Clinical Trials Directory

Trials / Completed

CompletedNCT00580931

Safety Study of Nicotinamide to Treat Alzheimer's Disease

Efficacy of Nicotinamide for the Treatment of Alzheimer's Disease

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
50 (actual)
Sponsor
University of California, Irvine · Academic / Other
Sex
All
Age
50 Years – 95 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether nicotinamide, or vitamin B3, is safe and effective in the treatment of Alzheimer's disease.

Detailed description

The goal of this proposal is to show that, nicotinamide (NA), a B3 vitamin, is safe and effective for the treatment of patients with mild to moderate Alzheimer's disease (AD). NA is known to block the ability of certain proteins to regulate other proteins by removing their acetyl groups. Recent evidence has demonstrated that inhibitors such as NA prevent nerve cell degeneration in models of Huntington's disease (HD), Parkinson's disease and Lou Gehrig's disease (or ALS). Despite these beneficial effects in many different animal models, there have been no studies to date using these inhibitors in AD. In some of our recent studies we found that the potent inhibitor, NA, significantly improves learning and memory in transgenic mice that develop AD. NA treatment also resulted in striking changes in tau, a protein that abnormally accumulates in AD. NA has been extensively used in clinical studies over the last 40 years and is generally safe and well-tolerated. As NA is a safe and readily available vitamin supplement, our recent results provide a strong argument for a study of NA in patients with AD. We therefore propose to treat 50 patients with mild to moderate AD with either NA (1500 milligrams twice a day) or an identical but inactive drug (placebo) for 24 weeks. At 6 week intervals we will assess functions such as learning and memory, and ability to carry out daily activities as well as caregiver reports using standardized tests. We will also perform spinal taps at the beginning and end of the study to measure the level of abnormal tau protein in the cerebrospinal fluid. Blood tests will periodically be done to assess liver function and complete blood counts. The results of this study may provide the basis for a more extensive study of NA for the treatment of mild to moderate AD.

Conditions

Interventions

TypeNameDescription
DRUGNicotinamide1500 mg twice a day for 6 months
DRUGEnduramide placebo1 tab twice a day

Timeline

Start date
2008-01-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2007-12-27
Last updated
2017-01-25

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00580931. Inclusion in this directory is not an endorsement.