Comparing Efficacy of 8-Week and 12-Week Faricimab Initial Follow-Up Treatment Intervals Following 4 Loading Doses - Prospective Randomised Study

Status: Recruiting
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This is a prospective, randomized study that compares 8-week and 12-week follow-up intervals after the 4 monthly injections in the loading phase. Patients with active CNV confirmed on optical coherence tomography (OCT) and OCT angiography (OCTA) will be randomized into two groups and followed for 44 to 56 weeks. Patients in the first group will receive 4 injections of faricimab every 4 weeks, with the next visit and injection after 8 weeks, followed by a treat-and-extend regimen with a minimal interval of 8 weeks and a maximal interval of 16 weeks. Patients in the second group will also receive 4 loading doses with the next visit after an extended 12-week interval. Following treatment, patients in this group will be on the same treat-and-extend regimen as patients in the first group. The study will compare best corrected visual acuity (BCVA), central retinal thickness (CRT) on OCT, and the number of injections between both groups.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Active treatment naïve CNV (Type 1, Type 2, or Type 3) in the macula including fovea diagnosed on OCT and OCTA

• BCVA between 70 to 35 ETDRS letters (approx. 20/40 to 20/200 Snellen equivalent) decrease in BCVA caused primarily by the CNV in the study eye

• presence of intra- or subretinal fluid or PED in the central 1 mm of the macula on the OCT

• patient capable of signing the informed consent

Contact Information
Primary
Martin Pencak, MD
martin.pencak@fnkv.cz
+420 267 16 3637
Backup
Patrik Rajs, MD
patrik.rajs@fnkv.cz
+420 267 16 3637
Time Frame
Start Date: 2023-03-31
Estimated Completion Date: 2026-04
Participants
Target number of participants: 100
Treatments
Experimental: Group 1, 8-Week
Patients in the first group will receive 4 injections of faricimab every 4 weeks, with the next visit and injection after 8 weeks (Week 20 Visit), followed by a treat-and-extend regimen with a minimal interval of 8 weeks and a maximal interval of 16 weeks.
Experimental: Group 2, 12-Week
Patients in the second group will also receive 4 loading doses with the next visit after an extended 12-week interval (Week 24 Visit). Following treatment, patients in this group will be on the same treat-and-extend regimen as patients in the first group.
Sponsors
Leads: Faculty Hospital Kralovske Vinohrady

This content was sourced from clinicaltrials.gov