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OpenTrials
Completed

NCT Number: NCT05171803

Investigating Immune Escape by SARS-CoV-2 Variants

The purpose of this protocol is to investigate the ability of pre-existing immunity by natural infection or vaccination to prevent infections by emerging SARS-CoV-2 variants.

Completed

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Key information

Age range

18 year–100 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Curative

San Dimas, California, 91773, United States

About this study

Several variants of the SARS-CoV-2 virus were identified in 2020 including the United Kingdom variant (known as 20I/501Y.V1, VOC 202012/01, or B.1.1.7), South Africa variant (known as 20H/501Y.V2 or B.1.35), and Brazil variant (known as P.1), with more variants still being discovered. There is concern that these variants, due to mutations in spike protein and receptor-binding domain of the spike protein, can be more infectious, lethal, and potentially escape the immune responses from vaccination or prior infection. Research is needed to understand the risks associated with currently known variants of SARS-CoV-2 as well as investigate if there is potential for new mutations to form that would allow SARS-CoV-2 variants to partially or entirely escape the immune mechanisms developed from vaccination and/or prior infection from the wild-type strain of SARS-CoV-2.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • People who have been fully vaccinated for COVID-19 2-12 weeks prior to enrollment or individuals <3 months post-COVID-19 infection.
  • Collection of samples for blood samples will be done only from healthy, nonpregnant adults who weigh at least 110 pounds.
  • Participants must be able to provide informed consent.

Exclusion criteria

-Subjects considered vulnerable including children, pregnant women, nursing home residents, or other institutionalized persons, fetuses, prisoners, and persons without decisional capacity.

Treatment and study plan

No intervention

Other

No intervention, prospective, cohort study.

Primary outcomes

  1. Assessing immunity

    Time frame: 1 year

    Assess immune escape among people with vaccination or natural immunity

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Collaborators

  • Advarra

Registry information

Important dates

Study start
2021
Primary completion
2022
Study completion
2023
First posted
Dec 29, 2021
Registry last updated
Nov 8, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.