Clinical TrialsUBX1325 demonstrated outperformance of aflibercept for patients with less aggressive disease, suggesting a prospective option for 2L treatment.
Efficacy DataUBX1325 achieved non-inferiority to aflibercept for 9 out of 10 time points through 36 weeks, reflecting a completely novel approach in retinal disease.
Treatment EfficacyApproximately 40% of UBX1325 patients did not require supplemental anti-VEGF through week 36, supporting the novel retinal mechanism.