Integrated results from the COPERNICUS and GALILEO studies.

ABSTRACT:

Objectives

To report on the efficacy and safety of intravitreal aflibercept in patients with macular edema secondary to central retinal vein occlusion (CRVO) in an integrated analysis of COPERNICUS and GALILEO.

Patients and methods

Patients were randomized to receive intravitreal aflibercept 2 mg every 4 weeks or sham injections until week 24. From week 24 to week 52, all intravitreal aflibercept-treated patients in both studies and sham-treated patients in COPERNICUS were eligible to receive intravitreal aflibercept based on prespecified criteria. In GALILEO, sham-treated patients continued to receive sham treatment through week 52.

Results

At week 24, mean gain in best-corrected visual acuity and mean reduction in central retinal thickness were greater for intravitr

SUBMITTER: Pielen A 

PROVIDER: S-EPMC5574701 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature