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OpenTrials
Completed

NCT Number: NCT04854980

Serologic Response to the SARS-CoV-2 (COVID-19) MRNA-1273 Vaccine in Select Subsets of Oncology Patients

To explore the immune response to the COVID-19 vaccine in cancer patients and compare to the general population.

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Key information

Age range

50 year–75 year

Sex eligibility

All sexes

Study type

Observational

Primary location

University of Rochester

Rochester, New York, 14642, United States

About this study

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.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subjects are between 50 and 75 years of age;
  • Have not had known or suspected infection with SARS-CoV-2 at any time;
  • Subjects must fall into one of the following subsets of cancer patients:
  • Localized prostate cancer on radiotherapy or have completed radiotherapy in the last three months
  • Prostate cancer on androgen-deprivation therapy for biochemical recurrence
  • Colon cancer on adjuvant chemotherapy for stage III disease
  • CLL on a BTK inhibitor as a first-line single agent for at least 3 months
  • Melanoma patients on adjuvant immunotherapy with PD-1 checkpoint inhibitors for at least 3 months
  • Have received both doses of SARS-CoV-2 mRNA-1273 vaccine with proof of vaccination or are scheduled to do so;
  • Have at least a one-year life expectancy;
  • Prior radiation therapy is allowed, as long as it was completed more than 6 months prior to vaccination

Exclusion criteria

  • Subjects have a known hypersensitivity to a vaccine component;
  • Have had known or suspected infection with SARS-CoV-2 at any time;
  • Are organ transplant recipient on immunosuppression;
  • Had received or are scheduled to receive a live virus vaccine in the period from 4 weeks prior to Dose 1 through 28 days post second dose;
  • Had received or are scheduled to receive an inactivated vaccine in the period ranging from 7 days prior to Dose 1 through 7 days post second dose;
  • Received high-dose corticosteroids at any time after receiving the vaccine;
  • Are unable to give informed consent;
  • Are receiving treatment for CLL with another agent (such as rituximab) in addition to a BTK inhibitor

Treatment and study plan

blood sample

Other

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.

Primary outcomes

  1. Immunological response to the vaccine

    Time frame: 1 year

    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

Sponsors and collaborators

Lead sponsor

University of Rochester

Other

Registry information

Official study title

Serologic Response to the SARS-CoV-2 MRNA-1273 Vaccine in Select Subsets of Oncology Patients - a Pilot Study

Important dates

Study start
2021
Primary completion
2022
Study completion
2024
First posted
Apr 22, 2021
Registry last updated
Mar 30, 2025

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.

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