跳至主要内容
临床试验/EUCTR2007-001646-40-DE
EUCTR2007-001646-40-DE进行中(未招募)1 期

A Phase III Open-Label, Single-Group Extension Study to Obtain Long-Term Safety and Tolerability Data of Idebenone in the Treatment of Friedreich's Ataxia Patients - MICONOS EXTENSIO

Santhera Pharmaceuticals (Switzerland) Limited0 个研究点目标入组 232 人开始时间: 2007年4月25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
232

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

  • Completion of 52 weeks in study SNT-III-001
  • Body weight = 25kg
  • Negative urine pregnancy test
  • Eligibility to participate in the present extension study as confirmed by the investigator
  • Are the trial subjects under 18? yes
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Safety or tolerability issues arising during the course of SNT-III-001 which in the
  • opinion of the investigator preclude further treatment with idebenone
  • Clinically significant abnormalities of haematology or biochemistry including, but
  • not limited to, elevations greater than 1.5 times the upper limit of SGOT, SGPT or
  • Parallel participation in another clinical drug trial
  • Pregnancy or breast-feeding
  • Abuse of drugs or alcohol

研究者

发起方
Santhera Pharmaceuticals (Switzerland) Limited

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