drugset / Trial / NCT01027650

Safety and Efficacy of AGN208397 in the Treatment of Macular Edema Associated With Retinal Vein Occlusion (RVO)

NCT01027650 ↗

Phase 1/2 Completed 121 enrolled Allergan
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will evaluate the safety and efficacy of a single intravitreal injection of AGN208397 to treat Macular Edema associated with Retinal Vein Occlusion. This study is being conducted in two stages: Stage 1 will enroll approximately 21 subjects who will receive a single open label intravitreal injection of either 75 ug, 300 ug, 600 ug or 900 ug of AGN208397 and be followed for 12 months post treatment; based on Stage 1 results, Stage 2 will enroll approximately 96 subjects who will receive a single masked intravitreal injection of one of three doses of AGN208397 or Ozurdex® and be followed for 12 months post treatment.

Timeline

Start
2010-03
Primary completion
2012-04
Completion
2013-02

Drugs

EvaluationDrugModalityDoseRoute
Subject AGN208397 Unknown 75 ug Intravitreal
Subject AGN208397 Unknown 300 ug Intravitreal
Subject AGN208397 Unknown 450 ug Intravitreal
Subject AGN208397 Unknown 600 ug Intravitreal
Subject AGN208397 Unknown 900 ug Intravitreal
Comparator Dexamethasone Small molecule 700 ug Intravitreal