Eylea Post Marketing Surveillance(PMS)

NCT01783925 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 3206

Last updated 2023-11-07

No results posted yet for this study

Summary

The objective of this PMS is to gain information about safety and efficacy in real practice as a regulatory commitment required by MFDS

Conditions

  • Macular Degeneration

Interventions

DRUG

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

Patients in daily life clinical practice treatment receiving EYLEA according to indication on the label.

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-04-29
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • South Korea

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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 NCT01783925 on ClinicalTrials.gov