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临床试验/NCT00093951
NCT00093951已完成2 期

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase II Study of the Efficacy and Safety of SGS742 in Subjects With Mild to Moderate Alzheimer's Disease

Saegis Pharmaceuticals101 个研究点 分布在 1 个国家目标入组 280 人开始时间: 2004年4月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
280
试验地点
101

研究概览

简要总结

The purpose of this trial is to determine the effect of a new drug, SGS742, on memory and cognition in patients with mild to moderate Alzheimer's disease.

详细描述

SGS742 is a GABA(B) receptor antagonist. It is an orally active drug and possesses neurochemical and psychopharmacologic features that suggest it could improve memory and cognition in humans. The primary objective of the SGS742 clinical trial will be to determine the effect of SGS742 on memory and cognition in individuals diagnosed with mild to moderate Alzheimer's disease. The duration of the study is 3 months with 5 clinic visits.

研究设计

研究类型
Interventional
分配方式
Randomized
主要目的
Treatment
盲法
Double

入排标准

年龄范围
55 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 55 to 90 years of age
  • Diagnosed with mild to moderate Alzheimer's disease
  • Willing caregiver
  • In general good health

排除标准

  • Call 1-877-MY-MEMORY and ask to be referred to a study center located near you for entry criteria information.
  • Prohibited Meds:
  • Alzheimer's medications (Aricept, Exelon, Remydl, Nemenda)

研究者

发起方
Saegis Pharmaceuticals
申办方类型
Industry

研究点 (101)

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