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
| Type | Name | Description |
|---|---|---|
| DRUG | Olanzapine Tablets 20 mg | 20mg, single dose fasting |
| DRUG | Zyprexa® Tablets 20 mg | 20mg, 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.