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Efficacy and Safety Study of SLC022 in Treating Pain Associated With Post Herpetic Neuralgia

Postherpetic Neuralgia Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study Evaluating the Efficacy and Tolerability of Oral SLC022 300 mg TID, a Glial Cell Modulating Agent, Versus Placebo in the Treatment of Post Herpetic Neuralgia

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of SLC022 in treating pain associated with post-herpetic neuralgia (PHN) in recently diagnosed patients.

Clinical Trial Description

This study will enroll subjects with established PHN, a stable pain intensity and that meet all other eligibility criteria. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00813826
Study type Interventional
Source Solace Pharmaceuticals
Contact
Status Active, not recruiting
Phase Phase 2
Start date January 2009
Completion date November 2009
View Details
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