Study to Evaluate the Safety and Immunogenicity of Poly ICLC (Hiltonol) in Healthy Volunteers

Inclusion Criteria:

1. Healthy adult males and females, as assessed by a medical history, physical exam, and laboratory tests
2. Age of at least 18 years on the day of screening and no greater than 60 years at time of drug/placebo administration
3. Willing to comply with the requirements of the protocol and available for follow-up for the planned duration of the study (screening plus 4 weeks)
4. In the opinion of the principal investigator or designee, has understood the information provided. Written informed consent needs to be given before any study-related procedures are performed
5. Willing to undergo HIV testing and counseling, and receive HIV test results
6. If a sexually active male, willing to use an effective method of contraception (condoms, anatomical sterility) throughout the study period and will be advised not to get his partner pregnant for 6 weeks after study drug administration

7. Females of child-bearing potential must agree to use one of the following methods of contraception for 2 weeks prior to date of screening evaluation through 6 weeks after study drug administration:

   • Be surgically sterile Be abstinent (or willing to be)
   • Use oral contraceptives, or other form of hormonal birth control including hormonal vaginal rings or transdermal patches
   • Use an intra-uterine device (IUD)
   • Use (by ensuring her male partner(s) uses) barrier contraception (condom) with spermicide
   • Any other equivalent (as judged by the investigative team) methods of contraception

Exclusion Criteria:

1. Any clinically significant abnormality on history or examination including history of immunodeficiency or autoimmune disease; use of systemic corticosteroids, immunosuppressive, anticancer, or other medications considered significant by the trial physician within the last 6 months
2. Confirmed HIV-1 or HIV-2 infection
3. A medical history that includes any chronic medical problem that requires daily topical nasal medications, prior nasal or sinus surgery (including trans-nasal approaches of other organs such as pituitary, allergic rhinitis, chronic sinusitis, or any other nasal inflammatory disease that requires daily intranasal or oral medication)
4. A medical history that includes any chronic pulmonary conditions including but not limited to asthma, chronic obstructive pulmonary disease and chronic bronchitis
5. Any clinically significant acute or chronic medical conditions requiring care of a physician (e.g., diabetes, coronary artery disease, rheumatologic illness, malignancy, substance abuse) that in the opinion of the investigator would preclude participation
6. Any laboratory value outside of reference range, with the exception of any non-clinically significant Grade 1 elevations of liver function tests (AST, ALT, direct/total bilirubin), CBC, as determined by the Principal Investigator or her designee
7. Confirmed diagnosis of hepatitis B (surface antigen, HbsAg); hepatitis C (HCV antibodies) or active syphilis
8. If female, pregnant, planning a pregnancy during the trial period or lactating
9. Receipt of a live attenuated vaccine within 30 days or other vaccine within 14 days of poly ICLC administration
10. Receipt of blood transfusion or blood products 6 months prior to drug administration