drugset / Trial / NCT00760955

Efficacy and Safety of TAK-583 in Subjects With Diabetic Peripheral Neuropathy

NCT00760955 ↗

Phase 2 Completed 338 enrolled Takeda
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the safety and effectiveness of TAK-583, once daily (QD), in the treatment of neuropathy caused by diabetes mellitus.

Timeline

Start
2006-09
Primary completion
2008-02
Completion
2008-02

Drugs

EvaluationDrugModalityDoseRoute
Subject TAK-583 Unknown 5 mg Oral
Subject TAK-583 Unknown 50 mg Oral
Subject TAK-583 Unknown 100 mg Oral