Trials / Completed
CompletedNCT01511770
Bioavailability Study of Fluconazole Tablets 200 mg Under Fasting Conditions
Comparative,Randomized,Single-dose,2-way Crossover Bioavailability Study of Dr.Reddy's Laboratories Limited Fluconazole Tablets 200 mg and PFIZER (DIFLUCAN) 200 MG in Healthy Males Under Fasting Condition.
- Status
- Completed
- Phase
- Phase 1
- Study type
- Interventional
- Enrollment
- 17 (actual)
- Sponsor
- Dr. Reddy's Laboratories Limited · Industry
- Sex
- Male
- Age
- 18 Years – 45 Years
- Healthy volunteers
- Accepted
Summary
The objective of this study was an open-label, randomized, 2-way crossover to compare the single-dose relative bioavailability of Dr. Reddy's Laboratories, Ltd. and Pfizer (Diflucan®) 200 mg fluconazole tablets under fasting conditions.
Detailed description
Detailed Description : The study was conducted as an open-label, randomized, single-dose, 2-way crossover, relative bioavailability study performed on 18 healthy adult male volunteers. A total of 17 subjects completed the clinical phase of the study. In each period, subjects were housed from the morning dosing until after the 72-hour blood draw. Single oral 200 mg doses were separated by a washout period of 21 days.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Fluconazole | Fluconazole Tablets, 200 mg |
| DRUG | Fluconazole | Fluconazole 200 mg tablets |
Timeline
- Start date
- 2002-08-01
- Primary completion
- 2002-08-01
- Completion
- 2002-09-01
- First posted
- 2012-01-19
- Last updated
- 2012-01-19
Locations
1 site across 1 country: Canada
Source: ClinicalTrials.gov record NCT01511770. Inclusion in this directory is not an endorsement.