Clinical Trials Directory

Trials / Completed

CompletedNCT00694187

Bioequivalency Study of Zaleplon 10 mg Capsules Under Fasting Conditions

A Single Dose, Two-Period, Two-Treatment, 2-Way Crossover Bioequivalency Study of Zaleplon 10 mg Capsules Under Fasting Conditions.

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

Summary

The objective of this study was to show the bioequivalence of a Roxane Laboratories' Zaleplon Capsules, 10 mg, to Sonata ® Capsules, 10 mg (Jones Pharma) under fasting conditions using a single-dose, randomized, 2-treatment, 2-period, 2-sequence crossover design

Conditions

Interventions

TypeNameDescription
DRUGZaleplon

Timeline

Start date
2004-01-01
Primary completion
2004-02-01
Completion
2004-02-01
First posted
2008-06-10
Last updated
2018-01-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00694187. Inclusion in this directory is not an endorsement.