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Real-Life Clinical Outcomes of Aflibercept Biosimilar MY-1701P in the Treatment of Exudative Age-Related Macular Degeneration

Real-Life Clinical Outcomes of Aflibercept Biosimilar MY-1701P in the Treatment of Exudative Age-Related Macular Degeneration

Recruiting
45-90 years
All
Phase N/A

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Overview

In this study, patients receiving Eylea treatment will be treated with Yesafili, a biosimilar molecule, and routine examination results will be noted.

Eligibility

Inclusion Criteria:

  • Patients aged between 45 and 90 years with active neovascular age-related macular degeneration (nAMD)
  • who show signs of disease activity on routine ophthalmologic examination and optical coherence tomography (OCT)
  • for whom intravitreal injection has already been clinically indicated

Exclusion Criteria:

  • Patients younger than 45 years or older than 90 years
  • History of stroke, cerebrovascular event, myocardial infarction, or coronary stent placement within the last six months
  • Presence of uveitis
  • Media opacity preventing adequate retinal imaging (e.g., corneal opacity, mature cataract)
  • Coexistence of other retinal vascular diseases (e.g., branch retinal vein occlusion, diabetic macular edema)
  • Presence of hereditary retinal dystrophies
  • Presence of optic atrophy

Study details
    Age Related Macular Degeneration
    Exudative Age-Related Macular Degeneration
    Anti Vascular Endothelial Growth Factor

NCT07235527

Saglik Bilimleri Universitesi

1 February 2026

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