Drug intelligence / Profile preview

P-AML-2025

Development stage
Preclinical
Lead developer
Institute of Hematology and Blood Diseases Hospital
Modality
Small Molecules
01

Overview

**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.

Other names
P-AML-2025 regimenP-AML2025 regimenP-AML 2025 regimen
02

Targets

TOP2A (DNA topoisomerase II)DNA at Topoisomerase II cleavage sites

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