A Double-Blind Placebo-Control Dose Escalating Study to Evaluate the Safety and Immunogenicity of dmLT by Oral, Sublingual and Intradermal Vaccination in Adults Residing in an Endemic Area

Exclusion Criteria

• •1. Women who are pregnant or lactating or have a positive urine pregnancy test at screening or on the day of vaccinations.
• •Note: all women presenting for screening will have urine pregnancy testing. "Females of childbearing potential must agree to use an efficacious hormonal or barrier method of birth control from screening and through 28 days post last dose of vaccine. Abstinence is also acceptable."
• •2. Presence or history of a chronic medical condition\* that would, in the opinion of the investigator, render vaccination unsafe or interfere with the evaluation of the vaccine.
• •\*Note: this may include, but is not limited to: significant renal disease, unstable or progressive neurological disorders, diabetes, heart disease, asthma, lung disease, liver disease, organ transplant recipients and cancer.
• •3. Presence of a significant dermatologic condition\*, or tattoo(s), scarring or significant skin damage at the vaccination site that would impede evaluation of local reactogenicity.
• •\*Note: this may include severe eczema, psoriasis or history of keloid formation. Participants with history of squamous cell or basal cell skin cancer that has been surgically excised and considered cured may be enrolled in the study if the skin cancer site is healed and is not at proposed vaccine administration site.
• •4. Any developmental abnormality of the palate.
• •5. Participants diagnosed with autoimmune disorders, chronic inflammatory disorders or neurological disorders with a potential autoimmune correlation.
• •6. Use of long-term (\> / = 2 weeks) oral steroids, intranasal or topical prednisone (or equivalent), parenteral steroids, or high-dose inhaled steroids (\> 800 microgram/day of beclomethasone dipropionate or equivalent) within the preceding 6 months.
• •7. Has major psychiatric illness\* during last 12 months that in the investigator's opinion would preclude participation.
• •\*Note: Participants taking antipsychotic or antimanic drugs should not be enrolled. These include: aripiprazole, clozapine, ziprasidone, haloperidol, molindone, lamotrigine, gabapentin, topiramate, loxapine, thioridazine, thiothixene, pimozide, fluphenazine, risperidone, mesoridazine, quetiapine, trifluoperazine, chlorprothixene, chlorpromazine, perphenazine, olanzapine, carbamazepine, divalproex sodium, lithium carbonate, or lithium citrate. Participants taking a single antidepressant drug and are stable without de-compensating symptoms in the preceding 3 months can be enrolled in the study.
• •8. Use of prescription or over-the-counter (OTC) anti-inflammatory medications\* 48 hours prior to receiving the investigational product.
• •\*Note: This includes naproxen, aspirin, ibuprofen, and other non-steroidal anti-inflammatory drugs.
• •9. Gastrointestinal symptoms\* in the past 24 hours or abdominal pain lasting for more than 2 weeks in the past 6 months.
• •\*Note: this may include, but is not limited to: abdominal pain or cramps, loss of appetite, nausea, general ill-feeling or vomiting.
• •10. Moderate or severe diarrheal illness\* during the 6 weeks prior to enrollment.
• •\*Note: Moderate or severe diarrheal illness is defined by the passage of \> / = 4 unformed or loose stools (mix of liquid and solid components) in a 24 hour period
• •11. History of chronic gastrointestinal illness\*.
• •\*Note: this includes severe dyspepsia or gastroesophageal reflux disease, constipation, irritable bowel syndrome (IBS), hemorrhoids, diverticular disease, colitis, colon polyps, colon cancer, and inflammatory bowel disease. Mild or moderate heartburn or epigastric pain occurring no more than three times per week is permitted.
• •12. Regular use (weekly or more often) of laxatives, anti-diarrheal, anti-constipation, or antacid therapy.
• •13. History of major gastrointestinal surgery, excluding uncomplicated appendectomy or cholecystectomy.
• •14. History of systemic antimicrobial treatment (i.e., topical treatments are not an exclusion) during the week prior to any administration of dmLT.
• •15. Acute febrile illness (body temperature \> / = 38 degrees Celsius) during the week prior to enrollment.
• •16. Abnormal screening laboratories. Note: screening labs include white blood cell count (WBC), absolute neutrophil count (ANC), hemoglobin (Hg), platelet count, serum creatinine, serum albumin, alanine aminotransferase (ALT, also known as SGPT), and serologic testing for Hepatitis B virus surface antigen (HBsAg) and Hepatitis C virus (HCV) antibody. Abnormal vital signs.
• •17. Isolation of specific bacteria\* from screening stool cultures.
• •\*Note: bacteria include ETEC, Vibrio cholerae, and Shigella spp. Salmonella and Campylobacter will not be evaluated as part this criterion.
• •18. Received an inactivated licensed vaccine within 2 weeks of enrollment or live licensed vaccine within 4 weeks of enrollment.
• •19. Received a cholera (licensed or experimental) vaccine, E. coli vaccine, or Shigella vaccine in the last 3 years.
• •20. History of receiving immune globulin or other blood product within the 3 months before enrollment in this study.
• •21. Currently enrolled in another study, involving an experimental agent. Participants involved in observational studies or surveys remain eligible.
• •22. Any condition that would, in the opinion of the Site Investigator, place the participant at an unacceptable risk of injury or render the participant unable to meet the requirements of the protocol.
• •23. Known allergies to study compound or components of the study vaccine.
• •24. Donating blood in the 8 weeks prior to study entry.