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
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
How this study is categorized
These labels come from structured fields and exact terms in the public record.
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.
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.