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Clinical Trial Summary

A randomized, single-dose, two-way crossover study to evaluate bioequivalence of two formulations of micafungin (50 mg/vial) after intravenous infusion of 50 mg micafungin in healthy volunteers under fasting conditions


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05496725
Study type Interventional
Source Yung Shin Pharm. Ind. Co., Ltd.
Contact
Status Completed
Phase Phase 4
Start date January 6, 2022
Completion date July 28, 2022

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