Chikungunya Virus Vaccine Trial in Healthy Adults

This is an interventional prevention trial for Viral Vaccines focused on measuring Vaccine-Mediated Protection, Antibody Response, Chikungunya Virus, Immune Response, Healthy Volunteer, Humoral Inmunity, Virus-like Particles Read More

INCLUSION CRITERIA:

A participant must meet all of the following criteria:

1. 18 to 50 years old
2. Available for clinical follow-up through Week 44
3. Able to provide proof of identity to the satisfaction of the study clinician completing the enrollment process
4. Complete an Assessment of Understanding prior to enrollment and verbalize understanding of all questions answered incorrectly
5. Able and willing to complete the informed consent process
6. Willing to donate blood for sample storage to be used for future research
7. In good general health, with a BMI less than or equal to 40, without clinically significant medical history, and has satisfactorily completed screening

8. Physical examination and laboratory results without clinically significant findings within the 56 days prior to enrollment

   Laboratory Criteria within 56 days prior to enrollment:

9. Hemoglobin greater than or equal to11.5 g/dL for women; greater than or equal to13.5 g/dL for men
10. WBC: 3,000-12,000 cells/mm(3).
11. Differential either within institutional normal range or accompanied by physician approval
12. Total lymphocyte count: greater than or equal to 800 cells/mm(3)
13. Platelets = 125,000-500,000/mm(3)
14. Alanine aminotransferase (ALT) less than or equal to 1.25 times upper limit of normal range
15. Serum creatinine less than or equal to1x upper limit of normal (less than or equal to1.3 mg/dL for females; less than or equal to1.4 mg/dL for males).

16. Negative FDA-approved HIV blood test

    Female-Specific Criteria

17. Negative Beta-HCG pregnancy test (urine or serum) on day of enrollment for women presumed to be of reproductive potential
18. A woman of childbearing potential must agree to use an effective means of birth control from at least 21 days prior to enrollment through 12 weeks after last study vaccination

EXCLUSION CRITERIA:

A participant will be excluded if one or more of the following conditions apply:

Female-Specific Criteria

1. Woman who is breast-feeding or planning to become pregnant during the time projected for individual study participation
2. Systemic immunosuppressive medications or cytotoxic medications within 12 weeks prior to enrollment [with the exceptions that a short course of corticosteroids (less than or equal to10 days duration or a single injection) for a self-limited condition at least 2 weeks prior to enrollment will not exclude study participation]
3. Blood products within 16 weeks prior to enrollment
4. Immunoglobulin within 8 weeks prior to enrollment
5. Prior vaccinations with an investigational CHIKV vaccine
6. Investigational research agents within 4 weeks prior to enrollment
7. Live attenuated vaccines within 4 weeks prior to enrollment
8. Medically indicated subunit or killed vaccines, e.g. influenza, pneumococcal, or allergy treatment with antigen injections, within 2 weeks prior to enrollment

9. Current anti-TB prophylaxis or therapy

   Subject has a history of any of the following clinically significant conditions:

10. A history of confirmed or suspected CHIKV infection
11. A history of immune-mediated or clinically significant arthritis
12. Serious reactions to vaccines that preclude receipt of study vaccinations as determined by the investigator
13. Hereditary angioedema (HAE), acquired angioedema (AAE), or idiopathic forms of angioedema
14. Asthma that is unstable or required emergent care, urgent care, hospitalization or intubation during the past two years or that is expected to require the use of oral or intravenous corticosteroids
15. Diabetes mellitus (type I or II), with the exception of gestational diabetes
16. Idiopathic urticaria within the past year
17. Bleeding disorder diagnosed by a doctor (e.g. factor deficiency, coagulopathy, or platelet disorder requiring special precautions) or significant bruising or bleeding difficulties with IM injections or blood draws
18. Malignancy that is active, or treated malignancy for which there is not reasonable assurance of sustained cure, or malignancy that is likely to recur during the period of the study
19. Seizure disorder other than: 1) febrile seizures, 2) seizures secondary to alcohol withdrawal more than 3 years ago, or 3) seizures that have not required treatment within the last 3 years
20. Asplenia, functional asplenia or any condition resulting in the absence or removal of the spleen
21. Psychiatric condition that may preclude compliance with the protocol; past or present psychoses; disorder requiring lithium; or within five years prior to enrollment, a history of suicide plan or attempt
22. Any medical condition (such as thyroid disease or hypertension that are not well controlled by medication, or viral hepatitis) that, in the judgment of the investigator, is a contraindication to protocol participation or impairs a volunteer's ability to give informed consent