Evaluate Bioequivalence of Burotam (1/1 g/Vial)

Clinical Trial Summary

A randomized, single-dose, two-way crossover study to evaluate bioequivalence of two formulations of cefoperazone sodium and sulbactam sodium combination (1/1 g/vial) after intravenous infusion of 1 g cefoperazone sodium and 1 g sulbactam sodium in healthy volunteers under fasting conditions

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NCT number	NCT05654090
Study type	Interventional
Source	Yung Shin Pharm. Ind. Co., Ltd.
Contact
Status	Active, not recruiting
Phase	Phase 4
Start date	August 25, 2022
Completion date	February 20, 2023

Evaluate Bioequivalence of Burotam (1/1 g/Vial)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms