Viewing Study NCT00124111



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Last Modification Date: 2024-10-26 @ 9:12 AM
Study NCT ID: NCT00124111
Status: COMPLETED
Last Update Posted: 2010-02-26
First Post: 2005-07-25

Brief Title: A Study of CyclophosphamideMethotrexate5-Fluorouracil CMF With Pegfilgrastim in Subjects With Breast Cancer
Sponsor: Amgen
Organization: Amgen

Study Overview

Official Title: A Single-arm Study Evaluating the Relative Dose Intensity of IV CMF Given on Day 1 and Day 8 With Pegfilgrastim Support in Subjects With Stage I-III Breast Cancer
Status: COMPLETED
Status Verified Date: 2010-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None