26
Participants
Start Date
May 17, 2022
Primary Completion Date
May 12, 2023
Study Completion Date
June 16, 2023
LAT8881
"In Part A, LAT8881 will be given as a single intravenous infusion at doses of 0.8, 1.2 and 1.8 mg/kg.~In Part B, a single intravenous infusion of LAT8881 will be given, the dose to be determined by the results in Part A"
Placebo
Matching placebo'given as a single intravenous infusion at all dose levels
PARC Clinical Research, Adelaide
Lead Sponsor
Collaborators (1)
Southern Star Research
INDUSTRY
Lateral Pharma Pty Ltd
INDUSTRY