JPRN-jRCT2080221669UnknownPhase 3
An open-label long-term extension study to evaluate the safety and efficacy of venlafaxine ER in adult outpatients with major depressive disorder(B2411264)
Trial Snapshot
- Phase
- Phase 3
- Sponsor
- Pfizer Japan Inc.
- Enrollment
- 50
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- >= 20age old to ot applicable (—)
- Sex
- All
Inclusion Criteria
- •Outpatients who have completed 8 weeks double-blind study (B2411263), without major protocol violations or tolerability concerns in the opinion of the investigator.
Exclusion Criteria
- •-Clinically important abnormalities on baseline (Week 8 of the double-blind study) physical examination, or any unresolved clinically significant abnormalities on electrocardiogram (ECG), laboratory test results, or vital signs recorded before Week 8 in the previous double-blind study.
- •-Significant risk of suicide based on clinical judgment.
- •-Use of prohibited treatments
Investigators
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