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临床试验/EUCTR2007-002365-13-NL
EUCTR2007-002365-13-NL进行中(未招募)1 期

Sorafenib as adjuvant to radioiodine therapy in non-medullary thyroid carcinoma

Bayer B.V.0 个研究点目标入组 0 人开始时间: 2007年5月11日最近更新:
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试验速览

阶段
1 期
状态
进行中(未招募)
发起方

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 with non-medullary thyroid carcinoma
  • ·The patients must have undergone total thyroidectomy
  • ·Presence of metastases or inoperable recurrent disease, as proven by elevated serum thyroglobulin levels (Tg) in combination with radiological evidence for tumor.
  • ·No or insufficient RaI uptake in tumor as proven by RaI scintigraphy, performed after prior RaI therapy.
  • 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

  • ·Other active malignancies
  • ·Active kidney, liver or pancreatic disease or dysfunction
  • ·Unstable angina pectoris or recent (<3 months) myocardial infarction.
  • ·Coagulopathy

研究者

发起方
Bayer B.V.

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