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Ataluren use in patients with nonsense mutation Duchenne muscular dystrophy: patient demographics and characteristics from the STRIDE Registry.
Muntoni, Francesco; Desguerre, Isabelle; Guglieri, Michela; Osorio, Andrés Nascimento; Kirschner, Janbernd; Tulinius, Már; Buccella, Filippo; Elfring, Gary; Werner, Christian; Schilling, Traci; Trifillis, Panayiota; Zhang, Olivia; Delage, Abdallah; Santos, Claudio L; Mercuri, Eugenio.
Afiliación
  • Muntoni F; Dubowitz Neuromuscular Centre & MRC Centre for Neuromuscular Diseases, University College London, Institute of Child Health & Great Ormond Street Hospital for Children Foundation Trust, 30 Guildford Street, London WC1N 1EH, UK.
  • Desguerre I; NIHR Great Ormond Street Hospital Biomedical Research Centre, Great Ormond Street Institute of Child Health, University College London, Great Ormond Street Hospital Trust, London, UK.
  • Guglieri M; APHP Necker - Enfants Malades Hospital, Paris V Descartes University, Neuromuscular Network FILNEMUS, Paris, France.
  • Osorio AN; The John Walton Muscular Dystrophy Research Centre, Newcastle University & Newcastle Upon Tyne Hospitals, Newcastle Upon Tyne, UK.
  • Kirschner J; Hospital Sant Joan de Déu Unidad de Patología Neuromuscular, Universidad de Barcelona, CIBERER, ISCIII, Barcelona, Spain.
  • Tulinius M; Medical Center - University of Freiburg, Faculty of Medicine, Freiburg, Germany.
  • Buccella F; Department of Pediatrics, Gothenburg University, Queen Silvia Children's Hospital, Gothenburg, Sweden.
  • Elfring G; Parent Project Italy APS, Rome, Italy.
  • Werner C; PTC Therapeutics Inc., South Plainfield, NJ 07080-2449, USA.
  • Schilling T; PTC Therapeutics Germany GmbH, Frankfurt, Germany.
  • Trifillis P; PTC Therapeutics Inc., South Plainfield, NJ 07080-2449, USA.
  • Zhang O; PTC Therapeutics Inc., South Plainfield, NJ 07080-2449, USA.
  • Delage A; PTC Therapeutics Inc., South Plainfield, NJ 07080-2449, USA.
  • Santos CL; PTC Therapeutics Switzerland GmbH, Zug, Switzerland.
  • Mercuri E; PTC Therapeutics Inc., South Plainfield, NJ 07080-2449, USA.
J Comp Eff Res ; 8(14): 1187-1200, 2019 10.
Article en En | MEDLINE | ID: mdl-31414621
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxadiazoles / Distrofia Muscular de Duchenne Tipo de estudio: Clinical_trials Límite: Adolescent / Aged / Animals / Child / Child, preschool / Humans / Infant / Male Idioma: En Revista: J Comp Eff Res Año: 2019 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oxadiazoles / Distrofia Muscular de Duchenne Tipo de estudio: Clinical_trials Límite: Adolescent / Aged / Animals / Child / Child, preschool / Humans / Infant / Male Idioma: En Revista: J Comp Eff Res Año: 2019 Tipo del documento: Article Pais de publicación: Reino Unido