Study Evaluating Desvenlafaxine Sustained-Release (DVS-SR) in Adult Outpatients With Major Depressive Disorder

Completed · Phase 3 · Has a placebo group

Conditions studied: Major Depressive Disorder

In brief

The purpose of this study is to compare the antidepressant efficacy, safety, and tolerability of DVS-SR in subjects receiving daily doses of 50 mg or 100 mg of DVS-SR versus subjects receiving placebo.

Key facts

Study ID

NCT00277823

Run by

Wyeth is now a wholly owned subsidiary of Pfizer

People needed

480

Starts

2006-02-01

Expected to finish

2007-01-01

Last updated by the study team

2007-12-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Clinical diagnosis of major depressive disorder
• Must be able to swallow tablets
• Must be at least 18 years of age.

You may not qualify if…

• Clinical diagnosis of other psychiatric disorders
• Significant risk of suicide
• Unstable medical conditions.

Where it is running

• Study site — Beverly Hills, California, United States
• Study site — Northridge, California, United States
• Study site — Farmington, Connecticut, United States
• Study site — Washington D.C., District of Columbia, United States
• Study site — Miami, Florida, United States
• Study site — St. Petersburg, Florida, United States
• Study site — Marietta, Georgia, United States
• Study site — Smyrna, Georgia, United States
• Study site — Libertyville, Illinois, United States
• Study site — New Orleans, Louisiana, United States
• Study site — Farmington Hills, Michigan, United States
• Study site — Clementon, New Jersey, United States
• Study site — Moorestown, New Jersey, United States
• Study site — New York, New York, United States
• Study site — New York, New York, United States
• Study site — Dayton, Ohio, United States
• Study site — Toledo, Ohio, United States
• Study site — Oklahoma City, Oklahoma, United States
• Study site — Portland, Oregon, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Charleston, South Carolina, United States
• Study site — Columbia, South Carolina, United States
• Study site — Salt Lake City, Utah, United States
• Study site — Seattle, Washington, United States
• Study site — Brown Deer, Wisconsin, United States

Full record on ClinicalTrials.gov

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