Inherited Retinal Dystrophies (IRDs), such as Stargardt’s disease (STGD), lack effective treatments. STGD is characterised by mutations in the ABCA4 gene, leading to lipofuscin accumulation, oxidative stress (OS) and Ca2+ dysregulation, ultimately causing photoreceptor death. This study evaluates the therapeutic potential of MP-004, a small molecule designed to modulate OS and maintain Ca2+ homeostasis through […]