drugset / Trial / NCT01080209

Safety Extension Study to Evaluate the Biodegradation of the Brimonidine Tartrate Posterior Segment Drug Delivery System

NCT01080209 ↗

Phase 2 Completed 215 enrolled Allergan
Non-randomizedSingle-groupSingle-blind

Summary

This study will evaluate the biodegradation of the brimonidine tartrate posterior segment drug delivery system.

Timeline

Start
2010-02
Primary completion
2014-02
Completion
2014-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Brimonidine Unknown 50 ug Intravitreal
Subject Brimonidine Unknown 100 ug Intravitreal
Subject Brimonidine Unknown 200 ug Intravitreal
Subject Brimonidine Unknown 400 ug Intravitreal

Indications

No indication recorded.