跳至主要内容
临床试验/CTIS2024-513904-33-00
CTIS2024-513904-33-00进行中(未招募)1 期

ongterm Follow-up of Subjects with Cerebral Adrenoleukodystrophy Who Were Treated with Lenti-D Drug Product - LTF-304

Bluebird Bio Inc.0 个研究点目标入组 64 人开始时间: 2024年7月3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
入组人数
64

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 17(—)
性别
Male

入选标准

  • 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, Have received Lenti-D Drug Product in a parent clinical study.

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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