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Clinical Trial Summary

The study is designed to evaluate the bioequivalence and the within-subject variability between the test formulation of extended-release tablet of cilostazol (PMR) administered once daily and the reference formulation of immediate- release tablet of cilostazol (Cilostazol) administered twice-daily in normal healthy male and female subjects under fasting conditions.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06167265
Study type Interventional
Source Genovate Biotechnology Co., Ltd.,
Contact
Status Completed
Phase Phase 1
Start date November 28, 2023
Completion date January 18, 2024

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