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临床试验/NCT04422509
NCT04422509已完成1 期

Lanadelumab for Treatment of COVID-19 Disease

Radboud University Medical Center4 个研究点 分布在 1 个国家目标入组 43 人开始时间: 2020年10月30日最近更新:
适应症

试验速览

阶段
1 期
状态
已完成
入组人数
43
试验地点
4
主要终点
oxygen

研究概览

简要总结

So far little is very few drugs have demonstrated positive results for treatment of COVID19.

Recently the researchers have shown that the use of icatibant in COVID-19 results in a potent decrease in oxygen use. Yet the effect of the three dosages as according to the label dose was insufficient to maintain the clinical improvement in a small group of patients. The researchers argue that with the use of lanadelumab a more lasting effect can be reached due to its longer half life.

研究设计

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

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patient is SARS-COV2 positive (PCR)
  • Without oxygen a saturation below 90%
  • At least 3L/min oxygen dependent
  • Patient is 16 years and older

排除标准

  • Has previously participated in this study
  • Acute myocardial or cerebral ischemic event at time of enrolment
  • Receiving ACE or ARB inhibitor or comparable drugs that is specified as an intervention in this domain as a usual medication prior to this hospitalization will exclude a patient from receiving that agent
  • A baseline alanine aminotransferase or an aspartate aminotransferase that is more than five times the upper limit of normal
  • Patient is known hypersensitive to full human monoclonal antibodies
  • Patient is pregnant or breast feeding

结局指标

主要结局

oxygen

时间窗: 2 weeks

oxygen use in L/min

次要结局

  • adverse events(2 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (4)

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