About Infantile neuroaxonal dystrophy
Infantile neuroaxonal dystrophy is a rare disease catalogued by Orphanet (ORPHA:35069). It is associated with the PLA2G6 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 neuroaxonal dystrophy trials.
Search ClinicalTrials.gov for "Infantile neuroaxonal dystrophy" or filter by Orphanet code ORPHA:35069 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 neuroaxonal dystrophy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Infantile neuroaxonal dystrophy. Updated daily.