drugset / Trial / NCT00755807

Duloxetine for Multiple Sclerosis Pain

NCT00755807

Phase 3 Completed 239 enrolled Eli Lilly and Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study is designed to primarily assess the efficacy and safety of duloxetine 60-120 mg once daily (QD) compared with placebo on the reduction of pain severity in participants with central neuropathic pain due to Multiple Sclerosis.

Timeline

Start
2008-10
Primary completion
2010-08
Completion
2010-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Duloxetine Small molecule 60 mg Oral
Subject Duloxetine Small molecule 90 mg Oral
Subject Duloxetine Small molecule 120 mg Oral

Indications