Overview

Dosage and Efficacy of Probucol-induced apoE to Negate Cognitive Deterioration

Status:
Completed
Trial end date:
2017-03-01
Target enrollment:
Participant gender:
Summary
DEPEND is an open-label but dosage-masked trial of the retired cholesterol-lowering drug probucol as an agent to increase availability of apolipoprotein E (apoE) in the cerebrospinal fluid (CSF) of cognitively intact older persons at risk of Alzheimer's dementia. Absorption of oral probucol is variable. In a sample of 23 cognitively intact persons over age 55, DEPEND will therefore develop an algorithm to prescribe individualized dosing to achieve plasma concentration that will likely increase availability of CSF apoE. These persons will then use their individualized dosage for 12 months to assess longer-term effects of the drug on CSF apoE concentration, while monitoring closely for evidence of adverse consequences of use.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Douglas Mental Health University Institute
Collaborators:
McGill University
Weston Brain Institute
Treatments:
Probucol