drugset / Trial / NCT03339700

Addition of Gemcitabine to Pre Allo-HSCT Conditioning for Acute Lymphoblastic Leukemia

NCT03339700 ↗

NaSingle-groupOpen-labelTreatment

Summary

The main purpose of the project is to evaluate the disease free survival and overall survival in patients diagnosed with acute lymphoblastic leukemia undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) adding gemcitabine to the standard institutional conditioning regimen based on two alkylating drugs, reduced busulfan and cyclophosphamide (reduced BUCY 2).

Timeline

Start
2018-09-15
Primary completion
2020-09
Completion
2021-09

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Gemcitabine Small molecule 1200 mg/m2 Intravenous
Background Busulfan Small molecule 3 mg/kg Oral
Background Cyclophosphamide Other / unclassified 40 mg/kg Intravenous