This was an open-label, multi-center, FIH study with a single ascending dose (SAD) design that assessed the safety, tolerability and pharmacokinetics (PK) of a single IVT dose of MHU650 in up to 24 participants with macular edema.
Age range
18 Years – 90 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.
Number of participants with ocular and nonocular adverse events
Timeframe: Day 1 to Day 60
Change from baseline in Best Correct Visual Acuity (BCVA ) by dose level and timepoint - Study Eye
Timeframe: Day 1 to Day 60
Change from baseline in Central subfield thickness (CSFT) (µm) in the study eye by dose level and timepoint
Timeframe: Day 1 to Day 60
Change from baseline in Intraocular pressure (IOP) (mmHg) in the study eye by dose level and timepoint
Timeframe: Day 1 to Day 60