Disease Directory Chronic eosinophilic leukemia
Blood

Chronic eosinophilic leukemia

Type

Disease

Gene

FIP1L1, PDGFRA

About Chronic eosinophilic leukemia

Chronic eosinophilic leukemia is a rare disease catalogued by Orphanet (ORPHA:168940). It is associated with the FIP1L1, PDGFRA 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 Chronic eosinophilic leukemia trials.

Search ClinicalTrials.gov for "Chronic eosinophilic leukemia" or filter by Orphanet code ORPHA:168940 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

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:168940)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Chronic eosinophilic leukemia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Chronic eosinophilic leukemia. Updated daily.