Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Study of ISU104, Targeting ERBB3 in Patients With Advanced Solid Tumors

3 de mayo de 2021 actualizado por: ISU Abxis Co., Ltd.

A Phase I, Open-label, Dose-finding Study to Assess the Safety, Tolerability and Pharmacokinetics of ISU104, a Human Monoclonal Antibody Targeting ErbB3 in Patients With Advanced Solid Tumors

A phase I, open-label, dose-finding study to assess the safety, tolerability and pharmacokinetics of ISU104, a human monoclonal antibody targeting erbB3 in patients with advanced solid tumors.

Descripción general del estudio

Estado

Activo, no reclutando

Condiciones

Intervención / Tratamiento

Descripción detallada

[Part 1 Dose-escalation]

This study ams to evaluate the safety, tolerability, and pharmacokinetics of ISU104 in patients with advanced solid tumors.

Primary objective To determine recommended Phase II dose (RP2D) of ISU104 based on the results of its safety and tolerability in patients with advanced solid tumors.

Secondary objectives

  1. To evaluate pharmacokinetics (PK) of ISU104 in patients with advanced solid tumors.
  2. To evaluate efficacy of ISU104 in patients with advanced solid tumors.

Exploratory purpose To identify the expression of explorable multiple tumor biomarkers and to analyze the relationship between biomarkers and antitumor activity of ISU104.

[Part 2 dose-expansion] The purpose of this study is to evaluate the safety, tolerability, and pharmacokinetics of ISU104 in patients with recurrent/metastatic HNSCC (except for nasopharyngeal cancer), when administered intravenously ISU104 alone or ISU104 in combination with cetuximab.

Primary objective To determine RP2D of ISU104 based on results of its safety and tolerability in patients with recurrent/metastatic HNSCC (except for nasopharyngeal cancer), when administered intravenously ISU104 only or ISU104 in combination with cetuximab.

Secondary objectives

  1. To evaluate the pharmacokinetics of ISU104 in patients with recurrent/metastatic HNSCC (except for nasopharyngeal cancer), when administered intravenously ISU104 only or ISU104 in combination with cetuximab.
  2. To evaluate the efficacy of ISU104 in patients with recurrent/metastatic HNSCC (except for nasopharyngeal cancer), when administered intravenously ISU104 only or ISU104 in combination with cetuximab.

Exploratory purpose To explore a variety of detectable tumor biomarkers and evaluate the relationship between these biomarkers and antitumor activity of ISU104.

Tipo de estudio

Intervencionista

Inscripción (Actual)

33

Fase

  • Fase 1

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

      • Busan, Corea, república de
        • Kosin University Gospel Hospital
      • Daegu, Corea, república de
        • Kyungpook National University Chilgok Hospital
      • Seoul, Corea, república de
        • Seoul National University Hospital
      • Seoul, Corea, república de
        • Asan Medical Center
      • Seoul, Corea, república de
        • Samsung Medical Center

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

19 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

Common

  1. Male or Female with ≥ 19 years of age
  2. Histologically or Cytologically confirmed a diagnosis of an advanced solid tumor that was refractory to standard treatment or for which no standard therapy existed, or patients declined any treatment options
  3. Eastern Cooperative Oncology Group (ECOG) performance status ≤ 2
  4. Life Expectancy ≥ 12 weeks
  5. Adequate Hematological, Renal and Hepatic function
  6. According to Response Evaluation Criteria in Solid Tumors Criteria (RECIST) version 1.1, the patient had at least one measurable lesion

Exclusion Criteria:

  1. Severe hypersensitivity or a history of any hypersensitivity to the similar drug class of IP
  2. Patients underwent the major surgery or procedure, or had the medical history (as blow):

    • Major surgery requiring systemic anesthesia or respiratory assist device within 4 weeks prior to baseline [2 weeks in case of video-assisted thoracoscopic surgery (VATS) or open-and-closed (ONC) surgery)]
    • Severe cardiovascular disease within 24 weeks prior to baseline
    • Severe cerebrovascular disease within 24 weeks prior to baseline
    • Pulmonary thromboembolism, deep vein thrombosis (DVT) or other clinically and significantly severe lung disease within 24 weeks prior to baseline
  3. Patients had the following concurrent diseases at baseline:

    • Hematologic malignancies including lymphoma
    • Clinically significant symptom or uncontrolled central nervous system (CNS) or brain metastases
    • Pleural effusion and ascites drainage
    • Uncontrolled hypertension (SBP/DBP > 160/100 mmHg)
    • Active hepatitis B or C virus
    • Human immunodeficiency virus (HIV) that is positive
    • Thromboembolic disease or bleeding diatheses
    • Interstitial lung disease (ILD)
  4. Left ventricular ejection fraction (LVEF) value, when measured by echocardiogram, multiple gated acquisition (MUGA) scan or a standard procedure in the institution within 4 weeks prior to the study entry
  5. Patients with the following medication history:

    • anti-ErbB3 targeted therapies
    • small-molecule tyrosine kinase inhibitors within 2 weeks prior to baseline
    • any anti-cancer therapy, including chemotherapy, radiotherapy, biologic therapy, retinoid therapy, or therapeutic/palliative radiotherapy for the treatment of advanced solid tumors within 4 weeks prior to baseline
    • Granulocyte-Colony Stimulating Factor (G-CSF), packed red cell or platelet transfusion within 2 weeks prior to the first injection of IP to correct the abnormal values of absolute neutrophil count (ANC) or platelet count
  6. Pregnant woman, breastfeeding woman, or women of childbearing age and men with partners of childbearing age, unless they are willing to follow abstinence or use effective forms of contraception* from the study entry until at least 16 weeks after the EOT visit
  7. Subjects receiving any other investigational products or medical devices within 4 weeks prior to screening
  8. Principal investigator's opinion

[Part 1 Dose-escalation cohort]

  1. Patients with severe hypersensitivity or history of hypersensitivity to the similar drug class of the investigational product.
  2. Patients receiving anti-cancer therapy, including chemotherapy, radiotherapy, biologic therapy, retinoid therapy, or therapeutic/palliative radiotherapy for treatment of advanced solid tumors within four weeks prior to baseline.

[Part 2 dose-expansion cohort]

  1. Patients with history of allergy or hypersensitivity to the investigational product (ISU104 or cetuximab) or any excipients of the investigational product or its similar derivatives.
  2. Patients with primary malignant neoplasm, including head and neck cancer as specified in inclusion criteria of Part 2 dose-expansion cohort. However, an exception may be allowed for the following:

    • For respective malignancy, treatment-naïve or disease-free patients for at least three years (however, patients undergoing radical resection on papillary thyroid carcinoma may be eligible for this clinical trial, even though three years have not passed).
    • Total dissection of skin basal cell carcinoma/squamous cell carcinoma or at least one year had passed since successful treatment of cervical intraepithelial neoplasia.
  3. Patients receiving anti-cancer therapy, including chemotherapy, radiotherapy, biologic therapy, retinoid therapy, therapeutic/palliative radiotherapy, or hormone therapy for treatment of advanced solid tumors within four weeks prior to baseline.

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Dose-Escalation of ISU104 (Dose-Level 1)
1 mg/kg; Administered single-dose first week and observation for 4-weeks and then Administered once weekly in a 28-days Cycle
Intravenous Infusion for 1 hour.
Otros nombres:
  • A human monoclonal antibody targeting ErbB3
Experimental: Dose-Escalation of ISU104 (Dose-Level 2)
3 mg/kg; Administered single-dose first week and observation for 4-weeks and then Administered once weekly in a 28-days Cycle
Intravenous Infusion for 1 hour.
Otros nombres:
  • A human monoclonal antibody targeting ErbB3
Experimental: Dose-Escalation of ISU104 (Dose-Level 3)
5 mg/kg; Administered single-dose first week and observation for 4-weeks and then Administered once weekly in a 28-days Cycle
Intravenous Infusion for 1 hour.
Otros nombres:
  • A human monoclonal antibody targeting ErbB3
Experimental: Dose-Escalation of ISU104 (Dose-Level 4)
10 mg/kg; Administered single-dose first week and observation for 4-weeks and then Administered once weekly in a 28-days Cycle
Intravenous Infusion for 1 hour.
Otros nombres:
  • A human monoclonal antibody targeting ErbB3
Experimental: Dose-Escalation of ISU104 (Dose-Level 5)
20 mg/kg; Administered single-dose first week and observation for 4-weeks and then Administered once weekly in a 28-days Cycle
Intravenous Infusion for 1 hour.
Otros nombres:
  • A human monoclonal antibody targeting ErbB3
Experimental: Dose-Expansion of ISU104 (Group 1: Monotherapy)
ISU104 20 mg/kg to be administered every three weeks (Q3W) as monotherapy
Intravenous Infusion for 1 hour.
Otros nombres:
  • A human monoclonal antibody targeting ErbB3
Experimental: Dose-Expansion of ISU104 (Group 2: Combination therapy)
ISU104 20 mg/kg (or decreased dose) Q3W in combination with cetuximab* 250 mg/m2 QW (*Initial dose: 400 mg/m2)
Intravenous Infusion for 1 hour.
Otros nombres:
  • A human monoclonal antibody targeting ErbB3
Intravenous Infusion for 1 hour (2 hours at initial dose)
Otros nombres:
  • Erbitux
  • Epidermal Growth Factor Receptor (EGFR) inhibitor

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Determine the Maximum Tolerated Dose Dependent on Reports of Dose-limiting Toxicities
Periodo de tiempo: From date of first dose to 4 weeks after administration.
Determination of MTD is dependent upon number of cohorts and patients required
From date of first dose to 4 weeks after administration.

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Toxicity Evaluation
Periodo de tiempo: through the study completion, an average of 1 year
To determine the occurrence of Adverse Events (AEs)
through the study completion, an average of 1 year
Determine Immunogenicity of ISU104
Periodo de tiempo: through the study completion, an average of 1 year
To measure the level of Anti-Drug Antibody (ADA) and/or Neutralizing Antibody (NAb) of ISU104
through the study completion, an average of 1 year
Determine the Peak Plasma Concentration (Cmax) of ISU104
Periodo de tiempo: up to 12 weeks
To measure the Peak Plasma Concentration (Cmax) of ISU104
up to 12 weeks
Determine the Area Under the Curve (AUC) of ISU104
Periodo de tiempo: up to 12 weeks
To measure the Area under the plasma concentration versus time curve (AUC) of ISU104
up to 12 weeks
Explore Overall Response Rate (ORR) of ISU104 or ISU104+Cetuximab
Periodo de tiempo: up to progression, an average 6 months
To determine the number of patients reporting an objective response using RECIST v 1.1 where a Partial Response (PR) is defined as >30% decrease in tumor burden from baseline and a Complete Response (CR) is defined as complete disappearance from tumor burden from baseline
up to progression, an average 6 months
Explore Disease Control Rate (DCR) of ISU104 or ISU104+Cetuximab
Periodo de tiempo: up to progression, an average 6 months
To determine the number of patients reporting an objective response using RECIST v 1.1 where a Partial Response (PR) is defined as >30% decrease in tumor burden from baseline, a Complete Response (CR) is defined as complete disappearance from tumor burden from baseline, and Stable Disease (SD) is defined as neither sufficient shrinkage to qualify for Partial Response nor sufficient increase to qualify for Partial Response (defined as >20% decrease in tumor burden from baseline)
up to progression, an average 6 months
Explore Progression-Free Survival (PFS) of ISU104 or ISU104+Cetuximab
Periodo de tiempo: up to progression, an average 6 months
To measure the length of time during and after the treatment of a disease, such as cancer, that a patient lives with the disease but it does not get worse
up to progression, an average 6 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Director de estudio: Jaehyeon Juhn, Ph.D, ISU Abxis Co., Ltd.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

27 de abril de 2018

Finalización primaria (Actual)

19 de octubre de 2020

Finalización del estudio (Anticipado)

31 de diciembre de 2021

Fechas de registro del estudio

Enviado por primera vez

2 de mayo de 2018

Primero enviado que cumplió con los criterios de control de calidad

29 de mayo de 2018

Publicado por primera vez (Actual)

11 de junio de 2018

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

6 de mayo de 2021

Última actualización enviada que cumplió con los criterios de control de calidad

3 de mayo de 2021

Última verificación

1 de mayo de 2021

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • ISU104-001

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

No

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Ensayos clínicos sobre Tumor solido

3
Suscribir