Alzheimer's Disease
Conditions
Brief summary
The objectives of this study are to assess the safety, tolerability and pharmacokinetics of ABT-126 in elderly subjects.
Interventions
DRUGABT-126
See arm for details
Sponsors
Abbott
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Healthy male or female subjects 65 years or greater. * Has a MMSE score of 27 or higher.
Exclusion criteria
* History of dementia including by not limited to Alzheimer's disease, Parkinson's disease and mult-infarct dementia. * History of any significant neurological disease. * Has an estimated creatinine clearance \< 30 mL/min
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety and Tolerability Assessments (i.e., ECG, clinical laboratory tests, vital signs, weight, AE assessment, physical and brief neurological examinations) | Study Days -1 thru Day 28 |
| Assess the Pharmacokinetics | Study Days -1 thru Day 28 |
Countries
United States
Outcome results
None listed