Trials / Completed
CompletedNCT00775918
Bioequivaelnce Study of Doxycycline Monohydrate 100mg Tablets Under Fed Conditions
Single Dose Two-Way Crossover Fed Bioequivalence Study of Doxycycline Monohydrate 100 mg Tablets in Healthy Volunteers
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 32 (actual)
- Sponsor
- Ranbaxy Laboratories Limited · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study was to determine the bioequivalence of Doxycycline monohydrate formulations after administration of single doses to normal healthy subjects under fed 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 Doxycycline monohydrate comparing Doxycycline monohydrate 100mg tablets of Ranbaxy Pharmaceuticals Inc with Adoxa ® 100 mg tablets of Bradley Pharmaceuticals Inc. in healthy, adult, human, subjects under fed conditions. A total of 32 non-smoking subjects (21 men and 11 women) were included in this study, of which 32 finished the study according to the protocol.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Doxycycline monohydrate 100mg tablets | Bioequiavelnce Doxycycline monohydrate 100mg tablets fed conditions |
Timeline
- Start date
- 2005-06-01
- Primary completion
- 2005-06-01
- Completion
- 2005-08-01
- First posted
- 2008-10-20
- Last updated
- 2008-10-20
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT00775918. Inclusion in this directory is not an endorsement.