drugset / Trial / NCT00630201

Extension to Safety and Efficacy of Probuphine in the Treatment of Opioid Dependence

NCT00630201

Phase 3 Completed 62 enrolled Titan Pharmaceuticals
NaSingle-groupOpen-labelTreatment

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.

Timeline

Start
2007-10
Primary completion
2009-02
Completion
2009-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Buprenorphine Other / unclassified 4 unknown Subcutaneous

Indications