drugset / Trial / NCT01363440

Study of Intravitreal Aflibercept Injection (IAI; EYLEA®; BAY86-5321) in Patients With Diabetic Macular Edema

NCT01363440 ↗

Phase 3 Completed 466 enrolled Regeneron Pharmaceuticals Bayer · collab
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine the efficacy of Intravitreal Aflibercept Injection (IAI; EYLEA®; BAY86-5321) on the best corrected visual acuity (BCVA) assessed by the early treatment diabetic retinopathy study (ETDRS) chart in patients with diabetic macular edema (DME) with central involvement.

Timeline

Start
2011-05
Primary completion
2013-01
Completion
2014-11

Outcome

Met primary endpoint

registry analysis (superiority or other test); Control vs Intravitreal Aflibercept Injection (IAI;EYLEA®;BAY86-5321) 2Q4; p <.0001; Mean Difference (Net) 12.19 (97.5% CI 9.35 to 15.04); ANCOVA NCT01363440 ↗

registry analysis (superiority or other test); Control vs Intravitreal Aflibercept Injection (IAI;EYLEA®;BAY86-5321) 2Q8; p <.0001; Mean Difference (Net) 10.45 (97.5% CI 7.73 to 13.17); ANCOVA NCT01363440 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Aflibercept Protein / enzyme biologic 2 mg Intravitreal