drugset / Trial / NCT00322595

Efficacy and Safety Study of Seroquel SR in the Treatment of Generalized Anxiety Disorder

NCT00322595 ↗

Phase 3 Completed 800 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to evaluate the efficacy of (SEROQUEL SR™ ) quetiapine fumarate sustained-release (SR) compared to placebo in the treatment of anxiety symptoms in patients with generalized anxiety disorder (GAD). PLEASE NOTE: Seroquel SR and Seroquel XR refer to the same formulation. The SR designation was changed to XR after consultation with FDA.

Timeline

Start
2006-05
Primary completion
—
Completion
2007-05

Outcome

Met primary endpoint

paper At week 8, all active agents produced significant improvements in HAMA total and psychic subscale scores vs. placebo; PMID 19691907 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Paroxetine Small molecule 20 mg —
Subject Quetiapine Small molecule 50 mg —
Subject Quetiapine Small molecule 150 mg —