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临床试验/EUCTR2013-002701-56-NL
EUCTR2013-002701-56-NL进行中(未招募)1 期

A Phase 2, multicenter, multinational, open-label, dose-escalation study to evaluate the safety and efficacy of ORGN001 (formerly ALXN1101) in pediatric patients with Molybdenum Cofactor Deficiency (MoCD) Type A currently treated with recombinant Escherichia coli-derived Cyclic Pyranopterin Monophosphate (rcPMP)

Origin Biosciences, Inc.0 个研究点目标入组 8 人开始时间: 2014年1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

  • - Male or female patients with a genetically confirmed diagnosis of MoCD Type A (MOCS1 mutation)
  • - Currently treated with rcPMP infusions
  • Are the trial subjects under 18? yes
  • Number of subjects for this age range: 8
  • 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

  • - Current or planned treatment with another investigational drug or device, with the exception of rcPMP treatment through Day -1

研究者

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