drugset / Trial / NCT00693485

Safety and Effects of Brimonidine Intravitreal Implant in Patients With Glaucomatous Optic Neuropathy

NCT00693485

Phase 2 Completed 70 enrolled Allergan
RandomizedParallel-groupTriple-blindTreatment

Summary

A multicenter, randomized, patient-masked, sham-controlled evaluation of the safety and effects on visual function of brimonidine intravitreal implant in patients with glaucomatous optic neuropathy. Patients will be followed for up to 1 year.

Timeline

Start
2008-09
Primary completion
2011-01
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Brimonidine Small molecule 200 ug Intravitreal
Subject Brimonidine Small molecule 400 ug Intravitreal

Indications