- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04494893
ImmuneRACE - Immune Response Action to COVID-19 Events
Study Overview
Status
Conditions
Detailed Description
PURPOSE Aim 1. Compare disease-specific TCR signatures in patients vs. controls Aim 2. Identify antigens that elicit a T-cell response Aim 3. Risk Stratification based on immune signature Aim 4. Early detection
Secondary Aim:
Aim 5. Identify and/or confirm antigenic binding (BCR PairSEQ/neutralizing antibodies)
STUDY POPULATION Approximately 1000 individuals, between the ages of 18 - 89 Cohort 1. EXPOSED to someone with a confirmed diagnosis of COVID-19 Cohort 2. ACTIVE COVID-19
Individuals with a confirmed diagnosis of COVID-19:
Clinical diagnosis made by a medical professional, or Positive laboratory test Cohort 3. RECOVERED from COVID-19
Individuals with a previously confirmed diagnosed and cleared from active infection by either:
Testing negative on two consecutive swab tests, or Cleared by a healthcare professional, or Resolution of symptoms
METHODS Decentralized study (visits occur at participant's houses) Utilizing remote phlebotomy to collect (1) whole blood, (2) serum, (3) nose or throat swab Collection of relevant metadata by electronic questionnaire
Option for longitudinal collection of up to 4 additional blood draws and questionnaires
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Washington
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Seattle, Washington, United States, 98102
- Adaptive Biotechnologies
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Cohort 1. Exposed to coronavirus disease
Inclusion criteria
Participants must satisfy the following criteria to be enrolled in the study:
Individuals exposed to someone with a confirmed diagnosis of coronavirus disease within 2 weeks of exposure (or at the discretion of the investigator) Male and female participants of any race and ethnicity between 18 to 89 years of age (inclusive) at the time of enrolling in the study Must be able to communicate with the investigator, understand and comply with the requirements of the study
Exclusion Criteria
The presence of any of the following will exclude a participant from enrollment:
Individuals who have not been exposed to a person with a confirmed diagnosis of coronavirus disease within 2 weeks of exposure (or at the discretion of the investigator) Protected populations including minors, pregnant women, prisoners, mentally disabled persons, and wards-of-the state Any significant condition, laboratory abnormality, or psychiatric illness that would prevent the participant from safely participating in the study Donated more than 500cc or 1 pint of blood in the past 60 days prior to the blood draw (at the discretion of the investigator)
Cohort 2. Active coronavirus disease Inclusion criteria
Participants must satisfy the following criteria to be enrolled in the study:
Individuals with a diagnosis of coronavirus disease:
Either by clinical diagnosis made by a medical professional, or By positive laboratory test, including but not limited to naso- or oropharyngeal swab (or at the discretion of the investigator) Male and female participants of any race and ethnicity between 18 to 89 years of age (inclusive) at the time of enrolling in the study Must be able to communicate with the investigator, understand and comply with the requirements of the study
Exclusion Criteria
The presence of any of the following will exclude a participant from enrollment:
Individuals without a diagnosis of coronavirus disease Protected populations including minors, pregnant women, prisoners, mentally disabled persons, and wards-of-the state Any significant condition, laboratory abnormality, or psychiatric illness that would prevent the participant from safely participating in the study Donated more than 500cc or 1 pint of blood in the past 60 days prior to the blood draw (at the discretion of the investigator)
Cohort 3. Recovered from coronavirus disease Inclusion criteria
Participants must satisfy the following criteria to be enrolled in the study:
Individuals previously diagnosed with coronavirus disease and cleared from active infection by:
Testing negative on two consecutive naso- or oropharyngeal swab tests following initial diagnosis, or Cleared by a healthcare professional or public health authority, or Resolution of symptoms related to COVID-19 (or at the discretion of the investigator) Male and female participants of any race and ethnicity between 18 to 89 years of age (inclusive) at the time of enrolling in the study Must be able to communicate with the investigator, understand and comply with the requirements of the study
Exclusion Criteria
The presence of any of the following will exclude a participant from enrollment:
Individuals without a previous diagnosis of coronavirus disease at the discretion of the investigator Protected populations including minors, pregnant women, prisoners, mentally disabled persons, and wards-of-the state Any significant condition, laboratory abnormality, or psychiatric illness that would prevent the participant from safely participating in the study Donated more than 500cc or 1 pint of blood in the past 60 days prior to the blood draw (at the discretion of the investigator)
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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Cohort 1
Exposed to coronavirus disease
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Cohort 2
Active coronavirus disease
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Cohort 3
Recovered from coronavirus disease
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Comparison of disease-specific TCR signatures in patients and controls
Time Frame: Baseline
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We will run immunoSEQ on approximately 1000 patient samples with disease status unblinded.
After sequencing these samples, we will quantitatively describe the compartment of the T-cell repertoire specific for the disease of interest.
We will then use these data to construct a classifier that accurately distinguishes patients from controls.
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Baseline
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Identify the immunodominant antigens that elicit a T-cell response to COVID-19
Time Frame: Baseline
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We developed technology to query the antigen specificity of the T-cell repertoire to hundreds of peptide epitopes in a single blood sample5.
This technology not only allows us to parse out immunodominant epitopes of a given infection from irrelevant epitopes, but also allows us to determine the TCR sequences of the T cells responding to these immunodominant epitopes.
We will use this technology to determine which peptide epitopes derived from the SARS-CoV-2 genome commonly elicit an immunodominant T-cell response in different samples.
The TCR sequence data generated from these studies will be used to boost the diagnostic classifier obtained in Aim 1.
In addition, the identification of immunodominant epitopes can be disseminated to fuel studies in vaccine design and antigen specific T-cell responses relating to clinical outcome in other labs.
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Baseline
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Risk Stratification based on an individual's immune signature
Time Frame: Baseline
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There is a critical need for a reliable risk stratification test to enable treatment prioritization given the potentially massive number of symptomatic patients.
Despite an emerging understanding of the diagnosis of COVID-19, how it spreads, and the death rate, there is no currently available way to predict who needs hospitalization beyond age associated risk and limited epidemiologically linked comorbidities.
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Baseline
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Determine whether an immune signature can be detected in individuals exposed to SARS-CoV-2 earlier than currently available tests
Time Frame: Baseline
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Another critical need to contain the spread of SARS-CoV-2 is to determine the false negative rate of the RNA test in asymptomatic people and offer an alternative diagnostic that is more sensitive in this cohort.
For example, it is possible that early stage disease is not picked up by RNA tests because the virus may be isolated to regions such as the lower respiratory cavity that are not assessed by standard testing methods.
We aim to determine whether the immune response can be used to detect the virus from a simple blood test thereby providing a more sensitive test in asymptomatic people even if the virus itself is not directly detectable in the upper respiratory region.
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Baseline
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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Explore whether additional research assays could potential identify and/or confirm antigenic binding
Time Frame: Baseline
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As a secondary aim, Adaptive will perform explorational research with additional sequencing-based research assays to profile the adaptive immune system, such as, but not limited to TCR pairSEQ26 and B-cell receptor (BCR) pairSEQ3.
These assays use a combinatorial method for pairing TCR alpha and beta chain sequences and BCR heavy and light chain sequences.
The output is a large set of full length paired BCR or TCR sequences, which allows reconstruction of a functional antibody or TCR.
We regularly utilize the results of our pairSEQ assays to identify and/or confirm antigenic binding.
For the case of BCR pairSEQ, the resulting antibody sequences could potentially have therapeutic value for imparting passive immunity.
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Baseline
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ADAP-006
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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