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临床试验/EUCTR2019-000337-39-IT
EUCTR2019-000337-39-IT进行中(未招募)1 期

An Open-Label Safety, Tolerability, and Efficacy Study of Eteplirsen in Patients with Duchenne Muscular Dystrophy Who Have Completed Study 4658-102 - Not applicable

SAREPTA THERAPEUTICS, INC.0 个研究点目标入组 0 人开始时间: 2021年2月1日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)

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. Patient has successfully completed 96 weeks of treatment in Study 4658-102.
  • 2. Parent(s) or legal guardian(s) who is/are able to understand and comply with the study requirements.
  • 3. Patient and/or their parent(s)/legal guardian(s) are willing and able to provide signed informed consent.
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range:
  • 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

  • 1. Patient has a prior or ongoing medical condition that, in the Investigator’s opinion, could adversely affect the safety of the patient, or make it unlikely that the course of treatment or follow-up would be completed, or impair the assessment of study results.

研究者

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