A study to investigate the process by which ABT-126 is absorbed, distributed, metabolized and eliminated by the body of stable schizophrenic volunteers receiving treatment with an atypical antipsychotic.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
16
ABT-126 Low Dose \& ABT-126 High Dose
Matching Placebo for Arms 1 \& 2
Site Reference ID/Investigator# 25423
Glendale, California, United States
Site Reference ID/Investigator# 24322
San Antonio, Texas, United States
Adverse Events
Time frame: Duration of study
ABT-126 levels in blood (plasma)
Time frame: Pre-dose to 144 hours post-dose
Clinical laboratory tests, vital signs and electrocardiogram (ECG)
Time frame: Pre-dose to 72 hours post-dose
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