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临床试验/EUCTR2013-003321-28-NL
EUCTR2013-003321-28-NL
进行中(未招募)
1 期

An open-label, multicenter, multinational extension study of the long-term safety and pharmacokinetics of repeated biweekly infusions of neoGAA in patients with Pompe disease

Genzyme Corporation0 个研究点目标入组 21 人2014年7月16日

概览

阶段
1 期
干预措施
未指定
疾病 / 适应症
Pompe disease (acid alpha-glucosidase deficiency)
发起方
Genzyme Corporation
入组人数
21
状态
进行中(未招募)
最后更新
2年前

概览

简要总结

暂无简介。

注册库
who.int
开始日期
2014年7月16日
结束日期
待定
最后更新
2年前
研究类型
Interventional clinical trial of medicinal product
性别
All

研究者

入排标准

入选标准

  • Patients with Pompe disease who previously completed a neoGAA study.
  • The patient and/or their parent/legal guardian is willing and able to provide signed informed consent, and the patient, if \<18 years of age, is willing to provide assent if deemed able to do so.
  • The patient (and patient’s legal guardian if patient is \<18 years of age) must have the ability to comply with the clinical protocol.
  • The patient, if female and of childbearing potential, must have a negative pregnancy test \[urine beta\-human chorionic gonadotropin] at baseline
  • 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 17
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 4

排除标准

  • The patient is concurrently participating in another clinical study using investigational treatment.
  • The patient, in the opinion of the Investigator, is unable to adhere to the requirements of the study.
  • The patient has clinically significant organic disease (with the exception of symptoms relating to Pompe disease), including clinically significant cardiovascular, hepatic, pulmonary, neurologic, or renal disease, or other medical condition, serious intercurrent illness, or extenuating circumstance that, in the opinion of the Investigator, precludes participation in the study or potentially decreases survival.

结局指标

主要结局

未指定

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