drugset / Trial / NCT02961816

Panobinostat Combined With High-Dose Gemcitabine/Busulfan/Melphalan With Autologous Stem Cell Transplant for Patients With Refractory/Relapsed Lymphoma

NCT02961816

Phase 2 Withdrawn M.D. Anderson Cancer Center
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The goal of this clinical research study is to learn about the safety and effectiveness of the combination of panobinostat, gemcitabine, busulfan, and melphalan, either with or without rituximab, in patients who have non-Hodgkin's or Hodgkin's lymphoma and are receiving a stem cell transplant.

Timeline

Start
2017-06
Primary completion
2021-06
Completion
2021-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Busulfan Small molecule Intravenous
Subject Gemcitabine Small molecule 2700 mg/m2 Intravenous
Subject Melphalan Small molecule 60 mg/m2 Intravenous
Subject Panobinostat Small molecule 20 mg Oral
Subject Rituximab Monoclonal antibody 375 mg/m2 Intravenous
Background Dexamethasone Small molecule 8 mg Intravenous
Background G-CSF Unknown Subcutaneous
Background Glutamine Other / unclassified 15 g Oral
Background Palifermin Protein / enzyme biologic Intravenous
Background Pyridoxine Unknown 100 mg Intravenous

Indications