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**P-AML-2025** is an investigator-initiated, named treatment regimen/protocol for children with newly diagnosed acute myeloid leukemia, excluding acute promyelocytic leukemia and several secondary or genetically defined AML subgroups. It is being evaluated by the Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College in the prospective ChiCTR study ChiCTR2500096333. The public registry identifies the regimen but does not disclose its individual active pharmaceutical components, doses, or target-specific mechanism. Study endpoints include complete remission, measurable residual disease negativity, event-free survival, overall survival, safety, and exploratory RNA-sequencing correlates of response and resistance.
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