Study Evaluating the Clinical Benefit of SEROQUEL XR in Subjects With Schizophrenia

PHASE3CompletedINTERVENTIONAL
Enrollment

331

Participants

Timeline

Start Date

March 31, 2008

Primary Completion Date

July 31, 2010

Study Completion Date

July 31, 2010

Conditions
Schizophrenia
Interventions
DRUG

Quetiapine Fumarate Extended- Release

Open-label seroquel XR tablets: On Day 1 Patients received 300 mg, on Day 2 600 mg, on Day 3 600-800 mg and between Day 4-168 400-800 mg Seroquel XR, according to clinical judgement of investigator. Dose changes were in 200 mg fixed doses. Investigational product (IP) was supplied in open label wallet blister cards and subjects were instructed to take the IP once daily in the evening.

Trial Locations (36)

Unknown

Research Site, Garran

Research Site, Newcastle

Research Site, Brisbane

Research Site, Meadowbrook

Research Site, Dandenong

Research Site, Calgary

Research Site, Claresholm

Research Site, Red Deer

Research Site, Vancouver

Research Site, Victoria

Research Site, Miramichi

Research Site, St. John's

Research Site, Sydney

Research Site, Belleville

Research Site, Brantford

Research Site, Chatham

Research Site, Cornwall

Research Site, Greater Sudbury

Research Site, London

Research Site, Markham

Research Site, Mississauga

Research Site, Newmarket

Research Site, Oakville

Research Site, Orléans

Research Site, Toronto

Research Site, Windsor

Research Site, Gatineau

Research Site, Greenfield Park

Research Site, Montreal

Research Site, Québec

Research Site, Rouyn-Noranda

Research Site, Verdun

Research Site, Prince Albert

Research Site, Saskatoon

Research Site, Hong Kong

Research Site, Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY