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Clinical Trial Summary

This study is intended to assess the safety, tolerability and evidence of pharmacodynamic activity of a single intravitreal (IVT) injection of UBX1325 in patients with diabetic macular edema (DME)


Clinical Trial Description

This is a Phase 2a Proof-of-Concept (POC) study. The study will enroll approximately 62 patients randomized 1:1 into either the UBX1325 or sham study arms, in order to assess the primary objective. All patients will be followed for approximately 24 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04857996
Study type Interventional
Source Unity Biotechnology, Inc.
Contact Medical Monitor
Phone 650-513-0096
Email [email protected]
Status Not yet recruiting
Phase Phase 2
Start date May 2021
Completion date June 2022

See also
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Not yet recruiting NCT04739306 - Study to Compare Efficacy and Safety of CT-P42 in Comparison With Eylea in Patients With Diabetic Macular Edema Phase 3