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Crossover Study of CNV1014802 in Subjects With Neuropathic Pain From Lumbosacral Radiculopathy

Lumbosacral Radiculopathy Clinical Trial

Official title:
A Randomized, Double Blind, Cross-over Study to Evaluate the Safety and Efficacy of CNV1014802 in Subjects With Neuropathic Pain From Lumbosacral Radiculopathy

Clinical Trial Summary

The study is a randomized, double blind, cross-over study to evaluate the safety and efficacy of CNV1014802 in subjects with neuropathic pain from lumbosacral radiculopathy.

Clinical Trial Description

The study consists of two treatment periods of 22 days with randomized CNV1014802 350mg or placebo administered twice daily. In addition, single blind placebo will be administered during a two week run-in, a two week wash-out period between the two treatment periods, and a one week run-out phase.

This study was previously posted by Convergence Pharmaceuticals, Ltd., which has been acquired by Biogen. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01561027
Study type Interventional
Source Biogen
Contact
Status Completed
Phase Phase 2
Start date April 30, 2011
Completion date August 31, 2012
View Details
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