About Intermediate nemaline myopathy
Intermediate nemaline myopathy is a rare disease catalogued by Orphanet (ORPHA:171433). It is associated with the TPM3, ACTA1, NEB 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 Intermediate nemaline myopathy trials.
Search ClinicalTrials.gov for "Intermediate nemaline myopathy" or filter by Orphanet code ORPHA:171433 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 Intermediate nemaline myopathy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Intermediate nemaline myopathy. Updated daily.