An Integrated Analysis of the Effectiveness of Intravitreal (IVT) Aflibercept (Eylea) in Routine Clinical Practice Based on Two Large Observational Studies

NCT ID: NCT03521895

Last Updated: 2020-01-10

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 1000 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2018-05-01
• Study Completion Date: 2018-11-30

Brief Summary

The aim of this integrated analysis is to describe the effectiveness of Eylea in an integrated pooled analysis using existing individual patient data of two non-interventional studies RAINBOW and PERSEUS.

The primary objective of this integrated analysis is to describe the effectiveness of Eylea on the mean change from baseline in visual acuity (VA) at 12 months in Wet age-related macular degeneration (wAMD) treatment naïve patients.

Conditions

Macular Degeneration

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: RETROSPECTIVE

Study Groups

Treatment naïve wAMD

Treatment naïve patients with wAMD treated with IVT aflibercept from the two underlying studies PERSEUS and RAINBOW

Eylea (Aflibercept, VEGF Trap-Eye, BAY86-5321)

Intervention Type: DRUG

Patients observed with regular and irregular treatment course

Interventions

Eylea (Aflibercept, VEGF Trap-Eye, BAY86-5321)

Patients observed with regular and irregular treatment course

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

PERSEUS

• Patients with wet AMD treated with Eylea (in accordance with the local Summary of Product Characteristics, SPC)
• Documentation of at least one Aflibercept (Eylea) injection
• Assessment of at least one visual acuity measurement with available VA letter score for the study eye at baseline and at least one post-baseline assessment of visual acuity with available VA letter score for the study eye and valid for analysis, i.e. measured at least 5 days after an injection RAINBOW
• Patient with a diagnosis of wet AMD will be enrolled after the decision for treatment with Aflibercept (Eylea) has been made
• Patient who meet the local indication criteria for Eylea treatment
• At least one BCVA after the 1st Eylea injection
• BCVA at baseline
• Patient with no history of retinal disease
• Patient not previously treated with any macular laser or any anti-VEGF intravitreal injections for the study eye (for fellow eye allowed).
• For patients with both eyes treated, the eye firstly treated at initial visit will be considered as study eye. If both eyes are treated during initial visit, the treated eye with worst Best-Corrected Visual Acuity (BCVA) at M0 will be retained. If the two conditions are similar the study eye is the Right eye by convention

Exclusion Criteria

• Scar, fibrosis, or atrophy involving the center of the fovea in the study eye
• All patients previously treated with any macular laser or any anti-VEGF intravitreal injections for the study eye will additionally be excluded for this integrated analysis
• Any concomitant therapy with another agent to treat wet AMD in the study eye RAINBOW
• Patient who does not meet the local indication criteria for Eylea treatment. Contraindications listed in the SmPCs must be taken into account
• Patient with another retinal disease: diabetic retinopathy, diabetic macular oedema (DME), myopic choroidal neovascularization, retinal vein occlusion (RVO), central serous chorioretinopathy (CSC), angioid streaks
• Patient who has previously been treated with any macular laser (laser and/or visudyne/PDT) or any anti-VEGF intravitreal injections for the study eye
• Patient taking part in an interventional study at the time of enrolment

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Bayer

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Many locations

Multiple Locations, , Germany

Countries

Germany

Related Links

http://clinicaltrials.bayer.com/

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Other Identifiers

19694

Identifier Type: -

Identifier Source: org_study_id