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Open access · US-GOV via ClinicalTrials.gov Clinical trial

Two-Year Prospective Study of Antibody Response and Longevity Post SARS-CoV-2 Vaccine and Their Correlation With Humoral Factors

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IRCCS San Camillo, Venezia, Italy · 2021

Abstract

Longitudinal study on healthy subjects to investigate the longevity of the antibody response to the Pfizer-BioNTech COVID-19 vaccine. Venous blood samples will be collected on an outpatient basis from 400 adults at regular intervals (1, 2, 4, 6, 12, 18 and 24 months) after the second dose of the vaccine. In the event of the administration of a third dose, the participants already recruited will be subjected to a venous blood sample immediately before administration and subsequently at regular intervals (1, 2, 4, 6, 8 and 12 months). A laboratory serological test will be performed for each sample. The expression of humoral biomarkers will be evaluated with the Luminex methodology with the aim of identifying prognostic and predictive biomarkers of the response to the vaccine.

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ClinicalTrials.gov
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2026-10-18 MST

Cite this

APA
Anonymous. (2021). Two-Year Prospective Study of Antibody Response and Longevity Post SARS-CoV-2 Vaccine and Their Correlation With Humoral Factors. <em>IRCCS San Camillo, Venezia, Italy</em>. https://clinicaltrials.gov/study/NCT05515081
Vancouver
Anonymous. Two-Year Prospective Study of Antibody Response and Longevity Post SARS-CoV-2 Vaccine and Their Correlation With Humoral Factors. IRCCS San Camillo, Venezia, Italy. 2021.
BibTeX
@misc{anon2021TwoYea, title = {Two-Year Prospective Study of Antibody Response and Longevity Post SARS-CoV-2 Vaccine and Their Correlation With Humoral Factors}, author = {Anonymous}, journal = {IRCCS San Camillo, Venezia, Italy}, year = {2021}, }

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