drugset / Trial / NCT04857996

Safety, Tolerability and Evidence of Activity Study of UBX1325 in Patients With Diabetic Macular Edema (BEHOLD)

NCT04857996

Phase 2 Completed 65 enrolled Unity Biotechnology, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is intended to assess the exposure, safety, biological activity, and durability of UBX1325, a phosphate pro-drug, and its active parent molecule (UBX0601) following a single intravitreal (IVT) injection of UBX1325 in patients with diabetic macular edema (DME).

Timeline

Start
2021-06-25
Primary completion
2023-04-06
Completion
2023-04-06

Drugs

EvaluationDrugModalityDoseRoute
Subject foselutoclax Small molecule 10 ug Intravitreal