Trials / Completed
CompletedNCT00776542
Bioequivalence Study of Minocycline 100mg Tablets Under Fasting Conditions
Single Dose Two-Way Crossover Fasted Bioequivalence Study of Minocycline 100 mg Capsules in Healthy Volunteers
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 28 (actual)
- Sponsor
- Ranbaxy Laboratories Limited · Industry
- Sex
- All
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study was to determine the bioequivalence of Minocycline formulations after administration of single doses to normal healthy subjects under fasted conditions. These data were to be evaluated statistically to determine if the products meet bioequivalence criteria.
Detailed description
The study was conducted as an open label, balanced, randomised, two-treatment, two-period, two-sequence, single-dose, crossover , bioequivalence study on minocycline comparing minocycline 100mg tablets of Ranbaxy pharmaceuticals inc with Minocin 100mg capsules of in healthy, adult, human, subjects under fasting conditions. A total of 28 non-smoking subjects (16 men and 12 women) were included in this study, of which 28 finished the study according to the protocol,
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Minocycline 100mg Tablets |
Timeline
- Start date
- 2002-10-01
- Primary completion
- 2002-11-01
- Completion
- 2003-01-01
- First posted
- 2008-10-21
- Last updated
- 2008-10-21
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00776542. Inclusion in this directory is not an endorsement.