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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

研究概览

研究类型

介入性

注册 (估计的)

493

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Tianjin Municipality
      • Tianjin、Tianjin Municipality、中国、300060
        • 招聘中
        • Tianjin Medical University Cancer Institute and Hospital
        • 首席研究员:
          • Yi Hu
        • 首席研究员:
          • Jihui Hao
        • 接触:

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

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.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:治疗
  • 分配:不适用
  • 介入模型:顺序分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
实验性的: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

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
体检结果出现临床显着变化的受试者人数
大体时间:最长 3 年
研究者报告的具有临床意义的异常体检结果。
最长 3 年
心电图出现临床显着变化的受试者数量
大体时间:最长 3 年
研究者报告的具有临床意义的异常心电图结果。
最长 3 年
生命体征临床显着变化的受试者数量
大体时间:最多3年
生命体征在内,包括体温,脉搏,呼吸速率,静止时脉冲血氧饱和度和血压的氧气饱和
最多3年
剂量限制毒性(DLTS)
大体时间:长达21天
剂量限制毒性(DLT)以建立MTD和/或RP2D。
长达21天
实验室参数有显着变化的受试者数量
大体时间:最多3年
研究人员报告的临床意义异常实验室参数发现。
最多3年
Numbers of subjects with adverse events
大体时间: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
大体时间: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
大体时间: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 reduction
大体时间:Up to 3 years
AEs leading to dose reduction reported by the investigator
Up to 3 years
Number of AEs leading to permanent discontinuation
大体时间:Up to 3 years
AEs leading to permanent discontinuation reported by the investigator
Up to 3 years
Objective response rate (ORR) in dose expansion
大体时间:Up to 3 years
Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria.
Up to 3 years

次要结果测量

结果测量
措施说明
大体时间
Area under the curve (AUC)
大体时间:Up to 3 years
Area under the curve (AUC) of single and multiple doses of IBI3028
Up to 3 years
Maximum concentration (Cmax)
大体时间:Up to 3 years
Maximum concentration (Cmax) of single and multiple doses of IBI3028
Up to 3 years
Time to maximum concentration (Tmax)
大体时间:Up to 3 years
Time to maximum concentration (Tmax) of single and multiple doses of IBI3028
Up to 3 years
Clearance (CL)
大体时间:Up to 3 years
Clearance (CL) of single and multiple doses of IBI3028
Up to 3 years
Apparent volume of distribution (V)
大体时间:Up to 3 years
apparent volume of distribution (V) of single and multiple doses of IBI3028
Up to 3 years
Half-life (t1/2)
大体时间:Up to 3 years
Half-life (t1/2) of IBI3020 to the last administration of IBI3028
Up to 3 years
Anti-drug antibody (ADA)
大体时间:Up to 3 years
Incidence and characterization of anti-drug antibody (ADA)
Up to 3 years
Neutralizing antibody (NAb)
大体时间:Up to 3 years
Incidence and characterization of neutralizing antibody (NAb)
Up to 3 years
Objective response rate (ORR)
大体时间:Up to 3 years
Objective response rate (ORR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Duration of response (DoR)
大体时间:Up to 3 years
Duration of response (DoR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Disease control rate (DCR)
大体时间:Up to 3 years
Disease control rate (DCR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Time to response (TTR)
大体时间:Up to 3 years
Time to response (TTR) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Progression-free survival (PFS)
大体时间:Up to 3 years
progression-free survival (PFS) as evaluated per the RECIST v1.1 criteria
Up to 3 years
Overall survival (OS)
大体时间: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

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2026年3月31日

初级完成 (估计的)

2027年6月30日

研究完成 (估计的)

2028年6月30日

研究注册日期

首次提交

2026年4月27日

首先提交符合 QC 标准的

2026年5月11日

首次发布 (实际的)

2026年5月15日

研究记录更新

最后更新发布 (实际的)

2026年7月23日

上次提交的符合 QC 标准的更新

2026年7月21日

最后验证

2026年7月1日

更多信息

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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