drugset / Trial / NCT00226512

To Determine the Role of Adding Campath-1H or ATG Given In-vivo in Addition to Fludarabine and Low Dose Busulfex on Outcome in Patients Treated With Reduced Intensity Conditioning

NCT00226512

Phase 3 Withdrawn 203 enrolled Hadassah Medical Organization Bayer · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

Multi-institutional randomized phase III trial of a non-myeloablative preparative regimen with fludarabine and busulfex with or without anti-lymphocyte antibodies (monoclonal humanized Campath-1H administered s.c. or polyclonal rabbit anti-T lymphocyte antibodies (ATG), combined with low dose and short course cyclosporine A (CSA) and methotrexate (MTX) as the sole agent for prevention of graft-vs-host disease (GVHD) for patients with acute myelogenous leukemia or myelodysplastic syndrome undergoing allogeneic stem cell transplantation from an HLA compatible donor.

Timeline

Start
2004-07
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject ATG Protein / enzyme biologic
Subject Alemtuzumab Monoclonal antibody Subcutaneous