NCT00658762

A 10-week Study Evaluating the Efficacy and Safety of PD 0332334 for the Treatment of Generalized Anxiety Disorder (3)

A Phase 3, Randomized, Double-Blind, Parallel Group, 10-Week Placebo Controlled Fixed Dose Study of PD 0332334 and Paroxetine Evaluating the Efficacy and Safety of PD 0332334 for the Treatment of Generalized Anxiety Disorder

• Status: Terminated
• Phase: Phase 3
• Study type: Interventional
• Enrollment: 286 (actual)
• Sponsor: Pfizer · Industry
• Sex: All
• Age: 18 Years – 65 Years
• Healthy volunteers: Not accepted

Summary

This is a 10-week trial that evaluates the efficacy and safety of PD 0332334 in subjects ages 18 and older with generalized anxiety disorder.

Detailed description

Termination reason: On February 23rd 2009, a decision to terminate further development for PD 0332334 was communicated to investigators in this study. The decision to terminate this study was not based on any safety concerns.

Conditions

• Generalized Anxiety Disorder

Interventions

Type	Name	Description
DRUG	PD 0332334	Capsules, oral, 225 mg BID, 8 weeks, with 2 week taper
DRUG	PD 0332334	Capsules, oral, 300 mg BID, 8 weeks, with 2 week taper
DRUG	paroxetine	Capsules, oral, 20 mg q am, 8 weeks, with 2 week taper
DRUG	Placebo	Capsules, oral, BID, 8 weeks, with 2 week taper

Timeline

• Start date: 2008-05-01
• Primary completion: 2009-04-01
• Completion: 2009-04-01
• First posted: 2008-04-15
• Last updated: 2012-11-16

Locations

28 sites across 2 countries: United States, Hungary