跳至主要内容
临床试验/NCT04381091
NCT04381091No Longer Available不适用

Expanded Access Program for Idebenone in Patients With Leber's Hereditary Optic Neuropathy Who Completed the LEROS Study

Santhera Pharmaceuticals0 个研究点开始时间: 2020年5月8日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
No Longer Available

研究概览

简要总结

Expanded Access Program for Idebenone in Patients with Leber's Hereditary Optic Neuropathy who completed the LEROS Study

详细描述

see above

研究设计

研究类型
Expanded Access

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients who completed the LEROS study, who attended the end of study visit in LEROS and who in the opinion of investigator could benefit from continuation of idebenone treatment.
  • Signed and dated Informed Consent Form (to be obtained at the Enrollment Visit from patient or parent/legal guardian (if applicable) prior to dispensing idebenone to the patient).

排除标准

  • Patients who, in the opinion of the LEROS investigator, had unacceptable tolerability of idebenone treatment in LEROS trial.
  • Patients who prematurely discontinued the LEROS study.

研究者

申办方类型
Industry
责任方
Sponsor

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