drugset / Trial / NCT00139737

Extension Study: Evaluating the Safety of Oral Ziprasidone in the Treatment of Subjects With Schizophrenia

NCT00139737

Phase 3 Completed 344 enrolled Viatris Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To provide treatment to eligible subjects who have successfully completed one of the following phase III ziprasidone studies, A1281028, A1281044, A1281045 (NCT00136994) or A1281088 (NCT00143351).

Timeline

Start
2002-03
Primary completion
2009-06
Completion
2009-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Ziprasidone Small molecule 20 mg Oral
Subject Ziprasidone Small molecule 40 mg Oral
Subject Ziprasidone Small molecule 60 mg Oral
Subject Ziprasidone Small molecule 80 mg Oral

Indications