Safety, Tolerability, and Efficacy Study of UBX1325 in Patients With Neovascular Age-Related Macular Degeneration (ENVISION)

PHASE2CompletedINTERVENTIONAL
Enrollment

51

Participants

Timeline

Start Date

March 2, 2022

Primary Completion Date

February 15, 2023

Study Completion Date

July 25, 2023

Conditions
Neovascular Age-related Macular Degeneration
Interventions
DRUG

UBX1325 injection 50 μL

Patients randomized to the UBX1325 arm will receive UBX1325 on Day 1, Weeks 4, 24, and 28

DRUG

EYLEA® (aflibercept) Injection 2 mg (0.05mL)

Patients randomized to the active-control aflibercept arm will receive aflibercept per label every 8 weeks starting from day 1 until Week 40. In addition, these patients will receive UBX1325 on Week 24 and Week 32; and a sham procedure at Week 4 and Week 28.

Trial Locations (14)

33064

Rand Eye Institute, Deerfield Beach

33711

Retina Vitreous Associates of Florida, St. Petersburg

46290

Midwest Eye, Carmel

55905

Mayo Clinic-Rochester, Rochester

60439

University Retina and Macula Associates, Lemont

61615

Illinois Eye Center, Peoria

78503

Valley Retina Institute, McAllen

78681

Austin Retina Associates, Round Rock

79606

Retina Research Institution of Texas, Abilene

80503

Advanced Vision Research Institute, Longmont

89502

Sierra Eye Associates, Reno

90211

Retina-Vitreous Associates Medical Group, Beverly Hills

92647

Salehi Retina Institute, Huntington Beach

97225

EyeHealth Northwest, Portland

All Listed Sponsors
lead

Unity Biotechnology, Inc.

INDUSTRY