Arrowhead Pharmaceuticals Reports Fiscal 2026 Third Quarter Results
A Priority Review designation would accelerate FDA action timelines to 6 months. Arrowhead also announced an exclusive worldwide license agreement with Madrigal Pharmaceuticals for ARO-PNPLA3, with potential milestone payments up to $975 million. The company acquired an FDA priority review voucher it plans to use with its upcoming plozasiran sNDA submission before end of 2026, aiming to expand the approved indication to severe hypertriglyceridemia.