The Canberra Study
A randomized, double-masked, 48-week, parallel-group, placebo-controlled, proof-of-concept study to investigate the efficacy and safety of RG7774 in patients with diabetes mellitus type 1 or type 2 with treatment-naïve diabetic retinopathy.
This study investigates the efficacy and safety of RG7774, an oral medication, for patients with moderately severe to severe non-proliferative diabetic retinopathy. The 48-week duration of the study allowed a comprehensive evaluation of RG7774.