drugset / Trial / NCT00191685

Duloxetine in the Treatment of Melancholic Depression

NCT00191685

Phase 3 Completed 200 enrolled Eli Lilly and Company
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the optimal treatment strategy for MDD patients with melancholic features who do not respond to a standard daily dose. This study will allow investigators to mimic standard clinical practice. During the first 2 weeks of treatment, clinical evaluation of individual patient tolerability and efficacy will enable the dose of duloxetine to be adjusted. Patients allocated to the Flex group may have their daily dose of duloxetine adjusted in the attempt to elicit a clinical response.

Timeline

Start
2004-05
Primary completion
Completion
2005-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Duloxetine Small molecule