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

2021년 5월 3일 업데이트: 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.

연구 개요

상태

모집하지 않고 적극적으로

정황

상세 설명

[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.

연구 유형

중재적

등록 (실제)

33

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

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

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

19년 이상 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.
다른 이름들:
  • A human monoclonal antibody targeting ErbB3
실험적: 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.
다른 이름들:
  • A human monoclonal antibody targeting ErbB3
실험적: 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.
다른 이름들:
  • A human monoclonal antibody targeting ErbB3
실험적: 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.
다른 이름들:
  • A human monoclonal antibody targeting ErbB3
실험적: 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.
다른 이름들:
  • A human monoclonal antibody targeting ErbB3
실험적: 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.
다른 이름들:
  • A human monoclonal antibody targeting ErbB3
실험적: 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.
다른 이름들:
  • A human monoclonal antibody targeting ErbB3
Intravenous Infusion for 1 hour (2 hours at initial dose)
다른 이름들:
  • 얼비툭스
  • Epidermal Growth Factor Receptor (EGFR) inhibitor

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Determine the Maximum Tolerated Dose Dependent on Reports of Dose-limiting Toxicities
기간: 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.

2차 결과 측정

결과 측정
측정값 설명
기간
Toxicity Evaluation
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

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

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2018년 4월 27일

기본 완료 (실제)

2020년 10월 19일

연구 완료 (예상)

2021년 12월 31일

연구 등록 날짜

최초 제출

2018년 5월 2일

QC 기준을 충족하는 최초 제출

2018년 5월 29일

처음 게시됨 (실제)

2018년 6월 11일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2021년 5월 6일

QC 기준을 충족하는 마지막 업데이트 제출

2021년 5월 3일

마지막으로 확인됨

2021년 5월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • ISU104-001

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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