Study to compare the pharmacokinetics and pharmacodynamics of VHX-896 and iloperidone and evaluate the safety and tolerability of VHX-896 and iloperidone in patients with schizophrenia or bipolar I disorder under steady state conditions.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
26
oral tablet
oral tablet
Vanda Investigational Site
Los Alamitos, California, United States
Vanda Investigational Site
Gaithersburg, Maryland, United States
Vanda Investigational Site
Marlton, New Jersey, United States
Bioequivalence between VHX-896 tablets relative to iloperidone tablets
As measured by plasma concentrations
Time frame: 12 hours
Assessment of safety and tolerability of VHX-896 and iloperidone
As measured by spontaneous reporting of adverse events (AEs).
Time frame: 24 days
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