Trials / Completed
CompletedNCT00601315
Bioequivalency Study of Clarithromycin Tablets Under Fasting Conditions
A Single Dose, Two-Treatment, Two-Period, Two-Sequence Crossover Bioequivalency Study of 250 mg Clarithromycin Tablets Under Fasting Conditions
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 40 (actual)
- Sponsor
- Roxane Laboratories · Industry
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The objective of this study was the bioequivalence of a potential generic 250 mg clarithromycin tablet formulation compared with Abbott Laboratories 250 mg clarithromycin tablet, Biaxin® following a single 250 mg dose, administered in the fasted state.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Clarithromycin |
Timeline
- Start date
- 2003-04-01
- Primary completion
- 2003-05-01
- Completion
- 2003-05-01
- First posted
- 2008-01-28
- Last updated
- 2018-01-23
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00601315. Inclusion in this directory is not an endorsement.