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

3 maggio 2021 aggiornato da: 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.

Panoramica dello studio

Stato

Attivo, non reclutante

Condizioni

Descrizione dettagliata

[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 di studio

Interventistico

Iscrizione (Effettivo)

33

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

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

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

19 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Altri nomi:
  • A human monoclonal antibody targeting ErbB3
Sperimentale: 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.
Altri nomi:
  • A human monoclonal antibody targeting ErbB3
Sperimentale: 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.
Altri nomi:
  • A human monoclonal antibody targeting ErbB3
Sperimentale: 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.
Altri nomi:
  • A human monoclonal antibody targeting ErbB3
Sperimentale: 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.
Altri nomi:
  • A human monoclonal antibody targeting ErbB3
Sperimentale: 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.
Altri nomi:
  • A human monoclonal antibody targeting ErbB3
Sperimentale: 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.
Altri nomi:
  • A human monoclonal antibody targeting ErbB3
Intravenous Infusion for 1 hour (2 hours at initial dose)
Altri nomi:
  • Erbitux
  • Epidermal Growth Factor Receptor (EGFR) inhibitor

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Determine the Maximum Tolerated Dose Dependent on Reports of Dose-limiting Toxicities
Lasso di tempo: 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.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Toxicity Evaluation
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Jaehyeon Juhn, Ph.D, ISU Abxis Co., Ltd.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

27 aprile 2018

Completamento primario (Effettivo)

19 ottobre 2020

Completamento dello studio (Anticipato)

31 dicembre 2021

Date di iscrizione allo studio

Primo inviato

2 maggio 2018

Primo inviato che soddisfa i criteri di controllo qualità

29 maggio 2018

Primo Inserito (Effettivo)

11 giugno 2018

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

6 maggio 2021

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 maggio 2021

Ultimo verificato

1 maggio 2021

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • ISU104-001

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

No

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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