研究项目库 / NCT07619235

Iparomlimab and Toripalimab用于胆道癌的IV 期研究

这是一项关于胆道癌的IV 期研究,登记的药物或干预包括Iparomlimab and Toripalimab;Bevacizumab;Gemcitabine (1000 mg/m2);Cisplatin,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。

一分钟看懂

这是一项关于胆道癌的IV 期研究,登记的药物或干预包括Iparomlimab and Toripalimab;Bevacizumab;Gemcitabine (1000 mg/m2);Cisplatin,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 Toripalimab;Bevacizumab;Gemcitabine (1000 mg/m2);Cisplatin · IV 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。

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

公开的入选条件

  • * Informed Consent: Patients voluntarily join this study and sign the informed consent form.
  • * Age: 18 to 75 years old, male or female.
  • * Histologically or cytologically confirmed, unresectable locally advanced or metastatic biliary tract cancer (BTC), including cholangiocarcinoma (intrahepatic and extrahepatic) and gallbladder carcinoma.
  • * No prior systemic anti-tumor therapy for locally advanced or metastatic BTC.
  • * At least one measurable lesion according to RECIST v1.1 that is suitable for accurate repeated measurement. Lesions previously irradiated or brain metastases are not eligible as target lesions.
  • * Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0 or 1.
  • * Adequate organ function
  • * For HBsAg positive subjects: HBV DNA must be \< 2000 IU/mL (or \< 10⁴ copies/mL), and effective antiviral therapy (e.g., Entecavir, Tenofovir, TAF, or Tenofovir Amibufenamide) must be administered throughout the study.

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:NCT07619235;登记信息更新于 2026-09-15。

查看原始登记记录