跳至主要内容
临床试验/NCT00033813
NCT00033813已完成2 期

KUL0401: An Open-label Pilot Study of Oxatomide in Steroid-Naive Duchenne Muscular Dystrophy

Cooperative International Neuromuscular Research Group2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2002年1月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
15
试验地点
2

研究概览

简要总结

This study will help to determine the safety and efficacy of the mast cell stabilizer Oxatomide as a treatment for Duchenne muscular dystrophy (DMD). Boys with DMD who are enrolled in this study will should not have taken steroids to treat DMD for at least twelve months, and should not have taken any nutritional supplements for at least three months. Subjects will complete a two screening visits within a one-week period, and if enrolled will then have their strength tested monthly for three months before beginning therapy with Oxatomide. Once Oxatomide therapy is started, participants will have their strength tested monthly for six months. Following the six month treatment period, participants will be given the option to remain on Oxatomide until the study is completed.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
5 Years 至 10 Years(Child)
性别
Male
接受健康志愿者

入选标准

  • Subject Inclusion Criteria
  • 5 to 10 years of age
  • diagnosis of DMD confirmed by at least one of the following:
  • Positive x-linked family history of DMD in older male relatives (onset by 5 years, wheelchair bound by 12 years), or;
  • Dystrophin immunofluorescence and/or immunoblot showing complete dystrophin deficiency, and clinical picture consistent with typical DMD, or;
  • Gene deletion test positive (missing one or more exons) in the central rod domain (exons 25-60) of dystrophin, where reading frame can be predicted as 'out of frame', and clinical picture consistent with typical DMD.
  • glucocorticosteroid-naive (i.e. has not been treated with prednisone or deflazacort within the past year)
  • Evidence of muscle weakness by MRC score or clinical functional evaluation
  • QMT biceps score variability no greater than 10% between screening visits

排除标准

  • Failure to achieve one or more of the inclusion criteria listed above
  • Inability to suitably cooperate with strength assessments
  • Symptomatic DMD carrier
  • Use of oxatomide (or other anti-histamine drugs) within the last 6 months for DMD or any other disease
  • Use of creatine monohydrate or glutamine within the last 6 months
  • Use of carnitine, Coenzyme Q10, other amino acids or any herbal medications within the last 3 months
  • History of symptomatic cardiomyopathy
  • History of impairment of hepatic function
  • History of significant concomitant illness or significant impairment of renal function.

研究者

发起方
Cooperative International Neuromuscular Research Group
申办方类型
Network
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验