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临床试验/EUCTR2019-003595-38-GB
EUCTR2019-003595-38-GB进行中(未招募)1 期

FORTIS: A Phase 1/2, Open-Label, Ascending-Dose Clinical Study to Evaluate the Safety and Preliminary Efficacy of AT845, an AAV8-Delivered Gene Transfer Therapy in Patients with Late Onset Pompe Disease - FORTIS

Audentes Therapeutics, Inc.0 个研究点目标入组 8 人开始时间: 2020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)
入组人数
8

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

  • Subjects must meet all of the following inclusion criteria to be eligible for enrollment:
  • 1. Subject is aged = 18 years (ambulatory or nonambulatory).
  • 2. Subject has a documented clinical diagnosis of Pompe disease by genetic testing.
  • 3. Subject has received ERT with rhGAA for the previous = 2 years.
  • 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 6
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 2

排除标准

  • 1. Subject is currently participating in an interventional study or has received gene or cell therapy
  • 2. Subject tests positive for AAV8 antibodies

研究者

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FORTIS: AAV8-Delivered Gene Therapy in Late Onset... | 临床试验