The Wake Forest School of Medicine Alzheimer’s Disease Prevention Program offers patients a chance to participate in clinical trials that may impede the development of mild cognitive impairment or Alzheimer’s disease and help the functioning of the aging brain.
Therapeutic Effects of Intranasally-administered Insulin in Adults with Mild Cognitive Impairment or Mild Alzheimer’s Disease (INI Study)
This 18-month study investigates whether a type of insulin (Humulin® R) improves memory when administered intranasally (as a “nasal spray”) to adults with a mild memory impairment or early Alzheimer’s disease.
Anti-amyloid Treatment in Asymptomatic Alzheimer’s Disease (A4 Study)
This 36-month study is testing an investigational drug in older people who have evidence of elevated amyloid build-up in their brains, but who do not yet show symptoms of Alzheimer’s disease.
Alzheimer’s Disease Prevention Participant Repository (ADPPR)
The Alzheimer’s Disease Prevention Participant Repository is an observational study that will be used to identify and characterize early risk factors that predict memory decline and dementia in adults, with or without early signs of memory impairment.
Study of Nasal Insulin to Fight Forgetfulness – Short-Acting Insulin Aspart – 12 weeks (SNIFF-QUICK Study)
The purpose of this three-month research study is to find out whether insulin aspart improves memory when administered as a spray into the nasal passages of adults with mild memory impairment or early Alzheimer’s disease.
Brain Energy And Memory Study (BEAM)
The purpose of this 24-week research study is to find out how adults
with abnormal insulin sensitivity and those with memory/thinking problems respond
to different diets.
A Phase 2a Multi-Center Study of
18F-FDG PET, Safety and Tolerability of AZD0530 in Mild Alzheimer’s Disease
(FYN Connect Study)
The purpose of this research study is to determine whether AZD0530 is safe and effective in slowing decline in brain metabolism, memory and daily function in
people Alzheimer’s disease (AD).
in Dementia Methylphenidate Trial 2 (ADMET II)
This 6 month study
investigates the efficacy of methylphenidate for the treatment of clinically
significant apathy in participants with Alzheimer’s disease.
AVID 18F-AV-1451: A Clinico-Pathological Study of the Correspondence Between 18F-AV-1451 PET
Imaging and Post-Mortem Assessment of Tau Pathology (AVID)
Pictures of the brain made using the study drug during
the life of study participants will be compared to results of brain autopsy
EMERGE Study / Biogen 221AD302 - A Phase 3 Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of aducanumab (BIIB037) in Subjects with Early Alzheimer's Disease
The purpose of the study is to find out whether aducanumab has the potential to be a helpful treatment that slows down disease progression in subjects with early Alzheimer’s Disease (AD) by comparing it to placebo and to evaluate its safety (side effects), and to find out more about aducanumab. About 1350 people from150 research sites world-wide between 50 and 85 years old will take part in this 18 month study.
Alzheimer's Steadfast Study / A Phase 3 Multi-Center, Randomized, Double Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of TTP-488 in Patients with Mild Alzheimer’s Disease Receiving Acetylcholinesterase Inhibitors and/or Memantine
The purpose of this research study is to determine whether an investigational drug, azeliragon (TTP488) is safe and beneficial in delaying or altering the decline in memory and daily functioning when given to people with mild Alzheimer’s disease (AD). In this study, participants will be given either active study drug, azeliragon or placebo. A total of 800 people at least 50 years old, have mild Alzheimer's Disease (AD) and are experiencing memory problems will take part in this study. Participants must be currently taking a cholinesterase inhibitor (such as donepezil, Aricept, rivastigmine, Exelon, galantamine or Razadyne) and/or memantine for the treatment of AD.
EXERT Study / Phase 3 Multi-Center Study of Therapeutic Effects of Exercise in Adults with Amnestic Mild Cognitive Impairment
The EXERT study will examine the effects of aerobic exercise on cognition, functional status, brain atrophy and blood flow, and cerebrospinal fluid biomarkers of Alzheimer’s disease in 300 adults with amnestic Mild Cognitive Impairment. Adults will be between 65 and 89 years old. Participants will be randomized to one of two interventions: supervised and structured moderate/high intensity aerobic training vs.stretching/balance control for 12 months, followed by a 6-month unsupervised extension.
ADNI-2: Alzheimer’s Disease Neuroimaging Initiative 2 – Recruitment closed
ADNI 2 builds upon the successes of earlier ADNI
phases to identify the earliest signs of AD and will help define the subtle
changes that may take place in the brains of older people many years before
overt symptoms of the disease appear.
Noble-TCAD Study - Recruitment closed
The purpose of this research study is to evaluate whether an investigational drug (T-817MA) is safe and beneficial in delaying or altering the decline in memory and daily function when given to people with mild to moderate Alzheimer’s disease.