| Literature DB >> 31414621 |
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
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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