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

Author:

Muntoni Francesco12,Desguerre Isabelle3,Guglieri Michela4,Osorio Andrés Nascimento5,Kirschner Janbernd6,Tulinius Már7,Buccella Filippo8,Elfring Gary9,Werner Christian10,Schilling Traci9,Trifillis Panayiota9,Zhang Olivia9,Delage Abdallah11,Santos Claudio L9,Mercuri Eugenio1213

Affiliation:

1. 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

2. 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

3. APHP Necker – Enfants Malades Hospital, Paris V Descartes University, Neuromuscular Network FILNEMUS, Paris, France

4. The John Walton Muscular Dystrophy Research Centre, Newcastle University & Newcastle Upon Tyne Hospitals, Newcastle Upon Tyne, UK

5. Hospital Sant Joan de Déu Unidad de Patología Neuromuscular, Universidad de Barcelona, CIBERER, ISCIII, Barcelona, Spain

6. Medical Center – University of Freiburg, Faculty of Medicine, Freiburg, Germany

7. Department of Pediatrics, Gothenburg University, Queen Silvia Children’s Hospital, Gothenburg, Sweden

8. Parent Project Italy APS, Rome, Italy

9. PTC Therapeutics Inc., South Plainfield, NJ 07080-2449, USA

10. PTC Therapeutics Germany GmbH, Frankfurt, Germany

11. PTC Therapeutics Switzerland GmbH, Zug, Switzerland

12. Department of Pediatric Neurology, Catholic University, Rome, Italy

13. Centro Clinico Nemo, Policlinico Universitario A Gemelli IRCCS, Rome, Italy

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.

Publisher

Future Medicine Ltd

Subject

Health Policy

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