72
Participants
Start Date
July 15, 2024
Primary Completion Date
February 2, 2025
Study Completion Date
February 25, 2025
zelicapavir (therapeutic dose)
Subjects will receive zelicapavir (TD) once per treatment period.
zelicapavir (supratherapeutic dose)
Subjects will receive zelicapavir (SD) once per treatment period.
Placebo
Subjects will receive zelicapavir matching placebo once per treatment period.
moxifloxacin
Subjects will receive moxifloxin once per treatment period.
ICON, Lenexa
ICON Early Phase, LLC, San Antonio
Lead Sponsor
Enanta Pharmaceuticals, Inc
INDUSTRY