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BL-M07D1 (Trastuzumab Brengitecan T-bren) vs Standard of Care Platinum-based Chemotherapy (PBC) for HER2-expressing Metastatic Urothelial Cancer After Progression on Anti-PD-(L)1-based Therapy

2026年11月9日 更新者:SystImmune Inc.

A Phase 3 Open-Label, Randomized Controlled Trial of T-bren (BL M07D1) vs. Platinum-based Chemotherapy in Patients With HER2 Expressing Metastatic Urothelial Cancer With Disease Progression on or After Anti-PD-(L)1-based Therapy

The objective of the study is to evaluate the efficacy and safety of T-bren in participants with HER2 expressing metastatic UC with progression on or after anti-PD-(L)1-based therapy.

研究概览

详细说明

This study is a Global Phase 3, randomized, open-label, multicenter study of T-bren for the treatment of metastatic UC. This study will assess the efficacy and safety of T-bren versus PBC in adult participants with HER2-expressing UC after progression on anti-PD-(L)1-based therapy.

研究类型

介入性

注册 (估计的)

520

阶段

  • 第三阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Georgia
      • Macon、Georgia、美国、31210
        • 招聘中
        • Central Georgia Cancer Center
        • 首席研究员:
          • Bradley Sumrall, MD
        • 接触:
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Histologically or cytologically documented metastatic or surgically unresectable transitional cell carcinoma (TCC) of the urothelium involving the renal pelvis, ureter, bladder, or urethra. Minor histologic variants (ie, <50% overall) are acceptable, provided that TCC is the dominant histology.
  • Disease progression or recurrence during or following anti-PD-(L)1-based therapy.
  • Fresh biopsy or archival tumor samples.
  • Documented HER2 expression by central laboratory testing.
  • Eligible to receive carboplatin or cisplatin in combination with gemcitabine.
  • At least 1 measurable lesion based on RECIST v1.1.
  • An Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 to 1.
  • Adequate organ function.
  • Adequate coagulation parameters.

Exclusion Criteria:

  • Prior topoisomerase inhibitor-based ADC therapy.
  • Primary tumors in the central nervous system (CNS), active or untreated CNS metastases, or carcinomatous meningitis.
  • Bladder cancers with small cell histology.
  • Other prior or concurrent malignancies except for certain localized cancers or low-grade prostate cancer (if approved by sponsor), or other malignancy treated with curative intent with a disease-free interval of at least 3 years.
  • Prior history of clinically significant bleeding, or perforation of the gastrointestinal tract within 6 months of randomization.
  • Active autoimmune diseases and inflammatory diseases.
  • History of noninfectious interstitial lung disease (ILD)/pneumonitis that required treatment with steroids, have current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at Screening.
  • Advanced/clinically significant lung disease (eg, poorly controlled chronic obstructive pulmonary disease or asthma, restrictive lung disease, or pulmonary hypertension) within 6 months prior to randomization.
  • Known human immunodeficiency virus infection.
  • Active hepatitis B virus (HBV) infection.
  • Active hepatitis C virus (HCV) infection.
  • Active or latent tuberculosis.
  • Other protocol-specified inclusion/ exclusion criteria apply

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Arm A, T-bren Dose Level 1

T-bren administered intravenously

T-bren: Administered intravenously on day 1 of each 21-day cycle

其他名称:
  • T-Bren
  • BL-M07D1
  • Trastuzumab Brengitecan
实验性的:Arm B, T-bren Dose Level 2

T-bren administered intravenously

TBren administered intravenously on day 1 of each 21-day cycle

其他名称:
  • T-Bren
  • BL-M07D1
  • Trastuzumab Brengitecan
有源比较器:Arm C, Control Arm, Platinum-based Chemotherapy (PBC)
  1. Gemcitabine Administered intravenously
  2. Cisplatin or Carboplatin Administered intravenously

Gemcitabine administered intravenously on Day 1 and Day 8 of each 21-day cycle and Cisplatin or Carboplatin administered intravenously on Day 1 of each 21-day cycle

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Progression-Free Survival (PFS)
大体时间:Approximately 5 years

Progression-Free Survival (PFS) by Blinded Independent Central Review (BICR) per RECIST v1.1 in the primary population

Approximately 5 years

次要结果测量

结果测量
措施说明
大体时间
Overall Survival (OS)
大体时间:Approximately 5 years

Overall Survival (OS) in primary population

Approximately 5 years
Progression-Free Survival (PFS) in the ITT population
大体时间:Approximately 5 years

Progression-Free Survival (PFS) by BICR per RECIST v1.1 in the ITT (Intent-to-Treat) Population

Approximately 5 years
Overall Survival (OS) in the ITT population
大体时间:Approximately 5 years
Approximately 5 years
Progression-Free Survival (PFS) by Investigator Assessment
大体时间:Approximately 5 years

Progression-Free Survival (PFS) by Investigator Assessment per RECIST v1.1

Approximately 5 years
Objective Response Rate (ORR) per RECIST v1.1
大体时间:Approximately 5 years
Approximately 5 years
Disease Control Rate (DCR) per RECIST v1.1
大体时间:Approximately 5 years
Approximately 5 years
Duration of Response (DOR) per RECIST v1.1
大体时间:Approximately 5 years
Approximately 5 years
Time to Response (TTR) per RECIST v1.1
大体时间:Approximately 5 years
Approximately 5 years
Adverse Events (AEs) and Serious Adverse Events (SAEs)
大体时间:Approximately 5 years
Approximately 5 years

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Jimmy Liu Zhao, MD, PhD、SystImmune Inc.

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月1日

初级完成 (估计的)

2028年12月1日

研究完成 (估计的)

2029年12月1日

研究注册日期

首次提交

2026年10月6日

首先提交符合 QC 标准的

2026年10月6日

首次发布 (实际的)

2026年10月13日

研究记录更新

最后更新发布 (实际的)

2026年11月10日

上次提交的符合 QC 标准的更新

2026年11月9日

最后验证

2026年11月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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