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Becotatug Vedotin Plus Cisplatin and Radiotherapy in LA-ESCC

2026年7月6日 更新者:Jun wang、Hebei Medical University Fourth Hospital

A Phase Ib, Open-Label, Single-Arm Study of Becotatug Vedotin Combined With Cisplatin and Concurrent Radiotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma

This study is a prospective, single-arm, single-center Phase Ib clinical trial of Becotatug Vedotin in combination with cisplatin and concurrent radiotherapy for locally advanced esophageal squamous cell carcinoma. The primary objectives are to investigate the maximum tolerated dose (MTD), dose-limiting toxicity (DLT), and recommended Phase II dose (RP2D) of Becotatug Vedotin in combination with cisplatin and concurrent radiotherapy for locally advanced esophageal squamous cell carcinoma. The secondary objectives are to assess the efficacy and safety of this combination regimen.

研究概览

详细说明

This study is a prospective, open-label, single-center, dose-escalation Phase I clinical trial. During the dose-escalation phase, the classic "3+3" design will be used to guide dose escalation in order to determine the maximum tolerated dose (MTD) and recommended Phase II dose (RP2D). Eligible subjects who meet the inclusion and exclusion criteria will receive two cycles of Becotatug Vedotin in combination with cisplatin and concurrent radiotherapy, followed by subsequent systemic therapy per the investigator's discretion. The dose levels of Becotatug Vedotin are 1.5 mg/kg, 2.0 mg/kg, and 2.3 mg/kg (D1,IV,Q3W). Cisplatin is administered at a dose of 75 mg/m² (D1,IV,Q3W). The total radiotherapy dose is 50.4 Gy, delivered in 28 fractions of 1.8 Gy each. Dose-limiting toxicities (DLTs) will be observed during the treatment period until the completion of the entire concurrent chemoradiotherapy phase.

研究类型

介入性

注册 (估计的)

12

阶段

  • 阶段1

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

    • Hebei
      • Shijiazhuang、Hebei、中国、050000
        • The Fourth Hospital of Hebei Medical University
        • 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

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  • Subjects who are able to understand and voluntarily sign informed consent forms (ICFs).
  • Male and female subjects at the age of ≥18 and ≤75 at the time of screening.
  • Histologically confirmed esophageal squamous cell carcinoma staged as cT2-T4a, N0-N+, M0-M1 (M1 limited to supraclavicular lymph node metastasis only).
  • Patients must have at least one measurable lesion as defined by RECIST version 1.1 criteria.
  • Patients who have not received any prior anti-tumor treatment for esophageal cancer.
  • ECOG score of 0 or 1.
  • Life expectancy ≥ 3 months.
  • Adequate organ function (no blood transfusion and no use of granulocyte colony-stimulating factor, or other hematopoietic stimulator support within 2 weeks before the first administration of the study drug) confirmed as evidenced by:

    1. Absolute Neutrophil Count (ANC) ≥ 1.5×10^9/L;
    2. Hemoglobin (Hgb) ≥ 90 g/dl;
    3. Platelets (Plt) ≥ 75×10^9/L;
    4. Bilirubin total ≤ 1.5 x ULN, or bilirubin direct < ULN for patients with bilirubin total levels >1.5 ULN;
    5. AST/ALT ≤ 2.5 x ULN or ≤ 5.0 x ULN if liver metastases are present;
    6. Serum creatinine < 1.5 x ULN or creatinine clearance > 50 mL/min (as calculated via Cockcroft-Gault formula based on the actual body weight of the subject ;
  • Female subjects must not be pregnant or breastfeeding. Female or male subjects of childbearing potential must agree to practice effective contraceptive measures throughout the study period and for 6 months after completion of study treatment.

Exclusion Criteria:

  • Diagnosis of any other malignancy within the past 5 years (excluding carcinoma in situ, basal cell carcinoma, etc.).
  • Anyone allergic to any drug or any of its components in this regimen.
  • Patients with a prior history of surgery for esophageal squamous cell carcinoma.
  • Patients with a prior history of fistula caused by primary tumor infiltration.
  • Patients at high risk of gastrointestinal bleeding, esophageal fistula, or esophageal perforation.
  • Subjects with poor nutritional status, defined as BMI < 18.5 kg/m² or PG-SGA score ≥ 9.
  • Patients with a diagnosis of pulmonary fibrosis or interstitial pneumonia within 28 days prior to enrollment.
  • Active infections such as HIV; active chronic HBV/HCV (e.g., HBV DNA ≥ 10⁴ copies/mL or ≥ 2000 IU/mL) requiring antiviral and hepatoprotective therapy before enrollment. Enrollment is allowed only when HBV DNA decreases to < 10⁴ copies/mL or < 2000 IU/mL, with continued antiviral therapy and regular monitoring of liver function and HBV DNA levels.
  • Presence of major cardiovascular disease, including any of the following conditions:

    1. Congestive heart failure (defined as New York Heart Association [NYHA] Class III or IV), myocardial infarction, unstable angina, coronary angioplasty, stent implantation, coronary artery bypass grafting, cerebrovascular accident (CVA), or hypertensive crisis within 6 months prior to enrollment.
    2. History of clinically significant ventricular arrhythmias (e.g., sustained ventricular tachycardia, ventricular fibrillation, torsade de pointes).
    3. Fridericia-corrected QT interval (QTcF) > 450 msec in males or > 470 msec in females.
    4. History or family history of congenital long QT syndrome.
    5. Arrhythmias requiring antiarrhythmic therapy (subjects with atrial fibrillation that has been controlled for more than 30 days prior to randomization may be enrolled).
    6. History of deep vein thrombosis, pulmonary embolism, or any other serious thromboembolic event within 3 months prior to enrollment (thrombosis related to an implanted venous access port or catheter, or superficial venous thrombosis, is not considered "serious" thromboembolism).
  • Severe chronic diarrhea.
  • Severe psychiatric disorder.
  • Use of strong inhibitors or inducers of CYP3A4, CYP2C8, and UGT1A1.
  • Participation in another clinical trial within 4 weeks prior to enrollment.
  • Patients who, in the opinion of the investigator, are unsuitable for participation in this study.

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:不适用
  • 介入模型:单组作业
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的:Becotatug vedotin + Cisplatin + Radiotherapy
Participants receive Becotatug vedotin (MRG003) in combination with Cisplatin and concurrent radiotherapy. During the dose-escalation phase, the classic "3+3" design will be used to guide dose escalation in order to determine the maximum tolerated dose (MTD) and recommended Phase II dose (RP2D). Eligible subjects who meet the inclusion and exclusion criteria will receive two cycles of Becotatug Vedotin in combination with cisplatin and concurrent radiotherapy, followed by subsequent systemic therapy per the investigator's discretion.
  • Becotatug Vedotin:1.5mg/kg 、2.0mg/kg、2.3mg/kg,d1;IV; Q3W
  • Cisplatin:75mg/m2,d1;IV; Q3W
  • Radiotherapy:50.4Gy/28f/1.8Gy

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
Maximum Tolerated Dose (MTD)
大体时间:Cycle 1 (21 days)
MTD is defined as the highest dose level at which DLT is observed in ≤ 1/6 subjects at one single dose group
Cycle 1 (21 days)
Recommended Phase 2 Dose (RP2D)
大体时间:Cycle 1 (21 days)
RP2D will be a dose either below or equal to MTD
Cycle 1 (21 days)
Dose Limiting Toxicity (DLT)
大体时间:Cycle 1 (21 days)
DLT will be evaluated according to NCI-CTCAE V5.0 criteria
Cycle 1 (21 days)

次要结果测量

结果测量
措施说明
大体时间
Objective response rate(ORR)
大体时间:From first treatment date until disease progression or death, assessed every 6 weeks, up to approximately 36 months
Objective response rate (ORR) is the proportion of subjects with the best overall response being CR or PR (assessed by investigator per RECIST v1.1)
From first treatment date until disease progression or death, assessed every 6 weeks, up to approximately 36 months
Disease Control Rate (DCR)
大体时间:From first treatment date until disease progression or death, assessed every 6 weeks, up to approximately 36 months
Disease Control Rate (DCR) is defined as the proportion of patients who achieve a best overall response of Complete Response (CR), Partial Response (PR), or Stable Disease (SD) according to RECIST 1.1 criteria, among the total number of evaluable patients.
From first treatment date until disease progression or death, assessed every 6 weeks, up to approximately 36 months
Progression free survival (PFS)
大体时间:From first treatment date to disease progression or death, up to 36 months
Progression-Free Survival (PFS) is defined as the time from randomization (or first dose of study treatment) to the first documented disease progression per RECIST 1.1 criteria, or death from any cause, whichever occurs first.
From first treatment date to disease progression or death, up to 36 months
2-year overall survival (OS) rate
大体时间:From first treatment date to death from any cause, assessed up to 36 months
The 2-year overall survival (OS) rate is defined as the percentage of patients who remain alive at 2 years after the start of study treatment.
From first treatment date to death from any cause, assessed up to 36 months
Incidence and severity of adverse events (AEs)
大体时间:From first dose date through study completion, up to 36 months
severity determined according to National Cancer Institute Common Terminology Criteria for Adverse Events [NCI CTCAE] Version [v] 5.0
From first dose date through study completion, up to 36 months

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。

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7月1日

初级完成 (估计的)

2029年7月1日

研究完成 (估计的)

2029年12月31日

研究注册日期

首次提交

2026年6月20日

首先提交符合 QC 标准的

2026年7月6日

首次发布 (实际的)

2026年7月10日

研究记录更新

最后更新发布 (实际的)

2026年7月10日

上次提交的符合 QC 标准的更新

2026年7月6日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

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