跳至主要内容
临床试验/NCT00351156
NCT00351156已完成不适用

A Multicenter Study to Evaluate and Characterize the Ex Vivo Effect of Pharmacological Chaperone Therapy in Blood Cell Lines Derived From Patients With Gaucher Disease

Amicus Therapeutics7 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2006年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
试验地点
7

研究概览

简要总结

The purpose of this study is to learn more about Gaucher disease. The information we collect from medical histories and a blood sample from people with Gaucher disease may help us pinpoint certain things that are different between people who have Gaucher disease and people who do not have Gaucher disease. This information may be useful in the future to help find new treatments for Gaucher disease.

详细描述

This study is designed to evaluate the ex vivo response to pharmacological chaperone therapy by testing blood samples from previously treated and untreated patients with Gaucher disease. The study will include patients with non-neuropathic Gaucher disease (type I) and neuropathic Gaucher disease (types II and/or III).

All subjects will participate in one study visit. Clinical information will be collected retrospectively from medical records. Information collected will include Gaucher disease diagnosis and history, medical history, family history, assessments of clinical severity, and genotype. A blood sample will be collected and various cells will be isolated for laboratory testing and research.

研究设计

研究类型
Observational

入排标准

性别
All
接受健康志愿者

入选标准

  • Willing and able to provide written informed consent by subject or legal guardian
  • Male or female of any age
  • Confirmed diagnosis of Gaucher disease with known genotype
  • Clinically stable and either treatment naïve or on a stable dose of enzyme replacement therapy and/or substrate reduction therapy for at least 6 months prior to study entry
  • Available medical records for collection of retrospective clinical information

排除标准

  • Received any investigational product within 30 days prior to study entry
  • Other significant disease or be otherwise unsuitable for the study, as determined by the investigator

研究者

申办方类型
Industry

研究点 (7)

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