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临床试验/NCT04522817
NCT04522817撤回1 期

CLBS119 (Autologous Peripheral Blood Derived CD34+ Cells) for Repair of COVID-19 Induced Pulmonary Damage

Lisata Therapeutics, Inc.1 个研究点 分布在 1 个国家开始时间: 2020年10月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
撤回
试验地点
1
主要终点
Adverse events

研究概览

简要总结

This clinical trial will explore the safety and potential efficacy of CLBS119 for the repair of COVID-19 induced pulmonary damage in adults.

详细描述

This open-label clinical trial will explore the safety and potential efficacy of peripheral blood derived autologous CD34+ cells for the repair of COVID-19 induced pulmonary damage in adults. Eligible subjects will receive a single administration of CLBS119.

研究设计

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

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

  • Initial diagnosis with COVID-19 based on nasopharyngeal, oropharyngeal, or tracheobronchial aspirate SARS CoV-2 RT-PCR test
  • Receiving or received ventilatory support for COVID-19 pneumonia/ARDS
  • Evidence for ongoing pulmonary involvement based on P/F ratio <300
  • Able to provide informed consent

排除标准

  • Immunocompromised or current use of immunosuppressive agents other than corticosteroids
  • History of autoimmune disease
  • Evidence of multiorgan failure
  • Subject is pregnant or lactating at the time of signing the consent
  • Participation in any other clinical trial of an experimental treatment for COVID-19
  • History of sickle cell disease

研究组 & 干预措施

CLBS119 Active Treatment

Experimental

Single administration of CLBS119

干预措施: CLBS119 (Biological)

结局指标

主要结局

Adverse events

时间窗: Through end of study (6 months)

次要结局

  • Change in oxygen saturation(Change from baseline)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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