CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 183 enrolled
Drug / intervention
Intravitreal Aflibercept Injection (IAI;EYLEA®;BAY86-5321) +1 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01521559
NCT01521559Phase 3Completed

A Double-Masked, Randomized, Active-Controlled Study of the Efficacy, Safety, and Tolerability of Intravitreal Administration of VEGF Trap-Eye (Intravitreal Aflibercept Injection [IAI]) in Patients With Macular Edema Secondary to Branch Retinal Vein Occlusion

Regeneron Pharmaceuticals·interventional·Posted Jan 30, 2012·Updated Nov 13, 2014

In Brief

A Phase 3 clinical trial evaluating Macular Laser Photocoagulation and Intravitreal Aflibercept Injection (IAI;EYLEA®;BAY86-5321) for Branch Retinal Vein Occlusion. Completed, enrolled 183 participants across 56 sites in 3 countries.

Detailed Summary

This is a phase III, double-masked, randomized, active-controlled, parallel-group, 52-week study to assess the efficacy and safety of Intravitreal Aflibercept Injection (IAI;EYLEA®;BAY86-5321) compared to laser treatment in patients with macular edema secondary to BRVO.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada, Japan, United States
CollaboratorsBayer

Timeline

Phase 3CompletedFinished
201220132014201520162017201820192020202120222023202420252026
First PostedJan 30, 2012
Enrollment StartApr 1, 2012
Primary CompletionAug 1, 2013
Study CompletionMar 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 14.4 years ago

Interventions

Macular Laser Photocoagulationprocedure

Intravitreal Aflibercept Injection (IAI;EYLEA®;BAY86-5321)drug