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Study Evaluating Long-Term Safety of Effexor XR in Patients With Major Depression.

Phase 3
Completed
Conditions
Depression
Registration Number
NCT00225524
Lead Sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Brief Summary

Phase III long-term safety study of Effexor XR in patients with major depression.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Patients who complete the Phase III double-blind study (Protocol Number 0600B1-816)
Exclusion Criteria
  • Patients with schizophrenia or any other psychotic disorder
  • Patients with history or presence of bipolar disorder

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Incidence of adverse events
Secondary Outcome Measures
NameTimeMethod
Quantitative data for laboratory data

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