Clinical Trials Logo

Clinical Trial Summary

The primary objective of the study is to characterize the pharmacokinetics of 3 formulations of olanzapine. A secondary objective is to evaluate the safety and tolerability of 3 formulations of olanzapine. Another secondary objective is to characterize the pharmacokinetics of ZYPREXA. The planned duration of the study for each participant is 19 weeks.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06319170
Study type Interventional
Source Teva Branded Pharmaceutical Products R&D, Inc.
Contact Teva U.S. Medical Information
Phone 1-888-483-8279
Email USMedInfo@tevapharm.com
Status Recruiting
Phase Phase 1
Start date March 28, 2024
Completion date December 11, 2024

See also
  Status Clinical Trial Phase
Completed NCT04512066 - A Trial of the Efficacy and the Safety of RO6889450 (Ralmitaront) vs Placebo in Patients With an Acute Exacerbation of Schizophrenia or Schizoaffective Disorder Phase 2
Completed NCT02192593 - Computerized Cognitive-Behavioral Therapy for Auditory Hallucinations N/A
Completed NCT00224315 - Clozapine-Augmentation With Ziprasidone or Risperidone, a Randomized, Prospective Trial Phase 4
Recruiting NCT02808533 - Topiramate and Schizophrenia: Effects on Weight and Psychopathology N/A
Terminated NCT03669640 - A Study to Assess the Effects of RO6889450 (Ralmitaront) in Participants With Schizophrenia or Schizoaffective Disorder and Negative Symptoms Phase 2