Status:
COMPLETED
Study Evaluating DVS-233 SR and Venlafaxine ER in Adult Outpatients With Major Depressive Disorder
Lead Sponsor:
Wyeth is now a wholly owned subsidiary of Pfizer
Conditions:
Major Depressive Disorder
Eligibility:
All Genders
18-75 years
Phase:
PHASE3
Brief Summary
To compare the antidepressant efficacy and safety of DVS-233 SR versus placebo in adult outpatients with MDD.
Eligibility Criteria
Inclusion
- Outpatients.
- Sexually active individuals participating in the study must use a medically acceptable form of contraception during the study and for at least 15 days after the last dose of test article
- Subjects must have a primary diagnosis of major depressive disorder
Exclusion
- Treatment with DVS-233 SR at any time in the past
- Treatment with venlafaxine (immediate release \[IR\] or ER) within 90 days of study day 1
- Known hypersensitivity to venlafaxine (IR or ER)
Key Trial Info
Start Date :
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 1 2005
Estimated Enrollment :
369 Patients enrolled
Trial Details
Trial ID
NCT00087737
End Date
May 1 2005
Last Update
August 19 2009
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