跳至主要内容
临床试验/EUCTR2013-003439-31-CZ
EUCTR2013-003439-31-CZ进行中(未招募)1 期

A 24-week Double-blind Treatment and 24-week Follow-up, Randomized, Multicenter, Placebo-controlled, Phase IIa/IIb Study to Evaluate Safety and Efficacy of i.v. Bimagrumab on Total Lean Body Mass and Physical Performance in Patients After Surgical Treatment of Hip Fracture

ovartis Pharma Services AG0 个研究点目标入组 250 人开始时间: 2015年4月22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
250

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

  • Must have had surgical fixation or arthroplasty for a fracture of the proximal femur as confirmed by radiography;
  • Must have completed surgical wound healing;
  • Must be able to complete a 4 m gait speed test;
  • Must weigh at least 35 kg.
  • Other protocol-defined inclusion criteria may apply.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • 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) yes
  • F.1.3.1 Number of subjects for this age range 245

排除标准

  • Must not have history of any other lower limb fractures in the past 6 months;
  • Must not have certain cardiovascular conditions;
  • Must not have a chronic active infection (e.g. HIV, hepatitis B or C, etc);
  • Must not have used high-dose corticosteroid medications for at least 3 months in the past year;
  • Other protocol-defined inclusion and exclusion criteria may apply

研究者

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