Clinical trial Recruiting at 1 site Phase 4 Interventional Ages 50 and up

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

PhasePhase 4
Study typeInterventional
Ages50 Years and up
SexAll
Enrollment40 (estimated)
SponsorHospital Authority, Hong Kong
Government
Drugs / interventionsfaricimab
Locations1 site (Hong Kong)
StatusRecruiting
StartedAugust 21, 2025
Main results expectedOctober 1, 2026
Study endsFebruary 1, 2027
Registry record updatedOctober 1, 2025
Trial IDNCT06742307 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.