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临床试验/EUCTR2014-002480-15-NL
EUCTR2014-002480-15-NL进行中(未招募)不适用

A Phase II, Open-Label, Multicenter Study of Vemurafenib plus Cobimetinib (GDC-0973) in Unresectable Stage IIIc or Metastatic Melanoma; Response Monitoring and Resistance Prediction with Positron Emission Tomography and Tumor Characteristics. - REPOSIT

The Dutch Working Group on Immunotherapy of Oncology (WIN-O)0 个研究点开始时间: 2014年10月15日最近更新:
适应症
相关药物

试验速览

阶段
不适用
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 histologically confirmed melanoma, either unresectable stage IIIc or stage IV metastatic melanoma, as defined by AJCC 7th edition.
  • Patients must be naïve to treatment for locally advanced unresectable or metastatic disease. Prior adjuvant immunotherapy (including ipilimumab) is allowed.
  • Documentation of BRAFV600 mutation-positive status in melanoma tumor tissue (archival or newly obtained tumor samples).
  • Measurable disease per RECIST v1.1 (50), which are accessible to biopsies.
  • Biopsy lesion is within scan reach of diagnostic CT and PET-CT (thorax- abdomen-pelvis)
  • ECOG performance status of 0 or 1.
  • Male or female patient aged = 18 years.
  • Life expectancy = 12 weeks.
  • Adequate hematologic and end organ function within 14 days prior to first dose of study drug treatment.
  • 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 70
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 20

排除标准

  • History of prior RAF or MEK pathway inhibitor treatment.
  • Palliative radiotherapy, major surgery or traumatic injury within 14 days prior to the first dose of study treatment.
  • Active malignancy within the past 3 years other than melanoma that could potentially interfere with the interpretation of efficacy measures.
  • History of or evidence of retinal pathology, clinically significant cardiac dysfunction, patients with active CNS lesions, renal or liver dysfunction as described in main protocol (REPOSIT NL48639.031.14).
  • Pregnant, lactating, or breast-feeding.
  • Unwillingness or inability to comply with study and follow-up procedures (i.e. severe anxiety disorder preventing PET/CT imaging.

研究者

发起方
The Dutch Working Group on Immunotherapy of Oncology (WIN-O)

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