drugset / Trial / NCT00124111

A Study of Cyclophosphamide/Methotrexate/5-Fluorouracil (CMF) With Pegfilgrastim in Subjects With Breast Cancer

NCT00124111

Phase 2 Completed Amgen
Non-randomizedSingle-groupOpen-label

Summary

The purpose of this study is to assess the relative dose intensity (RDI) of intravenous (IV) CMF on a Day 1 and 8 schedule given every 28 days with pegfilgrastim support in subjects with stage I-III breast cancer.

Timeline

Start
Primary completion
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 600 mg/m2 Intravenous
Subject Methotrexate Small molecule 40 mg/m2 Intravenous
Subject Pegfilgrastim Protein / enzyme biologic 6 mg Subcutaneous
Subject fluorouracil Small molecule 600 mg/m2 Intravenous

Indications