Literature DB >> 32519222

Viltolarsen: First Approval.

Sohita Dhillon1.   

Abstract

Viltolarsen (Viltepso® in Japan) is a phosphorodiamidate morpholino antisense oligonucleotide being developed by Nippon Shinyaku, in collaboration with the National Center of Neurology and Psychiatry (NCNP), for the treatment of Duchenne muscular dystrophy (DMD). Viltolarsen binds to exon 53 of the dystrophin mRNA precursor and restores the amino acid open-reading frame by skipping exon 53, resulting in the production of a shortened dystrophin protein that contains essential functional portions. In March 2020, intravenous viltolarsen received its first global approval in Japan for the treatment of DMD in patients with confirmed deletion of the dystrophin gene that is amenable to exon 53 skipping. Viltolarsen is under regulatory review in the USA and clinical trials continue in the USA, Canada and globally. This article summarizes the milestones in the development of viltolarsen leading to the first approval for DMD.

Entities:  

Mesh:

Substances:

Year:  2020        PMID: 32519222     DOI: 10.1007/s40265-020-01339-3

Source DB:  PubMed          Journal:  Drugs        ISSN: 0012-6667            Impact factor:   9.546


  34 in total

Review 1.  Antisense technology: an overview and prospectus.

Authors:  Stanley T Crooke; Brenda F Baker; Rosanne M Crooke; Xue-Hai Liang
Journal:  Nat Rev Drug Discov       Date:  2021-03-24       Impact factor: 84.694

2.  Evaluation of Exon Skipping and Dystrophin Restoration in In Vitro Models of Duchenne Muscular Dystrophy.

Authors:  Andrea López-Martínez; Patricia Soblechero-Martín; Virginia Arechavala-Gomeza
Journal:  Methods Mol Biol       Date:  2022

3.  Antisense RNA Therapeutics: A Brief Overview.

Authors:  Virginia Arechavala-Gomeza; Alejandro Garanto
Journal:  Methods Mol Biol       Date:  2022

4.  "Bind, cleave and leave": multiple turnover catalysis of RNA cleavage by bulge-loop inducing supramolecular conjugates.

Authors:  Bahareh Amirloo; Yaroslav Staroseletz; Sameen Yousaf; David J Clarke; Tom Brown; Harmesh Aojula; Marina A Zenkova; Elena V Bichenkova
Journal:  Nucleic Acids Res       Date:  2022-01-25       Impact factor: 16.971

5.  Targeting Alternative Splicing for Therapeutic Interventions.

Authors:  Jessica L Centa; Michelle L Hastings
Journal:  Methods Mol Biol       Date:  2022

6.  Low human dystrophin levels prevent cardiac electrophysiological and structural remodelling in a Duchenne mouse model.

Authors:  Gerard A Marchal; Maaike van Putten; Arie O Verkerk; Simona Casini; Kayleigh Putker; Shirley C M van Amersfoorth; Annemieke Aartsma-Rus; Elisabeth M Lodder; Carol Ann Remme
Journal:  Sci Rep       Date:  2021-05-07       Impact factor: 4.379

7.  Fully automated fast-flow synthesis of antisense phosphorodiamidate morpholino oligomers.

Authors:  Chengxi Li; Alex J Callahan; Mark D Simon; Kyle A Totaro; Alexander J Mijalis; Kruttika-Suhas Phadke; Genwei Zhang; Nina Hartrampf; Carly K Schissel; Ming Zhou; Hong Zong; Gunnar J Hanson; Andrei Loas; Nicola L B Pohl; David E Verhoeven; Bradley L Pentelute
Journal:  Nat Commun       Date:  2021-07-20       Impact factor: 14.919

Review 8.  Therapeutic Strategies for Duchenne Muscular Dystrophy: An Update.

Authors:  Chengmei Sun; Luoan Shen; Zheng Zhang; Xin Xie
Journal:  Genes (Basel)       Date:  2020-07-23       Impact factor: 4.096

9.  Targeting KIT by frameshifting mRNA transcripts as a therapeutic strategy for aggressive mast cell neoplasms.

Authors:  Douglas B Snider; Greer K Arthur; Guido H Falduto; Ana Olivera; Lauren C Ehrhardt-Humbert; Emmaline Smith; Cierra Smith; Dean D Metcalfe; Glenn Cruse
Journal:  Mol Ther       Date:  2021-08-08       Impact factor: 11.454

10.  Muscle and cardiac therapeutic strategies for Duchenne muscular dystrophy: past, present, and future.

Authors:  Agnieszka Łoboda; Józef Dulak
Journal:  Pharmacol Rep       Date:  2020-07-20       Impact factor: 3.024

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.