Clinical Trials Directory

Trials / Completed

CompletedNCT01581866

Bioequivalence Study of Ziprasidone HCL Capsules, 20 mg Under Fasting Conditions

Randomized, 2-way Crossover, Bioequivalence Study of Ziprasidone HCL Capsules, 20 mg in Healthy Subjects Under Fasting Conditions.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
56 (actual)
Sponsor
Dr. Reddy's Laboratories Limited · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to compare the rate and extent of absorption of ziprasidone 20 mg capsules versus Geodon 20 mg capsules under fasting conditions.

Detailed description

Randomized, 2-way crossover, bioequivalence study of Ziprasidone 20 mg capsules and Geodon 20 mg capsules in healthy subjects under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGZiprasidone HydrochlorideZiprasidone HCL Capsules, 20 mg

Timeline

Start date
2004-11-01
Primary completion
2004-11-01
Completion
2005-01-01
First posted
2012-04-20
Last updated
2012-04-20

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01581866. Inclusion in this directory is not an endorsement.