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A Bioavailability and Safety Study of Probuphine Versus Sublingual Buprenorphine in Patients With Opioid Dependence (PRO-810)

This study has been terminated.
(This study was terminated for reasons not related to efficacy or safety)
Sponsor:
Information provided by (Responsible Party):
Braeburn Pharmaceuticals
ClinicalTrials.gov Identifier:
NCT00768482
First received: October 7, 2008
Last updated: June 12, 2017
Last verified: June 2017
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been terminated.
  Study Completion Date: December 2008
  Primary Completion Date: December 2008 (Final data collection date for primary outcome measure)
  Certification or Request for Extension to Delay Results Received: January 5, 2011