* individuals with body temperature \>37.8°c (axillary), or any acute illness at baseline (day 1) or within 3 days prior to randomization. * body mass index at screening \>30 kg/m2 * individuals with laboratory-confirmed sars-cov-2 infection \[as defined by reverse transcriptase polymerase chain reaction (rt-pcr) assay or rapid covid antigen test or an equivalent\] at the screening visit or with known history of covid-19 within 6 months prior to day 1 * individuals who have received an investigational or authorized covid-19 vaccine within 6 months prior to day 1, or plan to receive covid-19 vaccine during the study period * any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease \[e.g., malignancy, human immunodeficiency virus (hiv) infection\] or immunosuppressive/cytotoxic therapy (e.g., systemic corticosteroids, medications used for cancer chemotherapy, organ transplantation or to treat autoimmune disorders) within 3 months prior to day 1. * individuals with any progressive unstable or uncontrolled clinical conditions * individuals who are pregnant, or breastfeeding, or planning to become pregnant while enrolled in this study or during the study period * individuals who have a history of severe adverse reaction associated with a vaccine or severe allergic reaction, e.g., anaphylaxis to any components of the study vaccines * individuals who have a history of malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix which have been cured, or other malignancies with minimal risk of recurrence). * individuals who have received any other investigational product within 30 days prior to day 1 or intend to participate in another clinical study at any time during the conduct of this study * individuals who have received any other licensed vaccines within 14 days prior to enrollment in this study or who are planning to receive any vaccine up to 28 days after the second vaccination * individuals with known bleeding disorder that would, in the opinion of the investigator, contraindicate i.m. injection * individuals who have received treatment with rituximab or any other anti-cd20 monoclonal antibodies within 9 months prior to day 1 or planned during the study period * administration of intravenous immunoglobulins and/or any blood products within 3 months prior to enrollment or planned administration during the study period * individuals with positive test result for hepatitis b surface antigen, hepatitis c virus antibody, or human immunodeficiency virus types 1 or 2 antibodies at screening * individuals with safety laboratory test results (hematology, biochemistry, and coagulation) with a toxicity score of grade ≥2 at screening. * the participant has a reported or documented history of alcohol abuse or drug addiction (excluding nonprescription health supplements and herbal remedies) within 1 year before the planned day of dose administration * the participant has a positive test result for drugs of abuse at screening * individuals with any condition that, in the opinion of the investigator, would interfere with the primary study objectives or pose additional risk to the participant

* individuals with body temperature \>37.8°c (axillary), or any acute illness at baseline (day 1) or within 3 days prior to randomization. * body mass index at screening \>30 kg/m2 * individuals with laboratory-confirmed sars-cov-2 infection \[as defined by reverse transcriptase polymerase chain reaction (rt-pcr) assay or rapid covid antigen test or an equivalent\] at the screening visit or with known history of covid-19 within 6 months prior to day 1 * individuals who have received an investigational or authorized covid-19 vaccine within 6 months prior to day 1, or plan to receive covid-19 vaccine during the study period * any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease \[e.g., malignancy, human immunodeficiency virus (hiv) infection\] or immunosuppressive/cytotoxic therapy (e.g., systemic corticosteroids, medications used for cancer chemotherapy, organ transplantation or to treat autoimmune disorders) within 3 months prior to day 1. * individuals with any progressive unstable or uncontrolled clinical conditions * individuals who are pregnant, or breastfeeding, or planning to become pregnant while enrolled in this study or during the study period * individuals who have a history of severe adverse reaction associated with a vaccine or severe allergic reaction, e.g., anaphylaxis to any components of the study vaccines * individuals who have a history of malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix which have been cured, or other malignancies with minimal risk of recurrence). * individuals who have received any other investigational product within 30 days prior to day 1 or intend to participate in another clinical study at any time during the conduct of this study * individuals who have received any other licensed vaccines within 14 days prior to enrollment in this study or who are planning to receive any vaccine up to 28 days after the second vaccination * individuals with known bleeding disorder that would, in the opinion of the investigator, contraindicate i.m. injection * individuals who have received treatment with rituximab or any other anti-cd20 monoclonal antibodies within 9 months prior to day 1 or planned during the study period * administration of intravenous immunoglobulins and/or any blood products within 3 months prior to enrollment or planned administration during the study period * individuals with positive test result for hepatitis b surface antigen, hepatitis c virus antibody, or human immunodeficiency virus types 1 or 2 antibodies at screening * individuals with safety laboratory test results (hematology, biochemistry, and coagulation) with a toxicity score of grade ≥2 at screening. * the participant has a reported or documented history of alcohol abuse or drug addiction (excluding nonprescription health supplements and herbal remedies) within 1 year before the planned day of dose administration * the participant has a positive test result for drugs of abuse at screening * individuals with any condition that, in the opinion of the investigator, would interfere with the primary study objectives or pose additional risk to the participant

individuals with body temperature >37.8°c (axillary), or any acute illness at baseline (day 1) or within 3 days prior to randomization. body mass index at screening >30 kg/m2 individuals with laboratory-confirmed sars-cov-2 infection [as defined by reverse transcriptase polymerase chain reaction (rt-pcr) assay or rapid covid antigen test or an equivalent] at the screening visit or with known history of covid-19 within 6 months prior to day 1 individuals who have received an investigational or authorized covid-19 vaccine within 6 months prior to day 1, or plan to receive covid-19 vaccine during the study period any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease [e.g., malignancy, human immunodeficiency virus (hiv) infection] or immunosuppressive/cytotoxic therapy (e.g., systemic corticosteroids, medications used for cancer chemotherapy, organ transplantation or to treat autoimmune disorders) within 3 months prior to day 1. individuals with any progressive unstable or uncontrolled clinical conditions individuals who are pregnant, or breastfeeding, or planning to become pregnant while enrolled in this study or during the study period individuals who have a history of severe adverse reaction associated with a vaccine or severe allergic reaction, e.g., anaphylaxis to any components of the study vaccines individuals who have a history of malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix which have been cured, or other malignancies with minimal risk of recurrence). individuals who have received any other investigational product within 30 days prior to day 1 or intend to participate in another clinical study at any time during the conduct of this study individuals who have received any other licensed vaccines within 14 days prior to enrollment in this study or who are planning to receive any vaccine up to 28 days after the second vaccination individuals with known bleeding disorder that would, in the opinion of the investigator, contraindicate i.m. injection individuals who have received treatment with rituximab or any other anti-cd20 monoclonal antibodies within 9 months prior to day 1 or planned during the study period administration of intravenous immunoglobulins and/or any blood products within 3 months prior to enrollment or planned administration during the study period individuals with positive test result for hepatitis b surface antigen, hepatitis c virus antibody, or human immunodeficiency virus types 1 or 2 antibodies at screening individuals with safety laboratory test results (hematology, biochemistry, and coagulation) with a toxicity score of grade ≥2 at screening. the participant has a reported or documented history of alcohol abuse or drug addiction (excluding nonprescription health supplements and herbal remedies) within 1 year before the planned day of dose administration the participant has a positive test result for drugs of abuse at screening individuals with any condition that, in the opinion of the investigator, would interfere with the primary study objectives or pose additional risk to the participant

individuals with body temperature >37.8°c (axillary), or any acute illness at baseline (day 1) or within 3 days prior to randomization. body mass index at screening >30 kg/m2 individuals with laboratory-confirmed sars-cov-2 infection [as defined by reverse transcriptase polymerase chain reaction (rt-pcr) assay or rapid covid antigen test or an equivalent] at the screening visit or with known history of covid-19 within 6 months prior to day 1 individuals who have received an investigational or authorized covid-19 vaccine within 6 months prior to day 1, or plan to receive covid-19 vaccine during the study period any confirmed or suspected immunosuppressive or immunodeficient condition resulting from disease [e.g., malignancy, human immunodeficiency virus (hiv) infection] or immunosuppressive/cytotoxic therapy (e.g., systemic corticosteroids, medications used for cancer chemotherapy, organ transplantation or to treat autoimmune disorders) within 3 months prior to day 1. individuals with any progressive unstable or uncontrolled clinical conditions individuals who are pregnant, or breastfeeding, or planning to become pregnant while enrolled in this study or during the study period individuals who have a history of severe adverse reaction associated with a vaccine or severe allergic reaction, e.g., anaphylaxis to any components of the study vaccines individuals who have a history of malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix which have been cured, or other malignancies with minimal risk of recurrence). individuals who have received any other investigational product within 30 days prior to day 1 or intend to participate in another clinical study at any time during the conduct of this study individuals who have received any other licensed vaccines within 14 days prior to enrollment in this study or who are planning to receive any vaccine up to 28 days after the second vaccination individuals with known bleeding disorder that would, in the opinion of the investigator, contraindicate i.m. injection individuals who have received treatment with rituximab or any other anti-cd20 monoclonal antibodies within 9 months prior to day 1 or planned during the study period administration of intravenous immunoglobulins and/or any blood products within 3 months prior to enrollment or planned administration during the study period individuals with positive test result for hepatitis b surface antigen, hepatitis c virus antibody, or human immunodeficiency virus types 1 or 2 antibodies at screening individuals with safety laboratory test results (hematology, biochemistry, and coagulation) with a toxicity score of grade ≥2 at screening. the participant has a reported or documented history of alcohol abuse or drug addiction (excluding nonprescription health supplements and herbal remedies) within 1 year before the planned day of dose administration the participant has a positive test result for drugs of abuse at screening individuals with any condition that, in the opinion of the investigator, would interfere with the primary study objectives or pose additional risk to the participant