Clearside Biomedical Shares Key CLS-AX Trial Insights at Angiogenesis 2025
Clearside’s ODYSSEY Phase 2b results shape the future of CLS-AX for wet AMD treatment.

.webp&w=1920&q=75&dpl=dpl_DvHKTkTrxtw9jHK6MpkEndZCmmr3)
Clearside Biomedical recently presented critical findings from its ODYSSEY Phase 2b clinical trial at the Angiogenesis 2025 conference. The study evaluated CLS-AX, a targeted therapy for wet age-related macular degeneration (wet AMD), using Clearside’s innovative suprachoroidal injection technology. Dr. Roger Goldberg highlighted two key subgroup analyses that informed the design of the upcoming Phase 3 trial. The first analysis suggested that treatment-naïve patients showed promising stability in vision and retinal thickness, with 67% avoiding rescue treatment for six months. The second analysis recommended excluding participants with non-disease-related vision fluctuations, ensuring more reliable clinical outcomes.
Dr. Victor Chong, Clearside’s Chief Medical Officer, emphasized CLS-AX’s potential to provide long-lasting benefits while maintaining visual acuity. The findings indicate that refining patient selection could lead to more precise, real-world-applicable results in the Phase 3 trials. With CLS-AX’s highly selective mechanism and innovative delivery method, Clearside aims to set a new standard for durable and effective wet AMD treatment.

My international experience as a researcher in Taiwan for three years has equipped me with a global perspective, enabling me to create content that resonates with an international audience.
Plus dans Pharma News
Tous les articles →
Medicus Pharma soumet à la FDA le protocole de Phase 2b/3 pour Teverelix

Fresenius Kabi reçoit une lettre d’avertissement de la FDA après des défaillances d’enquête sur le traitement aseptique dans l’établissement de Melrose Park

Discussion