About Mixed phenotype acute leukemia with t(v;11q23.3)
Mixed phenotype acute leukemia with t(v;11q23.3) is a rare disease catalogued by Orphanet (ORPHA:589595). It is associated with the FLT3, KMT2A, AFF1 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 Mixed phenotype acute leukemia with t(v;11q23.3) trials.
Search ClinicalTrials.gov for "Mixed phenotype acute leukemia with t(v;11q23.3)" or filter by Orphanet code ORPHA:589595 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 Mixed phenotype acute leukemia with t(v;11q23.3) trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Mixed phenotype acute leukemia with t(v;11q23.3). Updated daily.