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Clinical Trial Summary

Primary Objective: To compare the bioavailability of a single dose of fluconazole 150 mg capsules (Test product) with the bioavailability of a single dose of Diflucan™ capsules, 150 mg (Reference) administered under fasting conditions in order to assess bioequivalence Secondary Objectives: To assess safety and tolerability in form of adverse events and clinical parameters (systolic/diastolic blood pressure, pulse rate, body temperature, physical examination, electrocardiogram, clinical laboratory testing, and overall tolerability) and to assess further pharmacokinetic parameters of fluconazole


Clinical Trial Description

Clinical pharmacology ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03929861
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 1
Start date July 31, 2012
Completion date September 10, 2012

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