Literature DB >> 31414621

Ataluren use in patients with nonsense mutation Duchenne muscular dystrophy: patient demographics and characteristics from the STRIDE Registry.

Francesco Muntoni1,2, Isabelle Desguerre3, Michela Guglieri4, Andrés Nascimento Osorio5, Janbernd Kirschner6, Már Tulinius7, Filippo Buccella8, Gary Elfring9, Christian Werner10, Traci Schilling9, Panayiota Trifillis9, Olivia Zhang9, Abdallah Delage11, Claudio L Santos9, Eugenio Mercuri12,13.   

Abstract

Aim: Strategic Targeting of Registries and International Database of Excellence (STRIDE) is an ongoing, multicenter registry providing real-world evidence regarding ataluren use in patients with nonsense mutation Duchenne muscular dystrophy (DMD) in clinical practice (NCT02369731). Here, we describe the initial demographic characteristics of the registry population. Patients & methods: Patients will be followed up from enrollment for ≥5 years or until study withdrawal. Results & conclusion: As of 9 July 2018, 213 DMD boys were enrolled from 11 countries. Mean (standard deviation) ages at first symptoms and at study treatment start were 2.7 (1.7) years and 9.8 (3.7) years, respectively. Corticosteroids were used by 190 patients (89.2%) before data cut-off. Mean (standard deviation) ataluren exposure was 639.0 (362.9) days. Six patients withdrew. STRIDE is the first drug registry for patients with DMD and represents the largest real-world registry of patients with nmDMD to date.

Entities:  

Keywords:  STRIDE Registry; ataluren; demographics; dystrophin; nonsense mutation Duchenne muscular dystrophy

Mesh:

Substances:

Year:  2019        PMID: 31414621     DOI: 10.2217/cer-2019-0086

Source DB:  PubMed          Journal:  J Comp Eff Res        ISSN: 2042-6305            Impact factor:   1.744


  6 in total

1.  A Chinese boy with familial Duchenne muscular dystrophy owing to a novel hemizygous nonsense mutation (c.6283C>T) in an exon of the DMD gene.

Authors:  Xing-Chuan Li; Song Wang; Jia-Rui Zhu; Yu-Shan Yin; Ni Zhang
Journal:  SAGE Open Med Case Rep       Date:  2022-05-21

Review 2.  Therapeutic opportunities and clinical outcome measures in Duchenne muscular dystrophy.

Authors:  Giulia Ricci; Luca Bello; Francesca Torri; Erika Schirinzi; Elena Pegoraro; Gabriele Siciliano
Journal:  Neurol Sci       Date:  2022-05-24       Impact factor: 3.830

3.  Read-through approach for stop mutations in Duchenne muscular dystrophy. An update.

Authors:  Luisa Politano
Journal:  Acta Myol       Date:  2021-03-31

4.  Safety and effectiveness of ataluren: comparison of results from the STRIDE Registry and CINRG DMD Natural History Study.

Authors:  Eugenio Mercuri; Francesco Muntoni; Andrés Nascimento Osorio; Már Tulinius; Filippo Buccella; Lauren P Morgenroth; Heather Gordish-Dressman; Joel Jiang; Panayiota Trifillis; Jin Zhu; Allan Kristensen; Claudio L Santos; Erik K Henricson; Craig M McDonald; Isabelle Desguerre
Journal:  J Comp Eff Res       Date:  2020-01-30       Impact factor: 1.744

5.  Ataluren delays loss of ambulation and respiratory decline in nonsense mutation Duchenne muscular dystrophy patients.

Authors:  Craig M McDonald; Francesco Muntoni; Vinay Penematsa; Joel Jiang; Allan Kristensen; Francesco Bibbiani; Elizabeth Goodwin; Heather Gordish-Dressman; Lauren Morgenroth; Christian Werner; James Li; Richard Able; Panayiota Trifillis; Már Tulinius
Journal:  J Comp Eff Res       Date:  2021-11-18       Impact factor: 2.040

6.  Genetic Profile of the Dystrophin Gene Reveals New Mutations in Colombian Patients Affected with Muscular Dystrophinopathy.

Authors:  Paula Triana-Fonseca; Juan Fernando Parada-Márquez; Claudia T Silva-Aldana; Daniela Zambrano-Arenas; Laura Lucia Arias-Gomez; Natalia Morales-Fonseca; Esteban Medina-Méndez; Carlos M Restrepo; Daniel Felipe Silgado-Guzmán; Dora Janeth Fonseca-Mendoza
Journal:  Appl Clin Genet       Date:  2021-10-01
  6 in total

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