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Longterm Safety Study of BEMA Buprenorphine in Subjects With Chronic Pain

Pain Clinical Trial

Official title:
A 52-Week, Open Label, Longterm Treatment Evaluation of the Safety and Efficacy of BEMA® Buprenorphine in Subjects With Moderate to Severe Chronic Pain

Clinical Trial Summary

The purpose of this study is to determine whether BEMA Buprenorphine is safe in the treatment of chronic pain.

Clinical Trial Description

This is an open label study of up to approximately 52 weeks duration to assess the safety and effectiveness of BEMA Buprenorphine in the management of moderate to severe chronic pain.

BEMA Buprenorphine is an oral transmucosal form of the opioid analgesic, buprenorphine hydrochloride, intended for application to the buccal mucosa. Buprenorphine is a synthetic opioid that is classified as a partial μ-receptor agonist and a Schedule III controlled substance in the United States. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01298765
Study type Interventional
Source BioDelivery Sciences International
Contact
Status Completed
Phase Phase 3
Start date March 2011
Completion date August 2012
View Details
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