5
Participants
Start Date
October 31, 2008
Primary Completion Date
February 28, 2009
Study Completion Date
April 30, 2010
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.
Paroxetine
FDA Approved medication for generalized anxiety disorder, oral tablet, at 20mg, once daily for 8 weeks and then 2 weeks of dose tapering.
Placebo
inactive substance, oral tablet, once per day, for 10 weeks.
Cedars-Sinai Medical Center Department of Psychiatry and Behavioral Neurosciences, Los Angeles
Collaborators (1)
Pfizer
INDUSTRY
Cedars-Sinai Medical Center
OTHER