About POMT1-related limb-girdle muscular dystrophy R11
POMT1-related limb-girdle muscular dystrophy R11 is a rare disease catalogued by Orphanet (ORPHA:86812). It is associated with the POMT1 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 POMT1-related limb-girdle muscular dystrophy R11 trials.
Search ClinicalTrials.gov for "POMT1-related limb-girdle muscular dystrophy R11" or filter by Orphanet code ORPHA:86812 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 POMT1-related limb-girdle muscular dystrophy R11 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for POMT1-related limb-girdle muscular dystrophy R11. Updated daily.