Disease Directory Acute myeloblastic leukemia with maturation
Blood

Acute myeloblastic leukemia with maturation

Type

Disease

Gene

FLT3, KIT, NPM1

About Acute myeloblastic leukemia with maturation

Acute myeloblastic leukemia with maturation is a rare disease catalogued by Orphanet (ORPHA:98834). It is associated with the FLT3, KIT, NPM1 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 Acute myeloblastic leukemia with maturation trials.

Search ClinicalTrials.gov for "Acute myeloblastic leukemia with maturation" or filter by Orphanet code ORPHA:98834 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:98834)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Acute myeloblastic leukemia with maturation trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Acute myeloblastic leukemia with maturation. Updated daily.