The study will determine the safety, tolerability, and pharmacokinetics of aripiprazole lauroxil in adults with schizophrenia or schizoaffective disorder.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
47
Intramuscular (IM) injection, single dose
Alkermes Investigational Site
Cerritos, California, United States
Alkermes Investigational Site
Lemon Grove, California, United States
Alkermes Investigational Site
Oakland, California, United States
Alkermes Investigational Site
Hoffman Estates, Illinois, United States
Maximum plasma concentration (Cmax)
Time frame: Up to 7 days
Time to Cmax (Tmax)
Time frame: Up to 7 days
Area under the concentration-time curve from time zero to the last quantifiable time interval (AUCl0-last)
Time frame: Up to 7 days
Area under the concentration-time curve from time zero to time t (AUC0-t)
Time frame: Up to 7 days
Terminal elimination half-life (t½)
Time frame: Up to 7 days
Safety will be determined by incidence of adverse events
Time frame: Up to 7 days
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Alkermes Investigational Site
Marlton, New Jersey, United States
Alkermes Investigative Site
Dallas, Texas, United States