Clinical Trials Directory

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

TypeNameDescription
DRUGIntramuscular Olanzapine Depot
DRUGOral 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.

Comparison of Intramuscular Olanzapine Depot to Oral Olanzapine and Low-Dose Depot in Patients With Schizophrenia (NCT00088491) · Clinical Trials Directory