Starting with nAMD, the stats show we are not administering sufficient injections during the first year, with seven yielding the best VA result, Prof Guymer said, adding undertreatment is causing vision loss. Even if we succeed in preserving VA in the short-term, real-life data show a drop off over time, which might be less significant with a longer lasting anti-VEGF agent. Neither do we have anything to address the formation of fibrosis or atrophy, Prof Guymer added.
Enter faricimab (Vabysmo), approved by Australia’s Therapeutic Goods Administration in August and now awaiting inclusion in the Pharmaceutical Benefits Scheme. In addition to blocking VEGF, it targets the Ang2 signalling associated with retinal vascular destabilisation and microvascular inflammation, elevated in eyes with nAMD. Faricimab, currently in Tenaya and Lucerne phase 3 clinical trials, is promising as it potentially offers a longer-acting drug while reducing scarring and atrophy, she said. Two-year results also suggest it might be possible to allow longer intervals between treatments (from 1-2 months to 3-4 months), but this remains to be confirmed by real-life data.
A different strategy to tackle the nAMD treatment burden is an implantable, reservoir-based slow-release platform. It sits in the sclera, delivering modified ranibizumab (Lucentis) and only needs refilling every six months, said Prof Guymer. Clinical phase 3 results from US Archway study indicated this system achieved its primary endpoint, being as effective as monthly injections. While short- and long-term safety issues might limit widespread availability, Prof Guymer said it may have a place for patients requiring a high frequency of intravenous injections (IVI).
A new era
We are at the dawn of a new era, Prof Guymer said, with GA treatments targeting the complement pathway being most common and in the later stages of trials. While frequent IVI is the delivery mode, other options are being explored, including long-duration therapy and gene therapy, she said. Wrapping up an afternoon of intense learning, Prof Guymer highlighted the challenge to the profession is to confidently diagnose GA and the early signs of atrophy on OCT to enable conversations with patients about these forthcoming treatments. She also encouraged optometrists to refer GA patients for imaging and baseline diagnosis and to participate in the many active trials (see CERA’s website).