drugset / Trial / NCT00948753

Maraviroc in Patients Undergoing Non-Myeloablative Allogeneic Stem-Cell Transplantation

NCT00948753

Phase 1/2 Completed 38 enrolled Abramson Cancer Center at Penn Medicine
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study investigates the effectiveness and safety of Maraviroc (an oral medication given twice daily given in addition to the standard GVHD prophylaxis) in preventing Graft versus Host Disease (GVHD) in patients undergoing non-myeloablative allogeneic stem-cell transplantation (SCT). Subjects will receive Maraviroc bid (in addition to standard GVHD prophylaxis) beginning after the last dose of the chemotherapy conditioning regimen until day 30 after stem-cell infusion.

Timeline

Start
2009-06
Primary completion
2011-04
Completion
2011-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Maraviroc Other / unclassified 150 mg Oral
Subject Maraviroc Other / unclassified 300 mg Oral