Viewing Study NCT00210002



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Last Modification Date: 2024-10-26 @ 9:18 AM
Study NCT ID: NCT00210002
Status: TERMINATED
Last Update Posted: 2006-11-14
First Post: 2005-09-12

Brief Title: Evaluation of Iron Supplementation During Darbepoetin Alfa Treatment in Prophylaxis of Severe Anaemia Chemo-Induced
Sponsor: Institut Claudius Regaud
Organization: Institut Claudius Regaud

Study Overview

Official Title: Evaluation of Systematic Intravenous Iron Supplementation During Darbepoetin Alfa Treatment in Prophylaxis of Severe Anaemia Chemo-Induced
Status: TERMINATED
Status Verified Date: 2006-11
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 evaluate the response rate obtained in an heterogeneous oncologic population treated by chemotherapy and either by Darbepoetin alfa classic treatment or by association of Darbepoetin alfa -ferric saccharose systematic supplementation administered concomitantly with chemotherapy
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