drugset / Trial / NCT05536973

Safety and Efficacy of ADVM-022 in Treatment-Experienced Patients With Neovascular Age-related Macular Degeneration [LUNA]

NCT05536973

Phase 2 Active not recruiting 69 enrolled Adverum Biotechnologies, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

Neovascular or wet age-related macular degeneration (nAMD) is a degenerative ocular disease associated with the infiltration of abnormal blood vessels in the retina from the underlying choroid layer and is a leading cause of blindness in patients over 65 years of age. The abnormal angiogenic process in nAMD is stimulated and modulated by vascular endothelial growth factor (VEGF). Treatment of nAMD requires frequent intravitreal (IVT) injections of VEGF inhibitors (anti-VEGF) administered every 4-16 weeks. ADVM-022 (AAV.7m8-aflibercept) is a gene therapy product being developed for the treatment of nAMD and offers the potential for sustained intraocular expression of aflibercept following a single IVT injection. ADVM-022 is designed to reduce the current treatment burden which often results in undertreatment and vision loss in patients with nAMD receiving anti-VEGF therapy in clinical practice.

Timeline

Start
2022-08-23
Primary completion
2024-08-26
Completion
2028-08

Drugs

EvaluationDrugModalityDoseRoute
Subject ADVM-022 Gene therapy (AAV / viral vector) 6e+10 vg Intravitreal
Subject ADVM-022 Gene therapy (AAV / viral vector) 2e+11 vg Intravitreal