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Clinical Trials/NCT00087737
NCT00087737
Completed
Phase 3

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Flexible-Dose Study of DVS-233 SR and Venlafaxine ER in Adult Outpatients With Major Depressive Disorder

Wyeth is now a wholly owned subsidiary of Pfizer0 sites369 target enrollmentJuly 16, 2004
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ConditionsMajor Depressive Disorder
DrugsDVS-233 SRVenlafaxine ER

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Major Depressive Disorder
Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Enrollment
369
Status
Completed
Last Updated
16 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

To compare the antidepressant efficacy and safety of DVS-233 SR versus placebo in adult outpatients with MDD.

Registry
clinicaltrials.gov
Start Date
July 16, 2004
End Date
May 2005
Last Updated
16 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer

Eligibility Criteria

Inclusion Criteria

  • •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 Criteria

  • •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)

Outcomes

Primary Outcomes

Not specified

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