跳至主要内容
临床试验/NCT00842673
NCT00842673已完成2 期

A Double-Blind Placebo-Controlled Preliminary Study of the Efficacy, Safety and Tolerability of ST101 Tablets in the Treatment of Alzheimer's Disease

Sonexa Therapeutics, Inc.0 个研究点目标入组 168 人开始时间: 2009年2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
入组人数
168
主要终点
Alzheimer's Disease Assessment Scale, Cognitive Subscale (ADAS-cog)

研究概览

简要总结

This study will investigate the ability of ST101 to improve memory in people with Alzheimer's disease. This study also will examine the safety and tolerability of the drug. This study is evaluating 3 different dose levels of ST101 and placebo. Patients will have a 1 in 4 chance of getting placebo.

详细描述

Alzheimer's disease (AD) is a progressive and fatal neurological illness. It produces changes in the brain that include loss of cells and accumulation of abnormal protein deposits. Initial symptoms are cognitive, with deficiencies in short-term memory the most common symptom. As the disease progresses so does the severity of cognitive deficiency. Loss of speech and immobility occur in the terminal stages There is no cure for AD and no marketed treatment that modifies the underlying disease process. Available therapies improve some symptoms of AD by increasing brain concentrations of molecules involved in cognition. ST101 differs from marketed therapies in that it has demonstrated two actions in animal research testing. It improves cognition and it also reduces the accumulation of abnormal protein deposits in the brain. These two properties suggest that ST101 may be a promising agent for the treatment of AD. This study is designed as a preliminary dose exploration/proof-of-concept investigation of the ability of ST101 to improve cognition during 12 weeks of administration.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnostic evidence of mild to moderate Alzheimer's disease.
  • CT or MRI results within the past 12 months that rule out dementia due to non-Alzheimer's etiology.
  • A reliable and capable caregiver.

排除标准

  • Subjects who reside in a skilled nursing facility.
  • Subjects with B12 or folate deficiency.
  • Subjects with chronic hepatic disease.
  • Subjects with a recent history of hematologic/oncologic disorders.
  • Subjects who have experienced a myocardial infarction with the past year.
  • Dementia caused or complicated by other organic disease

研究组 & 干预措施

2

Experimental

90 mg ST101

干预措施: ST101 (Drug)

1

Experimental

30 mg ST101

干预措施: ST101 (Drug)

3

Experimental

180 mg ST101

干预措施: ST101 (Drug)

4

Placebo Comparator

Placebo

干预措施: Placebo (Drug)

结局指标

主要结局

Alzheimer's Disease Assessment Scale, Cognitive Subscale (ADAS-cog)

时间窗: Baseline, 4 weeks, 8 weeks,12 weeks

次要结局

  • Alzheimer's Disease Cooperative Study - Activities of Daily Living (ADCS-ADL)(Baseline, 4 weeks, 8 weeks, 12 weeks)
  • Neuropsychiatric Inventory (NPI)(Baseline, 4 weeks, 8 weeks, 12 weeks)
  • Alzheimer's Disease Cooperative Study- Clinical Global Impression (ADCS-CGI)(Baseline (severity); 4 weeks, 8 weeks, 12 weeks (change))

研究者

申办方类型
Industry
责任方
Sponsor

相似试验

Preliminary Efficacy and Safety Study of ST101 in... | 临床试验