Related Experiment Video
Updated: Aug 6, 2026

Characterization of Vascular Morphology of Neovascular Age-Related Macular Degeneration by Indocyanine Green Angiography
Published on: August 11, 2023
Faricimab for High-Need Aflibercept 2 mg-Treated Neovascular Age-Related Macular Degeneration: A Randomized
Monja Michelitsch1, Regina Riedl2, Sanja Strini1
1Department of Ophthalmology, Medical University of Graz, Graz, Austria.
Purpose:
To assess whether "high-need" treated neovascular age-related macular degeneration (nAMD) eyes, requiring aflibercept 2 mg every 3 to 5 weeks, can be extended in their treatment interval when switched to faricimab.
Design:
A monocenter, randomized, double-masked, 2-part clinical trial (NCT05941715) with a comparator-controlled period of 32 weeks, followed by a single-arm open-label treatment period of up to 56 weeks.
Participants:
Patients with nAMD treated with aflibercept 2 mg, exhibiting retinal fluid at ≤6-week treatment intervals within a treat-and-extend (T&E) regimen, were recruited at the Medical University of Graz between July 2023 and January 2024.
Methods:
Seventy participants were randomized 1:1 to receive either faricimab T&E (comparator group, n = 35) or aflibercept 2 mg (control group, n = 35) T&E until week 32. From week 32 until week 56, both groups received faricimab T&E. Treatment intervals, change in central subfield thickness (CST), and visual acuity were assessed.
Main Outcome Measure:
The proportion of eyes with at least 1 successful extension, meaning no retinal fluid at a 6-week treatment interval, up to ≤32 weeks.
Results:
In the comparator-controlled period, 12 (34.3%) faricimab-treated eyes versus 3 (8.6%) aflibercept 2 mg-treated eyes were successfully extended by ≥2 weeks (P = 0.018). At 56 weeks, after both groups were treated with faricimab, 14 (40%) and 13 (37.1%) eyes, respectively, were successfully extended. Least square mean difference (LSMD) CST significantly reduced in the comparator group from baseline to 32 weeks by -36.4 μm (95% confidence interval [CI], -56.0 to -16.8; P < 0.001) and to 56 weeks by -43.7 μm (95% CI, -64.3 to -23.2; P < 0.001). In the control group, LSMD CST remained stable from baseline to 32 weeks with +2.7 μm (95% CI, -17.5 to 22.8; P = 0.793); when switched to faricimab, it significantly reduced at 56 weeks by -47.0 μm (95% CI, -67.7 to -26.4; P < 0.001). Visual acuity remained stable for both groups.
Conclusions:
In this first randomized clinical trial comparing faricimab with aflibercept 2 mg in "high-need" aflibercept 2 mg-treated nAMD eyes, switching to faricimab was effective in extending treatment intervals in more than a third of eyes.
Financial Disclosure(S):
Proprietary or commercial disclosure may be found in the Footnotes and Disclosures at the end of this article.
Related Concept Videos
Open Angle Glaucoma: Treatment
Drugs such as carbonic anhydrase inhibitors, α2- and...
Angle Closure Glaucoma: Treatment
Diabetic Retinopathy
Drugs for Treatment of Crohn's Disease in IBD Using Immunomodulatory Agents
Drugs for Treatment of Crohn's Disease in IBD Using Biologic Agents: Anti-TNF
Treatment for Pulmonary Arterial Hypertension: Prostacyclin Receptor Agonists
These agonists bind to the IPR receptor situated on the plasma membrane of the pulmonary artery smooth muscle cells. This binding triggers a cascade of reactions known as the GS-AC-cAMP-PKA pathway. This pathway results in the relaxation of smooth muscle...