drugset / Trial / NCT00645515

A Study Comparing the Safety and Efficacy of Ziprasidone and Risperidone for the Treatment of Chronic Schizophrenia

NCT00645515 ↗

Phase 3 Terminated 240 enrolled Viatris Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the safety of ziprasidone and risperidone for the treatment of chronic schizophrenia. The primary purpose is to differentiate the effects of ziprasidone and risperidone on extrapyramidal side effects and the secondary purpose is to compare their tolerability and efficacy.

Timeline

Start
2003-06
Primary completion
—
Completion
2003-12

Outcome

Outcome not reported

Stopped (Enrollment): “This study was terminated on November 20, 2003 because of poor recruitment. This study was not terminated due to safety/efficacy.”

Drugs

EvaluationDrugModalityDoseRoute
Comparator Risperidone Other / unclassified 3 mg —
Comparator Risperidone Other / unclassified 9 mg —
Subject Ziprasidone Small molecule 40 mg —
Subject Ziprasidone Small molecule 80 mg —

Indications