A Study Assessing AR-13503 Implant in Subjects With nAMD or DME

PHASE1CompletedINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

June 24, 2019

Primary Completion Date

May 12, 2022

Study Completion Date

May 12, 2022

Conditions
Neovascular Age-related Macular DegenerationDiabetic Macular Edema
Interventions
DRUG

AR-13503 Implant 10.6 Dose

AR-13503 Implant 10.6 Dose (10.6 µg) administered as an intravitreal implant into a single eye

DRUG

AR-13503 Implant 21.2 Dose

AR-13503 Implant 21.2 Dose (21.2 µg) administered as intravitreal implants into a single eye

DRUG

AR-13503 42.4 Dose

AR-13503 Implant 42.4 Dose (42.4 µg) administered as intravitreal implants into a single eye

DRUG

AR-13503 63.6 Dose

AR-13503 Implant 63.6 Dose (63.6 µg) administered as intravitreal implants into a single eye

Trial Locations (6)

78240

Medical Center Ophthamology Associates, San Antonio

78550

Valley Retina Institute, P.A., Harlingen

85296

Retinal Research Institute, LLC, Gilbert

90211

Retina-Vitreous Associates Medical Group, Beverly Hills

94598

Bay Area Retina Associates, Walnut Creek

97401

Sterling Vision, PC dba Oregon Retina, Eugene

Sponsors
All Listed Sponsors
lead

Aerie Pharmaceuticals

INDUSTRY

NCT03835884 - A Study Assessing AR-13503 Implant in Subjects With nAMD or DME | Biotech Hunter | Biotech Hunter