跳至主要内容
临床试验/EUCTR2006-002275-40-SE
EUCTR2006-002275-40-SE进行中(未招募)不适用

Prospective study of patients treated with pegylated interferon-alpha 2b (PegIntron) for metastasizing ileal/coecal carcinoids - NA

ppsala University Hospital, Dept. of Medical Sciences0 个研究点目标入组 90 人开始时间: 2006年12月5日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
90

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

  • Patients suffering from metstasizing, histopathologically verified (chromogranin A and serotonin immunohistochemistry must be positive), highly differentiated NE carcinomas of the jejunum/ileum/valvula Bauhini and the adjacent parts of coecum/colon ascendens. Patients with NE carcinomas of the duodenum, the appendix (including also goblet-cell carcinoids) are not included, neither those with poorly differentiated NE carcinomas (proliferation index higher than 15 %)
  • Measurable disease as diagnosed by means of CT or MRI according to the RECIST criteria
  • U-5-HIAA > 2 x upper normal limit and/or P-Chromogranin A > 2 x upper normal limit
  • Age >18 years.
  • Life expectancy of more than 12 months
  • Patients must be willing to give written informed consent
  • 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
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • Previous or present interferon treatment
  • Previous radioactive tumour-targeting treatment
  • Other active or previous neoplasms within 5 years (except non-melanoma skin cancer or in situ cervical cancer)
  • Liver embolization or radiofrequency ablation within 3 months prior to screening
  • Patients who have severe cardiovascular disease, i.e., arrhythmias requiring chronic treatment, congestive heart failure (NYHA Class III or IV) or symptomatic ischemic heart disease
  • Contraindications to the investigational product, e.g. known or suspected hypersensitivity

研究者

发起方
ppsala University Hospital, Dept. of Medical Sciences

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