Study Evaluating the Effects of DVS SR and Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects

Completed · Phase 3

Conditions studied: Depression, Depressive Disorder, Depressive Disorder, Major

In brief

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.

Key facts

Study ID

NCT00366652

Run by

Wyeth is now a wholly owned subsidiary of Pfizer

People needed

20

Starts

2006-09-01

Expected to finish

2006-09-01

Last updated by the study team

2007-05-28

Who can join

Age: 18 and older, up to 55. Sex: any. Healthy volunteers: accepted.

Where it is running

• Study site — Neptune City, New Jersey, United States

Full record on ClinicalTrials.gov

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