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临床试验/NCT07324629
NCT07324629招募中2 期

A Phase II Clinical Study of Sacituzumab Tirumotecan in Participants With Locally Advanced or Metastatic Thymic Carcinoma With Treatment Failure After Platinum-Based Therapy

Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd.1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2026年3月13日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
30
试验地点
1
主要终点
ORR

研究概览

简要总结

The goal of this clinical trial is to learn if drug Sac-TMT works to treat Thymic Carcinoma. It will also learn about the safety of Sac-TMT. The main questions it aims to answer are:

  • How effective is drug Sac-TMT in treating Thymic Carcinoma?
  • What adverse events (AEs) do participants have when taking drug Sac-TMT?

Participants will:

  • Progress after at least one platinum-based chemotherapy treatment.
  • Take drug Sac-TMT every 2 weeks.
  • Take tumor response assessments every 6 weeks.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Males or females aged ≥ 18 to ≤ 75 years at the time of signing the Informed Consent Form;
  • •Participants with histologically or cytologically confirmed thymic carcinoma, and locally advanced or metastatic thymic carcinoma who are not suitable for curative intent therapy;
  • •Participants with advanced thymic carcinoma who have progressed after at least one prior platinum-based chemotherapy;
  • •Able to provide a tumor tissue sample at the time of or after the diagnosis of locally advanced or metastatic tumor;
  • •At least one measurable target lesion that has not received radiotherapy according to RECIST v1.1;
  • •ECOG performance status score of 0 or 1;
  • •Expected survival ≥ 12 weeks;
  • •Adequate organ and bone marrow function.

排除标准

  • •Participants with histologically or cytologically confirmed thymoma or thymic neuroendocrine tumor;
  • •Participants with known metastases to meninges, brainstem metastases, spinal cord metastases and/or compression, active or untreated brain metastases;
  • •Participants with other malignant tumors within 3 years prior to the first dose;
  • •Presence of any of conditions or risk factors related to cardiovascular and cerebrovascular diseases;
  • •Uncontrolled systemic disease as judged by the investigator;
  • •History of interstitial lung disease/noninfectious pneumonitis requiring steroid therapy;
  • •Clinically severe pulmonary impairment due to lung disorder;
  • •Presence of active hepatitis B or hepatitis C;
  • •Known active tuberculosis;
  • •Known hypersensitivity to the study drug or any of its components.

研究组 & 干预措施

Sac-TMT 5mg/kg Q2W

Experimental

干预措施: Sacituzumab tirumotecan (Drug)

结局指标

主要结局

ORR

时间窗: From enrollment to the end of treatment at 24 months

To evaluate the objective response rate (ORR) of sac-TMT as assessed by the investigator based on RECIST v1.1.

ORR

时间窗: From enrollment to the end of treatment at 24 months

To evaluate the objective response rate (ORR) of sac-TMT as assessed by the investigator based on RECIST v1.1.

次要结局

  • PFS(From enrollment to the end of treatment at 24 months)
  • OS(From enrollment to the end of treatment at 24 months)
  • Incidence and severity of AEs and SAEs, and abnormal laboratory values.(From enrollment to the end of treatment at 24 months)
  • PFS(From enrollment to the end of treatment at 24 months)
  • OS(From enrollment to the end of treatment at 24 months)
  • Incidence and severity of AEs and SAEs, and abnormal laboratory values.(From enrollment to the end of treatment at 24 months)
  • DCR(From enrollment to the end of treatment at 24months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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