Learn languages naturally with fresh, real content!

Popular Topics
Explore By Region
FDA approves first siRNA drug for rare genetic disorder, reducing triglycerides and pancreatitis risk.
The FDA has approved plozasiran, sold as REDEMPLO, the first siRNA therapy for familial chylomicronemia syndrome (FCS), a rare genetic disorder.
The drug, developed by Arrowhead Pharmaceuticals, reduces triglycerides by targeting apoC-III and is administered as a subcutaneous injection every three months.
Approved based on phase 3 PALISADE trial results, it showed an 80% median triglyceride reduction and 83% lower pancreatitis risk versus placebo, with a favorable safety profile.
The drug is expected to be available in the U.S. before year-end.
8 Articles
La FDA aprueba el primer fármaco siRNA para un trastorno genético raro, reduciendo los triglicéridos y el riesgo de pancreatitis.