EUCTR2006-006824-20-DE进行中（未招募）1 期
Monocenter, double blinded, exploratory, randomized, study investigating the influence of Pasireotide on the hormonal activity of Pheochromocytoma – proof of concept study
niversitätsklinikum Essen - Zentrum für Innere Medizin - Klinik für Endokrinologie0 个研究点目标入组 12 人开始时间: 2007年7月23日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 12
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
- •Male and female patients.
- •Age: 18-80 years
- •Patients with malignant/ non-malignant Pheochromocytoma and/ or
- •Paraganglioma as shown by: - increased plasma values of metanephrines and
- •- confirmation by MRT/ CT not older than 3 months
- •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
- •Clinically significant renal or hepatic abnormalities.
- •Evidence of drug/alcohol abuse.
- •The patient has received any unlicensed drug within 30 days prior to screening.
- •Known hypersensitivity to somatostatin analogs
- •Karnovsky-Index <60
- •Pregnancy or breast-feeding
- •Known immunosuppression
- •Other malignant diseases, except Basalioma or in-situ Cervix carcinoma
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