About Galactokinase deficiency
Galactokinase deficiency is a rare disease catalogued by Orphanet (ORPHA:79237). It is associated with the GALK1 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 Galactokinase deficiency trials.
Search ClinicalTrials.gov for "Galactokinase deficiency" or filter by Orphanet code ORPHA:79237 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 Galactokinase deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Galactokinase deficiency. Updated daily.