drugset / Trial / NCT06385808

Efficacy and Safety of MTBF Conditioning Regimen for Salvageable Allo-HSCT in the Treatment of R/R AML

NCT06385808

NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study was to evaluate the efficacy of MTBF conditioning regimen of salvageable allo-HSCT in patients with relapsed or refractory acute myeloid leukemia. The secondary purpose of the study was to observe the safety of MTBF regimen in these patients.

Timeline

Start
2024-05-01
Primary completion
2026-12-31
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Busulfan Small molecule 0.8 mg/kg Intravenous
Subject Fludarabine Small molecule 50 mg/m2 Intravenous
Subject Mitoxantrone hydrochloride liposome Unknown 24 mg/m2 Intravenous
Subject Thiotepa Other / unclassified 5 mg/kg Intravenous