48
Participants
Start Date
May 6, 2025
Primary Completion Date
January 30, 2026
Study Completion Date
January 30, 2026
Placebo
Monitor for a minimum of 24 hours to assess whether the safety and tolerability are acceptable according to the investigator.
AK111
The study will use dose escalation scheme. Before proceeding to randomize the next group of subjects, the safety data from all subjects in the previous dose group must be reviewed and confirmed.
Zhejiang Xiaoshan Hospital, Hangzhou
Lead Sponsor
Akeso
INDUSTRY