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Neovascular Age Related Macular Degeneration

nAMD is an advanced form of age-related macular degeneration, a progressive retinal disease, characterised by choroidal neovascularization (or ocular angiogenesis) and vascular leakage into the retina, resulting in rapid and severe loss of central vision. Roche is committed to the development of new treatments and treatment strategies that optimize vision outcomes to improve the lives of patients and their caregivers.

What's new

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Apr 7 / Roche and Genentech
Key Clinical Outcomes with Faricimab▼ in Treatment-naïve Patients with Neovascular Age-Related Macular Degeneration (nAMD): Results from the TENAYA/LUCERNE Trials and Real-World FARETINA/FARWIDE Studies
This presentation described results From the TENAYA/LUCERNE Trials and Real-World FARETINA/FARWIDE Studies. Anatomic biomarkers of disease, including CST, retinal fluid and PED demonstrated greater improvement with faricimab▼ compared with aflibercept during head-to-head dosing in TENAYA/LUCERNE. Real-world results from FARETINA and FARWIDE were consistent with clinical trial results, showing vision gains, anatomical improvement and extended durability.

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Apr 7 / Roche and Genentech
Early Fluid Resolution is Associated with Short- and Long-Term Extended Durability in Patients with Neovascular Age-Related Macular Degeneration Treated with Faricimab▼: A post hoc analysis of the TENAYA/LUCERNE Trials
This presentation summarized a post hoc analysis of the impact of maintaining extended faricimab▼ treatment intervals on visual and anatomical outcomes in the TENAYA and LUCERNE trials. Results show that faricimab▼ demonstrated greater and faster resolution of fluid vs aflibercept. The results emphasize the importance of early drying as it relates to extended durability for the patient.

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Apr 5 / Roche and Genentech
Response of Large or Serous Pigment Epithelial Detachment to Faricimab▼ versus Aflibercept in Patients with Neovascular Age-related Macular Degeneration: A Subgroup Analysis from TENAYA and LUCERNE
This subgroup analysis demonstrates that faricimab▼ results in greater and faster reductions Pigment Epithelial Detachment (PED) thickness compared with aflibercept in patients with nAMD from the TENAYA and LUCERNE trials.

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Apr 5 / Roche and Genentech
Long-Term Efficacy and Safety of the Port Delivery Platform with Ranibizumab (PDS) in Patients With Neovascular Age-Related Macular Degeneration (nAMD): Ladder to Portal 5-Year Subgroup Analysis
The presentation described ongoing phase 3 Portal extension trial, evaluating long-term safety and tolerability of PDS with 100 mg/mL ranibizumab in patients who completed the Ladder or Archway trials, or who will have participated in Velodrome. The PDS 100 mg/mL demonstrated stable BCVA and CPT from Ladder baseline to Portal data cut-off (60 months from implant insertion procedure). The efficacy and safety profile of PDS 100 mg/mL was maintained over 5 years of follow-up.

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Apr 3 / Roche and Genentech
Treatment Patterns Among Medicare Advantage Plan Beneficiaries Diagnosed with Neovascular Age-Related Macular Degeneration Who Initiated Faricimab▼ Treatment
This presentation reports the real-world baseline characteristics, treatment patterns, and HCRU in patients initiating faricimab▼ for neovascular age-related macular degeneration (2022–2023). Treatment patterns and HCRU were evaluated for the 12 months before and after faricimab▼ initiation using claims analysis; results were stratified according to history of prior anti-VEGF therapy (VEGF-experienced vs VEGF-naive).

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Feb 16 / Roche and Genentech
Implementation of Optimized Surgical Steps for the PDS and the Incidence of Endophthalmitis and Associated Patient Outcomes
This presentation decribes results from a retrospective analysis which examined the impact of surgical improvements on endophthalmitis incidence and patient outcomes over time in patients receiving the Port Delivery Platform with ranibizumab (PDS) in the PDS clinical development program from 2016 to 2024. A trend for improvement in endophthalmitis incidence and patient outcomes was observed after June 2020. Key updates, increased awareness, better monitoring and management in the PDS clinical trial program have all contributed to this positive trend.

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