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NCT01783925

Eylea Post Marketing Surveillance(PMS)

Completed Last updated 7 November 2023
What this trial tests

trial testing Aflibercept (Eylea, VEGF Trap-Eye, BAY86-5321) in Macular Degeneration in 3,206 participants. Completed in 31 December 2018.

Timeline
29 April 2014
Primary endpoint
31 December 2018
31 December 2018

Quick facts

Lead sponsorBayer
StatusCompleted
Study typeOBSERVATIONAL
Enrollment3,206
Start date29 April 2014
Primary completion31 December 2018
Estimated completion31 December 2018
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

Bayer — full company profile →

Who can join

Eligibility, any sex, with Macular Degeneration. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Real-World Outcomes of Intravitreal Aflibercept for Neovascular Age-Related Macular Degeneration: A Large-Scale Postmarketing Surveillance in Korea.
    Ryu G, Noh D, Moon G, Sagong M. · · 2021 · cited 3× · PMID 34471345 · DOI 10.2147/opth.s324600

Verify or expand the search:

Other trials of Aflibercept (Eylea, VEGF Trap-Eye, BAY86-5321)

Trials testing the same drug.

Other recruiting trials for Macular Degeneration

Currently open trials in the same condition.

Other Bayer trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01783925.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing