This is an efficacy and safety study evaluating an experimental treatment for cognitive deficits in adults with schizophrenia.
This is a Phase 2 study designed to evaluate the efficacy and safety of ABT-288 in approximately 210 adults with schizophrenia. Subjects will be randomized to one of three treatment groups (ABT-288 Dose 1, ABT-288 Dose 2 or placebo) for a 12-week Treatment Period. The purpose of this research study is to find out whether ABT-288 compared to placebo can improve cognition and what side effects ABT 288 may cause. Cognition is the way a person thinks, and it includes abilities like paying attention, focusing, remembering things, and solving problems. Acronyms listed in the Outcomes and/or Eligibility sections for this study are defined below: * MCCB: Measurement and Treatment Research to Improve Cognition in Schizophrenia (MATRICS) Consensus Cognitive Battery * UPSA-2: University of California at San Diego (UCSD) Performance-Based Skills Assessment-2 * CANTAB: Cambridge Neuropsychological Test Automated Battery * PANSS: Positive and Negative Syndrome Scale * NSA-16: Negative Symptom Assessment-16 * CGI-S: Clinical Global Impression - Severity
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
214
Cognition: MCCB
Time frame: Measurements from screening period through 12-week treatment period
Functioning: UPSA-2
Time frame: Measurements from screening period through 12-week treatment period
Cognition: CANTAB
Time frame: Measurements from screening period through 12-week treatment period
Symptom Severity: PANSS, NSA-16, CGI-S
Time frame: Measurements from screening period through 12-week treatment period
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Site Reference ID/Investigator# 21662
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National City, California, United States
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