研究项目库 / NCT07842276

UTD2 + tislelizumab + doxorubicin用于肉瘤的II 期研究

这是一项关于肉瘤的II 期研究,登记的药物或干预包括UTD2 + tislelizumab + doxorubicin,当前状态为尚未开始招募。登记地点显示中国成都有研究中心记录。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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这是一项关于肉瘤的II 期研究,登记的药物或干预包括UTD2 + tislelizumab + doxorubicin,当前状态为尚未开始招募。登记地点显示中国成都有研究中心记录。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

UTD2 + tislelizumab + doxorubicin · II 期

登记条件中文摘要

登记的基本范围为不限性别,年龄18 岁至70 岁;另列出8项专业入选条件,需结合英文原文并由研究团队确认。

登记记录列出8项主要排除条件,具体医学含义需结合英文原文并由研究团队确认。

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。

  • West China Hospital Sichuan University · 成都

公开的入选条件

  • 1. Fully understand the purpose, content, process of the trial and possible adverse reactions, voluntarily participate as a subject, and sign the informed consent form;
  • 2. Age of 18-70 years old (including 18 and 70 years old) at the time of informed consent (ICF) signing, regardless of gender.
  • 3. Histopathologically /cytologically confirmed unresectable locally advanced or metastatic soft tissue sarcoma (classified per the 5th WHO classification, including leiomyosarcoma, liposarcoma, angiosarcoma, epithelioid sarcoma, synovial sarcoma, undifferenti
  • 4. No prior systemic anti-tumor therapy for advanced soft tissue sarcoma. For participants with prior neoadjuvant or adjuvant therapy, disease progression must occur \>6 months after the last treatment.
  • 5. At least one measurable lesion according to RECIST v1.1 definition.
  • 6. ECOG performance status of 0 or 1, with an expected survival of more than 12 weeks.
  • 7. Within 1 week before enrollment, the participant's blood routine examination was basically normal, and within 2 weeks before enrollment, the participant did not receive recombinant human granulocyte colony-stimulating factor (rhG-CSF) or blood products/eryt
  • Absolute neutrophil count (ANC) ≥1.5×10⁹/L;

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:NCT07842276;登记信息更新于 2026-09-25。

查看原始登记记录