We plan in healthy volunteers to characterize for E2020: the single oral dose peripheral and central compartment (P.&C.C) pharmacokinetic profile; the P.&C.C steady state, pharmacokinetic profile of 5 mg and 10 mg dosages; the terminal phase pharmacokinetic profile (last dose at steady-state); the magnitude and duration of plasma and CSF acetylcholinesterase (AChE) inhibition. We hypothesize that: E2020 will cross the blood-brain barrier with sufficient penetration to achieve measurable levels in the CSF and inhibit AChE; peripheralplasma E2020 and metabolite concentrations and markers of cholinesterase inhibition will correlate with CSF AChE activity.

Project Start
Project End
Budget Start
Budget End
Support Year
36
Fiscal Year
1996
Total Cost
Indirect Cost
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