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NCT00384033 · ClinicalTrials.gov registry record · Phase 3
Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) In The Treatment Of Major Depressive Disorder
A Phase 3 study, sponsored by Pfizer.
- Completed
- Registry status
- Phase 3
- Development phase
- 638
- Enrollment target
NCT00384033 is a Phase 3 study that has completed, run by Pfizer. The registered enrollment target is 638 participants.
The verdict
NCT00384033, a Phase 3 study, has completed, sponsored by Pfizer.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 638 participants
- Enrollment target
Study Summary
The primary purpose of this study is to evaluate the efficacy and safety of two doses of DVS SR (50 and 100 mg/day) in the treatment of adults with Major Depressive Disorder.
Interventions
- DRUG Placebo
- DRUG Desvenlafaxine Succinate Sustained-Release (DVS SR)
- DRUG Duloxetine 60 mg/day
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 638 participants |
| Start Date | 2006-09 |
| Est. Completion | 2007-09 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00384033
The ClinicalTrials.gov registry entry for NCT00384033 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 638 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 1,845 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.
NCT00384033 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00384033 about?
NCT00384033 is a clinical study titled "Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) In The Treatment Of Major Depressive Disorder". The primary purpose of this study is to evaluate the efficacy and safety of two doses of DVS SR (50 and 100 mg/day) in the treatment of adults with Major Depressive Disorder.
What is the current status of trial NCT00384033?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 638 participants. The study started on 2006-09. Estimated completion is 2007-09.
What interventions are being tested in trial NCT00384033?
The interventions under investigation include: Placebo (DRUG), Desvenlafaxine Succinate Sustained-Release (DVS SR) (DRUG), Duloxetine 60 mg/day (DRUG).
Who is sponsoring clinical trial NCT00384033?
This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.
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