Alzheimer Disease Clinical Trial
Official title:
Effects of an 8 Component Botanical Supplement on Mild and Moderate Alzheimer's Patients
This placebo-controlled, double blind study evaluates the treatment effects of adding a multi-pathway botanical dietary supplement (ReBuilder) to the standard treatment regimens of subjects diagnosed with mild or moderate stage Alzheimer's Disease. The objective of the study is to determine if mild and moderate AD patients exhibit improved or stabilized cognitive function when this supplement is added to maximum tolerated doses of their standard treatments.
Currently, there is no treatment that can stop the progression of Alzheimer's Disease. The
investigators in this study have used transgenic Drosophila melanogaster models and machine
learning to develop an eight component botanical mixture (Geneaireâ„¢* ReBuilderâ„¢) that targets
multiple genetic pathways involved in brain aging and dementia that are homologous between
Drosophila and humans.
While beta-amyloid plaques and phosphorylated-tau tangles are diagnostic for AD, the cause(s)
of their soluble precursors that kill neurons has not been determined. The majority of AD
patients are diagnosed after 60 years of age. Many studies point to aging related processes
like inflammation, neural vascular damage, neural stress, altered cell metabolism,
inefficient cellular autophagy, microglial dysfunction, mitochondrial dysfunction, and poor
diet as potential causal factors in the decline of brain function over the decades that
precede an actual AD diagnosis. AD is a multifaceted pathology involving many biochemical
pathways and thus a multifaceted therapeutic approach may prove beneficial.
The goal of this study was to test ReBuilder on human cognitive function. During the 12-month
pilot study, the subjects were evaluated quarterly on the Mini Mental State Exam (MMSE),
Alzheimer's Disease Cooperative Study's Activities of Daily Living (ADCS-ADL), and the
Clinical Dementia Rating Sum of Boxes (CDR-SB).
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