Queen Silvia Children's Hospital

Gothenburg SE-416 85

1 studies enrolling now · 14 studies all time

What they study most

Becker Muscular Dystrophy, Duchenne Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Genetic Diseases, Inborn, Genetic Diseases, X-Linked, Heart Block Complete, Heart Block Second Degree, Muscular Diseases, Muscular Disorders, Atrophic, Muscular Dystrophies, Muscular Dystrophy, Duchenne, Musculoskeletal Diseases

Studies at this site

• Slow Heart Registry of Fetal Immune-mediated High Degree Heart Block — Recruiting now
• Real World Data Collection Pediatric Neuroblastoma Treated With Lorlatinib — Stopped early
• A Study to Assess the Efficacy and Safety of Vamorolone in Boys With Duchenne Muscular Dystrophy (DMD) — Completed
• Phase III Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy — Completed
• Long-term Extension Study to Assess Vamorolone in Boys With Duchenne Muscular Dystrophy (DMD) — Completed
• An Open-Label Extension Study of Edasalonexent in Boys With Duchenne Muscular Dystrophy — Stopped early
• An Extension Study of Ataluren (PTC124) in Participants With Nonsense Mutation Dystrophinopathy — Stopped early
• Phase 3 Study of Ataluren in Participants With Nonsense Mutation Duchenne Muscular Dystrophy (nmDMD) — Completed
• Phase 2B Extension Study of Ataluren (PTC124) in Duchenne/Becker Muscular Dystrophy (DMD/BMD) — Stopped early
• Phase 2B Study of PTC124 (Ataluren) in Duchenne/Becker Muscular Dystrophy (DMD/BMD) — Completed
• An Extension Study to Assess Vamorolone in Boys With Duchenne Muscular Dystrophy (DMD) — Completed
• A Study to Assess Vamorolone in Boys With Duchenne Muscular Dystrophy (DMD) — Completed
• A Multicenter Collaborative Study on the Clinical Features, Expression Profiling, and Quality of Life of Infantile Onset FSHD — Completed
• Longitudinal Study of the Natural History of Duchenne Muscular Dystrophy (DMD) — Status unconfirmed