Trials / Completed
CompletedNCT00088491
Comparison of Intramuscular Olanzapine Depot to Oral Olanzapine and Low-Dose Depot in Patients With Schizophrenia
A Double-Blind, Randomized Study Comparing Intramuscular Olanzapine Depot to Oral Olanzapine and Low-Dose Depot in the Maintenance Therapy of Patients With Schizophrenia
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 1,205 (actual)
- Sponsor
- Eli Lilly and Company · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
This is a randomized, double-blind study to determine how well intramuscular (IM) olanzapine depot works compared to oral olanzapine; evaluate the safety and tolerability of IM olanzapine depot compared to oral olanzapine; evaluate different doses of IM olanzapine depot; and determine the blood levels of IM olanzapine depot in patients at different points in time after an injection.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Intramuscular Olanzapine Depot | |
| DRUG | Oral Olanzapine |
Timeline
- Start date
- 2004-06-01
- Completion
- 2006-10-01
- First posted
- 2004-07-28
- Last updated
- 2007-06-22
Locations
4 sites across 2 countries: Finland, Turkey (Türkiye)
Source: ClinicalTrials.gov record NCT00088491. Inclusion in this directory is not an endorsement.