Clinical Trials Directory

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

TypeNameDescription
DRUGPD 0332334Capsules, oral, 300 mg BID, 8 weeks with 2 week taper.
DRUGPlaceboCapsules, oral, placebo BID, 8 weeks with 2 week taper.
DRUGPD 0332334Capsules, oral, 225 mg BID, 8 weeks with 2 week taper.
DRUGPD 0332334Capsules, 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.