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临床试验/NL-OMON39828
NL-OMON39828已完成不适用

An open label phase I dose finding study of BI 853520 administered orally in a continuous dosing schedule in patients with various advanced or metastatic non-hematologic malignancies - BI 853520 in solid tumours

Boehringer Ingelheim0 个研究点目标入组 45 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
45

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - Patients with a confirmed diagnosis of advanced, measurable or evaluable, non-resectable and/or metastatic non-hematologic malignancy, which has shown to be progressive in the last 6 months as demonstrated by serial imaging;
  • - Patients who have failed conventional treatment or for whom no therapy of proven efficacy exists or who are not amenable to established treatment options;
  • -Tumour tissue must be available for the determination of E-cadherin expression (archived tissue or fresh biopsy);
  • - Recovery from reversible toxicities (alopecia excluded) of prior anti-cancer therapies (CTCAE grade < 2);
  • - Age >= 18 years;
  • - Written informed consent in accordance with International Conference on Harmonisation/Good Clinical Practice (ICH/GCP) and local legislation;
  • - Eastern Cooperative Oncology Group (ECOG), performance score 0-1;
  • Additional inclusion criteria in the expansion phase:
  • - Patients must have measurable progressive disease within the last 6 months, according to Response Evaluation Criteria in Solid Tumours (RECIST) criteria;
  • - Patients must be willing to provide paired tumour biopsies for PD determination. Refer to section 5.6.3;
  • - Patients should fit into one of the categories described below:;
  • I. Metastatic adenocarcinoma of the pancreas;
  • Patients should have preferably received at least one line of systemic treatment for metastatic disease and preferably not more than 2 prior regimens for metastatic disease.;
  • II. Platinum-resistant ovarian carcinoma, defined as recurrence within 6 months after completion of prior platinum-based chemotherapy;
  • Patients should have preferably received no more than 5 previous lines of systemic treatment for metastatic disease;
  • III. Oesophageal carcinoma;
  • Patients with oesophageal carcinoma of adenocarcinoma- or squamous cell histology who have received preferably not more than 2 previous lines of systemic treatment for metastatic disease;
  • IV. Soft tissue sarcoma;
  • Patients should preferably have received no more than 2 previous lines of systemic treatment for metastatic disease.;

排除标准

  • - Serious concomitant non-oncological disease/illness;- Pregnancy or breastfeeding;- Active/symptomatic brain metastases;- Second malignancy;- Women or men who are sexually active and unwilling to use a medically acceptable method of contraception ;- Treatment with cytotoxic anti-cancer-therapies or investigational drugs within four weeks of the first treatment with the study medication

研究者

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