Clinical Study ResultsUBX1325 demonstrated vision gains comparable and statistically non-inferior to aflibercept at week 36 considering difficult to-treat DME patients with favorable safety and tolerability.
Subgroup PerformanceUBX1325 generally outperformed aflibercept in the pre-specified subgroup entering the study with CST <400 microns, reflecting 60% of enrolled patients.
Treatment EfficiencyApproximately 40% of UBX1325 patients did not require supplemental anti-VEGF through week 36, supporting the novel retinal mechanism.