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临床试验/NCT04347226
NCT04347226终止2 期

A Randomized Phase 2 Study of Anti-IL-8 Therapy Versus Standard of Care in the Treatment of Hospitalized Patients With Severe COVID-19

Columbia University1 个研究点 分布在 1 个国家目标入组 43 人开始时间: 2020年4月16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
43
试验地点
1
主要终点
Time to Improvement in the 7-point Ordinal Scale

研究概览

简要总结

This study is for patients that are hospitalized for Coronavirus Disease 2019 (COVID-19). The purpose of this study is to see whether neutralizing interleukin-8 (IL-8) with BMS-986253 can help improve the health condition of participants infected with COVID-19. This is the first in-human study of this investigational product specifically in patients with severe COVID-19. Currently there are no FDA approved medications that improve the chance of survival in patients diagnosed with COVID-19. However there are usual treatments currently being used to help treat COVID-19 patients and BMS-986253 will be compared to these standard of care treatments in this study.

详细描述

This is a single center, randomized, open-label, phase 2 trial to evaluate the time-to-improvement in the 7 point ordinal scale following treatment with anti-IL-8 therapy (BMS-986253) compared to standard of care in hospitalized patients with COVID-19 respiratory disease. Patients will be randomized 2:1 to receive either BMS-986253 or standard of care. Patients randomized to treatment with BMS-986253 will receive between 1-3 doses of therapy depending on their clinical status. Participants will be assessed daily while in the hospital and with then be followed for up to 1 year after discharge.

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

BMS-986253

Experimental

BMS-986253 2400mg IV

干预措施: BMS-986253 (Drug)

结局指标

主要结局

Time to Improvement in the 7-point Ordinal Scale

时间窗: Up to 10.5 months

The time to improvement in the 7-point ordinal scale in patients treated with anti-IL-8 therapy compared to standard of care/controls. Measured from baseline to 2 point or greater improvement in 7-point ordinal scale.

次要结局

  • Proportion of Patients Requiring ICU Admission(Up to 10.5 months)
  • Mortality at 1 Month(1 month)
  • Time to Death(Up to 10.5 months)
  • Time to Intubation(Up to 10.5 months)

研究者

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

Mark Stein

Associate Professor of Medicine at the Columbia University Medical Center

Columbia University

研究点 (1)

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