This is a Phase 1, randomized, double-blind (with open-label sentinel cohorts), placebo-controlled, single-ascending-dose study designed to evaluate the safety, tolerability, and pharmacokinetics (PK) of MI226 Injection in participants with abdominal fat accumulation.
Age range
18 Years – 65 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 and severity of treatment-emergent adverse events (TEAEs) as assessed by NCI CTCAE v6.0
Timeframe: Up to Day 28
Number of participants with clinically significant abnormal physical examination findings
Timeframe: Up to Day 28
Number of participants with clinically significant changes in vital signs
Timeframe: Up to Day 28
Number of participants with clinically significant abnormal laboratory test results
Timeframe: Up to Day 7
Number of participants with clinically significant abnormal 12-lead electrocardiogram (ECG) findings
Timeframe: Up to Day 7