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临床试验/2024-512828-12-00
2024-512828-12-00招募中4 期

An open-label study to collect safety and effectiveness information on long-term treatment with vamorolone in boys with Duchenne Muscular Dystrophy who have completed prior studies with vamorolone (The GUARDIAN Study)

Santhera Pharmaceuticals (Schweiz) AG10 个研究点 分布在 6 个国家目标入组 26 人开始时间: 2024年10月4日最近更新:
适应症

试验速览

阶段
4 期
状态
招募中
入组人数
26
试验地点
10
主要终点
Number of vertebral fractures per 1000 person-years based on X- ray central reading

研究概览

简要总结

To evaluate the safety of long-term treatment with vamorolone in boys with DMD regarding vertebral fractures

入排标准

年龄范围
0 years 至 17 years(0-17 Years)
性别
Male
接受健康志愿者

入选标准

  • Subject and/or subject’s parent(s) or legal guardian has provided written informed consent
  • Subject has previously completed either the VBP15-LTE or VBP15-004 study, and transitioned through the CUP, NPP or EAP
  • Subject is on vamorolone on the day of enrolment
  • Subject and parent / legal guardian are willing and able to comply with the protocol schedule, assessments and requirements

排除标准

  • Any medical condition, which in the opinion of the Investigator, would affect study participation, performance or interpretation of study assessments
  • Vamorolone treatment discontinued for ≥6 months within the year prior to enrolment for a non-safety reason, or vamorolone treatment previously discontinued at any time for a safety reason
  • Severe hepatic impairment

结局指标

主要结局

Number of vertebral fractures per 1000 person-years based on X- ray central reading

Number of vertebral fractures per 1000 person-years based on X- ray central reading

次要结局

  • Time to first vertebral fractures (cumulative incidence)
  • Number of non-vertebral fractures per 1000 person-years based on investigator reporting
  • Time to first non-vertebral fractures (cumulative incidence)
  • Number of cataracts per 1000 person-years based on ophthalmologist assessment
  • Number of subjects not reaching Tanner stage 2 by 15 years of age
  • Frequency of adverse events (AEs) and serious adverse events (SAEs)
  • Change from baseline in body weight, height and body mass index (BMI)
  • Number of subjects with clinically relevant laboratory abnormalities including glycosylated haemoglobin (HbA1c), and morning cortisol
  • Change from baseline in Time to Stand Test (TTSTAND) velocity
  • 6-Minute Walk Test (6MWT) distance
  • Change from baseline in 6MWT distance
  • NorthStar Ambulatory Assessment (NSAA) scores
  • Age at ambulatory and non-ambulatory milestones

研究者

申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Santhera General Inquiries

Scientific

Santhera Pharmaceuticals (Schweiz) AG

研究点 (10)

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