drugset / Trial / NCT00206115

SR-Registration Study 1, ROW: Efficacy and Safety of Seroquel® in the Treatment of Patients With Schizophrenia

NCT00206115 ↗

Phase 3 Completed 535 enrolled AstraZeneca
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this 6-week study is to determine whether treatment with Seroquel® Sustained Release (SR) is more effective than placebo in the treatment of acute schizophrenia. PLEASE NOTE: Seroquel SR and Seroquel XR refer to the same formulation. The SR designation was changed to XR after consultation with FDA.

Timeline

Start
2004-11
Primary completion
—
Completion
2005-12

Outcome

Met primary endpoint

paper Improvement in PANSS total score at week 6 was significant versus placebo (-18.8) in all groups: -24.8 (p = .03), -30.9 (p < .001), and -31.3 (p < .001) PMID 17592906 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Quetiapine Small molecule 400 mg —
Subject Quetiapine Small molecule 600 mg —
Subject Quetiapine Small molecule 800 mg —

Indications