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

3. maj 2021 opdateret af: 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.

Studieoversigt

Status

Aktiv, ikke rekrutterende

Betingelser

Detaljeret beskrivelse

[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.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

33

Fase

  • Fase 1

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Busan, Korea, Republikken
        • Kosin University Gospel Hospital
      • Daegu, Korea, Republikken
        • Kyungpook National University Chilgok Hospital
      • Seoul, Korea, Republikken
        • Seoul National University Hospital
      • Seoul, Korea, Republikken
        • Asan Medical Center
      • Seoul, Korea, Republikken
        • Samsung Medical Center

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

19 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

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.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: 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.
Andre navne:
  • A human monoclonal antibody targeting ErbB3
Eksperimentel: 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.
Andre navne:
  • A human monoclonal antibody targeting ErbB3
Eksperimentel: 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.
Andre navne:
  • A human monoclonal antibody targeting ErbB3
Eksperimentel: 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.
Andre navne:
  • A human monoclonal antibody targeting ErbB3
Eksperimentel: 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.
Andre navne:
  • A human monoclonal antibody targeting ErbB3
Eksperimentel: 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.
Andre navne:
  • A human monoclonal antibody targeting ErbB3
Eksperimentel: 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.
Andre navne:
  • A human monoclonal antibody targeting ErbB3
Intravenous Infusion for 1 hour (2 hours at initial dose)
Andre navne:
  • Erbitux
  • Epidermal Growth Factor Receptor (EGFR) inhibitor

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Determine the Maximum Tolerated Dose Dependent on Reports of Dose-limiting Toxicities
Tidsramme: 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.

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Toxicity Evaluation
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Studieleder: Jaehyeon Juhn, Ph.D, ISU Abxis Co., Ltd.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

27. april 2018

Primær færdiggørelse (Faktiske)

19. oktober 2020

Studieafslutning (Forventet)

31. december 2021

Datoer for studieregistrering

Først indsendt

2. maj 2018

Først indsendt, der opfyldte QC-kriterier

29. maj 2018

Først opslået (Faktiske)

11. juni 2018

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

6. maj 2021

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

3. maj 2021

Sidst verificeret

1. maj 2021

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • ISU104-001

Plan for individuelle deltagerdata (IPD)

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