Safety & Efficacy Study of Quetiapine Fumarate (SEROQUEL®) vs. Placebo & Active Control in Generalized Anxiety Disorder

• Status: Completed
• Trial end date: 2007-09-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to demonstrate that quetiapine SR (SEROQUEL®) is efficacious and safe in the acute treatment of patients with Generalized Anxiety Disorder.

PLEASE NOTE: Seroquel SR and Seroquel XR refer to the same formulation. The SR designation was changed to XR after consultation with FDA.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: AstraZeneca
• Treatments: Citalopram; Quetiapine Fumarate

Criteria

Inclusion Criteria:

• Patient has a documented clinical diagnosis of Generalized Anxiety Disorder.

• Be able to understand and comply with the requirements of the study.

• Able to understand and provide written informed consent

Exclusion Criteria:

• Patients (female) must not be pregnant or lactating

• Current or past diagnosis of stroke or transient ischemic attack (TIA).