About Autosomal dominant spastic paraplegia type 37
Autosomal dominant spastic paraplegia type 37 is a rare disease catalogued by Orphanet (ORPHA:171612). It is associated with the SPG37, KPNA3 genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.
Clinical Trial Eligibility Tips
What to know before applying to Autosomal dominant spastic paraplegia type 37 trials.
Search ClinicalTrials.gov for "Autosomal dominant spastic paraplegia type 37" or filter by Orphanet code ORPHA:171612 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Autosomal dominant spastic paraplegia type 37 trials
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