drugset / Trial / NCT03835884

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

NCT03835884 ↗

Phase 1 Completed 18 enrolled Aerie Pharmaceuticals
RandomizedSequentialOpen-labelTreatment

Summary

First-in-Human Study of the Safety of AR-13503 Sustained Release Intravitreal Implant in Subjects with Neovascular Age-Related Macular Degeneration (nAMD) and Subjects with Diabetic Macular Edema (DME)

Timeline

Start
2019-06-24
Primary completion
2022-05-12
Completion
2022-05-12

Drugs

EvaluationDrugModalityDoseRoute
Subject AR-13503 Unknown 10.6 ug Intravitreal
Subject AR-13503 Unknown 21.2 ug Intravitreal
Subject AR-13503 Unknown 42.4 ug Intravitreal
Subject AR-13503 Unknown 63.6 ug Intravitreal