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临床试验/NCT05379478
NCT05379478已完成不适用

An Evaluation of Immune Responses to SARS-CoV-2 Infection or Vaccination

Aditxt, Inc.1 个研究点 分布在 1 个国家目标入组 403 人开始时间: 2020年12月1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
Aditxt, Inc.
入组人数
403
试验地点
1
主要终点
Laboratory assessment of SARS-CoV-2 antibody profiles

研究概览

简要总结

The overall purpose of this observational cohort study is to characterize COVID-specific immune responses to SARS-CoV-2 exposure or COVID vaccination in a real-world setting. Participants will be asked to provide blood samples (either a normal venous blood draw, a few drops of blood obtained with a small finger-stick device, or both), as well as saliva or nasal swab sample at a series of visits. Subjects will receive results of the testing that is approved for routine clinical use (i.e., their AditxtScore), while residual samples from each visit will be stored for future testing. These efforts will support ongoing AditxtScore test development and enhance the effectiveness of its interpretation - aiding efforts to maximize benefits of clinical laboratory testing in the pandemic response.

详细描述

  1. Background and Overview Aditxt, Inc, in collaboration with researchers at Stanford University, has laboratory-developed tests (LDTs) for simultaneously monitoring anti-SARS-COV2 antibodies (IgG, IgA, and IgM) directed against 3 different SARS-CoV-2 antigens (RBD, S1, and NP) as well as assessing SARS-CoV-2 neutralizing antibody activity.

These tests are currently being offered routinely to the public as the AditxtScoreTM at Aditxt's CLIA certified, CAP accredited clinical laboratory in Richmond, VA. Aditxt also performs these tests for research and development purposes at a facility in Mountain View, CA. The AditxtScore provides an ideal platform for real- world investigations of immune responses to SARS-CoV-2 exposure as well as to the COVID-19 vaccines.

The overall purpose of this observational cohort study is to characterize COVID-specific immune responses to SARS-CoV-2 exposure or COVID vaccination in a real-world setting. Participants will be asked to provide blood samples (either a normal venous blood draw, a few drops of blood obtained with a small finger-stick device, or both), as well as saliva or nasal swab sample at a series of visits. Subjects will receive results of the testing that is approved for routine clinical use (i.e., their AditxtScore), while residual samples from each visit will be stored for future testing. These efforts will support ongoing AditxtScore test development and enhance the effectiveness of its interpretation - aiding efforts to maximize benefits of clinical laboratory testing in the pandemic response. 2. Objectives • To characterize immune responses (e.g., magnitude/strength and temporal dynamics of antibody generation, class switching, and antibody persistence) following exposure to the SARS-CoV-2 virus or COVID-19 vaccination.

• To investigate between group (eg vaccine vs. natural exposure) and within group (i.e., individual variation) differences in immune responses.

• To determine the relationship between AditxtScore components and neutralizing antibody activity and other potential correlates of protection, and to describe possible clinical correlates of immune response characteristics.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Willingness to participate
  • 18 years and older

排除标准

  • Refusal or inability to provide informed consent

结局指标

主要结局

Laboratory assessment of SARS-CoV-2 antibody profiles

时间窗: 2 years

Antibody profiles consist of quantitative determination of IgG, IgM, and IgA levels to the SARs-CoV-2 spike protein (S), receptor binding domain (RBD), and nucleocapsid protein (NP) by flow cytometry. Also, Neutralizing Antibody (NAb) concentrations were determined with a novel flow cytometry based competitive inhibition assay for the measurement of total neutralizing antibodies to different variants of SARS-CoV-2.

次要结局

未报告次要终点

研究者

发起方
Aditxt, Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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