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临床试验/EUCTR2005-000063-25-GB
EUCTR2005-000063-25-GB进行中(未招募)1 期

A 26 week double-blind extension to a 26 week randomised, double-blind placebo-controlled study that evaluated the safety and efficacy of two different doses of phenserine-tartrate in patients with probable mild to moderate Alzheimer's disease.

Axonyx Inc0 个研究点目标入组 450 人开始时间: 2005年3月2日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Axonyx Inc
入组人数
450

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • After successfully completing the AX-CL-09 study, patients will be enrolled in the extension study and will continue to receive study medication without a break (i.e. rollover directly into the extension study).
  • In order to be eligible for inclusion in this extension study, patients must have successfully completed the AX-CL-09 study and continue to fulfil the inclusion criteria for the AX-CL-09 study.
  • In addition, patients must fulfil the following:
  • General health status acceptable for participation in a 6 month extension study;
  • Are capable of understanding and have given written informed consent for the extension study [or this has been provided by their acceptable representative (according to local requirements)] and a separate caregiver responsibilities and consent form has also been signed by the patient’s caregiver;
  • Have a reliable caregiver available, and if not living in the same household, the caregiver sees the patient at least 4 times a week or a total of 15 to 20 hours per week;
  • Agrees to comply with the protocol requirements of the extension study.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Patients who complete the AX-CL-09 study may have received the investigational drug phenserine-tartrate, which is an acetylcholinesterase inhibitor. These patients are eligible for enrolment in the AX-CL-09e extension study providing they have not received any other acetylcholinesterase inhibitor in the 3 months before study entry, and providing they do not fulfil any other exclusion criteria from the AX CL-09 study.

研究者

发起方
Axonyx Inc

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