Arrowhead Pharmaceuticals Sues Ionis Pharmaceuticals Over Patent Dispute
PorAinvest
viernes, 12 de septiembre de 2025, 10:27 am ET1 min de lectura
ARWR--
Arrowhead's lawsuit does not seek monetary compensation but rather a declaratory decree establishing that the patent is invalid and not infringed by the manufacture, use, sale, or offer for sale of plozasiran. The company's President and CEO, Christopher Anzalone, stated that the lawsuit is aimed at protecting the interests of patients with familial chylomicronemia syndrome (FCS), a severe and rare disease characterized by extremely high triglyceride levels [2].
Plozasiran is a first-in-class investigational RNA interference (RNAi) therapeutic designed to reduce the production of apolipoprotein C-III (APOC3), a key regulator of triglyceride metabolism. The drug has been granted Breakthrough Therapy Designation, Orphan Drug Designation, and Fast Track Designation by the U.S. Food and Drug Administration (FDA) for the treatment of FCS [2].
Ionis Pharmaceuticals has previously claimed that its patent No. 9,593,333 would be infringed if plozasiran were to be marketed. However, Arrowhead maintains that its patents covering plozasiran are based entirely on work developed internally and that Ionis had no contribution to the development of the drug [1].
The lawsuit is a significant development in the ongoing competition between Arrowhead and Ionis for the treatment of FCS. If Arrowhead's candidate gains FDA approval, it will face competition from Ionis' Tryngolza, which was approved for FCS in December 2024 [1].
IONS--
Arrowhead Pharmaceuticals has sued Ionis Pharmaceuticals in a Delaware District Court over a patent dispute related to its lead candidate, plozasiran. The lawsuit seeks a declaratory judgment determining the validity of Ionis' U.S. Patent No. 11,477,579, which Ionis claims covers the same technology as Arrowhead's product. Arrowhead's lawsuit does not seek monetary compensation.
Arrowhead Pharmaceuticals has filed a lawsuit against Ionis Pharmaceuticals in the U.S. District Court for the District of Delaware. The suit seeks a declaratory judgment determining the validity of Ionis' U.S. Patent No. 11,477,579, which Ionis claims covers the same technology as Arrowhead's investigational drug plozasiran [1].Arrowhead's lawsuit does not seek monetary compensation but rather a declaratory decree establishing that the patent is invalid and not infringed by the manufacture, use, sale, or offer for sale of plozasiran. The company's President and CEO, Christopher Anzalone, stated that the lawsuit is aimed at protecting the interests of patients with familial chylomicronemia syndrome (FCS), a severe and rare disease characterized by extremely high triglyceride levels [2].
Plozasiran is a first-in-class investigational RNA interference (RNAi) therapeutic designed to reduce the production of apolipoprotein C-III (APOC3), a key regulator of triglyceride metabolism. The drug has been granted Breakthrough Therapy Designation, Orphan Drug Designation, and Fast Track Designation by the U.S. Food and Drug Administration (FDA) for the treatment of FCS [2].
Ionis Pharmaceuticals has previously claimed that its patent No. 9,593,333 would be infringed if plozasiran were to be marketed. However, Arrowhead maintains that its patents covering plozasiran are based entirely on work developed internally and that Ionis had no contribution to the development of the drug [1].
The lawsuit is a significant development in the ongoing competition between Arrowhead and Ionis for the treatment of FCS. If Arrowhead's candidate gains FDA approval, it will face competition from Ionis' Tryngolza, which was approved for FCS in December 2024 [1].

Divulgación editorial y transparencia de la IA: Ainvest News utiliza tecnología avanzada de Modelos de Lenguaje Largo (LLM) para sintetizar y analizar datos de mercado en tiempo real. Para garantizar los más altos estándares de integridad, cada artículo se somete a un riguroso proceso de verificación con participación humana.
Mientras la IA asiste en el procesamiento de datos y la redacción inicial, un miembro editorial profesional de Ainvest revisa, verifica y aprueba de forma independiente todo el contenido para garantizar su precisión y cumplimiento con los estándares editoriales de Ainvest Fintech Inc. Esta supervisión humana está diseñada para mitigar las alucinaciones de la IA y garantizar el contexto financiero.
Advertencia sobre inversiones: Este contenido se proporciona únicamente con fines informativos y no constituye asesoramiento profesional de inversión, legal o financiero. Los mercados conllevan riesgos inherentes. Se recomienda a los usuarios que realicen una investigación independiente o consulten a un asesor financiero certificado antes de tomar cualquier decisión. Ainvest Fintech Inc. se exime de toda responsabilidad por las acciones tomadas con base en esta información. ¿Encontró un error? Reportar un problema

Comentarios
Aún no hay comentarios