1. availability of a signed and dated informed consent of the volunteer to participate in a clinical trial, prior to any of the study procedures. 2. verified diagnosis is "healthy" according to the data of the standard clinical, laboratory and instrumental examination methods. 3. age from 18 to 60 years old inclusive. 4. body mass index from 18.5 to 30 kg / m3. 5. ability to attend all scheduled visits and all planned procedures and examinations. 6. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.

1. availability of a signed and dated informed consent of the volunteer to participate in a clinical trial, prior to any of the study procedures. 2. verified diagnosis is "healthy" according to the data of the standard clinical, laboratory and instrumental examination methods. 3. age from 18 to 60 years old inclusive. 4. body mass index from 18.5 to 30 kg / m3. 5. ability to attend all scheduled visits and all planned procedures and examinations. 6. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.

availability of a signed and dated informed consent of the volunteer to participate in a clinical trial, prior to any of the study procedures. verified diagnosis is "healthy" according to the data of the standard clinical, laboratory and instrumental examination methods. age from 18 to 60 years old inclusive. body mass index from 18.5 to 30 kg / m3. ability to attend all scheduled visits and all planned procedures and examinations. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.

availability of a signed and dated informed consent of the volunteer to participate in a clinical trial, prior to any of the study procedures. verified diagnosis is "healthy" according to the data of the standard clinical, laboratory and instrumental examination methods. age from 18 to 60 years old inclusive. body mass index from 18.5 to 30 kg / m3. ability to attend all scheduled visits and all planned procedures and examinations. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.

1. availability of a signed and dated informed consent of the volunteer to participate in a clinical trial, prior to any of the study procedures. 2. verified diagnosis is "healthy" according to the data of the standard clinical, laboratory and instrumental examination methods. 3. age from 18 to 60 years old inclusive. 4. body mass index from 18.5 to 30 kg / m3. 5. ability to attend all scheduled visits and all planned procedures and examinations. 6. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.

1. availability of a signed and dated informed consent of the volunteer to participate in a clinical trial, prior to any of the study procedures. 2. verified diagnosis is "healthy" according to the data of the standard clinical, laboratory and instrumental examination methods. 3. age from 18 to 60 years old inclusive. 4. body mass index from 18.5 to 30 kg / m3. 5. ability to attend all scheduled visits and all planned procedures and examinations. 6. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.