A Study of SII Yellow Fever Vaccine to Compare Safety and Immunogenicity With STAMARIL

This is an interventional prevention trial for Yellow Fever Read More

Inclusion Criteria:

1. Male or female volunteers aged ≥ 1 to < 60 years
2. Healthy volunteers as determined by medical history and clinical examination
3. Participants willing to adhere to the protocol requirements and to provide informed consent for participants ≥ 18 years of age. For participants < 18 years of age, parental/guardian ability and willingness to provide informed consent (as per local requirements/procedures) and additional informed assent from participants, as appropriate for participating community (i.e. participants at least 7 years of age in Kenya)
4. Intend to remain residing in study area throughout the study participation
5. Female participants of childbearing potential* must have practiced adequate contraception** and agree to continue adequate contraception till Day 28 post-vaccination.
6. Female participants of childbearing potential must have a negative pregnancy test within 24 hours prior to IP administration.
7. Be willing to avoid the use of traditional/herbal local medications and treatments for the duration of the study

Exclusion Criteria:

1. Fever (> 37.5°C) or any clinically significant acute infection at time of vaccination [Temporary exclusion criteria - participants may be re-screened at least 48 hours after the last recorded fever]
2. Use of systemic (oral or parenteral) antibiotics or antiviral agents within the past 7 days. [Temporary exclusion criteria - participants may be re-screened at least 7 days after last dose of antibiotics or antiviral agents]
3. Use of traditional/herbal local medications and treatments in the past 7 days [Temporary exclusion criteria - participants may be re-screened at least 7 days after last consumption of traditional/herbal local medications and treatment]
4. Previous history of laboratory confirmed infection with yellow fever and other flaviviruses e.g., dengue fever, tick-borne-encephalitis (TBE), Japanese encephalitis (JE), West Nile virus (WNV), zika virus, etc.
5. Previous vaccination against yellow fever, TBE, JE, or dengue fever.
6. Receipt of any vaccine within past 28 days or planned vaccination until completion of Day 28 visit
7. Known or suspected impairment of immunological function based on medical history and physical examination.
8. Presence of any systemic disorder (cardiovascular, pulmonary, hepatic, renal, gastrointestinal, hematological, endocrine, immunological, dermatological, neurological, cancer, or autoimmune disease) as determined by medical history and / or physical examination which would compromise the participant's health or is likely to result in nonconformance to the protocol
9. History of chronic administration (defined as more than 14 consecutive days) of immunosuppressant (> 0.5 mg/kg/day of prednisolone or equivalent) or other immune modifying drugs including the use of glucocorticoids. The use of topical/inhaled/per nasal glucocorticoids will be permitted.
10. A known hypersensitivity to any of the vaccine components (including gelatin, eggs, egg products, or chicken protein) or history of a life-threatening reaction to any past vaccine.
11. Receipt of any immunoglobulin therapy and / or blood products in the past 60 days or planned administration until completion of Day 28 visit.
12. Participation in a drug research study, involving investigational products, within past 3 months or planned participation during the entire study period
13. Receipt of any investigational or unlicensed medication (drug or vaccine) in the preceding 28 days, or planned use until completion of Day 28 visit
14. Uncontrolled coagulopathy or blood disorder contraindicating subcutaneous injections or blood sampling
15. Be an employee of, or direct descendant (child or grandchild) of any person employed by the investigator or sponsor.
16. Pregnant or lactating women
17. Requirement of Yellow Fever vaccination certificate for travelling purpose
18. History of thymus dysfunction including myasthenia gravis, thymoma, thymectomy
19. History or presence of significant alcoholism or drug abuse in the past one year
20. Major congenital or genetic defect
21. Any other condition which in the opinion of the investigator will jeopardize the safety of the participant or compromise the assessment of the study objectives