Part A Primary objective: • To evaluate the safety, tolerability, and pharmacokinetic profile of a single dose of YZJ-4729 tartrate injection. Secondary objectives: * To investigate the PK/PD profile of YZJ-4729 tartrate injection administered as a single dose; * To investigate the metabolic transformation characteristics of YZJ-4729 tartrate; * To assess the relationship between plasma concentrations and change in QT interval (C-QT) and the effect on QT interval in subjects after a single dose of YZJ-4729 tartrate injection. Part B Primary objective: • To evaluate the safety, tolerability and pharmacokinetic profile of YZJ-4729 tartrate injection administered at the same dose and at different infusion rates . Secondary objectives: • To investigate the PK/PD profile of YZJ-4729 tartrate injection administered at the same dose and at different infusion rates.
Age range
18 Years – 45 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Incidence of adverse events (AEs) and serious adverse events (SAEs)
Timeframe: Part A: From Day 1 to Day 5 Part B: From Day 1 to Day 17
Incidence of participants with clinical laboratory abnormalities
Timeframe: Part A: From Day 1 to Day 5 Part B: From Day 1 to Day 17
Incidence of participants with vital signs abnormalities
Timeframe: Part A: From Day 1 to Day 5 Part B: From Day 1 to Day 17
Incidence of participants with physical exam abnormalities
Timeframe: Part A: From Day 1 to Day 5 Part B: From Day 1 to Day 17
Cmax
Timeframe: Pre-dose to 72 hours post-dose
AUCinf
Timeframe: Pre-dose to 72 hours post-dose
AUC0-24h
Timeframe: Pre-dose to 72 hours post-dose
AUC0-t
Timeframe: Pre-dose to 72 hours post-dose
t1/2z
Timeframe: Pre-dose to 72 hours post-dose
Tmax
Timeframe: Pre-dose to 72 hours post-dose
CL
Timeframe: Pre-dose to 72 hours post-dose
Vz
Timeframe: Pre-dose to 72 hours post-dose
MRT
Timeframe: Pre-dose to 72 hours post-dose
Ae0-t
Timeframe: Pre-dose to 72 hours post-dose
Cumulative excretion percentage of drug through urine and feces
Timeframe: Pre-dose to 72 hours post-dose