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临床试验/NCT00355550
NCT00355550已完成2 期

A Double-Blind, Placebo-Controlled Study of Tricaprilin (AC-1202) Administered For Ninety Days In Subjects With Age-Associated Memory Impairment

Cerecin5 个研究点 分布在 1 个国家目标入组 156 人开始时间: 2006年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
156
试验地点
5
主要终点
Number of subjects with treatment related adverse events

研究概览

简要总结

The purpose of this study is to determine whether tricaprilin, a compound that increases energy availability in the brain, improves memory in older adults with "normal" loss of memory abilities since early adult life.

详细描述

One physiological hallmark of aging in mammals is a decreased uptake and metabolism of glucose within the brain. The impaired glucose metabolism in the brain may contribute or exacerbate the cognitive deficits observed during normal aging. Facilitation of memory in elderly individuals occurs when glucose levels are elevated by the administration of carbohydrate. However, such a treatment poses challenges since elevated blood glucose levels are difficult to maintain and must be within a relatively narrow window, as excessive hyperglycemia is associated with cognitive impairments. The purpose of this study is to explore whether increasing levels of other substrates for the brain improves cognitive functioning in normal aged individuals with memory disorders.

Study participants will be 120 men and women aged 50-85 who have been diagnosed as having Age-Associated Memory Impairment (AAMI). During the double-blind period of the protocol, 60 participants will receive tricaprilin and 60 participants will receive a matching placebo. Tricaprilin or the matching placebo will be administered once a day for ninety days by mixing powder in 8 ounces of a liquid. Each participant will be seen six (6) times: at Screening; Baseline; treatment days Days 30, 60, 90; and 14 days after the conclusion of treatment (Day 104).

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
Double (Participant, Investigator)

入排标准

年龄范围
50 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Complaints that memory has declined since young adult life
  • Scores on standardized tests that are at least one standard deviation below the mean score of young adults

排除标准

  • Dementia, including Alzheimer's disease and Mild Cognitive Impairment (MCI)
  • Drugs that impair cognition
  • Psychiatric conditions that may impair cognition (e.g.,depression etc.)

研究组 & 干预措施

AC-1202

Active Comparator

Tricaprilin formulation, once daily. Administered orally

干预措施: Tricaprilin (Drug)

Matching Placebo to AC-1202

Placebo Comparator

Placebo formulation, once daily. Administered orally

干预措施: Placebo (Other)

结局指标

主要结局

Number of subjects with treatment related adverse events

时间窗: 90 days

AE incidence rate per treatment group

Changes in Psychologix and Cogscreen Test Batteries, RAVLT (Rey Auditory Verbal Learning Test)

时间窗: 90 days

次要结局

  • Self-reported memory improvement(90 days)

研究者

发起方
Cerecin
申办方类型
Industry
责任方
Sponsor

研究点 (5)

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