About Iminoglycinuria
Iminoglycinuria is a rare disease catalogued by Orphanet (ORPHA:42062). It is associated with the SLC6A20, SLC36A2, SLC6A18 genes. 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 Iminoglycinuria trials.
Search ClinicalTrials.gov for "Iminoglycinuria" or filter by Orphanet code ORPHA:42062 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 Iminoglycinuria trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Iminoglycinuria. Updated daily.