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.
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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