Trials / Completed
CompletedNCT00236015
A 10-Week Efficacy and Safety Study of Gabitril in the Treatment of Adults With Generalized Anxiety Disorder
A 10-Week, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Gabitril at 4, 8, and 12 mg/Day in the Treatment of Adults With Generalized Anxiety Disorder.
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 880 (planned)
- Sponsor
- Cephalon · Industry
- Sex
- All
- Age
- 18 Years – 64 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the safety and efficacy of an investigational anti-anxiety medication relative to placebo in patients with generalized anxiety disorder (GAD).
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Gabitril |
Timeline
- Start date
- 2004-11-01
- Completion
- 2006-03-01
- First posted
- 2005-10-12
- Last updated
- 2014-05-09
Locations
54 sites across 2 countries: United States, Canada
Source: ClinicalTrials.gov record NCT00236015. Inclusion in this directory is not an endorsement.