Safety and Efficacy of F2695 SR in Major Depressive Disorder



Status:Archived
Conditions:Depression, Major Depression Disorder (MDD)
Therapuetic Areas:Psychiatry / Psychology, Pulmonary / Respiratory Diseases
Healthy:No
Age Range:Any
Updated:7/1/2011
Start Date:September 2009

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Trial Summary
Trial Overview
Inclusion Criteria

A Double-blind, Placebo-Controlled, Fixed-Dose Study of F2695 SR in Patients With Major Depressive Disorder


The purpose of this study is to evaluate the efficacy, safety, and tolerability of F2695 SR
fixed doses versus placebo in the treatment of outpatients with major depressive disorder.



We found this trial at
18
sites
Forest Investigative Site
Wichita, Kansas 67206
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Wichita, KS
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Forest Investigative Site
Baltimore, Maryland 21285
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Baltimore, MD
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Sheppard Pratt Health System
Baltimore, Maryland 21285
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Baltimore, MD
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Forest Investigative Site
Bellevue, Washington 98007
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Bellevue, WA
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Forest Investigative Site
Boca Raton, Florida 33432
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Boca Raton, FL
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Forest Investigative Site
Chicago, Illinois 60608
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Chicago, IL
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Forest Investigative Site
Cleveland, Ohio 44106
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Cleveland, OH
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Forest Investigative Site
Cromwell, Connecticut 06416
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Cromwell, CT
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Forest Investigative Site
Dallas, Texas 75230
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Dallas, TX
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Forest Investigative Site
Denver, Colorado 80239
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Denver, CO
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Lincoln Medical Center
Lincoln, Nebraska 68506
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Lincoln, NE
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Forest Investigative Site
Lincoln, Rhode Island 02865
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Lincoln, RI
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Forest Investigative Site
Manhasset, New York 11030
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Manhasset, NY
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Forest Investigative Site
Memphis, Tennessee 38119
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Memphis, TN
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Forest Investigative Site
Pittsburgh, Pennsylvania 15203
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Pittsburgh, PA
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Forest Investigative Site
Portland, Oregon 97210
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Portland, OR
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Forest Investigative Site
Raleigh, North Carolina 27607
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Raleigh, NC
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Forest Investigative Site
Sacramento, California 95817
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Sacramento, CA
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