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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


Study Design

Related Conditions & MeSH terms

NCT number NCT05191862
Study type Interventional
Source Genovate Biotechnology Co., Ltd.,
Contact Tony Lo
Phone +886 (2) 2321-1978
Email [email protected]
Status Recruiting
Phase Phase 1
Start date April 2022
Completion date July 2022

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