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临床试验/NCT04555096
NCT04555096终止2 期

A Pilot, Randomized, Placebo-Controlled Trial of GC4419 (Avasopasem Manganese) in Patients With Critical Illness Due to SARS-CoV-2 Infection (COVID-19)

Galera Therapeutics, Inc.3 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2020年9月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
16
试验地点
3
主要终点
28 Day All-cause Mortality

研究概览

简要总结

A Trial of GC4419 in Patients with Critical Illness due to COVID-19

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Male or female subjects at least 18 years of age.
  • Ability to understand and the willingness to sign a written informed consent.
  • Laboratory-confirmed SARS-CoV-2 infection as determined by a positive PCR test documented prior to randomization
  • Requirement for intensive inpatient hospital care
  • Acute hypoxemic respiratory failure typifying ARDS
  • Adequate liver function
  • Use of effective contraception

排除标准

  • Expected survival for less than 48 hours after randomization
  • Child-Pugh stage C hepatic impairment and/or portal hypertension secondary to cirrhosis
  • Stage IV chronic kidney disease or end-stage kidney disease on maintenance hemodialysis
  • Requirement for extra-corporeal membrane oxygenation (ECMO)
  • Acute Myocardial Infarction (AMI)
  • Active bleeding requiring transfusion
  • Concurrent participation in another clinical trial of experimental treatment for SARSCoV-2
  • Female patients who are pregnant or breastfeeding
  • Requirement for concurrent treatment with nitrates

研究组 & 干预措施

Active GC4419

Experimental

Arm A

干预措施: GC4419 (Drug)

Placebo

Placebo Comparator

Arm B

干预措施: Placebo (Drug)

结局指标

主要结局

28 Day All-cause Mortality

时间窗: 28 days

Death rate of patients with critical illness due to COVID-19 28 days after initiation of therapy.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (3)

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