About Infantile-onset ascending hereditary spastic paralysis
Infantile-onset ascending hereditary spastic paralysis is a rare disease catalogued by Orphanet (ORPHA:293168). It is associated with the ALS2 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 Infantile-onset ascending hereditary spastic paralysis trials.
Search ClinicalTrials.gov for "Infantile-onset ascending hereditary spastic paralysis" or filter by Orphanet code ORPHA:293168 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 Infantile-onset ascending hereditary spastic paralysis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Infantile-onset ascending hereditary spastic paralysis. Updated daily.