Market PreparationLaunch preparations are already complete, with payer interactions covering more than 85% of U.S. lives, and Arrowhead’s One-REDEMPLO pricing strategy anchoring long-term value in high-risk sHTG.
Regulatory ApprovalsThe FDA approved REDEMPLO (plozasiran) as the first siRNA therapy for familial chylomicronemia syndrome (FCS), marking a transformative entry into the APOC3 landscape with a best-in-class profile.
Strategic PartnershipsArrowhead announced a global license and collaboration agreement with NVS for ARO-SNCA and additional collaboration targets, which brings in additional capital and potential future revenue.