About X-linked sideroblastic anemia and spinocerebellar ataxia
X-linked sideroblastic anemia and spinocerebellar ataxia is a rare disease catalogued by Orphanet (ORPHA:2802). It is associated with the ABCB7 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 X-linked sideroblastic anemia and spinocerebellar ataxia trials.
Search ClinicalTrials.gov for "X-linked sideroblastic anemia and spinocerebellar ataxia" or filter by Orphanet code ORPHA:2802 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 X-linked sideroblastic anemia and spinocerebellar ataxia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for X-linked sideroblastic anemia and spinocerebellar ataxia. Updated daily.