Clinical Trials Directory

Trials / Completed

CompletedNCT00000320

Buprenorphine Formulation Comparison: Sublingual Tablet vs. Solution - 1

Buprenorphine Formulation Comparison: Sublingual Tablet vs. Solution

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
120 (actual)
Sponsor
National Institute on Drug Abuse (NIDA) · NIH
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare subject response to liquid vs. tablet formulations, to assess bioequivalency of liquid vs. tablet, to compare subject preference, and to evaluate if dose response curve for tablet is equal to liquid form."

Detailed description

1\) Compare subjects response to liquid vs tablet formulation 2) Assess bioequivalency of liquid vs tablet 3)Compare subject preference 4) Evaluate if dose response curve for tablet = to liquid form

Conditions

Interventions

TypeNameDescription
DRUGBuprenorphine formulation: liquid vs. tabletrandom assignment to liquid buprenorphine or tablet buprenorphine

Timeline

Start date
1997-10-01
Primary completion
1999-08-01
Completion
1999-08-01
First posted
1999-09-21
Last updated
2017-01-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00000320. Inclusion in this directory is not an endorsement.