Study of GLS-5700 in Healthy Volunteers

GLS-5700 contains a single plasmid containing DNA encoding for pre-membrane and envelope
(prME) proteins of the Zika virus.

Inclusion Criteria:

1. Age 18-65 years;

2. Able to provide consent to participate and having signed an Informed Consent Form
(ICF);

3. Able and willing to comply with all study procedures;

4. Women of child-bearing potential agree to use medically effective contraception (oral
contraception, barrier methods, spermicide, etc.) or have a partner who is sterile
from enrollment to 3 months following the last injection, or have a partner who is
medically unable to induce pregnancy.

5. Sexually active men who are considered sexually fertile must agree to use either a
barrier method of contraception during the study, and agree to continue the use for at
least 3 months following the last injection, or have a partner who is permanently
sterile or is medically unable to become pregnant;

6. Normal screening ECG or screening ECG with no clinically significant findings;

7. Screening laboratory must be within normal limits or have only Grade 0-1 findings;

8. No history of clinically significant immunosuppressive or autoimmune disease.

9. No history of dengue virus vaccination or illness; no history of yellow fever
vaccination.

10. Dengue seronegative at baseline by screening laboratory evaluation

11. Not currently or within the previous 4 weeks taking immunosuppressive agents
(excluding inhaled, topical skin and/or eye drop-containing corticosteroids, low-dose
methotrexate, or corticosteroids at a dose less than 20 mg/day).

Exclusion Criteria:

1. Administration of an investigational compound either currently or within 30 days of
first dose;

2. Previous receipt of an investigational product for the treatment or prevention of Zika
virus except if participant is verified to have received placebo;

3. Administration of any vaccine within 4 weeks of first dose;

4. Administration of any monoclonal or polyclonal antibody product within 4 weeks of the
first dose

5. Administration of any blood product within 3 months of first dose;

6. Pregnancy or breast feeding or plans to become pregnant during the course of the
study;

7. Positive serologic result for dengue virus (any serotype) or history of receipt of
either dengue virus or yellow fever virus vaccination at any time in the past;

8. Positive serologic test for HIV, hepatitis B surface antigen (HBsAg); or any
potentially communicable infectious disease as determined by the Principal
Investigator or Medical Monitor;

9. Positive serologic test for hepatitis C (exception: successful treatment with
confirmation of sustained virologic response);

10. Baseline evidence of kidney disease as measured by creatinine greater than 1.5 (CKD
Stage II or greater);

11. Baseline screening lab(s) with Grade 2 or higher abnormality, except for Grade 2
creatinine;

12. Chronic liver disease or cirrhosis;

13. Immunosuppressive illness including hematologic malignancy, history of solid organ or
bone marrow transplantation;

14. Current or anticipated concomitant immunosuppressive therapy (excluding inhaled,
topical skin and/or eye drop-containing corticosteroids, low-dose methotrexate, or
corticosteroids at a dose less than 20 mg/day);

15. Current or anticipated treatment with TNF-α inhibitors such as infliximab, adalimumab,
etanercept;

16. Prior major surgery or any radiation therapy within 4 weeks of group assignment;

17. Any pre-excitation syndromes, e.g., Wolff-Parkinson-White syndrome;

18. Presence of a cardiac pacemaker or automatic implantable cardioverter defibrillator
(AICD)

19. Metal implants within 20 cm of the planned site(s) of injection;

20. Presence of keloid scar formation or hypertrophic scar as a clinically significant
medical condition at the planned site(s) of injection.

21. Prisoner or participants who are compulsorily detained (involuntary incarceration) for
treatment of either a physical or psychiatric illness;

22. Active drug or alcohol use or dependence that, in the opinion of the investigator,
would interfere with adherence to study requirements or assessment of immunologic
endpoints; or

23. Not willing to allow storage and future use of samples for Zika virus related research

24. Any illness or condition that in the opinion of the investigator may affect the safety
of the participant or the evaluation of any study endpoint.