NL-OMON39088已完成不适用
The influence of time of administration on tamoxifen pharmacokinetics. - Different times of tamoxifen administration.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 18
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •-Histological or cytological confirmed diagnosis of breast cancer, for which treatment with tamoxifen is indicated (to be evaluated by the treating physician);
- •-Use of tamoxifen for at least 4 weeks and willing to continue the treatment until the end of the study;
- •-Age > 18 years;
- •-WHO performance <= 1;
- •-Written informed consent;
- •-Adequate renal and hepatic functions (see protocol);
- •-Adequate hematological blood counts (see protocol);
- •-No chemotherapy within the last 4 weeks before start;
- •-No radiotherapy within the last 4 weeks before start.
排除标准
- •-Pregnant or lactating patients;
- •-Serious illness or medical unstable condition requiring treatment, symptomatic CNS metastases or history of psychiatric disorder that would prohibit the understanding and giving of informed consent;
- •-More than one tamoxifen dose per day (20 or 40 mg);
- •-Non-compliance.
研究者
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