Clinical Trials Directory

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

TypeNameDescription
DRUGMinocycline 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.