CompletedNot applicableNCT04865133

Efficacy and Safety of COVID-19 Vaccine in Cancer Patients

This study gathers information about how a cancer patient responds to COVID-19 vaccine during cancer treatment compared to healthy individuals. The information gained may help determine how effective currently available COVID-19 vaccines are in cancer patients receiving chemotherapy and learn more regarding how long an immune response will last compared to healthy individuals.

Checked against the public recordLast updated Dec 10, 2024 · Source: ClinicalTrials.gov

StatusCompleted
PhaseNot applicable
U.S. locations1
SponsorMayo Clinic
01
Study overview

What this study is about

Purpose
Not specified
Study type
Observational
Phase
Not applicable
Sponsor
Mayo Clinic
Interventions being studied
Procedure: Biospecimen Collection; Other: Electronic Health Record Review
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

Treatment approach
03
Public criteria

Who may be able to participate

Inclusion Criteria: * Willing to receive COVID-19 vaccination as per standard of care or has already received one or both COVID-19 vaccine injections as long as it has not been longer than three months since their second injection (or the only injection if they receive the types of COVID019 vaccines that do not require the second injection) * Willing and able to provide research blood samples * Capable of providing valid informed consent * For cancer patient cohort: * Male or female age \>= 18 years * Histologically confirmed solid malignancy on or will be starting on systemic cytotoxic chemotherapy * For healthy individual cohort: * Male or female age \>= 18 years * No history of active malignancy =\< 3 years * EXCEPTIONS: Adequately treated non-melanotic skin cancer (adequate wound healing is required prior to study entry) or carcinoma-in-situ of the cervix * NOTE: If there is a history of prior solid tumor malignancy, it must have been treated curatively with no evidence of recurrence =\< 3 years * PATIENTS WITH PREVIOUS COVID-19 INFECTION: Willing and able to provide research blood samples * PATIENTS WITH PREVIOUS COVID-19 INFECTION: Capable of providing valid informed consent * PATIENTS WITH PREVIOUS COVID-19 INFECTION: Male or female age \>= 18 years * PATIENTS WITH PREVIOUS COVID-19 INFECTION: Previous history of COVID-19 infection with positive SARS-CoV-2 ribonucleic acid (RNA) by polymerase chain reaction (PCR) or anti-SARS-CoV-2 nucleocapsid antibody Exclusion Criteria: * Immunocompromised patients including patients known to be human immunodeficiency virus (HIV) positive or those on immunosuppressive therapy other than chemotherapy in the judgment of the investigator

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

  • Mayo Clinic in FloridaJacksonville, Florida

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Dec 10, 2024. Always confirm current availability with the study team.

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