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| Sponsor: | AstraZeneca |
|---|---|
| Information provided by: | AstraZeneca |
| ClinicalTrials.gov Identifier: | NCT00034905 |
Purpose
The purpose of this study is to show equal efficacy of both quetiapine and risperidone in subjects treated with study medication for up to 8 weeks.
| Condition | Intervention | Phase |
|---|---|---|
|
Schizophrenia |
Drug: quetiapine fumarate vs risperidone |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Primary Purpose: Treatment |
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Exclusion Criteria
Contacts and Locations
Show 64 Study Locations
More Information
| ClinicalTrials.gov Identifier: | NCT00034905 History of Changes |
| Other Study ID Numbers: | 5077US/0043 |
| Study First Received: | May 2, 2002 |
| Last Updated: | January 25, 2011 |
| Health Authority: | United States: Food and Drug Administration |
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders Risperidone Quetiapine Serotonin Antagonists Serotonin Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Pharmacologic Actions |
Physiological Effects of Drugs Antipsychotic Agents Tranquilizing Agents Central Nervous System Depressants Central Nervous System Agents Therapeutic Uses Psychotropic Drugs Dopamine Antagonists Dopamine Agents |