The primary aim of this study is to assess the effect of EDP-323 on the pharmacokinetics and safety of midazolam, caffeine, and rosuvastatin in healthy adult participants.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
24
ICON, plc
San Antonio, Texas, United States
Cmax of midazolam, caffeine, and rosuvastatin with and without the coadministration of EDP-323
Time frame: Up to 17 Days
AUC of midazolam, caffeine, and rosuvastatin with and without the coadministration of EDP-323
Time frame: Up to 17 Days
Safety measured by adverse events
Time frame: Up to 22 days
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Subjects will receive rosuvastatin once daily on Days 2 and 13