About Benign Samaritan congenital myopathy
Benign Samaritan congenital myopathy is a rare disease catalogued by Orphanet (ORPHA:324581). It is associated with the RYR1 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 Benign Samaritan congenital myopathy trials.
Search ClinicalTrials.gov for "Benign Samaritan congenital myopathy" or filter by Orphanet code ORPHA:324581 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 Benign Samaritan congenital myopathy trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Benign Samaritan congenital myopathy. Updated daily.