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A phase I study to establish the safety and tolerability of ARC1905 (Anti-C5 Aptamer) in subjects with dry age-related macular degeneration 31/12/2011

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The objectives of this study are to evaluate the safety and tolerability of ARC1905 intravitreous injections in subjects with geographic atrophy secondary to dry age-related macular degeneration(AMD). Patients were assigned in an alternating fashion to one of two dose levels of ARC1905: 0.3 or 1 mg/eye. Patients were treated with 3 initial intravitreal injections of ARC1905 at Day 0,Week 4,Week 8, and a followup visit at Week 16. They then received 2 subsequent injections at Week 24 and Week 36, with a final follow-up visit at Week 48. There was a maximum of 5 ARC1905 injections.

RESULTS: Pending analysis data. No safety concerns in this phase I intravitreal use for the first time of aptamer anti C5 for geographic atrophy.

Inyecciones intravítreasDMAE seca o atróficaDMAE exudativa o húmedaRetinografíaAutofluorescenciaMicroperimetríaAngiografía fluoresceínicaTomografía de coherencia óptica

Autor

Dr. Jordi Monés, M.D., Ph.D.
Número de Colegiado COMB: 22.838
Director
Doctor en Medicina y Cirugía
Especialista en Oftalmología
Especialista en Retina, Mácula y Vítreo

Última modificación: 29 Noviembre, 2021 - 13:07