drugset / Trial / NCT00483730

Actovegin® Versus Placebo in Patients With Diabetic Polyneuropathy (AV-007-IM)

NCT00483730

Phase 3 Completed 569 enrolled Nycomed
RandomizedParallel-groupDouble-blindTreatment

Summary

To assess clinical efficacy and safety of Actovegin in type 2 diabetic patients with symptomatic diabetic peripheral polyneuropathy after 250 ml i.v. infusions once daily for 20 days followed by oral treatment 600 mg × 3 daily for 140 days.

Timeline

Start
2006-12
Primary completion
2008-05
Completion
2008-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Actovegin Protein / enzyme biologic 600 mg Intravenous