About Charcot-Marie-Tooth disease type 1F
Charcot-Marie-Tooth disease type 1F is a rare disease catalogued by Orphanet (ORPHA:101085). It is associated with the NEFL 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 Charcot-Marie-Tooth disease type 1F trials.
Search ClinicalTrials.gov for "Charcot-Marie-Tooth disease type 1F" or filter by Orphanet code ORPHA:101085 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 Charcot-Marie-Tooth disease type 1F trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Charcot-Marie-Tooth disease type 1F. Updated daily.