跳至主要内容
临床试验/NL-OMON44680
NL-OMON44680已完成2 期

Optimizing abiraterone (zytiga®)therapy by exploring the relation between an early biomarker-drug exposure-as a predictor for drug response in patients with mCRPC (OPTIMUM study) - OPTIMUM

Afdeling Apotheek0 个研究点目标入组 34 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
34

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

  • * patients with metastatic castration resistant prostate cancer who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated * OR * who have been treated upfront with 6 cycles of docetaxel: conform the Chaarted or Stampede trials
  • *Age *18 years
  • *Feasible to collect blood samples from
  • *Life expectancy of > 6 months
  • *Measurable disease
  • - Able and willing to give written informed consent prior to screening and enrollment

排除标准

  • Patients will be treated with abiraterone acetate in agreement with the drug label. Therefore the contra*indications of the drug label will be respected and no addi*tional strict exclusion criteria will be used in this study.

研究者

发起方
Afdeling Apotheek

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