drugset / Trial / NCT02599064

Evaluating RXI-109 to Reduce the Progression of Subretinal Fibrosis in Subjects With NVAMD

NCT02599064 ↗

Phase 1/2 Unknown 9 enrolled RXi Pharmaceuticals, Corp.
NaSingle-groupOpen-labelTreatment

Summary

This study is designed to evaluate the safety, tolerability and clinical activity of RXI-109 administered by intravitreal injection to reduce the progression of subretinal fibrosis in subjects with advanced neovascular age-related macular degeneration (NVAMD).

Timeline

Start
2015-11
Primary completion
2018-04
Completion
2018-05

Drugs

EvaluationDrugModalityDoseRoute
Subject RXI-109 Unknown — Intravitreal