This study is designed to evaluate the safety, tolerability and pharmacokinetics of multiple doses of ABT-957 in subjects with mild to moderate Alzheimer's disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
19
ABT-957 administered twice-daily for 7 days
Placebo for ABT-957 administered twice-daily for 7 days
Site Reference ID/Investigator# 129545
Glendale, California, United States
Site Reference ID/Investigator# 129435
Orlando, Florida, United States
Site Reference ID/Investigator# 129641
New York, New York, United States
Site Reference ID/Investigator# 144825
Salt Lake City, Utah, United States
Pharmacokinetic evaluation of the two ABT-957 diastereomers
maximum observed plasma concentration (Cmax), time to Cmax (peak time, Tmax), plasma concentration at the end of the dosing interval (Ctrough), the area under the plasma concentration-time curve (AUC) during each dosing interval (AUC0-12 and AUC12-24)
Time frame: Day 7
Number of subjects with adverse events
Subjects will be monitored for clinical and laboratory evidence of adverse events throughout the study
Time frame: Routinely for the duration of the study, about 7 months
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