Study to Assess the Efficacy, Safety, and Tolerability of AZD8529 in Adult Schizophrenia Patients
Completed · Phase 2 · Has a placebo group
Conditions studied: Schizophrenia
In brief
The purpose of this study is to determine whether treatment with daily oral dose of AZD8529 40 mg administered over 28 days is safe, well tolerated and improves main symptoms of schizophrenia in adult schizophrenia patients.
Key facts
- Study ID
- NCT00921804
- Run by
- AstraZeneca
- People needed
- 296
- Starts
- 2009-06-01
- Expected to finish
- 2010-05-01
- Last updated by the study team
- 2010-06-30
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient will need to read, understand and sign an informed consent prior to any study specific procedures
- Patient will have certain schizophrenia symptoms deemed by the investigator as appropriate for the study entry
You may not qualify if…
- Patients will be excluded based on recent history of significant illness or current disease as assessed by the investigator during screening process (based on physical examination, laboratory studies and electrocardiogram studies)
- Patients will be excluded if urine drug screen test show positive results
- Smoking of more than 2 packs of cigarettes a day
Where it is running
- Research Site — Garden Grove, California, United States
- Research Site — Glendale, California, United States
- Research Site — Rockville, Maryland, United States
Full record on ClinicalTrials.gov
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