Clinical Trial to Evaluate the Efficacy, Safety, and Tolerability of RO7239361 in Ambulatory Boys With Duchenne Muscular Dystrophy
Duchenne Muscular Dystrophy
About this trial
This is an interventional treatment trial for Duchenne Muscular Dystrophy focused on measuring muscular dystrophy, Duchenne's Muscular Dystrophy, DMD
Eligibility Criteria
Inclusion Criteria:
- Diagnosed with DMD by confirmed medical history and genetic testing
- Able to walk without assistance
- Minimum North Star Ambulatory Assessment score of 15 at screening
- Able to walk up 4 stairs in 8 seconds or less
- Weigh at least 15 kg (33 lbs)
- Taking corticosteroids for DMD
Exclusion Criteria:
- Any behavior or mental issue that will affect the ability to complete the required study procedures
- Previously or currently taking medications like androgens or human growth hormone
- Use of a ventilator during the day
- Unable to have blood samples collected or receive an injection under the skin
- Concomitant or previous participation at any time in a gene therapy study
Other protocol defined Inclusion/Exclusion Criteria could apply.
Sites / Locations
- Neuromuscular Research Center
- Stanford University
- University of California Davis Medical Center
- Yale University School of Medicine ; Pulmonary & Critical Care
- University of Florida
- Nemours Children's Hospital
- Rare Disease Research, LLC
- Rush University Medical Center - PPDS
- University of Iowa
- University of Kansas Medical Center
- Kennedy Krieger Institute
- University of Massachusetts Memorial Childrens Medical Center; Department of Neurology
- Saint Louis Children's Hospital
- Las Vegas Clinic
- Cincinnati Childrens Hospital Medical Center;Investigational Pharmacy
- Nationwide Childrens Hospital; Research Institute at Nationwide Childrens Hospital
- Seattle Children's Hospital
- Instituto centenario
- Children's Hospital Westmead; Paediatrics & Child Health
- Lady Cilento Children's Hospital; Neurosciences Department
- Royal Children's Hospital
- UZ Gent
- London Health Sciences Centre; Children's Hospital; Pediatrics
- Children'S Hospital of Eastern Ontario
- Hospices Civils de Lyon
- Hotel Dieu; Service Pharmacie Essais Cliniques
- Hopital Armand Trousseau; centre reference Maladies Neuro-musculaires Est parisien Neuropediatrie
- Hopitaux Universitaires de Strasbourg
- Universitatsklinikum Essen; Innere Klinik
- Fondazione Serena Onlus - CENTRO CLINICO NEMO
- Fondazione Policlinico Universitario A Gemelli; Servizio di Farmacia
- Az. Osp. Universitaria Pol. G. Martino; Dip. Neuroscienze, Scienze Psichiatriche e Anest.
- Hyogo College of Medicine Hospital
- Miyagi Children's Hospital
- Shinshu University Hospital
- National Hospital Organization Osaka Toneyama Medical Center
- National Center of Neurology and Psychiatry
- Leids Universitair Medisch Centrum
- Radboud University Nijmegen Medical Centre; Ophthalmology
- Hospital Sant Joan De Deu
- Hospital Universitari i Politecnic La Fe de Valencia; Servicio de Farmacia
- Drottning Silvias Barn- och ungdomssjukhus; Kliniken for barnmedicin
- Alder Hey Children s Hospital; Department of Pediatrics
- UCL Institute of Child Health & Great Ormond Street Hospital for Children
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Experimental
Placebo Comparator
RO7239361 Low Dose
RO7239361 High Dose
Placebo
Participants received low dose RO7239361 SC on specified days of the 48-week DB period. Following the DB period participants received low dose RO7239361 on specified days for up to 192 weeks during the open-label period followed by 24 weeks of follow-up.
Participants received high dose RO7239361 SC on specified days of the 48-week DB period. Following the DB period participants received high dose RO7239361 on specified days for up to 192 weeks during the open-label period followed by 24 weeks of follow-up.
Participants received matching placebo solution subcutaneously (SC) on specified days of the 48-week double-blind (DB) period. Following the DB period participants received low dose or high dose RO7239361 on specified days for up to 192 weeks during the open-label period followed by 24 weeks of follow-up.