Real Life of Aflibercept In FraNce: oBservatiOnnal Study in Wet AMD

NCT02279537 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 593

Last updated 2023-11-07

No results posted yet for this study

Summary

The purpose of this study is to collect real-life data on patients with wet age related macular degeneration (AMD) for whom treatment with Eylea was initiated

Conditions

  • Wet Macular Degeneration

Interventions

DRUG

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

Administration by intravitreal injection

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-02
Primary Completion
2019-04-17
Completion
2019-04-17

Countries

  • France

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02279537 on ClinicalTrials.gov