Clinical trial · Observational
Serologic Response to the SARS-CoV-2 (COVID-19) MRNA-1273 Vaccine in Select Subsets of Oncology Patients
Serologic Response to the SARS-CoV-2 MRNA-1273 Vaccine in Select Subsets of Oncology Patients - a Pilot Study
NCT04854980CI-TRIAL-00087895completedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
To explore the immune response to the COVID-19 vaccine in cancer patients and compare to the general population.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
| Covid19 | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood Sample | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- label
- Experimental:
- description
- Blood Sample Taken
- interventionNames
- Other: Blood Sample
Primary outcomes (1)
- measure
- Immunological response to the vaccine
- timeFrame
- 1 year
- description
- 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
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 50 Years
- Maximum age
- 75 Years
Show eligibility criteria text
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
References
Publications (0)
Data not yet available
No reference posted for this study.