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临床试验/EUCTR2014-003856-30-BE
EUCTR2014-003856-30-BE进行中(未招募)1 期

Sandostatin (Octreotide LAR) may lead to clinical improvement through receptor occupation optimisation.A prospective interventional trial of patients with neuro-endocrine tumors with carcinoid syndrome receiving octreotide LAR. - SCIROCCO

Cliniques Universitaires Saint Luc0 个研究点目标入组 50 人开始时间: 2015年10月7日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
50

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

  • Written informed consent
  • GEP NET Ki 67 = 10 %
  • Histologically or cytologically confirmed GEP NET
  • Appearance of carcinoid syndrome maximum 6 months before the inclusion
  • Evaluable or measurable disease (RECIST 1.1)
  • WHO ECOG performance status 0-2
  • Positive somatostatin receptor scintigraphy
  • Life expectancy of at least 12 weeks
  • 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 35
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 15

排除标准

  • Uncontrolled concurrent disease which prevents the adequate management and follow-up of the NET.
  • Previous malignancy in the last past 3 years except malignancies estimated as completely cured.
  • Current pregnancy or breast feeding
  • Concomitant anti-tumoral treatment, except external beam radiotherapy

研究者

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