EUCTR2012-004053-88-GB进行中（未招募）1 期
Second International Inter-Group Study for Classical Hodgkin's Lymphoma in Children and Adolescents - EuroNet-PHL-C2
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 2,200
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
- •* Histologically confirmed primary diagnosis of classical Hodgkin’s lymphoma
- •* Patients under 18 years of age on the date of written informed consent. In specialised Teenage and Young Adult (TYA) units in France, Italy and UK patients under 25 years of age can also be enrolled. Lower age limits will be country specific according to national laws or formal insurance requirements that may preclude very young Patients.
- •* Written informed consent of the Patient and/or the Patient’s Parents or Guardian according to national laws
- •* Negative pregnancy test within 2 weeks prior to starting treatment for female Patients with childbearing potential
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 0
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 0
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 0
排除标准
- •Patients with one or more of the following criterion are excluded:
- •* Prior chemotherapy or radiotherapy for other malignancies
- •* Pre-treatment of Hodgkin’s lymphoma (except for 7-10 days steroid pre-phase of a large mediastinal tumour)
- •* Diagnosis of lymphocyte-predominant Hodgkin’s lymphoma
- •* Other (simultaneous) malignancies
- •* Contraindication or known hypersensitivity to study drugs
- •* Severe concomitant diseases (e.g. immune deficiency syndrome)
- •* Known HIV-positivity
- •* Residence outside the participating countries where long term follow-up cannot be guaranteed
- •* Pregnancy and/or lactation
- •* Patients who are sexually active and are unwilling to use adequate contraception during therapy and for one year after last trial treatment
- •* Current or recent (within 30 days prior to date of written informed consent) treatment with another investigational drug or participation in another interventional clinical trial
研究者
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已完成
3 期
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