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临床试验/DRKS00017765
DRKS00017765已完成2 期

Genotype and phenotype guided supplementation of TAMoxifen standard therapy with ENDOXifen in breast cancer patients - TAMENDOX

Robert Bosch Gesellschaft für medizinische Forschung mbH (RBMF)0 个研究点目标入组 356 人开始时间: 2019年8月30日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
356

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled study
盲法
Blinded (masking used)

入排标准

年龄范围
18 Years 至 one(—)
性别
Female

入选标准

  • Main Inclusion Criteria: Pre- and postmenopausal female patients with DCIS or stage I, IIA, IIB or IIIA invasive breast cancer who have received at least three months standard tamoxifen treatment before baseline visit.

排除标准

  • Main Exclusion Criteria: Locally advanced (Stadium IIIB or IIIC) or metastatic (Stage IV) breast cancer, ongoing chemotherapy and/or treatment with trastuzumab within the last three months, other active second malignancy, pregnancy, breast feeding/lactation, severe chronic or acute respiratory, cardiac, renal or endocrine diseases.

研究者

发起方
Robert Bosch Gesellschaft für medizinische Forschung mbH (RBMF)

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