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Efficacy and tolerability of extended release quetiapine fumarate (quetiapine XR) monotherapy in patients with generalised anxiety disorder: an analysis of pooled data from three 8‐week placebo‐controlled studies
Author(s) -
Stein Dan J.,
Bandelow Borwin,
Merideth Charles,
Olausson Bengt,
Szamosi Johan,
Eriksson Hans
Publication year - 2011
Publication title -
human psychopharmacology: clinical and experimental
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.461
H-Index - 78
eISSN - 1099-1077
pISSN - 0885-6222
DOI - 10.1002/hup.1256
Subject(s) - quetiapine , tolerability , placebo , clinical global impression , pittsburgh sleep quality index , medicine , hamilton anxiety rating scale , quetiapine fumarate , adverse effect , nausea , somnolence , anxiety , insomnia , atypical antipsychotic , psychology , anesthesia , psychiatry , antipsychotic , sleep quality , pathology , schizophrenia (object oriented programming) , alternative medicine
Objective Prospectively planned pooled analysis evaluating efficacy and tolerability of acute quetiapine XR monotherapy in generalised anxiety disorder. Methods Data from three 10‐week, randomised, double‐blind, placebo‐controlled studies of similar design were analysed. Results At Week 8, Hamilton Anxiety Rating Scale (HAM‐A) total score significantly improved with quetiapine XR: least squares means change −13.31, p < 0.001 (50 mg/day, n = 452), −14.39, p < 0.001 (150 mg/day, n = 673) and −12.50, p < 0.05 (300 mg/day, n = 444) versus −11.30 placebo; significant ( p < 0.001, n = 665) improvements versus placebo were observed with each dose at Week 1. Significant improvements versus placebo at Week 8 are as follows: HAM‐A psychic symptom subscale, Montgomery‐Åsberg Depression Rating Scale total, Pittsburgh Sleep Quality Index global scores for all quetiapine XR doses; HAM‐A response and remission rates, HAM‐A somatic symptom subscale score, Clinical Global Impression‐Severity of Illness total score, % patients with Clinical Global Impression‐Improvement score ≤2 with quetiapine XR 50 and 150 mg/day; and Quality of Life Enjoyment and Satisfaction Questionnaire short form % maximum total score with quetiapine XR 150 mg/day. In the quetiapine XR 50, 150 and 300 mg/day and placebo groups, 13.2%, 16.5%, 24.0% and 5.4% of patients discontinued because of an adverse event, and 1.9%, 1.4%, 3.7% and 1.8% of patients experienced clinically significant changes in glucose. The most common adverse events with quetiapine XR included dry mouth, somnolence, sedation and constipation. Conclusion Quetiapine XR monotherapy reduced the symptoms of generalised anxiety disorder, with improvement from Week 1. Adverse events were consistent with the known tolerability profile of quetiapine. Copyright © 2011 John Wiley & Sons, Ltd.