Trials / Completed
CompletedNCT00366652
Study Evaluating the Effects of DVS SR and Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects
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
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 20 (estimated)
- Sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer · Industry
- Sex
- All
- Age
- 18 Years – 55 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the effects of multiple doses of DVS SR and duloxetine on the pharmacokinetics of a single dose of desipramine in healthy subjects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | desvenlafaxine SR | |
| DRUG | desipramine | |
| DRUG | duloxetine |
Timeline
- Start date
- 2006-09-01
- Completion
- 2006-09-01
- First posted
- 2006-08-21
- Last updated
- 2007-05-28
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00366652. Inclusion in this directory is not an endorsement.