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临床试验/ISRCTN48334111
ISRCTN48334111已完成不适用

Randomised, Double-Blind, Placebo Controlled, Cross Over Trial of a Parenteral Modified Cobratoxin in Adrenomyeloneuropathy

ReceptoPharm Inc. (USA)0 个研究点目标入组 0 人开始时间: 2005年3月10日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
All

入选标准

  • 1. Male or female age =18 years
  • 2. Diagnosis of AMN either biochemically or genetically
  • 3. Have some motor disability that affects their gait
  • 4. Willing and able to provide written informed consent
  • 5. Willing and able to comply with study procedures

排除标准

  • Not provided at time of registration.

研究者

发起方
ReceptoPharm Inc. (USA)

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