1. previous medications intervention for the prophylaxis or prevention of covid-19 (including vaccination with any licensed sars-cov-2 vaccines other than 2 doses of coronavac® ). 2. history of severe acute respiratory syndrome (sars), middle east respiratory syndrome (mers) or other coronavirus infections. 3. history of a previous laboratory-confirmed diagnosis of sars-cov-2 infection or covid-19. 4. history of allergy to any component of the study vaccine or history of severe allergic reaction to the vaccine or drug (including but not limited to anaphylaxis, allergic laryngeal oedema, anaphylactic purpura, thrombocytopenic purpura, or localized allergic necrosis (arthus reaction)). 5. positive nucleic acid for sars-cov-2 in nasopharyngeal/oropharyngeal swab specimens. 6. positive hiv test result. 7. a history or family history of convulsions, epilepsy, encephalopathy and psychosis. 8. malignant tumors in the active phase, malignant tumors not receiving adequate treatment, malignant tumors at potential risk of recurrence during the study period. 9. congenital or functional splenic deficiency, complete or partial splenectomy for any reason. 10. prolonged (defined as more than 14 days) use of immunosuppressive or other immunomodulatory drugs (e.g., corticosteroids, ≥20 mg/d prednisone or equivalent; however, inhaled and topical steroids are permitted) within 6 months prior to the vaccine. 11. any other licensed vaccines given within 28 days prior to the study vaccination, or planned administration of vaccine(s) within 28 days after vaccination. 12. have received immunoglobulin or other blood products within 3 months prior to enrollment or plan to receive them during the study period. 13. blood donation or blood loss ≥ 450 ml within 1 month prior to enrolment, or planned donation during the study period. 14. participants who have received any other investigational product within 1 month prior to enrollment or intent to participate in another clinical study at any time during the conduct of this study. 15. female participants who are pregnant or breastfeeding. 16. participants deemed unsuitable for participation in this study based on the investigator's assessment.

1. previous medications intervention for the prophylaxis or prevention of covid-19 (including vaccination with any licensed sars-cov-2 vaccines other than 2 doses of coronavac® ). 2. history of severe acute respiratory syndrome (sars), middle east respiratory syndrome (mers) or other coronavirus infections. 3. history of a previous laboratory-confirmed diagnosis of sars-cov-2 infection or covid-19. 4. history of allergy to any component of the study vaccine or history of severe allergic reaction to the vaccine or drug (including but not limited to anaphylaxis, allergic laryngeal oedema, anaphylactic purpura, thrombocytopenic purpura, or localized allergic necrosis (arthus reaction)). 5. positive nucleic acid for sars-cov-2 in nasopharyngeal/oropharyngeal swab specimens. 6. positive hiv test result. 7. a history or family history of convulsions, epilepsy, encephalopathy and psychosis. 8. malignant tumors in the active phase, malignant tumors not receiving adequate treatment, malignant tumors at potential risk of recurrence during the study period. 9. congenital or functional splenic deficiency, complete or partial splenectomy for any reason. 10. prolonged (defined as more than 14 days) use of immunosuppressive or other immunomodulatory drugs (e.g., corticosteroids, ≥20 mg/d prednisone or equivalent; however, inhaled and topical steroids are permitted) within 6 months prior to the vaccine. 11. any other licensed vaccines given within 28 days prior to the study vaccination, or planned administration of vaccine(s) within 28 days after vaccination. 12. have received immunoglobulin or other blood products within 3 months prior to enrollment or plan to receive them during the study period. 13. blood donation or blood loss ≥ 450 ml within 1 month prior to enrolment, or planned donation during the study period. 14. participants who have received any other investigational product within 1 month prior to enrollment or intent to participate in another clinical study at any time during the conduct of this study. 15. female participants who are pregnant or breastfeeding. 16. participants deemed unsuitable for participation in this study based on the investigator's assessment.

previous medications intervention for the prophylaxis or prevention of covid-19 (including vaccination with any licensed sars-cov-2 vaccines other than 2 doses of coronavac® ). history of severe acute respiratory syndrome (sars), middle east respiratory syndrome (mers) or other coronavirus infections. history of a previous laboratory-confirmed diagnosis of sars-cov-2 infection or covid-19. history of allergy to any component of the study vaccine or history of severe allergic reaction to the vaccine or drug (including but not limited to anaphylaxis, allergic laryngeal oedema, anaphylactic purpura, thrombocytopenic purpura, or localized allergic necrosis (arthus reaction)). positive nucleic acid for sars-cov-2 in nasopharyngeal/oropharyngeal swab specimens. positive hiv test result. a history or family history of convulsions, epilepsy, encephalopathy and psychosis. malignant tumors in the active phase, malignant tumors not receiving adequate treatment, malignant tumors at potential risk of recurrence during the study period. congenital or functional splenic deficiency, complete or partial splenectomy for any reason. prolonged (defined as more than 14 days) use of immunosuppressive or other immunomodulatory drugs (e.g., corticosteroids, ≥20 mg/d prednisone or equivalent; however, inhaled and topical steroids are permitted) within 6 months prior to the vaccine. any other licensed vaccines given within 28 days prior to the study vaccination, or planned administration of vaccine(s) within 28 days after vaccination. have received immunoglobulin or other blood products within 3 months prior to enrollment or plan to receive them during the study period. blood donation or blood loss ≥ 450 ml within 1 month prior to enrolment, or planned donation during the study period. participants who have received any other investigational product within 1 month prior to enrollment or intent to participate in another clinical study at any time during the conduct of this study. female participants who are pregnant or breastfeeding. participants deemed unsuitable for participation in this study based on the investigator's assessment.

previous medications intervention for the prophylaxis or prevention of covid-19 (including vaccination with any licensed sars-cov-2 vaccines other than 2 doses of coronavac® ). history of severe acute respiratory syndrome (sars), middle east respiratory syndrome (mers) or other coronavirus infections. history of a previous laboratory-confirmed diagnosis of sars-cov-2 infection or covid-19. history of allergy to any component of the study vaccine or history of severe allergic reaction to the vaccine or drug (including but not limited to anaphylaxis, allergic laryngeal oedema, anaphylactic purpura, thrombocytopenic purpura, or localized allergic necrosis (arthus reaction)). positive nucleic acid for sars-cov-2 in nasopharyngeal/oropharyngeal swab specimens. positive hiv test result. a history or family history of convulsions, epilepsy, encephalopathy and psychosis. malignant tumors in the active phase, malignant tumors not receiving adequate treatment, malignant tumors at potential risk of recurrence during the study period. congenital or functional splenic deficiency, complete or partial splenectomy for any reason. prolonged (defined as more than 14 days) use of immunosuppressive or other immunomodulatory drugs (e.g., corticosteroids, ≥20 mg/d prednisone or equivalent; however, inhaled and topical steroids are permitted) within 6 months prior to the vaccine. any other licensed vaccines given within 28 days prior to the study vaccination, or planned administration of vaccine(s) within 28 days after vaccination. have received immunoglobulin or other blood products within 3 months prior to enrollment or plan to receive them during the study period. blood donation or blood loss ≥ 450 ml within 1 month prior to enrolment, or planned donation during the study period. participants who have received any other investigational product within 1 month prior to enrollment or intent to participate in another clinical study at any time during the conduct of this study. female participants who are pregnant or breastfeeding. participants deemed unsuitable for participation in this study based on the investigator's assessment.