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NCT06124677Completed

Single Injection of Faricimab for nAMD With Persisting Fluid Despite Frequent Aflibercept Treatments

Anatomical and Visual Outcomes Following a Single Injection of Intravitreal Faricimab in Patients With Neovascular Age-related Macular Degeneration and Persisting Fluid Despite Frequent Aflibercept Treatments

Source: ClinicalTrials.gov · Last updated 11 Dec 2023

Brief summary (registry, in English)

The goal of this retrospective single-center chat review is to establish the efficacy and safety of a single dose of intravitreal faricimab (Vabysmo®) injection in patients with neovascular age-related macular degeneration (AMD), who were previously treated with aflibercept (Eylea®) and had persisting intraretinal or subretinal fluid despite frequent treatments.

Status (registry)
Completed
Study type
Observational
Enrollment
46 (actual)
First submitted
1 Nov 2023
Start date
1 Nov 2023
Primary completion date
15 Nov 2023
Lead sponsor
Copenhagen University Hospital, Rigshospitalet
NCT number
NCT06124677

What you commit to

  • Study type: Observational
  • Participants enrolled: 46
  • From 1 Nov 2023 to the primary completion date, 15 Nov 2023
  • 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.

Prior treatment

  • Intraocular surgery in the study eye 3 months before or within 1 month after the treatment switch

Other illness

  • Neovascular conditions other than AMD (e.g., choroidal neovascularisation due to other causes) or co-existence of other retinal disease in the study eye

Other

  • Significant optical media opacities that would result in poor imaging quality on OCT scans in the study eye

Who the study is looking for

  • Presence of neovascular age-related macular degeneration (AMD) in the study eye
  • \>50 years of age
  • Previous intravitreal anti-VEGF treatment with aflibercept (Eylea®) or with aflibercept and ranibizumab (Lucentis®) in the study eye
  • Minimum of 6 monthly aflibercept injections
  • Persisting intraretinal or subretinal fluid or both, despite at least 3 consecutive monthly aflibercept injections in the study eye before switching to faricimab

Age in the registry: 50 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Miklos Schneider
Coordinator of this site? Confirm its status
Glostrup MunicipalityDenmarkUnknown status

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