About X-linked spastic paraplegia type 34
X-linked spastic paraplegia type 34 is a rare disease catalogued by Orphanet (ORPHA:171607). It is associated with the SPG34 gene. 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 X-linked spastic paraplegia type 34 trials.
Search ClinicalTrials.gov for "X-linked spastic paraplegia type 34" or filter by Orphanet code ORPHA:171607 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 X-linked spastic paraplegia type 34 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for X-linked spastic paraplegia type 34. Updated daily.