About SMPX-related distal myopathy
SMPX-related distal myopathy is a rare disease catalogued by Orphanet (ORPHA:700163). It is associated with the SMPX 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 SMPX-related distal myopathy trials.
Search ClinicalTrials.gov for "SMPX-related distal myopathy" or filter by Orphanet code ORPHA:700163 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 SMPX-related distal myopathy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for SMPX-related distal myopathy. Updated daily.