The objective is to evaluate the efficacy and safety of two doses of SSR149415 (250 mg and 100 mg twice daily) compared to placebo and paroxetine 20 mg once daily in outpatients with generalized anxiety disorder
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
325
Oral administration (capsules of 50 and 100 mg)
Oral administration (capsules)
Oral administration (capsules)
Sanofi-Aventis Administrative Office
Bridgewater, New Jersey, United States
Change from baseline to Day 56 in the 14-item Hamilton Anxiety Rating Scale (HAM-A) total score.
Time frame: 8 weeks
Change from baseline to Day 56 in the Clinical Global Impression (CGI) Severity of Illness score.
Time frame: 8 weeks
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