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Clinical Trial Summary

This study will evaluate the safety, tolerability, and pharmacokinetics of MK-4334 administered once daily (QD) in participants with Alzheimer's clinical syndrome receiving a stable, daily dose of donepezil 10 mg, taken orally (PO). This includes participants with symptoms of mild cognitive impairment (MCI) or mild to moderate Alzheimer's disease (AD). It is hypothesized that the true geometric mean minimum plasma concentration at 24 hours (C24) is at least 60 nM at steady state in the presence of steady-state donepezil 10 mg.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03740178
Study type Interventional
Source Merck Sharp & Dohme Corp.
Contact
Status Not yet recruiting
Phase Phase 1
Start date September 27, 2019
Completion date February 28, 2020

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