Viewing StudyNCT00152191



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Last Modification Date: 2024-10-26 @ 9:14 AM
Study NCT ID: NCT00152191
Status: COMPLETED
Last Update Posted: 2011-07-07
First Post: 2005-09-07

Brief Title: A Randomized Controlled Study of Postoperative Adjuvant Therapy of Uracil-tegafur UFT Compared With CyclophosphamideMethotrexate5-fluorouracil CMF in Breast Cancer NSAS-BC
Sponsor:
Organization: Taiho Pharmaceutical Co Ltd

Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention: None
Bio Spec Description: None
Enrollment Count: 1300
Enrollment Type: ESTIMATED
Design Primary Purpose:
Design Masking:
Phases:
Name
PHASE3
Observational Models:
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