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A Study of Risvutatug Rezetecan in Combination With Ivonescimab in Participants With Advanced Solid Tumors (EMBOLD PanTumour-103)

2026年9月4日 更新者:GlaxoSmithKline

A Phase 1/2 Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Clinical Activity of Risvutatug Rezetecan in Combination With Ivonescimab in Participants With Advanced Solid Tumors

This is an early-phase clinical study investigating a new combination treatment, Risvutatug rezetecan (Ris-Rez) given with ivonescimab for adults with advanced solid cancers. The study aims to determine:

  • What dose(s) of Ris-Rez given with ivonescimab is safe and what are the side effects?
  • How does the body handle the drug(s)?
  • What dose of Ris-Rez given with ivonescimab may work best and can improve the treatment of cancer?

研究概览

研究类型

介入性

注册 (估计的)

184

阶段

  • 阶段2
  • 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

研究联系人备份

学习地点

      • Osaka、日本、573-1191
        • GSK Investigational Site
        • 接触:
        • 接触:
        • 首席研究员:
          • Toshio Shimizu

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:

Participants are eligible to be included in the study only if all the following criteria apply:

  • Male or female participants at least 18 years of age (≥18 years) at the time of signing the informed consent form (ICF).
  • Participants with histologically confirmed advanced/metastatic solid tumors, irrespective of mutational status, as defined per cohort, as follows:

ES-SCLC

  • Histologically or cytologically confirmed SCLC (prior pathological diagnosis of complex SCLC [such as mixed SCLC and NSCLC] or transformed SCLC [NSCLC to SCLC] is not allowed)
  • ES-SCLC [per Veterans Administration Lung Study Group (VALG) criteria] at study entry Squamous NSCLC or non-squamous NSCLC
  • Histologically or cytologically confirmed Squamous or Non-squamous NSCLC.
  • Metastatic NSCLC (Stage IV), according to American Joint Committee on Cancer (AJCC) 8th edition,
  • Has at least 1 target lesion per RECIST 1.1, as determined by the investigator. Measurable lesions that have been previously irradiated and have been shown to be progressing following irradiation may be considered as TLs.
  • Has an ECOG performance status of 0 or 1, with no deterioration in the 2 weeks before first dose.
  • Has a life expectancy of ≥ 3 months with ability to complete at least 4 cycles of study intervention.
  • Has adequate organ function
  • Is willing to use adequate contraception (contraceptive use by male and female participants should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies).
  • For dose expansion only: Tumor tissue (archival tumor tissue or a fresh biopsy) is required for all participants at screening. Tissue from a newly obtained fresh biopsy is preferred. If it is not feasible to obtain a fresh biopsy at screening, archival tumor tissue, (from the most recent biopsy (within 1 year), Formalin Fixation and Paraffin Embedding FFPE) block (preferred), or freshly cut slides is acceptable. If archival tissue is unavailable and it is not medically feasible to obtain fresh tissue, the medical monitor should be informed and exemption to the tissue requirement may be granted on a case-by-case basis. Tumor tissue is necessary for retrospective detection of B7 homolog 3 protein (B7-H3) expression and other biomarker analysis

Exclusion Criteria:

Participants are excluded from the study if any of the following criteria apply:

• Has ongoing adverse reaction(s) from prior therapy that has (have) not recovered to ≤Grade 1 or to baseline status preceding prior therapy (excluding alopecia, hearing loss, vitiligo, endocrinopathy managed with replacement therapy, and Grade 1 neuropathy).

Has had major surgical procedures or serious trauma within 4 weeks prior to first dose, or plans for major surgical procedures within 4 weeks after the first dose (as determined by the investigator), or minor local procedures (excluding central venous catheterization and port implantation) within 3 days prior to first dose.

  • Has symptomatic Central Nervous System (CNS) metastases, CNS metastases with hemorrhagic features, CNS metastasis ≥ 1.5 cm, CNS radiation within 7 days prior to first dose, potential need for CNS radiation within the first cycle, or leptomeningeal disease. Patients must have stopped corticosteroids or be on physiologic corticosteroid replacement therapy (prednisone ≤ 10 mg daily or equivalent).
  • Has any of the following:

    • QTc >450 msec or QTc >480 msec for participants with bundle branch block.
    • Evidence of current clinically significant arrhythmias or ECG abnormalities (e.g., complete left bundle branch block, third-degree atrioventricular block, second-degree atrioventricular block, PR interval >250 msec).
    • Risk factors of prolonged QTc or arrhythmia events, such as heart failure, refractory hypokalemia, congenital long QT syndrome, family history of long QT syndrome, or unexplained sudden death of any direct relative under 40 years old or any concomitant medications that prolong the QT interval.
    • Left Ventricular Ejection Fraction (LVEF) <50%.
  • Has severe, uncontrolled or active CV disorders
  • Serious or poorly controlled hypertension; adjustment of antihypertensive medications due to poor blood pressure control within 2 weeks prior to the first dose; recurrent systolic blood pressure ≥150 mmHg or diastolic blood pressure ≥100 mmHg during screening period.
  • History of bleeding tendencies or coagulopathy and/or clinically significant bleeding symptoms or risk within 4 weeks prior to first dose, including but not limited to:

    • Hemoptysis (defined as coughing up ≥ 1 teaspoon of fresh blood or small blood clots)
    • Transient hemoptysis associated with diagnostic bronchoscopy is allowed.
    • Nasal bleeding/epistaxis (bloody nasal discharge is allowed)
    • Current use of prophylactic or full-dose anticoagulants or anti-platelet agents for therapeutic purposes that is not stable prior to first dose is not allowed.
  • Participants with a history of esophageal or gastric varicose vein, severe ulcer, unhealed wound, gastrointestinal perforation, abdominal fistula, gastrointestinal obstruction, intra-abdominal abscess, or acute gastrointestinal hemorrhage within 6 months prior to first dose.
  • History of any grade arterial thromboembolic event, Grade 3 and above venous thromboembolic event, as specified in National Cancer Institute-Common Terminology Criteria for Adverse Events (NCI-CTCAE) 6.0, hypertensive crisis, or hypertensive encephalopathy, within 12 months prior to the first dose.
  • Serious infections within 4 weeks prior to the first dose, including but not limited to infectious complications, bacteremia, severe pneumonia treated with IV antibiotics for ≥ 2 weeks; active infections with therapeutic IV antibiotics within 2 weeks prior to the first dose or oral antibiotics within 1 week prior to the first dose. Participants who are receiving or have received prophylactic antibiotics (e.g., prophylaxis against urinary infections) are allowed.
  • Any evidence of current Interstitial Lung Disease (ILD)/non-infectious pneumonitis OR a prior history of ILD/non-infectious pneumonitis requiring high-dose glucocorticoids OR suspected ILD/non-infectious pneumonitis that cannot be ruled out by imaging. Examples of suspected ILD/pneumonitis by imaging include the presence of lung parenchymal fibrosis, such as combined pulmonary fibrosis and emphysema (CPFE) and any radiographic features consistent with interstitial lung abnormalities, including but not limited to, extensive ground glass opacities, reticular opacities, traction bronchiectasis, and honeycombing.
  • Participants with moderate to severe pulmonary disease or current clinically significant pulmonary compromise that, in the investigator's judgment, could jeopardize safety or study conduct. Examples include severe/poorly controlled asthma or Chronic Obstructive Pulmonary Disease (COPD) (including acute exacerbation of COPD within 4 weeks before first dose), restrictive lung disease, significant pleural effusion (clinically significant pleural effusion on Study Day 1. Baseline oxygen saturation < 90% on room air.) or structural lung abnormalities, pulmonary involvement from autoimmune/connective tissue disorders (e.g., rheumatoid arthritis, Sjögren's, sarcoidosis), or any condition requiring continuous supplemental oxygen or causing marked respiratory impairment (e.g., dyspnea at rest, greatly reduced exercise tolerance, or significantly decreased lung function). Treatment of pleural effusions to meet eligibility is permitted.
  • History of allergy or hypersensitivity to Ris-Rez (antibody-drug conjugate (ADC), antibody, payload [GSK5757810]). History of severe allergies (e.g., anaphylactic shock), or severe infusion-related reactions (IRRs), or idiosyncrasy to recombinant humanized or mouse proteins.
  • Has received prior anticancer therapy within 14 days of the first dose of study intervention or having to continue these medications during the study. Participants that had any macromolecular anticancer drug (including immunotherapies such as monoclonal antibodies and bispecific antibodies) within 28 days prior to the first dose of study intervention are excluded.
  • History of local radiotherapy within 2 weeks prior to the first dose of study intervention; more than 30% of bone marrow irradiation or extensive radiotherapy within 4 weeks before the first dose of study intervention
  • Has received any transfusion of blood products (including platelets or red blood cells) or administration of colony-stimulating factors (including granulocyte colony-stimulating factor (G-CSF), granulocyte macrophage colony-stimulating factor (GM-CSF), or recombinant erythropoietin) within 14 days before enrollment. G-CSF prophylaxis prior to administration of Ris-Rez is permitted.
  • Has received immunosuppressive agents within 30 days prior to first dose of study treatment (or requires long-term (30 days or longer) glucocorticoid therapy). Low-dose corticosteroids (prednisone ≤10 mg/day or equivalent) may be administered. Use of inhaled or topical steroids and prophylactic corticosteroids for procedures and pre-infusion prophylaxis are permitted.
  • Participant with history of nephrotic syndrome or Grade 3 proteinuria or protein urine >1+ on dipstick or 24-h urine protein quantitation ≥ 1.0 g at Screening.
  • History of abdominal or gastrointestinal fistula, tracheoesophageal fistula or any Grade 4 fistula, gastrointestinal perforation, or intra-abdominal abscess.
  • Has any active renal condition (e.g., requirement for dialysis, or any other significant renal condition that could affect the participant's safety). Renal obstruction successfully managed by stenting is permitted.

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:顺序分配
  • 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:Phase 1: Dose escalation
Ivonescimab will be administered
Risvutatug rezetecan will be administered
实验性的:Phase 2: Dose expansion
Ivonescimab will be administered
Risvutatug rezetecan will be administered

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
Phase 1 and Phase 2 Number of participants with Adverse events (AEs), Serious Adverse Events (SAEs) and Adverse events of special interest (AESIs)
大体时间:Up to approximately 143 weeks
Up to approximately 143 weeks
Phase 1 and Phase 2: Number of participants with AEs leading to dose modifications including study intervention discontinuation
大体时间:Up to approximately 130 weeks
Up to approximately 130 weeks
Phase 2: Number of participants with AEs leading to dose modifications or study intervention discontinuation
大体时间:Up to approximately 130 weeks
Up to approximately 130 weeks
Phase 1 and Phase 2: Number of participants with changes in safety parameters
大体时间:Up to approximately 143 weeks
Up to approximately 143 weeks
Phase 1: Number of participants with Dose Limiting Toxicities (DLT)
大体时间:Up to 21 days
Up to 21 days
Phase 1 and Phase 2: Number of participants with a change from baseline in vital signs
大体时间:Baseline (Day -1) and up to approximately 143 weeks
Number of participants will be assessed
Baseline (Day -1) and up to approximately 143 weeks
Phase 1 and Phase 2: Number of participants with a change from baseline in body weight
大体时间:Baseline (Day -1) and up to approximately 143 weeks
Number of participants will be assessed
Baseline (Day -1) and up to approximately 143 weeks
Phase 1 and Phase 2: Number of participants with a change from baseline in laboratory parameters (hematology, clinical chemistry and urinalysis)
大体时间:Baseline (Day -1) and up to approximately 143 weeks
Number of participants will be assessed
Baseline (Day -1) and up to approximately 143 weeks
Phase 1 and Phase 2: Number of participants with a change from baseline in cardiac function [Electrocardiogram (ECG) and Echocardiogram (ECHO)]
大体时间:Baseline (Day -1) and up to approximately 143 weeks
Number of participants will be assessed
Baseline (Day -1) and up to approximately 143 weeks
Phase 1 and Phase 2: Number of participants with a change from baseline in Eastern Cooperative Oncology Group (ECOG) performance status
大体时间:Baseline (Day -1) and up to approximately 143 weeks
Number of participants will be assessed
Baseline (Day -1) and up to approximately 143 weeks
Phase 2:Confirmed Objective Response Rate (cORR)
大体时间:Up to approximately 143 weeks
cORR is defined as the proportion of participants who have confirmed Complete Response (CR) or Partial Response (PR), assessed by the investigator according to Response Evaluation Criteria in Solid Tumors (RECIST) version (v) 1.1
Up to approximately 143 weeks

次要结果测量

结果测量
措施说明
大体时间
Phase 1: Maximum observed plasma concentration (Cmax) of Ris-Rez, rezetecan and ivonescimab
大体时间:Up to approximately 169 weeks
Up to approximately 169 weeks
Phase 1: Time to reach maximum concentration (Tmax) of Ris-Rez, GSK5757810 and ivonescimab
大体时间:Up to approximately 169 weeks
Up to approximately 169 weeks
Phase 1: Area under the curve (AUC) of Ris-Rez, GSK5757810 and ivonescimab
大体时间:Up to approximately 169 weeks
Up to approximately 169 weeks
Phase 1: Trough concentration (Ctrough) of Ris-Rez, GSK5757810 and ivonescimab
大体时间:Up to approximately 169 weeks
Up to approximately 169 weeks
Phase 1: Confirmed Objective Response Rate (cORR)
大体时间:Up to approximately 143 weeks
cORR is defined as the proportion of participants who have confirmed Complete Response (CR) or Partial Response (PR), assessed by the investigator according to Response Evaluation Criteria in Solid Tumors (RECIST) version (v) 1.1
Up to approximately 143 weeks
Phase 1 and Phase 2:Disease control rate at 12 weeks (DCR12)
大体时间:At week 12
DCR12 is as the proportion of participants who have achieved CR or PR, or stable disease (SD) for a duration of at least 11 weeks, per RECIST 1.1 by investigator assessment
At week 12
Phase 1and Phase 2: Duration of Response (DoR)
大体时间:Up to approximately 169 weeks
DoR is defined as the time from the date of first documented objective response (CR/PR) per RECIST 1.1 by investigator assessment to the date of first documented PD or death due to any cause, whichever comes first
Up to approximately 169 weeks
Phase 2: Progression-free survival (PFS)
大体时间:Up to approximately 169 weeks
PFS is defined as the time from the date of first dose until the earliest date of documented disease progression according to RECIST 1.1 per investigator assessment
Up to approximately 169 weeks
Phase 1 and Phase 2: Overall Survival (OS)
大体时间:Up to approximately 169 weeks
OS is defined as the time from first dose to death from any cause
Up to approximately 169 weeks
Phase 2: Observed plasma concentration of Ris-Rez, GSK5757810 and ivonescimab
大体时间:Up to approximately 169 weeks
Up to approximately 169 weeks
Phase 2: Number of participants with Anti-drug antibodies (ADA) and Neutralizing antibody (NAb) for Ris-Rez and ivonescimab
大体时间:Up to approximately 169 weeks
Up to approximately 169 weeks
Phase 2: Titers of ADA to Ris-Rez and ivonescimab
大体时间:Up to approximately 169 weeks
Up to approximately 169 weeks

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9月8日

初级完成 (估计的)

2029年6月21日

研究完成 (估计的)

2029年12月21日

研究注册日期

首次提交

2026年5月15日

首先提交符合 QC 标准的

2026年5月15日

首次发布 (实际的)

2026年5月22日

研究记录更新

最后更新发布 (实际的)

2026年9月10日

上次提交的符合 QC 标准的更新

2026年9月4日

最后验证

2026年8月1日

更多信息

与本研究相关的术语

其他研究编号

  • 307890
  • 2026-525721-20 (其他标识符:EU CT Number)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

Study Sponsor will assess requests from qualified researchers for anonymized individual patient-level data and related study documents. Data sharing is subject to certain criteria, conditions, and exceptions. For further information, refer to https://www.gsk-studyregister.com/gsk-patient-level-data-sharing-july2025.pdf

IPD 共享时间框架

Anonymized IPD will be made available within 6 months of publication of primary, key secondary and safety results for studies in product with approved indication(s) or asset(s) with development terminated across all indications.

IPD 共享访问标准

Anonymized IPD is shared with researchers whose proposals are approved by an Independent Review Panel and after a Data Sharing Agreement is in place. Access is provided for an initial period of 12 months, but an extension may be granted, when justified, for up to 6 months.

IPD 共享支持信息类型

  • 研究方案
  • 树液
  • 国际碳纤维联合会
  • 企业社会责任

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

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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