The Isis 696844-CS5 Study
A phase 2, randomized, placebo-controlled, double-masked study to assess safety and efficacy of multiple doses of Ionis- FB0LRX, an antisense inhibitor of complement factor B, in patients with Geographic Atrophy secondary to Age-Related Macular Degeneration.
The study’s primary purpose was to assess both the safety and efficacy of multiple doses of Ionis-FB0LRX, an antisense inhibitor specifically targeting complement factor B. Patients who were diagnosed with Geographic Atrophy were enrolled in the study. The Ionis-FB0LRX is administered subcutaneously. This study is 57 weeks long.