56
Participants
Start Date
November 21, 2024
Primary Completion Date
March 31, 2025
Study Completion Date
May 7, 2025
HC002 SAD
"Part 1 will enroll 32 participants across 4 cohorts.~Route of administration: Oral Dose interval and frequency: Single oral dose range across 4 cohorts."
HC002 MAD
"Part 2 will enroll 24 participants across 3 cohorts.~Route of administration: Oral Dose interval and frequency: Once daily for 7 days"
Placebo
Matching placebo will be administered across SAD and MAD
CMAX Clinical Research Pty Ltd, Adelaide
Holoclara Aus Pty Ltd
INDUSTRY