Clinical trial
Study Evaluating the Effects of DVS SR and Duloxetine on the Pharmacokinetics of…
NCT00366652 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Completed
Key facts
| NCT number | NCT00366652 |
|---|---|
| Title | Study Evaluating the Effects of DVS SR and Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects |
| Official title | A Randomized, Open-Label, Crossover, Drug Interaction Study to Evaluate the Effects of DVS SR And Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects |
| Lead sponsor | Wyeth is now a wholly owned subsidiary of Pfizer, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Depression, Depressive Disorder, Major |
| Intervention type | Drug |
| Interventions | desvenlafaxine SR, desipramine, duloxetine |
| Enrollment | 20 |
| Start date | Sep 1, 2006 |
| Completion | Sep 1, 2006 |
| First posted | Aug 21, 2006 |
| Last update posted | May 28, 2007 |
| Countries | United States |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: