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临床试验/NCT00580931
NCT00580931已完成1 期

Efficacy of Nicotinamide for the Treatment of Alzheimer's Disease

University of California, Irvine1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2008年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
50
试验地点
1
主要终点
Alzheimer's Disease Assessment Scale-Cognitive Subscale

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
50 Years 至 95 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of probable AD according to DSM-IV criteria
  • Mild to moderate dementia based on Mini-Mental State Examination [MMSE] score between 13-25
  • Minimum age 50 years
  • Brain imaging (computed tomographic scan or magnetic resonance image) within 12 months consistent with a diagnosis of probable AD
  • Hachinski Ischemic Score of <
  • Stable doses of concomitant medications, including cholinesterase inhibitors (ChEIs) and/or memantine.

排除标准

  • Dementia due to another cause
  • Other neurological or psychiatric diseases
  • Pseudodementia
  • Unstable medical condition
  • Initial treatment within 30 days of screening with a ChEI, memantine or any investigational drug
  • History of alcoholism, drug abuse, liver disease, peptic ulcer disease
  • Pregnancy, or the potential to become pregnant.

研究组 & 干预措施

1

Experimental

Subjects will receive experimental drug in a blinded fashion.

干预措施: Nicotinamide (Drug)

2

Placebo Comparator

Identical in size, shape and color to experimental drug.

干预措施: Enduramide placebo (Drug)

结局指标

主要结局

Alzheimer's Disease Assessment Scale-Cognitive Subscale

时间窗: Baseline, 6 wk, 12 wk, 18 wk, 24 wk

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Steven Schreiber

Professor of Neurology

University of California, Irvine

研究点 (1)

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