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临床试验/EUCTR2012-005371-13-GB
EUCTR2012-005371-13-GB进行中(未招募)1 期

A Phase 3, Randomized, Double- Blind Study of Nivolumab Monotherapy or Nivolumab Combined with Ipilimumab Versus Ipilimumab Monotherapy in Subjects with Previously Untreated, Unresectable or Metastatic MelanomaPharmacogenetics Blood Sample Protocol Amendment 01, version 1.0, dated 19-Mar-2013

Bristol-Myers Squibb International Corporation0 个研究点目标入组 1,144 人开始时间: 2013年5月15日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
入组人数
1,144

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

  • Histologically confirmed stage III (unresectable) or stage IV melanoma
  • Treatment naïve patients
  • Measurable disease by CT or MRI per RECIST 1.1 criteria.
  • Tumor tissue from an unresectable or metastatic site of disease for biomarker analyses.
  • ECOG PS 0 or 1
  • 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 795
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 349

排除标准

  • Active brain metastases or leptomeningeal metastases
  • Ocular melanoma
  • Subjects with active, known or suspected autoimmune disease
  • Subjects with a condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalents) or other immunosuppressive medications within 14 days of treatment
  • Prior treatment with an anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 antibody

研究者

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