inclusion criteria: 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. volunteers (men and women) above the age of 18 years with stable indicators of basic vital functions. 3. ability to attend all scheduled visits and all planned procedures and examinations. 4. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.

inclusion criteria: 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. volunteers (men and women) above the age of 18 years with stable indicators of basic vital functions. 3. ability to attend all scheduled visits and all planned procedures and examinations. 4. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.

inclusion criteria: availability of a signed and dated informed consent of the volunteer to participate in a clinical trial, prior to any of the study procedures. volunteers (men and women) above the age of 18 years with stable indicators of basic vital functions. 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.

inclusion criteria: availability of a signed and dated informed consent of the volunteer to participate in a clinical trial, prior to any of the study procedures. volunteers (men and women) above the age of 18 years with stable indicators of basic vital functions. 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.

inclusion criteria: 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. volunteers (men and women) above the age of 18 years with stable indicators of basic vital functions. 3. ability to attend all scheduled visits and all planned procedures and examinations. 4. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.

inclusion criteria: 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. volunteers (men and women) above the age of 18 years with stable indicators of basic vital functions. 3. ability to attend all scheduled visits and all planned procedures and examinations. 4. consent of volunteers to use effective contraceptive methods throughout the study, including the observation period for possible post-vaccination reactions.