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A Safety and Tolerability Study of ABT-126 in Elderly

A Multiple Dose Study of Safety, Tolerability and Pharmacokinetics of ABT-126 in Elderly Subjects

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00867399
Enrollment
30
Registered
2009-03-23
Start date
2009-03-31
Completion date
Unknown
Last updated
2010-11-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's Disease

Brief summary

The objectives of this study are to assess the safety, tolerability and pharmacokinetics of ABT-126 in elderly subjects.

Interventions

See arm for details

Sponsors

Abbott
Lead SponsorINDUSTRY

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

MeasureTime 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 PharmacokineticsStudy Days -1 thru Day 28

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026