About 3-methylglutaconic aciduria type 1
3-methylglutaconic aciduria type 1 is a rare disease catalogued by Orphanet (ORPHA:67046). It is associated with the AUH 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 3-methylglutaconic aciduria type 1 trials.
Search ClinicalTrials.gov for "3-methylglutaconic aciduria type 1" or filter by Orphanet code ORPHA:67046 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 3-methylglutaconic aciduria type 1 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for 3-methylglutaconic aciduria type 1. Updated daily.