This study will assess the safety, tolerability and pharmacokinetics (PK) of Bemnifosbuvir in healthy adult Japanese subjects
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
14
BEM administered BID for 4 days and QD on Day 5 (9 consecutive doses)
Atea Study Site
Cypress, California, United States
Pharmacokinetics (PK) of BEM Maximum plasma concentration (Cmax)
Time frame: Day 1, Day 5
Pharmacokinetics (PK) of BEM Area under the plasma concentration-time curve (AUC)
Time frame: Day 1, Day 5
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