Special Drug Use Investigation of EYLEA for Myopic Choroidal Neovascularization

NCT02260687 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 353

Last updated 2019-09-19

No results posted yet for this study

Summary

The objectives of this study are to investigate the safety and effectiveness of EYLEA.

Conditions

  • Choroidal Neovascularization

Interventions

DRUG

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

Administration by intravitreal injection

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-12-05
Primary Completion
2018-04-02
Completion
2018-08-22

Countries

  • Japan

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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 NCT02260687 on ClinicalTrials.gov