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NCT07235527Completed

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

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

Source: ClinicalTrials.gov · Last updated 1 Sept 2026

Brief summary (registry, in English)

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

Status (registry)
Completed
Study type
Observational
Enrollment
54 (actual)
First submitted
14 Nov 2025
Start date
20 Nov 2025
Primary completion date
20 Aug 2026
Lead sponsor
Saglik Bilimleri Universitesi
NCT number
NCT07235527

What you commit to

  • Study type: Observational
  • Participants enrolled: 54
  • From 20 Nov 2025 to the primary completion date, 20 Aug 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • History of stroke, cerebrovascular event, myocardial infarction, or coronary stent placement within the last six months
  • Coexistence of other retinal vascular diseases (e.g., branch retinal vein occlusion, diabetic macular edema)

Age

  • Patients younger than 45 years or older than 90 years

Other

  • Presence of uveitis
  • Media opacity preventing adequate retinal imaging (e.g., corneal opacity, mature cataract)
  • Presence of hereditary retinal dystrophies
  • Presence of optic atrophy

Who the study is looking for

  • 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

Age in the registry: 45 years to 90 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Prof. Dr. Cemil Taşcıoğlu City Hospital
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

This page is information, not medical advice. Discuss any trial with your doctor.