The purpose of this study is to determine whether a live, oral, combined Shigella-ETEC vaccine candidate, known as strain CVD 1208S-122, is safe and immunogenic.
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Participants Experiencing Fever, Diarrhea, or Dysentery; Solicited Local Adverse Events; Solicited Systemic Adverse Events; and Clinical Safety Laboratory Adverse Events
Timeframe: Solicited AEs: Cohorts 1-3 during 4 days of inpatient and memory aid for another 3 days; Cohort 4 memory aid over 7 days after each dose of study product Clinical Safety Labs: Cohorts 1-3: Day 1 and Day 8; Cohort 4: Days 1 and 29 and Days 8 and 36
Vaccine Organisms Shed in Stools in Cohorts 1-3 - Cohorts 1-3
Timeframe: 7 days
Vaccine Organisms Shed in Stools in Cohort 4
Timeframe: 2 days
Number of Participants With Genetically Stable Fecal Shed Organisms
Timeframe: 7 days