Viewing Study NCT00189579



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00189579
Status: TERMINATED
Last Update Posted: 2007-08-17
First Post: 2005-09-12

Brief Title: Addition of Herceptin to a Carboplatin-Paclitaxel Regimen in Patients With Ovarian Cancer
Sponsor: ARCAGY GINECO GROUP
Organization: ARCAGY GINECO GROUP

Study Overview

Official Title: A Phase II Study Designed to Evaluate the Safety and Efficacy of the Addition of Herceptin to a Carboplatin-Paclitaxel Regimen in Early Relapse Patients 6 Months With Ovarian Cancer Overexpressing HER2 Previously Treated With Carboplatin-Paclitaxel
Status: TERMINATED
Status Verified Date: 2007-08
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 whether or not the addition of Herceptin may be of benefit to a standard regimen of carboplatin-paclitaxel
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