ABT-126
DrugABT-126 Low Dose
NCT Number: NCT01678755
This is an efficacy study evaluating a experimental treatment for cognitive deficits in adults with schizophrenia.
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Notify Me20 year–55 year
All sexes
Interventional
Phase 2
Site Reference ID/Investigator# 74436, Chino, California, United States
Safety and Efficacy Study for Cognitive Deficits in Adult Subjects with Schizophrenia.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
ABT-126 Low Dose
Placebo
Time frame: Change from baseline to week 12
Rater based interview
Time frame: Measurements from screening period up through week 12
Rater based interview
Time frame: Measurements from screening period up through week 12
Rater based interview
Time frame: Measurements from screening period up through week 12
Rater based interview
AbbVie (prior sponsor, Abbott)
Industry
A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 2 Study of the Safety and Efficacy of ABT-126 in the Treatment of Cognitive Deficits in Schizophrenia (CDS) in Smokers
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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