drugset / Trial / NCT00161590

Study of CHOP + Campath for T-Cell, Null Cell, or Natural Killer (NK)-Cell Lymphoma

NCT00161590

Non-randomizedSingle-groupOpen-labelTreatment

Summary

Primary Objective: * To determine the toxicity profile and tolerability of alemtuzumab (Campath) when administered in combination with cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) chemotherapy (C-CHOP) in patients with T-cell, null-cell and NK-cell lymphomas. Secondary Objectives: * To evaluate response rate, overall survival, and disease-free survival in patients with T-cell, null-cell, and NK-cell lymphomas treated with Campath + CHOP chemotherapy. * To assess the incidence of cytomegalovirus (CMV) reactivation in patients with these lymphomas treated with the Campath + CHOP combination. * To determine features which might be predictive of resistance to treatment or predictive of relapse, including the absence of glycosylphosphatidylinositol (GPI)-linked proteins.

Timeline

Start
2004-07
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Alemtuzumab Monoclonal antibody
Background Cyclophosphamide Other / unclassified
Background Doxorubicin Other / unclassified
Background Prednisone Other / unclassified
Background Vincristine Small molecule