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
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
地位
条件
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
注册 (估计的)
阶段
- 第三阶段
联系人和位置
学习联系方式
- 姓名:Christine LaRock
- 电话号码:425-453-6841
- 邮箱:Christine.LaRock@systimmune.com
学习地点
-
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Georgia
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Macon、Georgia、美国、31210
- 招聘中
- Central Georgia Cancer Center
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首席研究员:
- Bradley Sumrall, MD
-
接触:
- Mackenzie Sanders, Study Coordinators
- 电话号码:478-743-7068
- 邮箱:mackenzie.sanders@aoncology.com
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接触:
- Rachel Warfield, Study Coordinators
- 电话号码:478-743-7068
- 邮箱:rachel.warfield@aoncology.com
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
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
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:
|
|
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:
|
|
有源比较器:Arm C, Control Arm, Platinum-based Chemotherapy (PBC)
|
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
调查人员
- 研究主任:Jimmy Liu Zhao, MD, PhD、SystImmune Inc.
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- BL-M07D1-UC-301
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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