Arrowhead says EU grants marketing authorization for REDEMPLO in adult FCS patients
Arrowhead Pharmaceuticals, Inc.
Arrowhead Pharmaceuticals, Inc. ARWR | 0.00 |
- Arrowhead Pharmaceuticals won European Commission marketing authorization for REDEMPLO (plozasiran) to cut triglycerides in adults with familial chylomicronemia syndrome.
- Approval covers patients diagnosed by clinical criteria or genetic testing, widening eligibility versus therapies requiring genetic confirmation.
- Phase 3 PALISADE showed median triglyceride reduction of 80% with 25 mg versus 17% with placebo.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Arrowhead Pharmaceuticals Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20260622025442) on June 22, 2026, and is solely responsible for the information contained therein.
