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- Ensaio Clínico NCT07602855
A Study of Risvutatug Rezetecan in Combination With Ivonescimab in Participants With Advanced Solid Tumors (EMBOLD PanTumour-103)
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?
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 2
- Fase 1
Contactos e Locais
Contato de estudo
- Nome: US GSK Clinical Trials Call Center
- Número de telefone: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
Estude backup de contato
- Nome: EU GSK Clinical Trials Call Center
- Número de telefone: +44 (0) 20 89904466
- E-mail: GSKClinicalSupportHD@gsk.com
Locais de estudo
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Osaka, Japão, 573-1191
- GSK Investigational Site
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Contato:
- US GSK Clinical Trials Call Center
- Número de telefone: 877-379-3718
- E-mail: GSKClinicalSupportHD@gsk.com
-
Contato:
- EU GSK Clinical Trials Call Centre
- Número de telefone: +44 (0) 20 8990 4466
- E-mail: GSKClinicalSupportHD@gsk.com
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Investigador principal:
- Toshio Shimizu
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
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.
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição sequencial
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Phase 1: Dose escalation
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Ivonescimab will be administered
Risvutatug rezetecan will be administered
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Experimental: Phase 2: Dose expansion
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Ivonescimab will be administered
Risvutatug rezetecan will be administered
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Phase 1 and Phase 2 Number of participants with Adverse events (AEs), Serious Adverse Events (SAEs) and Adverse events of special interest (AESIs)
Prazo: Up to approximately 143 weeks
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Up to approximately 143 weeks
|
|
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Phase 1 and Phase 2: Number of participants with AEs leading to dose modifications including study intervention discontinuation
Prazo: Up to approximately 130 weeks
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Up to approximately 130 weeks
|
|
|
Phase 2: Number of participants with AEs leading to dose modifications or study intervention discontinuation
Prazo: Up to approximately 130 weeks
|
Up to approximately 130 weeks
|
|
|
Phase 1 and Phase 2: Number of participants with changes in safety parameters
Prazo: Up to approximately 143 weeks
|
Up to approximately 143 weeks
|
|
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Phase 1: Number of participants with Dose Limiting Toxicities (DLT)
Prazo: Up to 21 days
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Up to 21 days
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Phase 1 and Phase 2: Number of participants with a change from baseline in vital signs
Prazo: Baseline (Day -1) and up to approximately 143 weeks
|
Number of participants will be assessed
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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
Prazo: 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)
Prazo: 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)]
Prazo: 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
Prazo: 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)
Prazo: 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
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Phase 1: Maximum observed plasma concentration (Cmax) of Ris-Rez, rezetecan and ivonescimab
Prazo: Up to approximately 169 weeks
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Up to approximately 169 weeks
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|
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Phase 1: Time to reach maximum concentration (Tmax) of Ris-Rez, GSK5757810 and ivonescimab
Prazo: Up to approximately 169 weeks
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Up to approximately 169 weeks
|
|
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Phase 1: Area under the curve (AUC) of Ris-Rez, GSK5757810 and ivonescimab
Prazo: Up to approximately 169 weeks
|
Up to approximately 169 weeks
|
|
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Phase 1: Trough concentration (Ctrough) of Ris-Rez, GSK5757810 and ivonescimab
Prazo: Up to approximately 169 weeks
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Up to approximately 169 weeks
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|
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Phase 1: Confirmed Objective Response Rate (cORR)
Prazo: Up to approximately 143 weeks
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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
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Up to approximately 143 weeks
|
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Phase 1 and Phase 2:Disease control rate at 12 weeks (DCR12)
Prazo: At week 12
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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
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At week 12
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Phase 1and Phase 2: Duration of Response (DoR)
Prazo: 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
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Up to approximately 169 weeks
|
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Phase 2: Progression-free survival (PFS)
Prazo: 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
|
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Phase 1 and Phase 2: Overall Survival (OS)
Prazo: Up to approximately 169 weeks
|
OS is defined as the time from first dose to death from any cause
|
Up to approximately 169 weeks
|
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Phase 2: Observed plasma concentration of Ris-Rez, GSK5757810 and ivonescimab
Prazo: Up to approximately 169 weeks
|
Up to approximately 169 weeks
|
|
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Phase 2: Number of participants with Anti-drug antibodies (ADA) and Neutralizing antibody (NAb) for Ris-Rez and ivonescimab
Prazo: Up to approximately 169 weeks
|
Up to approximately 169 weeks
|
|
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Phase 2: Titers of ADA to Ris-Rez and ivonescimab
Prazo: Up to approximately 169 weeks
|
Up to approximately 169 weeks
|
Colaboradores e Investigadores
Patrocinador
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Estimado)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Palavras-chave
Termos MeSH relevantes adicionais
Outros números de identificação do estudo
- 307890
- 2026-525721-20 (Outro identificador: EU CT Number)
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
Prazo de Compartilhamento de IPD
Critérios de acesso de compartilhamento IPD
Tipo de informação de suporte de compartilhamento de IPD
- PROTOCOLO DE ESTUDO
- SEIVA
- CIF
- CSR
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