About Lipoic acid synthetase deficiency
Lipoic acid synthetase deficiency is a rare disease catalogued by Orphanet (ORPHA:401859). It is associated with the LIAS 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 Lipoic acid synthetase deficiency trials.
Search ClinicalTrials.gov for "Lipoic acid synthetase deficiency" or filter by Orphanet code ORPHA:401859 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 Lipoic acid synthetase deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Lipoic acid synthetase deficiency. Updated daily.