Now that a treatment for geographic atrophy (GA) is entering the US market, retina specialists will need to be familiar with the safety and efficacy data of the pivotal trials evaluating this therapy. Drs. Kaiser, Kuppermann, and Loewenstein examine the data for the first US FDA-approved treatment for GA as well as other complement inhibitors in the pipeline. The faculty also discuss risk factors that drive this disease, imaging modalities that are best suited for GA evaluation, and the type of lesion patterns that place patients at high risk for progression.
This program was recorded at the Congress on Controversies in Ophthalmology (COPHy).
This activity is supported by an unrestricted educational grant from Iveric Bio.
































