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临床试验/CTIS2023-508635-31-00
CTIS2023-508635-31-00进行中(未招募)1 期

CA209-9DW - A Randomized, Multi-center, Phase 3 Study of Nivolumab in Combination with Ipilimumab Compared to Sorafenib or Lenvatinib as First-Line Treatment in Participants with Advanced Hepatocellular Carcinoma - CA209-9DW

Bristol Myers Squibb International Corporation0 个研究点目标入组 763 人开始时间: 2024年1月31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
763

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Participants must have a diagnosis of HCC based on histological confirmation, Participants must have an advanced HCC, Participants must have at least one Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 measurable previously untreated lesion, Child-Pugh score 5 or 6, Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1

排除标准

  • Known fibrolamellar HCC, sarcomatoid HCC, or mixed cholangiocarcinoma and HCC, Prior liver transplant, Episodes of hepatic encephalopathy (greater than or equal to [>=] Grade 2) within 12 months prior to randomization, Active brain metastases or leptomeningeal metastases

研究者

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