About SIM1-related Prader-Willi-like syndrome
SIM1-related Prader-Willi-like syndrome is a rare disease catalogued by Orphanet (ORPHA:398079). It is associated with the SIM1 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 SIM1-related Prader-Willi-like syndrome trials.
Search ClinicalTrials.gov for "SIM1-related Prader-Willi-like syndrome" or filter by Orphanet code ORPHA:398079 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 SIM1-related Prader-Willi-like syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for SIM1-related Prader-Willi-like syndrome. Updated daily.