- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07619339
A Study of Tepotinib and Ivonescimab in People With Non-Small Cell Lung Cancer
A Pilot Study of Tepotinib + Ivonescimab in Patients With Advanced METex14 Skipping Positive NSCLC
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 1
Contactos e Locais
Contato de estudo
- Nome: Paul Paik, MD
- Número de telefone: 646-608-3759
- E-mail: paikp@mskcc.org
Estude backup de contato
- Nome: Helena Yu, MD
- Número de telefone: 646-608-3912
Locais de estudo
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New Jersey
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Basking Ridge, New Jersey, Estados Unidos, 07920
- Recrutamento
- Memorial Sloan Kettering Basking Ridge (All Protocol Activities)
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Contato:
- Paul Paik, MD
- Número de telefone: 646-608-3759
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Middletown, New Jersey, Estados Unidos, 07748
- Recrutamento
- Memorial Sloan Kettering Monmouth (All Protocol Activities)
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Contato:
- Paul Paik, MD
- Número de telefone: 646-608-3759
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Montvale, New Jersey, Estados Unidos, 07645
- Recrutamento
- Memorial Sloan Kettering Bergen (All Protocol Activities)
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Contato:
- Paul Paik, MD
- Número de telefone: 646-608-3759
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New York
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Commack, New York, Estados Unidos, 11725
- Recrutamento
- Memorial Sloan Kettering Suffolk-Commack (All Protocol Activities )
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Contato:
- Paul Paik, MD
- Número de telefone: 646-608-3759
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Harrison, New York, Estados Unidos, 10604
- Recrutamento
- Memorial Sloan Kettering Westchester (All Protocol Activities)
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Contato:
- Paul Paik, MD
- Número de telefone: 646-608-3759
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New York, New York, Estados Unidos, 10065
- Recrutamento
- Memorial Sloan Kettering Cancer Center (All Protocol Activities)
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Contato:
- Paul Paik, MD
- Número de telefone: 646-608-3759
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Uniondale, New York, Estados Unidos, 11553
- Recrutamento
- Memorial Sloan Kettering Nassau (All Protocol Activities)
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Contato:
- Paul Paik, MD
- Número de telefone: 646-608-3759
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Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
Criteria:
Documentation of Disease
- Patients must have pathologically confirmed non-small cell lung cancer. This includes, but is not limited, to histologies such as adenocarcinoma, squamous cell carcinoma, sarcomatoid carcinoma, and poorly differentiated carcinoma.
- Patients must have documentation of MET exon 14 skipping present in their cancer using an FDA-approved assay done within a laboratory with CLIA, ISO/IEC, CAP, or similar certification.
Definition of Disease
Patients must have advanced or recurrent disease.
- Advanced disease is defined as stage IV disease or stage IIIB/C disease not amenable to local therapy such as radiation or surgery.
- Patients must have measurable disease as defined by RECIST 1.1 criteria.
- Must not have other known actionable oncogenic alterations, such as (but not limited to) EGFR sensitizing mutations, EGFR T790M mutation, ALK gene fusion, ROS1 gene rearrangement, RET gene rearrangement, NTRK rearrangement, HER2 mutation, KRAS activating mutations, and BRAF V600E mutation.
Must not have leptomeningeal disease or brain metastases unless: 1) metastases have been locally treated and have remained clinically controlled and asymptomatic for at least 3 days following the stereotactic radiation and/or 14 days following whole brain radiation, and prior to sub-study randomization, AND 2) participant has no residual neurological dysfunction and has been off corticosteroids for at least 24 hours prior to start of study therapy.
- Small/asymptomatic brain metastasis for which stereotactic radiation is indicated must be treated.
Prior Treatment
- No prior angiogenesis inhibitor therapy (i.e. bevacizumab or ramucirumab)
- Patients can have received prior MET inhibitor therapy
- Patients can have received prior ICI therapy.
If applicable, patients must have progressed on their most recent line of therapy.
- Must have not had prior systemic therapy within 21 days of the start of protocol therapy
- Must not have received radiation therapy within 7 days of starting protocol therapy
- Age ≥ 18
- ECOG Performance Status of ≤ 2
Not Pregnant and Not Nursing
- Female patients of childbearing age must have negative serum pregnancy test results before randomization.
- Female patient of childbearing potential having sex with an unsterilized male partner must agree to use a highly effective method of contraception from the beginning of screening until 90 days after the last dose of ivonescimab or until 1 week after last dose of tepotinib (whichever is longer).
- Unsterilized male patient having sex with a female partner of childbearing potential must agree to use an effective method of contraception from the beginning of screening until Day 90 after the last dose of ivonescimab
Required Organ Function
Adequate hematologic function defined as follows:
- Absolute neutrophil count (ANC) ≥ 1,500 cells/mm3
- Platelets ≥ 100,000 cells/mm3
- Hemoglobin ≥ 9 g/d
Adequate renal function defined as follows:
- Creatinine clearance (CrCL) of ≥50 mL/min by the Cockcroft-Gault formula or estimated glomerular filtration rate (eGFR) value ≥ 50 mL/min using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation (adjustment by BSA is not required for eGFR)
- Urine protein < 2+ or 24-hour urine protein < 1.0g
Adequate hepatic function defined as follows:
- Total bilirubin ≤ 1.5 x institutional upper limit of normal (ULN) (patients with known Gilbert's disease who have bilirubin level ≤ 3 x ULN may be enrolled)
- AST and ALT ≤2.5x institutional ULN. For patients with liver metastases, AST and ALT ≤ 5 x ULN.
- Coagulation: PT or INR ≤ 1.5 ULN, and PTT or aPTT ≤ 1.5 x ULN (unless abnormalities are unrelated to coagulopathy or prophylactic anticoagulation)
Comorbid Conditions No history of interstitial lung disease requiring steroid treatment
- Prior history of Grade ≥3 irAE
- Must not have evidence of major blood vessel invasion or tumor invading into organs or risk of esophagotracheal or esophagopleural fistula Must not have active autoimmune or lung disease requiring systemic therapy (prednisone ≤ 10mg allowed) within 2 years of treatment
- Poorly controlled hypertension with repeated systolic blood pressure ≥ 150 mmHg or diastolic blood pressure ≤ 100 mmHg after oral antihypertensive therapy
- Severe infection within 4 weeks prior to randomization, including but not limited to comorbidities requiring hospitalization, sepsis, or severe pneumonia; active infection (as determined by the investigator) requiring systemic anti-infective therapy within 2 weeks prior to randomization (excluding antiviral therapy for hepatitis B or C)
- Active or prior history of inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis, or chronic diarrhea)
- Must not have a history of unstable angina, MI, CHF (NYHA grade ≥ 2) requiring hospitalization in the preceding 6 months
- Must not have a history of gastric or esophageal varices, severe ulcers, or wounds that do not heal, or fistulas, or abscesses, or acute GI bleeding within 6 months of therapy
- Must not have a history of arterial thromboembolic event, venous thromboembolic event grade ≥ 3, CVA/TIA, HTN crisis or HTN encephalopathy within 6 months of therapy
Must not have a history of bleeding tendencies or coagulopathy or clinically significant bleeding symptoms or risk within 4 weeks of therapy
- Hemoptysis (defined as coughing up ≥ 0.5 teaspoon of fresh blood or small blood clots)
- Note: 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 randomization is not allowed. The use of full-dose anticoagulants is permitted as long as the international normalized ratio (INR) or activated partial thromboplastin time (aPTT) is within therapeutic limits according to the medical standard of the enrolling institution.
- Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial.
For patients with known HIV, HBV, and/or HCV infection:
- HIV-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial.
- Patients with active hepatitis B are required to have stable or declining levels of hepatitis B DNA by polymerase chain reaction (PCR) on appropriate anti-viral therapy with acceptable tolerability for one month prior to randomization.
- All patients with active hepatitis C (hepatitis C virus [HCV] antibody positive with HCV RNA levels above the lower limit of detection) are excluded.
- Allergies o No history of allergic reaction to the study agent(s), compounds of similar chemical or biologic composition to the study agent (s) (or any of its excipients).
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
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Experimental: Tepotinib and Ivonescimab
The study is divided into an initial dose finding phase and subsequent dose expansion phase.
A total of 16 patients will be enrolled across these two phases.
The sample size for this study was not based on formal power calculations for efficacy, instead focusing on the qualitative description of safety for the combination of tepotinib + ivonescimab.
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Tepotinib will be administered at 225mg or 450mg oral daily continuously in every 3 week cycles.
Ivonescimab is administered IV Q3W on Day 1 of each cycle.
The total duration of ivonescimab treatment is up to 24 months.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Dose finding
Prazo: 2 years
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The primary objective of the dose finding phase is determination of the recommended dose expansion dose using a standard 3+3 design based on dose-limiting toxicities (DLT).
DLT definition: any grade ≥ 3 immune-related adverse event attributable to synergistic combinatorial toxicity from tepotinib and ivonescimab.
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2 years
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Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
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Overall Survival (OS)
Prazo: 5 years
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defined as the duration of time from the start of treatment to time of death
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5 years
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Paul Paik, MD, Memorial Sloan Kettering Cancer Center
Publicações e links úteis
Links úteis
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
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
- 26-120
Plano para dados de participantes individuais (IPD)
Planeja compartilhar dados de participantes individuais (IPD)?
Descrição do plano IPD
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