Condition: Acute Myeloid Leukemia With T(8;21)(Q22;Q22) · Acute Myeloid Leukemia With T(16;16)(P13;Q22) · KIT Gene Mutation · Sponsor: The First Affiliated Hospital of Soochow University
The goal of this clinical trial is to learn if avapritinib combined with standard induction therapy works to treat newly diagnosed adult acute myeloid leukemia (AML) patients with KIT mutations and t(8;21)(q22;q22.1); inv(16)(p13.1q22) or t(16;16)(p13.1;q22). It will also investigate the safety and tolerability of this combination therapy. The main questions it aims to answer are: To determine the maximum tolerated dose (MTD) and/or recommended Phase II dose (RP2D) of avapritinib combined with chemotherapy by Dose-limiting toxicity (DLT). Does this combination therapy improve the rates of minimal residual disease (MRD) negativity and long-term survival outcomes?
This description comes directly from the study's public registry record.
Su-ning Chen, M.D. · 008613814881746 · chensuning@sina.com
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| The First Affiliated Hospital of Soochow University | Suzhou, Jiangsu, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07028073