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
| Type | Name | Description |
|---|---|---|
| DRUG | Buprenorphine formulation: liquid vs. tablet | random 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.