drugset / Trial / NCT00117897

Treatment for Subjects With Non-Hodgkin's Lymphoma

NCT00117897

Phase 2 Completed Amgen
RandomizedParallel-groupOpen-labelTreatment

Summary

This multicenter, open-label, randomized, parallel study was designed to evaluate whether a single fixed-dose subcutaneous (SC) administration of pegfilgrastim or daily administration of Filgrastim for absolute neutrophil count (ANC) support would assist in allowing the planned dose-on-time (PDOT) of cyclophosphamide, doxorubicin, vincristine, prednisolone (CHOP) chemotherapy with Rituximab every 14 days in subjects with aggressive B-cell Non-Hodgkin's Lymphoma by reducing the duration of neutropenia and incidence of febrile neutropenia.

Timeline

Start
2002-07
Primary completion
Completion
2004-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Pegfilgrastim Protein / enzyme biologic Subcutaneous
Subject filgrastim Protein / enzyme biologic

Indications