Viewing Study NCT00309569



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Last Modification Date: 2024-10-26 @ 9:24 AM
Study NCT ID: NCT00309569
Status: COMPLETED
Last Update Posted: 2020-10-14
First Post: 2006-03-31

Brief Title: Randomized Study Comparing Pre- and Postoperative vs Conventional Adjuvant Treatment in Receptor-negative Patients
Sponsor: Austrian Breast Colorectal Cancer Study Group
Organization: Austrian Breast Colorectal Cancer Study Group

Study Overview

Official Title: A Randomized Phase III Study Comparing Pre- and Postoperative vs Conventional Adjuvant Treatment Hormone Receptor-negative Breast Cancer Patients
Status: COMPLETED
Status Verified Date: 2020-10
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: Primarily this clinical investigation compared overall survival and recurrence-free survival in patients with hormone receptor-negative breast cancer treated with pre- and postoperative chemotherapy vs conventional postoperative treatment
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