Clinical Trials Directory

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

TypeNameDescription
DRUGFluconazoleFluconazole Tablets, 200 mg
DRUGFluconazoleFluconazole 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.