已完成 NCT04567615

Relatlimab联合Nivolumab用于曾接受酪氨酸激酶抑制剂治疗后、从未接受免疫肿瘤治疗的晚期肝癌参与者的研究

肝癌胆道癌肉瘤Phase IIIII 期IV 期

本研究旨在评估relatlimab联合nivolumab在曾接受酪氨酸激酶抑制剂治疗后、从未接受免疫肿瘤治疗的晚期肝癌参与者中的疗效及安全性。

适应症:Hepatocellular Carcinoma、Hepatoma、Liver Cancer, Adult、Liver Cell Carcinoma、Liver Cell Carcinoma, Adult

入组条件

纳入标准

  • Must have a diagnosis of hepatocellular carcinoma (HCC) based on histological confirmation
  • Must have advanced/metastatic HCC
  • Have to be immunotherapy treatment-naive in the advanced/metastatic setting
  • Must have at least one Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 measurable untreated lesion
  • Child-Pugh score of 5 or 6
  • Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 for ECOG performance status scale

排除标准

  • Known fibrolamellar HCC, sarcomatoid HCC, combined hepatocellular cholangiocarcinoma
  • Prior organ allograft or allogeneic bone marrow transplantation
  • No uncontrolled or significant cardiovascular disease
  • No active known autoimmune disease
  • Have received one or two lines of tyrosine kinase inhibitor therapies
  • Evidence of radiographic progression on or after the last line of tyrosine kinase inhibitor therapy

入组条件维持 ClinicalTrials.gov 原始英文登记资料,实际入组资格以研究团队的正式评估与受试者知情同意书为准。资料来源:ClinicalTrials.gov,每两周自动更新,最后同步:2026年10月8日。