About Neuralgic amyotrophy
Neuralgic amyotrophy is a rare disease catalogued by Orphanet (ORPHA:2901). It is associated with the SEPTIN9 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 Neuralgic amyotrophy trials.
Search ClinicalTrials.gov for "Neuralgic amyotrophy" or filter by Orphanet code ORPHA:2901 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 Neuralgic amyotrophy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Neuralgic amyotrophy. Updated daily.