drugset / Trial / NCT04747197

First in Human Study to Evaluate the Safety and Tolerability of EYP-1901 in Patients With Wet Age Related Macular Degeneration (wAMD)

NCT04747197

Phase 1 Completed 17 enrolled EyePoint Pharmaceuticals, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

Phase 1 open-label study to assess the bioactivity, ocular and systemic safety, tolerability, and pharmacokinetics of a single dose injections of EYP-1901 at three dose levels: 440 µg, 2060 µg and 3090 µg in subjects with Wet Age Related Macular Degeneration (wAMD)

Timeline

Start
2021-01-20
Primary completion
2022-05-11
Completion
2022-05-11

Drugs

EvaluationDrugModalityDoseRoute
Subject CM082 Unknown 440 ug Intravitreal
Subject CM082 Unknown 1030 ug Intravitreal
Subject CM082 Unknown 2060 ug Intravitreal
Subject CM082 Unknown 3090 ug Intravitreal