drugset / Trial / NCT02022501

A Phase I/II Safety Study of DE-120 Injectable Solution for Age-related Macular Degeneration

NCT02022501

Phase 1/2 Completed 10 enrolled Santen Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety, tolerability, bioactivity and pharmacokinetics of three concentrations of DE-120 after a single intravitreal injection in subjects with late stage exudative age-related macular degeneration.

Timeline

Start
2014-01
Primary completion
2016-04-21
Completion
2016-04-21

Drugs

EvaluationDrugModalityDoseRoute
Subject DE-120 Unknown 0.02 ml Intravitreal