跳至主要内容
临床试验/EUCTR2015-002805-13-NL
EUCTR2015-002805-13-NL进行中(未招募)1 期

ongterm Follow-up of Subjects With Cerebral Adrenoleukodystrophy Who Were Treated With Lenti-D Drug Product

bluebird bio, Inc0 个研究点目标入组 60 人开始时间: 2021年4月30日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
60

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
Male

入选标准

  • 1.Provision of written informed consent for this study by the subject or subject’s parent(s)/ legal guardian(s) and written informed assent by subject, if applicable
  • 2.Have received Lenti-D Drug Product in a parent clinical study.
  • 3.Able to comply with study requirements.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 60
  • F.1.2 Adults (18-64 years) no
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • There are no exclusion criteria for this Study.

研究者

发起方
bluebird bio, Inc

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