drugset / Trial / NCT00328978

Seroquel STACK Study in Schizophrenic or Schizoaffective Subjects

NCT00328978 ↗

Phase 3 Completed 330 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of the study is to assess and compare the side effect profile, safety, tolerability and efficacy of schizophrenic or schizoaffective subjects non- or partially- responsive to 800 mg/day of quetiapine treated with either 800 mg/day or more than 800 mg/day of quetiapine during 8 weeks.

Timeline

Start
2003-10
Primary completion
—
Completion
2005-09

Outcome

Met primary endpoint

paper a value that was within the a priori limit of 16% defined as noninferiority. PMID 21733490 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Quetiapine Small molecule 800 mg —
Subject Quetiapine Small molecule 1200 mg —