About Frontotemporal dementia with motor neuron disease
Frontotemporal dementia with motor neuron disease is a rare disease catalogued by Orphanet (ORPHA:275872). It is associated with the VCP, TARDBP, FUS 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 Frontotemporal dementia with motor neuron disease trials.
Search ClinicalTrials.gov for "Frontotemporal dementia with motor neuron disease" or filter by Orphanet code ORPHA:275872 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 Frontotemporal dementia with motor neuron disease trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Frontotemporal dementia with motor neuron disease. Updated daily.