Study of Two Formulations of Buprenorphine HCl in Opioid-dependent Subjects on Buprenorphine Maintenance Therapy (Study P04451) (COMPLETED)

Opioid Dependency Clinical Trial

Official title:
Evaluation of Preference Between Two Buprenorphine Sublingual Formulations, After a Switch From the Marketed Tablet (Subutex®) to the New Fast Dissolving Tablet (FDT), in Opioid-dependent Patients With Buprenorphine Maintenance Therapy

Status Completed

Clinical Trial Summary

This is a multi-center, open-label, preference study of two sublingual formulations of buprenorphine HCl, in opioid-dependent patients on buprenorphine maintenance therapy. The objectives of this study are to evaluate the overall preference between two buprenorphine sublingual formulations, after a switch from the marketed tablet (Subutex®) to the new fast dissolving tablet (FDT), in opioid-dependent patients with buprenorphine 8 mg or 16 mg daily maintenance therapy.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Opioid Dependency

Clinical Trial Details

NCT number	NCT01075971
Study type	Interventional
Source	Indivior Inc.
Contact
Status	Completed
Phase	Phase 2
Start date	September 2005
Completion date	November 2005

View Details

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