Clinical Trials Directory

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

TypeNameDescription
DRUGdesvenlafaxine SR
DRUGdesipramine
DRUGduloxetine

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.