研究项目库 / NCT07776080

Iparomlimab and Tuvonralimab (QL1706)用于肝细胞癌的II 期研究

这是一项关于肝细胞癌的II 期研究,登记的药物或干预包括Iparomlimab and Tuvonralimab (QL1706);Lenvatinib;Radiotherapy;hepatic arterial infusion chemotherapy (HAIC),当前状态为招募中。登记地点显示中国武汉有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

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这是一项关于肝细胞癌的II 期研究,登记的药物或干预包括Iparomlimab and Tuvonralimab (QL1706);Lenvatinib;Radiotherapy;hepatic arterial infusion chemotherapy (HAIC),当前状态为招募中。登记地点显示中国武汉有研究中心记录。是否仍有名额以及是否值得进一步询问,需要向研究中心确认。

药物或干预

Iparomlimab and Tuvonralimab (QL1706);Lenvatinib;Radiotherapy;hepatic arterial infusion chemotherapy (HAIC) · II 期

中国哪些地方有记录

以下地点来自登记信息,不代表此刻仍有名额;请向研究中心确认最新情况。

  • Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China · 武汉

公开的入选条件

  • 1. Age ≥18 and ≤75 years at the time of signing informed consent.
  • 2. Histologically or clinically confirmed hepatocellular carcinoma (HCC) according to the 2024 Chinese Guidelines for the Diagnosis and Treatment of Primary Liver Cancer.
  • 3. Radiologically confirmed portal vein tumor thrombus (PVTT), classified as Cheng type I-IV.
  • 4. No prior systemic or local treatment directed at PVTT, including targeted therapy, immunotherapy, or systemic chemotherapy.
  • 5. Child-Pugh class A or B with a Child-Pugh score ≤7.
  • 6. Considered unsuitable for curative surgery or liver transplantation after multidisciplinary evaluation, but suitable for radiotherapy.
  • 7. Adequate organ function, including: WBC ≥3.0 × 10⁹/L; PLT ≥50 × 10⁹/L; hemoglobin ≥80 g/L; ALT ≤5 × ULN; AST ≤5 × ULN; total bilirubin ≤3 × ULN; albumin ≥28 g/L; and creatinine clearance ≥80 mL/min.
  • 8. At least one measurable lesion according to mRECIST.

联系前需要确认

请继续确认中心是否启动、疾病分型、既往治疗、检查费用和知情同意安排。

查看登记信息

登记号:NCT07776080;登记信息更新于 2026-09-15。

查看原始登记记录