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临床试验/EUCTR2010-020611-36-NL
EUCTR2010-020611-36-NL进行中(未招募)不适用

A Phase 4 Prospective Exploratory Muscle Biopsy, Biomarker, and Imaging Assessment Study in Patients With Late-Onset Pompe Disease Treated With Alglucosidase Alfa - Exploratory Muscle Biopsy Assessment Study (EMBASSY)

Genzyme Europe B.V.0 个研究点目标入组 15 人开始时间: 2011年8月23日最近更新:
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试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
15

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

  • A patient must meet all of the following criteria to be eligible for this study.
  • 1.The patient is willing and able to provide signed informed consent.
  • 2.The patient is =18 years of age with confirmed acid a-glucosidase [GAA] enzyme deficiency from any tissue source and/or confirmed GAA gene mutations and without known cardiac hypertrophy.
  • 3.The patient is able to ambulate a distance without stopping and without an assistive device. Use of assistive device for community ambulation is appropriate.
  • 4.The patient has a certain forced vital capacity (FVC) in upright position.
  • 5.The patient, if female and of childbearing potential, must have a negative pregnancy test at baseline. Note: All female patients of childbearing potential and sexually mature males must agree to use a medically accepted method of contraception throughout the study.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 14
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 1

排除标准

  • A patient who meets any of the following criteria will be excluded from this study.
  • 1.The patient has had previous treatment with enzyme replacement therapy (ERT).
  • 2.The patient is wheelchair dependent.
  • 3.The patient requires invasive-ventilation (non-invasive ventilation is allowed).
  • 4.The patient is participating in another clinical study using investigational treatment.
  • 5.The patient cannot submit to MRI examination because of a formal contraindication such as a pacemaker, implanted ferromagnetic metals, etc.
  • 6.The patient, in the opinion of the Investigator, is unable to adhere to the requirements of the study.

研究者

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