Active, not recruitingPhase 4NCT06713135
A Study on Safety and Effectiveness of Long-term Treatment With Vamorolone in Boys With Duchenne Muscular Dystrophy
Studying Duchenne muscular dystrophy
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Santhera Pharmaceuticals
- Principal Investigator
- A Child, MDLeeds Teaching Hospital
- Intervention
- vamorolone 40 mg/mL oral suspension(drug)
- Enrollment
- 80 enrolled
- Eligibility
- MALE
- Timeline
- 2024 – 2028
Study locations (18)
- UZ Gent (Universitair Ziekenhuis Gent), Ghent, Belgium
- UZ Leuven (Universitair Ziekenhuis Leuven), Leuven, Belgium
- University Hospital Brno, Brno, Czechia
- Fakultni Nemocnice Motol, Prague, Czechia
- Children's Hospital Agia Sofia, Athens, Greece
- Children's Health Ireland at Tallaght, Tallaght University Hospital, Dublin, Ireland
- Schneider Children's Medical Center, Petah Tikva, Israel
- Leiden University Medical Center, Leiden, Netherlands
- Radboud University Nijmegen, Nijmegen, Netherlands
- Te Wao Nui - Child Health Service, Wellington Hospital, Wellington, New Zealand
- Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain
- Hospital Universitario y Politecnico de La Fe, Valencia, Spain
- Queen Elizabeth University Hospital, Glasgow, Lanarkshire, United Kingdom
- Alder Hey Children's Hospital, Liverpool, Merseyside, United Kingdom
- Leeds Teaching Hospitals NHS Trust, Leeds, West Yorkshire, United Kingdom
- +3 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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