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临床试验/EUCTR2016-000589-47-CZ
EUCTR2016-000589-47-CZ进行中(未招募)1 期

A Phase II Single-arm, Open-label Monotherapy Clinical Trial of Pembrolizumab (MK-3475) in Locally Advanced/Metastatic Renal Cell Carcinoma (mRCC) (KEYNOTE-427) - Pembrolizumab in advanced renal cell carcinoma

Merck Sharp & Dohme Corp.0 个研究点目标入组 255 人开始时间: 2016年8月19日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
255

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

  • - Provide written informed consent/assent for the trial
  • - Be > or = 18 years of age on day of signing informed consent
  • - Cohort A (clear cell cohort) must have histologically confirmed diagnosis of clear cell RCC or RCC with clear cell component (with or without sarcomatoid features)
  • - Cohort B (non-clear cell cohort) must have histologically confirmed diagnosis of non-clear cell RCC (with or without sarcomatoid features). Confirmation of the diagnosis of non-clear cell RCC by central histology review during the screening phase is required prior to allocation to Cohort B
  • - Have locally advanced/metastatic disease, i.e., Stage IV RCC per American Joint Committee on Cancer (AJCC) or have recurrent disease
  • - Have measurable disease per RECIST 1.1 as assessed by BICR. Target lesions situated in a previously irradiated area are considered measurable if progression has been demonstrated in such lesions
  • - Have received no prior systemic therapy for advanced RCC
  • - Provide adequate tissue for biomarker analysis for cohorts A and B
  • - Demonstrate adequate organ function
  • 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 120
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 135

排除标准

  • - Is currently participating in or has participated in a study of an investigational agent or using an investigational device within 4 weeks prior to allocation, has had major surgery within 4 weeks prior to allocation or radiation therapy within 2 weeks prior to allocation, or who has not recovered (i.e., < or = Grade 1 or at baseline) from adverse events due to prior treatment
  • - Had prior treatment with any anti-PD-1, or PD-L1, or PD-L2 agent or an antibody targeting any other immune-regulatory receptors or mechanisms. Examples of such antibodies include (but are not limited to) antibodies against IDO, PD-L1, IL-2R, GITR
  • - Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment, except in the case of central nervous system (CNS) metastases
  • - Has an active autoimmune disease requiring systemic treatment within the past 3 months or a documented history of clinically severe autoimmune disease, or a syndrome that requires systemic or immunosuppressive agents
  • - Has a known additional malignancy that has had progression or has required active treatment in the last 3 years. Note: Subjects with basal cell carcinoma of the skin, squamous cell carcinoma of the skin that has undergone potentially curative therapy or carcinoma in situ are not excluded
  • - Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis
  • - Has a history of (non-infectious) pneumonitis that required steroids or current pneumonitis
  • - Has had a prior solid organ transplant

研究者

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