跳至主要内容
临床试验/EUCTR2015-005784-17-NL
EUCTR2015-005784-17-NL进行中(未招募)1 期

The effects of the proton pump inhibitor esomeprazole on the bioavailability of regorafenib in patients with a metastatic colorectal cancer (mCRC) or gastrointestinal stromal tumour (GIST). - REGORA

Erasmus MC cancer institute0 个研究点目标入组 14 人开始时间: 2016年3月9日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
14

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • 1. Age = 18 years
  • 2. Histological or cytological confirmed diagnosis of mCRC or GIST
  • 3. ECOG Performance Status = 1
  • 4. Signed Informed Consent Form prior to screening evaluations
  • 5. No concurrent (over the counter) use of other acid reducing drugs, other than esomeprazole 40mg (PPIs, H2As and/or antacids) once daily during the study.
  • 6. No concurrent medication or supplements which can interact with esomeprazole or regorafenib during the study period.
  • 7. Abstain from grapefruit, grapefruit juice, herbal dietary supplements, and herbal tea during the study period.
  • 8. Adequate baseline patient characteristics
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 12
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 2

排除标准

  • 1. Pregnant or lactating patients.
  • 2. Patients with known impaired drug absorption (e.g. gastrectomy and achlorhydria).
  • 3. Known serious illness or medical unstable conditions that could interfere with this study
  • 4. Patients with evidence or history of any bleeding diathesis, irrespective of severity
  • 5. Cardiac history ( recent myocardial infarction, unstable or new-onset angina, uncontrolled cardiac arrhythmias)
  • 6. Uwillingness to abstain from grapefruit (juice), (herbal) dietary supplements, herbals, over-the-counter medication (except for paracetamol and ibuprofen) and other drugs known to seriously interact with esomeprazole and regorafenib during the study period.
  • 7. Unwillingness to abstain from acid beverages such as jus d’orange and other acidic beverages in the morning during regorafenib treatment in this study.
  • 8. Known hypersensitivity to any of the study drugs, study drug classes, or excipients in the formulation.
  • 9. Symptomatic CNS metastases or history of psychiatric disorder that would prohibit the understanding and giving of informed consent.

研究者

发起方
Erasmus MC cancer institute

相似试验