Clinical Trials Directory

Trials / Terminated

TerminatedNCT00647972

Fasting Study of Olanzapine Tablets 20 mg and Zyprexa® Tablets 20 mg

Single-Dose Fasting In Vivo Bioequivalence Study of Olanzapine Tablets (20 mg; Mylan) and Zyprexa® Tablets (20 mg; Eli Lilly) in Healthy Volunteers

Status
Terminated
Phase
Phase 1
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Mylan Pharmaceuticals Inc · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The objective of this study was to investigate the bioequivalence of Mylan olanzapine 20 mg tablets to Eli Lilly Zyprexa® 20 mg tablets following a single, oral 20 mg (1 x 20 mg) dose administration under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGOlanzapine Tablets 20 mg20mg, single dose fasting
DRUGZyprexa® Tablets 20 mg20mg, single dose fasting

Timeline

Start date
2003-05-01
Primary completion
2003-05-01
First posted
2008-04-01
Last updated
2024-04-23

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00647972. Inclusion in this directory is not an endorsement.