跳至主要内容
临床试验/NCT04486482
NCT04486482已完成不适用

An Exploratory, Open Label, Clinical Study to Evaluate the Physiologic Effects of KB109 in Adult Patients With Mild-to-Moderate COVID-19 on Gut Microbiota Structure and Function in the Outpatient Setting

Kaleido Biosciences24 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2021年1月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
49
试验地点
24
主要终点
Number of patients experiencing study-product related treatment-emergent adverse events (TEAEs)

研究概览

简要总结

This exploratory, open-label clinical study aims to explore the physiologic effects of KB109, a novel glycan, on adult patients with COVID-19 illness on gut microbiota structure and function in the outpatient setting.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Other
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

  • To be considered for enrollment into this study, each patient must meet all of the following Inclusion Criteria:
  • Be male or female, ≥18 years of age
  • Be willing and able to give informed consent
  • Screening/Randomization telemedicine visit within 2 days of testing positive test for COVID-19
  • Having self-reported fever or cough for not more than 72 hours prior to COVID-19 testing
  • Mild to moderate COVID-19
  • Able to adhere to the study visit schedule and other protocol requirements
  • Patients who meet any of the following

排除标准

  • at the Randomization Visit will not be enrolled into the study:
  • Patients who are hospitalized for in-patient treatment or currently being evaluated for potential hospitalization at the time of informed consent for conditions other than COVID-19
  • History of chronic lung disease
  • Ongoing requirement for oxygen therapy
  • Shortness of breath in resting position
  • Diagnosis of sleep apnea requiring Bilevel Positive Airway Pressure (BIPAP) / Continuous Positive Airway Pressure (CPAP)
  • Female patients who are pregnant, trying to become pregnant or lactating.
  • Is considered, in the opinion of the PI, to be unlikely for any reason to be able to comply with study procedures

结局指标

主要结局

Number of patients experiencing study-product related treatment-emergent adverse events (TEAEs)

时间窗: Day 1 to Day 35

次要结局

  • Relative abundance of microbial taxa in fecal samples as assessed by shotgun profiling based on shotgun sequencing.(Day 1 to Day 35)

研究者

发起方
Kaleido Biosciences
申办方类型
Industry
责任方
Sponsor

研究点 (24)

Loading locations...

相似试验

A Clinical Study to Assess the Physiologic Effects... | 临床试验