An observational study in Covid19 and Cancer, sponsored by University of Rochester. Completed at 1 site in United States. Open to participants aged 50 Years to 75 Years. Per ClinicalTrials.gov, last updated 2025-03-30.
Sponsored by University of Rochester · Observational
To explore the immune response to the COVID-19 vaccine in cancer patients and compare to the general population.
The purpose of this study is to measure the immune response to the COVID-19 vaccine in cancer patients and compare to the general population. This information can help optimize the timing of the mRNA-1273 vaccine relative to starting treatment for cancer, adding booster immunizations or incorporation of medications that to enhance the immune response.
7,640 studies on the registry are indexed under COVID-19; 488 are open to participants now.
This study's enrollment of 8 is below the median of 260 across 3,135 observational studies indexed under COVID-19.
Browse COVID-19 studies →University of Rochester is the lead sponsor of 715 studies on the registry; 116 are open to participants now.
Of its 56 completed or terminated interventional studies of FDA-regulated products, 44 (79%) have results posted.
Counted across the registry records on this site, refreshed daily.
Subjects are between 50 and 75 years of age
Subjects must fall into one of the following subsets of cancer patients:
Exclusion Criteria:
Blood Sample Taken
Other: Blood Sample
Blood sample, 2- to 5 tea spoon full (between 10 to 25 mL approximately) between 43 to 96 days after first dose of the vaccine.
Immunological response to the vaccine
Vaccine response, as determined by blood concentrations of serum IgG reactive to the RBD domain of spike protein from the original SARS-CoV-2 virus will be measured by ELISA
Time frame: 1 year
This study is completed, as verified in Sep 2023. You cannot join it, but the record below documents what was studied.
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University of Rochester