이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

Study of IBI3028 in Participants With Locally Advanced, Unresectable, or Metastatic Solid Tumors

A Phase 1, Multi-Center, Open-Label Study Evaluating IBI3028 Treatment in Participants With Locally Advanced, Unresectable, or Metastatic Solid Tumors

This is a phase 1 multi-center, open-label study evaluating IBI3028 Treatment in participants with locally advanced, unresectable, or metastatic solid tumors

연구 개요

연구 유형

중재적

등록 (추정된)

493

단계

  • 1단계

연락처 및 위치

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

연구 연락처

연구 장소

    • Tianjin Municipality
      • Tianjin, Tianjin Municipality, 중국, 300060
        • 모병
        • Tianjin Medical University Cancer Institute and Hospital
        • 수석 연구원:
          • Yi Hu
        • 수석 연구원:
          • Jihui Hao
        • 연락하다:

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

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria

  1. Be able to understand and sign written informed consent to participate in this study, including all assessments and procedures specified in this protocol;
  2. Male or female participants aged 18 years or older;
  3. Have histologically or cytologically confirmed unresectable locally advanced or metastatic solid tumors;
  4. Have at least one evaluable lesion (dose escalation) or measurable lesion (dose expansion) as per RECIST v1.1 within 28 days prior to the first dose of IBI3028;
  5. ECOG PS(Eastern Cooperative Oncology Group Performance Status)score of 0-1;
  6. Anticipated life expectancy of ≥ 12 weeks;
  7. Adequate bone marrow and organ function as evidenced by :

    1. Hematological function: ANC(Absolute neutrophil count) ≥ 1.5 × 10 9 /L; platelet count (PLT) ≥ 90 × 10 9 /L; hemoglobin ≥ 9.0 g/dL, and without receiving granulocyte-colony stimulating factor (G-CSF), granulocyte-macrophage colony stimulating factor (GM-CSF), thrombopoietin (TPO), interleukin-11, or other leukocyte/platelet stimulating growth factors (including red blood cell and platelet transfusions) within at least 7 days before the first dose of the study drug;
    2. Hepatic function: total bilirubin ≤ 1.5 × ULN (Upper Limit of Normal) (≤ 3 × ULN for participants with Gilbert's syndrome); AST(Aspartate Aminotransferase) and ALT (Alanine Aminotransferase)≤ 2.5 × ULN in the absence of liver metastases (≤ 5 × ULN if liver metastases are present); albumin ≥ 2.8 g/dL;
    3. Renal function: creatinine clearance ≥ 30 mL/min (using Cockcroft-Gault formula); urine protein < 2+ or 24-h total urine protein < 1 g;
    4. Cardiac function: Left ventricular ejection fraction (LVEF) ≥ 50%, no clinically significant pericardial effusion as determined by ECHO or MUGA(Multigated Acquisition), and no clinically significant ECG result;
    5. Coagulation function: International normalized ratio (INR) ≤ 1.5; activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN (participants receiving anticoagulant therapy with coagulation function within the range above are allowed);
    6. Pulmonary function: With at least the lowest level of pulmonary reserve, defined as Grade ≤ 1 dyspnea and blood oxygen saturation ≥ 95% in non-oxygen breathing state;
  8. Participants (both male and female participants) who will be not of childbearing potential or who agree to use at least 1 highly effective method of contraception during the study (from start of screening or within 2 weeks prior to first dose, whichever occurs first, and continue until 7 months for females and 4 months for males after the last dose of study drug).

Exclusion Criteria

  1. Participation in any other interventional clinical study other than an observational (non-interventional) study or during the follow-up period of an interventional study;
  2. Prior anti-tumor therapy:

    Participants who have received cytotoxic therapy within 3 weeks or 5 half-lives (whichever is shorter) prior to the first administration of study intervention ; Participants who have received PD-1/PD-L1 therapy within 4 weeks prior to the first administration of study drug; Participants who have received treatment with small molecule targeted therapy within 14 days or 5 half-lives (whichever is shorter) prior to the first dose of the study drug; Palliative radiation therapy within 2 weeks or radical radiation therapy within 4 weeks prior to the first dose of study drug; Participants who had received adoptive cell therapy within 8 weeks prior to the first administration of study intervention.

  3. Have received live vaccines within 4 weeks or tumor vaccines within 3 months prior to the first administration of the study drug, or plan to receive any live vaccines during the study;
  4. Use of strong cytochrome P450 3A4 (CYP3A4) enzyme inhibitors within 2 weeks or 5 half-lives (whichever is shorter) prior to the first dose of study drug;
  5. Adverse reactions caused by previous anti-tumor treatments that have not resolved to Grade 0 or 1 or baseline level according to NCI CTCAE v5.0 before the first dose of the study drug (except for alopecia, fatigue, pigmentation, and other conditions with no safety implications per the Investigator's clinical judgement);
  6. Known allergies, hypersensitivity, or intolerance to IBI3028 or its excipients (refer to the Investigator's Brochure);
  7. Have undergone major surgery (craniotomy, thoracotomy, or laparotomy, and other surgeries according to Investigators' opinion, excluding needle biopsy) within 4 weeks prior to the first dose of the investigational product, or are expected to undergo major surgery during the study, or have severe unhealed wounds, ulcers, etc.;
  8. Known symptomatic central nervous system (CNS) metastases. Participants with asymptomatic CNS metastases (ie, no neurologic syndrome and metastases ≤1.5 cm in diameter) or stable disease after treatment as judged by the investigator may be considered if: they have no metastases in the midbrain, pons, cerebellum, meninges, medulla oblongata, or spinal cord; stable status for at least 4 weeks prior to the first dose of study drug (≤1.5 mg/day dexamethasone or equivalent and baseline anticonvulsants are allowed), and have no new or enlarging CNS metastases as clearly demonstrated by clinical evidence; Note : CNS lesions are not considered target lesions.
  9. Uncontrolled disease or condition, including:

    1. Uncontrolled infection requiring systemic antibiotics, antivirals, or antifungals prior to the first dose of the study drug;
    2. With known human immunodeficiency virus (HIV) infection, or HIV positive (HIV 1/2 Ab positive), for participants outside mainland China, participants with positive HIV antibody test at screening are eligible to participate in the study under the premise of undetectable viral load, or well-controlled under antiretroviral therapy (defined as CD4+ T cell count ≥ 350 cells/μL and no history of AIDS-defining opportunistic infection within 12 months before the first dose);
    3. Acute or chronic active hepatitis B (HBsAg positive and/or HBcAb positive, and HBV DNA titer ≥ 10 4 copies/mL or ≥ 2000 IU/mL) or hepatitis C (HCV Ab positive, and HCV RNA > 10 3 copies/mL or above the lower limit of detection);
    4. Active tuberculosis infection, or still receiving anti-tuberculosis treatment, or receiving anti-tuberculosis treatment within 1 year before the first dose of the study drug;
    5. Uncontrolled myocarditis or symptomatic congestive heart failure Class II-IV (New York Heart Association ,NYHA), symptomatic or uncontrolled arrhythmia, QTc interval > 480 ms, or personal or family history of congenital long/short QT syndrome;
    6. Uncontrolled hypertension with SBP ≥ 160 mmHg or DBP ≥ 100 mmHg measured on 2 follow-up visits despite adequate standard treatment;
    7. Current gastrointestinal tract (muscle-derived tube from the oral cavity to the anus, including oral cavity, pharynx, esophagus, stomach, duodenum, jejunum, ileum, cecum, appendix, colon, rectum, and anus) or endotracheal stent implantation;
    8. Significant malnutrition, such as malnutrition requiring parenteral nutrition;
    9. Spinal cord compression that has not been radically cured by surgery and/or radiotherapy;
    10. Ascites, pleural effusion, or pericardial effusion that is symptomatic and requires intervention prior to the first dose of study intervention (participants who do not require treatment or who recover steadily without intervention are eligible).
  10. With a history of pneumonia requiring corticosteroid treatment, or a history of clinically significant lung diseases (such as interstitial lung disease, non-infectious pneumonitis, or uncontrolled lung diseases such as pulmonary fibrosis, severe radiation pneumonitis, and acute lung injury), or suspected of having these diseases by imaging during the screening period;
  11. Any history of arterial thromboembolic events within 6 months prior to the first dose of the study drug, including myocardial infarction, unstable angina, cerebrovascular stroke, or transient ischemic attack;
  12. Esophageal or gastric varices requiring immediate intervention (e.g., ligature or sclerotherapy) or at high risk of bleeding according to the opinion of the investigator or a gastroenterologist or hepatologist. Participants with evidence of portal hypertension (including imaging findings of hypersplenism) or a history of esophageal and gastric variceal bleeding must undergo endoscopic evaluation within 3 months prior to the first dose of the study drug;
  13. Any history of life-threatening hemorrhage or hemorrhage requiring blood transfusion, endoscopy, or surgery within 3 months prior to the first dose of the investigational product ;
  14. Unhealed gastrointestinal obstruction, perforation, or fistula. At risk of gastrointestinal obstruction or perforation (including but not limited to: acute diverticulitis, abdominal abscess, etc.), history of extensive bowel resection (segmental colectomy or extensive bowel resection accompanied with chronic diarrhea), active inflammatory bowel disease, or Grade ≥ 2 chronic diarrhea;
  15. History of immunodeficiency diseases, including congenital or acquired immunodeficiency diseases;
  16. History of allogeneic organ transplantation or allogeneic bone marrow transplantation, or autologous hematopoietic stem cell transplantation within 3 months prior to the first dose of the investigational drug, except for corneal transplantation;
  17. History of other malignancy within 2 years before the first dose of study drug(s), with the following exceptions:

    1. Malignancy (other than in situ) treated with curative therapy with no known active disease present for ≥ 2 years prior to the first dose of study drug and at low risk of recurrence according to the physician's opinion;
    2. Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of residual or recurrent disease;
    3. Adequately treated carcinoma in situ without evidence of residual or recurrent disease;
    4. Prostate intraepithelial neoplasia without evidence of prostate cancer;
    5. Adequately treated urothelial papillary non-invasive carcinoma.
  18. Presence of any indwelling tubes or drains (such as percutaneous nephrostomy tubes, indwelling Foley catheters, biliary drainage tubes, or peritoneal/pericardial catheters); Note: Thoracic catheters or dedicated central venous access catheters such as Port-A-Cath or Hickman catheters are allowed.
  19. Other acute or chronic diseases or laboratory abnormalities, which may increase the risk of participating in the study or receiving the investigational product, interfere with the interpretation of study results, and make the participant unsuitable for participating in the study based on the investigator's judgment;
  20. Neurological, mental, or social conditions that affect the compliance with trial requirements, significantly increase the risk of AEs, or affect the participants' signing of written informed consent (IC);
  21. Females who are pregnant, have a positive pregnancy test result, or are breastfeeding;
  22. Not fit to participate in this study at the discretion of the Investigator.

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: 해당 없음
  • 중재 모델: 순차적 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Drug: IBI3028
IBI3028 will be dosed until disease progression, toxicity intolerance, starting of new systemic anti-cancer treatment, withdrawal of consent, occurrence of other reasons for discontinuing study therapy, or treatment duration reaching the maximum of 24 months, whichever occurs first.
Recombinant anti-EGFR(Epidermal growth factor receptor) and c-Met antibodies-dual-payload conjugate for injection

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
신체검사 결과에 임상적으로 유의한 변화가 있는 피험자 수
기간: 최대 3년
조사자가 보고한 임상적으로 유의미한 비정상적인 신체 검사 소견.
최대 3년
심전도에 임상적으로 유의미한 변화가 있는 피험자 수
기간: 최대 3년
연구자가 임상적으로 유의미한 비정상 심전도 소견을 보고했습니다.
최대 3년
생명 징후의 임상 적으로 유의미한 변화가있는 피험자 수
기간: 최대 3 년
체온, 맥박, 호흡 속도, 휴식 및 혈압에서 맥박 산소 측정에 의한 산소 포화도를 포함한 활력 징후
최대 3 년
용량 제한 독성 (DLT)
기간: 최대 21 일
MTD 및/또는 RP2D를 확립하기위한 용량 제한 독성 (DLT).
최대 21 일
실험실 매개 변수의 임상 적으로 유의미한 변화가있는 피험자 수
기간: 최대 3 년
임상 적으로 유의 한 실험실 매개 변수 조사 결과 조사자가보고했습니다.
최대 3 년
Numbers of subjects with adverse events
기간: Up to 3 years
Defined as any untoward medical occurrence, whether or not there is a causal relationship with the study drug, in a clinical study subject from the time informed consent form is signed
Up to 3 years
Numbers of subjects with serious adverse events
기간: Up to 3 years
Defined as any serious untoward medical occurrence, whether or not there is a causal relationship with the study drug, in a clinical study subject from the time informed consent form is signed
Up to 3 years
Number of AEs(adverse events) leading to dose interruption
기간: Up to 3 years
AEs(adverse events) leading to dose interruption reported by the investigator
Up to 3 years
Number of AEs leading to dose delay
기간: Up to 3 years
AEs leading to dose delay reported by the investigator
Up to 3 years
Number of AEs leading to dose reduction
기간: Up to 3 years
AEs leading to dose reduction reported by the investigator
Up to 3 years
Number of AEs leading to permanent discontinuation
기간: Up to 3 years
AEs leading to permanent discontinuation reported by the investigator
Up to 3 years
Objective response rate (ORR) in dose expansion
기간: Up to 3 years
Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria.
Up to 3 years

2차 결과 측정

결과 측정
측정값 설명
기간
Area under the curve (AUC)
기간: Up to 3 years
Area under the curve (AUC) of single and multiple doses of IBI3028
Up to 3 years
Maximum concentration (Cmax)
기간: Up to 3 years
Maximum concentration (Cmax) of single and multiple doses of IBI3028
Up to 3 years
Time to maximum concentration (Tmax)
기간: Up to 3 years
Time to maximum concentration (Tmax) of single and multiple doses of IBI3028
Up to 3 years
Clearance (CL)
기간: Up to 3 years
Clearance (CL) of single and multiple doses of IBI3028
Up to 3 years
Apparent volume of distribution (V)
기간: Up to 3 years
apparent volume of distribution (V) of single and multiple doses of IBI3028
Up to 3 years
Half-life (t1/2)
기간: Up to 3 years
Half-life (t1/2) of IBI3020 to the last administration of IBI3028
Up to 3 years
Anti-drug antibody (ADA)
기간: Up to 3 years
Incidence and characterization of anti-drug antibody (ADA)
Up to 3 years
Neutralizing antibody (NAb)
기간: Up to 3 years
Incidence and characterization of neutralizing antibody (NAb)
Up to 3 years
Objective response rate (ORR)
기간: Up to 3 years
Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Duration of response (DoR)
기간: Up to 3 years
Duration of response (DoR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Disease control rate (DCR)
기간: Up to 3 years
Disease control rate (DCR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Time to response (TTR)
기간: Up to 3 years
Time to response (TTR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Progression-free survival (PFS)
기간: Up to 3 years
progression-free survival (PFS) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Overall survival (OS)
기간: Up to 3 years
OS is defined as the time from the date of first dose of study drug until the date of death from any cause.
Up to 3 years

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

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)

2026년 3월 31일

기본 완료 (추정된)

2027년 6월 30일

연구 완료 (추정된)

2028년 6월 30일

연구 등록 날짜

최초 제출

2026년 4월 27일

QC 기준을 충족하는 최초 제출

2026년 5월 11일

처음 게시됨 (실제)

2026년 5월 15일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 5월 15일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 5월 11일

마지막으로 확인됨

2026년 5월 1일

추가 정보

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. .

대장암에 대한 임상 시험

Drug: IBI3028에 대한 임상 시험

구독하다