Trial Profile

Randomized, Double-Masked, Active-Controlled, Phase 3 Study of the Efficacy and Safety of Aflibercept 8 mg in Macular Edema Secondary to Retinal Vein Occlusion

Status: Completed

Phase of Trial: Phase III

Latest Information Update: 11 Jun 2025

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At a glance

04 Jun 2025 Status changed from active, no longer recruiting to completed.
17 Apr 2025 According to a Regeneron Pharmaceuticals Inc. media release, the U.S. Food and Drug Administration (FDA) has accepted for Priority Review the supplemental Biologics License Application (sBLA) for EYLEA HD (aflibercept) based on the data from this study. The FDA target action date is August 19, 2025, following the use of a Priority Review voucher.
03 Apr 2025 Planned End Date changed from 16 May 2025 to 27 May 2025.

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