drugset / Trial / NCT06652685

Molecular Subtype Combined with Early Minimal Residual Disease to Optimize the Treatment of Newly Diagnosed Acute Myeloid Leukemia

NCT06652685

Phase 2 Not yet recruiting 218 enrolled Ruijin Hospital
Non-randomizedSequentialOpen-labelTreatment

Summary

This study aims to investigate the safety and efficacy of drug "X" in combination with intensive chemotherapy in subjects with newly diagnosed AML (excluding APL and CBF-AML). "X" drugs included BCL-2 inhibitor venetoclax and FLT3 inhibitor Gilteritinib. Subjects will receive standard intensive chemotherapy during induction and consolidation. Early induction response will be evaluated according to the results of peripheral blood blast clearance rate on the fifth day after induction therapy (D5-PBCR). Venetoclax will be added in D5-PBCR positive subjects. For subjects with FLT3 mutations, Gilteritinib will be combined. Subjects will be stratified based on the genetic risk classification of 2022 European LeukemiaNet recommendations (ELN risk) and MRD status to receive specific consolidation therapy after the induction therapy.

Timeline

Start
2024-10-30
Primary completion
2026-10-31
Completion
2027-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Venetoclax Small molecule 400 mg Oral
Background Cytarabine Small molecule 100 mg/m2 Intravenous
Background Cytarabine Small molecule 2000 mg/m2 Intravenous
Background Idarubicin Small molecule 10 mg/m2 Intravenous