CEBPA Biallelic Mutation
Associated Genetic Biomarkers
CEBPA Biallelic Mutation serves as an inclusion eligibility criterion in 1 clinical trial, of which 1 is open and 0 are closed. Of the trial that contains CEBPA Biallelic Mutation as an inclusion criterion, 1 is phase 2 (1 open).
Trials with CEBPA Biallelic Mutation in the inclusion eligibility criteria most commonly target acute myeloid leukemia .
Autologous hematopoietic stem cell transplatation, busulfan, and etoposide are the most frequent therapies in trials with CEBPA Biallelic Mutation as an inclusion criteria .
Significance of CEBPA Biallelic Mutation in Diseases
Acute Myeloid Leukemia +
CEBPA is mutated in 4.19% of acute myeloid leukemia patients .
CEBPA Biallelic Mutation is an inclusion criterion in 1 clinical trial for acute myeloid leukemia, of which 1 is open and 0 are closed. Of the trial that contains CEBPA Biallelic Mutation and acute myeloid leukemia as inclusion criteria, 1 is phase 2 (1 open) .
Autologous hematopoietic stem cell transplatation, busulfan, and etoposide are the most frequent therapies in trials for acute myeloid leukemia that contain CEBPA Biallelic Mutation .
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