Benfotiamine in Alzheimer's Disease: A Pilot Study

PHASE2CompletedINTERVENTIONAL
Enrollment

71

Participants

Timeline

Start Date

February 15, 2015

Primary Completion Date

July 20, 2020

Study Completion Date

September 8, 2020

Conditions
Alzheimer's Disease
Interventions
DRUG

Benfotiamine

"* To test whether increasing brain thiamine by administering 600 mg per day (300 mg/morning and 300 mg/evening) of benfotiamine for one year can slow cognitive decline in these patients as measured with the Alzheimer's Disease Assessment Scale (ADAS-COG).~* To determine whether increasing brain thiamine availability with 600 mg (300 mg/morning and 300 mg/evening) per day of benfotiamine for one year can slow the decline in brain glucose metabolism in these patients as measured with Fluorodeoxyglucose Positron Emission Tomography(FGPET) in the posterior cingulate."

Trial Locations (1)

10605

Burke, White Plains

All Listed Sponsors
collaborator

Burke Rehabilitation Hospital

OTHER

collaborator

Columbia University

OTHER

collaborator

National Institute on Aging (NIA)

NIH

collaborator

Alzheimer's Drug Discovery Foundation

OTHER

collaborator

Montefiore Medical Center

OTHER

lead

Burke Medical Research Institute

OTHER