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NCT00329147 · ClinicalTrials.gov registry record · Phase 3
Study Evaluating the Effects of DVS SR and Paroxetine on the Pharmacokinetics of Desipramine in Healthy Subjects
A Phase 3 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- Completed
- Registry status
- Phase 3
- Development phase
- 20
- Enrollment target
NCT00329147 is a Phase 3 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 20 participants.
The verdict
NCT00329147, a Phase 3 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 20 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the effects of multiple doses of DVS SR and paroxetine on the pharmacokinetics of a single dose of desipramine in healthy subjects.
Interventions
- DRUG paroxetine
- DRUG desipramine
- DRUG desvenlafaxine SR
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2006-05 |
| Est. Completion | 2006-06 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00329147
The ClinicalTrials.gov registry entry for NCT00329147 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which paroxetine is the first listed.
NCT00329147 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00329147 about?
NCT00329147 is a clinical study titled "Study Evaluating the Effects of DVS SR and Paroxetine on the Pharmacokinetics of Desipramine in Healthy Subjects". The purpose of this study is to evaluate the effects of multiple doses of DVS SR and paroxetine on the pharmacokinetics of a single dose of desipramine in healthy subjects.
What is the current status of trial NCT00329147?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 20 participants. The study started on 2006-05. Estimated completion is 2006-06.
What interventions are being tested in trial NCT00329147?
The interventions under investigation include: paroxetine (DRUG), desipramine (DRUG), desvenlafaxine SR (DRUG).
Who is sponsoring clinical trial NCT00329147?
This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.
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