The objectives of this study are to describe characteristics, treatment patterns, and outcomes of patients with schizophrenia newly initiated on 1 of 4 FDA-approved atypical Long Acting Injectable (LAI) antipsychotics (ABILIFY MAINTENA®, ARISTADA®, INVEGA SUSTENNA® or RISPERDAL CONSTA®)
This is a non-interventional, prospective, multi-center observational cohort study. Patients at behavioral health clinics will be enrolled and evaluated by health care professionals (e.g., psychiatrists) according to the standard of care. All patients will be followed for approximately 12 months from their enrollment visit.
Study Type
OBSERVATIONAL
Enrollment
338
Schizophrenia disease history
Including time (years) since diagnosis as assessed from clinical history
Time frame: Baseline
Number of comorbid conditions at baseline
Assessed from clinical history
Time frame: Baseline
Changes in comorbid conditions
The percent of patients experiencing each comorbid condition will be assessed at follow-up visits
Time frame: Up to 12 months
Number of LAI injections
Average number of injections during treatment period
Time frame: Up to 12 months
Number of patients switching or discontinuing LAI treatment
Time frame: Up to 12 months
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Alkermes Investigational Site
Tucson, Arizona, United States
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El Cajon, California, United States
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Granada Hills, California, United States
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Oceanside, California, United States
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Panorama City, California, United States
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San Bernardino, California, United States
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Dayville, Connecticut, United States
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Hialeah, Florida, United States
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Hialeah, Florida, United States
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