Active, not recruitingNot applicableNCT06419322
Acceptability, Feasibility, Safety and Efficacy of a Optimized Rehabilitation Program for Treated Patients With Spinal Muscular Atrophy (SMA).
Studying Autosomal dominant adult-onset proximal spinal muscular atrophy
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
- University of Oxford
- Principal Investigator
- Charlotte LilienUniversity of Oxford, Department of Paediatrics
- Intervention
- Optimized rehabilitation program(other)
- Enrollment
- 14 enrolled
- Eligibility
- 1-10 years · All sexes
- Timeline
- 2024 – 2026
Study locations (1)
- Oxford Brookes University, Oxford, Oxfordshire, United Kingdom
Collaborators
Oxford Brookes University · Oxford University Hospitals NHS Trust · ACE SMA Charity · Roche Products Limited · Scholar Rock, Inc. · Biohaven Therapeutics Ltd. · Rally Round Rupert Charity
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.
Open NCT06419322 on ClinicalTrials.govOther trials for Autosomal dominant adult-onset proximal spinal muscular atrophy
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