* had significant exposure to someone with sars-cov-2 infection or covid-19 in the past 14 days, defined by the us centers for disease control and prevention (cdc) as a close contact of someone who has covid-19. * is acutely ill or febrile (temperature ≥38.0 degree celsius \[°c\]/100.4 degree fahrenheit \[°f\]) less than 72 hours prior to or at the screening visit or day 1. * has a medical, psychiatric, or occupational condition that may pose additional risk as a result of participation, or that could interfere with safety assessments or interpretation of results according to the investigator's judgment. * has received systemic immunosuppressants or immune-modifying drugs for \>14 days in total within 6 months prior to screening (for corticosteroids ≥10 milligrams \[mg\]/day of prednisone equivalent) or is anticipating the need for immunosuppressive treatment at any time during participation in the study. * has received or plans to receive any licensed vaccine ≤28 days prior to the injection (day 1) or plans to receive a licensed vaccine within 28 days before or after the study injection, with the exception of influenza vaccines, which may be given 14 days before or after receipt of a study vaccine. * has received systemic immunoglobulins or blood products within 3 months prior to the screening visit, or plans to receive these during the study. * has donated ≥ 450 milliliters (ml) of blood products within 28 days prior to the screening visit or plans to donate blood products during the study. * plans to participate in an interventional clinical trial of an investigational vaccine or drug while participating in this study. note: other inclusion and exclusion criteria may apply.

* had significant exposure to someone with sars-cov-2 infection or covid-19 in the past 14 days, defined by the us centers for disease control and prevention (cdc) as a close contact of someone who has covid-19. * is acutely ill or febrile (temperature ≥38.0 degree celsius \[°c\]/100.4 degree fahrenheit \[°f\]) less than 72 hours prior to or at the screening visit or day 1. * has a medical, psychiatric, or occupational condition that may pose additional risk as a result of participation, or that could interfere with safety assessments or interpretation of results according to the investigator's judgment. * has received systemic immunosuppressants or immune-modifying drugs for \>14 days in total within 6 months prior to screening (for corticosteroids ≥10 milligrams \[mg\]/day of prednisone equivalent) or is anticipating the need for immunosuppressive treatment at any time during participation in the study. * has received or plans to receive any licensed vaccine ≤28 days prior to the injection (day 1) or plans to receive a licensed vaccine within 28 days before or after the study injection, with the exception of influenza vaccines, which may be given 14 days before or after receipt of a study vaccine. * has received systemic immunoglobulins or blood products within 3 months prior to the screening visit, or plans to receive these during the study. * has donated ≥ 450 milliliters (ml) of blood products within 28 days prior to the screening visit or plans to donate blood products during the study. * plans to participate in an interventional clinical trial of an investigational vaccine or drug while participating in this study. note: other inclusion and exclusion criteria may apply.

had significant exposure to someone with sars-cov-2 infection or covid-19 in the past 14 days, defined by the us centers for disease control and prevention (cdc) as a close contact of someone who has covid-19. is acutely ill or febrile (temperature ≥38.0 degree celsius [°c]/100.4 degree fahrenheit [°f]) less than 72 hours prior to or at the screening visit or day 1. has a medical, psychiatric, or occupational condition that may pose additional risk as a result of participation, or that could interfere with safety assessments or interpretation of results according to the investigator's judgment. has received systemic immunosuppressants or immune-modifying drugs for >14 days in total within 6 months prior to screening (for corticosteroids ≥10 milligrams [mg]/day of prednisone equivalent) or is anticipating the need for immunosuppressive treatment at any time during participation in the study. has received or plans to receive any licensed vaccine ≤28 days prior to the injection (day 1) or plans to receive a licensed vaccine within 28 days before or after the study injection, with the exception of influenza vaccines, which may be given 14 days before or after receipt of a study vaccine. has received systemic immunoglobulins or blood products within 3 months prior to the screening visit, or plans to receive these during the study. has donated ≥ 450 milliliters (ml) of blood products within 28 days prior to the screening visit or plans to donate blood products during the study. plans to participate in an interventional clinical trial of an investigational vaccine or drug while participating in this study. note: other inclusion and exclusion criteria may apply.

had significant exposure to someone with sars-cov-2 infection or covid-19 in the past 14 days, defined by the us centers for disease control and prevention (cdc) as a close contact of someone who has covid-19. is acutely ill or febrile (temperature ≥38.0 degree celsius [°c]/100.4 degree fahrenheit [°f]) less than 72 hours prior to or at the screening visit or day 1. has a medical, psychiatric, or occupational condition that may pose additional risk as a result of participation, or that could interfere with safety assessments or interpretation of results according to the investigator's judgment. has received systemic immunosuppressants or immune-modifying drugs for >14 days in total within 6 months prior to screening (for corticosteroids ≥10 milligrams [mg]/day of prednisone equivalent) or is anticipating the need for immunosuppressive treatment at any time during participation in the study. has received or plans to receive any licensed vaccine ≤28 days prior to the injection (day 1) or plans to receive a licensed vaccine within 28 days before or after the study injection, with the exception of influenza vaccines, which may be given 14 days before or after receipt of a study vaccine. has received systemic immunoglobulins or blood products within 3 months prior to the screening visit, or plans to receive these during the study. has donated ≥ 450 milliliters (ml) of blood products within 28 days prior to the screening visit or plans to donate blood products during the study. plans to participate in an interventional clinical trial of an investigational vaccine or drug while participating in this study. note: other inclusion and exclusion criteria may apply.