This study will include 4 cohorts of 14 ZIKV and DENV-naïve female and male subjects, 18 - 40 years of age (total: up to 56 subjects). Within each cohort, 10 subjects will receive ZIKV and 4 subjects will receive a placebo on Study Day 0. Cohorts 1 and 2 (Dose = 10\^2 PFU) will be enrolled first and will enroll only women. Cohorts 3 and 4 (Dose = 10\^2 PFU) will enroll men.
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Number of Solicited Adverse Events
Timeframe: Through 90 days post-inoculation
Severity of Adverse Events
Timeframe: Through 90 days post-inoculation
Number of Participants Infected by ZIKV
Timeframe: Through 90 days post-inoculation
Number of Participants With Zika Virus Recovered From Serum, Whole Blood, CVS, Semen, Urine, and Saliva
Timeframe: Through 90 days post-inoculation
Magnitude of ZIKV Recovered From Serum, Whole Blood, CVS, Semen, Urine, and Saliva
Timeframe: Through 90 days post-inoculation
Duration of ZIKV in Serum, Whole Blood, CVS, Semen, Urine, and Saliva
Timeframe: Through 90 days post-inoculation