About Fetal and neonatal alloimmune thrombocytopenia
Fetal and neonatal alloimmune thrombocytopenia is a rare disease catalogued by Orphanet (ORPHA:853). It is associated with the GP1BA, GP1BB, ITGA2B 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 Fetal and neonatal alloimmune thrombocytopenia trials.
Search ClinicalTrials.gov for "Fetal and neonatal alloimmune thrombocytopenia" or filter by Orphanet code ORPHA:853 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 Fetal and neonatal alloimmune thrombocytopenia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Fetal and neonatal alloimmune thrombocytopenia. Updated daily.