Arrowhead Pharmaceuticals IncEU approval for REDEMPLO, first siRNA treatment for familial chylomicronemia syndrome

Arrowhead Pharmaceuticals has received marketing authorization from the European Commission for REDEMPLO, the first and only siRNA treatment for adults with familial chylomicronemia syndrome that does not require genetic confirmation of the condition. The approval is supported by Phase 3 PALISADE study data showing that 25 mg REDEMPLO reduced triglycerides by a median of 80% from baseline versus 17% for placebo, and a pooled analysis of all doses demonstrated an 83% lower incidence of acute pancreatitis compared with placebo. REDEMPLO is designed to suppress production of apolipoprotein C-III and is self-administered via subcutaneous injection once every three months. Arrowhead is now engaging with national authorities across the European Union to bring the therapy to patients as quickly as possible.
Arrowhead Pharmaceuticals IncEU approval for REDEMPLO, first siRNA treatment for familial chylomicronemia syndrome