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Clinical Trial Summary

This is a randomized, double blind, placebo controlled study in opioid dependent subjects. Subjects meeting entry criteria will be treated with multiple doses of B-BNX or B-Placebo, with non-responders rescued within 6 hours. Open treatment B-BNX will be administered as follow-up therapy. Clinical efficacy assessments include the clinical opioid withdrawal scale (COWS), subject-rated assessments, and a urine drug screen.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01713803
Study type Interventional
Source BioDelivery Sciences International
Contact
Status Withdrawn
Phase Phase 3
Completion date May 1, 2017

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