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Clinical Trials in the EU / 2025-522701-38-00
Authorised, recruiting Phase IV

EFFICACY OF FARICIMAB IN PATIENTS WITH SUBRETINAL HYPERREFLECTIVE MATERIAL ASSOCIATED WITH TYPE 2 OR MIXED NEOVASCULAR MEMBRANES ASSESSED BY MULTIMODAL IMAGING

2025-522701-38-00 · tracked via the Priya Life Science EU tracker
Sponsor
Asociacion Instituto De Investigacion Sanitaria Biobizkaia
Sponsor type
Laboratory/Research/Testing facility
Therapeutic area
Eye Diseases
Decision date
15/12/2025
Enrollment target
100
Sites
Spain

Condition studied

SUBRETINAL HYPERREFLECTIVE MATERIAL

Investigational medicinal product(s)

Vabysmo 120 mg/mL solution for injection in pre-filled syringe

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Resolution of SHRM at week 16

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-522701-38-00 on CTIS ↗ ← All trials in the EU