Open-label, Multi-centre, Non-Inferiority Study of Safety and Immunogenicity of BIMERVAX for the Prevention of COVID-19 in Adolescents From 12 Years to Less Than 18 Years of Age.

Inclusion Criteria:

• Adolescents aged from 12 to less than 18 years at Screening.

• Participant's parent(s)/legal guardian(s) willing and able to sign the informedconsent and can comply with all study visits and procedures. A written assent willbe required for all participants in the study. Note: Participants are expected to beavailable for the duration of the study and whose parent(s)/legal guardian can becontacted by telephone during study participation.

• Participant must have received two previous doses of Comirnaty, last dose being atleast 6 months before screening.

• Participant has a body mass index at or above the third percentile according tolocal Child Growth Standards at Screening Visit.

• Healthy participants and participants with pre-existing, chronic and stable diseases (non-immunocompromised), if these are stable and well-controlled according to theinvestigator's judgment, are eligible for inclusion in the study. Note: Healthyparticipants are determined by medical history, physical examination, and clinicaljudgment of the investigator. Healthy participants with pre-existing stablediseases, are defined as diseases not requiring significant change in the therapy orhospitalisation for worsening disease during the 6 weeks before enrolment.

• Has a negative Rapid Antigen Test (RAT) at Day 0 before BIMERVAX® vaccineadministration.

• Participants biologically able to have children may be enrolled in the study if theparticipant fulfils all the following criteria:

• Has a negative urine pregnancy test at Screening (Day 0), only for thoseparticipants who are biologically able to become pregnant.

• Has practiced adequate contraception or has abstained from all activities that couldresult in pregnancy for at least 28 days prior to the booster dose, only for thoseparticipants who are biologically able to become pregnant.

• Has agreed to continue adequate contraception or abstinence through 3 monthsfollowing the booster dose.

1. Participants with female reproductive system:

2. Hormonal contraception (progestogen only or combined: oral, injectable ortransdermal (patch)

3. Intrauterine device.

4. Vasectomized partner (the vasectomized partner should be the sole partnerfor that participant).

5. Condom.

6. Participants with male reproductive system:

7. Vasectomized participants.

8. Agree to use a condom in partners biologically able to become pregnant.

• Participant must have a body weight >50 kg at Screening visit to be eligible for thecellular immunology assays.

Exclusion Criteria:

• Acute illness with fever ≥ 38.0°C at Screening or within 24 hours prior tovaccination. Participant can be rescheduled for Screening when they have completed 24 hours without fever. Afebrile participants with minor illnesses can be enrolledat the discretion of the investigator.

• Received medications intended to prevent or treat COVID-19 before Screening, exceptfor Comirnaty vaccines.

• Previous or current diagnosis of MIS-C.

• Other medical or psychiatric condition including recent (within the past year) oractive suicidal ideation/behaviour or laboratory abnormality that may increase therisk of study participation or, in the investigator's judgment, make the participantinappropriate for the study.

Note: This includes both conditions that may increase the risk associated with study intervention administration or a condition that may interfere with the interpretation of study results.

• History of severe adverse reaction associated with a vaccine and/or severe allergicreaction (e.g. anaphylaxis) to any component of the study intervention(s).

• Immunocompromised individuals defined as those with primary and secondary immunedeficiencies and those receiving chemotherapy or immunosuppressant drugs other thansteroids and glucocorticoids (maximum 1 mg/kg/day of prednisone or total dose of 20mg/day by any administration route for a maximum of 30 consecutive days), within 90 days prior to vaccination or during the study.

• Bleeding diathesis or condition associated with prolonged bleeding that would, inthe opinion of the investigator, contraindicate intramuscular injection.

• Female who is pregnant or breastfeeding.

• Receipt of blood/plasma products, immunoglobulin, monoclonal antibodies, or receiptof any passive antibody therapy, within 90 days prior to vaccination or during thestudy.

• Participation in other studies involving study intervention within 28 days prior toscreening and/or during study participation.

• Received any non-study vaccine (including seasonal Influenza vaccine) within 14 daysbefore or after screening. For live or attenuated vaccines, 4 weeks before or afterscreening.

• History of illegal substance use or alcohol abuse within the past 2 years.

• History of a diagnosis or other conditions that, in the judgment of theinvestigator, may affect study endpoint assessment or compromise participant safety.

• Individuals who are family members of the Investigators.

• Individuals with documented medical history of microbiologically confirmed COVID-19will not be eligible for the immunogenicity group.