About Inherited congenital spastic tetraplegia
Inherited congenital spastic tetraplegia is a rare disease catalogued by Orphanet (ORPHA:210141). It is associated with the KANK1, GAD1, ADD3 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 Inherited congenital spastic tetraplegia trials.
Search ClinicalTrials.gov for "Inherited congenital spastic tetraplegia" or filter by Orphanet code ORPHA:210141 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 Inherited congenital spastic tetraplegia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Inherited congenital spastic tetraplegia. Updated daily.