Hostname: page-component-848d4c4894-89wxm Total loading time: 0 Render date: 2024-07-06T15:17:43.506Z Has data issue: false hasContentIssue false

EPA-0423 - Efficacy of Lurasidone in the Treatment of Agitation Associated with Acute Schizophrenia

Published online by Cambridge University Press:  15 April 2020

M. Allen
Affiliation:
Department of Psychiatry, University of Colorado Anschutz Medical Campus, Aurora, USA
A. Pikalov
Affiliation:
Clinical Development, Sunovion Pharmaceuticals Inc, Fort Lee, USA
P. Werner
Affiliation:
Medical Affairs, Sunovion Pharmaceuticals Inc, Marlborough, USA
F. Jin
Affiliation:
Clinical Development, Sunovion Pharmaceuticals Inc, Fort Lee, USA
J. Cucchiaro
Affiliation:
Clinical Development, Sunovion Pharmaceuticals Inc., Fort Lee NJ, USA
A. Loebel
Affiliation:
Clinical Development, Sunovion Pharmaceuticals Inc, Fort Lee, USA

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Introduction:

Agitation is a common presentation among patients hospitalized for an acute exacerbation of schizophrenia. Rapid and effective control of agitation is an important early treatment goal.

Objectives:

The aim of this post-hoc analysis was to evaluate the efficacy of lurasidone in reducing agitation in patients with an acute exacerbation of schizophrenia.

Methods:

The analysis was performed on pooled data from 5 six-week, placebo-controlled trials in the subgroup of patients with an acute exacerbation of schizophrenia who met (n=773), or did not meet (n=754), criteria) for agitation (PANSS-Excited Component [EC] score ≥14 at baseline, Citrome, J Clin Psych 2007;68:1876-1885). Patients were randomized to fixed once-daily doses of lurasidone (40-160 mg).

Results:

The mean baseline PANSS-EC scores were similar for lurasidone vs. placebo in the high (16.7 vs. 16.8) and low (10.9 vs. 10.7) agitation subgroups. In the high agitation subgroup, treatment with lurasidone (vs. placebo) was associated with significantly greater improvement in PANSS-EC scores at days 3/4 (-2.0 vs. -1.3; p<0.001) and day 7 (-2.6 vs. -1.8; p<0.001). At week 6 endpoint, improvement on lurasidone vs. placebo was greater in the high vs. low agitation groups on the PANSS-EC score (effect size, 0.43 vs. 0.31), and comparable on the PANSS total score (effect size, 0.57 vs. 0.58).

Conclusions:

In this pooled post-hoc analysis, treatment with lurasidone significantly reduced agitation by day 3/4 in patients hospitalized with an acute exacerbation of schizophrenia. The magnitude of improvement at week 6 was similar in both the high and low agitation groups.

Type
EPW01 - Schizophrenia 1
Copyright
Copyright © European Psychiatric Association 2014
Submit a response

Comments

No Comments have been published for this article.