* clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºcelsius (c) (100.4°fahrenheit \[f\]) within 24 hours prior to the planned 1st dose of the janssen ad26.cov2.s vaccine; randomization at a later date is permitted at the discretion of the sponsor-investigator. * has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients (including specifically the excipients of the janssen ad26.cov2.s vaccine; refer to the investigative brochure). * subject has received or plans to receive: * licensed live attenuated vaccines -within 28 days before or after planned administration of the 1st or subsequent janssen vaccinations. * other licensed (not live) vaccines -within 14 days before or after planned administration of the 1st or subsequent janssen vaccinations. * received an investigational drug within 30 days (including investigational drugs for prophylaxis of covid-19) or used an invasive investigational medical device within 30 days of the janssen ad26.cov2.s vaccine. received investigational ig or investigational monoclonal antibodies within 3 months, or received convalescent serum for covid-19 treatment within 4 months or received an investigational vaccine (including investigational adenoviral- vectored vaccines) within 6 months before the planned administration of the 1st dose of the janssen ad26.cov2.s vaccine or is currently enrolled or plans to participate in another investigational study within 3 months after the last jansen vaccination. note: participation in an observational clinical study is allowed at the sponsor-investigator's discretion; please notify the sponsor-investigator of this decision. efforts will be made to ensure inclusion of participants who have not been previously enrolled in coronavirus studies. in order to participate subject must agree and understand that they cannot enroll in other coronavirus focused studies while participating in this one. * is pregnant or planning to become pregnant at the time of consent and within 3 months of the last dose of the janssen ad26.cov2.s vaccine. * has a history of an underlying clinically significant acute or chronic medical condition or physical examination findings which, in the opinion of the sponsor-investigator, would make study participation not be in the participant's best interest (e.g., compromise the well- being) or that could prevent, limit, or confound the protocol-specified assessments. * has a contraindication to intramuscular (im) injections and blood draws. * has had major psychiatric illness, which in the sponsor-investigator's opinion would compromise the participant's safety or compliance with the study procedures. * cannot communicate reliably with the sponsor-investigator or comply with study procedures. * in the opinion of the sponsor-investigator, is unlikely to adhere to the requirements of the study or is unlikely to complete the full course of protocol required vaccination and observation. * history of cancer malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or other malignancies with minimal risk of recurrence). * history of acute polyneuropathy (e.g., guillain-barré syndrome) * chronic history of platelet count \<75,000/µl. * history of thrombosis with thrombocytopenia syndrome (tts) or heparin-induced thrombocytopenia (his). * history of capillary leak syndrome (cls). * received pre-exposure prophylactic medications for covid-19 that could interfere with assessments of any study-related endpoint * history of myocarditis or pericarditis

* clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºcelsius (c) (100.4°fahrenheit \[f\]) within 24 hours prior to the planned 1st dose of the janssen ad26.cov2.s vaccine; randomization at a later date is permitted at the discretion of the sponsor-investigator. * has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients (including specifically the excipients of the janssen ad26.cov2.s vaccine; refer to the investigative brochure). * subject has received or plans to receive: * licensed live attenuated vaccines -within 28 days before or after planned administration of the 1st or subsequent janssen vaccinations. * other licensed (not live) vaccines -within 14 days before or after planned administration of the 1st or subsequent janssen vaccinations. * received an investigational drug within 30 days (including investigational drugs for prophylaxis of covid-19) or used an invasive investigational medical device within 30 days of the janssen ad26.cov2.s vaccine. received investigational ig or investigational monoclonal antibodies within 3 months, or received convalescent serum for covid-19 treatment within 4 months or received an investigational vaccine (including investigational adenoviral- vectored vaccines) within 6 months before the planned administration of the 1st dose of the janssen ad26.cov2.s vaccine or is currently enrolled or plans to participate in another investigational study within 3 months after the last jansen vaccination. note: participation in an observational clinical study is allowed at the sponsor-investigator's discretion; please notify the sponsor-investigator of this decision. efforts will be made to ensure inclusion of participants who have not been previously enrolled in coronavirus studies. in order to participate subject must agree and understand that they cannot enroll in other coronavirus focused studies while participating in this one. * is pregnant or planning to become pregnant at the time of consent and within 3 months of the last dose of the janssen ad26.cov2.s vaccine. * has a history of an underlying clinically significant acute or chronic medical condition or physical examination findings which, in the opinion of the sponsor-investigator, would make study participation not be in the participant's best interest (e.g., compromise the well- being) or that could prevent, limit, or confound the protocol-specified assessments. * has a contraindication to intramuscular (im) injections and blood draws. * has had major psychiatric illness, which in the sponsor-investigator's opinion would compromise the participant's safety or compliance with the study procedures. * cannot communicate reliably with the sponsor-investigator or comply with study procedures. * in the opinion of the sponsor-investigator, is unlikely to adhere to the requirements of the study or is unlikely to complete the full course of protocol required vaccination and observation. * history of cancer malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or other malignancies with minimal risk of recurrence). * history of acute polyneuropathy (e.g., guillain-barré syndrome) * chronic history of platelet count \<75,000/µl. * history of thrombosis with thrombocytopenia syndrome (tts) or heparin-induced thrombocytopenia (his). * history of capillary leak syndrome (cls). * received pre-exposure prophylactic medications for covid-19 that could interfere with assessments of any study-related endpoint * history of myocarditis or pericarditis

clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºcelsius (c) (100.4°fahrenheit [f]) within 24 hours prior to the planned 1st dose of the janssen ad26.cov2.s vaccine; randomization at a later date is permitted at the discretion of the sponsor-investigator. has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients (including specifically the excipients of the janssen ad26.cov2.s vaccine; refer to the investigative brochure). subject has received or plans to receive: licensed live attenuated vaccines -within 28 days before or after planned administration of the 1st or subsequent janssen vaccinations. other licensed (not live) vaccines -within 14 days before or after planned administration of the 1st or subsequent janssen vaccinations. received an investigational drug within 30 days (including investigational drugs for prophylaxis of covid-19) or used an invasive investigational medical device within 30 days of the janssen ad26.cov2.s vaccine. received investigational ig or investigational monoclonal antibodies within 3 months, or received convalescent serum for covid-19 treatment within 4 months or received an investigational vaccine (including investigational adenoviral- vectored vaccines) within 6 months before the planned administration of the 1st dose of the janssen ad26.cov2.s vaccine or is currently enrolled or plans to participate in another investigational study within 3 months after the last jansen vaccination. note: participation in an observational clinical study is allowed at the sponsor-investigator's discretion; please notify the sponsor-investigator of this decision. efforts will be made to ensure inclusion of participants who have not been previously enrolled in coronavirus studies. in order to participate subject must agree and understand that they cannot enroll in other coronavirus focused studies while participating in this one. is pregnant or planning to become pregnant at the time of consent and within 3 months of the last dose of the janssen ad26.cov2.s vaccine. has a history of an underlying clinically significant acute or chronic medical condition or physical examination findings which, in the opinion of the sponsor-investigator, would make study participation not be in the participant's best interest (e.g., compromise the well- being) or that could prevent, limit, or confound the protocol-specified assessments. has a contraindication to intramuscular (im) injections and blood draws. has had major psychiatric illness, which in the sponsor-investigator's opinion would compromise the participant's safety or compliance with the study procedures. cannot communicate reliably with the sponsor-investigator or comply with study procedures. in the opinion of the sponsor-investigator, is unlikely to adhere to the requirements of the study or is unlikely to complete the full course of protocol required vaccination and observation. history of cancer malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or other malignancies with minimal risk of recurrence). history of acute polyneuropathy (e.g., guillain-barré syndrome) chronic history of platelet count <75,000/µl. history of thrombosis with thrombocytopenia syndrome (tts) or heparin-induced thrombocytopenia (his). history of capillary leak syndrome (cls). received pre-exposure prophylactic medications for covid-19 that could interfere with assessments of any study-related endpoint history of myocarditis or pericarditis

clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºcelsius (c) (100.4°fahrenheit [f]) within 24 hours prior to the planned 1st dose of the janssen ad26.cov2.s vaccine; randomization at a later date is permitted at the discretion of the sponsor-investigator. has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients (including specifically the excipients of the janssen ad26.cov2.s vaccine; refer to the investigative brochure). subject has received or plans to receive: licensed live attenuated vaccines -within 28 days before or after planned administration of the 1st or subsequent janssen vaccinations. other licensed (not live) vaccines -within 14 days before or after planned administration of the 1st or subsequent janssen vaccinations. received an investigational drug within 30 days (including investigational drugs for prophylaxis of covid-19) or used an invasive investigational medical device within 30 days of the janssen ad26.cov2.s vaccine. received investigational ig or investigational monoclonal antibodies within 3 months, or received convalescent serum for covid-19 treatment within 4 months or received an investigational vaccine (including investigational adenoviral- vectored vaccines) within 6 months before the planned administration of the 1st dose of the janssen ad26.cov2.s vaccine or is currently enrolled or plans to participate in another investigational study within 3 months after the last jansen vaccination. note: participation in an observational clinical study is allowed at the sponsor-investigator's discretion; please notify the sponsor-investigator of this decision. efforts will be made to ensure inclusion of participants who have not been previously enrolled in coronavirus studies. in order to participate subject must agree and understand that they cannot enroll in other coronavirus focused studies while participating in this one. is pregnant or planning to become pregnant at the time of consent and within 3 months of the last dose of the janssen ad26.cov2.s vaccine. has a history of an underlying clinically significant acute or chronic medical condition or physical examination findings which, in the opinion of the sponsor-investigator, would make study participation not be in the participant's best interest (e.g., compromise the well- being) or that could prevent, limit, or confound the protocol-specified assessments. has a contraindication to intramuscular (im) injections and blood draws. has had major psychiatric illness, which in the sponsor-investigator's opinion would compromise the participant's safety or compliance with the study procedures. cannot communicate reliably with the sponsor-investigator or comply with study procedures. in the opinion of the sponsor-investigator, is unlikely to adhere to the requirements of the study or is unlikely to complete the full course of protocol required vaccination and observation. history of cancer malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or other malignancies with minimal risk of recurrence). history of acute polyneuropathy (e.g., guillain-barré syndrome) chronic history of platelet count <75,000/µl. history of thrombosis with thrombocytopenia syndrome (tts) or heparin-induced thrombocytopenia (his). history of capillary leak syndrome (cls). received pre-exposure prophylactic medications for covid-19 that could interfere with assessments of any study-related endpoint history of myocarditis or pericarditis

clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºcelsius (c) (100.4°fahrenheit [f]) within 24 hours prior to the planned 1st dose of the janssen ad26.cov2.s vaccine; randomization at a later date is permitted at the discretion of the sponsor-investigator. has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients (including specifically the excipients of the janssen ad26.cov2.s vaccine; refer to the investigative brochure). subject has received or plans to receive: licensed live attenuated vaccines -within 28 days before or after planned administration of the 1st or subsequent janssen vaccinations. other licensed (not live) vaccines -within 14 days before or after planned administration of the 1st or subsequent janssen vaccinations. received an investigational drug within 30 days (including investigational drugs for prophylaxis of covid-19) or used an invasive investigational medical device within 30 days of the janssen ad26.cov2.s vaccine. received investigational ig or investigational monoclonal antibodies within 3 months, or received convalescent serum for covid-19 treatment within 4 months or received an investigational vaccine (including investigational adenoviral- vectored vaccines) within 6 months before the planned administration of the 1st dose of the janssen ad26.cov2.s vaccine or is currently enrolled or plans to participate in another investigational study within 3 months after the last jansen vaccination. note: participation in an observational clinical study is allowed at the sponsor-investigator's discretion; please notify the sponsor-investigator of this decision. efforts will be made to ensure inclusion of participants who have not been previously enrolled in coronavirus studies. in order to participate subject must agree and understand that they cannot enroll in other coronavirus focused studies while participating in this one. is pregnant or planning to become pregnant at the time of consent and within 3 months of the last dose of the janssen ad26.cov2.s vaccine. has a history of an underlying clinically significant acute or chronic medical condition or physical examination findings which, in the opinion of the sponsor-investigator, would make study participation not be in the participant's best interest (e.g., compromise the well- being) or that could prevent, limit, or confound the protocol-specified assessments. has a contraindication to intramuscular (im) injections and blood draws. has had major psychiatric illness, which in the sponsor-investigator's opinion would compromise the participant's safety or compliance with the study procedures. cannot communicate reliably with the sponsor-investigator or comply with study procedures. in the opinion of the sponsor-investigator, is unlikely to adhere to the requirements of the study or is unlikely to complete the full course of protocol required vaccination and observation. history of cancer malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or other malignancies with minimal risk of recurrence). history of acute polyneuropathy (e.g., guillain-barré syndrome) chronic history of platelet count <75,000/µl. history of thrombosis with thrombocytopenia syndrome (tts) or heparin-induced thrombocytopenia (his). history of capillary leak syndrome (cls). received pre-exposure prophylactic medications for covid-19 that could interfere with assessments of any study-related endpoint

clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºcelsius (c) (100.4°fahrenheit [f]) within 24 hours prior to the planned 1st dose of the janssen ad26.cov2.s vaccine; randomization at a later date is permitted at the discretion of the sponsor-investigator. has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients (including specifically the excipients of the janssen ad26.cov2.s vaccine; refer to the investigative brochure). subject has received or plans to receive: licensed live attenuated vaccines -within 28 days before or after planned administration of the 1st or subsequent janssen vaccinations. other licensed (not live) vaccines -within 14 days before or after planned administration of the 1st or subsequent janssen vaccinations. received an investigational drug within 30 days (including investigational drugs for prophylaxis of covid-19) or used an invasive investigational medical device within 30 days of the janssen ad26.cov2.s vaccine. received investigational ig or investigational monoclonal antibodies within 3 months, or received convalescent serum for covid-19 treatment within 4 months or received an investigational vaccine (including investigational adenoviral- vectored vaccines) within 6 months before the planned administration of the 1st dose of the janssen ad26.cov2.s vaccine or is currently enrolled or plans to participate in another investigational study within 3 months after the last jansen vaccination. note: participation in an observational clinical study is allowed at the sponsor-investigator's discretion; please notify the sponsor-investigator of this decision. efforts will be made to ensure inclusion of participants who have not been previously enrolled in coronavirus studies. in order to participate subject must agree and understand that they cannot enroll in other coronavirus focused studies while participating in this one. is pregnant or planning to become pregnant at the time of consent and within 3 months of the last dose of the janssen ad26.cov2.s vaccine. has a history of an underlying clinically significant acute or chronic medical condition or physical examination findings which, in the opinion of the sponsor-investigator, would make study participation not be in the participant's best interest (e.g., compromise the well- being) or that could prevent, limit, or confound the protocol-specified assessments. has a contraindication to intramuscular (im) injections and blood draws. has had major psychiatric illness, which in the sponsor-investigator's opinion would compromise the participant's safety or compliance with the study procedures. cannot communicate reliably with the sponsor-investigator or comply with study procedures. in the opinion of the sponsor-investigator, is unlikely to adhere to the requirements of the study or is unlikely to complete the full course of protocol required vaccination and observation. history of cancer malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or other malignancies with minimal risk of recurrence). history of acute polyneuropathy (e.g., guillain-barré syndrome) chronic history of platelet count <75,000/µl. history of thrombosis with thrombocytopenia syndrome (tts) or heparin-induced thrombocytopenia (his). history of capillary leak syndrome (cls). received pre-exposure prophylactic medications for covid-19 that could interfere with assessments of any study-related endpoint

clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºc (100.4°f) within 24 hours prior to the planned 1st dose of the janssen ad26.cov2.s vaccine; randomization at a later date is permitted at the discretion of the sponsor-investigator. has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients (including specifically the excipients of the janssen ad26.cov2.s vaccine; refer to the investigative brochure). subject has received or plans to receive: licensed live attenuated vaccines -within 28 days before or after planned administration of the 1st or subsequent janssen vaccinations. other licensed (not live) vaccines -within 14 days before or after planned administration of the 1st or subsequent janssen vaccinations. received an investigational drug within 30 days (including investigational drugs for prophylaxis of covid-19) or used an invasive investigational medical device within 30 days of the janssen ad26.cov2.s vaccine. received investigational ig or investigational monoclonal antibodies within 3 months, or received convalescent serum for covid-19 treatment within 4 months or received an investigational vaccine (including investigational adenoviral- vectored vaccines) within 6 months before the planned administration of the 1st dose of the janssen ad26.cov2.s vaccine or is currently enrolled or plans to participate in another investigational study within 3 months after the last jansen vaccination. note: participation in an observational clinical study is allowed at the sponsor-investigator's discretion; please notify the sponsor-investigator of this decision. efforts will be made to ensure inclusion of participants who have not been previously enrolled in coronavirus studies. in order to participate subject must agree and understand that they cannot enroll in other coronavirus focused studies while participating in this one. is pregnant or planning to become pregnant at the time of consent and within 3 months of the last dose of the janssen ad26.cov2.s vaccine. has a history of an underlying clinically significant acute or chronic medical condition or physical examination findings which, in the opinion of the sponsor-investigator, would make study participation not be in the participant's best interest (e.g., compromise the well- being) or that could prevent, limit, or confound the protocol-specified assessments. has a contraindication to im injections and blood draws. has had major psychiatric illness, which in the sponsor-investigator's opinion would compromise the participant's safety or compliance with the study procedures. cannot communicate reliably with the sponsor-investigator or comply with study procedures. in the opinion of the sponsor-investigator, is unlikely to adhere to the requirements of the study or is unlikely to complete the full course of protocol required vaccination and observation. history of cancer malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or other malignancies with minimal risk of recurrence). history of acute polyneuropathy (e.g., guillain-barré syndrome) chronic history of platelet count <75,000/µl. history of thrombosis with thrombocytopenia syndrome (tts) or heparin-induced thrombocytopenia (his). history of capillary leak syndrome (cls). received pre-exposure prophylactic medications for covid-19 that could interfere with assessments of any study-related endpoint

clinically significant acute illness (this does not include minor illnesses such as diarrhea or mild upper respiratory tract infection) or temperature ≥38.0ºc (100.4°f) within 24 hours prior to the planned 1st dose of the janssen ad26.cov2.s vaccine; randomization at a later date is permitted at the discretion of the sponsor-investigator. has a known or suspected allergy or history of anaphylaxis or other serious adverse reactions to vaccines or their excipients (including specifically the excipients of the janssen ad26.cov2.s vaccine; refer to the investigative brochure). subject has received or plans to receive: licensed live attenuated vaccines -within 28 days before or after planned administration of the 1st or subsequent janssen vaccinations. other licensed (not live) vaccines -within 14 days before or after planned administration of the 1st or subsequent janssen vaccinations. received an investigational drug within 30 days (including investigational drugs for prophylaxis of covid-19) or used an invasive investigational medical device within 30 days of the janssen ad26.cov2.s vaccine. received investigational ig or investigational monoclonal antibodies within 3 months, or received convalescent serum for covid-19 treatment within 4 months or received an investigational vaccine (including investigational adenoviral- vectored vaccines) within 6 months before the planned administration of the 1st dose of the janssen ad26.cov2.s vaccine or is currently enrolled or plans to participate in another investigational study within 3 months after the last jansen vaccination. note: participation in an observational clinical study is allowed at the sponsor-investigator's discretion; please notify the sponsor-investigator of this decision. efforts will be made to ensure inclusion of participants who have not been previously enrolled in coronavirus studies. in order to participate subject must agree and understand that they cannot enroll in other coronavirus focused studies while participating in this one. is pregnant or planning to become pregnant at the time of consent and within 3 months of the last dose of the janssen ad26.cov2.s vaccine. has a history of an underlying clinically significant acute or chronic medical condition or physical examination findings which, in the opinion of the sponsor-investigator, would make study participation not be in the participant's best interest (e.g., compromise the well- being) or that could prevent, limit, or confound the protocol-specified assessments. has a contraindication to im injections and blood draws. has had major psychiatric illness, which in the sponsor-investigator's opinion would compromise the participant's safety or compliance with the study procedures. cannot communicate reliably with the sponsor-investigator or comply with study procedures. in the opinion of the sponsor-investigator, is unlikely to adhere to the requirements of the study or is unlikely to complete the full course of protocol required vaccination and observation. history of cancer malignancy within 1 year before screening (exceptions are squamous and basal cell carcinomas of the skin and carcinoma in situ of the cervix, or other malignancies with minimal risk of recurrence). history of acute polyneuropathy (e.g., guillain-barré syndrome) chronic history of platelet count <75,000/µl. history of thrombosis with thrombocytopenia syndrome (tts) or heparin-induced thrombocytopenia (his). history of capillary leak syndrome (cls). received pre-exposure prophylactic medications for covid-19 that could interfere with assessments of any study-related endpoint