1. Male or female participants between the ages of 16 and above at randomization 2. Living in the area and planning to reside in the area for at least 6 months 3. Capable of giving personal signed informed consent/have parent(s)/legal guardian capable of giving signed informed consent as described in SOP-03 4. Healthy participants who are determined by the clinical judgment of the investigator to be eligible for inclusion in the study 5. Participants who are willing and able to comply with all scheduled visits, vaccination plans, laboratory tests (if randomised and consent given, lifestyle considerations, and other study procedures

1. Male or female participants between the ages of 16 and above at randomization 2. Living in the area and planning to reside in the area for at least 6 months 3. Capable of giving personal signed informed consent/have parent(s)/legal guardian capable of giving signed informed consent as described in SOP-03 4. Healthy participants who are determined by the clinical judgment of the investigator to be eligible for inclusion in the study 5. Participants who are willing and able to comply with all scheduled visits, vaccination plans, laboratory tests (if randomised and consent given, lifestyle considerations, and other study procedures