About Progressive non-fluent aphasia
Progressive non-fluent aphasia is a rare disease catalogued by Orphanet (ORPHA:100070). It is associated with the TMEM106B, PSEN1, CHMP2B 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 Progressive non-fluent aphasia trials.
Search ClinicalTrials.gov for "Progressive non-fluent aphasia" or filter by Orphanet code ORPHA:100070 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 Progressive non-fluent aphasia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Progressive non-fluent aphasia. Updated daily.