About Familial LCAT deficiency
Familial LCAT deficiency is a rare disease catalogued by Orphanet (ORPHA:79293). It is associated with the LCAT 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 Familial LCAT deficiency trials.
Search ClinicalTrials.gov for "Familial LCAT deficiency" or filter by Orphanet code ORPHA:79293 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 Familial LCAT deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Familial LCAT deficiency. Updated daily.