drugset / Trial / NCT00167180

Post Transplant Donor Lymphocyte Infusion

NCT00167180 ↗

Phase 2 Terminated 57 enrolled Masonic Cancer Center, University of Minnesota
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to test the hypothesis that a pre-infusion preparative regimen of cyclophosphamide and fludarabine will improve the effectiveness of DLI in patients with blood cancers.

Timeline

Start
2004-01
Primary completion
2017-11-21
Completion
2018-12-24

Outcome

Outcome not reported

Stopped (Enrollment): “Accrual Goal Met”

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 60 mg/kg Intravenous
Subject Fludarabine Small molecule 25 mg/m2 Intravenous