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A Randomized Controlled Study of Postoperative Adjuvant Therapy of Uracil-tegafur (UFT) Compared With Cyclophosphamide/Methotrexate/5-fluorouracil (CMF) in Breast Cancer (NSAS-BC).

Phase 3
Conditions
Breast caner
Registration Number
JPRN-jRCT1080220055
Lead Sponsor
Taiho Pharmaceutical Co., Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

Patients with Stage I, II or IIIA high-risk breast cancer negative for lymph node metastasis.

Exclusion Criteria

Not provided

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Efficacy and safety
Secondary Outcome Measures
NameTimeMethod
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