drugset / Trial / NCT05383209

Study of EYP-1901 in Patients With Nonproliferative Diabetic Retinopathy (NPDR)

NCT05383209

Phase 2 Completed 77 enrolled EyePoint Pharmaceuticals, Inc.
RandomizedParallel-groupTriple-blindTreatment

Summary

A prospective, randomized, double-masked study that evaluated the ocular efficacy and safety of two doses of the EYP-1901 intravitreal (IVT) insert compared to sham.

Timeline

Start
2022-09-28
Primary completion
2024-02-12
Completion
2024-05-06

Drugs

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

Indications