About Amish nemaline myopathy
Amish nemaline myopathy is a rare disease catalogued by Orphanet (ORPHA:98902). It is associated with the TNNT1 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 Amish nemaline myopathy trials.
Search ClinicalTrials.gov for "Amish nemaline myopathy" or filter by Orphanet code ORPHA:98902 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 Amish nemaline myopathy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Amish nemaline myopathy. Updated daily.