EUCTR2014-002123-10-DK进行中（未招募）1 期
Phase I/II open label, dose escalation trial to determine the MTD, safety, PK and efficacy of afatinib monotherapy in children aged =1 year to <18 years with recurrent/refractory neuroectodermal tumours, rhabdomyosarcoma and/or other solid tumours with known ErbB pathway deregulation regardless of tumour histology - Phase I/II trial of afatinib in pediatric tumours
SCS Boehringer Ingelheim Comm. V0 个研究点目标入组 55 人开始时间: 2015年5月4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）
- 发起方
- 入组人数
- 55
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
- •- Paediatric patients
- •- aged =1 year - <18 years at the time of informed consent
- •- who present with recurrent/refractory disease after they received at least one prior standard treatment regimen and for whom no effective conventional therapy exists
- •- Dose finding part: patients with a diagnosis of HGG, DIPG, low grade astrocytoma, neuroblastoma, ependymoma, medulloblastoma/PNET, RMS, and/or solid tumours with known ErbB pathway deregulation regardless of tumour histology.
- •- MTD expansion cohorts/Phase II part: Patients with HGG, DIPG, EM and other solid tumours than aforementioned which fulfil at least two of the below criteria:
- •o EGFR gene amplification (FISH): Either EGFR/Cen7 = 2.0 or =10% of cells with =15 copies or =40% of cells with = 4 copies or gene cluster in =10% of cells and/or
- •o HER2 gene amplification (DDISH): Her2/CEP17 = 2.0 and/or
- •o EGFR protein expression: H-score > 150 (membrane staining) and/or
- •o HER2 protein expression: H-score > 0 (membrane staining)
- •Inclusion will be based on biomarker assessment prior to inclusion, as detected by central laboratory analysis of tumour biopsy materia
- •- Patients with proven genomic, transcriptomic or proteomic ErbB alterations which are not defined in the above regardless of tumour histology
- •-Performance status >= 50% (Lansky for =<12ys; Karnofsky for >12ys)
- •Are the trial subjects under 18? yes
- •Number of subjects for this age range: 55
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •-relevant toxicity from previous treatment
- •-known pre-existing relevant cardiac , hepatic, renal, bone marrow dysfunction, ILD, keratitis
研究者
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