Development of siRNA Therapeutics for the Treatment of Liver Diseases

Anja Holm, Marianne Bengtson Løvendorf, Sakari Kauppinen

Publikation: Bidrag til bog/antologi/rapport/konference proceedingBidrag til bog/antologiForskningpeer review

6 Citationer (Scopus)

Abstract

Small interfering RNA (siRNA)-based therapeutics holds the promise to treat a wide range of human diseases that are currently incurable using conventional therapies. Most siRNA therapeutic efforts to date have focused on the treatment of liver diseases due to major breakthroughs in the development of efficient strategies for delivering siRNA drugs to the liver. Indeed, the development of lipid nanoparticle-formulated and GalNAc-conjugated siRNA therapeutics has resulted in recent FDA approvals of the first siRNA-based drugs, patisiran for the treatment of hereditary transthyretin amyloidosis and givosiran for the treatment of acute hepatic porphyria, respectively. Here, we describe the current strategies for delivering siRNA drugs to the liver and summarize recent advances in clinical development of siRNA therapeutics for the treatment of liver diseases.

OriginalsprogEngelsk
TitelDesign and Delivery of SiRNA Therapeutics
RedaktørerHenrik J. Ditzel, Martina Tuttolomondo, Sakari Kauppinen
Antal sider19
Vol/bind2282
ForlagSpringer
Publikationsdato2021
Sider57-75
ISBN (Trykt)978-1-0716-1297-2, 978-1-0716-1300-9
ISBN (Elektronisk)978-1-0716-1298-9
DOI
StatusUdgivet - 2021
NavnMethods in Molecular Biology
Vol/bind2282
ISSN1064-3745

Fingeraftryk

Dyk ned i forskningsemnerne om 'Development of siRNA Therapeutics for the Treatment of Liver Diseases'. Sammen danner de et unikt fingeraftryk.

Citationsformater