Chikungunya Vaccine (V184) Study in Previously Exposed Adults (V184-006)

Exclusion Criteria

• •Taking medication or other treatment for unresolved symptoms attributed to a previous chikungunya virus infection.
• •Prior receipt of any investigational chikungunya or other alphavirus vaccine. To date, no alphavirus vaccines have been commercially available in the United States.
• •Recent infection:
• •* self-limited upper respiratory infections until afebrile without medication for \>1 week;
• •* chikungunya unless/until asymptomatic (other than mild subjective symptoms not requiring treatment) for \>3 months;
• •* non-recurrent upper respiratory or urinary tract infections successfully treated with antibiotics, until asymptomatic for 1 month after full antibiotic course has been completed.
• •History of an acute allergic or anaphylactic reaction to any vaccine.
• •History of an immunosuppressive disorder (such as human immunodeficiency virus \[HIV\] infection, Common Variable Immune Deficiency), chronic infection (such as chronic hepatitis B or C), autoimmune disease (such as rheumatoid arthritis, systemic lupus erythematosus (SLE), autoimmune thyroid disease), or any medical condition that, in the opinion of the Investigator, could lead to an atypical immune response to the vaccine.
• •History of moderate or severe non-traumatic arthritis or arthralgia within 3 months of the Screening Visit.
• •Recent (within 30 days), current or anticipated use of any immunosuppressive or immune modifying medication including corticosteroids (excluding nasal, ophthalmic, and other topical preparations).
• •Other vaccination or planned vaccination within 4 weeks of either study dose (seasonal influenza vaccine excepted).
• •Receipt or planned receipt of blood products including immunoglobulins within 120 days of the Screening Visit.
• •Pregnant or lactating or planning pregnancy during the trial.
• •Known alcohol or other substance abuse that in the opinion of the Investigator affects the ability or willingness of the participant to understand and comply with the study protocol.
• •Participation in another clinical study within the past 30 days in which the participant was exposed to an investigational product (pharmaceutical product or placebo or device) or planned participation in another interventional clinical study while participating in this study.
• •Relevant history of any medical condition that, in the opinion of the Investigator, may interfere with the safety of the participant or aims of the study.
• •History of neoplastic disease (excluding successfully treated non-melanoma skin cancer or cervical intraepithelial neoplasia) within the past 5 years or a history of any hematological malignancy.
• •Behavioral or psychiatric disease or cognitive impairment that in the opinion of the Investigator affects the ability or willingness of the participant to understand and comply with the study protocol.
• •Non-consent to storage of blood specimens for future research.
• •Persons in direct relationship with the Sponsor or its contracted service providers, the contract research organisation (CRO) or its subcontractors, the Investigator, or study site staff. Direct relationship includes first degree relatives or dependents (children, spouse/partner, siblings or parents), as well as employees (site or Sponsor).