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Extension to Safety and Efficacy of Probuphine in the Treatment of Opioid Dependence — PRO-807  

Opioid Dependence Clinical Trial

Official title:
An Open-Label, Multi-Center Extension Study Of Probuphine in Patients With Opioid Dependence

Clinical Trial Summary

Buprenorphine (BPN) is an approved treatment for opioid dependence; however, in taking oral tablets, patients experience withdrawal and cravings when the variable BPN levels in the blood are low. Probuphine (buprenorphine implant) is an implant placed just beneath the skin that contains BPN. It is designed to provide 6 months of stable BPN blood levels. This study will test the safety and efficacy of Probuphine in the treatment of patient with opioid dependence. Patients who have completed 24 weeks of treatment in the Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study of Probuphine in Patients with Opioid Dependence, will be re-treated with Probuphine over an additional 24 weeks.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00630201
Study type Interventional
Source Titan Pharmaceuticals
Contact
Status Completed
Phase Phase 3
Start date October 2007
Completion date February 2009
View Details
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