Clinical Trials Directory

Trials / Completed

CompletedNCT00602407

Bioequivalency Study of 50 mg Cilostazol Tablets Under Fasting Conditions

A Single Dose, Randomized, Two-Period, Two-Treatment, Crossover Bioequivalency Study of Cilostazol 50 mg Tablets Under Fasting Conditions

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
36 (actual)
Sponsor
Roxane Laboratories · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The objective of this study was the bioequivalence of a Roxane Laboratories' Cilostazol Tablets, 50 mg, to PLETAL® Tablets, 50 mg (OTSUKA Pharmaceuticals) under fasting conditions using a single-dose, randomized, 2-treatment, 2-period, crossover design.

Conditions

Interventions

TypeNameDescription
DRUGCilostazol

Timeline

Start date
2004-02-01
Primary completion
2004-03-01
Completion
2004-03-01
First posted
2008-01-28
Last updated
2018-01-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00602407. Inclusion in this directory is not an endorsement.