drugset / Trial / NCT01200329

High-Dose Gemcitabine, Busulfan and Melphalan for Patients With Refactory Hodgkin's Disease

NCT01200329

Phase 2 Completed 81 enrolled M.D. Anderson Cancer Center
NaSingle-groupOpen-labelTreatment

Summary

The goal of this clinical research study is to learn if the combination of gemcitabine, busulfan, and melphalan, when given before a stem cell transplant, can help to control refractory Hodgkin's disease. The safety of this study treatment will also be studied.

Timeline

Start
2011-06
Primary completion
2018-12-06
Completion
2018-12-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Busulfan Small molecule 32 mg/m2 Intravenous
Subject Gemcitabine Small molecule 2775 mg/m2 Intravenous
Subject Melphalan Small molecule 60 mg/m2 Intravenous
Background Palifermin Protein / enzyme biologic 60 mg/kg Intravenous

Indications