Efficacy of Faricimab in Patients With Subretinal Hyper-reflective Material

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age50+
SponsorBiobizkaia Health Research Institute

About this trial

Whose aim is to:

Determine the percentage of patients with resolution of subretinal hyperreflective material (SHRM) at week 16.

This study is intended to be performed in the ophthalmology departments or ophthalmology clinics of the participating sites, located in Spain.

Macular degeneration is an eye disease characterised by progressive damage to the macula leading to a loss of central vision. There are two types of macular degeneration, dry and wet or exudative. The prevalence of the latter in Spain is 1.9% in people aged 65 and over. Among the subtypes of macular neovascularisation (MNV), type 2 is rare (9%), with the majority being mixed type 1 and 2 cases (13.5%). SHRM is present in about 77% of eyes with neovascular age-related macular degeneration (AMD).

Different anti-VEGF (vascular endothelial growth factor) drugs have been used for the treatment of type 2 and mixed 1 and 2 types of MNV. Following treatment, a reduction in SHRM has been observed, although results between studies vary between 34% and 56%. Improvements in best-corrected visual acuity are also achieved in eyes with type 2 MNV with anti-VEGF therapy.

Eligibility criteria

Qualifiers

People aged 50 and over.

Diagnosed with bilateral or unilateral AMD.

Eyes with SHRM and type 2 or mixed (type 1 and 2) neovascular membrane.

Näive eyes treated with Faricimab following SmPC (summary of product characteristic).

Disqualifiers

Eyes with type 1, aneurysmal type 1 and type 3 MNV.

Eyes with type 2 MNV and other macular diseases (myopia, posterior uveitis, systemic diseases, such as pseudoxanthoma elasticum).

Eyes with ocular media opacity.

Patients with other retinal diseases, such as central serous chorioretinopathy, diabetic retinopathy, retinal vascular occlusion, uveitis, myopic maculopathy or any other retinal disease that could compromise the best-corrected visual acuity and interfere with retinal parameters.

Trial design

Treatments tested in this trial

  • Vabysmo 6 MG in 0.05 ML Injection

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators