total score of 92.8 (13.0). Based on Young Mania Rating Scale and/or a 21-item Hamilton Rating Scale for Depression score of ≥16 at baseline, 79.5% and 66.9% of subjects presented with prominent manic and depressive symptoms, respectively, and 46.4% presented with mixed symptoms. Approximately half (45%) of subjects were taking adjunctive mood stabilizers and/or antidepressants. Paliperidone ER was found to be effective in improving psychotic and mood symptoms in these subjects. Paliperidone ER was also effective as monotherapy or adjunctive to mood stabilizers and/or antidepressants for subjects with prominent manic, depressive, or mixed symptoms at baseline. No new tolerability signals were observed in this population. To the best of our awareness, these pooled data provide the largest data set of patients with schizoaffective disorder, and extend our knowledge of disease characteristics and treatment response.

Acknowledgment

The authors wish to acknowledge Mariana Ovnic, Matthew Grzywacz, and ApotheCom (funding supported by Ortho- McNeil Janssen Scientific Affairs, LLC, Titusville, NJ) for technical assistance in the development and submission of this manuscript.

Disclosure

This study was supported by Ortho-McNeil Janssen Scientific Affairs, LLC. CM Canuso and I Turkoz are employees of Johnson & Johnson Pharmaceutical Research and Development, LLC, and Johnson & Johnson stockholders. CA Bossie and DJ Fu are employees of Ortho-McNeil Janssen Scientific Affairs, LLC, and Johnson & Johnson stockholders.