drugset / Trial / NCT01050218

Study Evaluating the Long-Term Safety of Desvenlafaxine Succinate Sustained-Release (DVS SR) in Subjects With Pain Associated With Diabetic Peripheral Neuropathy

NCT01050218

Phase 3 Terminated 237 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of the study is to learn if long-term treatment with DVS SR is safe for treating the pain and other symptoms associated with diabetic peripheral neuropathy.

Timeline

Start
2006-07
Primary completion
2009-01
Completion
2009-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Desvenlafaxine Other / unclassified 100 mg
Subject Desvenlafaxine Other / unclassified 200 mg
Subject Desvenlafaxine Other / unclassified 400 mg