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:
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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.
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