Quarterly faricimab maintenance for neovascular age-related macular degeneration
Official title: Faricimab Fixed Quarterly Maintenance for Neovascular Age Related Macular Degeneration: A Prospective Case Series
Run by Hospital Authority, Hong Kong · NCT06742307 · Data updated 2026-11-12
This test will see if faricimab injections every 12–16 weeks can keep neovascular age-related macular degeneration stable after 2–4 initial loading doses.
Quick facts
| Phase | Phase 4 |
|---|---|
| Study type | Interventional |
| Ages | 50 Years and up |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | Hospital Authority, Hong Kong Government |
| Drugs / interventions | faricimab |
| Locations | 1 site (Hong Kong) |
| Status | Recruiting |
| Started | August 21, 2025 |
| Main results expected | October 1, 2026 |
| Study ends | February 1, 2027 |
| Registry record updated | October 1, 2025 |
| Trial ID | NCT06742307 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are people over 50 with active subfoveal neovascular AMD (types 1–3) who achieve inactivity after 2–4 loading faricimab doses.
✕Probably not a fit
Patients who had anti-VEGF treatment in the prior six months, have other macular diseases, or recent ocular surgery are unlikely to qualify and may not benefit from this planned quarterly regimen.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This phase 4, single-centre program gives patients 2–4 initial faricimab loading injections and then attempts a planned quarterly maintenance schedule (every 12–16 weeks) for those who achieve disease inactivity. It enrolls patients over 50 with active subfoveal macular neovascularisation, including both treatment-naïve and recurrent cases, while excluding eyes with recent anti-VEGF, other macular diseases, or recent ocular surgery. The main outcome is stability without recurrence of neovascular activity on the quarterly regimen at a tertiary eye centre in Hong Kong. The work is positioned as a real-world evaluation of a lower-frequency dosing option to reduce treatment burden compared with PRN or treat-and-extend approaches.
Why it matters
Potential benefit: If successful, this approach could reduce injection frequency and clinic visits while maintaining retinal stability and vision.
How similar studies have gone: Phase 3 trials (TENAYA and LUCERNE) showed faricimab can be effective with individualized intervals up to 16 weeks compared with aflibercept, supporting this dosing concept.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: Subjects aged over 50 years, neovascular AMD with foveal involvement, both treatment-naïve and recurrent cases. There were no specific criteria for initial best-corrected visual acuity (BCVA). Only active subfoveal MNV are included, including types 1, 2, and 3. Exclusion Criteria: * eyes that received any anti-VEGF therapy in the prior six months, * eyes with other disease entities (e.g., diabetic macula oedema, retinal vein occlusions, central serous chorioretinopathy, myopicmacular neovascularisation), * concurrent macula laser (except photodynamic therapy) and ocular surgery (e.g., cataract surgery or vitrectomy) in the prior six months and the study period.
Where it's running
-
Department of Ophthalmology, United Chrisitian Hospital
Hong Kong, Hong Kong Recruiting
Study contacts
- Study coordinator: Daniel Ho Tak Wong, FRCOphth (UK)
- Email: WHT454@ha.org.hk
- Phone: +852 3949 3411
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Faricimab for CNV in Presumed Ocular Histoplasmosis Syndrome
This study tests whether Faricimab can safely and effectively treat choroidal neovascularization linked to presumed ocular histoplasmosis in adults over a 52-week period.
-
Early imaging changes with faricimab versus biosimilar ranibizumab for diabetic retinal disease
This trial will see if faricimab or a biosimilar ranibizumab causes different early OCT and OCTA imaging changes in adults with diabetic retinopathy or diabetic macular edema who need anti-VEGF injections.
-
Personalized treat-and-extend faricimab regimen for treatment-naive polypoidal choroidal vasculopathy
This tests whether a personalized treat-and-extend dosing schedule of faricimab (Vabysmo) helps people with newly diagnosed polypoidal choroidal vasculopathy keep or improve their vision.
-
RO7823653 injections, alone or with faricimab, for diabetic macular edema
This research tests injections of RO7823653, given alone or with faricimab, in people with diabetic macular edema to see if the medication is safe and how the eye handles it.
-
Faricimab for subretinal hyper-reflective material in AMD
This study tests whether Faricimab (Vabysmo) can help reduce subretinal hyper-reflective material in adults with age-related macular degeneration.
-
See If Faricimab Helps Neovascular Age-related Macular Degeneration
This study tests whether Faricimab injections every month for 4 months can help adults aged 50 and older with active neovascular AMD in at least one eye.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.