Identification of Molecular Signals in Vitreous Humor Associated With Suboptimal Response to VEGF Inhibition in nAMD Within a Clinical Trial Setting

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Neovascular age-related macular degeneration (nAMD), also called wet AMD, can cause serious vision loss. While anti-VEGF (anti Vascular Endothelial Growth Factor) treatments such as ranibizumab help many patients, about 20 40% have a suboptimal response. In this study, the investigators want to identify other factors (beyond VEGF) that might be driving the disease in these non-responding patients. By looking at samples from inside the eye (vitreous humor) and comparing good responders to suboptimal responders, the investigators hope to find potential new treatment approaches or biomarkers for nAMD.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: f
View:

• Patients aged ≥ 50 years old at the time of informed consent

• Willing and able to provide informed consent

• Willingness and ability to comply with all scheduled visits and study procedures

• Female subjects must be of non-childbearing potential or show a negative pregnancy test at screening and must agree to use appropriate methods of contraception during the study and for one month after the last dose.

• Confirmed diagnosis of symptomatic nAMD based on optical coherence tomography (OCT), fluorescein fundus angiography (FFA), and indocyanine green angiography (ICG-A)

• nAMD characteristics:

‣ Subfoveal CNV/PCV

⁃ Juxtafoveal/extrafoveal CNV/PCV with a subfoveal component related to the exudative activity.

• Treatment naïve- NO previous treatment with intravitreal anti-VEGF agents, regardless of the indication, NO previous thermal laser in the macular region, or verteporfin photodynamic therapy (vPDT), regardless of indication

• BCVA of 24-78 letters as measured by an Early Treatment Diabetic Retinopathy Study (ETDRS) chart (Snellen equivalent 20/32-20/320)

Locations
Other Locations
Singapore
Singapore National Eye Centre/Singapore Eye Research Institute
RECRUITING
Singapore
Contact Information
Primary
Gemmy Cheung
gemmy.cheung.c.m@singhealth.com.sg
63227460
Time Frame
Start Date: 2025-07-18
Estimated Completion Date: 2029-07
Participants
Target number of participants: 117
Treatments
Other: Ranibizumab
Other: Faricimab
Sponsors
Leads: Singapore National Eye Centre

This content was sourced from clinicaltrials.gov