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Safety and Efficacy Study of IPX159 in Restless Legs Syndrome (RLS)

Restless Legs Syndrome Clinical Trial

Official title:
A Randomized, Double-Blind, Placebo-Controlled Safety and Efficacy Study of IPX159 in the Treatment of Moderate to Severe Restless Legs Syndrome (RLS)

Clinical Trial Summary

The purpose of this study is to determine whether IPX159 is safe and effective in treating symptoms of RLS in subjects with Restless Legs Syndrome.

Clinical Trial Description

IPX159 was developed as an extended release formulation to reduce the fluctuation in nefopam concentration compared to IR and to reduce the incidence of peak or rate related side effects. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01521663
Study type Interventional
Source IMPAX Laboratories, Inc.
Contact
Status Completed
Phase Phase 2
Start date November 2011
Completion date February 2013
View Details
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