drugset / Trial / NCT02396316

Japanese Phase 3 Study of Aflibercept in Neovascular Glaucoma Patients

NCT02396316

Phase 3 Completed 54 enrolled Bayer Regeneron Pharmaceuticals · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

To assess the efficacy and safety of the administration of aflibercept by intravitreal injection in comparison to sham to control intraocular pressure in patients with neovascular glaucoma.

Timeline

Start
2015-04-02
Primary completion
2016-06-16
Completion
2016-09-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Aflibercept Protein / enzyme biologic 2 mg Intravitreal

Indications