Safety, Efficacy and Tolerability of Vilazodone in (GAD) Generalized Anxiety Disorder
| Status: | Completed |
|---|---|
| Conditions: | Anxiety, Psychiatric |
| Therapuetic Areas: | Psychiatry / Psychology |
| Healthy: | No |
| Age Range: | 18 - 70 |
| Updated: | 5/5/2014 |
| Start Date: | April 2013 |
| End Date: | July 2014 |
| Contact: | Sandra Beaird, Pharm.D |
| Email: | FRXClinTrials@frx.com |
| Phone: | 1-800-678-1605 |
A Double-Blind, Placebo-Controlled, Flexible-Dose Study of Vilazodone in Patients With Generalized Anxiety Disorder.
The purpose of this study is to evaluate the efficacy, safety, and tolerability of
vilazodone relative to placebo in the treatment of generalized anxiety disorder (GAD).
vilazodone relative to placebo in the treatment of generalized anxiety disorder (GAD).
Inclusion Criteria:
- Male or female outpatient, 18-70 years of age
- Currently meet the Diagnostic and Statistical Manual of Mental Disorders, Fourth
Edition, Text Revision (DSM-IV-TR) criteria for Generalized Anxiety Disorder
- Minimum score of 20 on Hamilton Rating Scale for Anxiety
Exclusion Criteria:
- Women who are pregnant or who will be breastfeeding during the study
- Patients with a history of:
1. Any manic or hypomanic or mixed episode, including bipolar disorder and
substance-induced manic, hypomanic or mixed episode
2. Any depressive episode with psychotic or catatonic features
3. Panic disorder with or without agoraphobia
We found this trial at
36
sites
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