Fixed Dose Study of PD 0332334 and Paroxetine for the Treatment of Generalized Anxiety Disorder

PHASE3TerminatedINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

October 31, 2008

Primary Completion Date

February 28, 2009

Study Completion Date

April 30, 2010

Conditions
Anxiety Disorders
Interventions
DRUG

No drug name provided by Sponsor; drug referenced as PD 0332334

Experimental study drug for generalized anxiety disorder, oral tablet, at a total daily dose of 450mg or 600mg, twice daily for 8 weeks and then 2 weeks of dose tapering.

DRUG

Paroxetine

FDA Approved medication for generalized anxiety disorder, oral tablet, at 20mg, once daily for 8 weeks and then 2 weeks of dose tapering.

DRUG

Placebo

inactive substance, oral tablet, once per day, for 10 weeks.

Trial Locations (1)

90048

Cedars-Sinai Medical Center Department of Psychiatry and Behavioral Neurosciences, Los Angeles

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Pfizer

INDUSTRY

lead

Cedars-Sinai Medical Center

OTHER