About Amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis is a rare disease catalogued by Orphanet (ORPHA:803). It is associated with the CCNF, TAF15, ANXA11 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 Amyotrophic lateral sclerosis trials.
Search ClinicalTrials.gov for "Amyotrophic lateral sclerosis" or filter by Orphanet code ORPHA:803 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 Amyotrophic lateral sclerosis trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Amyotrophic lateral sclerosis. Updated daily.