“This notification from the FDA allows us to begin a multiple-dose Phase 2b study of ARC-520, and we are working diligently to get treatment sites up and running. Our goal is to gain site IRB approvals and perform site initiation visits to begin recruiting and enrolling patients for this study in about a month, ” said Bruce Given, M.D., chief operating officer and head of R&D for Arrowhead. “We are also working with various regulatory agencies outside of the United States to initiate additional Phase 2b studies.”“We are also working with various regulatory agencies outside of the United States to initiate additional Phase 2b studies.”
Labels: ARC-520 Phase 2b Study Update, Arrowhead