Literature DB >> 32026421

Golodirsen: First Approval.

Young-A Heo1.   

Abstract

Golodirsen (Vyondys 53™), an antisense oligonucleotide of the phophorodiamidate morpholino oligomer (PMO) subclass designed to induce exon 53 skipping, has been developed by Sarepta Therapeutics for the treatment of Duchenne muscular dystrophy (DMD). In December 2019, intravenous golodirsen received its first global approval in the USA for the treatment of DMD in patients with a confirmed mutation of the DMD gene that is amenable to exon 53 skipping, based on positive results from a phase I/II clinical trial. Golodirsen is in phase III clinical development for the treatment of DMD worldwide. This article summarizes the milestones in the development of golodirsen leading to this first approval for DMD.

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Year:  2020        PMID: 32026421     DOI: 10.1007/s40265-020-01267-2

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


  53 in total

1.  Design of Bifunctional Antisense Oligonucleotides for Exon Inclusion.

Authors:  Haiyan Zhou
Journal:  Methods Mol Biol       Date:  2022

2.  Genetic correction strategies for Duchenne Muscular Dystrophy and their impact on the heart.

Authors:  Jamie R Johnston; Elizabeth M McNally
Journal:  Prog Pediatr Cardiol       Date:  2021-11-02

3.  "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

Review 4.  Pharmacology and toxicology of eteplirsen and SRP-5051 for DMD exon 51 skipping: an update.

Authors:  Omar Sheikh; Toshifumi Yokota
Journal:  Arch Toxicol       Date:  2021-11-19       Impact factor: 5.153

Review 5.  Restoring Protein Expression in Neuromuscular Conditions: A Review Assessing the Current State of Exon Skipping/Inclusion and Gene Therapies for Duchenne Muscular Dystrophy and Spinal Muscular Atrophy.

Authors:  Omar Sheikh; Toshifumi Yokota
Journal:  BioDrugs       Date:  2021-06-07       Impact factor: 5.807

6.  RNA Drugs and RNA Targets for Small Molecules: Principles, Progress, and Challenges.

Authors:  Ai-Ming Yu; Young Hee Choi; Mei-Juan Tu
Journal:  Pharmacol Rev       Date:  2020-10       Impact factor: 25.468

Review 7.  Current Status of Antisense Oligonucleotide-Based Therapy in Neuromuscular Disorders.

Authors:  Flavien Bizot; Adeline Vulin; Aurélie Goyenvalle
Journal:  Drugs       Date:  2020-09       Impact factor: 9.546

Review 8.  CRISPR technologies for the treatment of Duchenne muscular dystrophy.

Authors:  Eunyoung Choi; Taeyoung Koo
Journal:  Mol Ther       Date:  2021-04-03       Impact factor: 11.454

9.  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

10.  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

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