Efficacy and Safety Study of Seroquel SR in the Treatment of Generalised Anxiety Disorder

PHASE3CompletedINTERVENTIONAL
Enrollment

450

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

April 30, 2008

Study Completion Date

April 30, 2008

Conditions
Anxiety Disorders
Interventions
DRUG

Quetiapine XR

Quetiapine XR 50 mg tablets orally administered in flexible doses of 50 to 300 mg quetiapine XR once daily, in the evening for a 9-week treatment period.

DRUG

Placebo

Matching placebo tablets orally administered in flexible doses of 50 to 300 mg once daily, in the evening for a 9-week treatment period.

Trial Locations (43)

Unknown

Research Site, Fort Myers

Research Site, Gainsville

Research Site, Miami

Research Site, Sarasota

Research Site, Roswell

Research Site, Boston

Research Site, Brooklyn

Research Site, The Bronx

Research Site, Avon Lake

Research Site, Eugene

Research Site, Jenkintown

Research Site, Austin

Research Site, Houston

Research Site, San Antonio

Research Site, Tartu

Research Site, Tallinn

Research Site, Viljandi

Research Site, Bialystok

Research Site, Gorlice

Research Site, Katowice

Research Site, Krakow

Research Site, Leszno

Research Site, Skorzewo

Research Site, Torun

Research Site, Wroclaw

Research Site, Arkhangelsk

Research Site, Izhevsk

Research Site, Lipetsk

Research Site, Moscow

Research Site, Nizhny Novgorod

Research Site, Perm

Research Site, Saint Petersburg

Research Site, Saratov

Research Site, Stavropol

Research Site, Voronezh

Research Site, Hlevakha

Research Site, Dnipro

Research Site, Dnipropetrovsk

Research Site, Donetsk

Research Site, Kiev

Research Site, Luhansk

Research Site, Odesa

Research Site, Vinnitsa

Sponsors

Lead Sponsor

All Listed Sponsors
lead

AstraZeneca

INDUSTRY