Eplontersen is currently in development for the treatment of hereditary transthyretin-mediated amyloid polyneuropathy (hATTR-PN). Hereditary transthyretin amyloidosis with polyneuropathy (formerly known as Familial Amyloid Polyneuropathy) is a rare disease caused by mutations in the gene that codes for transthyretin and is characterised by a multisystem extracellular deposition of amyloid (abnormal fibrous, extracellular, proteinaceous deposits found in organs and tissues), leading to the dysfunction of different organs and tissues. Therefore, hATTR-PN is a debilitating disease that can cause life-threatening situations.
Eplontersen for hereditary transthyretin-mediated amyloid polyneuropathy
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Eplontersen is currently in development for the treatment of hereditary transthyretin-mediated amyloid polyneuropathy (hATTR-PN). Hereditary transthyretin amyloidosis with polyneuropathy (formerly known as Familial Amyloid Polyneuropathy) is a rare disease caused by mutations in the gene that codes for transthyretin and is characterised by a multisystem extracellular deposition of amyloid (abnormal fibrous, extracellular, proteinaceous deposits found in organs and tissues), leading to the dysfunction of different organs and tissues.
Interventions:
Eplontersen (ION-682884;AKCEA TTR-LRx)
Indications:
Transthyretin-mediated amyloid polyneuropathy
Therapeutic Areas:
Genetic Disorders
Year:
2023