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临床试验/EUCTR2016-004108-73-IT
EUCTR2016-004108-73-IT进行中(未招募)1 期

A Phase III, Open Label, Randomised, Controlled, Multi-Centre Study To Assess the Efficacy and Safety of Savolitinib versus Sunitinib in Patients with MET-Driven, Unresectable/Locally Advanced Or Metastatic Papillary Renal Cell Carcinoma (PRCC) - A phase III study to compare the efficacy and safety of a new anticancer medication, Savolitinib, wi

ASTRAZENECA SPA0 个研究点目标入组 180 人开始时间: 2020年2月11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)
入组人数
180

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

  • 1. Histologically confirmed PRCC, which is unresectable/locally advanced or metastatic with measurable disease as per RECIST 1.1.
  • 2. Confirmation of MET-driven PRCC without co-occurring FH or VHL mutations from an FFPE tumour sample using the sponsor-designated central laboratory
  • validated MET NGS assay
  • 3. Patients who have received no prior systemic therapy as well as those who have received prior systemic therapy for PRCC
  • 4. Adequate haematological, renal, cardiac and liver functions
  • 5. Karnofsky performance status = 80
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 1
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 90
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 90

排除标准

  • 1. Most recent cytotoxic chemotherapy, immunotherapy, chemo-immunotherapy, or investigational agents <21 days from the date of randomisation or 5 half-lives of the agent, whichever is longer. Most recent non-cytotoxic targeted therapy <14 days from the date of randomisation.
  • 2. Prior treatment with a MET inhibitor (e.g. foretinib, crizotinib, cabozantinib, onartuzumab or previous savolitinib) or sunitinb.
  • 3. Treatment with strong inducers or inhibitors of CYP3A4 or strong inhibitors of CYP1A2, taken within 2 weeks or not possible to be stopped for at least 2 week before the date of randomisation. Herbal medications cannot be taken within 7 days of the date of randomisation (3 weeks for St John’s wort).
  • 3. Wide field radiotherapy administered =28 days or limited field radiation for palliation =7 days prior to the date of randomisation
  • 4. Major surgical procedures =28 days of randomisation or minor surgical procedures =7 days. No waiting is required following port-a-cath placement.
  • 5. Previously untreated brain metastases
  • 6. Serious active infection or gastrointestinal disease
  • 7. Presence of other active cancers, or history of treatment for invasive cancer within the last 5 years.

研究者

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