Trials / Completed
CompletedNCT00542685
A 10-Week Study Evaluating the Efficacy And Safety of PD 0332334 for the Treatment of Generalized Anxiety Disorder
A Phase 3, Randomized, Double-Blind, Placebo Controlled, Parallel Group, 10-Week Study Evaluating the Efficacy And Safety of PD 0332334 for the Treatment of Generalized Anxiety Disorder
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 551 (actual)
- Sponsor
- Pfizer · Industry
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This study will evaluate the efficacy and safety of PD 0332334 for the treatment of generalized anxiety disorder.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | PD 0332334 | Capsules, oral, 300 mg BID, 8 weeks with 2 week taper. |
| DRUG | Placebo | Capsules, oral, placebo BID, 8 weeks with 2 week taper. |
| DRUG | PD 0332334 | Capsules, oral, 225 mg BID, 8 weeks with 2 week taper. |
| DRUG | PD 0332334 | Capsules, oral, 175 mg BID, 8 weeks with 2 week taper. |
Timeline
- Start date
- 2007-10-01
- Primary completion
- 2008-12-01
- Completion
- 2008-12-01
- First posted
- 2007-10-11
- Last updated
- 2012-11-16
Locations
43 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT00542685. Inclusion in this directory is not an endorsement.